OCTAPHYRIN-(1.0.1.0.1.0.1.0)

被引:102
作者
BRORING, M
JENDRNY, J
ZANDER, L
SCHMICKLER, H
LEX, J
WU, YD
NENDEL, M
CHEN, JG
PLATTNER, DA
HOUK, KN
VOGEL, E
机构
[1] UNIV COLOGNE, INST ORGAN CHEM, D-50939 COLOGNE, GERMANY
[2] HONG KONG UNIV SCI & TECHNOL, DEPT CHEM, CLEARWATER BAY, HONG KONG
[3] UNIV CALIF LOS ANGELES, DEPT CHEM & BIOCHEM, LOS ANGELES, CA 90095 USA
关键词
MACROCYCLES; OCTAPHYRIN; PORPHYRINOIDS;
D O I
10.1002/anie.199525151
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The formal exchange of the pyrrole units of porphyrin by bipyrrole units provides the title compound 1. The hexadecaethyl derivative of 1 is the only isolable product of a MacDonald condensation of tetrapyrrolic as well as of dipyrrolic components. The new cyclooctapyrrole adopts a figure‐eight conformation in the solid state as well as in solution. (Figure Presented.) Copyright © 1995 by VCH Verlagsgesellschaft mbH, Germany
引用
收藏
页码:2515 / 2517
页数:3
相关论文
共 35 条
[11]   SYNTHESIS OF A FOURFOLD ENLARGED PORPHYRIN WITH AN EXTREMELY LARGE, DIAMAGNETIC RING-CURRENT EFFECT [J].
GOSMANN, M ;
FRANCK, B .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1986, 25 (12) :1100-1101
[12]  
Gosmann M, 1986, ANGEW CHEM, V98, P1107
[13]  
GOSSAUER A, 1983, B SOC CHIM BELG, V92, P793
[14]  
GOSSAUER A, 1984, CHIMIA, V38, P45
[15]  
HOFER O, COMMUNICATION
[16]  
K?nig H., 1990, ANGEW CHEM, V102, P1437
[17]   NOVEL PORPHYRINOIDS .6. BIOMIMETIC SYNTHESIS OF AN OCTAVINYLOGOUS PORPHYRIN WITH AN AROMATIC [34]ANNULENE SYSTEM [J].
KNUBEL, G ;
FRANCK, B .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1988, 27 (09) :1170-1172
[18]  
KNUBEL G, 1988, ANGEW CHEM, V100, P1203
[19]   NOVEL PORPHYRINOIDS .10. SYNTHESIS OF A BISVINYLOGOUS OCTAETHYLPORPHYRIN [J].
KONIG, H ;
EICKMEIER, C ;
MOLLER, M ;
RODEWALD, U ;
FRANCK, B .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1990, 29 (12) :1393-1395
[20]   THE SYNTHESIS OF A NEW 22 PI-ELECTRON MACROCYCLE - PENTAPHYRIN [J].
REXHAUSEN, H ;
GOSSAUER, A .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1983, (06) :275-275