Mechanochemical Formation,Solution Rearrangements,and Catalytic Behavior of a Polymorphic Ca/K Allyl Complex |
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Authors: | Ross F. Koby Alicia M. Doerr Nicholas R. Rightmire Nathan D. Schley Dr. William W. Brennessel Prof. Brian K. Long Prof. Timothy P. Hanusa |
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Affiliation: | 1. Department of Chemistry, Vanderbilt University, Nashville, TN 37235 USA;2. Department of Chemistry, University of Tennessee, Knoxville, TN 37996–1600 USA;3. X-ray Crystallographic Facility, Department of Chemistry, University of Rochester, Rochester, NY 14627 USA |
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Abstract: | Without solvents present, the often far-from-equilibrium environment in a mechanochemically driven synthesis can generate high-energy, non-stoichiometric products not observed from the same ratio of reagents used in solution. Ball milling 2 equiv. K[A’] (A’=[1,3-(SiMe3)2C3H3]−) with CaI2 yields a non-stoichiometric calciate, K[CaA’3], which initially forms a structure ( 1 ) likely containing a mixture of pi- and sigma-bound allyl ligands. Dissolved in arenes, the compound rearranges over the course of several days to a structure ( 2 ) with only η3-bound allyl ligands, and that can be crystallized as a coordination polymer. If dissolved in alkanes, however, the rearrangement of 1 to 2 occurs within minutes. The structures of 1 and 2 have been modeled with DFT calculations, and 2 initiates the anionic polymerization of methyl methacrylate and isoprene; for the latter, under the mildest conditions yet reported for a heavy Group 2 species (one-atm pressure and room temperature). |
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Keywords: | Allyl ligands Calcium Mechanochemistry Polymerization Potassium |
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