REACTIVITY OF IRON(II) NONCLASSICAL HYDRIDES WITH ALKYNES

被引：26

作者：

ALBERTIN, G

ANTONIUTTI, S

DELMINISTRO, E

BORDIGNON, E

机构：

来源：

JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS | 1992年 / 22期

关键词：

D O I：

10.1039/dt9920003203

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The complex [FeH(eta2-H2){PPh(OEt)2}4]BPh4 reacts with terminal alkynes HC=CR (R = p-tolyl, Bu(t) or SiMe3) to give the corresponding alkenes H2C=CHR and the butenynyl derivative [Fe(eta3-RC3CHR){PPh(OEt)2}4]+. In contrast, the related complex [FeH(eta2-H2){P(OEt)3}4]BPh4 reacts with terminal alkynes to yield alkenes and sigma-acetylide [Fe(C=CR){P(OEt)3}5]+ derivatives. Activated alkynes such as HC=CCO2Me and MeO2CC=CCO2Me react with both [FeH(eta2-H2)L4]BPh4 [L = P(OEt)3 or PPh(OEt)2] to give vinyl derivatives [Fe{CH=CH(CO2Me)}L4]+ and [Fe{C(CO2Me)=CH(CO2Me)}L4]+, respectively. The characterization of the complexes by IR, H-1, C-13 and P-31 NMR spectroscopy is discussed.

引用

页码：3203 / 3208

页数：6

共 36 条

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