共查询到20条相似文献,搜索用时 46 毫秒
1.
Synthesis,Structure, and Magnetic Characterization of a Series of Iron(II) Coordination Frameworks with 2, 6‐Bis(1, 2,4‐triazole‐4‐yl)pyridine 下载免费PDF全文
Yue Liu Jian Zhong Huo Yuan Yuan Liu XiuMei Su Jian Hua Guo Bin Ding Xiu Guang Wang Jun Xia 《无机化学与普通化学杂志》2015,641(14):2422-2428
Based on the bis‐triazole ligand 2, 6‐bis(1, 2,4‐triazole‐4‐yl)pyridine (L), the triazole‐iron(II) complexes [Fe(L)2(dca)2(H2O)2] · 2H2O ( 1 ) (Nadca = sodium dicyanamide), {[Fe(μ2‐L)2(H2O)2]Cl2}n ( 2 ), and {[Fe(μ2‐L)2(H2O)2](ClO4)2 · L · H2O}n ( 3 ) were isolated by solvent diffusion methods. When iron(II) salts and Nadca were used, compound 1 was isolated, which contains mononuclear Fe(L)2(dca)2(H2O)2 units. When FeCl2 or FeClO4 were used, one‐dimensional (1D) cation iron(II) chains ( 2 ) and two‐dimensional (2D) cation iron(II) networks ( 3 ) were isolated indicating anion directing structural diversity. Moreover, variable‐temperature magnetic susceptibility data of 1 – 3 were recorded in the temperature range 2–300 K. The magnetic curve of complex 2 was fitted by using the classical spin Heisenberg chain model indicating anti‐ferromagnetic interactions (J = –5.31 cm–1). Obviously complexes 1 – 3 show no detectable thermal spin crossover behaviors, the lack of spin‐crossover behavior may be correlated with FeN4O2 coordination spheres in 1 – 3 . 相似文献
2.
Maria G. Babashkina Elmira R. Shakirova Dr. Damir A. Safin Felix D. Sokolov Axel Klein Łukasz Szyrwiel Maria Kubiak Henryk Kozlowski Dmitriy B. Krivolapov 《无机化学与普通化学杂志》2010,636(15):2626-2632
Reaction of O,O′‐diisopropylthiophosphoric acid isothiocyanate (iPrO)2P(S)NCS with 1,10‐diaza‐18‐crown‐6, 1,7‐diaza‐18‐crown‐6, or 1,7‐diaza‐15‐crown‐5 leads to the N‐thiophosphorylated bis‐thioureas N,N′‐bis[C(S)NHP(S)(OiPr)2]‐1,10‐diaza‐18‐crown‐6 ( H2LI ), N,N′‐bis[C(S)NHP(S)(OiPr)2]‐1,7‐diaza‐18‐crown‐6 ( H2LII ) and N,N′‐bis[C(S)NHP(S)(OiPr)2]‐1,7‐diaza‐15‐crown‐5 ( H2LIII ). Reaction of the potassium salts of H2LI–III with a mixture of CuI and 2,2′‐bipyridine ( bpy ) or 1,10‐phenanthroline ( phen ) in aqueous EtOH/CH2Cl2 leads to the dinuclear complexes [Cu2(bpy)2LI–III] and [Cu2(phen)2LI–III] . The structures of these compounds were investigated by 1H, 31P{1H} NMR spectroscopy, and elemental analysis. The crystal structures of H2LI and [Cu2(phen)2LI] were determined by single‐crystal X‐ray diffraction. Extraction capacities of the obtained compounds in comparison to the related compounds 1,10‐diaza‐18‐crown‐6, N,N′‐bis[C(=CMe2)CH2P(O)(OiPr)2]‐1,10‐diaza‐18‐crown‐6, N,N′‐bis[C(S)NHP(O)(OiPr)2]‐1,10‐diaza‐18‐crown‐6 towards the picrate salts LiPic, NaPic, KPic. and NH4Pic were also studied. 相似文献
3.
