Indenopyrans - synthesis and photoluminescence properties

被引:5
作者
Diac, Andreea Petronela [1 ]
Tepes, Ana-Maria [1 ]
Soran, Albert [1 ]
Grosu, Ion [1 ]
Terec, Anamaria [1 ]
Roncali, Jean [2 ]
Bogdan, Elena [1 ]
机构
[1] Univ Babes Bolyai, Ctr Supramol Organ & Organometall Chem CSOOMC Clu, 11 Arany Janos, Cluj Napoca 400028, Romania
[2] Univ Angers, CNRS Moltech Anjou, Grp Linear Conjugated Syst, 2 Blvd Lavoisier, F-49045 Angers, France
关键词
indenopyran-3-ones; organic fluorophores; pyrones; solid-state emission spectra; solution emission spectra; UV-vis spectra; DIELS-ALDER REACTIONS; HYDROGEN-BOND; 6H-1,3,4-OXADIAZIN-6-ONES 4,5-DIAZA-ALPHA-PYRONES; ELECTROLUMINESCENT DEVICES; BIOLOGICAL EVALUATION; FLUORESCENT DYES; INDOTECAN LMP400; RED; CYCLOADDITIONS; PYRAN;
D O I
10.3762/bjoc.12.81
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
New indeno[1,2-c]pyran-3-ones bearing different substituents at the pyran moiety were synthesized and their photophysical properties were investigated. In solution all compounds were found to be blue emitters and the trans isomers exhibited significantly higher fluorescence quantum yields (relative to 9,10-diphenylanthracene) as compared to the corresponding cis isomers. The solid-state fluorescence spectra revealed an important red shift of lambda(max) due to intermolecular interactions in the lattice, along with an emission-band broadening, as compared to the solution fluorescence spectra.
引用
收藏
页码:825 / 834
页数:10
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