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Hydrothermal Synthesis and Crystal Structure of One 3D Coordination Polymer of Cobalt(II) Achieved from 1,1′-Biphenyl-2,2′,6,6′-tetracarboxylic Acid Ligand 被引量:3
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作者 梅崇珍 杨光瑞 李凯慧 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2013年第2期225-230,共6页
A new three-dimensional coordination polymer {[Co(BPTC)0.5(bix)]′(H2O)}n (1, H4BPTC = 1,1′-biphenyl-2,2′,6,6′-tetracarboxylic acid, bix = 1,3-bis(imidazol-l-ylmethyl)-benzene) has been synthesized by the... A new three-dimensional coordination polymer {[Co(BPTC)0.5(bix)]′(H2O)}n (1, H4BPTC = 1,1′-biphenyl-2,2′,6,6′-tetracarboxylic acid, bix = 1,3-bis(imidazol-l-ylmethyl)-benzene) has been synthesized by the hydrothermal method and characterized by IR, elemental analysis, and single-crystal X-ray analysis. The crystal is of orthorhombic, space group Pbcn with a = 13.2975(10), b = 13.8424(12), c = 22.6367(17) A, CoC22H19N4Os, Mr = 478.34, V = 4166.7(6) A3, Dc = 1.525 g/cm^3, F(000) = 1968,μ = 0.867 mm^-1, S = 1.023 and Z = 8. The final R = 0.0683 and wR = 0.1529 for 3655 observed reflections with I 〉 20(I). In the title complex, the 2D Co-BPTC layer is formed through self-assembly of Co(II) ions and bridging BPTC4-ligands in a molar ratio of 2:1. The metal-organic lattice layers are further united together through the second bridging ligand bix to form a 3D metal-organic framework. The thermal stability of the title complex was studied by thermal gravimetric (TG) and differential thermal analysis (DTA). 展开更多
关键词 cobalt 1 1′-biphenyl-2 2′ 6 6′-tetracarboxyl acid 3D coordination polymer
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Synthesis and Structural Characterization of Co(Ⅱ) Coordination Polymer [Co(-phth)(imi_)2]_n
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作者 CHEN Yun LIU Ping② LIU Qing-Yan WANG Jian CHENG Wen-Dan (Fujian Institute of Research on the Structure of Matter, The Chinese Academy of Sciences, Fuzhou, Fujian 350002, China) 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2003年第3期313-317,共5页
