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  • 1,2,3,4-Diphosphadiboretane, isomerisation of  (1)
  • 1,3,2,4-Diphosphadiboretanes, 2,4-bis(dialkylamino)-  (1)
  • 1-Oxa-3-oxonia-5λD3-phospha-2-boratacyclohexadiene derivatives  (1)
  • Boron  (1)
  • 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
    ISSN: 0009-2940
    Keywords: Boron ; Phosphorus ; Spiro compounds ; Cage compounds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of 1-lithio · DME-2,4-bis(dialkylamino)-l,3,2,4-diphosphadiboretanes (1a, 1b) with SiCl4 followed by dehydrohalogenation with tBuLi produce spirocyclic compounds [(R2NB)2P2]2Si (2a, 2b). The compounds have been characterized by spectroscopic methods and X-ray crystallography. The assembly process has also been followed and one intermediate species [(iPr2NB)2P2][(iPr2NB)P(H)(iPr2NB)P]SiCl (3) has been isolated and fully characterized.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1923-1926 
    ISSN: 0009-2940
    Keywords: 1-Oxa-3-oxonia-5λD3-phospha-2-boratacyclohexadiene derivatives ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Monomeric B-[bis(trimethylsilyl)phosphanyl]-9-borabicyclo-[3.3.1]nonane (1) reacts with acyl chlorides 2 in a 1:2 ratio to afford deep red derivatives of six-membered oxaoxonia-s̰2,λD3-phosphaboratacyclohexadienes 3. In contrast, the (di-tert-butylboryloxy)phosphaethene 5 is obtained from tBu2BP-(SiMe3)2 (4) and PhC(O)Cl. It is assumed that both reactions proceed via a common intermediate, an (acylphosphanyl)bo-rane 6. The color of compounds 3, which feature a flat boat conformation, is due to a π-π* transition.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0009-2940
    Keywords: 1,2,3,4-Diphosphadiboretane-tetracarbonyliron complexes ; 1,3,2,4-Diphosphadiboretane-tetracarbonylchromium complexes ; 1,2,3,4-Diphosphadiboretane, isomerisation of ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,2-Di-tert-butyl-3-(diisopropylamino)-4-(dimethylamino)- 1,2,3,4-diphosphadiboretane (1) reacts with Fe2(CO)9 to give two isomeric tetracarbonyliron complexes 2, 3 with P-Fe bonds and a bis(tetracarbonyliron) complex 4. In contrast, 1 displaces the olefinic ligand from tetracarbonyl(η4-norbornadiene)metal (metal = Cr, Mo) to form the tetracarbonylmetal complexes 5 and 6 with a rearranged ligand molecule, i.e. a 1,3,2,4-diphosphadiboretane. This process is accompanied by a change of the tert-butyl groups from an anti orientation in 1 to a syn orientation in 5 as shown by X-ray crystallography.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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