Spectroscopic, redox and photophysical properties of push-pull fluoroarylporphyrins

被引:22
作者
Sen, A [1 ]
Krishnan, V
机构
[1] Indian Inst Sci, Dept Inorgan & Phys Chem, Bangalore 560012, Karnataka, India
[2] Jawaharlal Nehru Ctr Adv Sci Res, Bangalore 560064, Karnataka, India
来源
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS | 1997年 / 93卷 / 24期
关键词
D O I
10.1039/a704663d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Novel fluoroarylporphyrins bearing electron donor dimethylamino groups in the meso-aryl positions and an electron acceptor nitro group on one of the pyrrole carbons exhibit significant solvent dependent fluorescence spectra and time-resolved emission properties. These effects are suggestive of intramolecular charge transfer (ICT) in the singlet excited state of these porphyrins. Electrochemical redox behaviour of these porphyrins showed the presence of substantial donor-acceptor interactions in the nitro-amino porphyrins.
引用
收藏
页码:4281 / 4288
页数:8
相关论文
共 43 条
[41]   PUSH-PULL PORPHYRINS AS NONLINEAR OPTICAL-MATERIALS [J].
SUSLICK, KS ;
CHEN, CT ;
MEREDITH, GR ;
CHENG, LT .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (17) :6928-6930
[42]   THE FLUORESCENCE PROPERTIES OF (2-NITRO-5,10,15,20-TETRAPHENYLPORPHYRINATO)ZINC [J].
TAKAHASHI, K ;
HASE, S ;
KOMURA, T ;
IMANAGA, H ;
OHNO, O .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1992, 65 (06) :1475-1481
[43]   A PROTON NMR-STUDY OF THE REACTIONS WITH ACID OF MESO-TETRAPHENYLPORPHYRINS WITH VARIOUS NUMBERS OF 4-DIMETHYLAMINO GROUPS [J].
WALTER, RI ;
OJADI, ECA ;
LINSCHITZ, H .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (50) :13308-13312