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M+ + X-2(-) reaction system involves two potential energy surfaces, i.e., the covalence state(M+X-2) and the ionic state(M++X-2(-)) and their crossing effect, The working equations for calculating state-to-state probability have been derived based on the above two-state model, The selected-state reaction probabilities of collinear ion-pair formation process M+I-2 --> M+ +I-2(-) (M = Na, K, Cs) on Aten-Lanting-Los two-state potential energy surface have been calculated. The results show that the reaction probabilities are of resonance effect. [author_in] => [Ma, W.-Y] Institute of Theoretical Chemistry, Shandong University, Jinan, 250100, China, Department of Chemical Engineering, Shandong Institute of Light Industry, Jinan, 250100, China@@@[ Cai, Z.-T] Institute of Theoretical Chemistry, Shandong University, Jinan, 250100, China@@@[ Feng, D.-C] Institute of Theoretical Chemistry, Shandong University, Jinan, 250100, China@@@[ Deng, C.-H] Institute of Theoretical Chemistry, Shandong University, Jinan, 250100, China [pub_date] => MAY [format_title_en_publication_en_pub_year] => 01150d99dcf7cc7e89eb21937e27aa54-831692535 [from_id] => 76,74,73,80,78,85 [issue] => 5 [hx_id] => 2376,2378,2371 [classification_pub] => KTHPD [datebase] => Scopus [sys_level_num] => 1_4 [sys_jg_type] => 0,5 [format_issn_issue_page_pub_year] => dc1b6525eed0b9e672cd8ed3072b19f74238320 [title_en] => The quantum scattering study for ion-pair formation reaction with LCAC-SW method [volume] => 20 [author_fn] => Ma, WY; Cai, ZT; Feng, DC; Deng, CH [pub_year] => 1999 [article_id] => 213702,583486,3363,400978,497596,334140 [hints] => 37 [publisher] => HIGHER EDUCATION PRESS [language] => Chinese [source_type] => 351 [reference_No] => 6 [batch] => 3250,3241,3254,3246,3243,3252 [publication_en] => CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE [school_id] => 117 [sys_update_time] => 2018-09-05 15:28:36 [format_title_en_issn_pub_year] => 2e0aba09b12d8be864572c7482b7b742280124234 [format_ei_No] => 2b51d7438b637f14acc15d630ed12ea41321052191 [SYS_TAG] => 3 [page] => 138-140 [hb_type] => 2 [article_dt] => Letter [cite_wos] => 2 [check_3Y] => 0 [delivery_No] => 198MU [format_title] => 138d019b6bc006c5016ad404c9a3b481-798020738 [cauthor_ad] => [Ma, WY]Shandong Univ, Inst Theoret Chem, Jinan 250100, Peoples R China. [pages] => 3 [publication_29] => CHEM J CHINESE U [end_page] => 799 [publication_type] => J [begin_page] => 797 [get_data] => 2018-08-29 [keyword_en] => ion-pair formation; reaction probabilities; LCAC-SW method [format_publication_cn] => 112be9cb2f30361719ed2bc572ba4a22192440272 [publication_iso] => Chem. J. Chin. Univ.-Chin. [format_title_en] => 38f6d8c2b26a00e6f3b3e221e22baccb-1404889632 [publisher_city] => BEIJING [cite_awos] => 2 [wos_No] => WOS:000080428600031 [sys_priority_field] => 76 [wos_sub] => Chemistry, Multidisciplinary [research_area] => Chemistry [check_180] => 0 [publisher_ad] => SHATANHOU ST 55, BEIJING 100009, PEOPLES R CHINA [format_publication_en] => 4eabdd9afe3fe566a165b6e1c3e0dbbd-130083487 [jl_language] => chinese [jl_article_dt] => letter [jl_publication_en] => chemicaljournalofchineseuniversitieschinese [jl_country] => 中国 [jl_keyword_en] => reactionprobabilities,lcacswmethod,ionpairformation [jl_publisher] => highereducationpress [author_jg] => [马万勇,蔡政亭,冯大成,邓从豪]山东大学理论化学研究所,山东轻工业学院化工系 [keyword_cn] => 离子对生成;反应几率;LCAC-SW方法 [clc] => O643 [title_cn] => 离子对生成反应的LCAC-SW量子散射理论研究 [publication_cn] => 高等学校化学学报 [CSSN] => 22-1131/O6 [abstract_cn] => 离子对生成反应微观动力学的理论和实验研究有助于从本质上揭示气相、液相及上层空间大气化学反应机理.实验上已经发展到用激光-交叉分子束技术研究其态-态过程;理论上则主要是采用准经典轨迹法.由于这类反应是电子非绝热过程,涉及到共价态和离子态两个势能面及其耦... [author_cn] => 马万勇,蔡政亭,冯大成,邓从豪 [uri] => https://www.scopus.com/inward/record.uri?eid=2-s2.0-0345880689&partnerID=40&md5=01f341cefcc5e038e11305ccb0b90775 [jl_publication_cn] => 高等学校化学学报 [jl_keyword_cn] => 离子对生成,反应几率,lcacsw方法 [jl_clc] => o643 [company_id] => 0,0,0,0,0,0,0,0 [author_id] => [author_test] => Array ( ) [sys_author_id_arr] => [jl_publication_cn_publication_en] => chemicaljournalofchineseuniversitieschinese,高等学校化学学报 [jl_keyword_cn_keyword_en] => 离子对生成,反应几率,ionpairformation,lcacswmethod,lcacsw方法,reactionprobabilities [format_scopus_No] => 93d9b5bf09ce2cc5d06e2e952c4e33a2704217273 [format_wos_No] => 3c598c78e5a06731e00e41b30636c14a-1348391272 [standard_in] => Institute of Theoretical Chemistry, Shandong University, Jinan, 250100, China; Department of Chemical Engineering, Shandong Institute of Light Industry, Jinan, 250100, China [scopus_No] => 2-s2.0-0345880689 [format_title_cn_publication_cn_pub_year] => 74a93d03bed4819950721b59eff0b01893759334 [format_title_cn_issn_pub_year] => a72e6c26481cf94b5a1c0f3d26dff73a-1397311027 [sys_author_jg_last_arr] => 山东轻工业学院化工系 [sys_author_in_last_arr] => china [sys_author_id] => [id] => lQd5vWUBFjIhTVEbiEgl [tags] => 0 ) [7] => Array ( [issn] => 0251-0790 [delivery_No] => 102LD [batch2] => 1,2 [hb_batch] => 3241 [tag] => 0 [author_en] => Shao, W; Wang, JS; Wang, CX; Mi, GT; Wang, DQ [abstract_en] => The aim of this study was to improve the solubility of quercetin in aqueous solution. The inclusion compound of quercetin with P-cyclodextrin was obtained by saturated aqueous solution method. The formation of the inclusion compound was confirmed by IR spectroscopy and differential scanning calorimetry. The content of quercetin inclusion was determined by UV. The results indicated that the inclusion compound of quercetin with beta-cyclodextrin was formed. The dissolubility of quercetin in inclusion form increased from 2.78 mu g/mL to 23. 15 mu g/mL. The experimental data of inclusion compound fitted well to the molar ratio of 1 : 1. Through the thermodynamic study we got the constants and Delta(r)H(m)(o), Delta(r)S(m)(o), Delta(r)G(m)(o) of the inclusion at different temperatures. [publication_type] => J [author_in] => [Shao, W; Wang, JS; Wang, CX; Mi, GT; Wang, DQ]Shandong Med Univ, Fac Pharm, Jinan 250012, Peoples R China.@@@[Shao, W; Wang, JS; Wang, CX; Mi, GT; Wang, DQ] Shandong Teachers Univ, Jinan 250012, Peoples R China. [publisher_city] => BEIJING [cauthor_back] => Shao, W [get_data] => 2018-08-29 [format_title_en_publication_en_pub_year] => 196315db8b5bbf63286fe599abc857e4539869261 [pages] => 3 [cite_wos] => 3 [check_3Y] => 3 [cite_awos] => 3 [from_id] => 80,73 [cauthor_ad] => [Shao, W]Shandong Med Univ, Fac Pharm, Jinan 250012, Peoples R China. [school_id] => 117 [cauthor_order] => 1 [research_area] => Chemistry [sys_level_num] => 1_7 [publisher] => HIGHER EDUCATION PRESS [sys_jg_type] => 0,5 [format_issn_issue_page_pub_year] => 981b1a74abeff65829b3be224c422973-1278274045 [title_en] => Studies on inclusion compound of quercetin with beta-cyclodextrin [publication_29] => CHEM J CHINESE U [author_fn] => Shao, W; Wang, JS; Wang, CX; Mi, GT; Wang, DQ [pub_year] => 1998 [publisher_ad] => SHATANHOU ST 55, BEIJING 100009, PEOPLES R CHINA [check_180] => 1 [keyword_en] => quercetin; beta-cyclodextrin; inclusion compound; thermodynamics [end_page] => 1103 [pub_date] => JUL [begin_page] => 1101 [format_wos_No] => 9d28f05c34162aac05f14f9fb11440d1943566064 [hints] => 1 [volume] => 19 [language] => Chinese [source_type] => 351 [issue] => 7 [reference_No] => 4 [batch] => 3241,3252 [publication_en] => CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE [hx_id] => 2371 [sys_update_time] => 2018-09-05 15:29:30 [format_title_en_issn_pub_year] => b513324bf9556294d7ad9577c843487f448841499 [publication_iso] => Chem. J. Chin. Univ.-Chin. [article_id] => 334406,202875 [wos_sub] => Chemistry, Multidisciplinary [SYS_TAG] => 3 [wos_No] => WOS:000074925100022 [page] => 1101-1103 [hb_type] => 2 [article_dt] => Article [jl_language] => chinese [jl_article_dt] => 期刊论文 [jl_publication_en] => chemicaljournalofchineseuniversitieschinese [jl_country] => 中国,中国 [jl_keyword_en] => quercetin,inclusioncompound,betacyclodextrin,thermodynamics [jl_publisher] => highereducationpress [author_jg] => 山东医科大学药学系,济南,250012;山东师范大学,济南,250014 [keyword_cn] => 槲皮素;β-环糊精;包合物;热力学 [format_title] => 7b58cdb060449b2b18ab080b1aef620d49803885 [cite_wanfang] => 25 [clc] => O642.3 [title_cn] => 槲皮素-β-环糊精包合物的研究 [format_publication_cn] => 112be9cb2f30361719ed2bc572ba4a22192440272 [publication_cn] => 高等学校化学学报 [format_title_en] => 701f2820b60281f2c16ca6fc5118cd72637478474 [CSSN] => 22-1131/O6 [abstract_cn] => 槲皮素具有抗氧化、抗自由基、抗癌防癌、抗菌和抗过敏等作用[1],对由腺苷二磷酸、胶原或凝血酶引起的血小板聚集及血栓有抑制作用.但由于槲皮素几乎不溶于水、稳定性差等影响了其临床应用. [sys_priority_field] => 73 [author_cn] => 邵伟;王金山;王春香;米广太;王大庆 [format_publication_en] => 4eabdd9afe3fe566a165b6e1c3e0dbbd-130083487 [jl_publication_cn] => 高等学校化学学报 [jl_keyword_cn] => 槲皮素,β环糊精,热力学,包合物 [jl_clc] => o6423 [company_id] => 0,0,0,0,0,0,0,0,0,0,0,0 [author_id] => [author_test] => Array ( ) [sys_author_id_arr] => [jl_publication_cn_publication_en] => chemicaljournalofchineseuniversitieschinese,高等学校化学学报 [jl_keyword_cn_keyword_en] => inclusioncompound,thermodynamics,quercetin,槲皮素,betacyclodextrin,热力学,β环糊精,包合物 [sys_author_id] => [format_title_cn_publication_cn_pub_year] => 704ad344a98956c3a9671cec0b3400f8-700987043 [format_title_cn_issn_pub_year] => bc2f110cd9091f50e72b31301871f1cf1017692619 [id] => VQifvWUBFjIhTVEbUuIV [tags] => 0 ) [8] => Array ( [issn] => 0251-0790 [delivery_No] => 106YP [batch2] => 1,2,6 [hb_batch] => 3241 [tag] => 0 [author_en] => Fu, AP; Feng, DC; Deng, CH [abstract_en] => Ab initio molecular orbital method is used to theoretically investigate the interaction of water with the bridge site of graphite surface (0001). The adsorption energies in different directions are calculated at 6-31G* basis set level using C6H8 cluster. The results indicate that the interaction between water and graphite is weak and they belong to the physicosorption system. On the surface with no charge or with negative charges, when the atom H of the water is near the surface, there is a minimum point on the potential energy surface; while on the surface with the positive charges, when the atom O is near the surface, there exists a stable adsorption point. Whether the surface carries negative charges or positive charges, the interaction between the water and the graphite surface is strengthened. [publication_type] => J [keyword_plu] => CHEMISORPTION; HYDROGEN; ALUMINUM; CLUSTER; MODEL [author_in] => [Fu, A.-P] Institute of Theoretical Chemistry, Shandong University, Jinan 250100, China@@@[ Feng, D.-C] Institute of Theoretical Chemistry, Shandong University, Jinan 250100, China@@@[ Deng, C.