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

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    SYSNO ASEP0424221
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleCarbon insertion into borane clusters via nucleophilic addition reactions of borane and carborane anions
    Author(s) Štíbr, Bohumil (UACH-T) RID, SAI, ORCID
    Source TitleJournal of Organometallic Chemistry. - : Elsevier - ISSN 0022-328X
    Roč. 747, december (2013), s. 16-24
    Number of pages9 s.
    Languageeng - English
    CountryCH - Switzerland
    KeywordsBoron hydrides ; Carboranes ; Dicarbaboranes ; Heterocarboranes ; Tricarbaboranes
    Subject RIVCA - Inorganic Chemistry
    R&D ProjectsGAP207/11/0705 GA ČR - Czech Science Foundation (CSF)
    Institutional supportUACH-T - RVO:61388980
    UT WOS000326116500004
    DOI10.1016/j.jorganchem.2013.04.010
    AnnotationNew 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.
    WorkplaceInstitute of Inorganic Chemistry
    ContactJana Kroneislová, krone@iic.cas.cz, Tel.: 311 236 931
    Year of Publishing2014
Number of the records: 1  

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