标题：Synthesis, X-ray crystal structure and optical properties of novel 2-aryl-3-ethoxycarbonyl-4-phenylpyrido[1,2-a]benzimidazoles
作者：Chen, X.;Yang, H.;Ge, Y.;Feng, L.;Jia, J.;Wang, J.
作者机构：[Chen, X] School of Chemistry and Chemical Engineering, Shandong University Shandong, Jinan 250100, Shandong, China;[ Yang, H] School of Chemistry and 更多[Chen, X] School of Chemistry and Chemical Engineering, Shandong University Shandong, Jinan 250100, Shandong, China;[ Yang, H] School of Chemistry and Chemical Engineering, Shandong University Shandong, Jinan 250100, Shandong, China;[ Ge, Y] School of Chemistry and Chemical Engineering, Taishan Medical University Shandong, Taian 271016, China;[ Feng, L] School of Chemistry and Chemical Engineering, Shandong University Shandong, Jinan 250100, Shandong, China;[ Jia, J] School of Chemistry and Chemical Engineering, Shandong University Shandong, Jinan 250100, Shandong, China, State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100, China;[ Wang, J] School of Chemistry and Chemical Engineering, Shandong University Shandong, Jinan 250100, Shandong, China 收起 通讯作者：Jia, J
通讯作者地址：[Jia, J]Shandong Univ, Sch Chem & Chem Engn, Jinan 250100, Shandong, Peoples R China.
来源：Luminescence: The journal of biological and chemical luminescence
出版年：2012
卷：27
期：5
页码：382-389
DOI：10.1002/bio.1362
关键词：absorption;fluorescence;pyrido[1;2-a]benzimidazole;synthesis;X-ray
摘要：A series of novel 2-aryl-3-ethoxycarbonyl-4-phenylpyrido[1,2-a] benzimidazole derivatives were synthesized by the tandem reaction of 2-benzoyl benzimidazole and (Z)-ethyl 4-bromo-3-arylbut-2-enoate in the presence of potassium carbonate. The compounds were characterized using IR, ~1H-NMR, ~(13)C-NMR, HRMS and the structure of 6f was further determined by X-ray crystallography. Both absorption and fluorescence spectra characteristics of the compounds were investigated in acetonitrile and dichloromethane. The results showed that the absorption maxima of the compounds varied from 220 to 284 nm, depending on the structure of 2-aryl group. The fluorescence results revealed that these compounds exhibited blue-green fluorescence (463-475 nm) in dilute solutions and showed acceptable fluorescence quantum yields (_(PL) = 0.13-0.73) in dichloromethane.
收录类别：SCOPUS;SCIE
WOS核心被引频次：4
Scopus被引频次：3
资源类型：期刊论文
原文链接：https://www.scopus.com/inward/record.uri?eid=2-s2.0-84867232738&doi=10.1002%2fbio.1362&partnerID=40&md5=5481d52c5048a5736dbceb8fcb26a368
