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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 1923-1929 
    ISSN: 0009-2940
    Keywords: 1,3,2,4-Diphosphadisiletanes, 1,3-bis(tert-butylmercurio)-substituted ; Mercury - phosphorus bond ; 1,3-Diphospha-2,4-disilabicyclo[1.1.0]butanes ; Silicon inversion ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A Facile Synthesis of 1,3-Diphospha-2,4-disilabicyclo[1.1.0]butanes and Isomerization by Silicon InversionDilithiation of the PH positions of the P2Si2 cyclobutanes 2a - h with n-BuLi and treatment with tBuHgCl leads to the 1,3-bis(tert-butylmercurio) compounds 3a - h. According to NMR spectroscopy and X-ray structural analysis the tert-butylmercurio groups at phosphours occupy trans configuration. Photolysis of solutions of 3a - d and 3f, g in toluene yields the corresponding 1,3-diphospha-2,4-disilabicyclo[1.1.0]butanes 1a - d and 1f, g. Interestingly, the dimercury compound 3e (R = mesityl and tert-butoxy) is quite stable in visible light, probably due to intramolecular donor (tBuO) acceptor (Hg) stabilization. Starting from 3b, the light-induced elimination of the tBuHg groups gives the expected exo,endo-P2Si2-bicyclo[1.1.0]butane 1b only as intermediate. The final product of the latter photolysis is the CMe3/CMe3-exo,exo isomer 1b′. The formation of 1b′ from 1b is an irreversible silicon inversion process caused by unfavourable interaction of the endo substituents in 1b. In comparison, the exo,endo isomer of 1g (R = isityl and CMe3 at silicon) does not rearrange to the Me3C/Me3C-exo,exo derivative 1g′ under similar photolysis conditions or when heated at 140°C for several days. The route to 1,3-diphospha-2,4-disilabicyclo[1.1.0]butanes 1 described herein allows the synthesis of new derivatives which cannot be prepared from disilenes and white phosphorus.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 1931-1939 
    ISSN: 0009-2940
    Keywords: 1,3,2,4-Diphosphadisiletanes ; Hindered rotation of aryl group ; Inversion at phosphorus ; Silanes, diorganodi(phosphino)- and fluoro-diorgano(phosphino) ; Chromium complexes ; Tungsten complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reaction of the bulkily substituted dichlorodiorganosilanes R1R2SiCl2 (R1 = Mesityl, R2 = Mesityl, tBu, OtBu, Xylyl, iBu) with LiPH2. dme in a 1 : 2 molar ratio in THF at -30°C leads to the new organo-substituted 1,3,2,4-diphosphadisiletanes 1a - e. Compounds 1c - e are isolated as mixtures of diastereomers. The crowded dichlorosilane Is(tBu)SiCl2 (Is = 2,4,6- triisopropylphenyl) reacts with LiPH2. dme above 10°C to yield the disubstituted products Is(tBu)Si(PH2)2 (2f) in 87% yield and only minor amounts of the corresponding four-membered ring [Is(tBu)SiPH]2 (1f), detected by 31P- and 29Si-NMR spectroscopy. Treatment of 2f with 2 equivalents of nBuLi in Et2O gives Is(tBu)Si(PHLi)2 (3f), which with Is(tBu)SiCl2 forms 1f. The reaction of difluorodiisitylsilane with LiPH2.dme in THF leads to different products, depending on the reaction temperature. At  -  30°C Is2Si(PHLi)F (7g) is obtained as sole product, whereas at 28°C the air-stable diphosphino-substituted Is2Si(PH2)2 (2g) is formed. Elimination of LiF from 7g affords the tetraisityl-substituted P2Si2-cyclobutane 1g, and treatment with H2O and Me3SiCl leads to Is2Si(PH2)F (8g) and Is2Si(PHSiMe3)F (9g). The temperature-dependent 1H-NMR spectra of 1a  -  g exhibit two dynamic processes: hindered rotation of the aryl groups at silicon and inversion at phosphorus.  -  The solid state structures of 1a, 1b, 1g, and 2g are established by X-ray crystallography. Reaction of 1a with 2 equivalents of M(CO)5.thf (M = Cr, W) yields the P,P′-bis(pentacarbonylmetal) complexes 10a (M = Cr) and 11a (M = W). A single-crystal X-ray diffraction analysis of 10a is performed.Concerning New 1,3,2,4-Diphosphadisiletanes and Diorganodi(phosphino)silane Derivatives
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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