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1.
《Journal of Coordination Chemistry》2012,65(3):400-409
Two d10 group 12 metal complexes, 2-(2-methoxyphenyl)-1,10-phenanthroline zinc dichloride (2a) and 2-(2-methoxyphenyl)-1,10-phenanthroline mercury dichloride (2b) were synthesized and characterized by IR, 1H and 13C NMR as well as elemental analysis. Structure of 2b in the solid state was determined by single-crystal X-ray crystallography, revealing that 2b is four-coordinate in a distorted tetrahedral geometry with the methoxy group uncoordinated. Luminescent properties of 2a and 2b in solution and the solid state were studied. 相似文献
2.
Two hexanuclear zinc(II) complexes, [Zn6(L1)2(μ2-OH)2(μ2-CH3COO)8] · CH3CN (1 · CH3CN) and [Zn6(L2)2(μ2-OH)2(μ2-CH3COO)8] · 4CH3CN (2 · 4CH3CN), where HL1 = 4-methyl-2,6-bis(cyclohexylmethyliminomethyl)-phenol and HL2 = 4-methyl-2,6-bis(1-naphthalylmethyliminomethyl)-phenol, have been synthesized and characterized by elemental analysis, FT-IR and fluorescence spectroscopic methods, and by X-ray diffraction analysis. In the asymmetric unit of complex 1, two of the three zinc atoms have pentacoordinate geometries and the other is tetrahedrally coordinated, whereas the three distinct Zn atoms in complex 2 adopt three different coordination environments, namely distorted octahedral, trigonal bipyramidal and tetrahedral. The fluorescence properties of the ligands and complexes have been investigated. 相似文献
3.
The new zinc ternary complexes [Zn(cyclen)NO3]ClO4 (I), [Zn2(cyclen)2(m-nic)](ClO4)3 (II), [Zn2(cyclen)2(m-pic)](ClO4)3 (III) (cyclen=1,4,7,10-tetraazacyclododecane; nic=nicotinic acid; pic=picolinic acid) were synthesized and their spectral and thermal properties were investigated. The compounds were characterized
by elemental analysis, IR spectroscopy and TG/DTG, DTA methods. Moreover, the way of coordination of pyridinecarboxylate anions
was proposed on the basis of the spectral data and consequently proved with results of X-ray structure analysis.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
4.
A new ligand, 2-carboxybenzaldehyde-(4’-hydroxy)benzoylhydrazone(H2L) and its ZnII and NiII complexes have been synthesized and characterized on the basis of elemental analyses, molar conductivities, 1H-NMR, IR spectra and thermal analyses. In addition, DNA-binding properties of these two metal complexes were investigated
using spectrometric titrations, ethidium bromide displacement experiments, and viscosity measurements. The results show that
the two complexes, especially the NiII complex, strongly bind with calf-thymus DNA, presumably via an intercalation mechanism. The intrinsic binding constants of the ZnII and NiII complexes with DNA are 2.46 × 105 and 7.94 × 105
M
−1, respectively. 相似文献
5.
Wang Cong Wu Yancong Qu Yao Zhao Kun Xu Jianhua Xia Xinzhao Wu Huilu 《Transition Metal Chemistry》2020,45(8):523-529
Three new metal complexes, namely: [Mn(AIDB)Cl2]·DMF (1), [Zn(AIDB)Br2]·CH3OH (2) and [Co(AIDB)Cl2]·CH3OH (3) having a ligand bis(benzimidazol-2-ylmethyl)allylamine (AIDB), have been synthesized in high yields and characterized by elemental analyses, molar conductivities, IR, UV–Vis spectra and single-crystal X-ray diffraction. The structural analysis revealed that all the three complexes 1–3 have five-coordinated trigonal bipyramid geometry where the degree of distorting is 1>3>2. In vitro antioxidant activity assay demonstrates that the complexes 1 and 3 display high scavenging activity against hydroxyl (OH·) and superoxide (O2−·) radicals.
相似文献6.
