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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1373-1379 
    ISSN: 1434-1948
    Keywords: Sodium bis(borane)dimethylamide solvates ; X-ray structure ; Reduction ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of sodium metal with dimethylamine-borane in THF yields Na[(H3B)2NMe2] (1) which can be isolated as {Na[(H3B)2NMe2]}5·THF or as Na[(H3B)2NMe2]·15-crown-5 (2) and Na[(H3B)2NMe2]·benzo-15-crown-5 (3) after addition of the appropriate crown ether to the THF solution of 1. Reaction of 1 with ZrCl4 yields Me2HN-BH2-NMe2-BH3 (4), the structure of which has been determined. In THF solution, 1 reduces aldehydes, ketones, acyl chlorides, and esters to the corresponding alcohols. It also reacts slowly with nitriles and allylbenzene. Compound (1)5·THF crystallizes in an extended three-dimensional lattice, in which the Na atoms are coordinated by 6-9 hydridic H atoms, while 3 is a molecular compound in the solid state. Only one hydrogen atom of each BH3 group coordinates to the sodium center. On the other hand, 4 forms dimeric associates in the solid state through N-H···H-B interactions.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 941-949 
    ISSN: 1434-1948
    Keywords: Lithium tetrahydridoborate diethyl ether (1:1) ; Lithium tetrahydridoborate diveron (1:1) ; Lithium tetrahydridoborate dimethoxyethane (1:2) ; Lithium tetrahydridoborate triglyme (1:1) ; Lithium tetrahydridoborate tetrahydrofuran (1:3) ; Lithium tetrahydridoborate 1,3-dioxolane (1:1) ; Hydride-bridge bonding ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: LiBH4 · OEt2 (1) and LiBH4 · O(Me)CMe3 (2) form double-stranded chains in the solid state. While 3 hydrides of the BH4 group in 1 bind to three different Li atoms through Li···H-B interactions, the fourth H atom interacts with three adjacent Li centers. In contrast, in compound 2 there are two single Li···H-B bonds and two doubly bridging hydrogen atoms, the latter again interacting with three lithium centers. Moreover, the arrangements of the ether molecules in 1 and 2 are different. LiBH4 · 2 DME (3) (DME = dimethoxyethane) forms a molecular lattice, in which the BH4- anions are present in Li···H2BH2 bridges. The same structural feature is present in LiBH4 · TG (4) (TG = triglyme = triethylene glycol dimethyl ether), but the TG molecule coordinates to two Li centers through two of its four oxygen atoms in such a manner that a chain structure results. The compound LiBH4 · 3 THF (5) exists as discrete molecules in the lattice. Its BH4- anion is triply bridging to the Li center. In contrast, LiBH4·C3H6O2 (6) (1,3-dioxolane) is polymeric. Due to the presence of two μ22-BH4 groups, a chain of the type ···Li(H2BH2)Li(H2BH2)··· is formed, and the 1,3-dioxolane molecules connect the chains through Li-O coordination to form a three-dimensional array. In spite of the variations in the bonding of the BH4 group to Li centers, the Li atoms are hexacoordinated in 3 to 6 but are heptacoordinated in 1 and 2.
    Type of Medium: Electronic Resource
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