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Volumn 11, Issue 10, 2009, Pages 1681-1686

Highly water-soluble arene-ruthenium(II) complexes: Application to catalytic isomerization of allylic alcohols in aqueous medium

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EID: 70350064305     PISSN: 14639262     EISSN: 14639270     Source Type: Journal    
DOI: 10.1039/b914789f     Document Type: Article
Times cited : (60)

References (61)
  • 2
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    • B. Cornils and W. A. Herrmann, Wiley-VCH, Weinheim
    • Aqueous-Phase Organometallic Catalysis, ed. B. Cornils and W. A. Herrmann, Wiley-VCH, Weinheim, 2004.
    • (2004) Aqueous-Phase Organometallic Catalysis
  • 4
    • 84891498804 scopus 로고    scopus 로고
    • B. Cornils, W. A. Herrmann, I. T. Horváth, W. Leitner, S. Mecking, H. Olivier-Bourbigou and D. Vogt, Wiley-VCH, Weinheim
    • Multiphase Homogeneous Catalysis, ed. B. Cornils, W. A. Herrmann, I. T. Horváth, W. Leitner, S. Mecking, H. Olivier-Bourbigou and D. Vogt, Wiley-VCH, Weinheim, 2005.
    • (2005) Multiphase Homogeneous Catalysis
  • 28
    • 37049118608 scopus 로고
    • Preparation and characterization of the new compound 3c are described in the ESI. Complexes 3a–b and 3d–e were synthesized following the procedures previously reportedin ref. 11 and in
    • Preparation and characterization of the new compound 3c are described in the ESI. Complexes 3a–b and 3d–e were synthesized following the procedures previously reportedin ref. 11 and in: M. A. Bennett A. K. Smith J. Chem. Soc., Dalton Trans. 1974 233.
    • (1974) J. Chem. Soc., Dalton Trans. , pp. 233
    • Bennett, M.A.1    Smith, A.K.2
  • 31
    • 9144265784 scopus 로고    scopus 로고
    • For similar hydrolysis processes see for example
    • For similar hydrolysis processes see for example: P. Csabai F. Joó Organometallics 2004 23 5640.
    • (2004) Organometallics , vol.23 , pp. 5640
    • Csabai, P.1    Joó, F.2
  • 34
    • 85032769237 scopus 로고    scopus 로고
    • 3)] (details of X-ray diffraction study given in the ESI)
    • 3)] (details of X-ray diffraction study given in the ESI).
  • 38
    • 0001507732 scopus 로고
    • Redox potentials of some p-cymene and benzene ruthenium(II) complexes have been already reported but under different experimental conditions
    • Redox potentials of some p-cymene and benzene ruthenium(II) complexes have been already reported but under different experimental conditions: D. Devanne P. H. Dixneuf J. Organomet. Chem. 1990 390 371.
    • (1990) J. Organomet. Chem. , vol.390 , pp. 371
    • Devanne, D.1    Dixneuf, P.H.2
  • 42
    • 85032767700 scopus 로고    scopus 로고
    • Formal oxidation potentials (in V): 2a, 0.82; 2b, 0.77; 2c, 0.70; 2d, 0.86; 2e, 0.71; 3a, 0.71; 3b, 0.66; 3c, 0.61; 3d, 0.76; 3e, 0.60; 4a, 0.85; 4b, 0.83; 4c, 0.74; 4e, 0.81
    • Formal oxidation potentials (in V): 2a, 0.82; 2b, 0.77; 2c, 0.70; 2d, 0.86; 2e, 0.71; 3a, 0.71; 3b, 0.66; 3c, 0.61; 3d, 0.76; 3e, 0.60; 4a, 0.85; 4b, 0.83; 4c, 0.74; 4e, 0.81.
  • 58
    • 85032771848 scopus 로고    scopus 로고
    • 3: 107, 123, 128, 130 and 145°, respectively
    • 3: 107, 123, 128, 130 and 145°, respectively.
  • 61
    • 85032766633 scopus 로고    scopus 로고
    • Coordination of the C═C bond on the metal during the catalytic cycle is usually proposed for these processes. See, for example, ref. 24 and 26b
    • Coordination of the C═C bond on the metal during the catalytic cycle is usually proposed for these processes. See, for example, ref. 24 and 26b.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.