A new cobalt(Ⅱ) complex [Co(-phth)(imi)2]n (phth = o-phthalato, imi = imidazole) has been synthesized by the reaction of CoCl2 with disodium o-phthalate and imidazole. The crystal structure of the compound has been d... A new cobalt(Ⅱ) complex [Co(-phth)(imi)2]n (phth = o-phthalato, imi = imidazole) has been synthesized by the reaction of CoCl2 with disodium o-phthalate and imidazole. The crystal structure of the compound has been determined by single-crystal X-ray diffraction. The crystal is of monoclinic system, space group Pn with a = 8.405(1), b = 9.995(1), c = 9.996(2) ? b = 104.479(2), V = 813.0(2) ?, Dc = 1.467 g/cm3, C14H12N4O4Co, Mr = 359.21, F(000) = 366, m = 1.079 mm-1, Z = 2, R = 0.0483 and wR = 0.1209 for 1583 observed reflections (I > 2s(I)). In the title complex, the Co(Ⅱ) ions are bridged by o-phthalate ligands in a bidentate mode, producing a zigzag infinite chain structure. Each four-coordinated cobalt(Ⅱ) center was coordinated by two oxygen atoms and two nitrogen atoms to give a distorted tetrahedral geometry. The chains are linked by hydrogen bonds between oxygen atoms belonging to carboxylate groups and hydrogen atoms of imidazole molecules, forming an unusual two-dimensional coordination polymer. 展开更多
关键词 cobalt() complex o-phthalate complex SYNTHESIS crystal structure coordination polymer
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Synthesis, Crystal Structure and Electrochemical Properties of One-dimensional Chain Coordination Polymer [Co(II)(C_6H_5CH=CHCOOH)_2(4,4′-bipy)(H_2O)_5]_n
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作者 李薇 李昶红 +2 位作者 聂雪 杨颖群 匡云飞 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2007年第12期1486-1490,共5页
A one-dimensional chain coordination polymer [Co(Ⅱ)(C6H5CH--CHCOOH)2(4,4'- bipy)(H20)5]n has been synthesized with cinnamylic acid, 4,4'-bipy and cobaltous chloride as raw materials. Crystal data for this c... A one-dimensional chain coordination polymer [Co(Ⅱ)(C6H5CH--CHCOOH)2(4,4'- bipy)(H20)5]n has been synthesized with cinnamylic acid, 4,4'-bipy and cobaltous chloride as raw materials. Crystal data for this complex: monoclinic, space group P21/c, a = 1.1481(3), b = 1.1230(2), c = 1.1759(3) nm, β = 97.054(4)^o, V= 1.5046(6) nm^3, Mr= 617.50, Dc = 1.363 g/cm^3, Z = 2, ,u(MoKa) = 0.627 mm^-1, F(000) = 646, S = 1.062, R 0.0443 and wR = 0.1178. The crystal structure shows that two neighboring cobalt(ID ions are linked together by one 4,4'-bipy, and the whole complex molecule adopts a one-dimensional chain structure. Each cobalt(H) ion is coordinated with two nitrogen atoms from two 4,4'-bipy molecules and four oxygen atoms from four water molecules, giving a distorted octahedral coordination geometry. The electrochemical properties were analyzed by combining with the crystal structure. 展开更多
