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1.
Mary S. Thomas David C. Liles Maril Landman Elizabeth M. van der Merwe Simon Lotz 《Polyhedron》2006,25(18):3562-3568
The complexes [Zn2(S2CTR)4] (T = 2,5-disubstituted thiophene, R = C4H9 (1), C6H13 (2), C8H17 (3), C12H25 (4) and C16H33 (5)) have been synthesized and their structural features investigated. Compared to the analogous dithiobenzoate complexes, the crystal structure determination of 2 revealed that the thiophene induces a “step-rod” chain pattern instead of the linear, rodlike structure found for the corresponding dithiobenzoates. Complexes 1–5 did not display mesophases under thermal conditions, but an irregular melting pattern was observed for 3 and 4. 相似文献
2.
《Journal of Coordination Chemistry》2012,65(4):679-687
Cationic nickel(II) complexes containing chelating O,O′-donor maltolate or ethyl maltolate ligands in conjunction with bidentate bisphosphine ligands Ph2P(CH2) n PPh2 were prepared by a one-pot reaction starting from nickel(II) acetate, bisphosphine, maltol (or ethyl maltol), and trimethylamine, and isolated as their tetraphenylborate salts. An X-ray structure determination of [Ni(maltolate)(Ph2PCH2CH2PPh2)]BPh4 shows that the maltolate ligand binds asymmetrically to the (slightly distorted) square-planar nickel(II) center. The simplicity of the synthetic method was extended to the synthesis of the known platinum(II) maltolate complex [Pt(maltolate)(PPh3)2]BPh4 which was obtained in high purity. 相似文献
3.
A series of nickel(II) complexes having the (Me-Tp)2PMA ligand ((Me-Tp)2PMA = bis(5-methyl-2-thiophenemethyl)(2-pyridylmethyl)amine) with nitrates (1), chlorides (2), and perchlorates (3) as anions were synthesized and isolated. All these complexes were successfully characterized by physicochemical methods including X-ray crystallographic analysis. In complex 1, the ligand binds in a bidentate N2 fashion, whereas in the cases of 2 and 3 the ligand binds in the tridentate N2S form. The coordination geometry around the nickel(II) atoms in these complexes is distorted octahedral. 相似文献
4.
Damian C. Onwudiwe Anthony C. Ekennia Eric Hosten 《Journal of Coordination Chemistry》2016,69(16):2454-2468
Three Ni(II) dithiocarbamate complexes, [Ni(buphdtc)2] (1), [Ni(buphdtc)(PPh3)(NCS)] (2) and [Ni(buphdtc)(PPh3)(NC)] (3) (where bu = butyl and ph = phenyl), were synthesized and characterized by elemental analysis, UVvis, and FTIR spectroscopies. Complexes 1 and 2 were further characterized by single-crystal X-ray structural analysis. The single-crystal X-ray structural analysis indicates a slightly distorted square planar geometry. In 2 and 3, the influences of the auxiliary ligands (PPh3, NCS, and NC) on their steric and electronic properties were observed. Thermal studies of the complexes showed decomposition starting at 250–300 °C, leading to formation of nickel sulfide phases around 400 °C. The complexes were screened against some bacteria strains, Staphylococcus aureus, Streptococcus pneumoniae, Bacillus subtilis, Escherichia coli, Klebsiella oxytoca and Pseudomonas aeruginosa, and two fungi species, Aspergillus niger and Fusarium oxysporum. The complexes showed moderate-to-strong antimicrobial potentials, with [Ni(buphdtc)2] (1) displaying the best antimicrobial activity. Fluconazole and streptomycin were used as reference drugs for antifungal and antibacterial assays, respectively. 相似文献
5.
《Journal of Coordination Chemistry》2012,65(1):136-146
Ni(II) and Cu(II) metal complexes of simple unsymmetrical Schiff-base ligands derived from salicylaldehyde/5-methylsalicylaldehyde and ethylenediamine or diaminomaleonitrile (DMN) were synthesized. The ligands and their complexes were characterized by elemental analysis, 1H NMR, FT IR, and mass spectroscopy. The electronic spectra of the complexes show d–d transitions in the region at 450–600 nm. Electrochemical studies of the complexes reveal that all mononuclear complexes show a one-electron quasi-reversible reduction wave in the cathodic region. ESR spectra of the mononuclear copper(II) complexes show four lines, characteristic of square-planar geometry, with nuclear hyperfine spin 3/2. The copper(II) complexes show a normal room temperature magnetic moment value μ eff = 1.70–1.74 BM which is close to the spin only value of 1.73 BM. Kinetic studies on the oxidation of pyrocatechol to o-quinone using the copper(II) complexes as catalysts were also carried out. The in vitro antimicrobial activity of the investigated compounds was tested against human pathogenic bacterias such as Staphylococcus aureus, Bacillus subtilis, Klebsiella pneumonia, Pseudomonas aeruginosa and Escherichia coli. The antifungal activity was tested against Candida albicans. Generally, the metal complexes have higher antimicrobial activity than the free ligands. 相似文献
6.
