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1.
IntroductionIsonitrosoketonesandrelatedligandssuchasni trosophenolesareusedasanalyticalreagents .1Complexesofcobaltmetals2 ,3withisonitrosoketoneiminesarerelevanttothechemistryandbiochemistryofthevitaminB12 coen zymes .Isonitroso(oximino)groupofthoseligandsc… 相似文献
2.
<正>A new tetranuclear copper(II) compound containing dissymmetrical oxamidate ligand was synthesized and structurally characterized by IR spectroscopy, elemental analysis, single-crystal X-ray diffraction, and magnetic properties. The title compound 1 crystallizes in triclinic, space group P_1~- with a = 8.9547(9), b = 11.7018(9), c = 12.0288(10), α = 110.1790(10), β = 100.0700(10), γ = 100.6780(10)°, V = 1122.97(17) ~3, C_(34)H_(48)C_(l2)Cu_4N_(10)O_(16), M_r = 1177.92, D_c = 1.742 g/cm~3, μ(MoKα) = 2.067 mm~(-1), F(000) = 600, Z = 1, the final R = 0.0391 and wR = 0.1073 for 3904 observed reflections (I > 2σ(I)). In the structure, complex 1 consists of a tetranuclear unit and two perchlorate anions. Furthermore, its magnetic properties have also been investigated. 相似文献
3.
A dinuclear copper(Ⅱ) complex,[Cu2(HL)2(H2O)6] 1(H3L = 2,4,6-tri(3-carboxy-phenylthio)-1,3,5-triazine),was synthesized hydrothermally and characterized by single-crystal X-ray diffraction,IR and thermal analysis.Single-crystal X-ray diffraction reveals that complex 1 is a dinuclear copper(Ⅱ) complex,which is further extended to a 3D network by weak interactions such as O…H-O hydrogen bonds and noncovalent S...S interactions.The crystal of compound 1 belongs to monoclinic,space group C2/c,with a = 50.15(2),b = 6.789(3),c =15.667(8) ,β = 90.588(9)o,V = 5334(4) 3,Z = 4,C48H38Cu2N6O18S6,Mr = 1306.28,Dc = 1.627 g/cm3,F(000) = 2664,Rint = 0.0631,T = 293(2) K,μ = 1.112 mm-1,the final R = 0.0661 and wR = 0.1850 for 3782 observed reflections with I > 2σ(I). 相似文献
4.
Mixed-valencecopper(I,II)complexesplayanimportantroleinavastrangeofchemicalandbiochemicalcatalyticsystems'.Thecrystalstructuresofmixed-valencecopper(I,II)complexeshavebeenreceivedconsiderableattentionforwhattheymayrevealaboutstructuralchangesaccompanyingoxidationandreductionofcopperinmetalloenzymes'.Herewereportanovelstructureofmixed-valencecopper(I,II)complexcontainingbridgingcarboxylategroup,obviouslydifferentinstructurewiththemixed-valencecomplexesrepoFtedpreviously'-'.SynthesisMethanol… 相似文献
5.
《结构化学》2016,(5)
Two new Cu(Ⅰ) complexes [CuCl(3-PyOH)(PPh_3)_2](1) and [Cu_2(μ-Cl)_2(4-Stpy)(Ph_3P)_3](2)(PyOH = hydroxypyridine; stpy = styrylpyridine) with triphenylphosphine and pyridine derivatives have been synthesized and characterized by elemental analysis and X-ray single-crystal diffraction. Compound 1 crystallizes in monoclinic, space group P2_1/c with a = 9.8945(7), b = 37.266(2), c = 10.9461(7) ?, β = 116.0750(10)°, V = 3625.3(4) ?~3, Z = 4, D_c = 1.350 Mg/cm~(-3), μ = 0.801 mm~(-1), F(000) = 1528, the final R = 0.0320 and w R = 0.0729 for 18568 observed reflections(I 2σ(I)), R(all data) = 0.0413, wR(all data) = 0.0769, completeness to theta of 25.01 is 99.9% and GOF = 1.037. Compound 2 crystallizes in monoclinic, space group P2_1/c with a = 11.290(3), b = 20.388(5), c = 24.092(6) ?, β = 102.028(4)°, V = 5424(2) ?~3, Z = 4, D_c = 1.428 Mg/cm~(-3), μ = 1.016 mm~(-1), F(000) = 2408, the final R = 0.0568 and w R = 0.1486 for 27644 observed reflections(I 2σ(I)), R(all data) = 0.0716, wR(all data) = 0.1592, completeness to theta of 25.01 is 99.9% and GOF = 1.056. Two new Cu(I) complexes have been utilized as catalysts for N-arylation of imidazole and both showed good catalytic activity. 相似文献
6.