-H] Institute of Theoretical Chemistry, Shandong University, Jinan 250100, China [publisher_city] => BEIJING [cauthor_back] => Feng, DC [get_data] => 2018-08-29 [format_title_en_publication_en_pub_year] => 45b23f5f2e1fd22bb282e973dfb40da71109907777 [begin_page] => 792 [cite_wos] => 2 [check_3Y] => 0 [cite_awos] => 2 [from_id] => 76,80,73 [cauthor_ad] => [Feng, DC]Shandong Univ, Inst Theoret Chem, Jinan 250100, Peoples R China. [school_id] => 117 [cauthor_order] => 2 [research_area] => Chemistry [sys_level_num] => 1_7 [publisher] => HIGHER EDUCATION PRESS [sys_jg_type] => 0,5 [format_issn_issue_page_pub_year] => a0a6a02f01b577d6f6d0cf5469e523c51763300579 [title_en] => The quantum chemical study of molecular water adsorption on the bridge site of graphite surface (0001) [publication_29] => CHEM J CHINESE U [author_fn] => Fu, AP; Feng, DC; Deng, CH [pub_year] => 1998 [publisher_ad] => SHATANHOU ST 55, BEIJING 100009, PEOPLES R CHINA [check_180] => 0 [keyword_en] => ab initio method; graphite surface (0001); water; adsorption [end_page] => 795 [pub_date] => MAY [pages] => 4 [format_wos_No] => ee5fd285d5ee527afabea27fa248547d1505423520 [hints] => 2 [volume] => 19 [language] => Chinese [source_type] => 351 [issue] => 5 [reference_No] => 10 [batch] => 3243,3241,3252 [publication_en] => CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE [hx_id] => 2378,2371 [sys_update_time] => 2018-09-05 15:29:31 [format_title_en_issn_pub_year] => 64191aff4cd87c9f00730ea278690525-215459765 [publication_iso] => Chem. J. Chin. Univ.-Chin. [article_id] => 334457,497919,197335,214921 [wos_sub] => Chemistry, Multidisciplinary [SYS_TAG] => 3 [wos_No] => WOS:000075179300030 [page] => 792-795 [hb_type] => 2 [article_dt] => Article [jl_language] => chinese [jl_article_dt] => 期刊论文 [jl_publication_en] => chemicaljournalofchineseuniversitieschinese [jl_country] => 中国 [jl_keyword_en] => water,abinitiomethod,adsorption,graphitesurface0001 [jl_publisher] => highereducationpress [author_jg] => 山东大学理论化学研究室,济南,250100 [keyword_cn] => 从头计算;石墨(0001)表面;水;吸附 [format_title] => 0210f76c274de8e2ff646d3e6048aa76905627192 [cite_wanfang] => 9 [clc] => O647.3 [title_cn] => 水在石墨(0001)面簇模型桥位上吸附的量子化学研究 [format_publication_cn] => 112be9cb2f30361719ed2bc572ba4a22192440272 [publication_cn] => 高等学校化学学报 [format_title_en] => c7cfc21528461547ccc362b193cf3fdf1432072879 [CSSN] => 22-1131/O6 [abstract_cn] => 用从头计算方法对水在石墨(0001)面桥位上的吸附进行了研究.用C6H8原子簇模拟石墨表面,在6-31G*水平上计算了水在不同方向和位置上的吸附能量.研究表明:水在石墨面上的吸附很弱,属于物理吸附;在中性或带负电荷的石墨表面,当水分子中的氢原子靠近石墨面时,体系存在能量最小值,而在带正电荷的表面,当氧原子靠近石墨面时存在稳定的吸附点;不论表面带正电荷还是带负电荷,均对水分子的吸附起增强作用. [sys_priority_field] => 76 [author_cn] => 傅爱萍;冯大诚;邓从豪 [format_publication_en] => 4eabdd9afe3fe566a165b6e1c3e0dbbd-130083487 [jl_publication_cn] => 高等学校化学学报 [jl_keyword_cn] => 吸附,水,从头计算,石墨0001表面 [jl_clc] => o6473 [company_id] => [author_id] => [author_test] => Array ( ) [sys_author_id_arr] => [jl_publication_cn_publication_en] => chemicaljournalofchineseuniversitieschinese,高等学校化学学报 [jl_keyword_cn_keyword_en] => 从头计算,吸附,adsorption,water,石墨0001表面,水,graphitesurface0001,abinitiomethod [datebase] => Scopus [format_scopus_No] => cf159e8c144a4f6d857d2d1d453ab504426725960 [cite_scopus] => 4 [classification_pub] => KTHPD [uri] => https://www.scopus.com/inward/record.uri?eid=2-s2.0-0005249086&partnerID=40&md5=21a9f7fac81f23356fca0d209bc9aa83 [standard_in] => Institute of Theoretical Chemistry, Shandong University, Jinan 250100, China [scopus_No] => 2-s2.0-0005249086 [format_title_cn_publication_cn_pub_year] => d25096bc9acde4229a67ebdf3a8a7411-1704965903 [format_title_cn_issn_pub_year] => a29f11a7a3df163fd69ed680263d1e05-1083313438 [sys_author_jg_last_arr] => 250100 [sys_author_in_last_arr] => china [sys_author_id] => [id] => iAifvWUBFjIhTVEbUuIV [tags] => 0 ) [9] => Array ( [batch2] => 1,2 [batch] => 3241,3254,3252 [tag] => 0 [abstract_cn] => 测定了无机盐,单元及多元醇,有机酸及离子型表面活性剂对3种非离子表面活性剂十二烷基聚氧乙烯聚氧丙烯醚C12H25(EO)m(PO)nH(LS36,m=3,n=6;LS45,m=4,n=5,LS54,m=5,n=4)浊点的影响。 [keyword_cn] => 浊点;添加剂;LS;表面活性剂;非离子型; [clc] => O647.2 [author_jg] => [李英;李干佐]山东大学胶体和界面化学开放实验室,中国 [format_title_cn_publication_cn_pub_year] => 48466d5c1baf94368d0f5c5ee1e2b555909586000 [from_id] => 80,73,85 [issue] => 9 [sys_level_num] => 2_1 [sys_jg_type] => 5 [source_type] => 351 [pub_year] => 1998 [article_id] => 113153,197337,334551 [pages] => 5 [hints] => 4 [author_cn] => 李英;李干佐 [issn] => 0251-0790 [uri] => http://lib.cqvip.com/qk/90335X/199809/3326576.html [publication_cn] => 高等学校化学学报 [title_cn] => 添加剂对非离子十二烷基聚氧乙烯聚氧丙烯醚浊点的影响 [CSSN] => 22-1131/06 [SYS_TAG] => 3 [format_title_cn_issn_pub_year] => 8f7c87d612c48fe1ddd56481021e547d-191570387 [hb_type] => 2 [jl_publication_cn] => 高等学校化学学报 [jl_country] => 中国 [jl_keyword_cn] => ,添加剂,非离子型,ls,表面活性剂,浊点 [jl_clc] => o6472 [author_in] => [Li, Y; Li, GZ; Mu, JH; Xu, HK]Shandong Univ, Inst Colloid & Interface Chem, Jinan 250100, Peoples R China. [company_id] => 0,0,0,0,0 [author_id] => 21993,21994 [author_test] => Array ( [0] => Array ( [sure] => 0 [irmagnum] => 0 [u_index] => 1 [name] => 李英 [irtag] => 7 [t_index] => 0 [person_id] => 21993 ) [1] => Array ( [sure] => 0 [irmagnum] => 0 [u_index] => 1 [name] => 李英 [irtag] => 7 [t_index] => 0 [person_id] => 21994 ) ) [sys_author_id_arr] => [jl_publication_cn_publication_en] => 高等学校化学学报 [sys_author_id] => [hb_batch] => grant_no [publication_en] => CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE [cite_wos] => 6 [check_3Y] => 2 [language] => Chinese [delivery_No] => 121AP [format_title] => e4436f691f9e58a7f2c206618478b1e51045084056 [cauthor_ad] => [Li, Y]Shandong Univ, Inst Colloid & Interface Chem, Jinan 250100, Peoples R China. [author_fn] => Li, Y; Li, GZ; Mu, JH; Xu, HK [cite_wanfang] => 32 [format_title_en_issn_pub_year] => de71c8aed75ca993969980b81b2a27311308607296 [publication_29] => CHEM J CHINESE U [end_page] => 1461 [abstract_en] => The effects of additives, such as salts, alcohol, carboxylic acid and ionic surfactant on the cloud ponit of nonionic surfactant dodecylpolyoxyethylene polyoxypropylene ether were studied in the paper, It was found that the change of CP value coursed by salts followed the Schott additivity regulation and was determined by the characteristic of salts(such as charge of ions) and surfactants(such as group numbers of oxyethylene and oxypropylene); the effects of organic substances on the CP value of nonionic surfactant varied if the additives have a different kind of hydrophilic head or carbon chain length; the formation of mixmicell could be the reason why ionic surfactants greatly increased the CP value of nonionic surfactant, but more detail studies were needed to find the regulation. [publication_type] => J [begin_page] => 1457 [article_dt] => Article [author_en] => Li, Y; Li, GZ; Mu, JH; Xu, HK [volume] => 19 [get_data] => 2018-08-29 [publisher] => HIGHER EDUCATION PRESS [keyword_en] => dodecylpolyoxyethylene polyoxypropylene ether; cloud point; additives [page] => 1457-1461 [format_publication_cn] => 112be9cb2f30361719ed2bc572ba4a22192440272 [publication_iso] => Chem. J. Chin. Univ.-Chin. [format_title_en_publication_en_pub_year] => 45aa8f4eaf2ca9a8d64241b199cc7284-714211616 [format_title_en] => 8163ca574d4ac0862f70206a404b1dad1663995030 [publisher_city] => BEIJING [pub_date] => SEP [cauthor_order] => 1 [hx_id] => 2371 [reference_No] => 9 [format_issn_issue_page_pub_year] => 80f72dc9b7c1b90c4699c00d028556631408015333 [cite_awos] => 6 [wos_No] => WOS:000075990200025 [format_wos_No] => 889e6d802c2bfa524e6ec9ce307bd519-1067642062 [wos_sub] => Chemistry, Multidisciplinary [research_area] => Chemistry [cauthor_back] => Li, Y [check_180] => 0 [publisher_ad] => SHATANHOU ST 55, BEIJING 100009, PEOPLES R CHINA [title_en] => Effect of additives on cloud point of dodecylpolyoxyethylene polyoxypropylene ether nonionic surfactant [format_publication_en] => 4eabdd9afe3fe566a165b6e1c3e0dbbd-130083487 [jl_article_dt] => 期刊论文 [id] => SQkvvmUBFjIhTVEbC0eT [tags] => 0 ) [10] => Array ( [issn] => 0251-0790 [delivery_No] => ZH999 [batch2] => 1,2,6 [hb_batch] => 3241 [tag] => 0 [author_en] => Wang, YX; Deng, CH [abstract_en] => The Geometries of the two lacking electron fragments HPXF (X=Li, Na) have been investigated by using ab initio method at RHF/6-31G* level, and characteristics of all the geometries have also been analysed in terms of bonding concepts, By comparing with free phosphinidene ((HP)-H-1), reaction activities of HPXF(X=Li, Na) were discussed. Moreover, the effect of alkali metal atoms on the geometries and activities of HPXF(X=Li, Na) have been briefly discussed, The results indicate that both HPLiF and HPNaF have three types of equilibrium geometries among them, the three-membered ring geometry is the most stable one, and it may be the basic geometry taking part in chemical reactions. It is expected that HPXF(X = Li, Na) is a superior electrophilic intermediate to free phosphinidene in selectivity and control ability. [publication_type] => J [keyword_plu] => TERMINAL PHOSPHINIDENE COMPLEXES; PHOSPHIRENE [author_in] => [Lu, X.-H] Chemistry Department, Jinan University, Jinan 250002, China@@@[ Wang, Y.-X] Institute of Chemistry, Shandong University, Jinan 250100, China@@@[ Deng, C.-H] Institute of Chemistry, Shandong University, Jinan 250100, China [publisher_city] => BEIJING [cauthor_back] => Wang, YX [get_data] => 2018-08-29 [format_title_en_publication_en_pub_year] => 1fdcb270905b9f8d38c089d0b7ab6bb2282142944 [begin_page] => 617 [cite_wos] => 0 [check_3Y] => 0 [cite_awos] => 0 [from_id] => 76,80,73 [cauthor_ad] => [Wang, YX]Jinan Univ, Dept Chem, Jinan 250002, Peoples R China. [school_id] => 117 [cauthor_order] => 1 [research_area] => Chemistry [sys_level_num] => 1_7 [publisher] => HIGHER EDUCATION PRESS [sys_jg_type] => 0,5 [format_issn_issue_page_pub_year] => f7bfab709f2c4bcf7135733c7e2a55b7-1923247658 [title_en] => Ab initio study on the geometries and reaction activities of HPXF (X=Li, Na) [publication_29] => CHEM J CHINESE U [author_fn] => Wang, YX; Deng, CH [pub_year] => 1998 [publisher_ad] => SHATANHOU ST 55, BEIJING 100009, PEOPLES R CHINA [check_180] => 0 [keyword_en] => phosphinidene; reaction activity; ab initio [end_page] => 621 [pub_date] => APR [pages] => 5 [format_wos_No] => 87a0929c0688adef6644c34159888988-1604779448 [hints] => 3 [volume] => 19 [language] => Chinese [source_type] => 351 [issue] => 4 [reference_No] => 12 [batch] => 3243,3241,3252 [publication_en] => CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE [hx_id] => 2378,2371 [sys_update_time] => 2018-09-05 15:29:31 [format_title_en_issn_pub_year] => 9caecce15797183037e060806c1bb5d91326366239 [publication_iso] => Chem. J. Chin. Univ.