Novel ruthenium nitrosyl complexes formed by nitrosating the tris(violurato)- and tris(1,3-dimethylviolurato)-ruthenate(II) anions
作者:Claude Bremard、Maurice Muller、Guy Nowogrocki、St�phane Sueur
DOI:10.1039/dt9770002307
日期:——
3-dimethylviolurate). The complexes react with Na[NO2] in acidic aqueous solutions to afford a series of novel diamagnetic nitrosylruthenium complexes of the general type cis-[Ru(L–L)2(NO)X](L–L = bidentate H2va– or dmva–; X–= Cl–, Br–, or unidentate H2va– or dmva–). In water, acetomtrile, or dimethyl sulphoxide. the complexes cis-[Ru(L–;L)3(NO)] release the co-ordinated nitrosyl lirgand owing to the intramolecular
Na 2 [Ru(NO)(NO 2)4(OH)]盐与巴比妥酸在水中反应,生成Na [Ru(H 2 va)3 ](H 2 va – =戊二酸二齿戊酸酯),与1, 3-二甲基巴比妥酸生成Na [Ru(dmva)3 ](dmva – =二齿1,3-二甲基紫草酸酯)。络合物在酸性水溶液中与Na [NO 2 ]反应,得到一系列新型的顺式-[Ru(L–L)2(NO)X](L–L =双齿H 2 va –或dmva –; X – = Cl–,Br –或未知H 2 va –或dmva –)。在水中,乙腈或二甲基亚砜中。配合物的顺式- [茹(L-; L) 3(NO)]释放协调亚硝酰基lirgand由于分子内变换:顺式- [茹(L-L) 2(NO)(单齿L-L)] →[Ru(L–L) 2(二元L–L)] – + [NO] +。根据ir和1在H nmr光谱中,给出了络合物的最可能的结构,并且表明配位NO的高亲电性