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Activation of Dihydrogen by Masked Doubly Bonded Aluminum Species.
Nagata, Koichi; Murosaki, Takahiro; Agou, Tomohiro; Sasamori, Takahiro; Matsuo, Tsukasa; Tokitoh, Norihiro.
Afiliação
  • Nagata K; Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011, Japan.
  • Murosaki T; Department of Applied Chemistry, Faculty of Science and Engineering, Kindai University, 3-4-1 Kowakae, Higashi-Osaka, Osaka, 577-8502, Japan.
  • Agou T; Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011, Japan.
  • Sasamori T; Department of Biomolecular Functional Engineering, College of Engineering, Ibaraki University, 4-12-1 Nakanarisawa, Hitachi, Ibaraki, 316-8511, Japan.
  • Matsuo T; Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011, Japan.
  • Tokitoh N; Department of Applied Chemistry, Faculty of Science and Engineering, Kindai University, 3-4-1 Kowakae, Higashi-Osaka, Osaka, 577-8502, Japan.
Angew Chem Int Ed Engl ; 55(41): 12877-80, 2016 10 04.
Article em En | MEDLINE | ID: mdl-27529165
Activation of dihydrogen by masked dialumenes (Al=Al doubly bonded species) is reported. Reactions of barrelene-type dialumanes, which have the reactivity as masked equivalents of 1,2-diaryldialumenes ArAl=AlAr, with H2 afforded dihydroalumanes ArAlH2 at room temperature (Ar: bulky aryl groups). These dihydroalumanes form hydrogen-bridged dimers [ArHAl(µ-H)]2 in the crystalline state, while a monomer-dimer equilibrium was suggested in solution. The 1,2-diaryldialumenes generated from the barrelene-type dialumanes are the putative active species in the cleavage of H2 .
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Japão