共查询到20条相似文献,搜索用时 250 毫秒
1.
Ranjan Patra Israel Goldberg 《Acta Crystallographica. Section C, Structural Chemistry》2013,69(8):819-821
The synthesis is reported of the tricarboxylic acid 3‐(3,5‐dicarboxybenzyloxy)benzoic acid (H3L) and the product of its reaction under solvothermal conditions with ZnII cations, namely poly[[μ6‐3‐(3,5‐dicarboxylatobenzyloxy)benzoato](dimethylformamide)‐μ3‐hydroxido‐dizinc(II)], [Zn2(C16H9O7)(OH)(C3H7NO)]n, the formation of which is associated with complete deprotonation of H3L. Its crystal structure consists of a single‐framework coordination polymer of the organic L3− ligand with ZnII cations in a 1:2 ratio, with additional hydroxide and dimethylformamide (DMF) ligands coordinated to the ZnII centres. The ZnII cations are characterized by coordination numbers of 5 and 6, being bridged to each other by hydroxide ligands. In the polymeric framework, the carboxylate‐ and hydroxy‐bridged ZnII cations are arranged in coordination‐tessellated columns, which propagate along the a axis of the crystal structure, and each L3− ligand links to seven different ZnII centres via Zn—O bonds of two different columns. The coordination framework, composed of [Zn2(L)(OH)(DMF)]n units, forms an open architecture, the channel voids within it being filled by the zinc‐coordinating DMF ligands. This report provides the first structural evidence for the formation of coordination polymers with H3L via multiple metal–ligand bonds through its carboxylate groups.<!?tpb=21.5pt> 相似文献
2.
Levon A. Tavadyan Seyran H. Minasyan Makich V. Musaelyan Lusik H. Harutyunyan Hakob G. Tonikyan John R. J. Sorenson 《国际化学动力学杂志》2010,42(1):56-67
Absolute rate constants (keff) for the chemical reactions of Cu(II)2(3,5‐di‐iso‐propylsalicylate)4(H2O)3, Cu(II)2(3,5‐di‐tert‐butylsalicylate)4, Cu(II)2(3,5‐di‐tert‐butylsalicylate)4(H2O)4, Cu(II)2(3,5‐dimethylsalicylate)4(H2O)3, Cu(II)2(3‐ethylsalicylate)4(H2O), Cu(II)2(3‐phenylsalicylate)4, and Cu(II)(3,5‐di‐iso‐propylsalicylate)2(pyridine)2 with tert‐butylperoxyl radical were determined using kinetic electron paramagnetic resonance measurements in 10% toluene in the hexane medium at temperatures ranging from ?63°C to 2°C. These antioxidant (AO) chelates were ranked by their reactivity as follows: 2,6‐di‐tert‐butyl‐4‐methylphenol ? Cu(II)2(3,5‐di‐tert‐butylsalicylate)4 ? Cu(II)2(3‐phenylsalicylate)4 > Cu(II)2(3,5‐di‐iso‐propylsalicylate)4(H2O)3 ? Cu(II)2(3,5‐di‐tert‐butylsalicylate)4(H2O)4 ? Cu(II)2(3,5‐dimethylsalicylate)4(H2O)3 > Cu(II)2(3‐ethylsalicylate)4(H2O) ? Cu(II)(3,5‐di‐iso‐propylsalicylate)2(pyridine)2 at 20°C. Differential pulse voltammetry was used to determine redox behavior of these chelates in CH2Cl2. Two types of salicylic OH groups were detected in these Cu(II) salicylates, characterized by the presence or absence of AO reactivity. One of them was coordinate covalently bonded to Cu(II) via the oxygen atoms of the salicylic OH groups, displaying oxidation peak potentials in the range from +650 to 970 mV versus Ag/Ag+. The second type was intramolecularly hydrogen bonded to carboxylate oxygens, with an oxidation peak potential in the range from +1100 to 1200 mV versus Ag/Ag+. It was concluded that non–hydrogen‐bonded salicylic OH groups are responsible for the antiperoxyl radical reactivity of these chelates, while neither Cu(II) nor salicylate ligands displayed reactivity with peroxyl radical. It has been established in this research that axially bonded electron pair donors such as pyridine and water decrease H‐donating reactivity of Cu(II) salicylates by promoting the formation of intramolecular hydrogen bonding between the salicylic OH hydrogen atoms and carboxylate oxygen atoms in the salicylic ligands. Dependences of log keff at 20°C and the anodic oxidation potential (Epa) for the salicylic OH group on the difference between symmetric and asymmetric stretching frequencies of carboxylate groups (in Fourier transform infrared spectra) for the substituted Cu(II) salicylates were determined. © 2009 Wiley Periodicals, Inc. Int J Chem Kinet 42: 56–67, 2010 相似文献
3.
