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Volumn 32, Issue 4, 2011, Pages 195-218

Dual site catalysts for hydride manipulation

Author keywords

ammonia borane; bifunctional catalyst; hydride; hydrogen storage; ruthenium; Shvo catalyst

Indexed keywords


EID: 84857983731     PISSN: 02603594     EISSN: 15489574     Source Type: Journal    
DOI: 10.1080/02603594.2011.642087     Document Type: Article
Times cited : (7)

References (52)
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    • Reviews on biochemical methods: 3769-3826
    • Reviews on biochemical methods: (a) Jones, J. B. Tetrahedron 1986, 42 (13), 3351-3403. (b) Schoffers, E.; Golebiowski, A.; Johnson, C. R. Tetrahedron 1996, 52 (29), 3769-3826.
    • (1986) Tetrahedron , vol.42-52 , Issue.13-29 , pp. 3351-3826
    • Jones, J.B.1    Schoffers, E.2    Golebiowski, A.3    Johnson, C.R.4
  • 18
    • 84857956126 scopus 로고    scopus 로고
    • A process with contributions from breaking multiple hydrogen bonds in the transition state of the rate determining step results in a combined KIE that is equal to the product of the two individual isotope effects
    • A process with contributions from breaking multiple hydrogen bonds in the transition state of the rate determining step results in a combined KIE that is equal to the product of the two individual isotope effects.
  • 19
    • 84857976958 scopus 로고    scopus 로고
    • Note that values in Tables 1 and B differ, in part, because the former is a stoichiometric reaction and the latter is catalytic
    • Note that values in Tables 1 and B differ, in part, because the former is a stoichiometric reaction and the latter is catalytic.
  • 20
    • 84857969435 scopus 로고    scopus 로고
    • Unpublished results, University of Southern California
    • Williams, T. J.; Stutzman, J. 2008. Unpublished results, University of Southern California.
    • (2008)
    • Williams, T.J.1    Stutzman, J.2
  • 23
    • 33644888003 scopus 로고    scopus 로고
    • 3)H, which has been shown to also proceed through a concerted, outer-sphere mechanism
    • 3)H, which has been shown to also proceed through a concerted, outer-sphere mechanism. Casey, C. P.; Strotman, N. A.; Beetner, S. E.; Johnson, J. B.; Priebe, D. C.; Guzei, I. A. Organometallics 2006, 25 (5, 1236-1244. The Hammett parameter for benzaldehyde hydroboration with 23-Tol is ρ =+0.91, note 27).
    • (2006) Organometallics , vol.25 , Issue.5 , pp. 1236-1244
    • Casey, C.P.1    Strotman, N.A.2    Beetner, S.E.3    Johnson, J.B.4    Priebe, D.C.5    Guzei, I.A.6
  • 31
    • 34547363930 scopus 로고    scopus 로고
    • For a discussion of agostic bonding, see (a) 245-269
    • For a discussion of agostic bonding, see (a) Brookhart, M.; Green, M. L. H.; Parkin, G. Natl. Acad. Sci. (USA) 2007, 104 (17), 6908-6914. (b) Crabtree, R. H. Chem. Rev. 1985, 85 (4), 245-269.
    • (2007) Natl. Acad. Sci. (USA) , vol.85-104 , Issue.4-17 , pp. 6269-6908
    • Brookhart, M.1    Green, M.L.H.2    Parkin, G.3    Crabtree, R.H.4
  • 33
    • 84857969452 scopus 로고    scopus 로고
    • CCDC 738031, 738030, and 755444 contain supplementary crystallographic data for compounds 29, 28, and 33, respectively. CCDC 830936 contains supplementary crystallographic data for compound 31. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 738031, 738030, and 755444 contain supplementary crystallographic data for compounds 29, 28, and 33, respectively. CCDC 830936 contains supplementary crystallographic data for compound 31. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
  • 47
    • 84857970172 scopus 로고    scopus 로고
    • 2). For the four cycles at 2.0 mol% this is: [(78.4 mg)/(400.0 mg + 810.4 mg + 38.0 mg)] × (8.8 eq./12.0 eq) × 100% = 4.6 system wt%
    • 2). For the four cycles at 2.0 mol% this is: [(78.4 mg)/(400.0 mg + 810.4 mg + 38.0 mg)] × (8.8 eq./12.0 eq) × 100% = 4.6 system wt%.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.