Robyn E. Powell Carl H. Schwalbe Graham J. Tizzard Petra J. van Koningsbruggen 《Acta Crystallographica. Section C, Structural Chemistry》2014,70(6):595-598
The synthesis and crystal structure (at 100 K) of the title compound, Cs[Fe(C11H13N3O2S2)2]·CH3OH, is reported. The asymmetric unit consists of an octahedral [FeIII(L)2]− fragment, where L2− is 3‐ethoxysalicylaldehyde 4‐methylthiosemicarbazonate(2−) {systematic name: [2‐(3‐ethoxy‐2‐oxidobenzylidene)hydrazin‐1‐ylidene](methylamino)methanethiolate}, a caesium cation and a methanol solvent molecule. Each L2− ligand binds through the thiolate S, the imine N and the phenolate O atoms as donors, resulting in an FeIIIS2N2O2 chromophore. The O,N,S‐coordinating ligands are orientated in two perpendicular planes, with the O and S atoms in cis positions and the N atoms in trans positions. The FeIII cation is in the low‐spin state at 100 K. 相似文献
4.
Jong‐Ha Choi Takayoshi Suzuki Sumio Kaizaki 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(11):m539-m541
In the title compound, [CrBr2(C5H14N2)2]2Br2·HClO4·6H2O, there are two independent CrIII complex cations which are conformational isomers of each other. The Cr atoms lie respectively on a center of symmetry and on a mirror plane and have octahedral environments, coordinated by the N atoms of two 2,2‐dimethylpropane‐1,3‐diamine ligands and by two Br atoms in trans positions. The Cr—N and Cr—Br bond lengths are in the ranges 2.078 (3)–2.089 (3) and 2.4495 (9)–2.5017 (9) Å, respectively. The crystal structure consists of two CrIII complex cations, two Br? anions, a (ClO4)? anion and an [H13O6]+ hydrogen‐bonded cluster cation. 相似文献
5.
Two Heterometallic–Organic Frameworks Composed of Iron(III)‐Salen‐Based Ligands and d10 Metals: Gas Sorption and Visible‐Light Photocatalytic Degradation of 2‐Chlorophenol 下载免费PDF全文
Dr. Jing Li Dr. Jin Yang Dr. Ying‐Ying Liu Prof. Dr. Jian‐Fang Ma 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(11):4413-4421
Two examples of heterometallic–organic frameworks (HMOFs) composed of dicarboxyl‐functionalized FeIII‐salen complexes and d10 metals (Zn, Cd), [Zn2(Fe‐L)2(μ2‐O)(H2O)2] ? 4 DMF ? 4 H2O ( 1 ) and [Cd2(Fe‐L)2(μ2‐O)(H2O)2] ? 2 DMF ? H2O ( 2 ) (H4L=1,2‐cyclohexanediamino‐N,N′‐bis(3‐methyl‐5‐carboxysalicylidene), have been synthesized and structurally characterized. In 1 and 2 , each square‐pyramidal FeIII atom is embedded in the [N2O2] pocket of an L4? anion, and these units are further bridged by a μ2‐O anion to give an (Fe‐L)2(μ2‐O) dimer. The two carboxylate groups of each L4? anion bridge ZnII or CdII atoms to afford a 3D porous HMOF. The gas sorption and magnetic properties of 1 and 2 have been studied. Remarkably, 1 and 2 show activity for the photocatalytic degradation of 2‐chlorophenol (2‐CP) under visible‐light irradiation, which, to the best of our knowledge, is the first time that this has been observed for FeIII‐salen‐based HMOFs. 相似文献
6.