-Chin. [article_id] => 498083,202722,334529 [wos_sub] => Chemistry, Multidisciplinary [SYS_TAG] => 3 [wos_No] => WOS:000073169500032 [page] => 617-621 [hb_type] => 2 [article_dt] => Article [jl_language] => chinese [jl_article_dt] => 期刊论文 [jl_publication_en] => chemicaljournalofchineseuniversitieschinese [jl_country] => 中国 [jl_keyword_en] => abinitio,phosphinidene,reactionactivity [jl_publisher] => highereducationpress [author_jg] => 济南大学化学系,济南,250002;山东大学化学院,济南,250100 [keyword_cn] => 磷烯;反应活性;从头算 [format_title] => 0f2920883c77ab58639295d27367feb2370784412 [cite_wanfang] => 1 [clc] => O641 [title_cn] => HPXF(X=Li,Na)的构型及反应性能的从头算研究 [format_publication_cn] => 112be9cb2f30361719ed2bc572ba4a22192440272 [publication_cn] => 高等学校化学学报 [format_title_en] => a962ec11e7e902d63eaad832cb3d65b7-1958695364 [CSSN] => 22-1131/O6 [abstract_cn] => 用RHF/6-31G*从头算解析梯度法优化了类磷烯HPXF(X=Li,Na)的平衡构型,分析了各构型的结构特点及稳定性.通过与磷烯(1HP)相比较,探讨了HPXF(X=Li,Na)的反应活性,还简单讨论了碱金属原子对HPXF(X=Li,Na)三元环构型稳定性和反应活性的影响.结果表明,HPLiF和HPNaF均具有3种平衡构型,其中三元环构型最稳定,也是参加反应的基本构型:类磷烯与相应的1HP相比,可成为一种使反应容易控制、选择性好和易获得的亲电反应中间体. [sys_priority_field] => 76 [author_cn] => 卢秀慧;王沂轩;邓从豪 [format_publication_en] => 4eabdd9afe3fe566a165b6e1c3e0dbbd-130083487 [jl_publication_cn] => 高等学校化学学报 [jl_keyword_cn] => 磷烯,从头算,反应活性 [jl_clc] => o641 [company_id] => [author_id] => 24397,24325 [author_test] => Array ( [0] => Array ( [sure] => 0 [irmagnum] => 0 [u_index] => 1 [name] => 王月霞 [irtag] => 7 [t_index] => 1 [person_id] => 24397 ) [1] => Array ( [sure] => 0 [irmagnum] => 0 [u_index] => 1 [name] => 王延相 [irtag] => 7 [t_index] => 1 [person_id] => 24325 ) ) [sys_author_id_arr] => [jl_publication_cn_publication_en] => chemicaljournalofchineseuniversitieschinese,高等学校化学学报 [jl_keyword_cn_keyword_en] => phosphinidene,反应活性,reactionactivity,磷烯,从头算,abinitio [datebase] => Scopus [format_scopus_No] => fc2b3eda997a02e94ab34b13c5c95e08-150587792 [classification_pub] => KTHPD [uri] => https://www.scopus.com/inward/record.uri?eid=2-s2.0-2842568406&partnerID=40&md5=f4bf10ac791de5d6de1f16abedb7c034 [standard_in] => Chemistry Department, Jinan University, Jinan 250002, China; Institute of Chemistry, Shandong University, Jinan 250100, China [scopus_No] => 2-s2.0-2842568406 [format_title_cn_publication_cn_pub_year] => a79197235d8a7f6c20233888014ae9a7541935328 [format_title_cn_issn_pub_year] => d81da3f5059fa448fd61947346a329fe257952868 [jl_author_test] => unameuu738bu6708u971e,uirtstag0,uuindex1,usureu0,utindex1,upersonid24325,uirtag7,uirtypical1,uirinspecttag0,unameuu738bu5ef6u76f8,uirauthortype3,upersonid24397 [sys_author_jg_last_arr] => 250100 [sys_author_in_last_arr] => china [sys_author_id] => [id] => 0AifvWUBFjIhTVEbUuIW [tags] => 0 ) [11] => Array ( [issn] => 0251-0790 [delivery_No] => 102LD [batch2] => 1,2,6 [hb_batch] => 3241 [tag] => 0 [author_en] => Li, F; Li, GZ; Wang, HQ; An, YL [abstract_en] => Steady fluorescence and dynamic light-scattering measurement were reported for dodecyldimethylammoniopropanesulfonate (DDAPS)/NaCl aqueous micellar system. The results show that the aggregation number and the hydrodynamic radius of DDAPS micelles increase slightly with the increasing of NaCl concentration and decrease slightly as the temperature rises. For the zwitterionic surfactant system we infer repulsive intermicellar interactions in spite of the absence of net charges. DDAPS behaves somewhat like an ionic surfactant, Within the scope of our investigation, DDAPS micelles exist in spherical shape. Keywords Dodecylimethylammoniopropanesulfonate, Aggregation number , Hydrodynamic radius, Fluorescence, Light-scattering. [publication_type] => J [keyword_plu] => INTERMICELLAR INTERACTIONS; SURFACTANT SOLUTIONS; PROBE [author_in] => [Li, F] Inst. of Colloid/Interface Chemistry, Shandong University, Jinan 250100, China@@@[ Li, G.-Z] Inst. of Colloid/Interface Chemistry, Shandong University, Jinan 250100, China@@@[ Wang, H.-Q] Institute of Chemical Physics, Academia Sinica, Lanzhou 730000, China@@@[ An, Y.-L] Department of Polymer, Nankai University, Tianjin 300071, China [publisher_city] => BEIJING [cauthor_back] => Li, F [get_data] => 2018-08-29 [format_title_en_publication_en_pub_year] => 8a9547e7a946bb2691933a91f289010e1377656784 [begin_page] => 1117 [cite_wos] => 6 [check_3Y] => 2 [cite_awos] => 7 [from_id] => 76,80,73 [cauthor_ad] => [Li, F]Shandong Univ, Inst Colloid & Interface Chem, Jinan 250100, Peoples R China. [school_id] => 117 [cauthor_order] => 1 [research_area] => Chemistry [sys_level_num] => 1_7 [publisher] => HIGHER EDUCATION PRESS [sys_jg_type] => 0,5 [format_issn_issue_page_pub_year] => d766ef20e196db4116507be1e5e2f480629137260 [title_en] => Studies on the aggregation and interaction of DDAPS micelles with fluorescence and light-scattering methods [publication_29] => CHEM J CHINESE U [author_fn] => Li, F; Li, GZ; Wang, HQ; An, YL [pub_year] => 1998 [publisher_ad] => SHATANHOU ST 55, BEIJING 100009, PEOPLES R CHINA [check_180] => 1 [keyword_en] => dodecyldimethylammoniopropanesulfonate; aggregation number; hydrodynamic; radius; fluorescence; light-scattering [end_page] => 1120 [pub_date] => JUL [pages] => 4 [format_wos_No] => fcf84edf3af8b563a8e6b929bd5cfbc41062234345 [hints] => 4 [volume] => 19 [language] => Chinese [source_type] => 351 [issue] => 7 [reference_No] => 17 [batch] => 3243,3241,3252 [publication_en] => CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE [hx_id] => 2378,2371 [sys_update_time] => 2018-09-05 15:29:30 [format_title_en_issn_pub_year] => 879823e5c758ba6ffd70ececeef97a841096476564 [publication_iso] => Chem. J. Chin. Univ.-Chin. [article_id] => 214920,334407,202877,498019 [wos_sub] => Chemistry, Multidisciplinary [SYS_TAG] => 3 [wos_No] => WOS:000074925100026 [page] => 1117-1120 [hb_type] => 2 [article_dt] => Article [jl_language] => chinese [jl_article_dt] => 期刊论文 [jl_publication_en] => chemicaljournalofchineseuniversitieschinese [jl_country] => 中国 [jl_keyword_en] => fluorescence,radius,hydrodynamic,aggregationnumber,dodecyldimethylammoniopropanesulfonate,lightscattering [jl_publisher] => highereducationpress [author_jg] => 山东大学胶体与界面化学开放实验室,济南,250100;中国科学院兰州化学物理研究所,兰州,730000;南开大学吸附与分离功能高分子材料国家重点实验室,天津,300071 [keyword_cn] => N-十二烷基-N,N-二甲基氨基丙磺酸盐;聚集数;水力半径;荧光;光散射 [format_title] => a29be97d9032cde6701ede91c66b524e1739611507 [cite_wanfang] => 28 [clc] => O648 [title_cn] => 荧光和动态光散射方法研究两性表面活性剂胶束的聚集和相互作用 [format_publication_cn] => 112be9cb2f30361719ed2bc572ba4a22192440272 [publication_cn] => 高等学校化学学报 [format_title_en] => 857aa67c830514579779975c0a3a93f8-1222712837 [CSSN] => 22-1131/O6 [abstract_cn] => 以芘为荧光探针、二苯酮为猝灭剂,利用荧光方法测定了两性表面活性剂N-十二烷基-N,N-二甲基氨基丙磺酸盐(DDAPS)胶束在不同温度和不同NaCl浓度下的聚集数.利用动态光散射方法得到了胶束的水力半径Rh.结果表明,DDAPs的胶束聚集数和Rh值随NaCl浓度的升高略有增大;随温度的升高而稍有下降.DDAPS胶束之间的作用力以排斥力为主. [sys_priority_field] => 76 [author_cn] => 李方;李干佐;汪汉卿;安英丽 [format_publication_en] => 4eabdd9afe3fe566a165b6e1c3e0dbbd-130083487 [jl_publication_cn] => 高等学校化学学报 [jl_keyword_cn] => n十二烷基n,n二甲基氨基丙磺酸盐,荧光,聚集数,水力半径,光散射 [jl_clc] => o648 [company_id] => [author_id] => 21642,23902,21587,21645 [author_test] => Array ( [0] => Array ( [sure] => 0 [irmagnum] => 0 [u_index] => 1 [name] => 李飞 [irtag] => 7 [t_index] => 1 [person_id] => 21642 ) [1] => Array ( [sure] => 0 [irmagnum] => 0 [u_index] => 1 [name] => 黎峰 [irtag] => 7 [t_index] => 1 [person_id] => 21587 ) [2] => Array ( [sure] => 0 [irmagnum] => 0 [u_index] => 3 [name] => 王海庆 [irtag] => 7 [t_index] => 0 [person_id] => 23902 ) [3] => Array ( [sure] => 0 [irmagnum] => 0 [u_index] => 1 [name] => 李峰 [irtag] => 7 [t_index] => 1 [person_id] => 21645 ) ) [sys_author_id_arr] => [jl_publication_cn_publication_en] => chemicaljournalofchineseuniversitieschinese,高等学校化学学报 [jl_keyword_cn_keyword_en] => n二甲基氨基丙磺酸盐,fluorescence,聚集数,光散射,radius,hydrodynamic,n十二烷基n,aggregationnumber,dodecyldimethylammoniopropanesulfonate,水力半径,荧光,lightscattering [datebase] => Scopus [format_scopus_No] => 054b0e258f88bce043f0efb57370fa83-1337004689 [cite_scopus] => 4 [classification_pub] => KTHPD [uri] => https://www.scopus.com/inward/record.uri?eid=2-s2.0-2842559464&partnerID=40&md5=37e840f84acebaa929fa295218f5fc80 [standard_in] => Inst. of Colloid/Interface Chemistry, Shandong University, Jinan 250100, China; Institute of Chemical Physics, Academia Sinica, Lanzhou 730000, China; Department of Polymer, Nankai University, Tianjin 300071, China [scopus_No] => 2-s2.0-2842559464 [format_title_cn_publication_cn_pub_year] => bc6c02242fde051ddb5fc381f87e450b-1092650189 [format_title_cn_issn_pub_year] => 6f1a7488cf3f6e1394e7985bf295223f-778671723 [jl_author_test] => unameuu674eu5cf0,unameuu674eu98de,uirtstag0,upersonid23902,unameuu738bu6d77u5e86,upersonid21645,uuindex1,usureu0,utindex1,utindex0,uirtag7,uirtypical1,uirinspecttag0,unameuu9eceu5cf0,upersonid21642,uirauthortype0,uirauthortype3,uuindex3,upersonid21587 [sys_author_jg_last_arr] => 300071 [sys_author_in_last_arr] => china [sys_author_id] => [id] => VgifvWUBFjIhTVEbUuIV [tags] => 0 ) [12] => Array ( [batch2] => 1,2,6 [batch] => 3243,3241,3254,3252 [tag] => 0 [abstract_cn] => 通过流变参数,电泳淌度和PH值的测定,研究了NaCl、MgCl2、Na2SO4等电解质和阳离子表面活性剂(十六烷基三甲基溴化铵)对铝镁混合金属氢氧化物/钠土 体胶体性能的影响。 [keyword_cn] => 铝镁混合金属;氢氧化物;钠土悬浮液;MMH;胶体; [clc] => O648.22 [author_jg] => [孙德军;侯万国]山东大学胶体与界面化学研究所胶体与界面化学开放研究实验室,中国 [format_title_cn_publication_cn_pub_year] => 8790d2a6df50d76c25d2afde600bb5d81166915836 [from_id] => 76,80,73,85 [issue] => 2 [sys_level_num] => 2_1 [sys_jg_type] => 0,5 [source_type] => 351 [pub_year] => 1998 [article_id] => 113163,197340,334480,497985 [pages] => 5 [hints] => 2 [author_cn] => 孙德军;侯万国 [issn] => 0251-0790 [uri] => http://lib.cqvip.com/qk/90335X/199802/2912122.html [publication_cn] => 高等学校化学学报 [title_cn] => 电解质和阳离子表面活性剂对MMH/粘土体系胶体性能的影响 [CSSN] => 22-1131/06 [SYS_TAG] => 3 [format_title_cn_issn_pub_year] => 148bdcd530c8d649332d2f58cf355b071627622636 [hb_type] => 2 [jl_publication_cn] => 高等学校化学学报 [jl_country] => 中国 [jl_keyword_cn] => ,mmh,钠土悬浮液,氢氧化物,铝镁混合金属,胶体 [jl_clc] => o64822 [author_in] => [Sun, D.-J] Inst. of Colloid/Interface Chemistry, Key Lab. Colloid/Interface C.S.E.C., Shandong University, Jinan 250100, China@@@[ Hou, W.-G] Inst. of Colloid/Interface Chemistry, Key Lab. Colloid/Interface C.S.E.C., Shandong University, Jinan 250100, China@@@[ Han, S.-H] Inst. of Colloid/Interface Chemistry, Key Lab. Colloid/Interface C.S.E.C., Shandong University, Jinan 250100, China@@@[ Song, S.