Title

Structural characterization of MAO and related aluminum complexes. 1. Solid-state 27Al NMR with comparison to EFG tensors from ab initio molecular orbital calculations

Document Type

Article

Publication Date

12-5-2001

Abstract

Experimental and ab initio molecular orbital techniques are developed for study of aluminum species with large quadrupole coupling constants to test structural models for methylaluminoxanes (MAO). The techniques are applied to nitrogen- and oxygen-containing complexes of aluminum and to solid MAO isolated from active commercial MAO preparations. (Aminato)- and (propanolato)aluminum clusters with 3-, 4-, and 6-coordinate aluminum sites are studied with three 27Al NMR techniques optimized for large 27Al quadrupole coupling constants: field-swept, frequency-stepped, and high-field MAS NMR. Four-membered (aminato)-aluminum complexes with AlN4 coordination yield slightly smaller Cq values than similar AlN2C2 sites: 12.2 vs 15.8 MHz. Planar 3-coordinate AlN2C sites have the largest Cq values, 37 MHz. In all cases, molecular orbital calculations of the electric field gradient tensors yields Cq and η values that match with experiment, even for a large hexameric (aminato)aluminum cage. A D3d symmetry hexaaluminum oxane cluster, postulated as a model for MAO, yields a calculated Cq of -23.7 MHz, η = 0.7474, and predicts a spectrum that is too broad to match the field-swept NMR of methylaluminoxane, which shows at least three sites, all with Cq values greater than 15 MHz but less than 21 MHz. Thus, the proposed hexaaluminum cluster, with its strained four-membered rings, is not a major component of MAO. However, calculations for dimers of the cage complex, either edge-bridged or face-bridged, show a much closer match to experiment. Also, MAO preparations differ, with a gel form of MAO having significantly larger 27Al Cq values than a nongel form, a conclusion reached on the basis of 27Al NMR line widths in field-swept NMR spectra acquired from 13 to 24 T.

Publication Source (Journal or Book title)

Journal of the American Chemical Society

First Page

12009

Last Page

12017

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