Insight into Varied Reaction Pathways for O–H and N–H Bond Activation by Bis(imino)pyridine Complexes of Al(III)

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• 作者：Tobias J. Sherbow ; Cody R. Carr ; Tomoya Saisu ; James C. Fettinger ; Louise A. Berben
• 刊名：Organometallics
• 出版年：2016
• 出版时间：January 11, 2016
• 年：2016
• 卷：35
• 期：1
• 页码：9-14
• 全文大小：323K
• ISSN：1520-6041

文摘

The activation of O–H bonds in alcohol substrates is the initial step in acceptor-less catalytic dehydrogenation of alcohols. At room temperature, the bis(imino)pyridine-ligated aluminum hydride compound, denoted as (^PhI₂P^2–)AlH (1), activates O–H bonds in alcohols through a metal–ligand cooperative pathway to afford the phenoxide and benzyloxide complexes with protonated ligand: (^PhHI₂P^1–)Al(OR)H, where R = Ph, Bn. Thermochemical measurements indicate that the amido nitrogen of the protonated ligand in (^PhHI₂P^1–)Al(OPh)H is far more basic (pK_a = 36–45) than the analogous proton for the previously reported (^PhHI₂P^1–)Al(NHPh)H (pK_a = 10–14), and this is consistent with reactivity we observe, where (^PhHI₂P^1–)Al(OPh)H complexes do not intramolecularly liberate H₂. The inability of (^PhHI₂P^1–)Al(OR)H to release H₂ upon heating precludes access to a four-coordinate Al center and results in an inability of 1 to dehydrogenate benzyl alcohol to benzaldehyde. These observations also lend further support to the mechanism for benzylamine dehydrogenation that we have previously proposed and provide insights for future catalyst design using metal–ligand cooperative pathways with Al.