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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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