Search results for "Cyana"
showing 10 items of 585 documents
Synthesis of the first heterometalic star-shaped oxido-bridged MnCu3 complex and its conversion into trinuclear species modulated by pseudohalides (N…
2011
A tetra-nuclear, star-shaped hetero-metallic copper(II)-manganese(II) complex, [{CuL(H(2)O)}(2)(CuL)Mn](ClO(4))(2) (1) has been synthesized by reacting the "complex as ligand" [CuL] with Mn(ClO(4))(2) where H(2)L is the tetradentate di-Schiff base derived from 1,3-propanediamine and 2-hydroxyacetophenone. Upon treatment with the polyatomic anions azide, cyanate, or thiocyanate in methanol medium, complex 1 transforms into the corresponding trinuclear species [(CuL)(2)Mn(N(3))(2)] (2), [(CuL)(2)Mn(NCO)(2)] (3) and [(CuL)(2)Mn(NCS)(2)] (4). All four complexes have been structurally and magnetically characterized. In complex 1 the central Mn(II) ion is encapsulated by three terminal [CuL] unit…
Ferromagnetic Coupling Through the End-to-End Thiocyanate Bridge in Cobalt(II) and Nickel(II) Chains
2015
The preparation, spectroscopic characterization, and X-ray crystal structure of two novel one-dimensional compounds of formula [MII(tppz)(NCS)(μ-1,3-NCS)]n [tppz = 2,3,5,6-tetrakis(2-pyridyl)pyrazine and M = Co(1) and Ni (2)] are reported. 1 and 2 are isomorphous compounds, and they crystallize in the P21/n space group. Their structures are made up of zigzag chains of cobalt(II) (1) and nickel(II) ions (2) bridged by single end-to-end thiocyanate groups with a tridentate tppz molecule and a terminally bound thiocyanate-N ligand achieving distorted MN5S octahedral surroundings around each metal center. The main source of the distortion of the ideal octahedron is due to the geometrical constr…
Syntheses, crystal structures and magnetic properties of copper(II) polynuclear and dinuclear compounds with 2,3-bis(2-pyridyl)pyrazine (dpp) and pse…
2001
Abstract The preparation, crystal structures and magnetic properties of four heteroleptic copper(II) complexes with 2,3-bis(2-pyridyl)pyrazine (dpp) and azide, cyanate or thiocyanate as ligands are reported, [Cu(dpp)(N3)2]n (1), [Cu(dpp)(NCO)2]n (2), [Cu(dpp)(NCS)2]2 (3) and [Cu(H2O)(dpp)(NCS)2]2·2H2O (4). Compounds 1 and 2 are isomorphous, triclinic, space group P1, and consist of mononuclear building blocks featuring copper atoms with close to square planar coordination geometries. The mononuclear units are, however, associated into chains through weak axial Cu–N bonds formed by end-on asymmetrically bridging azido/cyanato groups and by pyridyl nitrogen atoms. Taking these contacts into a…
Thermal and Light-Induced Spin Transition in [Fe(bpen)X2] (bpen = 1,6-Bis(2-pyridyl)-2,5-diazahexane, X = NCS-, NCSe-)
1996
The thermal and light-induced spin transitions in [Fe(bpen)(NCS)2] and [Fe(bpen)(NCSe)2] have been investigated by means of magnetic susceptibility and Mossbauer measurements. The HS → LS transition in [Fe(bpen)(NCS)2] is detected at temperatures below 120 K (T1/2 [when the fraction of high-spin species γHS = 0.5] = 68 K) with a residual HS fraction of 8% at 20 K. The transition is fairly abrupt and no hysteresis is observed, in contrast to earlier studies (ref. [8]). The generation of metastable HS states in [Fe(bpen)(NCS)2] is achieved by rapid cooling of the sample and by irradiating the compound at low temperatures with light of appropriate wavelengths (LIESST). The HS → LS relaxation o…
Linkage isomerism in the metal complex hexa(thiocyanato)rhenate(IV): Synthesis and crystal structure of (NBu4)2[Re(NCS)6] and [Zn(NO3)(Me2phen)2]2[Re…
2008
Abstract The linkage isomers [Re(NCS)6]2− and [Re(NCS)5(SCN)]2− are obtained by the reaction of [ReBr6]2− with NCS− in dimethylformamide. Some differences in the chemical behavior allowed their separation and structural characterization in the form of (NBu4)2[Re(NCS)6] (1) and [Zn(NO3)(Me2phen)2]2[Re(NCS)5(SCN)] (2), respectively (Bu = n-C4H9 and Me2phen = 2,9-dimethyl-1,10-phenanthroline).
