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Studies on reactions of some ruthenium sulfoxide bipyridyl complexes with 1,4-bis(salicylidene)phenylenediamine ligand used as spacer

机译:某些亚砜钌联吡啶配合物与1,4-双(水杨基)苯二胺配体作为间隔基的反应研究

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A dinucleating spacer 1,4-bis(salicylidene)phenylenediamine (SALPHEN) derived from 1,4-phenylenediamine and salicylaldehyde has been synthesized and characterized. The ruthenium(II) sulfoxide derivative of 2,2′-bipyridine or 1,10-phenanthroline on reaction with this ligand resulted in the formation of eight dinuclear complexes, which were characterized by elemental analyses, conductivity measurements, magnetic susceptibility, FT-IR, fast atom bombardment-mass spectra, electronic spectroscopy, 1H-NMR, 13C{1H}-NMR, and 2D-NMR spectra (HETCOR). The prepared complexes have two different formulations, [{trans-RuCl2(so)(N-N′)}2(μ-SALPHEN)] and [{cis-RuCl2(so)(N-N′)}2(μ-SALPHEN)], where so = dimethyl sulfoxide (DMSO)/tetramethylene sulfoxide (TMSO), N-N′ = 2,2′-bipyridine/1,10-phenanthroline, and SALPHEN = 1,4-bis(salicylidene)phenylenediamine. Two moles of ruthenium sulfoxide bipyridine precursor were coordinated to the bidentate SALPHEN through nitrogen. All the complexes possess antibacterial activity against Escherichia coli in comparison to Chloramphenicol.View full textDownload full textKeywordsPhenyldiamine, 1,4-Bis(salicylidene)phenylenediamine, Ruthenium sulfoxide, BipyridineRelated var addthis_config = { ui_cobrand: "Taylor & Francis Online", services_compact: "citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,more", pubid: "ra-4dff56cd6bb1830b" }; Add to shortlist Link Permalink http://dx.doi.org/10.1080/00958972.2012.657630
机译:合成并表征了由1,4-苯二胺和水杨醛衍生的双核间隔基1,4-双(水杨基)苯二胺(SALPHEN)。与该配体反应的2,2'-联吡啶或1,10-菲咯啉的钌(II)亚砜衍生物导致形成八个双核配合物,其特征在于元素分析,电导率测量,磁化率,FT-红外,快速原子轰击质谱,电子光谱, 1 H-NMR, 13 C { 1 H} -NMR和 2 D-NMR光谱(HETCOR)。准备的配合物有两种不同的配方,[{反式RuCl 2 (so)(N-N′)} 2 (α-SALPHEN)]和[{cis -RuCl 2 (so)(N-N′)} 2 (α-SALPHEN)],其中==二甲基亚砜(DMSO)/丁烷亚砜(TMSO),N-N = 2,2-联吡啶/ 1,10-菲咯啉和SALPHEN = 1,4-双(水杨基)苯二胺。将两摩尔的亚砜钌联吡啶前体通过氮与双齿SALPHEN配位。与氯霉素相比,所有的复合物均具有抗大肠杆菌的抗菌活性。 citeulike,netvibes,twitter,technorati,美味,linkedin,facebook,stumbleupon,digg,google,更多”,发布:“ ra-4dff56cd6bb1830b”};添加到候选列表链接永久链接http://dx.doi.org/10.1080/00958972.2012.657630

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