Three new copper(Ⅰ) complexes, namely [Cu(DPEphos)(Biq)]CF_3SO_3(1) and [Cu(PPh_3)_2(Biq)]CF_3SO_3(2) and [Cu(PPh_3)_2(Biq)]ClO_4(3)(DPEphos = bis[2-(diphenylphosp hino)phenyl]ether, PPh_3 = triphenylphosphine and Biq = 2,2?-biquinoline), are synthesized and characterized by IR, ~1H NMR, ~(31) P NMR, fluorescence spectra and terahertz time-domain spectroscopy(THz-TDS). Complex 1 crystallizes in triclinic, space group P1 with a = 12.6997(5), b = 13.2813(5), c = 15.3593(6) ?, α = 80.211(3)°, β = 88.752(3)°, γ = 70.113(3)°, V = 2398.85(15) ?~3, C_(55)H_(41.2)CuF_3N_2O_(4.6)P_2S, Mr = 1018.27, Z = 2, Dc = 1.410 g/cm3, F(000) = 1048, μ = 0.628 mm-1, the final R = 0.0450 and w R = 0.1105 for 9419 observed reflections(I 2σ(I)). Complex 2 crystallizes in monoclinic, space group C2/c with a = 19.9961(7), b = 15.9774(5), c = 17.7908(6) ?, β = 119.758(4)°, V = 4982.8(3) ?~3, C_(56.47)H_(47.88)CuF_3N_2O_(4.47)P_2S, Mr = 1040.54, Z = 4, Dc = 1.387 g/cm~3, F(000) = 2154, μ = 0.606 mm-1, the final R = 0.0430 and w R = 0.1218 for 4897 observed reflections(I 2σ(I)). Complex 3 crystallizes in monoclinic, space group C2/c with a = 19.7534(8), b = 15.0797(5), c = 17.8097(7) ?, β = 116.400(5)°, V = 4751.8(3) ?~3, C_(56)H_(45)ClCuN_3O_4P_2, Mr = 984.88, Z = 4, Dc = 1.377 g/cm~3, F(000) = 2040, μ = 0.635 mm-1, the final R = 0.0731 and w R = 0.2180 for 4670 observed reflections(I 2σ(I)). In the emission spectra, shifts of emission peak are derived from ligand-centered(π-π*) transition. 相似文献
7.
《结构化学》2017,(7)
One novel Co(Ⅱ) coordination polymer, namely [Co_4(L)_6(NO_3)_2](1) was prepared by solvothermal reactions of Co(NO3)2 with a(E)-2-[2-(3-thienyl)ethenyl]-8-quinolinol ligand(HL), which has been determined by single-crystal X-ray diffraction analyses and further characterized by means of elemental analyses, IR spectra, PXRD and thermogravimetric analyses(TGA). The core structure of complex 1 is an incomplete dicubane-like tetranuclear Co(Ⅱ) cluster, which is surrounded by six 8-hydroxy-quinolinate-based ligands and two nitrate ligands. Weak S–O interactions between the thienyl groups and nitrate ligands extend the adjacent tetranuclear Co(Ⅱ) clusters into a supramolecular(4, 4) net structure. Magnetic measurement indicates that the coupling within both molecules is overall antiferromagnetic. 相似文献
8.
