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Synthesis,structure,and magnetic property of a cobalt(Ⅱ)complex based on pyridyl⁃substituted imino nitroxide radical
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作者 WANG Xiaoling ZHANG Hongwu LIU Daofu 《无机化学学报》 北大核心 2025年第2期407-412,共6页
A new cobalt(Ⅱ)-radical complex:[Co(im4-py)_(2)(PNB)_(2)](im4-py=2-(4'-pyridyl)-4,4,5,5-tetramethylimidazole-1-oxyl,HPNB=p-nitrobenzoic acid)has been synthesized and characterized by X-ray diffraction analysis,el... A new cobalt(Ⅱ)-radical complex:[Co(im4-py)_(2)(PNB)_(2)](im4-py=2-(4'-pyridyl)-4,4,5,5-tetramethylimidazole-1-oxyl,HPNB=p-nitrobenzoic acid)has been synthesized and characterized by X-ray diffraction analysis,elemental analysis,IR,and magnetic properties.X-ray diffraction analysis shows that the complex exists as mononuclear molecules and Co(Ⅱ)ion is four-coordinated with two radicals and two PNB-ligands.The magnetic susceptibility study indicates the complex exhibits weak ferromagnetic interactions between cobalt(Ⅱ)and im4-py radical.The magnetic property is explained by the magnetic and structure exchange mechanism.CCDC:976028. 展开更多
关键词 Co(Ⅱ)complex imino nitroxide radical crystal structure magnetic property
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一种新的生物分离方法——混合模式吸附层析 被引量:17
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作者 姚善泾 高栋 林东强 《化工学报》 EI CAS CSCD 北大核心 2007年第9期2169-2177,共9页
混合模式吸附层析是一种新型的生物分离方法,其功能配基兼有两种或两种以上的作用模式,主要为静电和疏水相互作用。在低盐和高盐条件下,都可以实现对目标物的有效吸附,具有明显的耐盐吸附的特性,可避免对料液的额外预处理,从而提高分离... 混合模式吸附层析是一种新型的生物分离方法,其功能配基兼有两种或两种以上的作用模式,主要为静电和疏水相互作用。在低盐和高盐条件下,都可以实现对目标物的有效吸附,具有明显的耐盐吸附的特性,可避免对料液的额外预处理,从而提高分离效率,减少分离成本,已获得一定的应用。本文对混合模式吸附技术的发展历程、类型及应用现状等进行综述,以推动该技术的发展和进一步应用。 展开更多
关键词 生物分离 层析 混合模式 耐盐吸附 疏水性电荷诱导层析 配基结构
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Ligand substitution of diiron hexacarbonyl complex with aminodiphosphine to prepare diiron aminophosphine complexes relevant to[FeFe]-hydrogenases
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作者 LIU Xufeng WANG Shaojie ZHAO Peihua 《无机化学学报》 2025年第9期1851-1858,共8页
To extend a new family of aminophosphine-coordinated[FeFe]-hydrogenase mimics for catalytic hydro-gen(H_(2))evolution,we carried out the ligand substitutions of diiron hexacarbonyl precursors[Fe_(2)(μ-X_(2)pdt)(CO)_(... To extend a new family of aminophosphine-coordinated[FeFe]-hydrogenase mimics for catalytic hydro-gen(H_(2))evolution,we carried out the ligand substitutions of diiron hexacarbonyl precursors[Fe_(2)(μ-X_(2)pdt)(CO)_(6)](X_(2)pdt=(SCH_(2))_(2)CX_(2),X=Me,H)with aminodiphosphines(Ph_(2)PCH_(2))_(2)NY(Y=(CH_(2))_(2)OH,(CH_(2))_(3)OH)to obtain two new diiron aminophosphine complexes[Fe_(2)(L1)(μ-Me_(2)pdt)(CO)_(5)](1)and[Fe_(2)(L2)(μ-H_(2)pdt)(CO)_(5)](2),where L1=3-[(diphe-nylphosphaneyl)methyl]oxazolidine,L2=3-[(diphenylphosphaneyl)methyl]-1,3-oxazinane.Moreover,the structures of 1 and 2 have been fully confirmed by elemental analysis,spectroscopic techniques,and single-crystal X-ray diffraction.Using cyclic voltammetry(CV),we investigated the electrochemical redox performance and proton reduc-tion activities of 1 and 2 in acetic acid(HOAc).The CV study indicates that diiron aminophosphine complexes 1 and 2 can be considered to be hydrogenase-inspired diiron molecular electrocatalysts for the reduction of protons into H 2 generation in the presence of HOAc.CCDC:2443967,1;2443969,2. 展开更多
关键词 [FeFe]-hydrogenases diiron model complexes aminophosphine ligand structure electrochemical performance
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