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Volumn 692, Issue 9, 2007, Pages 1859-1870

Monophosphine and diphosphine ligands for diplatinum polyynediyl complexes: Efficient syntheses of new functionality-containing systems and model compounds

Author keywords

Fluorous; Functionalized phosphine; Olefin metathesis; Platinum; Polyyne

Indexed keywords

CATALYSTS; CHEMICAL BONDS; NITROGEN COMPOUNDS; PHOTOCHEMICAL REACTIONS; PLATINUM COMPOUNDS; SYNTHESIS (CHEMICAL);

EID: 33947103524     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jorganchem.2006.12.023     Document Type: Article
Times cited : (21)

References (58)
  • 2
    • 0001722667 scopus 로고    scopus 로고
    • Angew. Chem. 114 (2002) 1951
    • (2002) Angew. Chem. , vol.114 , pp. 1951
  • 9
    • 33947186540 scopus 로고    scopus 로고
    • J. Stahl, W. Mohr, L. de Quadras, T.B. Peters, J.C. Bohling, J.M. Marti{dotless}́n-Alvarez, G.R. Owen, F. Hampel, J.A Gladysz (in preparation).
  • 10
    • 33947186065 scopus 로고    scopus 로고
    • L. de Quadras, E.B. Bauer, W. Mohr, J.C. Bohling, T.B. Peters, J.M. Marti{dotless}́n-Alvarez, F. Hampel, J.A. Gladysz (in preparation).
  • 11
    • 33947135170 scopus 로고    scopus 로고
    • L. de Quadras, E.B. Bauer, J. Stahl, F. Zhuravlev, F. Hampel, J.A. Gladysz (in preparation).
  • 15
    • 33947170800 scopus 로고    scopus 로고
    • J. Stahl, Doctoral Dissertation, Universität Erlangen-Nürnberg, 2004.
  • 16
    • 33947138973 scopus 로고    scopus 로고
    • L. de Quadras, Doctoral Dissertation, Universität Erlangen-Nürnberg, 2006.
  • 26
    • 33750996012 scopus 로고    scopus 로고
    • Angew. Chem. 118 (2006) 1949
    • (2006) Angew. Chem. , vol.118 , pp. 1949
  • 31
    • 33947105813 scopus 로고    scopus 로고
    • Gladysz J.A., Curran D.P., and Horváth I.T. (Eds), Wiley/VCH, Weinheim
    • In: Gladysz J.A., Curran D.P., and Horváth I.T. (Eds). Handbook of Fluorous Chemistry (2004), Wiley/VCH, Weinheim 1-4
    • (2004) Handbook of Fluorous Chemistry , pp. 1-4
  • 43
    • 33947189770 scopus 로고    scopus 로고
    • H. Kuhn, Work in progress, Universität Erlangen-Nürnberg.
  • 45
    • 33947182766 scopus 로고    scopus 로고
    • 13C NMR signals that have been assigned by 2D NMR experiments; see footnote 33 of Ref. [4].
  • 46
    • 33947131456 scopus 로고    scopus 로고
    • 2P assignments, see footnote 36 of Ref. [5a].
  • 47
    • 33947128948 scopus 로고    scopus 로고
    • note
    • EI (phosphines and organic compounds) or FAB (platinum complexes; 3-nitrobenzyl alcohol matrix); m/z for the most intense peak of the isotope envelope.
  • 48
    • 33947153615 scopus 로고    scopus 로고
    • note
    • 27 was not observed.
  • 51
    • 33947127917 scopus 로고    scopus 로고
    • - [30].
  • 52
    • 33947103362 scopus 로고
    • Prepared from the commercial α,ω-diol as described by This compound is also sometimes commercially available
    • Prepared from the commercial α,ω-diol as described by. Stone G.C.H. J. Am. Chem. Soc. 62 (1940) 571 This compound is also sometimes commercially available
    • (1940) J. Am. Chem. Soc. , vol.62 , pp. 571
    • Stone, G.C.H.1
  • 54
    • 33947184560 scopus 로고    scopus 로고
    • 5 signals were not observed.
  • 55
    • 0000314595 scopus 로고    scopus 로고
    • For virtual triplets the J values represent the apparent couplings between adjacent peaks
    • For virtual triplets. Hersh W.H. J. Chem. Educ. 74 (1997) 1485 the J values represent the apparent couplings between adjacent peaks
    • (1997) J. Chem. Educ. , vol.74 , pp. 1485
    • Hersh, W.H.1
  • 56
    • 33947161263 scopus 로고    scopus 로고
    • note
    • 195Pt = 33.8%), and is not reflected in the peak multiplicity given.
  • 58
    • 0000502737 scopus 로고
    • Angew Chem. 107 (1995) 1284
    • (1995) Angew Chem. , vol.107 , pp. 1284


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.