Neslihan ?ahin Hani El MollDavid Sémeril Dominique Matt ?smail ÖzdemirCemal Kaya Loïc Toupet 《Polyhedron》2011,30(12):2051-2054
Two dichlorido-tetrakis-(N-R-imidazole)nickel(II) complexes (R = 2,6-diisopropylphenyl (1); methyl (2)) have been synthesised. A single crystal X-ray diffraction study was carried out for 1, which revealed a centrosymmetric complex with the nickel centre placed in an octahedral coordination environment. Both complexes showed high activities (TOFs up to 60200 mol(ArBr) mol(Ni)−1 h−1) in Kumada-Tamao-Corriu cross-coupling of arylhalides with arylgrignards. No significant differences in activity were observed between the two complexes. 相似文献
7.
Animesh Patra Sandipan Sarkar Michael G.B. Drew Ennio Zangrando Pabitra Chattopadhyay 《Polyhedron》2009
Three new mononuclear complexes of nitrogen–sulfur donor sets, formulated as [FeII(L)Cl2] (1), [CoII(L)Cl2] (2) and [NiII(L)Cl2] (3) where L = 1,3-bis(2-pyridylmethylthio)propane, were synthesized and isolated in their pure form. All the complexes were characterized by physicochemical and spectroscopic methods. The solid state structures of complexes 1 and 3 have been established by single crystal X-ray crystallography. The structural analysis evidences isomorphous crystals with the metal ion in a distorted octahedral geometry that comprises NSSN ligand donors with trans located pyridine rings and chlorides in cis positions. In dimethylformamide solution, the complexes were found to exhibit FeII/FeIII, CoII/CoIII and NiII/NiIII quasi-reversible redox couples in cyclic voltammograms with E1/2 values (versus Ag/AgCl at 298 K) of +0.295, +0.795 and +0.745 V for 1, 2 and 3, respectively. 相似文献
8.
M. Dolores Santana Gabriel García Consuelo Vicente-Hernndez Luís García Jos Prez Tefilo Rojo Luís Lezama 《Journal of organometallic chemistry》2008,693(11):2009-2016
The preparation, spectroscopic characterization and magnetic study of N,N′-bis(substituted-phenyl)oxamidate-bridged nickel(II) dinuclear complexes of formula {[Ni(N3-mc)]2(μ-CONC6H4-X)}(PF6)2 (N3-mc = 2,4,4-trimethyl-1,5,9-triazacyclo-dodec-1-ene (Me3-N3-mc) or 2,4,4,9-tetramethyl-1,5,9-triazacyclododec-1-ene (Me4-N3-mc), X = 2-Cl, 4-Cl, 2-OCH3, 4-OCH3) are reported. These paramagnetic nickel(II) complexes have been characterized by both one- and two-dimensional (COSY) 1H NMR techniques. The COSY spectrum of 5 has allowed to achieve the assignment of the phenyl protons of the N,N′-diphenyloxamidate. The crystal structures of [Ni(Me3-N3-mc)(μ-CONC6H4-4-Cl)]2(PF6)2 (6), [Ni(Me3-N3-mc)(μ-CONC6H4-4-OMe)]2(PF6)2 (8) and [Ni(Me4-N3-mc)(μ-CONC6H4-2-Cl)]2(PF6)2 (9) have been determined and their magnetic properties have been studied. The value of magnetic coupling between the two nickel(II) ions across the oxamidate bridge [J = − 37.6 (6), −39.9 (8) and −39.7 cm−1 (9)] is sensitive to the distortion of the coordination sphere of the metal ions and the topology of the molecular bridge. 相似文献
9.
《Journal of Coordination Chemistry》2012,65(21):3700-3710
Nickel(II) and palladium(II) form neutral 1?:?2 chelates with aromatic thiohydrazides, for example. thiobenzhydrazide, o-hydroxythiobenzhydrazide, furan-2-thiohydrazide, and thiophen-2-thiohydrazide. All the compounds are diamagnetic and have been characterized by elemental analysis and spectroscopic methods. o-Hydroxythiobenzhydrazido complexes of nickel(II) and palladium(II) were crystallized from DMSO and their structures were solved by X-ray diffraction. The complexes are isostructural with planar structures. Metal ion is linked to two identical deprotonated ligands through trans hydrazinic nitrogen and sulfur. Hydrogen of OH is involved in intramolecular hydrogen-bonding. 相似文献
10.
