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Volumn 7, Issue 20, 2015, Pages 3350-3357

Decatungstate-Photocatalyzed Si-H/C-H Activation in Silyl Hydrides: Hydrosilylation of Electron-Poor Alkenes

Author keywords

photochemistry; radicals; reaction mechanisms; silanes; tungsten

Indexed keywords

ATOMS; CHEMICAL ACTIVATION; FREE RADICAL REACTIONS; HYDRIDES; HYDROCARBONS; HYDROSILYLATION; PHOTOCHEMICAL REACTIONS; PHOTOLYSIS; SILICON; TUNGSTEN;

EID: 84944179714     PISSN: 18673880     EISSN: 18673899     Source Type: Journal    
DOI: 10.1002/cctc.201500562     Document Type: Article
Times cited : (82)

References (92)
  • 10
    • 0000829913 scopus 로고
    • (Eds.: S. Patai, Z. Rappoport), Wiley, New York
    • I. Ojima, in The Chemistry of Organic Silicon Compounds (Eds.:, S. Patai, Z. Rappoport,), Wiley, New York, 1989, pp. 1479-1526;
    • (1989) The Chemistry of Organic Silicon Compounds , pp. 1479-1526
    • Ojima, I.1
  • 15
    • 33746188862 scopus 로고    scopus 로고
    • Angew. Chem. 2006, 118, 2807-2811;
    • (2006) Angew. Chem. , vol.118 , pp. 2807-2811
  • 24
    • 84921333419 scopus 로고    scopus 로고
    • Recently, silyl radicals have been obtained from trisubstituted silanes and used for the synthesis of 9-silafluorenes (see:) and silaindenes (see
    • Recently, silyl radicals have been obtained from trisubstituted silanes and used for the synthesis of 9-silafluorenes (see:, D. Leifert, A. Studer, Org. Lett. 2015, 17, 386-389) and silaindenes (see:
    • (2015) Org. Lett. , vol.17 , pp. 386-389
    • Leifert, D.1    Studer, A.2
  • 50
    • 84944170275 scopus 로고    scopus 로고
    • For representative examples, see
    • For representative examples, see:
  • 54
    • 78651229742 scopus 로고    scopus 로고
    • Angew. Chem. 2010, 122, 6027-6029;
    • (2010) Angew. Chem. , vol.122 , pp. 6027-6029
  • 63
    • 84908869908 scopus 로고    scopus 로고
    • Angew. Chem. 2014, 126, 4778-4781.
    • (2014) Angew. Chem. , vol.126 , pp. 4778-4781
  • 66
    • 84944153284 scopus 로고    scopus 로고
    • 3SiOH was formed in this case.
    • 3SiOH was formed in this case.
  • 79
    • 9444259053 scopus 로고
    • Excited TBADT is known to activate organic substrates by a one-electron oxidation in the reaction with easily oxidizable compounds. The oxidation potential of aromatic silanes 1a - c is estimated to be 2.1-2.3V vs. saturated calomel electrode (SCE), which is slightly lower than that of 1e (≈2.4V vs. SCE
    • Excited TBADT is known to activate organic substrates by a one-electron oxidation in the reaction with easily oxidizable compounds. The oxidation potential of aromatic silanes 1a-c is estimated to be 2.1-2.3V vs. saturated calomel electrode (SCE) (, J. M. Gaidis, P. R. Briggs, T. W. Shannon, J. Phys. Chem. 1971, 75, 974-980), which is slightly lower than that of 1e (≈2.4V vs. SCE;
    • (1971) J. Phys. Chem. , vol.75 , pp. 974-980
    • Gaidis, J.M.1    Briggs, P.R.2    Shannon, T.W.3
  • 81
    • 84865266089 scopus 로고    scopus 로고
    • references quoted therein) to allow an efficient electron transfer reaction to occur.
    • S. Montanaro, D. Ravelli, D. Merli, M. Fagnoni, A. Albini, Org. Lett. 2012, 14, 4218-4221 and references quoted therein) to allow an efficient electron transfer reaction to occur.
    • (2012) Org. Lett. , vol.14 , pp. 4218-4221
    • Montanaro, S.1    Ravelli, D.2    Merli, D.3    Fagnoni, M.4    Albini, A.5
  • 83
    • 0000336004 scopus 로고    scopus 로고
    • Angew. Chem. 2001, 113, 1380-1414.
    • (2001) Angew. Chem. , vol.113 , pp. 1380-1414


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