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1.
《Journal of Coordination Chemistry》2012,65(20):2133-2138
A single crystal of the copper(II) compound, [Cu(bdmpp)(SeCN)2], 2, was obtained and its crystal structure was determined by X-ray diffraction methods. The complex was characterized by elemental, thermal and FTIR analysis. The FTIR analysis of the complex clearly shows the SeCN peaks at 2096 and 2061?cm?1 which did not exist in the free organic ligand (bdmpp). X-ray analysis showed that 2 crystallized in the monoclinic space group P21/c. Cu(II) has a distorted trigonal bipyramidal coordination involving three N atoms from the ligand and two N atoms from the selenocyanate group. 相似文献
2.
The mercury complex of 2,6-bis(3,5-dimethyl-N-pyrazolyl)pyridine (bdmpp) has been synthesized and characterized by X-ray diffraction, IR, UV–Vis and TGA–DTA methods. The structure consists of units in which the mercury atom is pentacoordinate with two sulfur and three nitrogen atoms. [Hg(bdmpp)(SCN)2] has a distorted square pyramid geometry. 相似文献
3.
The reaction of Cu(ClO4)2·6H2O and Cd(ClO4)2 with di-(2-picolyl)sulfur (dps) leads to the formation of mononuclear complexes [Cu(dps)(H2O)(ClO4)](ClO4) (1) and [Cd(dps)2](ClO4)2 (2). The crystal structure of 1 exhibits a distorted square pyramidal geometry, coordinated by one sulfur and two nitrogen atoms from the dps ligand, one
water molecule and one perchlorate oxygen atom. For 2, the environment around cadmium atom is in a distorted octahedron with four nitrogen and two sulfur atoms from the dps ligand.
Cyclic voltammetric data show that complexes undergo two waves of a one-electron transfer corresponding to M(II)/M(III) and
M(II)/M(I) processes. Spectral and electrochemical behaviors of the complexes are also discussed. 相似文献
4.
Gabrijela Brađan Andrej Pevec Iztok Turel Igor N. Shcherbakov Milica Milenković Marina Milenković 《Journal of Coordination Chemistry》2016,69(18):2754-2765
Isothiocyanate complexes of Zn(II) and Cd(II) with the condensation product of 2,6-diacetylpyridine and trimethylammoniumacetohydrazide (Girard’s T reagent) were synthesized, characterized, and their antimicrobial activities were evaluated. The structures of the complexes were determined by elemental analysis, IR, and NMR spectroscopy. The crystal structure of the Zn(II) complex was also determined. Quantum-chemical calculations of the geometry and total energy of isomers of 2,6-diacetylpyridine-bis(trimethylammoniumacetohydrazone) were performed in vacuum and methanol solution, with the aim to explain conformational behavior and E/Z isomerism of this compound. DFT calculations of the molecular structures and the relative stabilities of linkage isomers of the Cd(II) complex showed that the isomer with N–Cd–N coordination of SCN? is the most stable. Complexes of Zn(II) and Cd(II) exhibited low to moderate activity against the tested microbial strains. 相似文献
5.
Three novel cadmium(II) complexes of 2-benzoylpyridine [Cd(bopy)2Cl2] (1), {[Cd(bopy)(μ1,1-N3)2]·bopy}n (2) and [Cd(bopy)2(SCN)2] (3) were synthesized and characterized by spectroscopic and crystallographic methods. Azide ions of 2 act as bridging ligands generating a 1D chain running along [0 1 0]. The zig-zag chains consisting of {Cd(bopy)(N3)2} units are separated by 2-benzoylpyridine molecules. The fluorescence properties of the complexes 1, 2 and 3 were examined both in solid state and solution, and compared with the free ligand. Additionally, the electronic spectrum of 3 were investigated at the TDDFT level employing B3LYP functional in combination with LANL2DZ. 相似文献
6.
《Journal of Coordination Chemistry》2012,65(2):298-307
The coordination chemistry and cationic binding properties of 2,6-bis(pyrazol-1-ylmethyl)pyridine (L1), 2,6-bis(3,5-dimethylpyrazol-1-ylmethyl)pyridine (L2), and 2,6-bis(3,5-ditertbutylpyrazol-1-ylmethyl)pyridine (L3) with zinc(II) and cadmium(II) have been investigated. Reactions of L2 with zinc(II) and cadmium(II) nitrate or chloride salts produced monometallic complexes [Zn(NO3)2(L2)] (1), [ZnCl2(L2)] (2), [Cd(NO3)2(L2)] (3), and [CdCl2(L2)] (4). Solid state structures of 1 and 3 confirmed that L2 binds in a tridentate mode. While the nitrates in the zinc complex (1) adopt monodentate binding fashion, in cadmium complex (3), they exhibit bidentate mode. L1–L3 show binding efficiencies of 99% for zinc(II), 60% for lead(II), and 30% for cadmium(II) cations from aqueous solutions of the metal ions. Theoretical studies using Density Functional Theory were consistent with the observed extraction results. 相似文献
7.
