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1.
1 INTRODUCTION During the last decade the manganese che- mistry has aroused great interest due to its diverse redox functions of enzymes in photosystem Ⅱ and its specially structural, magnetic and spectroscopic properties[1, 2]. A lot of manganese complexes involving carboxylate ligands have been reported, and their properties been fully explored[3, 4]. The coordination environment of the manganese site in biosystem often consists of oxygen and nitrogen atoms from the carboxylate groups…  相似文献   

2.
A novel Mn(Ⅱ) complex Mn2(phen)2(p-MBA)4(H2O) has been hydrothermally synthesized by the reaction of p-methyl benzoic acid (p-MBA) with 1,10-phenanthroline (phen). Crystal data for this complex: monoclinic, space group C2/c, a= 2.3328(3), b =1.5549(2), c = 1.5557(2) nm, β = 121.726(2)°, V= 4.7997(11) nm^3, Mr = 1028.85, Dc = 1.424 g/cm^3, Z = 4, F(000) = 2128, μ(MoKa) = 0.590mm^-1, GOOF = 1.060, R = 0.0333 and wR = 0.0767. In the crystal, each Mn(Ⅱ) ion is coordinated by two nitrogen atoms from one o-phenanthroline molecule, three oxygen atoms from three p-methyl benzoic acids and one oxygen atom from one water molecule, giving a six-coordinate distorted octahedral coordination geometry. Two neighboring Mn(Ⅱ) ions are bridged by two p-methyl benzoic acid groups and one water molecule, and their end positions are respectively coordinated by one 1,10-phenanthroline and one p-methyl benzoic acid molecule, giving a binuclear cage structure, of which the Mn(Ⅱ)…Mn(Ⅱ) distance is 0.3502 nm.  相似文献   

3.
1 INTRODUCTION The syntheses and structures of carboxyl complex- es have captured the interest of chemists for years due to their potential applications in many fields, such as materials, medicine, molecular electro-che- mistry and biochemistry[1~3]. So far, to the best of our knowledge, cadmium complexes with aromatic carboxylic acid as ligands have been intensively studied[4~7], but those with heterocyclic carboxylic acid as ligands are much less. α-Furoic acid is widely used in orga…  相似文献   

4.
5.
1 INTRODUCTION In the design of crystal molecule, inorganic crystal engineering is one of the focused fields that are ever developing[1]. The introduction of different metal ions and bridging ligands often gives rise to novel physical and chemical properties[2~4]. Conse- quently, the supramolecular compounds constructed from weak interactions, such as hydrogen bond, π-π stacking, C–H???O interaction, ion-π interaction and hy- drophobing interaction, have become the new focus of cryst…  相似文献   

6.
7.
1 INTRODUCTION Pronounced interest has recently been focused on the supramolecular chemistry and crystal enginee- ring of coordination compounds organized by coor- dinate covalent or molecular contacts like hydro- gen-bonding, π-π interactions, et al. because of their fascinating structure diversity and potential applica- tions as functional materials in catalysis and separa- tion[1]. A lot of infinite one-, two- and three-dimen- sional coordination frameworks have been synthe- sized, s…  相似文献   

8.
1 INTRODUCTION Transition-metal complexes supported by poly-dentate phosphine ligands have been widely studieddue to the unique photophysical properties andpotential applications as industrial catalysts, mole-cular sensors and drugs[1~3]. As known, oxidation ofphosphine ligands could happen in the synthesisreaction to result in novel complex with unexpectedstructure[4, 5]. For example, the structure of complexFe((OPPh2)2N)3[6] is an octahedral tris-chelate arrange-ment of the oxidized a…  相似文献   

9.
1 INTRODUCTION The design and assembly of organic-inorganic solid-state materials with active physical properties, such as materials with electrical, magnetic and opti- cal properties, has become a focus of a great deal of interest in recent years[1, 2].…  相似文献   

10.
1 INTRODUCTIONRareEarth (RE)elementsareappliedinagricultureandmedicine .Therfore,betterunderstandingofthebondingofREionsinthecomplexeswithaminoacidsisnecessary .ThecrystalstructureofREcomplexeswiththesimplestaminoacidglycinewerestudiedbefore[1- 4].Toresearch…  相似文献   

11.
0引言由于羧酸化合物具有丰富的配位结构类型,而且羧酸桥联多核配合物广泛存在于生物体内金属蛋白和金属酶的活性部位,使其在配位化学中占有重要地位[1]。尤其是近年来,研究发现羧酸配位聚合物具有潜在的光学、磁学、吸附分离、信息储存以及催化等性能,使得由苯二甲酸,均苯三甲  相似文献   

12.
1INTRODUCTIONTheorganicaromaticcarboxylatemetalcom-plexeshavearousedmuchattentionandbeenwidelyinvestigated.However,thestrategyofdesignandsynthesisofthesecomplexesismostlyfocusedonrigidligands,suchasterephthalicacidandbenzenetricarboxylicacid,etc.[1~5].Theassemblyofcom-plexesbyusingflexiblearomaticcarboxylateli-gandsisfarlessdeveloped[6,.Phenylenedioxydia-7]ceticacids(bdoaH2)withbiologicalactivitiesandwideapplicationsinagriculture[8]areafamilyofmultidentateflexibleligandswithversatilebind…  相似文献   

