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  • 1980-1984  (54)
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 23 (1984), S. 4147-4152 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 21 (1982), S. 706-716 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 22 (1983), S. 2700-2703 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Organometallics 2 (1983), S. 579-585 
    ISSN: 1520-6041
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 1235-1244 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Boron, CII. Synthesis and Reactions of 1-Stanna-4-bora-2,5-cyclohexadienesHydrostannation of (dialkylamino)dialkinylboranes 1 with dimethylstannane yields 1,1-dimethyl-1-stanna-4-bora-2,5-cyclohexadienes 2. Additional 4-amino derivatives are accessible via trans-amination reactions. Solvolysis of the amino derivatives by alcohols leads to alkoxy derivatives 3. These are alkylated by aluminium alkyls or tert-butyllithium to 4-alkyl-1,1-dimethyl-1-stanna-4-boracyclohexadienes 5. A considerable difference in the chemical behaviour of the 1,1-dimethyl-and the 1,1,2,6-tetramethyl derivatives has been observed.
    Notes: Die Hydrostannierung von (Dialkylamino)dialkinylboranen 1 mit Dimethylstannan führt zu 1,1-Dimethyl-1-stanna-4-bora-2,5-cyclohexadienen 2. Über Transaminierung sind weitere 4-Amino-Derivate zugänglich. Die Solvolyse der Amino-Derivate mit Alkoholen liefert die Alkoxyderivate 3, die mit Aluminiumalkylen bzw. mit tert-Butyllithium zu 4-Alkyl-1,1-dimethyl-1-stanna-4-boracyclohexadienen 5 alkyliert werden. Zwischen den 1,1-Dimethyl- und den 1,1,2,6-Tetramethyl-Derivaten bestehen beträchtliche Unterschiede im chemischen Verhalten.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 116 (1983), S. 3552-3558 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation and Molecular Structure of Tris(dimethyldithiocarbamato)aluminium, a Compound with Hexacoordinated AluminiumAl(NR2)3 and ClAl(NR2)2 (R = CH3) add CS2 with formation of the dimethyldithiocarbamates 1 and 2. 1 dissolves in benzene as a monomer in contrast to dimeric 2. 27Al NMR data indicate the presence of hexacoordinated Al atoms which are ascertained by an X-ray structure determination of 1: its Al atom is surrounded in a distorted trigonal antiprismatic fashion by six sulfur atoms. The C2NCS2 groups are planar. 2 possesses a structure containing two bridging Cl-atoms with four sulfur atoms each to complete hexacoordination for the two Al atoms in the molecule.
    Notes: Al(NR2)3 und ClAl(NR2)2 (R = CH3) addieren CS2 unter Bildung der Dimethyldithiocarbamate 1 und 2, von denen 1 in Benzol monomer, 2 hingegen dimer löslich ist. 27Al-NMR-Daten weisen hexakoordinierte Al-Atome aus, die durch die Röntgenstrukturanalyse von 1 bestätigt werden: das Al-Atom ist verzerrt trigonal antiprismatisch von sechs Schwefelatomen umgeben. Die C2NCS2-Gruppen sind planar. Für 2 folgt eine Struktur mit zwei brückenständigen Cl-Atomen, jeweils vier S-Atome ergänzen zur Hexakoordination der zwei Al-Atome im Molekül.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 117 (1984), S. 2495-2503 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Boron, 1401). Boron, Aluminium, and Gallium Halide Adducts of a Tetraaminodiboron CompoundThe tetraamino diboron compound 1 adds trihalides EX3 (E = B, Al, Ga, X = Cl, Br, I) to yield 1:1- and 1:2-coordination compounds. The BBr3 adduct 1b is thermally stable and shows nonfluxional behaviour in solution in contrast to the AlCl3 and GaCl3 adducts. The 1:2 adducts are nonfluxional and, according to NMR spectra, only the meso-form is present. The structure of the 1:1-adducts was ascertained by an X-ray structure determination of 1g. The single crystal contained R configurated molecules. A change from planar to the envelope conformation of the diazaborolidine ring occurs on adduct formation.
