STEREOCHEMICAL AND THERMOCHEMICAL STUDY OF 1,2 ALKYL SHIFTS FROM A CARBONYL GROUP TO A METAL ATOM

被引：21

作者：

EGGLESTONE, D ^{[1
]}

BAIRD, MC ^{[1
]}

机构：

[1] QUEENS UNIV,DEPT CHEM,KINGSTON,ONTARIO,CANADA

来源：

JOURNAL OF ORGANOMETALLIC CHEMISTRY | 1976年 / 113卷 / 02期

关键词：

D O I：

10.1016/S0022-328X(00)96139-4

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

引用

页码：C25 / C29

页数：5

共 16 条

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[2] ADDITION REACTIONS OF TRIS(TRIPHENYLPHOSPHINE)CHLORORHODIUM(I) - HYDRIDO- ALKYL AND ACYL COMPLEXES - CARBON MONOXIDE INSERTION AND DECARBONYLATION REACTIONS
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[3] DIRECT DETERMINATION OF ENTHALPY CHANGE FOR MIGRATION OF PARA-SUBSTITUTED BENZYL AND TRIFLUOROMETHYL GROUPS IN COORDINATIVELY UNSATURATED IRIDIUM(III) ACYL COMPLEXES
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[4] STEREOCHEMISTRY OF REACTIONS AT CARBON-TRANSITION METAL SIGMA BONDS - (CH3)3CCHDCHDFE(CO)2C5H5
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1974, 96 (09) : 2814 - 2825
[5] NUCLEAR MAGNETIC RESONANCE STUDIES ON METAL COMPLEXES .V. DIMETHYLPHENYLPHOSPHINE AND DIMETHYLPHENYLARSINE COMPLEXES OF RHODIUM(3)
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[6] PREPARATION OF RHODIUM(3) HALIDE COMPLEXES WITH TERTIARY PHOSPHINES + TERTIARY ARSINES
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[J]. JOURNAL OF THE CHEMICAL SOCIETY, 1964, (AUG): : 2508 - &
[7] Cotton F.A., 1973, INORG CHIM ACTA, V7, P161
[8] STEREOCHEMISTRY OF FORMATION AND REACTIONS OF CARBONYLDICHLORO-(THREO-ALPHA-BETA-DIDEUTERIOPHENETHYL)BIS(TRIPHENYLPHOSPHINE)-RHODIUM AND CARBONYLDICHLORO-(THREO-ALPHA-BETA-DIDEUTERIOPHENETHYL)BIS(TRIPHENYLPHOSPHINE-IRIDIUM COMPLEXES
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BAIRD, MC
[J]. JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1975, (09): : 774 - 779
[9] ELECTROPHILIC CLEAVAGE OF CARBON-ZIRCONIUM(IV) BOND - COMPARISON AND CONTRAST WITH OTHER TRANSITION-METAL ALKYL SYSTEMS
LABINGER, JA
HART, DW
SEIBERT, WE
SCHWARTZ, J
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1975, 97 (13) : 3851 - 3852
[10] P-31 NUCLEAR MAGNETIC-RESONANCE SPECTRA OF SOME COMPLEXES OF TYPE MER-[MX3L3] (M = RH OR IR - X = HALOGEN - L = TERTIARY PHOSPHINE)
MANN, BE
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SHAW, BL
[J]. JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1972, (06): : 704 - &

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