-E] Inst. of Colloid/Interface Chemistry, Key Lab. Colloid/Interface C.S.E.C., Shandong University, Jinan 250100, China@@@[ Zhang, C.-G] Inst. of Colloid/Interface Chemistry, Key Lab. Colloid/Interface C.S.E.C., Shandong University, Jinan 250100, China [company_id] => 0,0,0,0,0,0,0,0 [author_id] => 21153,23456 [author_test] => Array ( [0] => Array ( [sure] => 0 [irmagnum] => 0 [u_index] => 2 [name] => 侯万国 [irtag] => 7 [t_index] => 0 [person_id] => 21153 ) [1] => Array ( [sure] => 0 [irmagnum] => 0 [u_index] => 1 [name] => 孙德军 [irtag] => 7 [t_index] => 1 [person_id] => 23456 ) ) [sys_author_id_arr] => [jl_publication_cn_publication_en] => 高等学校化学学报 [hb_batch] => grant_no [cite_wos] => 6 [publication_en] => CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE [check_3Y] => 1 [language] => Chinese [delivery_No] => ZA790 [cauthor_ad] => [Sun, DJ]Shandong Univ, State Educ Commiss, Key Lab Colloid & Interface Chem, Inst Colloid & Interface Chem, Jinan 250100, Peoples R China. [format_title] => 7c061e1104f83493511ca03ce1666dcc1441772872 [author_fn] => Sun, DJ; Hou, WG; Han, SH; Song, SE; Zhang, CG [cite_wanfang] => 10 [format_title_en_issn_pub_year] => 9c411931eab98e7728ae7310c8241898-1591933654 [datebase] => Scopus [format_scopus_No] => d96975105c767bd4dd84e4829bdff34f174002464 [publication_29] => CHEM J CHINESE U [end_page] => 256 [abstract_en] => The effects of electrolytes (NaCl, Na2SO4 and MgCl2) and cationic surfactant (cetyltrimethylammonium bromide) on colloidal properties of mixed metal hydroxide (MMH)/montmorillonite (Mt) suspension were studied through measurements of electrophoretic mobilities, rheology and pH. The results show that all the electrolytes and surfactant studied in this work decreased Bingham yield point (YP) of MMH/Mt system, but exerted different effects on fluid loss (FL) and pH of MMH/Mt system. The results are interpreted as means that the cationic ions of electrolytes mainly displace the charge-balancing ions of Mt particles, such as H+ and Na+, so enhance their aggregation, leading to the decrease of pH and the increase of FL, but the anionic ions of these electrolytes mainly displace the charge-balancing ions of MMH particles, such as OH- and Cl-, so weaken the aggregation effects of MMH on Mt particles, therefore, cause the increase of pH and the decrease of FL. In another word, the overall effects of electrolytes on MMH/Mt system depend on the relative ability of anionic and cationic ions to exert the opposite effects on FL and pH. As for cetyltrimethylammonium bromide (CTAB), the adsorption of CTAB on Mt particles does not only displace H+ and cause the aggregation of Mt particles but also reverses their wetting ability, therefore, CTAB decrease FL and YP of MMH/Mt system to a larger extent than inorganic electrolytes although it can only decrease pH slightly. [article_dt] => Article [publication_type] => J [begin_page] => 252 [author_en] => Sun, DJ; Hou, WG; Han, SH; Song, SE; Zhang, CG [volume] => 19 [publisher] => HIGHER EDUCATION PRESS [get_data] => 2018-08-29 [keyword_en] => Al-Mg mixed metal hydroxide; Na-montmorillonite; rheology [page] => 252-256 [keyword_plu] => HYDROXIDE [format_publication_cn] => 112be9cb2f30361719ed2bc572ba4a22192440272 [publication_iso] => Chem. J. Chin. Univ.-Chin. [format_title_en_publication_en_pub_year] => ef1bb90f731731990b8b582027ec9f2712500402 [cite_scopus] => 5 [format_title_en] => 1474263a1f47921be681aef65e1633fd-1601513427 [publisher_city] => BEIJING [pub_date] => FEB [cauthor_order] => 1 [hx_id] => 2378,2371 [reference_No] => 13 [format_issn_issue_page_pub_year] => c0fdd58e2b491fdcfc39e010a05dab6e577072188 [cite_awos] => 6 [wos_No] => WOS:000072402000023 [classification_pub] => KTHPD [format_wos_No] => 1c01860f76c71ba57fd97771dcd16f73-4857568 [wos_sub] => Chemistry, Multidisciplinary [research_area] => Chemistry [cauthor_back] => Sun, DJ [check_180] => 0 [publisher_ad] => SHATANHOU ST 55, BEIJING 100009, PEOPLES R CHINA [standard_in] => Inst. of Colloid/Interface Chemistry, Key Lab. Colloid/Interface C.S.E.C., Shandong University, Jinan 250100, China [scopus_No] => 2-s2.0-0347170923 [title_en] => Effects of electrolytes and cationic surfactant on colloidal properties of MMH/Mt system [format_publication_en] => 4eabdd9afe3fe566a165b6e1c3e0dbbd-130083487 [jl_language] => chinese [jl_article_dt] => 期刊论文 [jl_author_test] => uirtypical3,uirtstag0,uuindex1,uuindex2,upersonid21153,unameuu4fafu4e07u56fd,usureu0,utindex0,uirtag6,uirinspecttag0,uirauthortype0,unameuu5b59u5fb7u519b,upersonid23456 [jl_publication_en] => chemicaljournalofchineseuniversitieschinese [sys_author_jg_last_arr] => 中国 [jl_keyword_en] => almgmixedmetalhydroxide,namontmorillonite,rheology [sys_author_in_last_arr] => china [jl_publisher] => highereducationpress [sys_author_id] => [id] => UwkvvmUBFjIhTVEbC0eT [tags] => 0 ) [13] => Array ( [batch2] => 1,2,6 [batch] => 3243,3241,3254,3252 [tag] => 0 [abstract_cn] => 利用从头计算法研究了二甲基锂氟类硅烯和二乙基锂氟类硅烯的各异构体的构型和能量。烷基的引入增加了Si的σ电子对Li的授与而降低了F对Si空p轨道的电子回授,使类硅烯的p-络合物构型热稳定性下降,而σ-络合物热稳定性增加。在上述两种作用的共同影响下,三元环构型的热稳定性只有很小的变化。 [keyword_cn] => 从头算;类硅烯;锂氟类硅烯;二甲基;二乙基; [clc] => O627.4 [author_jg] => [冯大诚;冯圣玉]山东大学理论化学研究室,中国 [format_title_cn_publication_cn_pub_year] => b49a8d19a200b5df31e92e9cddb108f9591975715 [from_id] => 76,80,73,85 [issue] => 3 [sys_level_num] => 2_1 [sys_jg_type] => 0,5 [source_type] => 351 [pub_year] => 1998 [article_id] => 334637,197342,497927,3359 [pages] => 4 [hints] => 2 [author_cn] => 冯大诚;冯圣玉 [issn] => 0251-0790 [uri] => http://lib.cqvip.com/qk/90335X/199803/2996315.html [publication_cn] => 高等学校化学学报 [title_cn] => 烷基对取代锂氟类硅烯R2SiLiF的构型和热稳定性的影响 [CSSN] => 22-1131/06 [SYS_TAG] => 3 [format_title_cn_issn_pub_year] => a4255dfdb10d95f12977f2ef7b28ce0f-1652820546 [hb_type] => 2 [jl_publication_cn] => 高等学校化学学报 [jl_country] => 中国 [jl_keyword_cn] => ,二乙基,二甲基,从头算,类硅烯,锂氟类硅烯 [jl_clc] => o6274 [author_in] => [Feng, D.-C] Institute of Theoretical Chemistry, Shandong University, Jinan 250100, China@@@[ Feng, S.-Y] Institute of Theoretical Chemistry, Shandong University, Jinan 250100, China@@@[ Deng, C.-H] Institute of Theoretical Chemistry, Shandong University, Jinan 250100, China [company_id] => 0,0,0,0,0,0,0,0 [author_id] => 20721 [author_test] => Array ( [0] => Array ( [sure] => 0 [irmagnum] => 0 [u_index] => 2 [name] => 冯圣玉 [irtag] => 7 [t_index] => 0 [person_id] => 20721 ) ) [sys_author_id_arr] => [jl_publication_cn_publication_en] => 高等学校化学学报 [jl_keyword_cn_keyword_en] => 类硅烯,二甲基,锂氟类硅烯,二乙基,从头算 [hb_batch] => grant_no [cite_wos] => 14 [publication_en] => CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE [check_3Y] => 0 [language] => Chinese [delivery_No] => ZD364 [cauthor_ad] => [Feng, DC]Shandong Univ, Inst Theoret Chem, Jinan 250100, Peoples R China. [format_title] => 711de9ec136d3111bdb2babe4885a8cb1645007298 [author_fn] => Feng, DC; Feng, SY; Deng, CH [cite_wanfang] => 10 [format_title_en_issn_pub_year] => 108dc08b3b018d0a565dca5defa535171073285824 [datebase] => Scopus [format_scopus_No] => 32712dec9b1a225e22fe8196212d3b4e283239433 [publication_29] => CHEM J CHINESE U [end_page] => 454 [abstract_en] => Isomeric structures and energies of dimethyllithoflurosilylenoid and diethyllithoflurosilylenoid were investigated by using ab initio molecular orbital theory. Alkyl groups increase the donor of sigma electrons of silicon to lithium atom and it leads to an increase of the thermal stability of sigma-complex. But alkyl groups decrease the donor of pi electrons of fluorine atom to silicon, leading to a decrease of the thermal stability of p-complex, However, because of the joint action of that two effect, alkyl groups change little the thermal stability of the three-membered ring. [article_dt] => Article [publication_type] => J [begin_page] => 451 [author_en] => Feng, DC; Feng, SY; Deng, CH [volume] => 19 [publisher] => HIGHER EDUCATION PRESS [get_data] => 2018-08-29 [keyword_en] => ab initio calculation; silylenoid; substituted lithofluro-silylenoids [page] => 451-454 [keyword_plu] => ISOMERIZATION; REACTIVITY [format_publication_cn] => 112be9cb2f30361719ed2bc572ba4a22192440272 [publication_iso] => Chem. J. Chin. Univ.-Chin. [format_title_en_publication_en_pub_year] => 0812bce4466aacdb7130f9ab6194429a-1599028535 [cite_scopus] => 14 [format_title_en] => f6b0c31cf91357aba1807af4b36d877c150654502 [publisher_city] => BEIJING [pub_date] => MAR [cauthor_order] => 1 [hx_id] => 2378,2371 [reference_No] => 6 [format_issn_issue_page_pub_year] => cf8df3995ffede29a436104556af52be2037031426 [cite_awos] => 14 [wos_No] => WOS:000072677800029 [classification_pub] => KTHPD [format_wos_No] => 0eb27260768102984f7b1da6785286fd-2059893653 [wos_sub] => Chemistry, Multidisciplinary [research_area] => Chemistry [cauthor_back] => Feng, DC [check_180] => 0 [publisher_ad] => SHATANHOU ST 55, BEIJING 100009, PEOPLES R CHINA [standard_in] => Institute of Theoretical Chemistry, Shandong University, Jinan 250100, China [scopus_No] => 2-s2.0-0346690362 [title_en] => Effect of alkyl group on the structures and thermal stability of substituted lithofluro-silylenoids R2SiLiF [format_publication_en] => 4eabdd9afe3fe566a165b6e1c3e0dbbd-130083487 [jl_language] => chinese [jl_article_dt] => 期刊论文 [jl_author_test] => uirtypical3,uirtstag0,upersonid20721,uuindex2,uirinspecttag0,usureu0,utindex0,uirtag6,unameuu51afu5723u7389,uirauthortype0 [jl_publication_en] => chemicaljournalofchineseuniversitieschinese [sys_author_jg_last_arr] => 中国 [jl_keyword_en] => silylenoid,abinitiocalculation,substitutedlithoflurosilylenoids [sys_author_in_last_arr] => china [jl_publisher] => highereducationpress [sys_author_id] => [id] => tQo0vmUBFjIhTVEbSvUX [tags] => 0 ) [14] => Array ( [batch2] => 1,2,6 [batch] => 3243,3241,3254,3252 [tag] => 0 [abstract_cn] => 用限制的HF/3-21G和HF/6-31G优化乙烯醇锂的几种可能构型,比较了它们的稳定性。用限制的HF/3-1G,从乙醛开始,探讨了气相反应生成乙烯醇锂的机理,并在MP2水平上用6-31G基组计算了反应热。 [keyword_cn] => 乙烯醇锂;结构优化;反应机理;从头算;构型; [clc] => O627.11 [author_jg] => [王义贵;孙昌俊]山东大学理论化学研究室,中国 [format_title_cn_publication_cn_pub_year] => 8a5e4eee251d073cf3429a7e671a3e6a-886987529 [from_id] => 76,80,73,85 [issue] => 3 [sys_level_num] => 2_1 [sys_jg_type] => 0,5 [source_type] => 351 [pub_year] => 1998 [article_id] => 84707,197341,497932,334636 [pages] => 5 [hints] => 3 [author_cn] => 王义贵;孙昌俊 [issn] => 0251-0790 [uri] => http://lib.cqvip.com/qk/90335X/199803/2996309.html [publication_cn] => 高等学校化学学报 [title_cn] => 乙烯醇锂的从头算研究 [CSSN] => 22-1131/06 [SYS_TAG] => 3 [format_title_cn_issn_pub_year] => c546885ea35beced2bd3dfbb8f18dc0b548084629 [hb_type] => 2 [jl_publication_cn] => 高等学校化学学报 [jl_country] => 中国 [jl_keyword_cn] => ,结构优化,从头算,乙烯醇锂,反应机理,构型 [jl_clc] => o62711 [author_in] => [Wang, Y.