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新型酰胺金属配合物的热力学稳定性研究 被引量:6
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作者 高东昭 郭延河 +2 位作者 朱守荣 林华宽 许新合 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2004年第4期740-742,共3页
N,N-Bis(2-pyridylmethyl)-amine-N-ethyl-2-pyridine-2-carboxamide was synthesized and characterized according to the literature. At 25 ℃, I=0.1 mol/L KNO 3, the stability constants of the binary system formed by the li... N,N-Bis(2-pyridylmethyl)-amine-N-ethyl-2-pyridine-2-carboxamide was synthesized and characterized according to the literature. At 25 ℃, I=0.1 mol/L KNO 3, the stability constants of the binary system formed by the ligand with metal ions in ethanol aqueous solution were studied by pH potentiometric titration and the appropriate structures with respect to the titration species were proposed. The results show that the stability order of divalent metals binding to the ligand is Co<Ni>Cu<Zn which does not conform to the order of the Irving-Williams series. Then the abnormal property of copper complex is discussed. 展开更多
关键词 酰胺 金属配合物 热力学稳定性 吡啶-2-甲酰胺配体 Irving—Williams序列
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氮氧自由基-锌配合物[Zn(NIT3Py)_2Cl_2]的合成、结构和磁行为(英文) 被引量:5
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作者 高东昭 赵为为 +1 位作者 陈毅雯 孙亚秋 《无机化学学报》 SCIE CAS CSCD 北大核心 2009年第4期738-741,共4页
A Zn(Ⅱ) complex with nitronyl nitroxide radicals [Zn(NIT3Py)2Cl2](1)(NIT3Py=2-(3'-pyridinyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide) has been synthesized and structurally characterized by X-ray diffraction... A Zn(Ⅱ) complex with nitronyl nitroxide radicals [Zn(NIT3Py)2Cl2](1)(NIT3Py=2-(3'-pyridinyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide) has been synthesized and structurally characterized by X-ray diffraction crystal structure determination method.The complex has a mononuclear-metal structure in which each Zn(Ⅱ) ion adopts a distorted tetrahedral geometry and is coordinated by two Cl-anions and two pyridyl-N atoms from two NIT3Py radical ligands.The magnetic measurements show the weak antiferromagnetic interaction between the nitroxide radicals through the diamagnetic Zn(Ⅱ) ion.CCDC:292363. 展开更多
关键词 锌配合物 氮氧自由基 晶体结构 磁行为
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氮-[双(2-吡啶)甲基]吡啶-2-甲酰胺金属配合物的热力学稳定性研究 被引量:1
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作者 高东昭 郭延河 +2 位作者 朱守荣 林华宽 许新合 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2004年第3期493-496,391,共5页
利用简单步骤合成了酰胺类配体氮 -[双 ( 2 -吡啶 )甲基 ]吡啶 -2 -甲酰胺 ( L) ,在 2 5℃ ,I=0 .1 mol/ LKNO3的 3 0 %乙醇 -水溶液中用 p H滴定法测定了其与不同金属离子组成的二元和三元配合物的稳定常数 ,结合单晶结构讨论了物种的... 利用简单步骤合成了酰胺类配体氮 -[双 ( 2 -吡啶 )甲基 ]吡啶 -2 -甲酰胺 ( L) ,在 2 5℃ ,I=0 .1 mol/ LKNO3的 3 0 %乙醇 -水溶液中用 p H滴定法测定了其与不同金属离子组成的二元和三元配合物的稳定常数 ,结合单晶结构讨论了物种的可能构型 ,并比较了配体与 Cu( )和 Fe( )形成配合物的热力学稳定性差异 。 展开更多
关键词 酰胺 配合物 热力学稳定性 线性自由能关系
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酰胺多胺配体Cu(Ⅱ)配合物的稳定性和酸分解动力学 被引量:3
