Synthesis and Structure of N,N,N?,N?‐Tetraisobutyl‐N′,N″‐isophthaloylbis(thiourea) and Dimethanol‐bis(N,N,N?,N?‐tetraisobutyl‐N′,N″‐isophthaloylbis(thioureato))dicobalt(II) The synthesis and the crystal structure of the ligand N,N,N?,N?‐tetraisobutyl‐N′,N″‐isophthaloylbis(thiourea) and its CoII‐complex are reported. The ligand co‐ordinates quadridentately forming a di‐bischelate. The donor atoms O and S are arranged in cis‐position around the central CoII ions. In addition the co‐ordination geometry is determined by methanol molecules resulting in the co‐ordination number five. The complex crystallizes in the space group P1 (Z = 1) with two additional methanol molecules per formula unit. The free ligand crystallizes in the space group P1 (Z = 2) with one methanol molecule per formula unit. It shows the typical keto form of N‐acylthioureas with a protonated central N atom. The structures of both acylthiourea fragments come close to E,Z′‐configurations. 相似文献
1‐tert‐Butyl‐1H‐1,2,4‐triazole (tbtr) was found to react with copper(II) chloride or bromide to give the complexes [Cu(tbtr)2X2]n and [Cu(tbtr)4X2] (X = Cl, Br). 1‐tert‐Butyl‐1H‐tetrazole (tbtt) reacts with copper(II) bromide resulting in the formation of the complex [Cu3(tbtt)6Br6]. The obtained crystalline complexes as well as free ligand tbtr were characterized by elemental analysis, IR spectroscopy, thermal and X‐ray analyses. For free ligand tbtr, 1H NMR and 13C NMR spectra were also recorded. In all the complexes, tbtr and tbtt act as monodentate ligands coordinated by CuII cations via the heteroring N4 atoms. The triazole complexes [Cu(tbtr)2Cl2]n and [Cu(tbtr)2Br2]n are isotypic, being 1D coordination polymers, formed at the expense of single halide bridges between neighboring copper(II) cations. The isotypic complexes [Cu(tbtr)4Cl2] and [Cu(tbtr)4Br2] reveal mononuclear centrosymmetric structure, with octahedral coordination of CuII cations. The tetrazole compound [Cu3(tbtt)6Br6] is a linear trinuclear complex, in which neighboring copper(II) cations are linked by single bromide bridges. 相似文献
Four new bridged silver(I) complexes, namely [Ag2(μ2‐teda)(μ2‐fbc)2] ( 1 ), [Ag2(μ2‐1,6‐dah)2](bpdc) · 4H2O ( 2 ), [Ag2(μ2‐2‐ap)(2‐ap)(bnb)] · 0.34H2O ( 3 ), [Ag2(μ2‐pyc)2(2‐apy)2] · 0.5H2O ( 4 ), have been synthesized and characterized by elemental analysis and crystallographic methods [fbc = 4‐fluorobenzoate, teda = triethylenediamine ( 1 ); bpdc = biphenyl‐4,4′‐dicarboxylate, 1,6‐dah = 1,6‐diaminohexane ( 2 ); bnb = 3,5‐binitrobenzoate, 2‐ap = 2‐aminopyrimidine ( 3 ); pyc = 3‐pyridinecarboxylate acid, 2‐apy = 2‐aminopyridine ( 4 )]. Complex 1 contains a 1D linear chain paralleling to the c‐axis, whereas in complex 2 silver(I) atoms were bridged by the 1,6‐dah ligand into a zigzag chain, further giving a 1D ribbon by weak Ag ··· Ag interactions. Complex 3 consists of a dinuclear silver(I) [Ag2(μ2‐2‐ap)(2‐ap)(bnb)] moiety and a lattice water molecule, forming a 3D network via a number of hydrogen‐bonding interactions such as N–H ··· O, N–H ··· N and C–H ··· O hydrogen bond and other weak interactions such Ag ··· Ag, Ag ··· N, N ··· O as well as O ··· O interaction. Similar to 3 , the asymmetric unit of 4 consists of one dinuclear silver(I) [Ag2(μ2‐pyc)2(2‐apy)2] moiety and half lattice water molecule, further generating a tetranuclear silver(I) {[Ag2(μ2‐pyc)2(2‐apy)2]2 · H2O} moiety. These moieties construct a 3D supramolecular network structure of 4 through N–H ··· O, O–H ··· O and C–H ··· O hydrogen bonds as well as other weak interactions such as Ag ··· O and N ··· O interactions. 相似文献
