Theoretical Designs for Organoaluminum CAlR with Well-Separated Al(I) and Al(III).

ACS Omega

Laboratory of Theoretical and Computational Chemistry, Institute of Theoretical Chemistry, Jilin University, Changchun 130023, China.

Published: September 2017

It is well-known that the chemistry of aluminum is dominated by Al(III) in the +3 oxidation state. Only during the past 2 decades has the chemistry of Al(I) and Al(II) been rapidly developed. However, if Al(I) and Al(III) are combined, the inherently high reactivities of Al(I) and Al(III) mostly result in their coupling with each other or interacting with surrounding elements, which easily results in significant deactivation or quenching of the desired oxidation states, as in the case of reported mixed valent Al-compounds. In this article, we report an unprecedented type of organoaluminum system, CAlR (R = H, SiH, Si(CH), SiPrDis, SiMe(SiBu)), whose lowest-energy structure, CAlR-, contains two Al(I) and two Al(III) atoms. The global nature and bonding motif of the parent CAlR- (R = H) were supported by an extensive global isomeric search, CBS-QB3 energy calculations, adaptive natural density partitioning, and bond order analysis. Interestingly and in sharp contrast to most organoaluminum species, CAlR- is associated with little multicenter bonding. CAlR- has a high feasibility of being observed either in the gas or condensed phases (with suitable substitutents). With well-separated Al(I) and Al(III), CAlR- (with suitable substitutents) could serve as the first Al/Al frustrated Lewis pair.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644568PMC
http://dx.doi.org/10.1021/acsomega.7b00487DOI Listing

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