-G] Theoretical Chemistry Institute, Shandong University, Jinan 250100, China@@@[ Sun, C.-J] Theoretical Chemistry Institute, Shandong University, Jinan 250100, China@@@[ Deng, C.-H] Theoretical Chemistry Institute, Shandong University, Jinan 250100, China [company_id] => 0,0,0,0,0,0,0,0 [author_id] => [author_test] => Array ( ) [sys_author_id_arr] => [jl_publication_cn_publication_en] => 高等学校化学学报 [hb_batch] => grant_no [cite_wos] => 1 [publication_en] => CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE [check_3Y] => 0 [language] => Chinese [delivery_No] => ZD364 [cauthor_ad] => [Wang, YG]Shandong Univ, Inst Theoret Chem, Jinan 250100, Peoples R China. [format_title] => d52636041f11c98363669ca367cc745d576074111 [author_fn] => Wang, YG; Sun, CJ; Deng, CH [cite_wanfang] => 1 [format_title_en_issn_pub_year] => efb5e3b0a24bf404e62fe01eace37f20-2110589553 [datebase] => Scopus [format_scopus_No] => d74659dcc02f7b8b1fd319b0b3081534824213986 [publication_29] => CHEM J CHINESE U [end_page] => 428 [abstract_en] => Two possible geometries of CH2 = CH-OLi and transition states between them were optimized by using RHF/3-21G and RHF/6-31G*. The stability of the two structures were discussed. The mechanism of producing CH2=CH-OLi from CH3-CH(=O) and Li-OH in gas phase was investigated under RHF/3-21G level. We found that the concerted mechanism was preferred. We also calculated the reaction heat by using 6-31G* basis sets at MP2 level. [article_dt] => Article [publication_type] => J [begin_page] => 424 [author_en] => Wang, YG; Sun, CJ; Deng, CH [volume] => 19 [publisher] => HIGHER EDUCATION PRESS [get_data] => 2018-08-29 [keyword_en] => lithium ethenolate; geometries optimization; reaction mechanism; ab; initio calculation [page] => 424-428 [keyword_plu] => REACTIVITY [format_publication_cn] => 112be9cb2f30361719ed2bc572ba4a22192440272 [publication_iso] => Chem. J. Chin. Univ.-Chin. [format_title_en_publication_en_pub_year] => 6b90f1621f4df79385d951ac666846be-1279362643 [cite_scopus] => 2 [format_title_en] => 744f591369eb853f3c62b3653887176d1441010843 [publisher_city] => BEIJING [pub_date] => MAR [cauthor_order] => 1 [hx_id] => 2378,2371 [reference_No] => 11 [format_issn_issue_page_pub_year] => 98647a7fc30517e98d575f417770f4cc-1927406570 [cite_awos] => 1 [wos_No] => WOS:000072677800023 [classification_pub] => KTHPD [format_wos_No] => 40d77cb7422f964525c35e296044e86d1710058869 [wos_sub] => Chemistry, Multidisciplinary [research_area] => Chemistry [cauthor_back] => Wang, YG [check_180] => 0 [publisher_ad] => SHATANHOU ST 55, BEIJING 100009, PEOPLES R CHINA [standard_in] => Theoretical Chemistry Institute, Shandong University, Jinan 250100, China [scopus_No] => 2-s2.0-0348149364 [title_en] => Ab initio studies of lithium ethenolate [format_publication_en] => 4eabdd9afe3fe566a165b6e1c3e0dbbd-130083487 [jl_language] => chinese [jl_article_dt] => 期刊论文 [jl_publication_en] => chemicaljournalofchineseuniversitieschinese [sys_author_jg_last_arr] => 中国 [jl_keyword_en] => lithiumethenolate,ab,initiocalculation,geometriesoptimization,reactionmechanism [sys_author_in_last_arr] => china [jl_publisher] => highereducationpress [sys_author_id] => [id] => SgkwvmUBFjIhTVEbgrPf [tags] => 0 ) [15] => Array ( [issn] => 0251-0790 [delivery_No] => 160YT [batch2] => 1,2,6 [hb_batch] => 3241 [tag] => 0 [author_en] => Fu, AP; Feng, DC; Deng, CH [abstract_en] => Ab initio molecular orbital method is used to theoretically investigate the interactions of water with the different sites of Cu(100) surface in this paper. Cu-5 cluster is used to simulate the surface, the adsorption energies and geometries in different directions are calculated at lanl1dz basis set level, The results show that water Lends to the surface through the oxygen atom, it prefers to adsorb on top site with the adsorption energy 70 kJ/mol and the equilibrium Cu-O distance 0. 213 nm, and hydrogen atoms are far away from the surface. Giving no consideration of the d orbitals of oxygen atom, the optimum structure is the water plane normal to the surface, H2O tilts of 50 degrees are found to require small amount of energy. When the d orbitals of oxygen atom is taken into account, the calculated structure of adsorption H2O monomer with an inclined molecular axis about 50 degrees is in agreement with the experimental results. Also the effect of charge on the adsorption system is discussed. The results indicate that on the surface with positive charges, the interactions between water and surface are strengthened, the charge transfer from the water to the surface increases, and Cu-O equilibrium distance decreases; On the surface with a negative charge, the results are opposite, the structure with Ii near the surface is the stable one. [publication_type] => J [keyword_plu] => CHEMISORPTION; SURFACES; AL(111); COPPER; H2O [author_in] => [Fu, A.-P] Institute of Theoretical Chemistry, Shandong University, Jinan 250100, China@@@[ Feng, D.-C] Institute of Theoretical Chemistry, Shandong University, Jinan 250100, China@@@[ Deng, C.-H] Institute of Theoretical Chemistry, Shandong University, Jinan 250100, China [publisher_city] => BEIJING [cauthor_back] => Feng, DC [get_data] => 2018-08-29 [format_title_en_publication_en_pub_year] => c0fc307189c6d888921c37e975ba3301-688231554 [begin_page] => 1654 [cite_wos] => 1 [check_3Y] => 0 [cite_awos] => 1 [from_id] => 76,80,73,85 [cauthor_ad] => [Feng, DC]Shandong Univ, Inst Theoret Chem, Jinan 250100, Peoples R China. [school_id] => 117 [cauthor_order] => 2 [research_area] => Chemistry [sys_level_num] => 1_7 [publisher] => HIGHER EDUCATION PRESS [sys_jg_type] => 5 [format_issn_issue_page_pub_year] => f288376d2c61ae0713b339ee40232851-1995319038 [title_en] => The ab initio study of molecular water adsorption on Cu(100) [publication_29] => CHEM J CHINESE U [author_fn] => Fu, AP; Feng, DC; Deng, CH [pub_year] => 1998 [publisher_ad] => SHATANHOU ST 55, BEIJING 100009, PEOPLES R CHINA [check_180] => 0 [keyword_en] => ab initio method; Cu(100) surface; water; adsorption [end_page] => 1658 [pub_date] => OCT [pages] => 5 [format_wos_No] => 4809b52e7443e95dedb3fa4014013e4a-875373913 [hints] => 1 [volume] => 19 [language] => Chinese [source_type] => 351 [issue] => 10 [reference_No] => 16 [batch] => 3243,3241,3254,3252 [publication_en] => CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE [hx_id] => 2378,2371 [sys_update_time] => 2018-09-05 15:29:30 [format_title_en_issn_pub_year] => 0981b1ac36836484fed0b857a643e22b1557145984 [publication_iso] => Chem. J. Chin. Univ.-Chin. [article_id] => 334332,98202,497920,197339 [wos_sub] => Chemistry, Multidisciplinary [SYS_TAG] => 3 [wos_No] => WOS:000078261500031 [page] => 1654-1658 [hb_type] => 2 [article_dt] => Article [jl_language] => chinese [jl_article_dt] => 期刊论文 [jl_publication_en] => chemicaljournalofchineseuniversitieschinese [jl_country] => 中国 [jl_keyword_en] => water,abinitiomethod,cu100surface,adsorption [jl_publisher] => highereducationpress [author_jg] => [傅爱萍;冯大诚]山东大学理论化学研究室,中国 [keyword_cn] => Cu(100)表面;水;吸附;铜表面;从头算; [format_title] => c25e6956745f66957d755758d193d187-606514514 [cite_wanfang] => 7 [clc] => O613.3 O614.121 [title_cn] => H2O在Cu(100)表面吸附的从头算研究 [format_publication_cn] => 112be9cb2f30361719ed2bc572ba4a22192440272 [publication_cn] => 高等学校化学学报 [format_title_en] => 6cc64b8da5db9df78adddae72957fb2f372631029 [CSSN] => 22-1131/06 [abstract_cn] => 用量子化学从头计算方法,以原子簇Cu5为模拟表面,研究了水在Cu(100)面上不同吸附位的吸附情况,结果表明:水分子通过氧原子与表面成键,顶位是其最佳吸附位,吸附能约为70kJ/mol,平衡距离为0.213nm,氢原子远离表面。在氧原子不加极化函数时,水分子的二次轴垂直于表面时能量最低,但倾斜至50°所需能量仅在10kJ/mol以内。 [sys_priority_field] => 76 [author_cn] => 傅爱萍;冯大诚 [format_publication_en] => 4eabdd9afe3fe566a165b6e1c3e0dbbd-130083487 [jl_publication_cn] => 高等学校化学学报 [jl_keyword_cn] => 吸附,水,从头计算,cu100表面 [jl_clc] => o6473 [company_id] => 0,0,0,0,0,0,0 [author_id] => [author_test] => Array ( ) [sys_author_id_arr] => [jl_publication_cn_publication_en] => chemicaljournalofchineseuniversitieschinese,高等学校化学学报 [jl_keyword_cn_keyword_en] => 从头计算,cu100表面,cu100surface,吸附,adsorption,water,水,abinitiomethod [datebase] => Scopus [format_scopus_No] => facae3c95f02c4c45bad60d887f75f9871012371 [cite_scopus] => 3 [classification_pub] => KTHPD [uri] => http://lib.cqvip.com/qk/90335X/199810/3176024.html [standard_in] => Institute of Theoretical Chemistry, Shandong University, Jinan 250100, China [scopus_No] => 2-s2.0-11744285402 [format_title_cn_publication_cn_pub_year] => 516c356137108d4e1698f07a656e60751661325146 [format_title_cn_issn_pub_year] => a92d3934ff95db247dfc59cace911d7464992610 [sys_author_jg_last_arr] => 250100 [sys_author_in_last_arr] => china [sys_author_id] => [id] => CwifvWUBFjIhTVEbUuIV [tags] => 0 ) [16] => Array ( [batch2] => 1,2,6 [batch] => 3243,3241,3254,3252 [tag] => 0 [abstract_cn] => 通过表面张力测定和13CNMR、ESR波谱研究了十二烷基甜菜碱(C12BE)与聚乙烯吡咯烷酮(PVP)的相互作用.表面张力测定表明,在pH=6.5及NaCI存在下,C12BE与PVP之间有明显的相互作用,可形成C12BE/PVP复合物,且C12BE-PVP混合溶液的β-lgc曲线出现2个转折点,第一个转折点时C12BE浓度c1(C12BE-PVP开始缔合)低于C12BE的cmc值;而第二个转折点时C12BE浓度c2(C12BE-PVP缔合达饱和)大于cmc值.(c2─c1)与PVP浓度呈线性关系.PVP降低C12BE胶束化标准自由能(△G0)随PVP浓度增加而增大.13CNMR测定表明,PVP骨架上α-CH、β-CH2和吡咯环上与N相连的亚甲基吸附于C12BE胶束表面的碳氢链部位,屏蔽了C12BE胶束表面碳氢链与水的接触.ESR波谱表明,PVP-C12BE聚集体\\\'界面\\\'的粘度高于C12BE胶束\\\'界面\\\'的粘度. [keyword_cn] => 十二烷基甜菜碱;聚乙烯吡咯烷酮;表面活性剂; [clc] => O647.2 [author_jg] => [赤京诚;梁芳珍;刘树海;任建成;鲁绍芬]山东师范大学表面与界面化学实验室,中国.@@@[李干佐]山东大学胶体与界面化学研究所,中国.@@@[汪汉卿]中国科学院兰州化学物理研究所,中国 [format_title_cn_publication_cn_pub_year] => 61faafa4f9c94015678a7575bb3fe3bc1675856680 [from_id] => 76,80,73,85 [issue] => 1 [sys_level_num] => 2_1 [sys_jg_type] => 0,5 [source_type] => 351 [pub_year] => 1998 [article_id] => 84706,202869,334521,498037 [pages] => 5 [hints] => 2 [author_cn] => 赤京诚[1];李干佐[2];梁芳珍[1];刘树海[1];任建成[1];鲁绍芬[1];汪汉卿[3]; [issn] => 0251-0790 [uri] => http://lib.cqvip.com/qk/90335X/199801/2911679.html [publication_cn] => 高等学校化学学报 [title_cn] => 十二烷基甜菜碱与聚乙烯吡咯烷酮相互作用的研究 [CSSN] => 22-1131/06 [SYS_TAG] => 3 [format_title_cn_issn_pub_year] => 60239ab7c1f3e9d32878d9381ef93cb2256181825 [hb_type] => 2 [jl_publication_cn] => 高等学校化学学报 [jl_country] => 中国 [jl_keyword_cn] => 聚乙烯吡咯烷酮,,表面活性剂,十二烷基甜菜碱 [jl_clc] => o6472 [author_in] => [Hao, J.-C] Laboratry of Surf./Interface Chem., Shandong Normal University, Jinan 250014, China@@@[ Liang, F.-Z] Laboratry of Surf./Interface Chem., Shandong Normal University, Jinan 250014, China@@@[ Liu, S.