Department of Chemistry, Ludwig-Maximilian-University Munich, Butenandtstraße 5-13 (House D), D-81377, Munich, Germany.
Dalton Trans. 2012 Feb 21;41(7):2176-86. doi: 10.1039/c1dt11696g. Epub 2011 Dec 20.
The synthesis, spectroscopic characterization and crystal structures of the first 1,4-bis(4-nitrosophenyl)piperazine (BNPP) (4) bridged dinuclear complexes of rhodium(III) and iridium(III) are presented. The reaction of the μ(2)-halogenido-bridged dimers (η(5)-C(5)Me(5))IrX(2) [X = Cl (5a), Br (5b), I (5c)] and (η(5)- C(5)Me(5))RhCl(2) (6a) with 4 yields the dinuclear complexes (η(5)-C(5)Me(5))IrX(2)-BNPP (7a-c) and (η(5)-C(5)Me(5))RhCl(2)-BNPP (8a). All new compounds were characterized by their NMR, IR and mass spectra. The X-ray structure analyses of the obtained half-sandwich complexes revealed a slightly distorted pseudo-octahedral configuration ("three-legged pianostool") for the metal(III) centers. The bridging BNPP ligand is σ-N coordinated by both nitroso groups and shows different conformations of the piperazine ring depending on the solvent used for crystallization. Moreover the crystal structures of 1,4-bis(4-nitrosophenyl)piperazine (4) and its precursor 1,4-diphenylpiperazine (3) are reported.
首次合成、光谱特性和晶体结构的 1,4-双(4-亚硝基苯基)哌嗪 (BNPP) (4) 桥联双核配合物的铑(III)和铱(III)。反应μ(2)-卤化物桥联二聚体(η(5)-C(5)Me(5))IrX(2) [X = Cl (5a), Br (5b), I (5c)]和(η(5)- C(5)Me(5))RhCl(2) (6a)与 4 生成双核配合物(η(5)-C(5)Me(5))IrX(2)-BNPP (7a-c)和(η(5)-C(5)Me(5))RhCl(2)-BNPP (8a)。所有新化合物都通过其 NMR、IR 和质谱进行了表征。获得的半夹心配合物的 X 射线结构分析表明,金属(III)中心呈现出略微扭曲的拟八面体构型(“三脚钢琴凳”)。桥联 BNPP 配体由两个亚硝基基团 σ-N 配位,根据用于结晶的溶剂呈现出不同的哌嗪环构象。此外,还报道了 1,4-双(4-亚硝基苯基)哌嗪 (4)及其前体 1,4-二苯基哌嗪 (3)的晶体结构。