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Carbene-induced synthesis of the first borironium cations using the [(η5-C5Me5)Fe(CO)2]− anion as an unlikely leaving group†
Holger Braunschweig,Rian D. Dewhurst,Katharina Ferkinghoff
Chemical Communications Pub Date : 10/29/2015 00:00:00 , DOI:10.1039/C5CC07503C
Abstract

Reaction of N-heterocyclic carbenes with ferroborirene complex [{(η5-C5Me5)Fe(CO)2}{BC2(SiMe3)2}] results in heterolytic Fe–B bond cleavage, yielding borironium ions, a new class of boron-containing heterocycles. The reaction rests on the surprising ability of the reactive [(η5-C5Me5)Fe(CO)2] anion to act as a leaving group. The properties of these species were investigated by multinuclear NMR spectroscopy, as well as single-crystal X-ray diffraction.

Graphical abstract: Carbene-induced synthesis of the first borironium cations using the [(η5-C5Me5)Fe(CO)2]− anion as an unlikely leaving group
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