Angel A. Recio Despaigne Jeferson G. da Silva Ana Cerúlia M. do Carmo Flavio Sives Oscar E. Piro Eduardo E. Castellano Heloisa Beraldo 《Polyhedron》2009,28(17):3797-3803
In the present work 2-formylpyridine-para-chloro-phenyl hydrazone (H2FopClPh) and 2-formylpyridine-para-nitro-phenyl hydrazone (H2FopNO2Ph) were obtained, as well as their copper(II) and zinc(II) complexes [Cu(H2FopClPh)Cl2] (1), [Cu(2FopNO2Ph)Cl] (2), [Zn(H2FopClPh)Cl2] (3) and [Zn(H2FopNO2Ph)Cl2] (4). Upon re-crystallization in DMSO:acetone conversion of 2 into [Cu(2FopNO2Ph)Cl(DMSO)] (2a) and of 4 into [Zn(2FopNO2Ph)Cl(DMSO)] (4a) occurred. The crystal structures of 1, 2a, 3 and 4a were determined. 相似文献
7.
Katarína Homzová Katarína Győryová Zuzana Bujdošová Daniela Hudecová Mária Ganajová Zuzana Vargová Jana Kovářová 《Journal of Thermal Analysis and Calorimetry》2014,116(1):77-91
New zinc(II) 4-hydroxybenzoate complex compounds with general formula [Zn(4-OHbenz)2Ln]·xH2O, where 4-OHbenz = 4-hydroxybenzoate; L = isonicotinamide, N-methylnicotinamide, N,N-diethylnicotinamide, thiourea, urea, phenazone, theophylline, methyl-3-pyridylcarbamate; n = 2, 3; x = 0–3, 5, were synthesized and characterised by elemental analysis, thermal analysis and IR spectroscopy. The thermal behaviour of the prepared compounds was studied by TG/DTG and DTA methods in argon atmosphere. The thermal decomposition of hydrated compounds started with dehydration. During the thermal decomposition, organic ligand, carbon monoxide, carbon dioxide and phenol were evolved. The final solid product of the thermal decomposition was zinc or zinc oxide. The volatile gaseous product, solid intermediate products and the final product of thermal decomposition were identified by IR spectroscopy, mass spectrometry, qualitative chemical analyses and X-ray powder diffraction method. The antimicrobial activity of zinc(II) carboxylate compounds was tested against various strains of bacteria, yeasts and filamentous fungi (S. aureus, E. coli, C. parapsilosis, R. oryzae, A. alternata, M. gypseum). The presence of zinc in complexes led to the increase in their antimicrobial activity in comparison with free 4-hydroxybenzoic acid. 相似文献
8.
Shyamapada Shit Madhusudan Nandy Dipankar Saha Lei Zhang Wolfgang Schmitt Corrado Rizzoli 《Journal of Coordination Chemistry》2016,69(16):2403-2414
Reactions of hydrated zinc(II) trifluoroacetate and sodium azide with two tridentate Schiff bases HL1 (2-((E)-(2-(dimethylamino)ethylimino)methyl)-4-chlorophenol) and HL2 (2-((E)-(2-(dimethylamino)ethylimino)methyl)-4-bromophenol) under the same reaction conditions yielded two dinuclear isostructural zinc(II) complexes, [Zn(L1)(N3)]2 (1) and [Zn(L2)(N3)]2 (2), respectively. The complexes were characterized systematically by elemental analysis, UV–Vis, FT-IR, and 1H NMR spectroscopic methods. Single-crystal X-ray diffraction studies reveal that each of the dinuclear complexes consists of two crystallographically independent zinc(II) ions connected by double bridging phenoxides. All zinc(II) ions in 1 and 2 are surrounded by similar donor sets and display distorted square–pyramidal coordination geometries. The ligands and complexes reveal intraligand 1(π → π*) flourescence. The enhancement of the fluorescence intensities for the complexes compared to the ligands indicates their potential to serve as photoactive materials. 相似文献
9.
S. A. Melkozerov I. G. Pervova G. N. Lipunova V. A. Barachevskii I. N. Lipunov E. A. Dvoskin 《Russian Journal of General Chemistry》2013,83(4):646-651
New zinc complexes of the salicylaldehyde benzazolyl- and pyrimidinylhydrazones were synthesized. Study of photophysical properties of the hydrazones and their complexes in solution showed that their structure and the luminescence intensities depend on the nature of the heterocyclic fragment included to the molecule. 相似文献
10.