关键词 cobalt coordination polymer crystal structure electrochemical propertyanalysis
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Two Novel Cobalt(Ⅱ)/nickel(Ⅱ) Metal-organic Coordination Polymers Based on Flexible Polycarboxylic Acids and Rigid Bis(imidazole) Mix Ligands
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作者 YANG Ming-Xing YAN Zhi-Wei +2 位作者 CHEN Li-Juan LIN Xing-Ye LIN Shen 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2020年第1期147-153,5,共8页
Two novel metal-organic coordination compounds, [Co2(OH)(chdc)1.5(bibp)]n(1) and [Ni(chdc)(bib)]n·2nH2O(2, H2chdc=1,4-cyclohexanedicarboxylic acid, bibp=4,4’-bis(1-imidazolyl)biphenyl, bib=1,4-bis(1-imidazolyl)b... Two novel metal-organic coordination compounds, [Co2(OH)(chdc)1.5(bibp)]n(1) and [Ni(chdc)(bib)]n·2nH2O(2, H2chdc=1,4-cyclohexanedicarboxylic acid, bibp=4,4’-bis(1-imidazolyl)biphenyl, bib=1,4-bis(1-imidazolyl)benzene), were synthesized and characterized. Compound 1 crystallizes in monoclinic system, space group PI with a=10.591(3), b=11.146(3), c=12.264(3) ?, α=89.009(6), β=88.397(4), γ=87.823(3)°, V=1446.0(6) ?3, Dc=1.554 g/cm3, C30H30Co2N4O7, Mr=676.44, F(000)=696, μ(MoKα)=1.202 mm-1, Z=2, R=0.0278 and wR=0.0718. In 1, it contains an interesting tetranuclear Co(Ⅱ) cluster. The neighboring {Co4} clusters are linked by chdc2-ligands to generate a 2D network. The bibp ligands connect adjacent layers to form an open 3 D metal-organic framework. Compound 2 crystallizes in monoclinic system, space group P21/n with a=8.8110(1), b=19.369(1), c=12.7379(4) ?, β=102.952(5)o, V=2118.5(2) ?3, Dc=1.490 g/cm3, C20H24N4NiO6, Mr=475.14, F(000)=992, μ(MoKα)=0.961 mm-1, Z=4, R=0.0306 and wR=0.0738. In 2, each deprotonated chdc 2-ligand links two Ni(Ⅱ) atoms to generate a 1 D chain along the a axis. The adjacent chains are further connected by bib ligands to build up an interesting two-dimensional network. Compound 1 shows antiferromagnetic property. 展开更多
关键词 coordination polymer magnetic properties cobalt()complex nickel()complex bis(imidazole)ligand
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以2,4,4′-联苯三羧酸及2,2′-联吡啶构筑的三维钴(Ⅱ)配位聚合物的合成、晶体结构及磁性质(英文)
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作者 高竹青 李红晋 顾金忠 《无机化学学报》 SCIE CAS CSCD 北大核心 2014年第6期1421-1426,共6页