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作者 郭延河 高东昭 +3 位作者 林海 林华宽 盖庆春 朱守荣 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2004年第1期103-107,共5页
合成了酰胺多胺配体 ( L) ,测定了 5,10 ,15和 2 5℃时其 Cu( )配合物的稳定常数 ,用标准摩尔焓变ΔH 0_m 和标准摩尔熵变ΔS0_m 解释了温度对稳定性的影响 ,并利用停流技术 ( Stopped- flow)研究了 Cu L配合物在 0 .0 4~ 2 .3m ol/L(... 合成了酰胺多胺配体 ( L) ,测定了 5,10 ,15和 2 5℃时其 Cu( )配合物的稳定常数 ,用标准摩尔焓变ΔH 0_m 和标准摩尔熵变ΔS0_m 解释了温度对稳定性的影响 ,并利用停流技术 ( Stopped- flow)研究了 Cu L配合物在 0 .0 4~ 2 .3m ol/L( I=2 .34 mol/L Na Cl)盐酸溶液中的酸分解动力学 .提出了反应机理 ,并求得了速控步骤的活化能 Ea,标准摩尔活化熵 Δ≠ S0_m 和标准摩尔活化焓 Δ≠ H0_m. 展开更多
关键词 酰胺多胺配体 Cu(Ⅱ)配合物 稳定性 酸分解 分解动力学
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N-乙基-1,10-菲罗啉-2-甲胺镍(Ⅱ) 配合物的合成、晶体结构及性质研究(英文)
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作者 李风华 吴红星 +2 位作者 高东昭 林华宽 朱守荣 《无机化学学报》 SCIE CAS CSCD 北大核心 2004年第4期483-487,共5页
A novel ligand N - ethyl - 1,10 - phenanthroline - 2 - methanamine and its Ni(Ⅱ)complex have been synthesized.The crystal structure of the complex has been determined by X - ray diffraction method.The Ni(Ⅱ)is five -... A novel ligand N - ethyl - 1,10 - phenanthroline - 2 - methanamine and its Ni(Ⅱ)complex have been synthesized.The crystal structure of the complex has been determined by X - ray diffraction method.The Ni(Ⅱ)is five - coordi - nated by three nitrogen atoms from the ligand and two Cl - anions in a distorted trigonal bipyramidal environment:the N(2),Cl(1)and Cl(2)in equatorial plane;the N(1)and N(3)in axial positions.The UV - spectra and IR - spectra of the ligand and its Ni(Ⅱ)complex were recorded and discussed.The thermodynamic properties of the ligand with various bivalent metals were studied by potentiometric titrations and the order of the stability constants is in a - greement with the Irving - Williams order in coordination chemistry.CCDC:221750. 展开更多
关键词 N-乙基-1 10-菲罗啉-2-甲胺 镍配合物 合成 晶体结构 性质
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一个锰(Ⅲ)Schiff碱配合物[Mn(napn)(CH_3OH)_2]ClO_4的合成与晶体结构
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作者 周北川 寇会忠 +3 位作者 高东昭 廖代正 王如骥 李亚栋 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2002年第5期549-552,共4页
合成了一个新配合物[Mn(napn)(CH3OH)2]ClO4 (C26H26 Cl N2O8Mn,Mr = 584.88,H2napn = 双a-萘酚醛缩乙二胺),并测定了其晶体结构。晶体属于三斜晶系,空间群P ,a = 7.813(1),b = 13.025(2),c = 14.089(2) ? = 64.89(3), = 83.98(3), = ... 合成了一个新配合物[Mn(napn)(CH3OH)2]ClO4 (C26H26 Cl N2O8Mn,Mr = 584.88,H2napn = 双a-萘酚醛缩乙二胺),并测定了其晶体结构。晶体属于三斜晶系,空间群P ,a = 7.813(1),b = 13.025(2),c = 14.089(2) ? = 64.89(3), = 83.98(3), = 78.11(3)海琕 = 1270.16 ?,Z = 2, Dc = 1.529 g/cm3, F(000) = 604, R = 0.0837, wR = 0.1636。锰(Ⅲ)离子的配位构型为拉长的八面体。Schiff碱配体napn2-中的N2O2在赤道平面与锰(Ⅲ)形成四配位,2个CH3OH中的O原子分别在赤道平面两侧轴向位置与锰(Ⅲ)配位。由于Jahn-Teller效应,轴向上的MnO平均键长为2.52 拧A硗猓О写嬖诜肿幽诤头肿蛹淝饧? 展开更多
关键词 锰(Ⅲ) SCHIFF碱 配合物 [Mn(napn)(CH3OH)2]ClO4 合成 JAHN-TELLER效应 氢键 晶体结构 锰超氧化物歧化酶
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{110}晶面取向Ag3PO4多面体的水热制备及可见光催化活性 被引量:3