Photomagnetism of a Series of Dinuclear Iron(II) Complexes
2009
International audience; The photomagnetic properties of a series of [{Fe(NCS)(py-X)}2(bpypz)2] (NCS=thiocyanate, py=pyridine, X=4-Mepy, py, 3-Mepy, 3-Clpy and 3-Brpy, and bpypz=3,5-bis(pyridine-2-yl)pyazolate) binuclear complexes are close to the antiferromagnetic response of [{Fe(NCS)(3,5-dmpy)}3(bpypz)2] (3,5-dmpy=3,5-dimethylpyrazine), which is characterised by two iron(II) metal ions in a high-spin (HS) electronic configuration . This paper describes the photomagnetic properties of a series of binuclear iron(II) complexes belonging to the [{Fe(NCS)(py-X)}2(bpypz)2] family (NCS=thiocyanate; py=pyridine; bpypz=3,5-bis(pyridine-2-yl)pyrazolate; and py-X=4-Mepy (1), py (3), 3-Mepy (4), 3-Cl…
Complexes of organometallic compounds
1972
Abstract The configurations of (CH 3 ) 3 PbNCS, (C 6 H 5 ) 3 PbNCS, (C 6 H 5 ) 2 Pb(NCS) 2 , (C 6 H 5 ) 3 Pb(NCS) 2 − and (C 6 H 5 ) 2 Pb(NCS) 4 2− have been investigated in the solid and (except for the insoluble diphenyl derivative) in solution. From infrared spectroscopy it is deduced that the compounds are isothiocyanates in both states, and there is evidence for a polymeric nature of the solid neutral species involving bridging through NCS. PMR and osmometric investigations show that five-coordinate species (CH 3 ) 3 Pb(NCS)·(CH 3 ) 2 CO are present in acetone solution. Possible configurations are discussed.
Unique copper ion catalyzed hydrolytic cleavage of C–N(2) bond of thiosemicarbazide
2006
Abstract For the first time, stable but coordinatively unsaturated Cu(II) complexes [Cu(2,2′-bpy)X2] · xH2O (X = ClO4, NO3, CH3COO and 2,2′-bpy = 2,2′-bipyridyl) have been found to promote the hydrolysis of C–N(2) bond of thiosemicarbazide (tsc) at 25 °C and at neutral pH yielding monomeric [Cu(2,2′-bpy)(NCS)2]. Direct reaction between [Cu(2,2′-bpy)2]Cl2 · 6H2O, KSCN and CuCl2 results in polymeric [Cu(2,2′-bpy)(NCS)2]n [1] [Inorg. Chim. Acta. 286 (1999) 108]. Similarly tsc is cleaved by Cu(I) complex [Cu(ϕ3P)2(CH3CN)2]ClO4 [ϕ3P = triphenylphosphine] which itself is converted into dimeric [Cu(ϕ3P)2(NCS)]2.
Synthesis, crystal structure and magnetic properties of the dinuclear manganese(II) complexes [Mn2(bpym)3(NCX)4] (bpym = 2,2′-bipyrimidine; X = S, Se)
1997
Abstract The dinuclear manganese(II) compounds of formula [Mn2(bpym)3(NCX)4], where bpym = 2,2′-bipyrimidine and X = S(1) and Se(2), have been prepared and their crystal structures determined by X-ray diffraction methods. 1 and 2 are isostructural. They crystallize in the triclinic P 1 space group with Z = 1, γ ( Mo K α ) = 0.71073 A , T = 295 K and a = 9.141(2), b = 9.248(2), c = 11.733(2) A , α = 74.88(2), β = 80.29(2), γ = 61.03(2)°, V = 836.7(3) A 3 , D c = 1.621 g cm −3 , M r = 316.7, F(000) = 412, and μ( Mo K α) = 10.54 cm −1 for 1 and a = 9.244(2), b = 9.278(2) A , c = 11.887(2) A , α = 75.19(2), β = 80.83(2), γ = 61.54(2)°, V = 865.7(3) A 3 , D c = 1.926 g cm −3 , M r = 1004.3, F(00…
Pseudohalide derivatives of manganese(II) and copper(II) complexes with mepirizole, a biologically active pyrimidyl-pyrazole ligand
1989
Abstract The synthesis and characterization of thiocyanate and azide derivatives of mepirizole(4-methoxy-2-(5-methoxy-3-methyl-pyrazol-1-yl)-6-methylpyrimidine, hereinafter L) with manganese(II) and copper(II) is reported. The compounds were characterized by IR, electronic and EPR spectra and analytical data. Spectroscopic results suggest the existence of dimeric neutral entities [L2Cu2(μ-X)2(X)2] (X = NCS or N3) with unsymmetrical end-to-end bridges and five-coordination geometry around the copper(II) ion. Magnetic susceptibility data show that in the azide derivative the copper atoms are antiferromagnetically coupled (J = −18 cm−1), but no magnetic exchange interaction could be detected i…