Three-coordinated chlorogermylenes of the type [Ph P(RN) ]GeCl (3: R= Bu; 4: R=Dip=2,6- Pr C H ), which bear an N,N-substituted iminophosphonamide ligand, were synthesized. The coordination behavior of 3 and 4 toward rhodium(I) complex was investigated. When 3 was treated with 1/2 of an equivalent of [RhCl(cod)] (cod=1,5-cyclooctadiene), the corresponding chlorogermylene-Rh(I) complex 5 was obtained as orange crystals. In contrast, the reaction of 4 with a half equivalent of [RhCl(cod)] under a CO atmosphere resulted in the formation of a five-membered germarhodacycle 7. Compounds 3, 4, 5, and 7 were characterized using NMR spectroscopies and single-crystal X-ray diffraction. Complex 5 can be employed as a catalyst for the hydrosilylation and hydroboration reactions of diphenylacetylene, thus demonstrating the utility of germylene ligands comparable to those of NHCs in the major transition metal catalytic processes.
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http://dx.doi.org/10.1002/asia.202300968 | DOI Listing |
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