Synthesis and photophysics of a linear non-covalently linked porphyrin-fullerene dyad

被引：78

作者：

Wilson, SR ^{[1
]}

MacMahon, S

Tat, FT

Jarowski, PD

Schuster, DI

机构：

[1] NYU, Dept Chem, New York, NY 10003 USA

[2] Uludag Univ, Dept Chem, TR-16059 Bursa, Turkey

来源：

CHEMICAL COMMUNICATIONS | 2003年 / 02期

关键词：

D O I：

10.1039/b208013c

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The synthesis and characterization of a new pyridinofullerene ligand capable of forming axially symmetric complexes with ZnTPP is reported; molecular modelling studies, H-1 NMR, UV-Vis spectroscopy and fluorescence quenching data support formation of a strong complex between the new ligand and ZnTPP.

引用

页码：226 / 227

页数：2

共 24 条

[1]

Armaroli N, 1998, CHEM-EUR J, V4, P406, DOI 10.1002/(SICI)1521-3765(19980310)4:3<406::AID-CHEM406>3.3.CO

[2]

2-R

[3] A new pyridyl-substituted methanofullerene derivative.: Photophysics, electrochemistry and self-assembly with zinc(II) meso-tetraphenylporphyrin (ZnTPP) [J].