通过水热方法,以2,4,4′-联苯三羧酸(H3btc)和2,2′-联吡啶(2,2′-bpy)与CoCl2·6H2O反应,合成了1个具有三核钴单元的三维配位聚合物[Co1.5(btc)(2,2′-bpy)0.5(2H2O)]n,并对其结构和磁性质进行了研究。结构分析结果表明该聚合物的... 通过水热方法,以2,4,4′-联苯三羧酸(H3btc)和2,2′-联吡啶(2,2′-bpy)与CoCl2·6H2O反应,合成了1个具有三核钴单元的三维配位聚合物[Co1.5(btc)(2,2′-bpy)0.5(2H2O)]n,并对其结构和磁性质进行了研究。结构分析结果表明该聚合物的晶体属于单斜晶系,I2/a空间群,a=1.774 4(4)nm,b=1.142 3(2)nm,c=1.890 8(4)nm,β=105.18(3)°,V=3.698 5(13)nm3,Dc=1.745 g·cm-3,Z=8,R=0.048 4,wR=0.085 2(I>2σ(I))。来自4个不同btc3-配体的4个羧基连接相邻的3个钴(Ⅱ)离子形成了1个三核钴(Ⅱ)的结构单元。这些三核钴(Ⅱ)的结构单元又通过btc3-配体与钴(Ⅱ)离子的配位作用形成了1个三维的框架。研究表明,该聚合物中相邻钴(Ⅱ)离子之间存在铁磁相互作用。 展开更多
关键词 配位聚合物 钴()配合物 磁性
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两个Mn(Ⅱ)/Co(Ⅱ)配位聚合物的脲热合成、结构和荧光性质 被引量:3
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作者 林星烨 杨明星 +2 位作者 陈丽娟 肖芷欣 林深 《无机化学学报》 SCIE CAS CSCD 北大核心 2020年第4期643-650,共8页
通过脲热合成法合成了2个金属配位聚合物[Mn3(Hidc)3(DMI)2]n(1)(H3idc=4,5-咪唑二羧酸,DMI=1,3-二甲基-2-咪唑啉酮),[Co(tbip)(DMPU)]n(2)(H2tbip=5-叔丁基间苯二甲酸,DMPU=N,N-二甲基丙烯基脲)。通过元素分析、红外光谱、X射线粉末衍... 通过脲热合成法合成了2个金属配位聚合物[Mn3(Hidc)3(DMI)2]n(1)(H3idc=4,5-咪唑二羧酸,DMI=1,3-二甲基-2-咪唑啉酮),[Co(tbip)(DMPU)]n(2)(H2tbip=5-叔丁基间苯二甲酸,DMPU=N,N-二甲基丙烯基脲)。通过元素分析、红外光谱、X射线粉末衍射、单晶X射线衍射等对配合物进行了结构表征。结果表明:配合物1属单斜晶系,空间群为P21/n。该配合物以DMI为模板剂,通过H3idc与Mn(Ⅱ)构筑成三维四方孔道结构,DMI填充在孔道中。配合物2属单斜晶系,空间群为P21/c。该配合物以DMPU为模板剂,通过H_2tbip与Co(Ⅱ)构筑成二维网状结构,DMPU分子通过与Co(Ⅱ)配位填充在网格中。固体荧光性能测试表明配合物1在462 nm处存在较强的荧光发射峰,说明具有良好的蓝光性质。 展开更多
关键词 锰配合物 钴配合物 脲热合成法 配位物聚合物 荧光性能
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一个二维同手性双苯并咪唑基樟脑酸钴(Ⅱ)配位聚合物的合成与荧光性质 被引量:1
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作者 刘滨秋 阚晓敏 +1 位作者 李小蕙 张巨文 《渤海大学学报(自然科学版)》 CAS 2016年第2期129-134,共6页
Co(NO3)2·6H2O与D-樟脑酸(D-H2cam)和4,4'-双(苯并咪唑-1-亚甲基)联苯(bbmmb)在水热条件下反应提供了一个配位聚合物[Co(D-cam)(bbmmb)]·H2O(1).通过单晶X-射线衍射、元素分析、红外、粉末X-射线衍射及热重分... Co(NO3)2·6H2O与D-樟脑酸(D-H2cam)和4,4'-双(苯并咪唑-1-亚甲基)联苯(bbmmb)在水热条件下反应提供了一个配位聚合物[Co(D-cam)(bbmmb)]·H2O(1).通过单晶X-射线衍射、元素分析、红外、粉末X-射线衍射及热重分析对配位聚合物1进行表征.结构分析揭示配位聚合物1结晶于正交空间群P212121,a=9.8786(9)A^°,b=17.5620(18)A^°,c=19.4752(19)A^°,α=90°,β=90°,γ=90°,V=3378.7(6)A^°3,Z=4,R1=0.0575,wR2=0.1097.配位聚合物1具有一个二维同手性层结构.bbmmb的柔韧性对配位聚合物1的同手性结构有重要影响.配位聚合物1的荧光性质被研究. 展开更多
关键词 同手性配位聚合物 樟脑酸 双苯并咪唑
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Synthesis, Crystal Structures and Photoluminescence Properties of Two 2D Coordination Polymer Compounds with Drug Ligand Enoxacin
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作者 禹良才 陈振锋 +3 位作者 谭明雄 梁宏 周春山 张勇 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2006年第7期899-902,共4页