13.
The title compound [Mn(DPMT)2Cl2(H2O)2] (DPMT = 1 -[[2-(2,4-dichlorophenyl)-1,3-dioxolan-2-yl]methyl]-1H-1,2,4-triazole) was synthesized by the reaction of MnCl2-4H2O and DPMT in ethanol solution and its structure was determined by single-crystal X-ray diffraction. The crystal belongs to monoclinic, space group P2/c with a=23.913(4), b=7.8883(13), c=8.6291(14) (A),β=95.816(3)°,V=1619.4(5)(A)3,Z=2,C24H26Cl6MnN6O6 Mr=762.15, Dc=1.563 g/cm3, μ=0.950 mm'1, S=1.045, F(000)=774, R=0.0462 and wR=0.0981. The molecular structure is a centrosymmetric conformation, and two ligands are symmetrically located on both sides of the Mn atom. The manganese atom is surrounded by two nitrogen atoms from ligands, two chlorine atoms and two oxygen atoms from water molecules to form a slightly distorted octahedral geometry.  相似文献   

14.
IntroductionThesupramolecularcomplexeformedbytheweakinteractions (electrostaticinteraction ,hydrogenbonds ,vanderWaalsforce ,short rangeexclusionforce ,etc .)ofmorethantwosortsofspeciesisanorganizingentitythatusuallypossessesspecialstructureandfunction .1Sup…  相似文献   

15.
A new nickel(II) coordination complex [Ni(phen)3]·(m-nitrobenzoic acid)2·(H2O) was synthesized by self-assembly of m-nitrobenzoic acid, 1,10-phenanthroline and nickelous per- chlorate. It crystallizes in the monoclinic system, space group C2/c, with a = 2.4596(6), b = 1.2124(3), c = 1.9824(5) nm, β = 97.088(5)o, V = 5.866(3) nm3, Dc = 1.474 g/cm3, Z = 4, Mr = 1301.82, μ(MoKα) = 0.417 mm-1 F(000) = 2688, R = 0.0493 and wR = 0.1025. Structural deter- mination indicates that the nickel(II) ion is coordinated with six nitrogen atoms from three phens, giving a distorted octahedral coordination geometry. The cyclic voltametric analysis shows that the electron transfer in the electrode reaction is irreversible.  相似文献   

16.
1 INTRODUCTION Multinuclear coordination compounds have attrac-ted much attention due to their distinctive optical, elec-tric and magnetic properties as well as enzyme ana-logue[1~4]. It is important for carboxylic acid to de-sign this compound[5~8]. EDTA is a useful titrant formetal determination because EDTA molecule is easyto coordinate with a metal atom (1:1). Other types ofEDTA-M compounds are seldom to know except Ln2-M3(EDTA)3(H2O)11?12H2O[5] and (UO2 )2EDTA[9]. …  相似文献   

17.
Synthesis and Crystal Structure of [{Cd(hmbdc)(H_2O)_3}·2H_2O]_n   总被引:1,自引:0,他引:1  
A novel coordination polymer [{Cd(hmbdc)(H2O)3}·2H2O]n (hmbdc = 5-hydroxy- isophthalic acid) has been synthesized and characterized by elemental analysis, IR spectra and single-crystal X-ray diffraction. The crystal belongs to monoclinic, space group P21/c, with a = 9.599(3), b = 18.699(5), c = 7.557(2) , β = 108.198(4)°, V = 1288.6(6) 3, Z = 4, Mr = 382.60, Dc = 1.972 g/cm3, F(000) = 760, μ = 1.740, the final R = 0.0555 and wR = 0.0995 for 1732 observed reflections with I > 2σ(I). The structural analysis shows that the intermolecular hydrogen bonds and π-π interactions result in a three-dimensional supramolecular framework.  相似文献   

18.
ZnCl2, PhONa和Et4NCl稨2O在乙腈溶剂中反应合成了一种二核锌配合物[Et4N]2[Zn2(OPh)2Cl4]。X射线衍射结果表明,晶体属单斜晶系,C2/m空间群,晶胞参数 a = 14.1366(2), b=13.6985(5), c=9.3308(3)牛?107.851(2)o, V=1719.92(9)?,C28H50O2N2Zn2Cl4,Mr=721.24,Z=2,Dx=1.393g/cm3,μ(MoKα)=1.732mm—1,F(000)=756, R=0.0552, wR=0.1534, S=1.027。 配合物是由2个阳离子Et4N+和1个阴离子[Zn2(OPh)2Cl4]2—组成。阴离子[Zn2(OPh)2Cl4]2—包含着1个中心Zn2O2菱形平面。配合物中的2个锌原子通过2个苯酚中的氧原子桥连,每个锌原子还与2个氯原子配位形成变形四面体结构。  相似文献   

19.
The pentanuclear complex, Cu5(SIP)2(HSIP)2(H2O)18(H2O)5(H3SIP = 5-sulfoi-sophthalic acid), has been synthesized by the hydrothermal reaction of CuCl2 with NaH2SIP at 160 ℃, and characterized by single-crystal X-ray diffraction and IR spectrum.The crystal of the complex crystallizes in a triclinic system, space group P1-, with a = 7.0018(5), b = 11.9725(8), c = 19.0424(13) , α = 78.8540(10), β = 85.1710(10), γ = 83.6080(10)o, V = 1553.24(19) 3, Z = 1, C32H60O51S4Cu5, Mr = 1706.74, Dc = 1.825 g/cm3, μ = 1.937 mm-1, F(000) = 869, the final R = 0.0709 and wR = 0.1503 for 4235 observed reflections with I > 2σ(I).The five Cu2+ ions are connected by two symmetry-related tridentate SIP3-ligands and charge-balanced by two monodentate HSIP2-ligands, giving a discrete pentanuclear structure.The pentanuclear copper molecules are linked by hydrogen bonds to form a three-dimensional supramolecular structure.The temperature-dependent magnetic susceptibility data revealed weak ferromagnetic magnetic interactions between the Cu2+ ions.  相似文献   

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