Jun Xia Xiao‐Lin Gong Xing Fan 《Acta Crystallographica. Section C, Structural Chemistry》2015,71(10):878-882
Assemblies of pyrazine‐2,3‐dicarboxylic acid and CdII in the presence of bis(1,2,4‐triazol‐1‐yl)butane or bis(1,2,4‐triazol‐1‐yl)ethane under ambient conditions yielded two new coordination polymers, namely poly[[tetraaqua[μ2‐1,4‐bis(1,2,4‐triazol‐1‐yl)butane‐κ2N4:N4′]bis(μ2‐pyrazine‐2,3‐dicarboxylato‐κ3N1,O2:O3)dicadmium(II)] dihydrate], {[Cd2(C6H2N2O4)2(C8H12N6)(H2O)4]·2H2O}n, (I), and poly[[diaqua[μ2‐1,2‐bis(1,2,4‐triazol‐1‐yl)ethane‐κ2N4:N4′]bis(μ3‐pyrazine‐2,3‐dicarboxylato‐κ4N1,O2:O3:O3′)dicadmium(II)] dihydrate], {[Cd2(C6H2N2O4)2(C6H8N6)(H2O)2]·2H2O}n, (II). Complex (I) displays an interesting two‐dimensional wave‐like structure and forms a distinct extended three‐dimensional supramolecular structure with the help of O—H...N and O—H...O hydrogen bonds. Complex (II) has a three‐dimensional framework structure in which hydrogen bonds of the O—H...N and O—H...O types are found. 相似文献
7.
pH Dependent Synthesis of NdIII Coordination Compounds Based on Bifunctional 5‐(4‐Pyridyl)tetrazole‐2‐acetic Acid 下载免费PDF全文
Meng Jie Cao Yue Kang Li Peng Peng Sun Chen Yi Zhang Jue Wang Qiao Yun Li Gao Wen Yang 《无机化学与普通化学杂志》2016,642(21):1218-1221
The NdIII coordination compounds [Nd(4‐pytza)3(H2O)2] · 2H2O ( 1 ) and [Nd(4‐pytza)2(H2O)4]Cl · 2H2O ( 2 ) [H4‐pytza = 5‐(4‐pyridyl)tetrazole‐2‐acetic acid] were synthesized by reactions of K4‐pytza and NdCl3 · 6H2O at different pH values. Single crystal X‐ray diffraction analysis reveals that 4‐pytza ligands in 1 in a μ1,3‐COO syn‐syn or μ1,1,3‐COO bridging mode coordinate to two central NdIII atoms to display a dinuclear unit, which is connected by one of these 4‐pytza ligands acting in end‐to‐end bridging mode to form a 1D ladder‐like chain. Different from 1 , each 4‐pytza in 2 with a μ1,3‐COO syn‐anti bridging mode coordinates to two NdIII atoms to display a 1D zigzag chain. Furthermore, the luminescence properties of 1 and 2 were investigated at room temperature in the solid state. 相似文献
8.
Trinuclear [CoIII2–LnIII] (Ln=Tb,Dy) Single‐Ion Magnets with Mixed 6‐Chloro‐2‐Hydroxypyridine and Schiff Base Ligands 下载免费PDF全文
Prof. Dr. Cai‐Ming Liu Prof. Dr. De‐Qing Zhang Prof. Dr. Xiang Hao Prof. Dao‐Ben Zhu 《化学:亚洲杂志》2014,9(7):1847-1853
The Schiff base ligand N1,N3‐bis(3‐methoxysalicylidene)diethylenetriamine (H2valdien) and the co‐ligand 6‐chloro‐2‐hydroxypyridine (Hchp) were used to construct two 3d–4f heterometallic single‐ion magnets [Co2Dy(valdien)2(OCH3)2(chp)2] ? ClO4 ? 5 H2O ( 1 ) and [Co2Tb(valdien)2(OCH3)2(chp)2] ? ClO4 ? 2 H2O ? CH3OH ( 2 ). The two trinuclear [CoIII2LnIII] complexes behave as a mononuclear LnIII magnetic system because of the presence of two diamagnetic cobalt(III) ions. Complex 1 has a molecular symmetry center, and it crystallizes in the C2/c space group, whereas complex 2 shows a lower molecular symmetry and crystallizes in the P21/c space group. Magnetic investigations indicated that both complexes are field‐induced single‐ion magnets, and the CoIII2–DyIII complex possesses a larger energy barrier [74.1(4.2) K] than the CoIII2–TbIII complex [32.3(2.6) K]. 相似文献
9.