The reaction of 2,2′‐Bis(2N‐(1,1′,3,3′‐tetramethyl‐guanidino))diphenylene‐amine (TMG2PA) ( 1 ) with CuI in MeCN results in the formation of [CuII(TMG2PAamid)I] ( 2 ) indicatingthat CuI is the target of an oxidative attack of the N‐H proton of the ligand which itself is converted to molecular hydrogen. In contrast, if [Cu(MeCN)4][PF6] is used as the CuI source, [CuI2(TMGbenz)2][PF6]2 ( 3 ) is obtained instead. The use of the non‐coordinating counterion [PF6]– apparently prevents CuI from oxidation but induces itself a cyclisation reaction within the ligand which results in the formation of a benzimidazole‐guanidine ligand. 相似文献
The synthesis of two new diphosphonic acid ligands,[ethane‐1, 2‐diylbis(azanediyl)]bis[(4‐chlorophenyl)methylene]diphosphonic acid (L1P), [ethane‐1, 2‐diylbis(azanediyl)]bis[(4‐bromophenyl)methylene]diphosphonic acid (L2P), and their corresponding copper complexes, Cu2(L1P)2 ( 1 ) and Cu2(L2P)2 ( 2 ) are described herein. Complex 2 was structurally characterized with X‐ray single crystal diffraction. The structure of 2 consists of five‐coordinatecopper(II) ions with a distorted square pyramidal arrangement doubly bridged by OPO from phosphonate groups. The Cu–Cu distance is 4.7810(2) Å. The crystal packing is determined by interdinuclear hydrogen bonds, which lead to one‐dimensional chains. The results of thermogravimetric investigations (TG‐DTA), UV/Vis diffuse reflectance, infrared and (1H and 13C) NMR spectroscopy, as well as elemental analyses of compounds 1 and 2 are also presented. 相似文献
The series of binuclear Cu(II) and Ni(II) complexes with an asymmetrical exchange fragment based on 2,6‐diformyl‐4‐methylphenol bishydrazone has been synthesized for the first time. The compositions and structures of both ligands and its complexes have been established with the data of IR, 1H NMR, and extended X‐ray absorption fine structure (EXAFS) spectroscopical studies as well as magnetic measurements. The structure of [Ni2L3(μ‐Pz)] · 2CH3OH (L = triply deprotonated form of bishydrazone, Pz = pyrazol) was confirmed by X‐ray crystallographic analysis. In this complex, the coordination environment of two nickel ions is quite different, one nickel atom is square‐planar and the other is distorted octahedral coordinated. The values of exchange parameter calculated in terms of HDVV theory have been compared with the features of an asymmetrical exchange fragment's electronic and geometrical structure. 相似文献
A novel chiral compound (C3N2H4)3CuSO4 ( 1 ) was synthesized at room temperature by using achiral organic amine imidazole as the structure‐directing agent, crystallizing in the chiral space group P212121. Single‐crystal structural analysis reveals that compound 1 consists of alternating CuO2N3 and SO4 units exhibiting a neutral one‐dimensional helical chain. 相似文献
Reaction of the carbene precursor 9,10‐bis(N‐ethylimidazoliummethyl)anthracene hexafluorophosphate ( 1 ) and Ag2O yielded the dinuclear metallocyclophane ( 2 ) in high yield. The structures of 1 and 2 were determined by X‐ray crystallography. 相似文献
