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The reactions of H2AlCl with [(dpp-Bian)Na(Et2O)n] and [(ArBIG-Bian)Na(THF)] produce respective aluminum hydrides supported by radical-anionic 1,2-bis(arylimino)acenaphthene ligands, [(dpp-Bian)AlH2] (1) and [(ArBIG-Bian)AlH2(THF)] (2) (dpp-Bian = 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene); ArBIG-Bian = 1,2-bis[(2,6-dibenzhydryl-4-methylphenyl)imino]acenaphthene). The reaction of 1 with CO2 proceeds with reduction of both CO bonds and results in diolate [{(dpp-Bian)Al(μ-O2CH2)}2] (3). Complex 2 reacts with CO2 to carbonate [{(ArBIG-Bian)Al(μ-OCH2OCO2)}2] (4) that is a result of the insertion of CO2 into the Al–O bond in diolate species formed initially. Aluminum monohydrides [(dpp-Bian)AlH(X)] (X = Cl, 5; Me, 6) react with CO2 to form respective alumoxanes [{(dpp-Bian)AlX}2(μ-O)] (X = Cl, 7 and X = Me, 8). Compounds 1–4, 7, and 8 have been characterized by ESR and IR spectroscopy, and their molecular structures have been determined by single-crystal X-ray analysis.
Sprache
Englisch
Identifikatoren
ISSN: 0020-1669
eISSN: 1520-510X
DOI: 10.1021/acs.inorgchem.1c02731
Titel-ID: cdi_proquest_miscellaneous_2614228691
Format
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