共查询到20条相似文献,搜索用时 15 毫秒
1.
The synthesis and properties of rhodium(I) complexes of formulae [“RhCl(diolefin)”2(L)] (or [Rh(Cl(diolefin)(L)]), and [Rh(diolefin)(L)]n(ClO4)n are reported. These complexes react with carbon monoxide to yield the related carbonyl derivatives. Ligands used were pyridazine, 4,6-dimethyl-pyrimidine, 4,6-bis(3,5-dimethylpyrazol-1-yl)pyrimidine, 3,6-bis(3,5-dimethylpyrazol-1-yl)pyridazine and 3-(3,5-dimethyl-pyrazol-1-yl)-6-chloropyridazine. Related iridium(I) and gold(I) compounds are also reported. 相似文献
2.
Virupaxappa H. Arali Vidyanand K. Revankar Vinayak B. Mahale 《Transition Metal Chemistry》1993,18(2):158-162
Summary Thirteen new complexes, MLX·nH2O and ML2(ClO4)2· nH2O [M = Co, Ni, Cu; X = Cl–, Br–, NO
f3
p–
, 1/2SO
f4
p2–
; n = 1 or 2; and L = 2-(3,5-dimethylpyrazol-1-yl)benzothiazole], have been synthesized, and characterized by elemental analysis, conductivity measurements, magnetic moments, thermal studies and electronic, i.r. and e.p.r. spectral studies. On the basis of available data probable structures have been proposed. In a few cases the antibacterial and antifungal activities increase on complexation of the ligand with metals. 相似文献
3.
Four new metal-radical complexes - [Cu(NIT3Py)2(DTB)2] 1, [Co(NIT3Py)2(DTB)2(CH3OH)2] 2, [Cu(NIT4Py)2(DTB)2(H2O)2] 3, [Co(NIT4Py)2(DTB)2(H2O)2] 4, (NIT3Py = 2-(3′-pyridyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide], NIT4Py = 2-(4′-pyridyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide], DTB = 3,5-dinitrobenzoic anion) have been synthesized by using transition metal ions, nitronyl nitroxide radicals as spin carriers, and incorporating 3,5-dinitrobenzoic acid (DTB) as a coligand. 相似文献
4.
The synthesis and structures of a mononuclear copper(I) carbonyl complex [Cu(OClO3)(CO)(H2CPz2')] (3) and a dinuclear copper(I) carbonyl complex [{Cu(CO)(H2CPz2')}2(mu-pyrazine)](ClO4)2 (4), where H2CPz2' = bis(3,5-dimethylpyrazol-1-yl)methane, are described. These two compounds were generated by the carbonylation of the corresponding copper(I)-acetonitrile complexes, [Cu(H2CPz2')(MeCN)](ClO4) (1) and [{Cu(H2CPz2')(MeCN)}2(mu-pyrazine)](ClO4)2 (2). Alternatively, treatment of mononuclear 1 and 3, respectively, with pyrazine in a molar ratio of 2:1 produces the pyrazine-bridged dinuclear Cu(I) complexes 2 and 4. Each of the complexes 1-4 can react with PPh3 to generate a common three-coordinated copper(I) complex [Cu(PPh3)(H2CPz2')](ClO4) (5). The structures of complexes 1-5 were all confirmed by X-ray crystallography. Comparison of the Cu(I)-C(CO) bond distances and the CO stretching frequencies of 3 and 4 indicates the back-donating properties of d pi(Cu)-pi*(pyrazine) bonds in 4, and accordingly, stabilizes the mixed-valence species generated from 2. Complex 3, stabilized by the strong interaction between copper(I) ion and perchlorate counteranion (Cu(I)-O(ClO4) = 2.240(3) A), is a potential precursor for polynuclear copper(I) carbonyl complexes. 相似文献
5.