《Acta Crystallographica. Section C, Structural Chemistry》2017,73(11):1010-1016
Because of their versatile coordination modes and strong coordination ability for metals, triazole ligands can provide a wide range of possibilities for the construction of metal–organic frameworks. Three transition‐metal complexes, namely bis(μ‐1,2,4‐triazol‐4‐ide‐3‐carboxylato)‐κ3N 2,O :N 1;κ3N 1:N 2,O‐bis[triamminenickel(II)] tetrahydrate, [Ni2(C3HN3O2)2(NH3)6]·4H2O, (I), catena‐poly[[[diamminediaquacopper(II)]‐μ‐1,2,4‐triazol‐4‐ide‐3‐carboxylato‐κ3N 1:N 4,O‐[diamminecopper(II)]‐μ‐1,2,4‐triazol‐4‐ide‐3‐carboxylato‐κ3N 4,O :N 1] dihydrate], {[Cu2(C3HN3O2)2(NH3)4(H2O)2]·2H2O}n , (II), (μ‐5‐amino‐1,2,4‐triazol‐1‐ide‐3‐carboxylato‐κ2N 1:N 2)di‐μ‐hydroxido‐κ4O :O‐bis[triamminecobalt(III)] nitrate hydroxide trihydrate, [Co2(C3H2N4O2)(OH)2(NH3)6](NO3)(OH)·3H2O, (III), with different structural forms have been prepared by the reaction of transition metal salts, i.e. NiCl2, CuCl2 and Co(NO3)2, with 1,2,4‐triazole‐3‐carboxylic acid or 3‐amino‐1,2,4‐triazole‐5‐carboxylic acid hemihydrate in aqueous ammonia at room temperature. Compound (I) is a dinuclear complex. Extensive O—H…O, O—H…N and N—H…O hydrogen bonds and π–π stacking interactions between the centroids of the triazole rings contribute to the formation of the three‐dimensional supramolecular structure. Compound (II) exhibits a one‐dimensional chain structure, with O—H…O hydrogen bonds and weak O—H…N, N—H…O and C—H…O hydrogen bonds linking anions and lattice water molecules into the three‐dimensional supramolecular structure. Compared with compound (I), compound (III) is a structurally different dinuclear complex. Extensive N—H…O, N—H…N, O—H…N and O—H…O hydrogen bonding occurs in the structure, leading to the formation of the three‐dimensional supramolecular structure. 相似文献
10.
Syntheses,Structures and Characterization of Four Metal‐Organic Frameworks constructed by 2,2′,6,6′‐Tetramethoxy‐4,4′‐biphenyldicarboxylic Acid 下载免费PDF全文
Four metal‐organic frameworks (MOFs), {[Mn3.5L(OH)(HCOO)4(DMF)] · H2O} ( 1 ), {[In2.5L2O(OH)1.5(H2O)2] · DMF · CH3CN · 2H2O} ( 2 ), {[Pb4L3O(DMA)] · CH3CN} ( 3 ), and {[LaL(NO3)(DMF)2] · 2H2O} ( 4 ) were synthesized by utilizing the ligand 2,2′,6,6′‐tetramethoxy‐4,4′‐biphenyldicarboxylic acid (H2L) via solvothermal methods. All MOFs were characterized by single‐crystal X‐ray diffraction, powder X‐ray diffraction, thermogravimetric analysis, and infrared spectroscopy. In 1 , the Mn2+ ions are interconnected by formic groups in situ produced via DMF decomposition to form a rare 2D macrocyclic plane, which is further linked by L2– to construct the final 3D network. In 2 , 1D zip‐like infinite chain is formed and then interconnected to build the 3D framework. In 3 , a [Pb6(μ4‐O)2(O2C)10(DMA)2] cluster with a centrosymmetric [Pb6(μ4‐O)2]8+ octahedral core is formed in the 3D structure. In 4 , the La3+ ions are connected with each other through carboxylate groups of L2– to generate 1D zigzag chain, which is further linked by L2– to construct a 3D network with sra topology. Solid photoluminescence properties of 3 and 4 were also investigated. 相似文献
11.