S. M. Zemskova L. A. Glinskaya V. B. Durasov R. F. Klevtsova S. V. Larionov 《Journal of Structural Chemistry》1994,34(5):794-802
We have synthesized novel mired-ligand complexes of zinc(I1) and cadmium(ZI) diethyldithiocarbamates ZnL2(2,2'-Bipy) (1), Zn2L4(4,4'-Bipy) (2), and CdL2(4,4'-Bipy) (3), where L = (C2H5NCS2
–. An X-ray structural study of zinc compleres 1 and 2 has been cam'ed out. The saucture of complex 1 is characterized by monomeric molecules of symmeby 2. In the crystal structure of complex 2, there are fwo independent binuclear molecules of the same point symmetry 2. It is shown that not only the mononuclear mixed-ligand complaes ML2 with Phen and 2,2'-Bipy (M = Zn, Cd) but also the binuclear Zn2L4(4,4'-Bipy) complex are volatile.Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences. Translated fromZhurnal Strukturnoi Khimii, Vol. 34, No. 5, pp. 157–166, September–October, 1993.Translated by T. Yudanova 相似文献
11.
Synthesis of four different types of ligands Ar[COC(NOH)R]
n
(Ar = biphenyl, n = 1, HL1; Ar = biphenyl, n = 2, H2L2; Ar = diphenylmethane, n = 1, HL3; Ar = diphenylmethane, n = 2, H2L4; R = furfurylamine in all ligands) and their dinuclear Co2+, Ni2+, Cu2+, and Zn2+ complexes is reported herein. These compounds were characterized by elemental analysis, ICP-OES, FT-IR spectra, and magnetic
susceptibility measurements. The ligands were further characterized by 1H NMR. The results suggest that dinuclear complexes of HL1 and HL3 have a metal to ligand mole ratio of 2: 2 and dinuclear complexes H2L2 and H2L4 have a metal to ligand mole ratio of 2: 1. Square pyramidal or octahedral structures are proposed for complexes of oxime
ligands. Furthermore, extraction abilities of the four ligands were also evaluated in chloroform using selected transition
metal picrates such as Mn2+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+, Hg2+, Pb2+. The ligands show strong binding ability towards Hg2+ and Cu2+ ions. 相似文献
12.
13.
14.
《Journal of Coordination Chemistry》2012,65(23):2597-2605
Two complexes [CuL2(H2O)2] (1) and [ZnL2(H2O)2] (2) (L?=?3-carboxyl-1,2,4-triazole (L)) have been synthesized and characterized by single-crystal X-ray diffraction analysis. Compound 1 crystallizes in the monoclinic space group P 2(1)/n, a?=?8.632(8)?Å, b?=?9.153(8)?Å, c?=?6.991(7)?Å, β?=?94.279(12)°, Z?=?2, R 1?=?0.0296, wR 2?=?0.0918. Compound 2 also crystallizes in the monoclinic space group P 2(1)/n, a?=?4.937(3)?Å, b?=?18.107(10)?Å, c?=?6.344(4)?Å, β?=?106.839(7)°, Z?=?2, R 1?=?0.0230, wR 2?=?0.0556. Extensive intermolecular hydrogen bonds assemble 1 and 2 into three-dimensional (3D) supramolecular architectures, with eight-member H-bonded synthons. Compounds 1 and 2 were also characterized by element analysis, FT–IR, luminescence and EPR studies. 相似文献
15.
N. Wannarit N. Chaichit C. Pakawatchai S. Youngme 《Russian Journal of Coordination Chemistry》2010,36(10):778-785
New trinuclear carbonato-bridged copper(II) complexes, [Cu3(Bipy)6(μ3-CO3)](CF3SO3)4(H2O)0.5 (I) and [Cu3(Phen)6(μ3-CO3)](CF3SO3)4(H2O)0.5 (II) (Bipy = 2,2′-bipyridine and Phen = 1,10-phenanthroline), have been synthesized and characterized by X-ray crystallography.
In the trinuclear units, a carbonate anion triply bridges three Cu atoms in a μ3-η1:η1:η1-CO3 mode. The environment around each copper(II) center is five-coordinate ranging between intermediate to distorted square-pyramidal
geometry. In the crystal packing, the molecule of I is involved in a variety of intra/intermolecular non-covalent interactions such as intra/intermolecular stacking and CH···π
interactions between the pyridine groups of the chelated ligand, leading to a one-dimensional arrangement of I. In complex II, the molecule is involved in both intra- and intermolecular Phen-Phen π-stacking, forming a three-dimensional network. The
spectroscopic (IR, diffuse reflectance, and EPR spectra) properties and the preliminary results of magnetic measurements of
both complexes are investigated and compared to other closely related trinuclear copper(II) complexes. 相似文献
16.
