Oxygen-atom transfer to a nucleophilic molybdenum complex

被引：0

作者：

Askari, Mohammad S. ^{[1
]}

Ottenwaelder, Xavier ^{[1
]}

机构：

[1] Concordia Univ, Dept Chem & Biochem, Montreal, PQ H4B 1R6, Canada

来源：

DALTON TRANSACTIONS | 2010年 / 39卷 / 10期

基金：

加拿大自然科学与工程研究理事会;

关键词：

EFFECTIVE CORE POTENTIALS; NONHEME IRON CATALYSTS; MOLECULAR CALCULATIONS; STRUCTURAL DYNAMICS; FLUXIONAL BEHAVIOR; OLEFIN EPOXIDATION; INTERMETAL OXYGEN; CYCLOPENTADIENYL; MECHANISM; OXO;

D O I：

10.1039/b921591c

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The reactivity of the imido-Mo(IV) species [(5-Cp)(2)Mo((NBu)-Bu-t)], 1, towards the iodine-based oxidant PhIO was investigated and yielded the m-oxodimolybdenum(V) dimer [{(eta(5)-Cp)(eta(1)-Cp)Mo((NBu)-Bu-t)}(2)O], 2. X-Ray crystallography and H-1-NMR of 2 indicate slipping of one of the eta(5)-Cp ring on each Mo center to eta(1)-Cp as the result of the coordination of the oxygen atom. DFT investigation of the OAT reaction to complex 1 revealed a transient Mo(IV)-oxo species as the most likely intermediate.

引用

页码：2644 / 2650

页数：7

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