EVIDENCE FOR CORRELATED ROTATION AND DIASTEREOISOMER DISCRIMINATION IN (ETA-4-DIENE)FE(CO)2L COMPLEXES - THE CRYSTAL AND SOLUTION STRUCTURES OF (CYCLOHEXADIENE)FE(CO)2P(ORTHO-TOLYL)3 AND (CYCLOHEPTADIENE)FE(CO)2(+)-PPH2(NEOMENTHYL)

被引：11

作者：

HOWELL, JAS

PALIN, MG

TIRVENGADUM, MC

CUNNINGHAM, D

MCARDLE, P

GOLDSCHMIDT, Z

GOTTLIEB, HE

机构：

[1] NATL UNIV IRELAND UNIV COLL GALWAY,DEPT CHEM,GALWAY,IRELAND

[2] BAR ILAN UNIV,DEPT CHEM,IL-52100 RAMAT GAN,ISRAEL

来源：

JOURNAL OF ORGANOMETALLIC CHEMISTRY | 1991年 / 413卷 / 1-3期

关键词：

D O I：

10.1016/0022-328X(91)80056-P

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The solid state structure of (cyclohexadiene)Fe(CO)2P(o-tolyl)3 reveals an exo2 conformation for the phosphine. In solution, arene ring exchange in the phosphine and exchange of phosphine between equivalent basal positions of the square pyramid occur at equal rates. In solution, (cycloheptadiene)Fe(CO)2(+)-PPh2(neomenthyl) exhibits a diastereoselection between basal isomers, and crystallizes as a single diastereoisomer which has been structurally characterized.

引用

页码：269 / 286

页数：18

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