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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 427-432 
    ISSN: 0009-2940
    Keywords: Chalcogenoboron hydride structure ; Adamantane ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: [(BH6)2]S4]2-, [(BH2)Se4]2-: New Chalcogenoboron Hydride Anions with Adamantane StructureThe reaction of THF·BH3/NaBH4 (2: 1) with H2S produces Na[H3B-μ2-S(B2H5)] (5) with hydrogen evolution. 5 reacts with an excess of H2S to give Na2[(BH2)6S4] (3a), which is also formed in the reaction of THF·BH3 with NaSH or anhydrous Na2S. These reactions proceed via 5 and the intermediates 7 or 8 by loss of BH-4 and cyclization. The analogous compound Na2[(BH2)6Se4] (4a) is obtained by the reaction of elemental selenium with NaBH4 (1:1) in triglyme. The primary product is Na2[H3B-Se-Se-BH3] (9). Treatment of 9 at 100 - 110°C yields 4a and polymers, 3a and 4a react with CsBr to form the crystalline compounds Cs2[(BH2)6Se4]·CsBr (3b) and Cs2-[(BH2)6Se4]·CsBr (4b), characterized by X-ray structure determinations. The anions of 3b and 4b consist of an adamantane skeleton. The Br- ion is octahedrally coordinated by Cs+ ions. The Cs6Br octahedra share faces to form columns along the hexagonal c axis. The crystal structures of the isotypic compounds 3b and 4b are closely related to the structure of CsNiCl3.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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