ACTIVATION AND DESULFURIZATION OF THIOPHENE AND BENZOTHIOPHENE BY IRON CARBONYLS

被引：163

作者：

OGILVY, AE ^{[1
]}

DRAGANJAC, M ^{[1
]}

RAUCHFUSS, TB ^{[1
]}

WILSON, SR ^{[1
]}

机构：

[1] UNIV ILLINOIS,SCH CHEM SCI,URBANA,IL 61801

来源：

ORGANOMETALLICS | 1988年 / 7卷 / 05期

关键词：

ORGANIC COMPOUNDS - Desulfurization;

D O I：

10.1021/om00095a024

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The synthesis, reactivity, and structure of thiaferroles Fe//2(R//2C//4H//2S)(CO)//6 and benzothiaferroles Fe//2(C//8H//6S)(CO)//6(1) are surveyed. These compounds are prepared by the reaction of Fe//3(CO)//1//2 with thiophenes and benzothiophenes. The benzothiaferrole 1 undergoes oxidative demetalation to give the cyclic thioester thiocoumarin C//9H//6OS. Solutions of 1 are stable at 185 degree C under N//2; at 160 degree C, high pressures of CO convert 1 into Fe(CO)//5 and benzothiophene, i. e. reductive elimination. Solutions of 1 react with H//2 to give primarily ethylbenzene together with 2-ethylbenzenethiol and bis(2-ethylphenyl) sulfide.

引用

页码：1171 / 1177

页数：7