| Literature DB >> 24864006 |
Julian Böhnke1, Holger Braunschweig, William C Ewing, Christian Hörl, Thomas Kramer, Ivo Krummenacher, Jan Mies, Alfredo Vargas.
Abstract
The complexation of two equivalents of a cyclic (alkyl)(amino)carbene (CAAC) to tetrabromodiborane, followed by reduction with four equivalents of sodium naphthalide, led to the formation of the CAAC-stabilized linear diboracumulene (CAAC)2B2. The capacity of the CAAC ligand to facilitate B2 →CAAC donation of π-electron density resulted in important differences between this species and a previously reported complex featuring a B≡B triple bond stabilized by cyclic di(amino)carbenes, including a longer B-B bond and shorter B-C bonds. Frontier orbital analysis indicated sharing of valence electrons across the entire linear C-B-B-C unit in (CAAC)2B2, which is supported by natural population analysis and cyclic voltammetry.Entities:
Keywords: boron; carbenes; cumulenes; main-group elements; multiple bonds
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Year: 2014 PMID: 24864006 DOI: 10.1002/anie.201403888
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336