Reaction of O,O′‐diisopropylthiophosphoric acid isothiocyanate (iPrO)2P(S)NCS with 1,10‐diaza‐18‐crown‐6, 1,7‐diaza‐18‐crown‐6, or 1,7‐diaza‐15‐crown‐5 leads to the N‐thiophosphorylated bis‐thioureas N,N′‐bis[C(S)NHP(S)(OiPr)2]‐1,10‐diaza‐18‐crown‐6 ( H2LI ), N,N′‐bis[C(S)NHP(S)(OiPr)2]‐1,7‐diaza‐18‐crown‐6 ( H2LII ) and N,N′‐bis[C(S)NHP(S)(OiPr)2]‐1,7‐diaza‐15‐crown‐5 ( H2LIII ). Reaction of the potassium salts of H2LI–III with a mixture of CuI and 2,2′‐bipyridine ( bpy ) or 1,10‐phenanthroline ( phen ) in aqueous EtOH/CH2Cl2 leads to the dinuclear complexes [Cu2(bpy)2LI–III] and [Cu2(phen)2LI–III] . The structures of these compounds were investigated by 1H, 31P{1H} NMR spectroscopy, and elemental analysis. The crystal structures of H2LI and [Cu2(phen)2LI] were determined by single‐crystal X‐ray diffraction. Extraction capacities of the obtained compounds in comparison to the related compounds 1,10‐diaza‐18‐crown‐6, N,N′‐bis[C(=CMe2)CH2P(O)(OiPr)2]‐1,10‐diaza‐18‐crown‐6, N,N′‐bis[C(S)NHP(O)(OiPr)2]‐1,10‐diaza‐18‐crown‐6 towards the picrate salts LiPic, NaPic, KPic. and NH4Pic were also studied. 相似文献
A new copper(II) phosphonatobenzenesulfonate incorporating 4,4′‐bipyridine (4,4′‐bipy) as auxiliary ligand has been discovered through systematic high‐throughput (HT) screening of the system Cu(NO3)2·3H2O/H2O3PC6H4SO3H/4,4′‐bipy using different solvents. The hydrothermal synthesis of [Cu(HO3PC6H4SO3)(C10H8N2)]·H2O ( 1 ) was further optimized by screening various copper(II) salts. The crystal structure of 1 was determined by single‐crystal X‐ray diffraction and unveiled the presence of isolated sixfold coordinated Jahn–Teller‐distorted Cu2+ ions. The isolated CuN2O4 octahedra are interconnected by phosphonate and sulfonate groups to form chains along the c‐axis. The organic groups, namely phenyl rings and 4,4′‐bipy molecules cross‐link the chains into a three‐dimensional framework. Water molecules are found in the narrow voids in the structure which are held by weak hydrogen bonds. Upon dehydration, the structure of 1 undergoes a phase transition, which was confirmed by TG measurements and temperature dependent X‐ray powder diffraction. The new structure of 1‐h was refined with Rietveld methods. Detailed inspection of the structure revealed the directional switching of the Jahn–Teller distortion upon de/rehydration. Weak ferro‐/ferrimagnetic interactions were observed by magnetic investigations of 1 , which switch to antiferromagnetic below 3.5 K. Compounds 1 and 1‐h are further characterized by thermogravimetric and elemental analysis as well as IR spectroscopy. 相似文献
Two copper(I) complexes of compositions [Cu(HL)I]2 · EtOH ( 1 ) and [Cu(HL)3]I · MeOH ( 2 ) were synthesized via the reactions of HL [HL = 2(4,5‐diphenyl‐1H‐imidazol‐2‐yl)pyridine] and CuI in EtOH and MeOH, respectively, under solvothermal conditions. The complexes were characterized by X‐ray single crystal diffraction, IR spectroscopy, and elemental analysis. Compounds 1 and 2 are catalytically active towards ketalization reaction, giving various ketals under mild conditions. 相似文献
Mono‐ and multinuclear complexes of ruthenium and [n]cycloparaphenylene (CPP, n=5 and 6) were synthesized in excellent yields through ligand exchange of the cationic complex [(Cp)Ru(CH3CN)3](PF6) with CPP. In the multinuclear complexes, ruthenium selectively coordinated to alternate paraphenylene units to give bis‐ and tris‐coordinated Ru complexes for [5] and [6]CPPs, respectively. Single‐crystal X‐ray analysis revealed the Ru was coordinated with η6‐hapticity on the convex surface of CPP. 相似文献