    Notes: Die Tetraaminodibor-Verbindung 1 lagert die Trihalogenide EX3 (E = B, Al, Ga; X = Cl, Br, I) zu 1:1- bzw. 1:2-Koordinationsverbindungen an. Von diesen zeigt nur das thermisch stabilere BBr3-Addukt 1b in Lösung im Gegensatz zu den AlCl3- und GaCl3-Addukten kein fluktuierendes Verhalten. Die 1:2-Addukte sind starr, und nach NMR-Spektren bildet sich nur die meso-Form. Die Struktur der 1:1-Addukte wurde durch Röntgenstrukturanalyse von 1g gesichert; die Einkristalle enthielten ein R-konfiguriertes Molekül. Durch die Addition nimmt der sonst planare Diazaborolidin-Ring Briefumschlag-Konformation an.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 117 (1984), S. 2504-2509 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Boron, 1411). Unexpected Formation of a Bis(amino)borane: Synthesis and Structure of Bis(benzyl-tert-butylamino)boraneThe reaction of BCl3 with 3 molar equivalents of lithium benzyl-tert-butylamide produces the bis(amino)borane 2 in 29% yield. According to an X-ray structure determination the compound crystallizes in the monoclinic system, space group C2/c, and the molecule possesses almost C2 symmetry. The mean BN bond lenght is 142 pm, and the C2N planes are twisted by an average of 23.8° versus the HBN2 plane.
    Notes: Die Umsetzung von BCl3 mit 3 mol Lithium-benzyl-tert-butylamid liefert mit 29% Ausbeute das Bis(amino)boran 2. Nach Röntgenstrukturanalyse der monoklin in der Raumgruppe C2/c kristallisierenden Verbindung besitzt das Molekül nahezu C2-Symmetrie. Der durchschnittliche BN-Abstand beträgt 142 pm, und die C2N-Ebenen sind gegen die HBN2-Ebenen um durchschnittlich 23.8° verdrillt.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 117 (1984), S. 2479-2494 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Boron, 139. Addition Compounds of Alkylhalogenoboranes with 1,3,2-Diazaborolidines: Structure, Stability, and Exchange ReactionsReactions of alkylhalogenoboranes RnBX3 - n (n = 0 - 2) with the 1,3-dimethyl-1,3,2-diazaborolidines 1 - 4 yield stable 1:1 addition compounds 1a - e, 2a, 3a - d, 4a irrespective of the boron substituents. Coordination of the borane moiety occurs at a ring N atom. An X-ray structure determination of the BCl3-adduct 3a shows two enantiomers in the asymmetric unit, envelope ring conformation, and strong π-bonding between the non-coordinated B an N atoms. - Equilibria of the 1:1 adducts with their ring cleavage products and their behaviour towards a second mol of BX3 was studied. In this case, replacement of the ring-BR group occurs. In contrast, haloboranes react with the 2-(dimethylamino)diazaborolidine 5 with R2N-substituent exchange while diborane yields in the first instance the (dimethylamino)borane adduct 5a.
    Notes: Umsetzungen von Alkylhalogenboranen RnBX3 - n (n = 0 - 2) mit den 1,3-Dimethyl-1,3,2-diazaborolidinen 1 - 4 führen unabhängig vom Bor-Substituenten zu stabilen 1:1-Additionsverbindungen 1a - e, 2a, 3a - d, 4a, wobei die Koordination über ein N-Atom des Fünfrings erfolgt. Die Röntgenstrukturanalyse des BCl3-Addukts 3a zeigt zwei enantiomere Formen in der asymmetrischen Einheit, “envelope”-Ringkonformation und eine starke π-Rückbindung des Ringbors zum nicht koordinierten Stickstoff. - Gleichgewichte der 1:1-Additionsverbindungen mit ihrem Ringöffnugsprodukt sowie ihr Verhalten gegenüber einem zweiten mol Lewis-Säure wurden untersucht. Hierbei wird die Ring-BR-Gruppe verdrängt. Im Gegensatz dazu tauscht das 2-(Dimethylamino)diazaborolidin 5 mit Halogenboranen den R2N-Substituenten aus, während die Umsetzung mit Diboran zunächst ein wenig stabiles (Dimethylamino)boran-Addukt 5a liefert.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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