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Article Abstract
Copper(I) complexes of isobutyl- () and isopropyl-substituted () proazaphosphatranes have been synthesized. Structural and computational studies of a series of monomeric complexes CuX (X = Cl, Br, I) and dimeric [CuCl] provide insight into the transannulation within and steric properties of the proazaphosphatrane ligand. These halide complexes are competent precatalysts in a model borylation reaction, and the silylamido complex CuN(TMS) catalyzes hydrosilylation of benzaldehyde under mild conditions.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11752512 | PMC |
| http://dx.doi.org/10.1021/acs.inorgchem.4c04779 | DOI Listing |
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