The chemistry of fluorescent bodipy dyes: Versatility unsurpassed

被引:2853
作者
Ulrich, Gilles [1 ]
Ziessel, Raymond [1 ]
Harriman, Anthony [2 ]
机构
[1] Univ Strasbourg, CNRS, LCM, ECPM,UMR 7509, F-67087 Strasbourg, France
[2] Newcastle Univ, Sch Nat Sci, Mol Photon Lab, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
关键词
bodipy; dyes/pigments; energy transfer; fluorescent probes; luminescence;
D O I
10.1002/anie.200702070
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The world of organic luminophores has been confined for a long time to fairly standard biological labeling applications and to certain analytical tests. Recently, however, the field has undergone a major change of direction, driven by the dual needs to develop novel organic electronic materials and to fuel the rapidly emerging nanotechnologies. Among the many diverse fluorescent molecules, the Bodipy family, first developed as luminescent tags and laser dyes, has become a cornerstone for these new applications. The near future looks extremely bright for porphyrin's little sister. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:1184 / 1201
页数:18
相关论文
共 126 条
[61]   Synthesis and spectroscopic properties of a new 4-bora-3a,4a-diaza-s-indacene (BODIPY®) dye [J].
Kim, H ;
Burghart, A ;
Welch, MB ;
Reibenspies, J ;
Burgess, K .
CHEMICAL COMMUNICATIONS, 1999, (18) :1889-1890
[62]   Correlations of structure and rates of energy transfer for through-bond energy-transfer cassettes [J].
Kim, TG ;
Castro, JC ;
Loudet, A ;
Jiao, JGS ;
Hochstrasser, RM ;
Burgess, K ;
Topp, MR .
JOURNAL OF PHYSICAL CHEMISTRY A, 2006, 110 (01) :20-27
[63]   INVIVO LABELING OF L-TYPE CA(2+) CHANNELS BY FLUORESCENT DIHYDROPYRIDINES - EVIDENCE FOR A FUNCTIONAL, EXTRACELLULAR HEPARIN-BINDING SITE [J].
KNAUS, HG ;
MOSHAMMER, T ;
FRIEDRICH, K ;
KANG, HC ;
HAUGLAND, RP ;
GLOSSMANN, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (08) :3586-3590
[64]   Electrogenerated chemiluminescence and proton-dependent switching of fluorescence: Functionalized difluoroboradiaza-s-indacenes [J].
Kollmannsberger, M ;
Gareis, T ;
Heinl, S ;
Breu, J ;
Daub, J .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1997, 36 (12) :1333-1335
[65]   Ultrafast charge transfer in amino-substituted boron dipyrromethene dyes and its inhibition by cation complexation: A new design concept for highly sensitive fluorescent probes [J].
Kollmannsberger, M ;
Rurack, K ;
Resch-Genger, U ;
Daub, J .
JOURNAL OF PHYSICAL CHEMISTRY A, 1998, 102 (50) :10211-10220
[66]  
Kollmannsberger M., 1999, US Patent, Patent No. 6001999
[67]  
KOLLMANNSBERGER M, 1997, ANGEW CHEM, V109, P1391
[68]   A novel fluorescent probe for zinc ion based on boron dipyrromethene (BODIPY) chromophore [J].
Koutaka, H ;
Kosuge, J ;
Fukasaku, N ;
Hirano, T ;
Kikuchi, K ;
Urano, Y ;
Kojima, H ;
Nagano, T .
CHEMICAL & PHARMACEUTICAL BULLETIN, 2004, 52 (06) :700-703
[69]   Electrogenerated chemiluminescence 71.: Photophysical, electrochemical, and electrogenerated chemiluminescent properties of selected dipyrromethene-BF2 dyes [J].
Lai, RY ;
Bard, AJ .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (21) :5036-5042
[70]   Design, synthesis, and photodynamics of light-harvesting arrays comprised of a porphyrin and one, two, or eight boron-dipyrrin accessory pigments [J].
Li, FR ;
Yang, SI ;
Ciringh, YZ ;
Seth, J ;
Martin, CH ;
Singh, DL ;
Kim, DH ;
Birge, RR ;
Bocian, DF ;
Holten, D ;
Lindsey, JS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (39) :10001-10017