Pure anhydrous Cu(CH3COO)2 was obtained both, by thermal dehydration of Cu(CH3COO)2 · H2O and by drying a commercially purchased mixture of Cu(CH3COO)2 · H2O and Cu(CH3COO)2 in a nitrogen atmosphere using P2O5 as drying agent. The crystal structure was solved ab initio from synchrotron X‐ray powder diffraction (XRPD) data at 150 °C and from laboratory XRPD data at ambient conditions and found to be isotypic to anhydrous chromium(II), molybdenum(II) and rhodium(II) acetate. Cu(CH3COO)2 crystallizes in space group P1 (no. 2) with lattice parameters of a = 5.1486(3) Å, b = 7.5856(6) Å, c = 8.2832(6) Å, α = 77.984(4)°, β = 75.911(8)°, γ = 84.256(6)° at ambient conditions. Cu2(CH3COO)4 paddle wheels with short (2.6 Å) Cu–Cu distances form chains in a direction, which is the main motif in the crystal structure. Due to their identical structural main motif Cu(CH3COO)2 · H2O and Cu(CH3COO)2 exhibit a similar bluish‐green color, almost identical UV/Vis spectra and comparable magnetic properties. The temperature dependent magnetic susceptibility also indicates only weak inter‐dimer spin exchange between neighbouring Cu2(CH3COO)4 paddle wheels. 相似文献
Y not? A unique, three‐coordinate Y‐shaped bis(silyl)platinum(II) complex was isolated and characterized (see structure; C light gray, N blue, Si pink, Pt dark gray). DFT studies on a model system shed light on the nature of this unusual coordination mode for platinum(II).
Reactions of [Cu(NCMe)4]+ with stoichiometric amount of diphosphine R2P–(C6H4)n–PR2, (R = NC4H4, n = 1; R = Ph, n = 1, 2, 3) or tri‐phosphine 1, 3, 5‐(PPh2–C6H4–)3–C6H3 ligands give the corresponding di‐ or trinuclear copper(I) acetonitrile‐phosphine complexes 1 – 5 . Substitution of the labile acetonitrile groups with chelating aromatic diimines – 2, 2′‐bipyridine (bpy), 1, 10‐phenanthroline (phen), 5, 6‐dimethyl‐1, 10‐phenanthroline (dmp), 5, 6‐dibromo‐1, 10‐phenanthroline (phenBr2) – gives the corresponding substituted compounds 6 – 16 . In all complexes 1 – 16 each central CuI atom has tetrahedral configuration completed with two N‐ and two P‐donor groups. The compounds obtained were characterized using elemental analysis, ESI‐MS, X‐ray crystallography, and NMR spectroscopy. All phosphine‐diimine compounds 6 – 16 are photoluminescent at room temperature both in dichloromethane solution and in solid state (λex = 385 nm). In CH2Cl2 solution the maxima of emission bands are found in a range 540–640 nm, and in solid in a similar range 538–620 nm. Emission of 6 – 16 is assigned to the triplet excited state dominated by the charge transfer transitions with contribution of the MLCT character. 相似文献
Two new oxamido‐bridged N4 macrocyclic complexes [(CuL)2Mn(C2H5OH)2](ClO4)2 · 2C2H5OH ( 1 ) and [(CuL)2Co‐(C2H5OH)2](ClO4)2 · 2C2H5OH ( 2 ) (H2L = 2,3‐dioxo‐5,6:14,15‐di‐benzo‐7,13‐diphenyl‐1,4,8,12‐tetraazacyclo‐pentadeca‐7,13‐diene) have been synthesized and structurally characterized by X‐ray crystallographic investigations. In the two complexes, all copper(II) ions adopt a slightly distorted square‐planar configuration and the central manganese(II) and cobalt(II) ions are set in a distorted octahedral coordination sphere, connected to the other CuL fragments through exo‐cis oxamido bridges. The analyses of the magnetic properties were carried out by means of the theoretical expression of the magnetic susceptibility deduced from the spin Hamiltonian ? = –2J?1?2, leading to J = –14.58 cm–1 for complex 1 and J = –26.95 cm–1 for complex 2 , respectively. 相似文献
