메뉴 건너뛰기




Volumn 667, Issue 1-2, 2003, Pages 167-175

2-(dimethylphosphinomethyl)- and 2-(methylthiomethyl)phenyl silicon compounds: Higher coordination with soft donors

Author keywords

2 (Dimethylphosphinomethyl)phenylsilanes; 2 (Dimethylphosphinomethyl)phenylsilyl triflate; 2 (Methylthiomethyl)phenylsilanes; 2 (Methylthiomethyl)phenylsilyl triflate; Si pentacoordination; Silicon; X ray structure

Indexed keywords

HYDROCARBON SUBSTITUENT; ION; ORGANOSILICON DERIVATIVE; PHOSPHORUS; SILICON DERIVATIVE; SULFUR;

EID: 0037415609     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-328X(02)02164-2     Document Type: Article
Times cited : (18)

References (45)
  • 6
    • 0013110279 scopus 로고    scopus 로고
    • Z. Rappoport, Y. Apeloig (Eds.), Wiley, Chichester, New York, Weinheim, Brisbane, Singapore, Toronto
    • D. Kost, I. Kalikhman, in: Z. Rappoport, Y. Apeloig (Eds.), The Chemistry of Organic Silicon Compounds, vol. 2, Wiley, Chichester, New York, Weinheim, Brisbane, Singapore, Toronto, 1998, p. 1436.
    • (1998) The Chemistry of Organic Silicon Compounds , vol.2 , pp. 1436
    • Kost, D.1    Kalikhman, I.2
  • 26
    • 0000490640 scopus 로고    scopus 로고
    • N. Auner, J. Weis (Eds.), Wiley-VCH, Weinheim, Berlin, New York
    • G. Müller, M. Waldkirch, A. Pape, in: N. Auner, J. Weis (Eds.), Organosilicon Chemistry III, Wiley-VCH, Weinheim, Berlin, New York, 1998, p. 452.
    • (1998) Organosilicon Chemistry III , pp. 452
    • Müller, G.1    Waldkirch, M.2    Pape, A.3
  • 30
    • 85064188771 scopus 로고    scopus 로고
    • 2 J (Si, P) couplings are in the range of 5-10 Hz, while 3J (Si, P) couplings are observable only in compounds with very special geometric conditions [see 22b]
    • 2 J (Si, P) couplings are in the range of 5-10 Hz, while 3J (Si, P) couplings are observable only in compounds with very special geometric conditions [see 22b].;
  • 31
    • 0001816089 scopus 로고
    • P. Diehl, E. Fluck, R. Kosfeld (Eds.), Springer-Verlag, New York
    • H. Marsmann, in: P. Diehl, E. Fluck, R. Kosfeld (Eds.), NMR Principles and Progress, Springer-Verlag, New York, 1981, p. 65.
    • (1981) NMR Principles and Progress , pp. 65
    • Marsmann, H.1
  • 35
    • 84922807510 scopus 로고    scopus 로고
    • Dissertation
    • Universität Bielefeld
    • U. Berlekamp, Dissertation, Universität Bielefeld, 1999.
    • (1999)
    • Berlekamp, U.1
  • 41
    • 0013104731 scopus 로고    scopus 로고
    • Crystallographic data
    • -3 . Crystallographic data for the structural analyses of 13 and 15 have been deposited with the Cambridge Crystallographic Data Centre, CCDC Nos. 184572 and 184573. Copies of this information may be obtained free of charge from The Director, CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (fax: +44-1223-336033; e-mail: depositγcdc.cam.ac.uk or www:http://www.ccdc.cam.ac.uk).
  • 42
    • 0013062726 scopus 로고
    • Si-Cl bonds are usually in the range of 201-204 pm: W.S. Sheldrick
    • S. Patai, Z. Rappoport (Eds.), Wiley, New York
    • Si-Cl bonds are usually in the range of 201-204 pm: W.S. Sheldrick, in: S. Patai, Z. Rappoport (Eds.), The Chemistry of Organic Silicon Compounds, Wiley, New York, 1989, p. 236.
    • (1989) The Chemistry of Organic Silicon Compounds , pp. 236
  • 45
    • 0013157757 scopus 로고    scopus 로고
    • In the reaction always a small amount of the corresponding silane containing two donor-functionalized aryl substituents is formed which can not be completely separated by distillation
    • In the reaction always a small amount of the corresponding silane containing two donor-functionalized aryl substituents is formed which can not be completely separated by distillation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.