NOVEL PORPHYRINOIDS .10. SYNTHESIS OF A BISVINYLOGOUS OCTAETHYLPORPHYRIN

被引：35

作者：

KONIG, H

EICKMEIER, C

MOLLER, M

RODEWALD, U

FRANCK, B

机构：

[1] UNIV MUNSTER,INST ORGAN CHEM,ORLEANSRING 23,W-4400 MUNSTER,GERMANY

[2] UNIV MUNSTER,INST ANORGAN CHEM,W-4400 MUNSTER,GERMANY

来源：

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH | 1990年 / 29卷 / 12期

关键词：

D O I：

10.1002/anie.199013931

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Hans Fischer's octaethylporphyrin (OEP) is so far the best available and most investigated of all synthetic porphyrins. The bisvinylogue OEP 1 has now been synthesized in high yields in a few steps. Owing to its chemical stability, good accessibility, and hitherto most intense UV/VIS absorption for an organic dye, this is a system with wide-ranging perspectives.

引用

页码：1393 / 1395

页数：3

共 14 条

[1] PYRROMETHANES AND PORPHYRINS THEREFROM [J].

ARSENAULT, GP ;

BULLOCK, E ;

MACDONALD, SF .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1960, 82 (16) :4384-4389

[2]

BREITMEIER E, 1990, NMR SPEKTRUM STRUKTU, P53

[3] SYNTHESIS, PROPERTIES, AND CRYSTAL-STRUCTURE OF OCTAETHYLPORPHIN BIS[CIS-DICARBONYLDICHLORORHODATE(I)] [OEPH4]2+2[RHCL2(CO)2]-AND SOME NEW REACTIONS OF CO(OEP) DERIVATIVES [J].

CETINKAYA, E ;

JOHNSON, AW ;

LAPPERT, MF ;

MCLAUGHLIN, GM ;

MUIR, KW .

JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1974, (11) :1236-1243

[4]

ENGEL J, 1976, LIEBIGS ANN CHEM, P1637

[5]

Fischer H, 1929, LIEBIGS ANN CHEM, V468, P58

[6]

FRANCK B, Patent No. 3635820

[7]

GARRATT PJ, 1986, AROMATICITY, P52

[8]

GOSMANN M, 1990, LIEBIGS ANN CHEM, P163

[9] 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

[10]

Gosmann M, 1986, ANGEW CHEM, V98, P1107

← 1 2 →