The reactions of Ln(NO3)3 · 6H2O and 4‐acetamidobenzoic acid (Haba) with 4,4′‐bipyridine (4,4′‐bpy) in ethanol solution resulted in three new lanthanide coordination polymers, namely {[Ln(aba)3(H2O)2] · 0.5(4,4′‐bpy) · 2H2O}∞ [Ln = Sm ( 1 ), Gd ( 2 ), and Er ( 3 ), aba = 4‐acetamidobenzoate]. Compounds 1 – 3 are isomorphous and have one‐dimensional chains bridged by four aba anions. 4,4′‐Bipyridine molecules don’t take part in the coordination with LnIII ions and occur in the lattice as guest molecules. Moreover, the adjacent 1D chains in the complex are further linked through numerous N–H ··· O and O–H ··· O hydrogen bonds to form a 3D supramolecular network. In addition, complex 1 in the solid state shows characteristic emission in the visible region at room temperature. 相似文献
12.
Four Complexes with the Rigid Ligand 1,4‐Bis(1H‐imidazol‐4‐yl)benzene and Varied Carboxylate Ligands
Four metal‐organic coordination polymers [Co2(L)3(nipa)2]·6H2O ( 1 ), [Cd(L)(nipa)]·3H2O ( 2 ), [Co(L) (Hoxba)2] ( 3 ) and [Ni2(L)2(oxba)2(H2O)]·1.5L·3H2O ( 4 ) were synthesized by reactions of the corresponding metal(II) salts with the rigid ligand 1,4‐bis(1H‐imidazol‐4‐yl)benzene (L) and different derivatives of 5‐nitroisophthalic acid (H2nipa) and 4,4′‐oxybis(benzoic acid) (H2oxba), respectively. The structures of the complexes were characterized by elemental analysis, FT‐IR spectroscopy and single‐crystal X‐ray diffraction. Complexes 1 and 3 have the same one‐dimensional (1D) chain while 2 is a 6‐connected twofold interpenetrating three‐dimensional (3D) network with α ‐Po 412·63 topology based on the binuclear CdII subunits. Compound 4 features a puckered two‐dimensional (2D) (4,4) network, and the large voids of the packing 2D nets have accommodated the uncoordinated L guest molecules. An abundant of N–H···O, O–H···O and C–H···O hydrogen bonding interactions exist in complexes 1–4 , which contributes to stabilize the crystal structure and extend the low‐dimensional entities into high‐dimensional frameworks. Lastly, the photoluminiscent properties of compounds 2 were also investigated. 相似文献
13.
