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Mendeleev Communications, 2020, Volume 30, Issue 1, Pages 94–96
DOI: https://doi.org/10.1016/j.mencom.2020.01.031
(Mi mendc1112)
 

This article is cited in 15 scientific papers (total in 15 papers)

Communications

One-step synthesis of new aluminum hydrides bearing a highly sterically hindered acenaphthene-1,2-diimine ligand

M. V. Moskalev, D. A. Razborov, A. A. Bazanov, V. G. Sokolov, T. S. Koptseva, E. V. Baranov, I. L. Fedushkin

G.A. Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences, Nizhnii Novgorod, Russian Federation
Abstract: Treatment of a bulky dbhmp-bian ligand (dbhmp-bian==1,2-bis[(2,6-dibenzhydryl-4-methylphenyl)imino]acenaphthene) by 1 equiv. of LiAlH4 or mixture of 3/4 equiv. LiAlH4 and 1/3 eqiuv. AlCl3 in tetrahydrofuran results in new hydrides [(dbhmp-bian)AlH2(THF)]-[Li(THF)4]+ and (dbhmp-bian)AlH(THF), respectively. Both complexes were characterized by spectroscopic (IR, NMR) and X-ray diffraction methods.
Keywords: aluminum hydrides, imines, acenaphthenes, sterically hindered ligands, diimine ligands, redox-active ligands.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.0 Mb)


Citation: M. V. Moskalev, D. A. Razborov, A. A. Bazanov, V. G. Sokolov, T. S. Koptseva, E. V. Baranov, I. L. Fedushkin, “One-step synthesis of new aluminum hydrides bearing a highly sterically hindered acenaphthene-1,2-diimine ligand”, Mendeleev Commun., 30:1 (2020), 94–96
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  • https://www.mathnet.ru/eng/mendc/v30/i1/p94
  • This publication is cited in the following 15 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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