Two new 2D coordination polymers of [M(Enox)2]·C2H5OH (M=Zn, 1 and Co, 2; HEnox=1,4-dihydro- 1-ethyl-6-fluoro-4-oxo-7-piperazine-1,8-naphtyridine-3-carboxylic acid) were synthesized under hydrothermal conditi... Two new 2D coordination polymers of [M(Enox)2]·C2H5OH (M=Zn, 1 and Co, 2; HEnox=1,4-dihydro- 1-ethyl-6-fluoro-4-oxo-7-piperazine-1,8-naphtyridine-3-carboxylic acid) were synthesized under hydrothermal conditions. The single crystal X-ray diffraction analyses showed that 1 and 2 are isostructural. The Zn(Ⅱ) in 1 and Co(Ⅱ) ions in 2 are six-coordinated in an octahedral environment with an equatorial plane composed of four oxygen atoms: two of them from the 4-oxo and the other two from 3-carboxylate of two coordinated Enox ligands, forming a stable six-membered chelating ring with the apical positions occupied by two N atoms of the piperazinyl rings. Thus, the molecules were self-assembled into a 2D neutral square grid with cavity dimensions of 1.3399 nm× 1.3399 nm for 1 and 1.3389 nm× 1.3389 nm for 2, respectively. Compound 1 emits strong blue fluorescence on irradiation by UV light in the solid state at room temperature. 展开更多
关键词 zinc( cobalt enoxacin hydrothermal synthesis coordination polymer crystal structure PHOTOLUMINESCENCE
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含有双螺旋链的配位聚合物[Co(dpa)prz_(0.5)]_n的合成、晶体结构及磁性质(英文) 被引量:5
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作者 顾金忠 高竹青 +2 位作者 窦伟 唐瑜 幺金丽 《无机化学学报》 SCIE CAS CSCD 北大核心 2009年第5期920-923,共4页
A coordination polymer [Co(dpa)prz0.5]n(1) with double-helix chains has been constructed hydrothermally using H2dpa(H2dpa=diphenic acid),prz(prz=piperazine) and Co(NO3)2.6H2O.The structure and magnetic properties of t... A coordination polymer [Co(dpa)prz0.5]n(1) with double-helix chains has been constructed hydrothermally using H2dpa(H2dpa=diphenic acid),prz(prz=piperazine) and Co(NO3)2.6H2O.The structure and magnetic properties of the complex were investigated.The complex crystallizes in triclinic system and P1 space group.Each Co atom is five-coordinated and takes a distorted tetragonal pyramid geometry.Two carboxylates of the H2dpa ligands bridge four Co(Ⅱ) ions to form infinite right-handed or left-handed helical-C-O-Co-chains.The two types of helical chains are interconnected to each other through the Co (Ⅱ) centers to produce double-helix chains.The chains form a 2D sheet through the coordination interaction of prz molecules between adjacent chains.The sheets are further interlinked by hydrogen bond interactions to generate 3D coordination frameworks.Magnetic studies for complex 1 show stronger antiferromagnetic coupling between the Co(Ⅱ) ions. 展开更多
关键词 螺旋链 配位聚合物 钴髤配合物 磁性