-H] Laboratry of Surf./Interface Chem., Shandong Normal University, Jinan 250014, China@@@[ Ren, J.-C] Laboratry of Surf./Interface Chem., Shandong Normal University, Jinan 250014, China@@@[ Lu, S.-F] Laboratry of Surf./Interface Chem., Shandong Normal University, Jinan 250014, China@@@[ Li, G.-Z] Inst. of Colloid/Interface Chemistry, Shandong University, Jinan 250100, China@@@[ Wang, H.-Q] Lanzhou Inst. of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, China [company_id] => [author_id] => [author_test] => Array ( ) [sys_author_id_arr] => [jl_publication_cn_publication_en] => 高等学校化学学报 [hb_batch] => grant_no [publication_en] => CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE [cite_wos] => 7 [check_3Y] => 1 [language] => Chinese [delivery_No] => YU597 [format_title] => 6c5210198002dbd9365f6a634b2b24aa-824862513 [cauthor_ad] => [Hao, JC]Shandong Normal Univ, Lab Surface & Interface Chem, Jinan 250014, Peoples R China. [author_fn] => Hao, JC; Liang, FZ; Liu, SH; Ren, JC; Lu, SF; Li, GZ; Wang, HQ [cite_wanfang] => 16 [format_title_en_issn_pub_year] => 5beb87a61993752ba298b243b8d16e6467208774 [datebase] => Scopus [format_scopus_No] => 8439439b227f7e653a19792e9f315f11-1722356576 [publication_29] => CHEM J CHINESE U [end_page] => 115 [abstract_en] => The association and standard free energy of formation of the complex between dodecyl betaine(C12BE) and polyvinylpyrrolidone (PVP) in aqueous solution have been investigated by using C-13 NMR, ESR and surface tension measurement on the air/water interface. It is found that the basic structure of the complex is a micelle-like aggregate, the C12BE molecules were assembled on the methine(alpha), methylene(beta) carbon in the backbone, and the methylene carbon attached to the nitrogen of PVP molecules, and shielding hydrocarbon groups on the surface of the micelle from contact with water. Our results also confirm that the micellization process in the presence of PVP occurs at a-lower concentration than that at the critical micelle concentration. The effectiveness of PVP in lowering the free energy of formation of the surfactant aggregates in aqueous solutions increases with the increasing concentrations of PVP. The interfacial viscosity of the aggregates of PVP-C12BE is higher than that of C12BE ones. [publication_type] => J [begin_page] => 111 [article_dt] => Article [author_en] => Hao, JC; Liang, FZ; Liu, SH; Ren, JC; Lu, SF; Li, GZ; Wang, HQ [volume] => 19 [get_data] => 2018-08-29 [publisher] => HIGHER EDUCATION PRESS [keyword_en] => dodecyl betaine; polyvinylpyrrolidone; NMR; ESR; surface tension [page] => 111-115 [format_publication_cn] => 112be9cb2f30361719ed2bc572ba4a22192440272 [publication_iso] => Chem. J. Chin. Univ.-Chin. [format_title_en_publication_en_pub_year] => 30a47c3df2d289caaf488e65e9e6bb90-1668834224 [cite_scopus] => 5 [format_title_en] => 0b4a0b6b36f648612a83fae7d41642a0-400366810 [publisher_city] => BEIJING [pub_date] => JAN [cauthor_order] => 1 [hx_id] => 2378,2371 [reference_No] => 10 [format_issn_issue_page_pub_year] => 82017e60f7622660b445fa4a4076537d1846199690 [cite_awos] => 7 [wos_No] => WOS:000071733800028 [classification_pub] => KTHPD [format_wos_No] => e6f390c75dadc58570d8211d23c5efd32121675092 [wos_sub] => Chemistry, Multidisciplinary [research_area] => Chemistry [cauthor_back] => Hao, JC [check_180] => 0 [publisher_ad] => SHATANHOU ST 55, BEIJING 100009, PEOPLES R CHINA [scopus_No] => 2-s2.0-3142558217 [standard_in] => Laboratry of Surf./Interface Chem., Shandong Normal University, Jinan 250014, China; Inst. of Colloid/Interface Chemistry, Shandong University, Jinan 250100, China; Lanzhou Inst. of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, China [title_en] => The interaction between dodecyl betaine and polyvinylpyrrolidone [format_publication_en] => 4eabdd9afe3fe566a165b6e1c3e0dbbd-130083487 [jl_language] => chinese [jl_article_dt] => 期刊论文 [jl_publication_en] => chemicaljournalofchineseuniversitieschinese [sys_author_jg_last_arr] => 中国,中国,中国 [jl_keyword_en] => nmr,surfacetension,dodecylbetaine,esr,polyvinylpyrrolidone [sys_author_in_last_arr] => china [jl_publisher] => highereducationpress [sys_author_id] => [id] => SQkwvmUBFjIhTVEbgrPf [tags] => 0 ) [17] => Array ( [issn] => 0251-0790 [delivery_No] => 106YP [batch2] => 1,2,6 [hb_batch] => 3241 [tag] => 0 [author_en] => Zhang, QZ; Sun, JR; Wang, DQ; Sheng, X; Yin, XY [abstract_en] => A novel complex - palladium-coordinated ate-type liquid crystalline dendrimer was synthesized by a divergent approach, The product showed liquid crystalline properties from 115 degrees C to 187 degrees C, and it belonged to dinuclear species, containing two palladium centers linked by two bridging Cl, each palladium atom completes its coordinations with N atom and a sigma bond to an ortho-carbon in the phenyl ring. The microanalytical values obtained for the product are in agreement with those of compound containing ligand, palladium:and chlorine in a molar ratio of 1 : 1 : 1 and 12 palladium atoms for every scaffold. [publication_type] => J [author_in] => [Zhang, Q.-Z] Department of Chemistry, Shandong University, Jinan 250100, China@@@[ Sun, J.-R] Department of Chemistry, Shandong University, Jinan 250100, China@@@[ Wang, D.-Q] Center of Analysis and Measurement, Shandong Normal University, Jinan 250014, China@@@[ Sheng, X] Department of Chemistry, Shandong University, Jinan 250100, China@@@[ Yin, X.-Y] Department of Chemistry, Shandong University, Jinan 250100, China@@@[ Zhao, X.-G] Changchun Inst. of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China@@@[ Li, G] Changchun Inst. of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China [publisher_city] => BEIJING [cauthor_back] => Zhang, QZ [get_data] => 2018-08-29 [format_title_en_publication_en_pub_year] => d2f6e84ddf24c47f196fd29b4ac13520 [pages] => 3 [cite_wos] => 13 [check_3Y] => 0 [cite_awos] => 13 [from_id] => 76,80,73,85 [cauthor_ad] => [Zhang, QZ]Shandong Univ, Dept Chem, Jinan 250100, Peoples R China. [school_id] => 117 [cauthor_order] => 1 [research_area] => Chemistry [sys_level_num] => 1_7 [publisher] => HIGHER EDUCATION PRESS [sys_jg_type] => 5 [format_issn_issue_page_pub_year] => 2735f494510d9e3b74be44bf8a621fc8 [title_en] => Studies on the organometallic palladium coordinated carbosillane liquid crystalline dendrimer [publication_29] => CHEM J CHINESE U [author_fn] => Zhang, QZ; Sun, JR; Wang, DQ; Sheng, X; Yin, XY [pub_year] => 1998 [publisher_ad] => SHATANHOU ST 55, BEIJING 100009, PEOPLES R CHINA [check_180] => 0 [keyword_en] => dendrimer; organometallic palladium complex; liquid crystalline [end_page] => 829 [pub_date] => MAY [begin_page] => 827 [format_wos_No] => 90d4564710c1e351dc42807e34145cfb [hints] => 5 [volume] => 19 [language] => Chinese [source_type] => 351 [issue] => 5 [reference_No] => 6 [batch] => 3243,3241,3254,3252 [publication_en] => CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE [hx_id] => 2378,2371 [sys_update_time] => 2018-09-05 15:29:31 [format_title_en_issn_pub_year] => 355b03cbdb3553713ac3e3be9ba6cb1c [publication_iso] => Chem. J. Chin. Univ.-Chin. [article_id] => 202879,113154,498030,334458 [wos_sub] => Chemistry, Multidisciplinary [SYS_TAG] => 3 [wos_No] => WOS:000075179300040 [page] => 827-829 [hb_type] => 2 [article_dt] => Article [jl_language] => chinese [jl_article_dt] => 期刊论文 [jl_publication_en] => chemicaljournalofchineseuniversitieschinese [jl_country] => 中国,纳米比亚,瑞士,印度 [jl_keyword_en] => organometallicpalladiumcomplex,liquidcrystalline,dendrimer [jl_publisher] => highereducationpress [author_jg] => [张其震;孙继润;盛昕;殷晓颍]山东大学化学系,中国.@@@[王大庆]山东师范大学测试中心,中国.@@@[赵晓光;李光]中国科学院长春应用化学研究所,中国 [keyword_cn] => 液晶;钯;树状化合物;配合物;碳桂烷;硅碳烷; [format_title] => c4acd484fa4bca549529ede280ca712e953263441 [cite_wanfang] => 31 [clc] => O614.823 [title_cn] => 有机金属钯硅碳烷树状分子液晶配合物研究 [format_publication_cn] => 112be9cb2f30361719ed2bc572ba4a22192440272 [publication_cn] => 高等学校化学学报 [format_title_en] => 95a56de28c87be3762651f25d50fed8b47820411 [CSSN] => 22-1131/06 [abstract_cn] => 树状分子具有规整结构,其分子体积、形状和功能基团可在分子水平上控制,金属有机树状分子及其超分子化学倍受关注[1].含锌、铁、钴、镍、铂、钌或铑的金属有机树状配合物的研究已有报道[2,3],但有机金属钯树状配合物则未见报道.传统的液晶分子为刚性棒状,按...更多还原 [sys_priority_field] => 76 [author_cn] => 张其震[1];孙继润[1];王大庆[2];盛昕[1];殷晓颍[1];赵晓光[3];李光[3]; [format_publication_en] => 4eabdd9afe3fe566a165b6e1c3e0dbbd-130083487 [jl_publication_cn] => 高等学校化学学报 [jl_keyword_cn] => 硅碳烷,液晶,碳桂烷,配合物,钯,树状化合物 [jl_clc] => o614823 [company_id] => 43,169 [sys_subject_sort] => 0,0 [college_parent_id] => 43,169 [company_test] => Array,Array [author_id] => 25613,25088,25608,25110,23827 [author_test] => Array ( [0] => Array ( [sure] => 0 [irmagnum] => 0 [u_index] => 1 [name] => 张群姿 [irtag] => 8 [t_index] => 1 [person_id] => 25613 ) [1] => Array ( [sure] => 0 [irmagnum] => 0 [u_index] => 1 [name] => 张庆竹 [irtag] => 7 [t_index] => 1 [person_id] => 25608 ) [2] => Array ( [sure] => 0 [irmagnum] => 0 [u_index] => 3 [name] => 王德强 [irtag] => 7 [t_index] => 0 [person_id] => 23827 ) [3] => Array ( [sure] => 0 [irmagnum] => 0 [u_index] => 5 [name] => 尹向勇 [irtag] => 7 [t_index] => 0 [person_id] => 25110 ) [4] => Array ( [sure] => 0 [irmagnum] => 0 [u_index] => 5 [name] => 殷向阳 [irtag] => 7 [t_index] => 0 [person_id] => 25088 ) ) [sys_author_id_arr] => [jl_publication_cn_publication_en] => 高等学校化学学报,chemicaljournalofchineseuniversitieschinese [jl_keyword_cn_keyword_en] => liquidcrystalline,液晶,树状化合物,有机金属钯络合物,organometallicpalladiumcomplex,dendrimer [datebase] => Scopus [format_scopus_No] => 6c8819ddb06cabab5be9777d7032f33e [classification_pub] => KTHPD [uri] => http://lib.cqvip.com/qk/90335X/199805/3063285.html [standard_in] => Department of Chemistry, Shandong University, Jinan 250100, China; Center of Analysis and Measurement, Shandong Normal University, Jinan 250014, China; Changchun Inst. of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China [scopus_No] => 2-s2.0-2842524722 [format_title_cn_publication_cn_pub_year] => 996e3fea3350552abc2d2d6839443464 [format_title_cn_issn_pub_year] => 67d72b495b3812e35465395d6835b9ae [jl_author_test] => uirtag7,usureu0,unameuu6bb7u5411u9633,unameuu5f20u5e86u7af9,uuindex3,uuindex1,upersonid25110,utindex1,utindex0,unameuu5f20u7fa4u59ff,unameuu5c39u5411u52c7,upersonid23827,unameuu738bu5fb7u5f3a,upersonid25608,upersonid25088,uuindex5,upersonid25613,uirtag8 [sys_author_jg_last_arr] => 中国 [jl_company_test] => uircu0,unameuu5316u5b66u4e0eu5316u5de5u5b66u9662,uparentidu43,uorgidu43,ulevelu1 [sys_author_in_last_arr] => china [sys_author_id] => [jl_pub_year] => 1998 [id] => iQifvWUBFjIhTVEbUuIV [tags] => 0 ) [18] => Array ( [batch2] => 1,2,6 [batch] => 3243,3241,3254,3252 [tag] => 0 [CSSN] => 22-1131/06 [keyword_cn] => HPMBP;萃取剂;缔合效应;螯合萃取剂; [clc] => O652.62 [author_jg] => [杨永会;薛淑云]山东大学化学院,中国 [format_title_cn_publication_cn_pub_year] => 029e3e06db5c43bc791d21e13e0b026f-510930651 [from_id] => 76,80,73,85 [issue] => 1 [sys_level_num] => 2_1 [sys_jg_type] => 0,5 [source_type] => 351 [pub_year] => 1998 [article_id] => 202871,334520,3358,498068 [pages] => 3 [hints] => 2 [author_cn] => 杨永会;薛淑云 [issn] => 0251-0790 [uri] => http://lib.cqvip.com/qk/90335X/199801/2911658.html [publication_cn] => 高等学校化学学报 [title_cn] => 1—苯基—3—甲基—4—苯甲酰基吡唑啉酮—5与胺类缔合研究 [SYS_TAG] => 3 [format_title_cn_issn_pub_year] => bf136e8a0e597c4d486b5fe7560ba9c8-1220432458 [hb_type] => 2 [jl_publication_cn] => 高等学校化学学报 [jl_country] => 中国 [jl_keyword_cn] => 萃取剂,螯合萃取剂,hpmbp,缔合效应, [jl_clc] => o65262 [author_in] => [Yang, Y.