Three novel compounds [Cu2(μ1,1-N3)2(N3)2(bdmpzm)2] (1) [Cd(N3)2(bdmpzm)]n (2) and [Ni(N3)2(bdmpzm)2] (3) have been synthesised and characterised structurally and spectroscopically. The structure 1 consists of a neutral dinuclear [Cu2(μ1,1-N3)2(N3)2(bdmpzm)2] entities, compound 2 has one-dimensional zigzag chain structure extending along the crystallographic direction [1 0 0] with alternating di-μ1,1-N3 and di-μ1,3-N3 bridges, and 3 is a mononuclear complex. The experimental studies on the nickel(II) complex have been accompanied computationally by the density functional theory (DFT) calculations. 相似文献
6.
Sodio C.N. Hsu Howard H.Z. Chen I-Jung Lin Jung-Jung Liu Po-Yu Chen 《Journal of organometallic chemistry》2007,692(17):3676-3684
The reaction of [Cu(NCMe)4](BF4) with equimolar amounts of the tris(substituted-pyrazolyl)methane ligand HCPz3 or HC(3,5-Me2Pz)3 yields the respective salts [Cu(HCPz3)(NCMe)](BF4) (1a) or [Cu(HC(3,5-Me2Pz)3)(NCMe)](BF4) (1). The acetonitrile ligand of 1 can be replaced by prazine, 4,4′-dipyridine or 1,4-diisocyanobenzene to yield related mononuclear complexes [Cu(HC(3,5-Me2Pz)3)(pyrazine)](BF4) (2), [Cu(HC(3,5-Me2Pz)3)(4,4′-bipyridine)] (BF4) (3) or [Cu(HC(3,5-Me2Pz)3)(1,4- CNC6H4NC)](BF4) (7), respectively. A series of binuclear copper(I) complexes {[Cu(HC(3,5-Me2Pz)3)]2(μ -BL)}(BF4)2 (4, BL = pyrazine; 5, BL = 4,4′-dipyridine; 8, BL = 1,4-diisocyanobenzene) were prepared by treating equal molar ratio of 1 with related mononuclear complexes 2, 3 and 7. In addition, binuclear copper(I) complexes were also prepared from treatment of 2 equiv of 1 with the related bridge ligand. Both of 4 and 5 reformed mononuclear starting complex 1 in acetonitrile solution. However, the more robust complex 8 was stable in acetonitrile solutions. The structure of complexes 1a, 4, 5, and 7 were confirmed by X-ray crystallography. The redox properties of 4 and 8 were examined by cyclic voltammetry and exhibited two quasi-reversible waves suggesting that no significant structural reorganization occurs during the redox process on the electrochemical time scale. 相似文献
7.
为研究吡唑硼类配体的配位行为, 合成了三(3,5-二甲基吡唑氢合硼酸钾[KHB(C~5H~7N~2)~3], 简称(KL)和双[三(3,5-二甲基吡唑)氢合硼酸根]合铜(II){Cu[HB(C~5H~7N~2)~3]~2}, 简称(CuL~2), 并测定了它们的晶体结构。化合物KL属空间群P2~1/n。a=1.0527(8), b=0.9464(3), c=1.7730(9)nm, β=94.51(5)°,Z=4, D~c=1.268g.cm~-~3, R=0.079。化合物CuL~2属空间群PI, a=0.8768(1),b=1.0170(2), c=1.0859(1)nm, α=62.45(1),β=83.78(1), γ=78.52(1)°, Z=2,D~c=1.298 g.cm~-~3, R=0.062。晶体结构测定结果表明: 化合物KL由钾离子和配体负离子组成, K~+与配体L中的B原子相距0.3634nm, 在配体负离子中B原子与三个吡唑环的N原子及H原子形成四面体构型。化合物CuL~2由孤立分子组成, 铜离子处于分子的对称中心且与两个配体分子中的六个N原子形成六配位的八面体构型, 并表现出明显的Jahn-Teller效应。 相似文献
8.
Transition Metal Chemistry - Two complexes based on isophthalic acid ligand were successfully synthesized and structurally characterized. Compound 1 exhibits a three-dimensional... 相似文献
9.