SHARMA Guruaribam Shashikumar SHEIKH Rayees Ahmad SHREAZ Sheikh HASHMI Athar Adil KHAN Luqman Ahmad 《中国化学》2009,27(7):1300-1306
A new organoborate ligand, hydro(benzoyl)(phthalyl)borate has been synthesized as its potassium salt (KL) and treatment of KL with one equivalent of MCl2•6H2O gave complexes ML(H2O)x•Cl [x=2, M=Co(II), Ni(II); x=1, M=Cu(II)]. All compounds were characterized by elemental analysis, FTIR, 1H NMR, ESI MS, UV-Vis techniques, conductivity and magnetic data measurements. Spectroscopic results suggest a square planar geometry in the Cu(II) complex, while the Co(II) and Ni(II) complexes possess an octahedral geometry. Antibacterial activities (in vitro) of the ligand and its metal complexes were studied against two Gram positive (B. subtillis and B. magterium) and two Gram negative bacteria (E. Coli and S. boydi) at a single concentration (75 μg/mL) by using the Disc diffusion method. Antifungal activities (in vitro) were also checked for the compounds by using the same method against Candida albicans 10261, Penicillium sp. and Asperjillius niger., at a single concentration (50 μg/mL). The results showed that all the metal complexes, specially the nickel(II) complex, have higher antibacterial and antifungal activities than the corresponding potassium salt. 相似文献
9.
IntroductionCopper(I)halidescanformoligomeric (normallydimersortetramers)andpolymericframeworksthem selves .Allthecopper(I)halidepolymericspeciesarebasedonone dimensionalchains ,noexamplesoftwo di mensionalsheetshavebeenfoundsofar .Inordertoin creasethedimens… 相似文献
10.
《Journal of Coordination Chemistry》2012,65(5):595-608
Three new binuclear w -oxalato copper(II) complexes of composition [(Cu(N,N' -dieten) H2O)2ox](ClO4)2 ·H2O (1) (N,N'-dieten = N,N'-diethylethylenediamine, H2ox = oxalic acid), [(Cu(trimeen)H2O)2ox](ClO4)2·2H2O (2) (trimeen = N,N,N'-trimethylethylenediamine) and [(Cu(trimeen)H2O)2ox](NO3)2 ·2H2O (3) have been isolated from the reactions of Cu(ClO4)2 ·6H2O (or Cu(NO3)2 ·3H2O), the appropriate amine and Na2ox in water and have been characterized by IR and electronic spectroscopy and magnetic measurements. The crystal structure of [(Cu(N,N' -dieten)H2O)2 ox](ClO4)2.H2O (1) has been determined by single-crystal X-ray analysis. The structure of ( 1 ) consists of binuclear cations [(N,N'-dieten)H2O)Cu(ox)Cu(N,N'-dieten)H2O)]2+, perchlorate anions and water molecules of crystallization. The copper atom is coordinated by two oxygen atoms of the oxalato ligand, two nitrogen atoms belonging to N,N'-dieten and one oxygen atom of water in a distorted square-pyramidal arrangement. The temperature dependence of magnetic susceptibilities (78-293 K) was measured for 1-3 . Magnetochemical measurements show that copper(II) ions in these compounds are antiferromagnetically coupled with J = -172 cm-1, -172 cm-1 and -168 cm-1 (H = -2JS 1 S 2, S 1= S 2 = 1/2) for 1, 2 and 3, respectively. 相似文献
11.
IntroductionInthepastseveralyears ,considerableprogresshasbeenachievedincontrollingtheassemblyofindividualbuildingblocksintostructureswithspecifictopologiesandinterestingpropertiessuchasmolecularrecognition ,ionexchangeandselectiveguestinclusion .1 3 Itis… 相似文献
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13.
Six different arylhydrazone derivatives of p-aminobenzoic hydrazide of vic-dioximes were synthesized by reaction of chloroglyoxime and dichloroglyoxime with N'-p-aminobenzoyl benzaldehyde, 4-hydroxybenzaldehyde and 4-methoxybenzaldehyde hydrazones, respectively. Metal-ligand (1 : 2) complexes of vic-dioxime derivatives with Cu(Ⅱ), Ni(Ⅱ) and Co(Ⅱ) were prepared from corresponding metal acetates. The ligands and their complexes were characterized on the basis of elemental analyses and spectral data. The complexing abilities of these new vic-dioximes toward transition metals of Co(Ⅱ), Cu(Ⅱ), Ni(Ⅱ), Zn(Ⅱ), Cd(Ⅱ), Mn(Ⅱ) and Cr(Ⅲ) were determined by solid-liquid extraction studies. 相似文献
14.