Hassan Hadadzadeh Ghobad Mansouri Ali RezvaniHamid R. Khavasi Brian W. SkeltonMohamed Makha Faramarz Rostami Charati 《Polyhedron》2011,30(15):2535-2543
Three mononuclear polypyridyl complexes of Ni(II), [Ni(Ph2phen)3](PF6)2·CH3CN (1), [Ni(dpa)2(phen)](PF6)2 (2) and [Ni(bpy)3](PF6)2 (3), where Ph2phen is 4,7-diphenyl-1,10-phenanthroline, dpa is 2,2′-dipyridylamine, bpy is 2,2′-bipyridine, and phen is 1,10-phenanthroline, were prepared and their solid state structures determined by single-crystal X-ray crystallography. The structural determination shows that the coordination geometry around the Ni(II) center is a distorted octahedron in each complex. The investigation of synthesis procedure and crystallographic data of complex 3 indicates the spontaneous resolution of supramolecular chirality. A careful inspection of the packing pattern in the lattice of each complex reveals that non-covalent interactions of two different types, viz. C-H?F and C-H?π interactions, are active in the lattice. The packing structures of 1-3 also show that the rings of the polypyridyl ligands, Ph2phen, dpa, bpy, and phen, are not located face-to-face and can not interact through π-π interactions. Cyclic voltammetry data of 1 and 3 show that the Ni(III/II) reduction couple is quasi-reversible and this reduction becomes progressively more difficult on passing from bpy to Ph2phen, while complex 2 shows an irreversible behavior with the peak-to-peak separation of about 500 mV. Magnetic susceptibility data derived from paramagnetic NMR revealed effective magnetic moments of 3.12 BM for 1, 3.27 BM for 2, and 3.14 for 3 at room temperature. 相似文献
11.
J. Titiš R. Boča L’. Dlháň T. Ďurčeková H. Fuess R. Ivaniková V. Mrázová B. Papánková I. Svoboda 《Polyhedron》2007
Heteroleptic nickel(II) complexes with the general formula Ni(L)m(H2O)n(X)k, have been synthesized and structurally characterized; L stands for neutral N-donor ligands: 4-benzofuropyridine (bzfupy), dimethylfuropyridine (Me2fupy) and 1,2-dimethylimidazole (Me2iz), X = acetate or Cl−. The structures of the complexes [Ni(bzfupy)2(ac)2(H2O)2], [Ni(Me2fupy)2(H2O)4](ac)2 and [Ni(Me2iz)4(H2O)2]Cl2 · 3H2O are formed from {NiO2O′2N2}, {NiO4N2} and {NiN4O2} chromophores, respectively. These complexes and two other previously characterized complexes, [Ni(pz)4(ac)2], pz – pyrazole, and [Ni(LNN)2(H2O)2], LNN – bidentate chelating ligand, were subjected to magnetochemical investigation down to 2 K (susceptibility and magnetization measurements). They show magnetic behaviour typical for zero-field splitting systems. The axial parameter of the zero-field splitting, D, adopts either positive or negative values and correlates with the axial distortion of the coordination polyhedra. 相似文献
12.
M. Dolores Santana Gabriel García Gregorio López Abel Lozano Consuelo Vicente Luís García José Pérez 《Polyhedron》2007
Substituted-benzoate complexes of nickel(II) of the types bidentate [Ni(mcN3)(Bz)](PF6) and monodentate [Ni(mcN3)(Bz)(H2O)](PF6) have been prepared by acid-base reaction between the hydroxo complexes [Ni(mcN3)(μ-OH)]2(PF6)2 (mcN3 = 2,4,4-trimethyl-1,5,9-triazacyclododec-1-ene (Me3-mcN3) or its 9-methyl derivative (Me4-mcN3)) and the corresponding benzoic acid. The paramagnetic nickel(II) complexes have been characterized in solution by NMR spectroscopy. The influence of the substituents on the hyperfine shift patterns for substituted-benzoate complexes of nickel(II) has been studied. The substituent effects upon the coordination mode of substituted benzoates have been established by X-ray diffraction. 相似文献
13.