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作者 刘春梅 张国英 +2 位作者 张欣 许艳艳 高东昭 《物理化学学报》 SCIE CAS CSCD 北大核心 2015年第10期1939-1948,共10页
采用简易水热法在聚乙二醇-6000(PEG-6000)辅助下合成了Ag3PO4多面体.系统考察了水热反应温度、时间及PEG-6000用量对产物形貌和结构的影响.通过X射线衍射(XRD),扫描电子显微镜(SEM),紫外-可见漫反射光谱(UV-Vis DRS)和荧光(PL)光谱等... 采用简易水热法在聚乙二醇-6000(PEG-6000)辅助下合成了Ag3PO4多面体.系统考察了水热反应温度、时间及PEG-6000用量对产物形貌和结构的影响.通过X射线衍射(XRD),扫描电子显微镜(SEM),紫外-可见漫反射光谱(UV-Vis DRS)和荧光(PL)光谱等测试手段对光催化剂进行了表征.结果表明,适宜的水热温度及PEG-6000用量是制备具有{110}活性晶面取向Ag3PO4多面体的必要条件,该多面体通过纳米颗粒的Ostwald熟化效应生长而成.可见光催化降解罗丹明B(Rh B)的实验表明,该Ag3PO4多面体活性明显优于其它水热条件下所制备的非{110}取向晶面样品和离子交换法所得纳米颗粒,其降解反应速率常数(k)为离子交换法所得Ag3PO4纳米颗粒的8.3倍.总有机碳含量(TOC)及循环实验证明,该Ag3PO4多面体可以有效地矿化Rh B并保持较好的循环稳定性.活性自由基捕获实验表明,空穴(h+)和羟基自由基(OH)是光催化氧化的主要活性物种.结合活性物种的氧化还原电位以及Ag3PO4的能带结构分析,提出了催化反应界面光生电子-空穴(e–-h+)对的分离及转移机制. 展开更多
关键词 Ag3PO4 PEG-6000 水热法 光催化 活性物种 光生载流子分离
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两个以大环草酰胺为主配体的多核铜及镍配合物的合成及晶体结构
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作者 刘晓旭 孙亚秋 +2 位作者 张国英 许艳艳 高东昭 《无机化学学报》 SCIE CAS CSCD 北大核心 2011年第9期1709-1714,共6页
本文利用大环草酰胺与2,2′-联吡啶、间苯二甲酸共配设计并合成了2个同多核配合物[Cu2L(2,2′-bipy)(H2O)(ClO4)]ClO4(1)和[Ni3L2(ipt)(H2O)]H2O(2)(ipt=isophthalic acid,H2L=2,3-dioxo-5,6,14,15-dibenzo-1,4,8,12-tetraazacyclo-pent... 本文利用大环草酰胺与2,2′-联吡啶、间苯二甲酸共配设计并合成了2个同多核配合物[Cu2L(2,2′-bipy)(H2O)(ClO4)]ClO4(1)和[Ni3L2(ipt)(H2O)]H2O(2)(ipt=isophthalic acid,H2L=2,3-dioxo-5,6,14,15-dibenzo-1,4,8,12-tetraazacyclo-pentadeca-7,13-diene),并利用单晶X-射线结构分析、红外对该配合物进行了结构表征,研究了其荧光性质。结构分析表明,配合物1为单斜晶系,空间群为P21/n,a=1.413 1(17)nm,b=1.091 7(13)nm,c=2.325 4(19)nm,β=119.35(5)°,Z=4。配合物2为单斜晶系,空间群为P21/c,a=1.159 7(2)nm,b=2.059 9(4)nm,c=1.847 7(4)nm,β=90.788(3)°,Z=4。配合物1和2分别是通过草酰胺桥联的双核、三核配合物,并通过氢键分别构成三维、二维超分子结构。 展开更多
关键词 大环草酰胺配合物 2 2′-联吡啶 间苯二甲酸 晶体结构 超分子
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一系列由柔性N,N′-双(3-吡啶甲基)胺构筑的螺旋配合物的合成、结构和性质(英文)
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作者 岳翠敏 高东昭 王修光 《无机化学学报》 SCIE CAS CSCD 北大核心 2015年第8期1609-1618,共10页
合成和表征了5个螺旋配位聚合物{[Cu(Hbpma)(H2O)4]2(SO4)3·3.5H2O}n(1)、{[Ni(Hbpma)(H2O)4]4(SO4)6·10.75H2O}n(2)、{[Mn(Hbpma)(H2O)4](SO4)1.5·3H2O}n(3)、{[Zn(Hbpma)(H2O)4]4(SO4)6... 合成和表征了5个螺旋配位聚合物{[Cu(Hbpma)(H2O)4]2(SO4)3·3.5H2O}n(1)、{[Ni(Hbpma)(H2O)4]4(SO4)6·10.75H2O}n(2)、{[Mn(Hbpma)(H2O)4](SO4)1.5·3H2O}n(3)、{[Zn(Hbpma)(H2O)4]4(SO4)6·4H2O·4CH3OH}n(4)和{[Cu(Hbpma)2(H2O)2](SO4)2·9H2O}n(5),其中bpma代表N,N′-双(3-吡啶甲基)胺。晶体结构分析表明配合物1~4为一维链状结构,配合物5为二维层状结构,其中金属离子由质子化的bpma配体桥连。值得注意的是,采取反-反式构象的柔性bpma配体使得配合物1和2为假螺旋链结构,配合物3和4为螺旋链结构,配合物5为螺旋层结构。同时研究了配合物的磁性和热稳定性。 展开更多
关键词 金属配合物 N N′-双(3-吡啶甲基)胺 螺旋结构 磁性 热稳定性
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Thermodynamic Stability Research of Metal Complexes with a Tripodal Amide Ligand and Crystal Structure of its Cobalt(Ⅲ) Complex
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作者 高东昭 陈毅雯 +2 位作者 赵为为 张国英 孙亚秋 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2009年第9期1136-1142,共7页
