摘要:
The binuclear nitropyrazole compound [Re2O3Cl2(PPh3)(2)(C3H2N3O2)(2)] (3) was synthesized by refluxing [ReOCl2(OEt)(PPh3)(2)] and 2-nitropyrazole in ethanol for 12 h. The octahedral {ReO2N2ClP} sites are linked by two bridging nitropyrazoles and an oxo group, with an Re-O-Re angle of 124.7(6)degrees. Compound 3 is electrochemically active, displaying a reversible one electron reduction at -0.55 V with respect to Ag/Ag+. Crystal data: C36H34Cl2N6O7P2Re2 (3), monoclinic C2/c, a=32.569(7), b=9.624(2), c=29.151(6) Angstrom, beta=109.33(3)degrees, V=8622(3) Angstrom(3), Z=8, D-calc=1.799 g cm(-3), structure solution and refinement based on 3364 reflections converged at R=0.056.