Ahmad R. Esmaeilbeig Hamid R. Samouei Mehdi Rashidi 《Journal of organometallic chemistry》2008,693(15):2519-2526
The phosphite complexes cis-[PtMe2L(SMe2)] in which L = P(OiPr)3, 1a, or L = P(OPh)3, 1b, were synthesized by the reaction of cis,cis-[Me2Pt(μ-SMe2)2PtMe2] with 2 equiv. of L. If 4 equiv. of L was used the bis-phosphite complexes cis-[PtMe2L2] in which L = P(OiPr)3, 2a, or L = P(OPh)3, 2b, were obtained. The reaction of cis-[Pt(p-MeC6H4)2(SMe2)2] with 2 equiv. of L gave the aryl bis-phosphite complexes cis-[Pt(p-MeC6H4)2L2] in which L = P(OiPr)3, 2a′, or L = P(OPh)3, 2b′. Use of 1 equiv. of L in the latter reaction gave the bis-phosphite complex along with the starting complex in a 1:1 ratio.The complexes failed to react with MeI. The reaction of cis,cis-[Me2Pt(μ-SMe2)2PtMe2] with 2 equiv. of the phosphine PPh3 gave cis-[PtMe2(PPh3)2] and cis-[PtMe2(PPh3)(SMe2)] along with unreacted starting material. Reaction of cis-[PtMe2L(SMe2)], 1a and 1b with the bidentate phosphine ligand bis(diphenylphosphino)methane, dppm = Ph2PCH2PPh2, gave [PtMe2(dppm)], 8, along with cis-[PtMe2L2], 2. The reaction of cis-[PtMe2L(SMe2)] with 1/2 equiv. of the bidentate N-donor ligand NN = 4,4′-bipyridine yielded the binuclear complexes [PtMe2L(μ-NN)PtMe2L] in which L = P(OiPr)3, 3a, or L = P(OPh)3, 3b.The complexes were fully characterized using multinuclear NMR (1H, 13C, 31P, and 195Pt) spectroscopy. 相似文献
8.
《Journal of Coordination Chemistry》2012,65(24):2649-2657
Reactions of imidazolidine-2-thione (Imt), 1,3-diazinane-2-thione (Diaz) and 1,3-diazipane-2-thione (Diap) with mercury(II) selenocyanate in acetonitrile resulted in formation of 2?:?1 complexes. Both solid state and solution NMR, confirm the exocyclic sulfur atom to be the donor in all cases. 199Hg shielding tensors and anisotropies were calculated from the solid-state NMR spectra. Based on the solid NMR data a distorted tetrahedral disposition of ligands around mercury is proposed. 相似文献
9.
Seven Zn(II) and Cd(II) complexes of ON donor acetone-N(4)-phenylsemicarbazone (HL) have been synthesized and physico-chemically characterized by partial elemental analyses, molar conductance measurements, infrared, electronic and 1H NMR spectral studies. The semicarbazone binds the metal as a neutral bidentate ligand in all the complexes. The crystal structures of acetone-N(4)-phenylsemicarbazone and [Cd(HL)2Cl2] have been determined by X-ray diffraction studies. The coordination geometry around cadmium(II) in the complex [Cd(HL)2Cl2] is distorted octahedral. 相似文献
10.
Mohammed FettouhiBassem A. Al-Maythalony M. Nasiruzzaman ShaikhMohammed I.M. Wazeer Anvarhusein A. Isab 《Polyhedron》2011,30(7):1262-1266
Complexes of cadmium(II)-selenocyanate with several alkyldiamine ligands have been synthesized and characterized by IR, 113Cd, 77Se, 15N and 13C NMR spectroscopy. The X-ray structure of the complex [Cd(SeCN)2-en] reveals two non-equivalent metal ion centers, both with a distorted octahedral geometry. The combined bridging modes of selenocyanate and ethylenediamine with the blocking mode of a chelating ethylenediamine generate a 2D metal-organic framework. 相似文献
11.
12.
《Thermochimica Acta》2001,370(1-2):29-36
The thermal properties of four copper(II) complexes with N,N′,N″,N-tetrakis(2-pyridylmethyl)-1,4,8,11-tetraazacyclotetradecane (tpmc) and several bidentate ligands N,S (thiosemicarbazide and thiourea) or N,O donors (semicarbazide and urea), of the general formula [Cu2(X)tpmc](ClO4)4, have been investigated by thermogravimetry (TG) and differential scanning calorimetry (DSC). The thermal stability order can be recognized for the examined complexes, depending on coordinated bidentate bridging N,S or N,O ligand. Kinetic data demonstrated first-order thermal decomposition. A plausible mechanism has been proposed which explains the major products of the degradation. 相似文献
13.