合成了3-硝基胍-6-(3,5-二甲基吡唑)-1,2,4,5-四嗪(NDT),在二甲基甲酰胺(DMF)中培养出NDT的单晶(NDT·DMF),该晶体属于三斜晶系,P-1空间群,晶胞参数为a=0.7070(4) nm,b=0.8468(6) nm,c=1.4123(9) nm,α=73.281(8)°,β=80.423(11)°,γ=81.740(9)°,Z=2。 利用DSC和TG-DTG研究了NDT的热分解行为,其放热过程的表观活化能和指前因子分别为288.245 kJ/mol和1029.04 s-1。 对NDT的热安全性进行了研究,获得NDT的自加速分解温度TSADT为212.19 ℃,热点火温度Tbe为213.52 ℃,热爆炸临界温度Tbp为214.95 ℃,绝热至爆时间范围在5.43~6.26 s。 相似文献
10.
以水合肼和硝酸胍为原料,经过环合、氧化和肼化,得到3-(3,5-二甲基-1H-吡唑-1-基)-6-肼基-1,2,4,5-四嗪(4),以此为原料和不同芳香醛发生腙化反应,得到系列1-芳基亚甲基-2-(6-(3,5-二甲基-1H-吡唑-1-基)-1,2,4,5-四嗪-3-基)肼(5),产物经元素分析、1H NMR、IR和MS表征。所合成的系列化合物抗菌活性测试表明,它们对大肠杆菌、金黄色葡萄球菌、枯草杆菌等3种细菌表现出一定程度的抑制活性。 相似文献
11.
12.
L. G. Lavrenova A. D. Strekalova A. I. Smolentsev D. Yu. Naumov A. S. Bogomyakov L. A. Sheludyakova S. F. Vasilevskii 《Russian Journal of Coordination Chemistry》2016,42(11):711-718
Coordination compounds of iron(II) thiocyanate with tris(3,5-dimethylpyrazol-1-yl)methane (HC(3,5-Me2Pz)3), [Fe(HC(3,5-Me2Pz)3)2](NCS)2] (I) and [Fe(HC(3,5-Me2Pz)3)(Рhz)(NCS)2] · H2O (II), where Рhz is phthalazine, are synthesized. The complexes are studied by X-ray diffraction analysis, diffuse reflectance and IR spectroscopy, and static magnetic susceptibility measurements. The single crystals are obtained, and the molecular and crystal structures of complex II and compounds [Fe(HC(3,5-Me2Pz)3)(3,5-Me2Pz)(NCS)2] · С2H5OH (III), where 3,5-Me2Pz is 3,5-dimethylpyrazole, and [Fe(HC(3,5-Me2Pz)3)2][Fe(HC(3,5-Me2Pz)3)(NCS)3]2 (IV) are determined (CIF files CCDC 1415452 (II), 1415453 (III), and 1415454 (IV)). The study of the temperature dependence μeff(Т) in a range of 2–300 K shows exchange interactions of the antiferromagnetic character between the iron(II) ions in complexes I and II. 相似文献
13.
Yuste C Armentano D Marino N Cañadillas-Delgado L Delgado FS Ruiz-Pérez C Rillema DP Lloret F Julve M 《Dalton transactions (Cambridge, England : 2003)》2008,(12):1583-1596
The preparation, crystal structures and magnetic properties of the copper(II) complexes of formula [Cu(pyim)(tcm)(2)](n) (1), [Cu(bpy)(tcm)(2)](n) (2), [Cu(4)(bpz)(4)(tcm)(8)] (3), {[Cu(terpy)(tcm)].tcm}(n) (4) and {[Cu(2)(tppz)(tcm)(4)].3/2H(2)O}(n) (5) [pyim = 2-(2-pyridyl)imidazole, tcm = tricyanomethanide, bpy = 2,2'-bipyridine, bpz = 2,2'-bipyrazine, terpy = 2,2':6',2'-terpyridine and tppz = 2,3,5,6-tetrakis(2-pyridyl)pyrazine] are reported. Complexes, 1, 2 and 4 are uniform copper(II) chains with single- (1 and 4) and double-(2) micro-1,5-tcm bridges with values of the intrachain copper-copper separation of 7.489(1) (1), 7.520(1) and 7.758(1) (2) and 7.469(1) A (4). Each copper atom in 1, 2 and 4 is five-coordinate with bidentate pyim (1)/bpy (2) and tridentate terpy (4) ligands and nitrile-nitrogen atoms from bridging (1,2 and 4) and terminal (1) tcm groups building a distorted square pyramidal surrounding. The structure of 3 is made up of neutral centrosymmetric rectangles of (2,2'-bipyrazine)copper(II) units at the corners, the edges being built by single- and double-micro-1,5-tcm bridges with copper-copper separations of 7.969(1) and 7.270(1) A, respectively. Five- and six-coordinated copper atoms with distorted square