O-H BOND ACTIVATION IN THE GAS-PHASE - THE REACTIONS OF WATER AND METHANOL WITH [FECH3]+
被引:42
作者:
BLUM, O
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机构:TECH UNIV BERLIN,INST ORGAN CHEM,STR DES 17 JUNI 135,W-1000 BERLIN 12,GERMANY
BLUM, O
STOCKIGT, D
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机构:TECH UNIV BERLIN,INST ORGAN CHEM,STR DES 17 JUNI 135,W-1000 BERLIN 12,GERMANY
STOCKIGT, D
SCHRODER, D
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机构:TECH UNIV BERLIN,INST ORGAN CHEM,STR DES 17 JUNI 135,W-1000 BERLIN 12,GERMANY
SCHRODER, D
SCHWARZ, H
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机构:TECH UNIV BERLIN,INST ORGAN CHEM,STR DES 17 JUNI 135,W-1000 BERLIN 12,GERMANY
SCHWARZ, H
机构:
[1] TECH UNIV BERLIN,INST ORGAN CHEM,STR DES 17 JUNI 135,W-1000 BERLIN 12,GERMANY
[2] WEIZMANN INST SCI,DEPT ORGAN CHEM,IL-76100 REHOVOT,ISRAEL
来源:
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH
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1992年
/
31卷
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05期
关键词:
D O I:
10.1002/anie.199206031
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
That even cationic fragments of late transition metals can activate O-H bonds in the gas phase is shown by studies of reaction (a) (R = H, CH3), in which a large deuterium isotope effect can be observed (k(H)/k(D) > 15). An oxidative addition mechanism is proposed for this transformation; the first step is the coordination of the dipolar H2O or CH3OH molecule to the [FeCH3]+ fragment, while the rate-determining step is the transfer of the H atom of the ROH group to the Fe atom.