A new Co(Ⅲ) complex with a tripodal amide ligand [CoL(N3)3] (L = N-acetyl- N',N'-bis-[(2-pyridyl)methyl]-ethylenediamine) has been synthesized and characterized structurally by X-ray diffraction. It crystal... A new Co(Ⅲ) complex with a tripodal amide ligand [CoL(N3)3] (L = N-acetyl- N',N'-bis-[(2-pyridyl)methyl]-ethylenediamine) has been synthesized and characterized structurally by X-ray diffraction. It crystallizes in orthorhombic, space group Pnma with a = 9.2515(19), b = 12.729(3), c = 17.273(4) A, V = 2034.0(7) A3, C16H20CoN13O, Mr = 469.38, Dc = 1.533 g/cm3, μ(MoKα) = 0.884 mm^-1, F(000) = 968, Z = 4, the final R = 0.0392 and wR = 0.0818 for 2430 observed reflections. In the complex, the amide ligand L acts as a tridentate fashion and coordinates to the Co(Ⅲ) ion through three nitrogen atoms, while the other three positions of the Co(Ⅲ) center are occupied by three terminal azide anions. The complex is connected as a 1D chain structure by intermolecular hydrogen bonds between the uncoordinated amide groups. In order to investigate the coordination ability, thermodynamic stability of the ligand L with the first-series transition metal ions (Co(Ⅱ), Ni(Ⅱ), Cu(Ⅱ) and Zn(Ⅱ)) has been studied by potentiometric titration, and the results show that the order of their stability constants conforms to the Irving-Williams sequence. 展开更多
关键词 thermodynamic stability TRIPODAL amide ligand Co(Ⅲ) complex
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A Novel Binuclear Cu(Ⅱ) Complex with Nitroxide Radicals Exhibiting Ferromagnetic Interactions 被引量:3
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作者 刘尚远 陈毅雯 高东昭 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2012年第1期39-44,共6页
A new binuclear Cu(Ⅱ) complex with nitronyl nitroxide radicals [Cu(NIT3Py)2Cl2]2(NIT3Py = 2-(3'-pyridinyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide) has been synthesized and structurally characterized b... A new binuclear Cu(Ⅱ) complex with nitronyl nitroxide radicals [Cu(NIT3Py)2Cl2]2(NIT3Py = 2-(3'-pyridinyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide) has been synthesized and structurally characterized by X-ray diffraction analysis.It crystallizes in monoclinic,space group C2/c with a = 38.483(4),b = 7.2450(8),c = 27.559(3) ,β = 134.0180(10)°,V = 5525.6(10) 3,C48H64Cl4Cu2N12O8,Mr = 1206.00,Z = 4,Dc = 1.450 g/cm3,μ(MoKα) = 1.025 mm-1,F(000) = 2504,S = 1.066,the final R = 0.0471 and wR = 0.1121 for 3286 observed reflections(I 2σ(I)).The title complex consists of centrosymmetric dinuclear units [Cu(NIT3Py)2Cl2]2,in which the copper ions are square-pyramidally coordinated by two pyridyl nitrogen atoms of two radical ligands and three chlorine anions,two of which bridge the copper ions.The magnetic measurements show ferromagnetic interactions between the copper ions and the radical ligands. 展开更多
