Coordination Chemistry of Rh(III) Porphyrins: Complexes with Hydrazine, Disulfide, and Diselenide Bridging Ligands
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Rh(III) porphyrin complexes with bridging hydrazine and substituted hydrazine ligands were characterized insolution by 1H NMR spectroscopy and in the solid state by X-ray diffraction. Addition of further ligand to thesespecies afforded 1:1 complexes in which methylhydrazine and N,N-dimethylhydrazine preferentially bound tothe Rh center through the substituted nitrogen atom, as evidenced by 1H NMR chemical shifts. An alkylatedRh(III) porphyrin was isolated as a decomposition product of the reaction of N,N-dimethylhydrazine with Rh(III)porphyrin in the presence of light and oxygen. Me2Se2 and Me2S2 formed bridging and nonbridging complexeswith Rh(III) porphyrin, analogous to that observed with N,N'-dimethylhydrazine.

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