pyramidal and elongated octahedral environments occur in . Compound 5 is a neutral copper(II) chain with regular alternating bis-tridentate tppz and double micro-1,5-tcm bridges, the intrachain copper-copper distances being 6.549(7) and 7.668(1) A, respectively. The two crystallographically independent copper atoms in 5 have an elongated octahedral geometry with three tppz nitrogen atoms and a nitrile-nitrogen atom from a bridging tcm group in the equatorial positions, and two nitrile nitrogen atoms from a terminal and a bridging tcm ligand occupying the axial sites. The investigation of the magnetic properies of 1-5 in the temperature range 1.9-295 K has shown the occurrence of weak ferro- [J = +0.11(1) cm(-1) (2)] and antiferromagnetic interactions [J = -0.093(1) (1), -0.083(1) (4), -0.04(1) and 1.21(1) cm(-1) (3)] across the micro-1,5-tcm bridges and intermediate antiferromagnetic coupling [-J = 37.4(1) cm(-1) (5)] through bis-tridentate tppz. The values of the magnetic interactions are analyzed through simple orbital symmetry considerations and compared with those previously reported for related systems. 相似文献
14.
Transition Metal Chemistry - The crystal structures and magnetic properties of three coordination compounds constructed from various nitroxide radicals L and MII(hfac)2(H2O)2 building blocks... 相似文献
15.
We have designed and synthesized a new Cu2Gd heterotrinuclear complex, [LCu2Gd(OAc)3] (1), where H4L is a bis(salen)-type tetraoxime ligand useful in the synthesis of discrete (3d)2(4f) complexes. Complex 1 crystallizes in the triclinic system, space group P1, with unit cell parameters a = 12.442(4) A, b = 13.397(3) A, c = 13.966(4) A, alpha = 77.052(8) degrees, beta = 88.656(10) degrees, gamma = 77.761(8) degrees, and Z = 2. In the crystal structure of 1, Cu-Gd distances are 3.3-3.5 A, whereas the two Cu atoms are separated by 6.08 A. The corresponding dinuclear CuGd complexes, 2 and 3, with mono(salen)-type chelate 3-MeOsalamo were also synthesized. Complex 2 crystallizes in the monoclinic system, space group P2(1)/c, with unit cell parameters a = 13.869(8) A, b = 13.688(7) A, c = 18.728(10) A, beta = 92.861(8) degrees, and Z = 4, and complex 3 crystallizes in the triclinic system, space group P1, with unit cell parameters a = 12.319(4) A, b = 13.989(4) A, c = 16.774(5) A, alpha = 64.699(14) degrees, beta = 66.672(13) degrees, gamma = 76.891(17) degrees, and Z = 4. Interaction between Cu(II) and Gd(III) in the dinuclear complexes 2 and 3 is ferromagnetic (J = 4.5 and 7.6 cm(-1), respectively, using spin Hamiltonian H = -JS(Cu) x S(Gd)) as observed in the previously prepared [LCuGdX3] complexes, where L is a salen-type chelate. Magnetic data for the Cu2Gd trinuclear complex can be reasonably interpreted with the use of a spin Hamiltonian H = -J(CuGd)S(Cu1) x S(Gd) - J(CuGd)S(Cu2) x S(Gd) - J(CuCu)S(Cu1) x S(Cu2) with J(CuGd) = 5.0 cm(-1) and J(CuCu) = 0 cm(-1). The S = 9/2 ground state resulted from the ferromagnetic interaction among the Cu(II)-Gd(III)-Cu(II) triad was also supported by the saturation magnetization at 1.8 K. 相似文献
16.
