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  • 1
    ISSN: 0009-2940
    Keywords: 1,3,2,4-Diphosphadiboretanes, 2,4-bis(dialkylamino)- ; Boranes, (dialkylamino)bis(alkylphosphanyl)- ; Chromium, pentacarbonyl[2,3-bis(dialkylamino)1-1,3,2,4-diphosphadiboretane] complexes ; Chromium, pentacarbonyl[(2,2,6,6-tetramethylpiperidino)phosphane-P]- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Contributions to the Chemistry of Boron, 216[1]. - On the Complex Formation of 1,3,2,4-Diphosphadiboretanes with Pentacarbonylchromium and the Preparation and Reactivity of Borylidenephosphane Complexes2,4-Bis(dialkylamino)1-1,3,2,4-diphosphadiboretanes (R2NBP-CMe3)2 with sterically undemanding amino substituents are prepared together with the corresponding bis(phosphanyl)1-boranes R2NB(PHCMe3)2 by the reaction of R2NBCl2 with Li-P(H)CMe3. Complexes of 1,3,2,4-diphosphadiboretanes with one or two pentacarbonylchromium fragments were obtained by the reaction of the ligands with Cr(CO)5·THF or Cr(CO)5·NMe3. If substituents are sterically demanding, cycloreversion is observed with formation of [(aminoborylidene)1-phosphanyl-P]pentacarbonylchromium compounds tmpB=PR[Cr(CO)5] (10, 29) with an allene-like structure. Complex 29 may also be prepared by HCl elimination from tmp-B(Cl)-P(H)CMe3[Cr(CO)5] (34) with lithium diisopropylamide. This reaction can by reversed be the addition of HCl. The diphosphadiboretane 11 reacts with HCl, ethanol, and secondary amines with cleavage of all BP bonds. The X-ray structures of complexes (Et2NB - PCMe3)2[Cr(CO)5]2 (23) and (iPr2NB - PCEt3)2 [Cr(CO)5] (25) as well as of the diphosphadi-boretanes (Me2NB - PCMe3)2 (11) and (iPr2NB - PCEt3)2 (24) are presented. The intra ring angles of 23 remain almost unchanged upon complexation. In contrast, the B2P2 ring of 25 is slightly folded and its noncoordinated P atom approaches a planar environment.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 611-618 
    ISSN: 0009-2940
    Keywords: Phosphanylboranes, tetraorganyl ; 1,3,2,4-Diphosphadiboracyclobutane ; Diboranes, μ1-phosphanyl- ; Thiophosphinate, S1-boryl ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Contributions to the Chemistry of Boron, 215[1]. - Synthesis and Reactions of Monomeric Tetraorganyl-phosphanyl-boranesThe reaction of diorganyl-chloroboranes with lithium diorganyl-or lithium bis(trimethylsilyl)phosphides leads to the monomeric phosphanylboranes tBu2BPtBu2 (1), tBu2BP(SiMe3)2 (2), 9-BBNPtBu2 (3), 9-BBNP(SiMe3)2 (4), and Cy2BPtBu2 (5). These species were studied by NMR-spectroscopic methods. For further characterization reactions of the compounds 1, 3, and 5 have been investigated. Heating of 1 and 5 results in the formation of the dimeric phosphanylboranes tBu(H)BPtBu2 (8) and Cy(H)BPtBu2 (9) by dehydroboration. Dimers 8 and 9 are present as cis- and trans1-isomers as confirmed by X-ray structure analyses. The trans1-isomer of 9 shows a planar (BP)2 four-membered ring, whereas the ring of the cis1-isomer of 8 is slightly folded. Furthermore, the reaction of 3 with 9H-9-BBN yields (μ1-H)(μ-tBu2P)[9-BBN]2 (14), whose bridged structure is proven by a crystal structure analysis. Oxidation of the phosphorus atom in 3 with sulfur leads to the S1-boryl thiophosphinate tBu2(S)PS-9-BBN (16).
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 855-859 
    ISSN: 1434-1948
    Keywords: Borazines ; Silyl borazines ; Oligomers ; Pyrolysis ; Ceramics ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of LiSi(SiMe3)3 with Cl(Me)2B3N3(Me)3, Cl2(Me)B3N3(Me)3, (ClBNMe)3, and (ClBNH)3 result in the formation of molecular species (Me3Si)3Si(Me)2B3N3(Me)3, [(Me3Si)3Si]2(Me)B3N3(Me)3, [(Me3Si)3SiBNMe]3, and [(Me3-Si)3SiBNH]3. The new compounds have been characterized by spectroscopic techniques, and a single-crystal X-ray diffraction analysis for [(Me3Si)3SiBNMe]3 has been completed. The monomer (Me3Si)3Si(Cl)2B3N3H3 was also prepared and combined with (Me3Si)2NH in hexane to form an organic solvent soluble oligomer. Pyrolysis of this oligomer provides composites containing BN and an SiXNYCZ phase that suppresses the crystallization of BN.
    Type of Medium: Electronic Resource
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