Push-Pull Amino Succinimidyl Ester Thiophene-Based Fluorescent Dyes: Synthesis and Optical Characterization

被引：22
|
作者：
Sotgiu, Giovanna [1 ]
Galeotti, Matteo [2 ]
Samori, Cristian [1 ]
Bongini, Alessandro [3 ]
Mazzanti, Andrea [4 ]
机构：
[1] Consiglio Nazl Ric CNR ISOF, I-40129 Bologna, Italy
[2] Mediteknology Srl, I-40129 Bologna, Italy
[3] Univ Bologna, Dept Chem G Ciamician, I-40122 Bologna, Italy
[4] Univ Bologna, Dept Organ Chem A Mangini, I-40136 Bologna, Italy
来源：
CHEMISTRY-A EUROPEAN JOURNAL | 2011年 / 17卷 / 28期
关键词：
dyes/pigments; fluorescent probes; oligothiophenes; singlet oxygen; sulfine; COPPER-CATALYZED AMINATION; AZO DYES; DONOR; OLIGOTHIOPHENES; CHROMOPHORES; FLUOROPHORES; BITHIOPHENE; DESIGN; BRIGHT;
D O I：
10.1002/chem.201100142
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
The design and synthesis of new fluorescent dyes with emission range at 490-650 nm are described. Their structural and electronic properties have been characterized by both experimental techniques and quantum-chemical calculations. The chromophores are donor-pi-bridge-acceptor push-pull compounds with a pi bridge of phenyl and thiophene rings and their combination. Compared with previous thiophene fluorophores, these dyes show significant redshift in the absorption and emission spectra and offer compact, red-emitting fluorophores. The dyes have amino succinimidyl active ester and can be readily conjugated to proteins, polymers and other amino-group-containing materials.
引用
收藏
页码：7947 / 7952
页数：6
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