4.1 Article

Thiophene-fused phospholo[3,2-b]phospholes and their dichalcogenides: Synthesis and structure-photophysical properties relationships

期刊

COMPTES RENDUS CHIMIE
卷 13, 期 8-9, 页码 1082-1090

出版社

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.crci.2010.04.021

关键词

Phosphorus; Fused-ring systems; Cyclization; Conjugation; Chromophores; Fluorescence

资金

  1. Ministry of Education, Culture, Sports, Science, and Technology, Japan [17069011, 19675001, 20750029]
  2. Grants-in-Aid for Scientific Research [17069011, 20750029] Funding Source: KAKEN

向作者/读者索取更多资源

The PCl3-promoted intramolecular cascade cyclization produced a series of thiophene-fused phospholo[3,2-b]phosphole derivatives, including non-oxidized 2, dioxides 3, and disulfides 4. These derivatives exhibit significantly red-shifted absorptions and fluorescences compared with their benzene-fused analogues. Among the thiophene-fused series, the non-oxidized 2 has the highest fluorescence quantum yield of 0.95. This trend is in contrast to that observed for the benzene analogues, in which a dioxide derivative shows the most intense fluorescence. (C) 2010 Academie des sciences. Published by Elsevier Masson SAS. All rights reserved.

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