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Volumn 36, Issue 19, 1997, Pages 4234-4240

Synthesis and Properties of Heterocyclic Substituted 1,2-Enedithiolates of Nickel, Palladium, and Platinum

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Indexed keywords


EID: 0001535342     PISSN: 00201669     EISSN: None     Source Type: Journal    
DOI: 10.1021/ic970194s     Document Type: Article
Times cited : (32)

References (48)
  • 2
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    • Catalysis by Molybdenum-Cofactor Enzymes
    • Reedijk, J., Ed.; Marcel Dekker Inc.: New York
    • Pilato, R. S.; Stiefel, E. I. Catalysis by Molybdenum-Cofactor Enzymes. In Bioinorganic Catalysis; Reedijk, J., Ed.; Marcel Dekker Inc.: New York, 1993; pp 133-88.
    • (1993) Bioinorganic Catalysis , pp. 133-188
    • Pilato, R.S.1    Stiefel, E.I.2
  • 6
    • 85038241000 scopus 로고
    • Metal Complexes Derived from cis-1,2-Dicyano-1,2-ethylenedithiolate and Bis(trifluoromethyl)-1,2-dithiete
    • McGraw-Hill, Inc.: New York
    • (b) Davison, A.; Holm, R. H. Metal Complexes Derived from cis-1,2-Dicyano-1,2-ethylenedithiolate and Bis(trifluoromethyl)-1,2-dithiete. Inorganic Synthesis; McGraw-Hill, Inc.: New York, 1967; Vol. 10, pp 8-25.
    • (1967) Inorganic Synthesis , vol.10 , pp. 8-25
    • Davison, A.1    Holm, R.H.2
  • 22
    • 0642263339 scopus 로고    scopus 로고
    • in press (Protonation State Dependent Excited State Electron Transfer Reactions of Pyridinium Substituted Metallo-1,2-enedithiolates)
    • (b) Kaiwar, S. P.; Vodacek, A; Blough, N. V.; Pilato, R. S. J. Am. Chem. Soc., in press. (Protonation State Dependent Excited State Electron Transfer Reactions of Pyridinium Substituted Metallo-1,2-enedithiolates).
    • J. Am. Chem. Soc.
    • Kaiwar, S.P.1    Vodacek, A.2    Blough, N.V.3    Pilato, R.S.4
  • 26
    • 77957065480 scopus 로고
    • Organosulfur Chemistry, Synthetic Aspects; Page, P., Ed.; Academic Press: San Diego, CA
    • Wood, W. Trends in the Chemistry of 1,3-Dithioacetal; Organosulfur Chemistry, Synthetic Aspects; Page, P., Ed.; Academic Press: San Diego, CA, 1995; pp 133-224.
    • (1995) Trends in the Chemistry of 1,3-Dithioacetal , pp. 133-224
    • Wood, W.1
  • 28
    • 0642263341 scopus 로고    scopus 로고
    • note
    • Pt-H = 53 Hz). There was no field or temperature dependence of the second-order line spacings.
  • 32
    • 0642294192 scopus 로고    scopus 로고
    • note
    • While complexes 24-37 were isolated analytically pure, no attempts to prepare 10-23 analytically pure were made. However, the protonation/deproto nation was repeated 10 times with no loss in absorption of either the protonated or deprotonated complexes.
  • 43
    • 85085783291 scopus 로고    scopus 로고
    • note
    • -1) correlate with the plot shown in Figure 4 unpublished results.
  • 45
    • 0642294188 scopus 로고
    • Progess in Physical Organic Chemistry; Streitwieser, A. J. Taft, R. W., Eds.; Interscience Publishers: New York
    • (b) Coetzee, J. F. Ionic Reactions in Acetonitrile; Progess in Physical Organic Chemistry; Streitwieser, A. J. Taft, R. W., Eds.; Interscience Publishers: New York, 1967, 45-92.
    • (1967) Ionic Reactions in Acetonitrile , pp. 45-92
    • Coetzee, J.F.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.