关键词 Cu(Ⅱ) complex nitroxide radical crystal structure ferromagnetic interaction
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Synthesis and Uncommon Structural Characterization of Novel Zinc and Cadmium Complexes with Imino Nitroxide Radical
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作者 王淑萍 高东昭 +2 位作者 廖代正 姜宗慧 阎世平 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2007年第4期472-476,共5页
Two novel complexes {[Zn(IM4py)2(tp)(H2O)]2H2O}. 1 and {[Cd(IM4py)2(tp)- (H2O)]1.25H2O},, 2 (IM4py = 2-(4'-pyridinyl)-4,4,5,5-tetramethylimidazoline-l-oxyl and tp = terephthalate dianion) have been sy... Two novel complexes {[Zn(IM4py)2(tp)(H2O)]2H2O}. 1 and {[Cd(IM4py)2(tp)- (H2O)]1.25H2O},, 2 (IM4py = 2-(4'-pyridinyl)-4,4,5,5-tetramethylimidazoline-l-oxyl and tp = terephthalate dianion) have been synthesized and characterized by elemental analyses, IR spectrum and single-crystal X-ray diffraction. Crystal data for complex I: monoclinic, space group C2/c, a = 20.648(7), b = 12.130(4), c = 14.036(4) A, β = 106.351(5)°, C32H42N6O9Zn, Mr = 720.09, V = 3373.3(2) A3, Z= 4, Dc = 1.418 g/cm^3μt(MoKα) = 0.790 mm^-1, F(000) = 1512, the final R = 0.0407 and wR = 0.0894 for 3480 independent reflections with Rint = 0.0432. Crystal data for complex 2: monoclinic, space group C2/c, a = 21.332(6), b = 12.063(3), c = 14.246(4) A, β = 106.704(4)°, C32H40.50N6O8.25Cd, Mr = 753.60, V= 3511.2(2) A^3, Z = 4, Dc = 1.426 g/cm^3,μ(MoKα) = 0.679 mm^--1, F(000) = 1554, the final R = 0.0419 and wR = 0.0961 for 3627 independent reflections with Rint = 0.0440. The framework structures of complexes 1 and 2 are 3-D networks via the hydrogen bonds among 1-D chains. The notable characteristics of the two complexes are that the coordination polyhedron of Zn(Ⅱ) adopts a rare distorted five-coordinate square pyramidal geometry in 1, and the Cd(Ⅱ) complex exhibits an unusual distorted seven-coordinate pentagonal bipyramid in 2. 展开更多
关键词 imino nitroxide radical zinc and cadmium complexes square pyramid pentagonal bipyramid
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Synthesis,Crystal Structure and Magnetic Property of a New Cd(Ⅱ) Complex with Four Nitronyl Nitroxide Radicals
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作者 崔志华 魏海霞 +3 位作者 高东昭 孙亚秋 张国英 许艳艳 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2011年第6期853-857,共5页
A new Cd(Ⅱ) complex with four nitronyl nitroxide radicals [Cd(NIT4Py)4Cl2](NIT4Py = 2-(4'-pyridinyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide) has been synthesized and structurally characterized by X-ra... A new Cd(Ⅱ) complex with four nitronyl nitroxide radicals [Cd(NIT4Py)4Cl2](NIT4Py = 2-(4'-pyridinyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide) has been synthesized and structurally characterized by X-ray diffraction analysis.It crystallizes in triclinic,space group P1 with a = 7.2441(4),b = 13.6964(8),c = 13.7354(8) ,α = 89.8610(10),β = 77.9180(10),γ = 87.2250(10)°,V = 1331.01(13) 3,C48H64CdCl2N12O8,Mr = 1120.41,Z = 1,Dc = 1.398 g/cm3,μ(MoKα) = 0.573 mm-1,F(000) = 582,S = 1.043,the final R = 0.0257 and wR = 0.0641 for 4333 observed reflections(I 〉2σ(I)).The title complex exists in the mononuclear-metal structures,in which each Cd(Ⅱ) ion adopts a distorted octahedral geometry and is coordinated by two Cl-anions and four pyridyl-N atoms from four NIT4Py ligands.The magnetic measurements show weak antiferromagnetic interactions between the nitroxide radicals. 展开更多
关键词 Cd(Ⅱ) complex nitronyl nitroxide radical crystal structure antiferromagnetic interaction
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Syntheses and Crystal Structures of Two One-dimensional Cobalt(Ⅱ) Compounds with the Flexible Dipyridyl Ligand
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作者 崔志华 王思思 +4 位作者 王修光 高东昭 孙亚秋 张国英 许艳艳 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2012年第6期769-776,共8页
Two one-dimensional cobalt(II) compounds {[Co(Hbpma)(H20)4]2·3SO4·4.5H2O}n 1 and {[Co(Hbpma)(NCS)3(H20)]·2.85H2O}n 2 (bpma = N,N'-bis(3-pyridylmethyl)amine) have been synthesized and st... Two one-dimensional cobalt(II) compounds {[Co(Hbpma)(H20)4]2·3SO4·4.5H2O}n 1 and {[Co(Hbpma)(NCS)3(H20)]·2.85H2O}n 2 (bpma = N,N'-bis(3-pyridylmethyl)amine) have been synthesized and structurally characterized by single-crystal X-ray diffraction. Complex 1 crystallizes in triclinic, space group Pi with a = 15.8780(5), b = 16.2187(5), c = 16.4858(5) A, α = 91.0420(10),β = 94.5190(10), γ = 101.4360(10)°, V = 4145.7(2) A3, C24H53Co2N6024.5083, Mr = 1031.76, Z = 4, Dc = 1.653 g/cm3, p(MoKa) = 1.046 mm-1, F(000) = 2148, S = 1.017, the final R = 0.0269 and wR = 0.0644 for 13032 observed reflections (I 〉 2a(/)). For complex 2, it belongs to triclinic, space group Pi with a = 9.3761(11), b = 10.5814(13), c = 11.2972(14)A, α= 85.472(2),β = 88.058(2),γ = 76.203(2)°, V= 1085.0(2) A3, C15Hzl.v0CoN603.85S3, Mr= 502.79, Z = 2, Dc = 1.539 g/cm3, p(MoKa) = 1.112 mm-1, F(000) = 519, S = 1.070, the final R = 0.0358 and wR = 0.0899 for 3466 observed reflections (I 〉 2σ(I)). Two complexes 1 and 2 are both found to be one-dimensional coordination polymers bridged by the protonated bpma ligands, which are assembled into three-dimensional supramolecular structures through the hydrogen bonding interactions and π-π packing interactions. 展开更多
关键词 cobalt(II) complex flexible dipyridyl ligand crystal structure
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Crystal Structure and Magnetic Properties of the Oxamidato-bridged Cu_3 Complex Containing Macrocyclic Ligands
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作者 王菁 孙亚秋 +1 位作者 许艳艳 高东昭 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2010年第9期1411-1415,共5页