The copper sulfide mineral flotation collector, N‐n‐butyl‐N′‐ethoxycarbonyl‐thiourea (H2bectu), and the 1:1 hexameric copper(I) thioureate complex, [Cu(Hbectu)]6, have been characterized by single crystal X‐ray diffraction. H2bectu crystallizes in the triclinic space group with a = 5.2754(4), b = 9.0042(7), c = 12.6030(9) Å, α = 80.528(6), β = 90.173(6), γ = 76.472(7)°. An intramolecular N‐H···O hydrogen bond between the thioamide proton and carbonyl oxygen forms a planar six‐membered ring in the central core of the molecule with C=O, C=S and C‐N bond lengths in accord with those reported for other N‐alkyl/aryl‐N′‐acyl‐thiourea compounds. [Cu(Hbectu)]6 crystallizes in the monoclinic space group C2/c with a = 23.269(5), b = 13.243(4), c = 23.037(7) Å, β = 91.81(2)° as discrete hexameric clusters disposed about a crystallographic centre of symmetry with a Cu6S6 core consisting of two Cu3S3 chair‐shaped rings linked by coordination of the deprotonated amide nitrogen atom to a copper atom in the adjacent ring. The six ligands assemble as a paddlewheel structure with the ethoxy and n‐butyl substituents packing in an alternating head to tail arrangement. Temperature dependent solution 1H NMR spectroscopic studies show that the hexameric structure of the complex is maintained in solution. 相似文献
Synthesis and characterization of seven new complexes [Cu(2‐MeSnic)2(CH3OH)]2 (where 2‐MeSnic is 2‐methylthionicotinate), [Cu(2‐MeSnic)2L2]2 (where L is pyridine — py, ethylnicotinate — Etnic and butylnicotinate — Bunic), [Cu(2‐MeSnic)2L2(H2O)2] (where L is py and nicotinamide — nia) and [Cu(2‐MeSnic)2(N‐Menia)2(H2O)2]·2H2O (where N‐Menia is N‐methylnicotinamide) are reported. The characterization were based on elemental analysis, infrared, electronic and EPR spectra, and magnetic susceptibility measurements over a temperature range of 1.8 — 300 K or 70 — 300 K. Three complexes of different type were studied by X‐ray analysis. The molecule of [Cu(2‐MeSnic)2(CH3OH)]2 has dimeric paddle‐wheel cage structure with a tetragonal pyramidal arrangement around CuII. The dimer results from the fact that carboxyl groups of four 2‐MeSnic anions function as bridging in a syn‐syn arrangement. On the other hand [Cu(2‐MeSnic)2(py)2]2 forms dimers with hexacoordinated CuII atoms in highly distorted coordination octahedra, each with two oxygen atoms of bridging carboxyl groups in an anti‐anti arrangement of two 2‐MeSnic anions, with two oxygen atoms of one asymmetrically chelating 2‐MeSnic anion and with two nitrogen atoms of two pyridine ligands. The temperature independent EPR spectrum for this complex exhibits an axial signal which corresponds to almost isolated S = 1/2 magnetic ions. Magnetic data for the dimer show a weak antiferromagnetic interaction between the two metal ions with J = —0.65 cm—1. The CuII atom in complex [Cu(2‐MeSnic)2(py)2(H2O)2] is hexacoordinated in an elongated centrosymmetrical tetragonal‐bipyramidal arrangement (4 + 2). Based on the molecular structure the electronic, infrared, electron paramagnetic resonance spectra and magnetic properties are discussed and stereochemistry as well as the mode of ligand coordination in new solid complexes under study have been determined. 相似文献