Issue 66, 2018

Reactivity of a trans-[H–Mo[quadruple bond, length as m-dash]Mo–H] unit towards alkenes and alkynes: bimetallic migratory insertion, H-elimination and other reactions

Abstract

Complex [Mo2(H)2{μ-HC(NDipp)2}2(THF)2], (1·THF), reacts with C2H4 and PhCH[double bond, length as m-dash]CH2 to afford hydrido-hydrocarbyl and bis(hydrocarbyl) derivatives of the Mo[quadruple bond, length as m-dash]Mo bond. Reversible migratory insertion and β-hydrogen elimination, as well as reductive elimination and other reactions, have been uncovered. PhC[triple bond, length as m-dash]CH behaves instead as a Brönsted–Lowry acid towards the strongly basic Mo–H bonds of 1·THF.

Graphical abstract: Reactivity of a trans-[H–Mo [[quadruple bond, length as m-dash]] Mo–H] unit towards alkenes and alkynes: bimetallic migratory insertion, H-elimination and other reactions

Supplementary files

Article information

Article type
Communication
Submitted
20 jun. 2018
Accepted
21 jul. 2018
First published
24 jul. 2018

Chem. Commun., 2018,54, 9186-9189

Reactivity of a trans-[H–Mo[quadruple bond, length as m-dash]Mo–H] unit towards alkenes and alkynes: bimetallic migratory insertion, H-elimination and other reactions

M. Pérez-Jiménez, J. Campos, J. López-Serrano and E. Carmona, Chem. Commun., 2018, 54, 9186 DOI: 10.1039/C8CC04945A

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