Meng Wen Zu‐Ping Xiao Chun‐Ya Wang Xi‐He Huang 《Acta Crystallographica. Section C, Structural Chemistry》2015,71(2):136-139
The title compound, {[Zn4(C8H4O4)3(OH)2(C12H6N2O2)2]·2H2O}n, has been prepared hydrothermally by the reaction of Zn(NO3)2·6H2O with benzene‐1,4‐dicarboxylic acid (H2bdc) and 1,10‐phenanthroline‐5,6‐dione (pdon) in H2O. In the crystal structure, a tetranuclear Zn4(OH)2 fragment is located on a crystallographic inversion centre which relates two subunits, each containing a [ZnN2O4] octahedron and a [ZnO4] tetrahedron bridged by a μ3‐OH group. The pdon ligand chelates to zinc through its two N atoms to form part of the [ZnN2O4] octahedron. The two crystallographically independent bdc2− ligands are fully deprotonated and adopt μ3‐κO:κO′:κO′′ and μ4‐κO:κO′:κO′′:κO′′′ coordination modes, bridging three or four ZnII cations, respectively, from two Zn4(OH)2 units. The Zn4(OH)2 fragment connects six neighbouring tetranuclear units through four μ3‐bdc2− and two μ4‐bdc2− ligands, forming a three‐dimensional framework with uninodal 6‐connected α‐Po topology, in which the tetranuclear Zn4(OH)2 units are considered as 6‐connected nodes and the bdc2− ligands act as linkers. The uncoordinated water molecules are located on opposite sides of the Zn4(OH)2 unit and are connected to it through hydrogen‐bonding interactions involving hydroxide and carboxylate groups. The structure is further stabilized by extensive π–π interactions between the pdon and μ4‐bdc2− ligands. 相似文献
14.
A novel dinuclear bismuth(III) coordination compound, [Bi2(C7H3NO4)2(N3)2(C12H8N2)2]·4H2O, has been synthesized by an ionothermal method and characterized by elemental analysis, energy‐dispersive X‐ray spectroscopy, IR, X‐ray photoelectron spectroscopy and single‐crystal X‐ray diffraction. The molecular structure consists of one centrosymmetric dinuclear neutral fragment and four water molecules. Within the dinuclear fragment, each BiIII centre is seven‐coordinated by three O atoms and four N atoms. The coordination geometry of each BiIII atom is distorted pentagonal–bipyramidal (BiO3N4), with one azide N atom and one bridging carboxylate O atom located in axial positions. The carboxylate O atoms and water molecules are assembled via O—H...O hydrogen bonds, resulting in the formation of a three‐dimensional supramolecular structure. Two types of π–π stacking interactions are found, with centroid‐to‐centroid distances of 3.461 (4) and 3.641 (4) Å. 相似文献
15.
A new type of naphthoxime‐based ligand, 1‐(1‐hydroxynaphthalen‐2‐yl)ethanone oxime (naphthsaoH2, 1a ), is introduced into the chemistry of manganese(III) complexes. First triangular [Mn3] compound with this ligand is presented: [Mn3O(naphthsao)3(CH3OH)5(CH2ClCOO)] ( 1 ). Also preliminary structural studies for [Mn3O(naphthsao)3(CH3OH)5(CH3COO)] ( A ) and 0.52[Mn3O(naphthsao)3(CH3OH)5(H2O)] · 0.48[Mn3O(naphthsao)3(CH3OH)6] ( B ) are mentioned. Compound 1 was characterized by X‐ray diffraction studies and by a preliminary investigation of the magnetic properties, showing antiferromagnetic coupling of the MnIII ions. Compound 1 displays a supramolecular motif of hydrogen‐bonded chains. 相似文献
16.
Synthesis,Structure, and Fluorescent Properties of Lanthanide Complexes Based on 8‐Hydroxyquinoline‐7‐carboxylic Acid 下载免费PDF全文
The lanthanide complex [Eu3(8‐HQCA)3(COOH)(OH)2(H2O)3]n · nH2O (8‐HQCA = 8‐hydroxyquinoline‐7‐carboxylic acid) was synthesized and characterized. Single‐crystal X‐ray diffraction shows that the trinuclear structures are linked by ligands to form 2D layers. The results of DFT calculation shows that energy can be transferred effectively from the ligand to EuIII ions. A series of heteronuclear complexes {[(Eu1–xYx)3(8‐HQCA)3(COOH) (OH)2(H2O)3]n · nH2O (x = 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8)} were synthesized and their luminescent properties were studied. The results showed that the doping of YIII ions could change the fluorescent intensity of the EuIII complex, but could not change their positions. 相似文献
17.