《Journal of Coordination Chemistry》2012,65(8):951-959
Synthesis and characterization, including data on thermal decomposition, are reported for the complexes of S,S'-methylenebis(cysteine) (djenkolic acid) with copper(II), zinc(II) and cadmium(II): CuC7H12N2O4S2 [I]; ZnC7H12N2O4S2 [II] and CdC7H12N2O4S2 [III]. X-ray diffraction showed that the compounds are isostructural and belong to a monoclinic system. According to IR spectra, COO, NH2 groups and bridging sulfur atoms are the main coordination sites. 相似文献
15.
1 INTRODUCTION The chemical properties of acylhydrazones Schiff bases and their complexes with some transition metal ions have been intensively investigated in several re- search areas because of their chelating capability and pharmacological applications[1~10]. Intriguingly, the copper(II) complexes are shown to be signifycantly more potent than the metal free chelate, suggesting that the metal complex is the biologically active species. Owing to the biological interest in these types … 相似文献
16.
Zidan A. S. A. El-Said A. I. El-Meligy M. S. Aly A. A. M. Mohammed O. F. 《Journal of Thermal Analysis and Calorimetry》2000,62(3):665-679
Ten mixed ligand complexes of the type [M(X-QA)(aa)] and [Ni(X-QA)2(Haa)(H2O)],where X-HQA=5-arylazo-8-hydroxyquinoline derivatives, M=Co(II) orCu(II) and Haa=glycine (gly), alanine (ala) or methionine (met), have been prepared. The complexes have been characterized by elemental
analysis, IR and electron spectra and thermal analysis. A tetrahedral structure has been proposed for the cobalt(II) and copper(II)
complexes with bidentate coordination of amino acids. The nickel(II) complexes have been assigned an octahedral structure
with the amino acids acting as monodentate ligands. The thermal behaviour of the complexes has been studied before and after
γ-irradiation.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
17.
Introduction Copper(I) complexes have received much attention for their being less expensive and environmentally friendly, various coordination geometry, rich photo-chemical and photophysical properties.1-7 It is well known that copper complexes with diimine (2,2'-bipy- ridine, 1,10-phenanthroline and their substituted deriva-tives designated as diimine) generally exhibit low en-ergy metal-to-ligand charge-transfer (MLCT) states lo-cated in the regions of 350650 nm (e ≈ 103—104 dm3昺ol-1昪… 相似文献
18.
The Co(II) complex [Co{C6H4–1,2-(N=CH–C6H4O)2}] (I) and Ni(II) complex [Ni{C6H4–1,2-(N=CH–C6H4O)2}] (II) with Schiff base of o-phenylenediamine and salicylaldehyde have been synthesized. The structure of the ligand and its complexes were derived on the basis of various techniques such as elemental analysis, mass, FT-IR, electronic spectra and magnetic susceptibility. From the Singal crystal X-ray diffraction (SCXRD) analysis techniques (CIF file CCDC no. 1498772 (II)), it has been confirmed that the Schiff base ligand (L), coordinates to the metal ion in a tetradentate fashion through the nitrogen and oxygen atom. In addition, the square planar geometry of Ni(II) complex also has been confirmed from SCXRD. Electronic spectra, mass spectra, and magnetic susceptibility measurements reveal square planar geometry for the Co(II) complex. Synthesized complexes were used in cross-coupling of arylhalides with phenylboronic acid. The transformation offers products in good yields using 0.02 mmol catalysts loading, thereby proving the efficiency of the complexes as catalysts for Suzuki–Miyaura reaction. 相似文献
19.
1 INTRODUCTION Coordination polymers are a family of materials composed of 1D chains, 2D sheets, and 3D networks of metal-organic building blocks connected via co- valent and hydrogen bonds. Recently, they have re- ceived increasing attention for their fascinating struc- tures and topological features[1~4]. The complex as ligands approach is one of the best strategies to de- sign and synthesize polynuclear species, and a good example of ‘complex ligand’ is represented by mono- nuclear… 相似文献