Rocío García-Bueno Gregorio Sánchez Gabriel García Luís García 《Journal of organometallic chemistry》2009,694(3):316-9511
Heteroleptic nickel pentacoordinate complexes with the macrocyclic ligands 2,4,4-trimethyl-1,5,9-triazacyclododec-1-ene (Me3-mcN3) or its 9-methyl derivative (Me4-mcN3), as ancillary ligands, and O,O′-(diphenylphosphineoxide)amidate ligands, [RC(O)NP(O)Ph2]¯ (R = C6H6 (1), C5H4N (2), C4H3S (3)), have been prepared as well as related acetylacetonate derivatives. The complexes have been studied by spectroscopic methods (IR, UV-Vis and 1H NMR). In acetone solution, the complexes exhibit isotropically shifted 1H NMR resonances. The full assignment of these resonances has been achieved using one- and two-dimensional 1H NMR techniques. The single-crystal structures of {(Me4-mcN3)Ni[OP(Ph2)NC(Tf)O]}[PF6] (9) and {(Me3-mcN3)Ni(acac)}[PF6] (10) have been established by X-ray diffraction. 相似文献
14.
Pulak K. Dhara Sandipan Sarkar Michael G.B. Drew Munirathinam Nethaji Pabitra Chattopadhyay 《Polyhedron》2008
Two sets of nickel(II) complexes of a series of tetradentate NSNO ligands were synthesized and isolated in their pure form. All these complexes, formulated as [Ni(L)Cl]2 and [Ni(L)(N3)]2 [HL = pyridylthioazophenols], were characterized using physicochemical and spectroscopic tools. The solid-state structures of two complexes (1a and 2a) were established by X-ray crystallography. The geometry about the nickel ion of the complexes is octahedral and the complexes are dimeric in nature. In 1, two Ni(II) ions are bridged by two Cl− anions while in 2 they are bridged by two azide ions in a μ-1,1-bridging fashion. 相似文献
15.
Two pincer-type nickel iminophosphinite complexes, [(2-(CHNR)-6-(OPR′2)C6H3)NiCl] (R = 2,6-iPr2C6H3, R′ = Ph (2a) or iPr (2b)), were synthesized from the reactions of bis(1,5-cyclooctadiene)nickel(0) and corresponding iminophosphinite ligands. The solid state structures of the nickel pincer complexes were determined by X-ray single crystal diffraction studies. They were successfully employed in the Kumada reaction of non-activated aryl chlorides and phenylmagnesium bromide at room temperature. 相似文献
16.
17.
Wen-Hua Sun Shu Zhang Wen Zhang Hongwei Ma Katrin Wedeking 《Journal of organometallic chemistry》2006,691(20):4196-4203
A series of nickel (II) complexes ligated by 2-imino-1,10-phenanthrolines were synthesized and characterized by elemental and spectroscopic analysis as well as by single-crystal X-ray crystallography. X-ray crystallographic analysis reveals complexes 3, 5, 7 and 11 as the five-coordinated distorted trigonal-bipyramidal geometry. Upon activation with Et2AlCl, these complexes exhibited considerably high activity for ethylene oligomerization (up to 3.76 × 107 g mol−1(Ni) h−1 for 12 with 10 equiv. of PPh3). The ligand environment and reaction conditions significantly affect the catalytic activity of their nickel complexes. 相似文献
18.
《Journal of Coordination Chemistry》2012,65(9):953-959
Hydrothermal treatments of ciprofloxacin with Ni(NO3)2·6H2O and Mn(ClO4)2·6H2O yield two metal complexes: [Ni(H-cip)2(H2O)2](NO3)2·2H2O (1) and [Mn(H-cip)2(H2O)2] (ClO4)2·2H2O (2), confirmed by elemental analysis, IR and single crystal X-ray diffraction analyses. Complexes 1 and 2 were screened for antibacterial activity against Staphylococcus aureas, E. coli, Pseudomonas aeruginos and Candidaalbicans. 相似文献
19.
《Journal of Coordination Chemistry》2012,65(14):2388-2398
The cobalt(II) and nickel(II) chelates of Schiff bases, derived by condensing 4-butyryl-3-methyl-1-phenyl-2-pyrazolin-5-one (BMPP) with o-, m-, p-phenylenediamine, benzidine, and ethylenediamine have been synthesized and characterized by elemental analyses, thermogravimetric analyses (TGA), conductance data, magnetic measurements, IR, 1H NMR, 13C NMR, mass, and electronic spectroscopies. Each of the Schiff bases was an ONNO donor to metal forming chelates formulated as [M(L)(H2O)2] n with M = Ni(II) and Co(II) and L is the di-anion of the Schiff base. The monomeric (n = 1) and dimeric (n = 2) species of these metal chelates, based on available evidence, are suggested. 相似文献