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An Aluminum Dihydride Working as a Catalyst in Hydroboration and Dehydrocoupling.
Yang, Zhi; Zhong, Mingdong; Ma, Xiaoli; Nijesh, Karikkeeriyil; De, Susmita; Parameswaran, Pattiyil; Roesky, Herbert W.
Afiliação
  • Yang Z; School of Chemical Engineering and Environment, Beijing Institute of Technology , 100081 Beijing, China.
  • Zhong M; School of Chemical Engineering and Environment, Beijing Institute of Technology , 100081 Beijing, China.
  • Ma X; School of Chemical Engineering and Environment, Beijing Institute of Technology , 100081 Beijing, China.
  • Nijesh K; Department of Chemistry, National Institute of Technology Calicut , NIT Campus P.O., Kozhikhode 673 601, Kerala, India.
  • De S; Department of Chemistry, National Institute of Technology Calicut , NIT Campus P.O., Kozhikhode 673 601, Kerala, India.
  • Parameswaran P; Department of Chemistry, National Institute of Technology Calicut , NIT Campus P.O., Kozhikhode 673 601, Kerala, India.
  • Roesky HW; Institut für Anorganische Chemie der Georg-August-Universität Göttingen , Tammannstrasse 4, D-37077 Göttingen, Germany.
J Am Chem Soc ; 138(8): 2548-51, 2016 Mar 02.
Article em En | MEDLINE | ID: mdl-26862789
ABSTRACT
The well-defined aluminum dihydride LAlH2 (L = HC(CMeNAr)2, Ar = 2,6-Et2C6H3) (1) operates in catalysis like a transition metal complex. The catalytic activity of 1 for hydroboration of terminal alkynes was investigated. Furthermore, catalyst 1 effectively initiated the dehydrocoupling of boranes with amines, thiols, and phenols, respectively, to form compounds with B-E bonds (E = N, S, O) under elimination of H2. Quantum mechanical calculations indicate that hydroboration and dehydrocoupling reactions occur via three consecutive cycloaddition reactions involving the activation of the X-H (X = Al, B, C, and O) σ-bonds.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Chem Soc Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Chem Soc Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China