-H] Department of Chemistry, Shandong University, Jinan 250100, China@@@[ Song, Q.-S] Department of Chemistry, Shandong University, Jinan 250100, China@@@[ Tian, X] Department of Chemistry, Shandong University, Jinan 250100, China@@@[ Sun, S.-X] Department of Chemistry, Shandong University, Jinan 250100, China@@@[ Xue, S.-Y] Department of Chemistry, Normal College, Qingdao University, Qingdao 266071, China [company_id] => 0,43,169 [sys_subject_sort] => 0,0 [college_parent_id] => 43,169 [company_test] => Array,Array [author_id] => [author_test] => Array ( ) [sys_author_id_arr] => [jl_publication_cn_publication_en] => 高等学校化学学报 [jl_keyword_cn_keyword_en] => 萃取剂,hpmbp,缔合效应,螯合萃取剂 [hb_batch] => grant_no [cite_wos] => 0 [publication_en] => CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE [check_3Y] => 0 [language] => Chinese [delivery_No] => YU597 [cauthor_ad] => [Sun, SX]Shandong Univ, Dept Chem, Jinan 250100, Peoples R China. [format_title] => c452d66be4e37e63d08e4c025f96ae74-1657653679 [author_fn] => Yang, YH; Song, QS; Tian, X; Sun, SX [cite_wanfang] => 9 [format_title_en_issn_pub_year] => 97ee7a2ae5856b57ee52de75afbff9441026439922 [datebase] => Scopus [format_scopus_No] => 8eb8566e332a65e9842a401dd29b8154-142691284 [publication_29] => CHEM J CHINESE U [end_page] => 26 [abstract_en] => Studies on association effect of HPMBP and different-amine extractants (N1923, DOA, TOA) in benzene and association constents of HPMBP and TOA in different diluents were carried out, The association compounds of TOA and amine extractants exist widely, which were associated through hydrogen bond into 1 : 1 compounds. The order of association ability (TOA>DOA>N1923) was consistent to their extraction abilities. Therefore, in different diluents, the association order of HPMBP and TOA was toluene>cyclohexane>n-hexane>benzene. [article_dt] => Article [publication_type] => J [begin_page] => 24 [author_en] => Yang, YH; Song, QS; Tian, X; Sun, SX [volume] => 19 [publisher] => HIGHER EDUCATION PRESS [get_data] => 2018-08-29 [keyword_en] => 1-phenyl-3-methyl-4-benzoylpyrazolone-5; association effect; amine [page] => 24-26 [format_publication_cn] => 112be9cb2f30361719ed2bc572ba4a22192440272 [publication_iso] => Chem. J. Chin. Univ.-Chin. [format_title_en_publication_en_pub_year] => 0717fe615c78d474904c73e56ebe7d42-1831210559 [format_title_en] => f803465450b7eb17c5df3b7aa05c8022-236797120 [publisher_city] => BEIJING [pub_date] => JAN [cauthor_order] => 4 [hx_id] => 2378,2371 [reference_No] => 8 [format_issn_issue_page_pub_year] => a136a45aa810e2eaad46547aac702e5b-1816732792 [cite_awos] => 0 [wos_No] => WOS:000071733800006 [classification_pub] => KTHPD [format_wos_No] => 9d670abb67516149e0e378217f1cd6fd-1409777967 [wos_sub] => Chemistry, Multidisciplinary [research_area] => Chemistry [cauthor_back] => Sun, SX [check_180] => 0 [publisher_ad] => SHATANHOU ST 55, BEIJING 100009, PEOPLES R CHINA [standard_in] => Department of Chemistry, Shandong University, Jinan 250100, China; Department of Chemistry, Normal College, Qingdao University, Qingdao 266071, China [scopus_No] => 2-s2.0-3142630486 [title_en] => Studies on the association of HPMBP with some amine extractants [format_publication_en] => 4eabdd9afe3fe566a165b6e1c3e0dbbd-130083487 [jl_language] => chinese [jl_article_dt] => 期刊论文 [jl_publication_en] => chemicaljournalofchineseuniversitieschinese [sys_author_jg_last_arr] => 中国 [jl_company_test] => uircu0,unameuu5316u5b66u4e0eu5316u5de5u5b66u9662,uparentidu43,uorgidu43,ulevelu1 [jl_keyword_en] => associationeffect,amine,1phenyl3methyl4benzoylpyrazolone5 [sys_author_in_last_arr] => china [jl_publisher] => highereducationpress [sys_author_id] => [id] => tAo0vmUBFjIhTVEbSvUX [tags] => 0 ) [19] => Array ( [issn] => 0251-0790 [delivery_No] => 160YW [batch2] => 1,2,6 [hb_batch] => 3241 [tag] => 0 [author_en] => Lu, XH; Wang, YX; Liu, CB [abstract_en] => The mechanism of singlet germylene and formaldehyde\'s cycloaddition reaction heve been studied by using ab initio method. We obtained the intermediate complex and transition state of this reaction, and then discussed the mechanism of the reaction, On the basis of ab initio and with the statistical thermodynamics method and transition-state theory we have calculated the reaction\'s change of thermodynamic functions and the quality of kinetic properties at different temperatures. The results show this reaction proceeds with two steps: (1) germylene and formaldehyde form an intermediate complex, which is a kind of exothermal reaction with no barrier; (2) the isomerized intermediate complex becomes the product, which after being corrected by zero-point energies, the barrier of reaction is 69. 6 kJ/mol(MP2/3-21G//3-21G), On account for dynamics and thermodynamies, it is found that the reaction will not only have the larger sponlaneous tendency and equilibrum constants, but also the quicker reaction rate in the range of 400 K similar to 500 K. [publication_type] => J [keyword_plu] => GERMANIUM; CHEMISTRY [author_in] => [Lu, X.-H] Chem. Dept., Jinan Univ., Jinan 250002, China@@@[ Wang, Y.-X] Institute of Chem., Shandong Univ., Jinan 250100, China@@@[ Liu, C.-B] Institute of Chem., Shandong Univ., Jinan 250100, China [publisher_city] => BEIJING [cauthor_back] => Lu, XH [get_data] => 2018-08-29 [format_title_en_publication_en_pub_year] => 29fc626aca705d44e2062abe1888eb77-481557582 [begin_page] => 2001 [cite_wos] => 6 [check_3Y] => 0 [cite_awos] => 7 [from_id] => 76,80,73,85 [cauthor_ad] => [Lu, XH]Jinan Univ, Dept Chem, Jinan 250002, Peoples R China. [school_id] => 117 [cauthor_order] => 1 [research_area] => Chemistry [sys_level_num] => 1_7 [publisher] => HIGHER EDUCATION PRESS [sys_jg_type] => 5 [format_issn_issue_page_pub_year] => 4d246ec25433c6c0c88698234c841f7b-1564822374 [title_en] => Theoretical study on the cycloaddition reaction of germylene and formaldehyde [publication_29] => CHEM J CHINESE U [author_fn] => Lu, XH; Wang, YX; Liu, CB [pub_year] => 1998 [publisher_ad] => SHATANHOU ST 55, BEIJING 100009, PEOPLES R CHINA [check_180] => 0 [keyword_en] => germylene; cycloaddition reaction; ab initio calculation; thermodynamic; and kinetic properties [end_page] => 2004 [pub_date] => DEC [pages] => 4 [format_wos_No] => 8924a685a85252e2bf39f1cb6924471b395002012 [hints] => 5 [volume] => 19 [language] => Chinese [source_type] => 351 [issue] => 12 [reference_No] => 11 [batch] => 3243,3241,3254,3252 [publication_en] => CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE [hx_id] => 2378,2371 [sys_update_time] => 2018-09-05 15:29:30 [format_title_en_issn_pub_year] => ec910f0aa1b24dbff793b9a4346df569-1963805958 [publication_iso] => Chem. J. Chin. Univ.-Chin. [article_id] => 1805,334281,202868,498070 [wos_sub] => Chemistry, Multidisciplinary [SYS_TAG] => 3 [wos_No] => WOS:000078261800028 [page] => 2001-2004 [hb_type] => 2 [article_dt] => Article [jl_language] => chinese [jl_article_dt] => 期刊论文 [jl_publication_en] => chemicaljournalofchineseuniversitieschinese [jl_country] => 中国 [jl_keyword_en] => andkineticproperties,thermodynamic,germylene,cycloadditionreaction,abinitiocalculation [jl_publisher] => highereducationpress [author_jg] => [卢秀慧]济南大学化学系,中国.@@@[王沂轩]山东大学化学学院,中国 [keyword_cn] => 锗烯;环加成反应;从头算;热力学;动力学;甲醛; [format_title] => a1df49775de7306cb10d59b3d0d22de7468947834 [cite_wanfang] => 9 [clc] => O621.146 O623.511 [title_cn] => 锗烯与甲醛环加成反应的理论研究 [format_publication_cn] => 112be9cb2f30361719ed2bc572ba4a22192440272 [publication_cn] => 高等学校化学学报 [format_title_en] => e72002ef3597f5a673b79f67447c434f-2027927896 [CSSN] => 22-1131/06 [abstract_cn] => 用从头算方法研究了单重态锗烯与甲醛环加成反应的机理,找到了反应的中间配合物和过渡态,并讨论了反应机理。在从头算的基础上,用统计热力学方法和过渡态理论计算了该反应在不同温度下的热力学函数的变化和动力学性质,结果表明,此反应由两步组成:(1)锗烯与甲醛反应生成了一中间配合物,是一无势垒的放热反应;(2)中间配合物异构化得到产物锗杂环氧甲烷,此步势垒经零点能校正后只有69.6kJ/mol(MP2/3-2 [sys_priority_field] => 76 [author_cn] => 卢秀慧[1];王沂轩[2] [format_publication_en] => 4eabdd9afe3fe566a165b6e1c3e0dbbd-130083487 [jl_publication_cn] => 高等学校化学学报 [jl_keyword_cn] => 锗烯,环加成反应,从头算,热力学和动力学性质 [jl_clc] => o641 [company_id] => 43,169 [author_id] => 24397,24325 [author_test] => Array ( [0] => Array ( [sure] => 0 [irmagnum] => 0 [u_index] => 2 [name] => 王月霞 [irtag] => 7 [t_index] => 0 [person_id] => 24397 ) [1] => Array ( [sure] => 0 [irmagnum] => 0 [u_index] => 2 [name] => 王延相 [irtag] => 7 [t_index] => 0 [person_id] => 24325 ) ) [sys_author_id_arr] => [jl_publication_cn_publication_en] => chemicaljournalofchineseuniversitieschinese,高等学校化学学报 [jl_keyword_cn_keyword_en] => 锗烯,环加成反应,andkineticproperties,cycloadditionreaction,从头算,热力学和动力学性质,germylene,abinitiocalculation,thermodynamic [datebase] => Scopus [format_scopus_No] => bb2010568f19521f73bf367e1e246a011163567678 [cite_scopus] => 1 [classification_pub] => KTHPD [uri] => http://lib.cqvip.com/qk/90335X/199812/3351199.html [standard_in] => Chem. Dept., Jinan Univ., Jinan 250002, China; Institute of Chem., Shandong Univ., Jinan 250100, China [scopus_No] => 2-s2.0-2842536854 [format_title_cn_publication_cn_pub_year] => 6194d09e67bdd084c3c51595c92ca4f11118093097 [format_title_cn_issn_pub_year] => 1fa661a204fd4462c62470cec2a2effb-587540464 [jl_author_test] => unameuu738bu6708u971e,uirtstag0,uuindex2,usureu0,unameuu738bu5ef6u76f8,utindex0,uirtag7,uirtypical1,uirinspecttag0,uirauthortype0,upersonid24325,upersonid24397 [sys_author_jg_last_arr] => 250100 [sys_author_in_last_arr] => china [sys_author_id] => [sys_subject_sort] => 0,0 [college_parent_id] => 43,169 [company_test] => Array,Array [id] => 2AifvWUBFjIhTVEbUuEV [tags] => 0 ) ) 1-->
141. 部分水解聚丙烯酰胺/柠檬酸铝胶态分散凝胶体系的剪切稠化现象 EI SCOPUS SCIE