Zun‐Ting Zhang Xin‐Li Cheng Yun He 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(10):m484-m487
In methylaminium 4′,7‐dihydroxyisoflavone‐3′‐sulfonate dihydrate, CH6N+·C15H9O7S−·2H2O, 11 hydrogen bonds exist between the methylaminium cations, the isoflavone‐3′‐sulfonate anions and the solvent water molecules. In hexaaquairon(II) bis(4′,7‐diethoxyisoflavone‐3′‐sulfonate) tetrahydrate, [Fe(H2O)6](C19H17O7S)2·4H2O, 12 hydrogen bonds exist between the centrosymmetric [Fe(H2O)6]2+ cation, the isoflavone‐3′‐sulfonate anions and the solvent water molecules. Additional π–π stacking interactions generate three‐dimensional supramolecular structures in both compounds. 相似文献
18.
Guo‐Qing Bian Takayoshi Kuroda‐Sowa Hisashi Konaka Masahiko Maekawa Megumu Munakata 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(7):m338-m340
The title compound, [Mn2(μ‐O)(C6H3NO3)2(C5H5N)4]·H2O, was isolated from the reaction of 2,6‐pyridinedicarboxylic acid with [Mn12O12(CH3COO)16(H2O)4] in pyridine. The dimanganese complex has twofold symmetry; the MnIII atoms are bridged by one oxo and two amidate ligands and show compressed octahedral Jahn–Teller distortion. The molecular packing comprises a three‐dimensional structure constructed by means of extensive intermolecular interactions, including three kinds of hydrogen bonds and π–π interactions. 相似文献
19.
Tong‐Hen Pan Kun‐Shan Huang Chong‐En Huang Fu‐Long Lai Chang‐Cang Huang 《Acta Crystallographica. Section C, Structural Chemistry》2011,67(2):m46-m49
The asymmetric unit of the title coordination polymer, [Gd2(C7H4O5S)2(C2O4)(H2O)6]n or [Gd(2‐SB)(ox)0.5(H2O)3]2n (2‐SB is 2‐sulfonatobenzoate and ox is oxalate), (I), consists of one GdIII ion, one 2‐SB anion, three coordinated water molecules and one half of an ox ligand. The ox ligand is located on a crystallographic inversion centre. The GdIII centre shows a distorted tricapped trigonal–prismatic coordination formed by nine O atoms from two 2‐SB anions, one ox ligand and three coordinated water molecules. The carboxylate and sulfonate groups of the 2‐SB anions adopt μ2‐η1:η2 and μ1‐η0:η0:η1 coordination modes to link two GdIII ions, generating a centrosymmetric binuclear [Gd2(2‐SB)2(H2O)6]2− subunit. The ox ligand acts as a bridge, linking the binuclear [Gd2(2‐SB)2(H2O)6]2− subunits into a one‐dimensional chain structure parallel to the b axis. Furthermore, extensive O—H...O hydrogen bonds connect the chains into a three‐dimensional supramolecular architecture. 相似文献
20.
Two mixed‐metal‐center inorganic‐organic hybrid frameworks incorporating N‐(Phosphonomethyl)iminodiacetate(H4pmida), [Zn2V2O2(pmida)2(H2O)10]·H2O ( 1 ) and [Zn2V2O2(pmida)2(H2O)12]·2H2O ( 2 ), were synthesized by hydrothermal reactions and characterized by elemental analysis, IR spectra, UV‐Vis spectra and single crystal X‐ray analysis. In complex 1 , the centrosymmetric dimeric [V2O2(pmida)2]4– unit connected to neighboring Zn2+ through the phosphonate group, while 2 the [V2O2(pmida)2]4– unit uncoordinated with the Zn2+ in the presence of NaOH. Magnetic measurements in the range 2‐300 K have shown weak antiferromagnetic interaction between the adjacent vanadium ions in complexes. 相似文献