Cherdantseva E. V. Nesterova A. V. Matern A. I. Buldakova L. Yu. Yanchenko M. Yu. Ishmetova R. I. Rusinov G. L. 《Russian Journal of General Chemistry》2010,80(9):1860-1863
Complex formation in the systems containing copper(II), cobalt(II) and nickel(II) ions (M) and 3-(3,5-dimethylpyrazol-1-yl)-6-R-1,2,4,5-tetrazines
(R = 2-hydroxyethylamino, piperidino) (L) was studied by voltammetry and spectrophotometry. Cu(II), Co(II) and Ni(II) were
found to form complex compounds with derivatives of 1,2,4,5-tetrazine with the ratio of the components M:L = 1:1. The complex
stability constants were determined. 相似文献
17.
18.
Tang Liang-Fu Wang Zhi-Hong Xu Yu-Ming Wang Ji-Tao Wang Hong-Gen Yao Xin-Kan 《Transition Metal Chemistry》1999,24(6):708-711
Bis(3,5-dimethylpyrazol-1-yl)ethane tetracarbonylmolybdenum (1a) and tungsten (1b) have been synthesized by the direct reaction of bis(3,5-dimethylpyrazolyl)ethane (bmpze) with M(CO)6 (M = Mo or W). The molecular structure (1b), determined by x-ray crystallography, showed the seven-membered ring W–N–N–C–C–N–N to be in the boat conformation. Upon treatment with RSnCl3 (R=Ph or Cl) in CH2Cl2 at room temperature, complexes (1a) and (1b) gave the seven-coordinate oxidative-addition products [(bmpze)M(CO)3(SnCl2R)Cl] [M = Mo, R = Ph, (2a); M = W, R=Ph, (2b); M = Mo, R = Cl, (2c); M = W, R = Cl, (2d)]. When complexes (1b) and (2b) were heated under reflux with 1,2-bis(diphenylphosphino)ethane (dppe), the ligand, bmpze, in these complexes was easily removed. The novel compounds were characterized by 1H-n.m.r., i.r. and elemental analysis. 相似文献
19.
《Journal of Coordination Chemistry》2012,65(24):4259-4270
One nonlinear and one linear trinuclear copper(II) complex [Cu3(dien)2(pdc)2CH3OH]2?·?6CH3OH (1) and [Cu3(pdc)2(CH3OH)6(H2O)4] (2) were prepared and characterized structurally, where dien is diethylenetriamine and pdc3? the trianion of 3,5-pyrazoledicarboxylic acid. Both complexes consist of 3,5-pyrazoledicarboxylato-bridged trinuclear copper(II) centers. In 1, copper(II) ions are five-coordinate in distorted square pyramids with bond angles 164.78° for Cu(1)–Cu(2)–Cu(3) and 164.51° for Cu(4)–Cu(5)–Cu(6). In 2, the three copper(II) ions are six-coordinate with elongated octahedral geometry. The trinuclear units of 1 and 2 interact through hydrogen bonds to form 3-D and 2-D supramolecular networks, respectively. Variable temperature magnetic susceptibility measurements show that 1 and 2 are antiferromagnetically coupled with J values of ?11.2 and ?13.3?cm?1. 相似文献
20.
Three dinuclear copper(II) complexes, [Cu2(L1)2(μ-ox)](ClO4)2?2(CH3CN), [Cu2(L2)2(μ-ox)](ClO4)2?H2O, and [Cu2(L3)2(μ-ox)](ClO4)2 where ox = oxalato; L = N,N-dimethyl,N′-benzylethane-1,2-diamine, L1, N,N-diethyl,N′-benzylethane-1,2-diamine, L2, N,N-diisoprophyl,N′-benzylethane-1,2-diamine, L3, were prepared and characterized by elemental analyses, spectral (IR, UV–Vis) data and molar conductance measurements. The crystal structures of [Cu2(L1)2(μ-ox)](ClO4)2?2(CH3CN) and [Cu2(L3)2(μ-ox)](ClO4)2 have been determined by single-crystal X-ray analysis. Solvatochromic behaviors were investigated in various solvents, showing positive solvatochromism. The effect of steric hindrance around the copper ion imposed by N-alkyl groups of the diamine chelates on the solvatochromism property of the complexes is discussed. Solvatochromism was also studied with different solvent parameter models using stepwise multiple linear regression method. 相似文献