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五角双锥构型的场诱导Co^(Ⅱ)单离子磁体
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作者 赵淑艳 《无机化学学报》 SCIE CAS CSCD 北大核心 2024年第8期1583-1591,共9页
利用CoCl_(2)·6H_(2)O和2,6-二乙酰吡啶双(氨基脲)(H_(2)dapsc)在水和乙醇的混合溶剂中回流反应得到一例具有五角双锥构型的单核Co~Ⅱ配合物[Co(H_(2)dapsc)(H_(2)O)Cl]Cl·2H_(2)O(1),其中中性的H_(2)dapsc配体分子提供5个配... 利用CoCl_(2)·6H_(2)O和2,6-二乙酰吡啶双(氨基脲)(H_(2)dapsc)在水和乙醇的混合溶剂中回流反应得到一例具有五角双锥构型的单核Co~Ⅱ配合物[Co(H_(2)dapsc)(H_(2)O)Cl]Cl·2H_(2)O(1),其中中性的H_(2)dapsc配体分子提供5个配位原子构成其赤道平面,1个水分子和1个Cl^(-)离子则占据其轴向位置,同时在其固态结构中包含1个价态平衡Cl^(-)离子和晶格水分子。直流磁化率研究表明,该配合物具有强的磁各向异性;交流磁性质表明其存在慢磁弛豫行为,直接和拉曼过程同时主导其弛豫,自旋翻转能垒为55.55 K。结合理论计算可以得出,导致该配合物慢磁弛豫行为的主要原因是五角双锥结构的面内各向异性,计算得到的D、E值为45.68、-0.32 cm^(-1)。 展开更多
关键词 Co^()配合 五角双锥 晶体结构 磁性质
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三元手性配位聚合物{[Fe~Ⅲ(L^1)_3][Fe_2~Ⅲ(L^2)_3]}_∞和{[M(HL^1)_3][M_2(L^2)_3]}_∞(M=Co~Ⅱ,Zn~Ⅱ)的合成、晶体结构及磁性研究 被引量:1
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作者 胡同亮 田金磊 +1 位作者 卜显和 童明良 《南开大学学报(自然科学版)》 CAS CSCD 北大核心 2007年第1期1-5,共5页
合成了草酸根桥联的三元手性配位聚合物:{[Fe(L^1)_3][Fe_2(L^2)_3]}_∞(1),{[Co(HL^1)_3][Co_2(L^2)_3]}_∞(2)和{[Zn(HL^1)_3][Zn_2(L^2)_3]}_∞(3)(HL^1=3-(2-吡啶基)吡唑;L^2=C_2O_4^(2-)),并用 X-射线单晶衍射法测定了它们的晶体结... 合成了草酸根桥联的三元手性配位聚合物:{[Fe(L^1)_3][Fe_2(L^2)_3]}_∞(1),{[Co(HL^1)_3][Co_2(L^2)_3]}_∞(2)和{[Zn(HL^1)_3][Zn_2(L^2)_3]}_∞(3)(HL^1=3-(2-吡啶基)吡唑;L^2=C_2O_4^(2-)),并用 X-射线单晶衍射法测定了它们的晶体结构.配合物1~3具有类似的结构:草酸根(L^2)与金属离子配位形成大孔洞三维骨架,而3-(2-吡啶基)吡唑(HL^1或 L^1)与金属离子形成的单核单元则填充在上述三维骨架中.配合物1中通过草酸根桥联的 Fe~Ⅲ离子之间存在反铁磁偶合作用. 展开更多
关键词 晶体结构 Fe^Ⅲ配合 Co^配合 Zn^配合 草酸根 磁性
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An EXAFS investigation of the mechanism of competitive sorption between Co(Ⅱ) and Ni(Ⅱ) at γ-alumina/solution interface 被引量:2
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作者 Wenxian Gou Junfeng Ji Wei Li 《Acta Geochimica》 EI CAS CSCD 2017年第3期462-464,共3页
Co(Ⅱ)and Ni(Ⅱ)are two common toxic heavy metals,and may simultaneously exist in contaminated water,soil,and sediment systems in Earth’s surface environment.Under this circumstance,competitive adsorption between the... Co(Ⅱ)and Ni(Ⅱ)are two common toxic heavy metals,and may simultaneously exist in contaminated water,soil,and sediment systems in Earth’s surface environment.Under this circumstance,competitive adsorption between the two metals may influence their migration,toxicity,and bioavailability.In this research,the competitive sorption of Co(Ⅱ)and Ni(Ⅱ)on γ-Al_2O_3was studied using both macroscopic sorption experiments and extended X-ray absorption fine structure(EXAFS)spectroscopy.Results suggest that Ni(Ⅱ)reduced the amount of Co(Ⅱ)sorption in a binary-solute system at pH 6.0.This is because both Co(Ⅱ)and Ni(Ⅱ)form inner-sphere surface complexes during sorption on γ-Al_2O_3and compete for the surface reactive sites.However,Co(Ⅱ)exhibited a negligible influence on sorption amount of Ni(Ⅱ)under the same conditions,which suggests Ni(Ⅱ)has a stronger affinity to alumina surface.At pH 7.5,Co(Ⅱ)and Ni(Ⅱ)sorption density were much higher than that at pH 6.0,but there no mutual competitive effect was observed.EXAFS analysis further revealed that formation of layered double-hydrated precipitates was the dominant sorption mechanism for both Co(Ⅱ)and Ni(Ⅱ)at pH 7.5.Because this type of sorption does not rely on surface reactive sites,there was no competition between Co(Ⅱ)and Ni(Ⅱ).This finding sheds light on risk assessment and remediation of Ni/Co pollution. 展开更多
关键词 Co( Ni( Γ-AL2O3 Competitive sorption EXAFS
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