One novel oxamido-bridged trinuclear complex [Cu(CuL)2(ClO4)2] has been syn-thesized and structurally determined.It crystallizes in the monoclinic system,space group P21/n with a = 10.636(4),b = 11.645(4),c = ... One novel oxamido-bridged trinuclear complex [Cu(CuL)2(ClO4)2] has been syn-thesized and structurally determined.It crystallizes in the monoclinic system,space group P21/n with a = 10.636(4),b = 11.645(4),c = 16.038(6) ,β = 91.029(5)°,V = 1986.2(12) 3,C38H32Cl2Cu3N8O12,Mr = 1054.24,Dc = 1.763 Mg/m3,μ(MoKα) = 1.802 mm-1,F(000) = 1066,Z = 2,the final R = 0.0328 and wR = 0.0882 for 3152 observed reflections.The crystal structure is a trinuclear complex in which the CuII ions are bridged by macrocyclic oxamide groups.C-H···O hydrogen bonding interactions link the trinuclear fragment to form a 2D supramolecular architecture.Magnetic measurements indicate that the compound is moderately antiferromagnetically coupled. 展开更多
关键词 macrocyclic oxamide complex crystal structure molecular magnetism
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Syntheses and Crystal Structures of Two Cadmium(Ⅱ) Compounds Linked by N,N-Bis(3-pyridylmethyl)amine
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作者 王思思 崔志华 +4 位作者 王修光 高东昭 孙亚秋 张国英 许艳艳 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2013年第1期89-95,共7页
Two cadmium(Ⅱ) compounds linked by a flexible dipyridyl ligand {[Cd2(Hbpma) Cl5(H2O)]·2H2O}n 1 and [Cd(Hbpma)Cl(H2O)2]2·2SO4·3H2O 2 (bpma = N,N-bis(3-pyridylmethyl)amine) have been synthe... Two cadmium(Ⅱ) compounds linked by a flexible dipyridyl ligand {[Cd2(Hbpma) Cl5(H2O)]·2H2O}n 1 and [Cd(Hbpma)Cl(H2O)2]2·2SO4·3H2O 2 (bpma = N,N-bis(3-pyridylmethyl)amine) have been synthesized and structurally characterized by single-crystal X-ray diffraction. Complex 1 crystallizes in triclinic, space group P with a = 9.5612(6), b = 11.3401(7), c = 11.5069(12), α = 112.8540(10), β = 106.5330(10), γ = 101.6680(10)°, V = 1030.77(14)3, C12H20Cd2Cl5N3O3, Mr = 656.36, Z = 2, Dc = 2.115 g/cm3, μ(MoKα) = 2.727 mm–1, F(000) = 636, S = 1.059, the final R = 0.0319 and wR = 0.0822 for 3443 observed reflections (I 2σ(I)). For complex 2, it belongs to triclinic, space group P with a = 10.9487(4), b = 11.4197(4), c = 15.4288(5), α = 94.7470(10), β = 104.1000(10), γ = 104.42°, V = 1790.76(11)3, C24H42Cd2Cl2N6O15S2, Mr = 1014.46, Z = 2, Dc = 1.881 g/cm3, μ(MoKα) = 1.529 mm–1, F(000) = 1020, S = 1.050, the final R = 0.0178 and wR = 0.0451 for 6026 observed reflections (I 2σ(I)). Complex 1 is found to have tetranuclear Cd(Ⅱ) clusters which are bridged by the protonated bpma ligands leading to one-dimensional coordination polymers, whereas complex 2 consists of binuclear Cd(Ⅱ) structures linked by the protonated bpma ligands. Both complexes are assembled into three-dimensional supramolecular structures through hydrogen bonding interactions. 展开更多
关键词 cadmium(Ⅱ) complex flexible dipyridyl ligand crystal structure
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