Thermal decomposition kinetics of ML2 (M = Ni(II) and Co(II); L = 5-(2-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)hydrazono)-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione) complexes were investigated by thermogravimetric analysis (TGA). The first decomposition process of the NiL2 and CoL2 complexes occurs in the temperature range of 320–350 °C. Kinetics parameters corresponding to this step, such as activation energy, Eα, and apparent pre-exponential factor, ln Aaap, were calculated from the thermogravimetric data at the heating rates of 5, 10, 15 and 20 K min−1 by differential (Friedman's equation) and integral (Flynn–Wall–Ozawa's equation) methods. The results show that the activation energy evidently depends on the extent of conversion. As far as their activation energy is concerned, NiL2 complex shows a higher thermal stability than the CoL2 complex. 相似文献
14.
《印度化学会志》2021,98(10):100168
The three new Cobalt(II) complexes [Co(L1)2(H2O)2] (1), [Co(L2)2(H2O)2] (2), and [Co(L3)2(H2O)2] (3) have been synthesized by interaction of acyl pyrazolone ligands, 4-(4-chlorobenzoyl)3-methyl1-phenyl1H-pyrazole5(4H)-one (HL1), 4-(4-chlorobenzoyl)1-(3-chlorophenyl)3-methyl1H-pyrazole5(4H)-one (HL2) and 5-methyl4-(4-methylbenzoyl)2-phenyl2,4-dihydro3H-pyrazole3-one (HL3) with CoCl2.6H2O. The complexes were screened using FTIR, UV–Vis, TGA, and Single Crystal X-ray diffraction spectroscopic techniques. A relative study of the ligands’ FTIR spectra and their metal complexes reveal the formation, sifting, and disappearance of several bands during complexation. Other interpretations stipulated that these three complexes are mononuclear and exhibited octahedral geometry around Co2+.Triclinic crystal system, Distortion in Octahedral geometry, and Intermolecular hydrogen bonding confirmed by Single-crystal XRD analysis of [Co(L3)2(EtOH)2] complex. 相似文献
15.
Urmila Pal Chaudhuri Lei Yang Laura R. Whiteaker Arunendu Mondal Matthew R. Fultz Douglas R. Powell Robert P. Houser 《Polyhedron》2007,26(18):5420-5431
Mononuclear copper(II) complexes of a family of pyridylmethylamide ligands HL, HLMe, HLPh, HLMe3 and HLPh3, [HL = N-(2-pyridylmethyl)acetamide; HLMe = N-(2-pyridylmethyl)propionamide; HLPh = 2-phenyl-N-(2-pyridylmethyl)acetamide; HLMe3 = 2,2-dimethyl-N-(2-pyridylmethyl)propionamide; HLPh3 = 2,2,2-triphenyl-N-(2-pyridylmethyl)acetamide], were synthesized and characterized. The reaction of copper(II) salts with the pyridylmethylamide ligands yields complexes [Cu(HL)2(OTf)2] (1), [Cu(HLMe)2](ClO4)2 (2), [Cu(HL)2Cl]2[CuCl4] (3), [Cu(HLMe3)2(THF)](OTf)2 (4), [Cu(HLMe3)2(H2O)](ClO4)2 (5a and 5b), [Cu(HLPh3)2(H2O)](ClO4)2 (6), [Cu(HL)(2,2′-bipy)(H2O)](ClO4)2 (7), and [Cu(HLPh)(2,2′-bipy)(H2O)](ClO4)2 (8). All complexes were fully characterized, and the X-ray structures vary from four-coordinate square-planar, to five-coordinate square-pyramidal or trigonal-bipyramidal. The neutral ligands coordinate via the pyridyl N atom and carbonyl O atom in a bidentate fashion. The spectroscopic properties are typical of mononuclear copper(II) species with similar ligand sets, and are consistent their X-ray structures. 相似文献
16.
The thermal properties of cyanatocopper complexes with pyridine, bipyridine and phenanthroline are described in this paper. It was found that the thermal stabilities of the complexes were found to increase in the order pybipy2(NCS)2 (L=pyridine and its methyl derivates) which are composed of the liberation of ligandsL and redox reactions of thiocyanate ligands with the central Cu(II) atom [1, 2]. The decomposition temperature of thiocyanate ligands depends on the properties of the ligandsL present in the coordination sphere. An analogous course of thermal decomposition was also observed for [Cu(bipy)2(NCX)](NCX) (X=S or Se) [3]. For the phenanthroline complexes [Cu(phen)2(NCX)2] (X=S or Se) the thermal stability was found to increase significantly (by about 140C) and the decomposition stoichiometry was also changed [3].The present paper contains the results of thermoanalytical studies on bipyridine and phenanthroline cyanatocopper complexes, and a comparison of the thermal properties of pyridine cyanato and isothiocyanatocopper complexes. 相似文献
17.
