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  • Artikel: DFG Deutsche Nationallizenzen  (3)
  • Calculations, ab initio  (2)
  • 1,3,2,4-Diazadiphosphetidinylium salts  (1)
  • 1,3-Diaza-2λ2-phosphonia-4λ4-gallatacyclobutanes  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 2397-2401 
    ISSN: 0009-2940
    Schlagwort(e): [Amino(imino)phosphane]gallium trichloride adduct ; 1,3-Diaza-2λ2-phosphonia-4λ4-gallatacyclobutanes ; Nickel tricarbonyl complexes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 1,3-Diaza-2λ2-phosphonia-4λ4-gallatacyclobutanesReaction of amino(imino)phosphanes 1a-c with gallium trichloride results in the formation of 1,3-diaza-2λ2-phosphonia-4λ4-gallatacyclobutanes 3a, b with elimination of chlorotrimethylsilane (1a) or tert-butyl chloride (1b, c). The intermediately formed amino(imino)phosphane/Lewis acid adducts R(Me3Si)NPN(GaCl3)R′ (2, R,R′ = tBu, Me3Si) can be isolated in the case of compound 2a (R = R′ = SiMe3). A diazaphosphasilacyclobutane - gallium trichloride adduct 4 is formed in a side reaction by isomerization of 2a. Reaction of compound 3b with Ni(CO)4 gives the corresponding transition metal complex 5. The NMR data and X-ray structures of compounds 2a, 4, and 5 are reported.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 0009-2940
    Schlagwort(e): 1,3-Diaza-2-phosphaallyllithium ; Calculations, ab initio ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Monomer and Dimer 1,3-Diaza-2-phosphaallyllithium Complexes: Structures and Ambident Reactivity*Metallation of the NH-functional amino(imino)phosphanes Mes*NPNHR (R = CPh3, Ad, tBu) 1a-c yields the 1,3-diaza-2-phosphaallyllithium compounds 2a-c. The crystal structure shows an ether-stabilized monomer of 2a and a solvent-free dimer with an eight-membered ring in the case of 2b, c. The reaction of 2b with chlorodiphenylphosphane yields, dependent on the reaction conditions, (phosphanylamino)iminophosphane 3 or bis(imino)phosphanylphosphorane 4. The structural and reactivity is discussed on the basis of ab initio calculations.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    ISSN: 0009-2940
    Schlagwort(e): [n + 2] Cycloadditions ; Calculations, ab initio ; Phosphenium ions ; 1,3,2,4-Diazadiphosphetidinylium salts ; Tetrazaphospholylium salts ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: [n + 2] Cycloaddition Reactions of the (Arylimino)phosphenium Ion, [P≡NAr]+-Kationic PN Heterocycles with Unusual Structure and Bonding SituationThe iminophosphenium ion [P≡NAr]+ (Ar=2,4,6-tBu3C6H2) (1) reacts with aminoiminophosphanes R2N-P=NtBu (R=iPr, Me3Si) (2) and alkyl azides RN3 (R=tBu, Et3C) (6) to yield the corresponding [n + 2] cycloadducts [R2NP (NAr)P(NtBu)+ (3) and [PN(Ar)NNN(R)]+ (7), respectively. Single-crystal X-ray diffraction studies show that 3a can be considered as an intramolecular donor-acceptor complex while 7 can be regarded as a cyclic diaminophosphenium cation coupled to a diimine fragment, which is in accordance with results of ab initio calculations.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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