Kesheng Shen Xintong Han Chuang Li Guozhen Huang Shanshan Mao Xinkui Shi 《Journal of Coordination Chemistry》2018,71(7):980-990
N,N-bis(N-methyl-2-ylmethylbenzimidazole)aniline (EtAIDB) and its transition metal complexes, [Cu(EtAIDB)Br2]·EtOH {dibromo[N,N-bis(N-methyl-2-ylmethylbenzimidazole)aniline] copper(II) ethanol} (1) and [Zn(EtAIDB)Br2] {dibromo[N,N-bis(N-methyl-2-ylmethylbenzimidazole)aniline] zinc(II)} (2), have been synthesized and characterized by elemental analysis, molar conductivity, UV–visible, and IR spectroscopy. The X-ray crystallographic studies of 1 and 2 have shown two different arrangements: 1 is distorted square-based pyramidal, while 2 can be treated as distorted tetrahedral. The cyclic voltammogram of 1 represents quasi-reversible Cu2+/Cu+ pairs. In vitro antioxidant tests showed that 1 had significant antioxidant activity against superoxide and hydroxy radicals. 相似文献
17.
Two new polynuclear complexes [Ni6(amox)6(mu6-O)(mu3-OH)2](Cl2).6H2O and [Cu3(amox)3(mu3-OH)(mu3-Cl)](ClO4).4H2O (amox- = anion of 4-amino-4-methyl-2-pentanone oxime) have been synthesized and characterized structurally and magnetically. The Ni(II) complex contains a novel Chinese-lantern-like Ni6 cage centered by an oxo ion. It contains the nearest octahedral Ni(II)...Ni(II) separation (<2.8 A) and exhibits strong antiferromagnetic properties. The Cu(II) complex has a cyclic trinuclear copper(II) core bridged by both mu3-OH(-) and mu3-Cl(-) ions. The magnetic susceptibilities of both antiferromagnetic complexes were fitted by using approximate models. 相似文献
18.
19.
V. P. Litvinov A. N. Sukiasyan Ya. L. Gol'dfarb 《Chemistry of Heterocyclic Compounds》1972,8(6):655-666
The review is devoted to the authors' research on the synthesis and study of the reactivities of selenides of the thiophene series, and, to a lesser extent, of selenides of the furan and selenophene series. The properties of the indicated compounds — their capacity for reaction with electrophilic agents and organolithium compounds — and their spectral characteristics are examined in order to compare them with the properties of the corresponding sulfides and alkoxy derivatives.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 723–737, June, 1972. 相似文献
20.
Pal Satyanarayan Pushparaju Jally Sangeetha Nimma Rajaiah Pal Samudranil 《Transition Metal Chemistry》2000,25(5):529-533
Copper(II) complexes [CuL2] of pyridine-N, imine-N and amide-O donor Schiff bases (HL) are reported. The Schiff bases Hpabh, Hpamh and Hpadh were prepared by condensation of 2-pyridinecarboxaldehyde with benzhydrazide, 4-methoxybenzhydrazide and 4-dimethylaminobenzhydrazide, respectively. The complexes were synthesised in MeOH media by reacting Cu(OAc)2 · H2O with HL in a 1:2 mole ratio. The X-ray structure of [Cu(pabh)2] was determined. The rhombically distorted octahedral CuN4O2 coordination sphere is formed by two mononegative meridionally spanning pyridine-N, imine-N and deprotonated amide-O donor ligands. Electronic spectra of the complexes display two d–d bands at ca. 700 and ca. 1300 nm and two strong absorptions due to charge transfer transitions in the 450–268 nm range. Room temperature (298 K) solid state magnetic moments (1.90–2.08 B) suggest an S = 1/2 spin state in each complex. The powder e.p.r. spectra of [Cu(pabh)2] and [Cu(pamh)2] at room temperature are consistent with a rhombic distortion of the N4O2 octahedron around the metal centre. However the spectrum of [Cu(padh)2] suggests a tetragonal elongation of the CuN4O2 octahedron. 相似文献