《Journal of Coordination Chemistry》2012,65(3):325-331
A novel one-dimensional complex, [Cd(NIT4py)2(DTB)2(H2O)2] (1), (where NIT4py is 2-(4′-pyridyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide and DTB is 3,5-dinitrobenzoate) has been synthesized and characterized by elemental analyses, IR and electronic spectra, single-crystal X-ray diffraction and magnetic measurements. The Cd(II) ion lies in a distorted octahedral environment with two nitrogen atoms from two NIT4py ligands and two oxygen atoms from two DTB molecules in the basal plane, and two oxygen atoms from two water molecules in axial positions. [Cd(NIT4py)2(DTB)2(H2O)2] units are connected to form one-dimensional chains by intermolecular hydrogen bonds. The complex exhibits intramolecular antiferromagnetic interactions. 相似文献
18.
《Journal of Coordination Chemistry》2012,65(6):529-537
Zinc(II), cadmium(II) and mercury(II) complexes of thiourea (TU) and selenourea (SeU) of general formula M(TU)2Cl2 or M(SeU)2Cl2 have been prepared. The complexes were characterized by elemental analysis and NMR (1H, 13C, 15N, 77Se and 113Cd) spectroscopy. A low-frequency shift of the C=S resonance of thiones in 13C NMR and high-frequency shifts of N–H resonances in 1H and 15N NMR are consistent with sulfur or selenium coordination to the metal ions. The Se nucleus in Cd(SeU)2Cl2 in 77Se NMR is deshielded by 87?ppm on coordination, relative to the free ligand. In comparison, the analogous Zn(II) and Hg(II) complexes show deshielding by 33 and 50?ppm, respectively, indicating that the orbital overlap of Se with Cd is better. Principal components of 77Se and 113Cd shielding tensors were determined from solid-state NMR data. 相似文献
19.
Tamara R. Todorović Alessia Bacchi Nenad O. Juranić Dušan M. Sladić Giancarlo Pelizzi Tatjana T. Božić Nenad R. Filipović Katarina K. Anđelković 《Polyhedron》2007
New complexes of Cd(II), Zn(II) and Ni(II) with 2-quinolinecarboxaldehyde selenosemicarbazone (Hqasesc) were synthesized and structurally characterized. The structure of the ligand, Cd(II) and Zn(II) complexes was determined by NMR and IR spectroscopy, elemental microanalysis and molar conductivity measurements. Both complexes occur in solution in two forms, the major tetrahedral and minor octahedral. In the major Cd(II) complex one qasesc− ligand is coordinated as a tridentate, the fourth coordination site being occupied by acetate, while in the major Zn(II) complex two qasesc− ligands are coordinated as bidentates. In both minor complexes two qasesc− ligands are coordinated as tridentates forming the octahedral geometry around the central metal ion. The only paramagnetic complex in the series is Ni(II) complex for which X-ray structure analysis was performed. The complex has the angularly distorted octahedral geometry with two qasesc− ligands coordinated as tridentates, in a similar way as in the minor complexes of Cd(II) and Zn(II). 相似文献
20.
The complex [Ru(II)(dcbpyH2)(bdmpp)NCS](PF6) (1) (where dcbpyH2 is 2,2′-bipyridine-4,4′-dicarboxylic acid, bdmpp is 2,6-bis(3,5-dimethyl-N-pyrazoyl)pyridine,) is synthesized and characterized extensively by 1H NMR and 13C NMR 1D and 2D, mass spectroscopy, cyclic voltammetry, electronic absorption spectroscopy and IR. The half-wave potential of the Ru(II)/Ru(III) redox couple was measured at E1/2=+0.795 V versus Ag/AgCl in CH3CN. The complex presents three intense metal-to-ligand charge transfer (MLCT) (dM→πL*) absorption bands centered at 383 (=21 300 M−1 cm−1), 432 (=22 400 M−1 cm−1) and 475 nm (=23 400 M−1 cm−1), respectively. The absorbance is extremely strong between 400 and 500 nm and even at 620 nm, the extinction coefficient is still high (=3768 M−1 cm−1). The strong π-acceptor property of the trans-isothiocyanate ligand compared with the Cl− ligand is probably the cause of the blue-shift observed in complex 1. These properties make the complex potentially promising for the photosensitization process. The incorporation of TiO2 photoelectrodes derivatized with this complex into a solar cell using a composite polymer/inorganic oxide solid-state electrolyte confirmed its sensitizing ability. Incident monochromatic photon-to-current conversion efficiency (IPCE) values of about 30% and overall energy conversion efficiency (η) of 1.7% were obtained. 相似文献