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由三羧基配体桥联的含有线性四核钴簇单元的二维层状配位聚合物的组装和性质(英文) 被引量:1
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作者 汪鹏飞 《无机化学学报》 SCIE CAS CSCD 北大核心 2018年第9期1747-1752,共6页
以金属钴盐、2-羟基-1,3,5-苯基三羧酸(OH-H_3BTC)为原料,在碱性条件下,通过水热方法合成了一个钴配位聚合物[Co_2(O-BTC)(H_2O)_5]_n(1),并利用X射线粉末和单晶衍射、红外光谱、元素分析以及热重等方法对该化合物进行了表征。化合物1... 以金属钴盐、2-羟基-1,3,5-苯基三羧酸(OH-H_3BTC)为原料,在碱性条件下,通过水热方法合成了一个钴配位聚合物[Co_2(O-BTC)(H_2O)_5]_n(1),并利用X射线粉末和单晶衍射、红外光谱、元素分析以及热重等方法对该化合物进行了表征。化合物1含有线性四核单元[Co_4O_7],四核单元内的金属离子是通过羧酸氧原子和羟基氧原子桥联的。该四核单元进一步通过O-BTC^(4-)配体在ab平面上形成一个二维层状结构,相邻的层与层通过氢键作用形成一个三维超分子结构。热重分析结果显示化合物1在100℃开始失重。磁性研究表明,化合物1中相邻的钴离子之间存在反铁磁性相互作用。 展开更多
关键词 配位聚合物 磁性 四核钴簇
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[Co(COOH)_2·2H_2O]的合成及晶体结构 被引量:1
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作者 苑蕾 《当代化工》 CAS 2017年第7期1361-1363,共3页
利用溶剂热法合成了新型甲酸钴配位聚合物[Co(COOH)_2·2H_2O]。采用单晶X射线、粉末X射线(XRD)、元素分析、红外光谱(IR)、热重分析(TGA)表征了该配合物的结构。结果表明[Co(COOH)_2·2H_2O]晶体属单斜晶系,P_(21)c空间群,a=8.... 利用溶剂热法合成了新型甲酸钴配位聚合物[Co(COOH)_2·2H_2O]。采用单晶X射线、粉末X射线(XRD)、元素分析、红外光谱(IR)、热重分析(TGA)表征了该配合物的结构。结果表明[Co(COOH)_2·2H_2O]晶体属单斜晶系,P_(21)c空间群,a=8.8334(11),b=7.2816(9),c=9.6103(12),α=90.00,β=97.666(2),γ=90.00,V=612.62-3,Z=4。 展开更多
关键词 甲酸钴 配位聚合物 晶体结构
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含对苯二甲酸根配位聚合物的合成和表征 被引量:2
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作者 肖洪平 《温州师范学院学报》 2003年第5期25-29,共5页
利用对苯二甲酸(H2BDC),三乙烯二胺(TED),CoCl2·6H2O为原料,采用溶液扩散混合法合成了三个新的配合物[Co(BDC)(0.5TED)]n(2nDMF)1.5nH2O)(Ⅰ), [Co(BDC)(TED)]n(nDMF)(1.5nH2O)(Ⅱ),[Ni(BDC)(0.5TED)]n(2nDMF)(1.5nH2O)(Ⅲ),并对... 利用对苯二甲酸(H2BDC),三乙烯二胺(TED),CoCl2·6H2O为原料,采用溶液扩散混合法合成了三个新的配合物[Co(BDC)(0.5TED)]n(2nDMF)1.5nH2O)(Ⅰ), [Co(BDC)(TED)]n(nDMF)(1.5nH2O)(Ⅱ),[Ni(BDC)(0.5TED)]n(2nDMF)(1.5nH2O)(Ⅲ),并对其进行了元素分析、红外光谱分析和热重分析,结果表明三个化合物是三维网络结构的配位聚合物. 展开更多
关键词 配位聚合物 对苯二甲酸 钴() 三乙烯二胺 网络结构
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一个生物相关单一手性二维金属有机鲱骨形分子网格:双-3-氨基-(S)-酪氨酸钴(英文) 被引量:1
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作者 高小勇 邢立新 +6 位作者 陈振锋 包燕雏 杨际虹 吴美芳 熊仁根 游效曾 范洪筠 《无机化学学报》 SCIE CAS CSCD 北大核心 2003年第8期802-806,共5页
The first example of homochiral two dimensional neutral cobalt? 3 amino (S) tyrosine (ATYR) coordination polymer, bis(3 amino (S) tyrosinato )cobalt? 1 was synthesized under the hydrothermal reaction of Co(ClO4)2 ... The first example of homochiral two dimensional neutral cobalt? 3 amino (S) tyrosine (ATYR) coordination polymer, bis(3 amino (S) tyrosinato )cobalt? 1 was synthesized under the hydrothermal reaction of Co(ClO4)2 ·6H2O with ATYR in which 1 displays modest second harmonic generation response. CCDC: 214275. 展开更多
