Carbon insertion into borane clusters via nucleophilic addition reactions of borane and carborane anions

0424221 - ÚACH 2014 RIV CH eng J - Journal Article
Štíbr, Bohumil
Carbon insertion into borane clusters via nucleophilic addition reactions of borane and carborane anions.
Journal of Organometallic Chemistry. Roč. 747, december (2013), s. 16-24. ISSN 0022-328X. E-ISSN 1872-8561
R&D Projects: GA ČR(CZ) GAP207/11/0705
Institutional support: RVO:61388980
Keywords : Boron hydrides * Carboranes * Dicarbaboranes * Heterocarboranes * Tricarbaboranes
Subject RIV: CA - Inorganic Chemistry
Impact factor: 2.302, year: 2013

New approaches to the synthesis of carboranes and heterocarboranes based on addition reactions of highly nucleophilic boron-cluster anions are briefly overviewed together with some mechanistic aspects. The anions, in which the negative charge is accumulated on the open face of the cage, become capable of coordinating to the most electrophilic center of the reacting substrate and are activated for addition reactions to multiply bonded substrates. Additions to cyanides, nitriles, isocyanides, aldehydes, and acyl chlorides lead usually to the insertion of one more carbon vertex into the boron framework, though the products may be in some cases unusual or unexpected. The methods based on nucleophilic addition have become an effective synthetic tool in the area of general carborane chemistry, though this specific field of cluster chemistry has still been far from being fully explored. One of the aims of this overview is to encourage a younger generation of chemists to return to building-up new borane clusters.
Permanent Link: http://hdl.handle.net/11104/0230259