作者:侯万国,朱维群,刘尚营,孙德军,盛永刚

作者机构:[侯万国,朱维群,刘尚营,孙德军,盛永刚]山东大学胶体与界面化学教育部重点实验室!济南,250100,山东大学胶体与界面化学教育部重点实验室!济南,250100,山东大学胶体与界面化学教育部重点实验室!济南,250100,山东大学胶体与界面化学教育部重点实验室!济南,250100,山东大学胶体与界面化学教育部重点实验室!济南,250100

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1999,Vol.20,Issue.12,1948-1950

WOS被引数:6

资源类型:期刊论文

WOS:000084320500028

142. ~1 HNMR及Raman光谱法研究十二烷基甜菜碱缔合体系的微观结构 SCIE

作者:李英,李干佐,郝树萱,李丽霞

作者机构:[李英,李干佐,郝树萱,李丽霞]山东大学胶体与界面化学研究所,山东大学实验中心

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1999,Vol.20,Issue.3,97-100

WOS被引数:1

资源类型:期刊论文

WOS:000081285900024

143. Mg—Fe—LDHs纳米颗粒的合成及其阴离子交换容量的研究 EI SCOPUS SCIE

作者:苏延磊;侯万国

作者机构:[苏延磊;侯万国]山东大学,中国

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1999,Vol.20,Issue.7,1015-1016

WOS被引数:23

资源类型:期刊论文

WOS:000081746300004

144. 中性介质中PbTiO3粉末的水热合成与表征 SCOPUS SCIE

作者:陈代荣[1];徐如人[2]

作者机构:[陈代荣]山东大学化学系,中国.;[徐如人]吉林大学化学系,中国

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1999,Vol.20,Issue.11,1685-1687

WOS被引数:1

资源类型:期刊论文

WOS:000083723600006

145. 二氯硅烯与乙烯和甲醛环加成反应机理的理论研究 EI SCOPUS SCIE

作者:卢秀慧,王沂轩,刘成卜

作者机构:[卢秀慧,王沂轩,刘成卜]济南大学化学系,山东大学化学院

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1999,Vol.20,Issue.4,119-122

WOS被引数:10

资源类型:期刊论文

WOS:000079767600029

146. 过渡金属和硅烯配体相互作用的理论研究(Ⅰ)——MSiH_2~+的从头算研究 SCOPUS SCIE

作者:李吉海,冯圣玉,高建军,刘少杰

作者机构:[李吉海,冯圣玉,高建军,刘少杰]山东大学化学院!济南,250100,山东大学化学院!济南,250100,山东大学化学院!济南,250100,山东大学化学院!济南,250100

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1999,Vol.20,Issue.12,1906-1909

WOS被引数:1

资源类型:期刊论文

WOS:000084320500019

147. 离子对生成反应的LCAC-SW量子散射理论研究 EI SCOPUS SCIE

作者:马万勇,蔡政亭,冯大成,邓从豪

作者机构:[马万勇,蔡政亭,冯大成,邓从豪]山东大学理论化学研究所,山东轻工业学院化工系

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1999,Vol.20,Issue.5,138-140

WOS被引数:2

资源类型:期刊论文

WOS:000080428600031

148. 槲皮素-β-环糊精包合物的研究 SCIE

作者:邵伟;王金山;王春香;米广太;王大庆

作者机构:山东医科大学药学系,济南,250012;山东师范大学,济南,250014

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1998,Vol.19,Issue.7,1101-1103

WOS被引数:3

资源类型:期刊论文

WOS:000074925100022

149. 水在石墨(0001)面簇模型桥位上吸附的量子化学研究 SCOPUS SCIE

作者:傅爱萍;冯大诚;邓从豪

作者机构:山东大学理论化学研究室,济南,250100

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1998,Vol.19,Issue.5,792-795

WOS被引数:2

资源类型:期刊论文

WOS:000075179300030

150. 添加剂对非离子十二烷基聚氧乙烯聚氧丙烯醚浊点的影响 SCIE

作者:李英;李干佐

作者机构:[李英;李干佐]山东大学胶体和界面化学开放实验室,中国

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1998,Vol.19,Issue.9,1457-1461

WOS被引数:6

资源类型:期刊论文

WOS:000075990200025

151. HPXF(X=Li,Na)的构型及反应性能的从头算研究 SCOPUS SCIE

作者:卢秀慧;王沂轩;邓从豪

作者机构:济南大学化学系,济南,250002;山东大学化学院,济南,250100

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1998,Vol.19,Issue.4,617-621

资源类型:期刊论文

WOS:000073169500032

152. 荧光和动态光散射方法研究两性表面活性剂胶束的聚集和相互作用 SCOPUS SCIE

作者:李方;李干佐;汪汉卿;安英丽

作者机构:山东大学胶体与界面化学开放实验室,济南,250100;中国科学院兰州化学物理研究所,兰州,730000;南开大学吸附与分离功能高分子材料国家重点实验室,天津,300071

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1998,Vol.19,Issue.7,1117-1120

WOS被引数:6

资源类型:期刊论文

WOS:000074925100026

153. 电解质和阳离子表面活性剂对MMH/粘土体系胶体性能的影响 SCOPUS SCIE

作者:孙德军;侯万国

作者机构:[孙德军;侯万国]山东大学胶体与界面化学研究所胶体与界面化学开放研究实验室,中国

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1998,Vol.19,Issue.2,252-256

WOS被引数:6

资源类型:期刊论文

WOS:000072402000023

154. 烷基对取代锂氟类硅烯R2SiLiF的构型和热稳定性的影响 SCOPUS SCIE

作者:冯大诚;冯圣玉

作者机构:[冯大诚;冯圣玉]山东大学理论化学研究室,中国

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1998,Vol.19,Issue.3,451-454

WOS被引数:14

资源类型:期刊论文

WOS:000072677800029

155. 乙烯醇锂的从头算研究 SCOPUS SCIE

作者:王义贵;孙昌俊

作者机构:[王义贵;孙昌俊]山东大学理论化学研究室,中国

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1998,Vol.19,Issue.3,424-428

WOS被引数:1

资源类型:期刊论文

WOS:000072677800023

156. H2O在Cu(100)表面吸附的从头算研究 SCOPUS SCIE

作者:傅爱萍;冯大诚

作者机构:[傅爱萍;冯大诚]山东大学理论化学研究室,中国

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1998,Vol.19,Issue.10,1654-1658

WOS被引数:1

资源类型:期刊论文

WOS:000078261500031

157. 十二烷基甜菜碱与聚乙烯吡咯烷酮相互作用的研究 SCOPUS SCIE

作者:赤京诚[1];李干佐[2];梁芳珍[1];刘树海[1];任建成[1];鲁绍芬[1];汪汉卿[3];

作者机构:[赤京诚;梁芳珍;刘树海;任建成;鲁绍芬]山东师范大学表面与界面化学实验室,中国.;[李干佐]山东大学胶体与界面化学研究所,中国.;[汪汉卿]中国科学院兰州化学物理研究所,中国

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1998,Vol.19,Issue.1,111-115

WOS被引数:7

资源类型:期刊论文

WOS:000071733800028

158. 有机金属钯硅碳烷树状分子液晶配合物研究 SCOPUS SCIE

作者:张其震[1];孙继润[1];王大庆[2];盛昕[1];殷晓颍[1];赵晓光[3];李光[3];

作者机构:[张其震;孙继润;盛昕;殷晓颍]山东大学化学系,中国.;[王大庆]山东师范大学测试中心,中国.;[赵晓光;李光]中国科学院长春应用化学研究所,中国

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1998,Vol.19,Issue.5,827-829

WOS被引数:13

资源类型:期刊论文

WOS:000075179300040

159. 1—苯基—3—甲基—4—苯甲酰基吡唑啉酮—5与胺类缔合研究 SCOPUS SCIE

作者:杨永会;薛淑云

作者机构:[杨永会;薛淑云]山东大学化学院,中国

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1998,Vol.19,Issue.1,24-26

资源类型:期刊论文

WOS:000071733800006

160. 锗烯与甲醛环加成反应的理论研究 SCOPUS SCIE

作者:卢秀慧[1];王沂轩[2]

作者机构:[卢秀慧]济南大学化学系,中国.;[王沂轩]山东大学化学学院,中国

来源:高等学校化学学报,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1998,Vol.19,Issue.12,2001-2004

WOS被引数:6

资源类型:期刊论文

WOS:000078261800028

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