关键词 生物相关 单一手性 二维金属有机鲱骨形分子网格 双-3-氨基-(S)-酪氨酸钴() 二价钴离子 配位聚合物
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两个含3,5-二羧酸吡啶配体的二维金属-有机骨架结构(英文)
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作者 王艳艳 王晓玲 +1 位作者 段泰轲 张千峰 《安徽工业大学学报(自然科学版)》 CAS 2010年第1期18-23,共6页
3,5-二羧酸吡啶(3,5-H2pydc)和四水氯化锰或六水氯化钴在水热条件反应得到了两个二维层状结构的配位聚合物[M(3,5-pydc)(H2O)2]n(M=Mn1,Co2),呈中性的金属-有机骨架结构是由三齿的3,5-pydc结构单元和水合金属离子构成的。这两个配合物... 3,5-二羧酸吡啶(3,5-H2pydc)和四水氯化锰或六水氯化钴在水热条件反应得到了两个二维层状结构的配位聚合物[M(3,5-pydc)(H2O)2]n(M=Mn1,Co2),呈中性的金属-有机骨架结构是由三齿的3,5-pydc结构单元和水合金属离子构成的。这两个配合物中的中心金属离子都是平面双锥体配位几何:配合物1为五角双锥,而配合物2为三角双锥。 展开更多
关键词 配位聚合物 晶体结构 3 5-吡啶二羧酸 锰() 钴()
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钴配位聚合物Co[2,4-bis(2-(benzylacid)thiophenylmethyl)-1,5-dimethylbenze]_2(pyridine)_2的水热合成、晶体结构及热稳定性
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作者 许玉敏 胡托平 胡晓琴 《广州化工》 CAS 2011年第3期59-60,共2页
在水、甲醇和N,N’-二甲基甲酰胺(DMF)的混合溶液中以2,4-双(2-(苯甲酸)苯巯甲基)-1,5-二甲苯(2,4-bis(2-(benzylacid)thiophenylmethyl)-1,5-dimethylbenze)、吡啶(pyridine)、硝酸钴为原料采用水热法合成了标题配合物Co[2,4-bis(2-(be... 在水、甲醇和N,N’-二甲基甲酰胺(DMF)的混合溶液中以2,4-双(2-(苯甲酸)苯巯甲基)-1,5-二甲苯(2,4-bis(2-(benzylacid)thiophenylmethyl)-1,5-dimethylbenze)、吡啶(pyridine)、硝酸钴为原料采用水热法合成了标题配合物Co[2,4-bis(2-(benzylacid)thiophenylmethyl)-1,5-dimethylbenze]2(pyridine)2。配合物晶体属正交晶系,空间群Pbcn。晶体结构表明:钴原子与两个吡啶的两个N原子、两个2,4-双(2-(苯甲酸)苯巯甲基)-1,5-二甲苯中的四个羧基氧原子配位,晶胞参数:a=1.6958 nm,b=0.959 6(2)nm,c=3.191 6 nm,V=5.193 8(5)cm3,Dc=1.397 g.cm-3,Z=4,F(000)=2 276,GooF=0.999,R1=0.036 9,wR2=0.096 2。对晶体进行了热稳定性分析,结果表明:配合物在420℃以前稳定存在。 展开更多
关键词 钴配位聚合物 晶体结构 热稳定性
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钴配位聚合物{Co(H2O)(phen)(C7H2O2F2Br)2}n的水热合成与结构表征
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作者 江玮 倪生良 《湖州师范学院学报》 2020年第2期46-50,共5页
新制备的CoCO3·xH2O加入溶有2,6-二氟-4-溴苯甲酸、邻菲咯啉的CH3OH/H2O(5∶1,V/V)混合溶剂中进行水热法反应,得到一新的钴配位聚合物{Co(H2O)(phen)(C7H2O2F2Br)2}n晶体.化合物结构经单晶X-衍射表征,结果表明配合物结晶于单斜晶系... 新制备的CoCO3·xH2O加入溶有2,6-二氟-4-溴苯甲酸、邻菲咯啉的CH3OH/H2O(5∶1,V/V)混合溶剂中进行水热法反应,得到一新的钴配位聚合物{Co(H2O)(phen)(C7H2O2F2Br)2}n晶体.化合物结构经单晶X-衍射表征,结果表明配合物结晶于单斜晶系,P21/c空间群,晶胞参数为:a=17.702(3)A,b=6.670(3)A,c=22.559(4)A,β=111.15(3)°,V=2484.2(8)A3,C26H14O5N2F4Br2Co,Mr=729.14,Z=4,Dc=1.950 g·cm-3,F(000)=1428.最后残余因子R1=0.0538,wR2=0.1334.晶体结构中,中心Co(Ⅱ)原子六配位模式形成畸变的八面体结构,分子间经过钴与其中一个2,6-二氟-4-溴苯甲酸羧基的2个O原子配位桥联作用沿b方向形成一维链聚合物,一维双链间存在π-π芳环堆积作用构筑形成bc层. 展开更多
关键词 钴配位聚合物 2 6-二氟-4-溴苯甲酸 结构表征
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