Zora Popovi Gordana Pavlovi Boris‐Marko Kukovec 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(5):m181-m183
The title compound, [Cu(C9H5N2O3)2(C2H6OS)2], consists of octahedrally coordinated CuII ions, with the 3‐oxo‐3,4‐dihydroquinoxaline‐2‐carboxylate ligands acting in a bidentate manner [Cu—O = 1.9116 (14) Å and Cu—N = 2.1191 (16) Å] and a dimethyl sulfoxide (DMSO) molecule coordinated axially via the O atom [Cu—O = 2.336 (5) and 2.418 (7) Å for the major and minor disorder components, respectively]. The whole DMSO molecule exhibits positional disorder [0.62 (1):0.38 (1)]. The octahedron around the CuII atom, which lies on an inversion centre, is elongated in the axial direction, exhibiting a Jahn–Teller effect. The ligand exhibits tautomerization by H‐atom transfer from the hydroxyl group at position 3 to the N atom at position 4 of the quinoxaline ring of the ligand. The complex molecules are linked through an intermolecular N—H...O hydrogen bond [N...O = 2.838 (2) Å] formed between the quinoxaline NH group and a carboxylate O atom, and by a weak intermolecular C—H...O hydrogen bond [3.392 (11) Å] formed between a carboxylate O atom and a methyl C atom of the DMSO ligand. There is a weak intramolecular C—H...O hydrogen bond [3.065 (3) Å] formed between a benzene CH group and a carboxylate O atom. 相似文献
4.
Trinuclear Cobalt(II) and Zinc(II) Salamo‐type Complexes: Syntheses,Crystal Structures,and Fluorescent Properties 下载免费PDF全文
Wen‐Kui Dong Fan Zhang Na Li Li Xu Yang Zhang Jing Zhang Li‐Chun Zhu 《无机化学与普通化学杂志》2016,642(7):532-538
Two trinuclear CoII and ZnII complexes, [(CoL)2(OAc)2Co] and [(ZnL)2(OAc)2Zn], with an asymmetric Salen‐type bisoxime ligand [H2L = 4‐(N,N‐diethylamine)‐2,2′‐[ethylenediyldioxybis(nitrilomethylidyne)]diphenol] were synthesized and characterized by elemental analyses, IR, UV/Vis, and fluorescent spectroscopy. The crystal structures of the CoII and ZnII complexes were determined by single‐crystal X‐ray diffraction methods. The CoII atom is pentacoodinated by N2O2 donor atoms from the (L)2– unit and one oxygen atom from the coordinated acetate ion, resulting in a trigonal bipyramid arrangement. With the help of intermolecular hydrogen bonding C–H ··· O and C–H ··· π interactions, a self‐assembled continual zigzag chain‐like supramolecular structure is formed. The ZnII atom is pentacoodinated by N2O2 donor atoms from the (L)2– unit and one oxygen atom from the coordinated acetate ion, resulting in an almost regular trigonal bipyramid arrangement. A self‐assembled continual 1D supramolecular chain‐like structure is formed by intermolecular hydrogen bonding C–H ··· O and C–H ··· π interactions. Additionally, the photophysical properties of the CoII and ZnII complexes were discussed. 相似文献
5.
Homo‐ and Heteronuclear Compounds with a Symmetrical Bis‐hydrazone Ligand: Synthesis,Structural Studies,and Luminescent Properties 下载免费PDF全文
Dr. Sabina Rodríguez‐Hermida Dr. Ana B. Lago Prof. Rosa Carballo Dr. Oscar Fabelo Prof. Ezequiel M. Vázquez‐López 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(17):6605-6616
Nine new coordination compounds have been synthesized by the reaction of salts of bivalent metal ions (a=ZnII, b=CuII, c=NiII, d=CoII) with the bis(benzoylhydrazone) derivative of 4,6‐diacetylresorcinol (H4L). Three kinds of complexes have been obtained: homodinuclear compounds [M2(H2L)2]?nH2O ( 1 a , 1 b , 1 c , and 1 d ), homotetranuclear compounds [M4(L)2]?n(solv) ( 2 a and 2 c ), and heterotetranuclear compounds [Zn2M2(L)2]?n(solv) ( 2 ab , 2 ac , and 2 ad ). The structures of the free ligand H4L?2 DMSO and its complexes [Zn2(H2L)2(DMSO)2] ( 1 a* ), [Zn4(L)2(DMSO)6] ( 2 a* ), and [Zn0.45Cu3.55(L)2(DMSO)6]?2 DMSO ( 2 ab* ) were elucidated by single‐crystal X‐ray diffraction. The ligand shows luminescence properties and its fluorimetric behavior towards MII metals (M=Zn, Cu, Ni and Co) has been studied. Furthermore, the solid‐state luminescence properties of the ligand and compounds have been determined at room temperature. 1H NMR spectroscopic monitoring of the reaction of H4L with ZnII showed the deprotonation sequence of the OH/NH groups upon metal coordination. Heteronuclear reactions have also been monitored by using ESI‐MS and spectrofluorimetric techniques. 相似文献
6.
Johannes E. M. N. Klein Robert J. Thatcher Adrian C. Whitwood Richard J. K. Taylor 《Acta Crystallographica. Section C, Structural Chemistry》2011,67(4):m108-m110
The title complex, [Cu4(C2H3O2)6(OH)2(C5H11N)4]·2H2O, possesses an unusual inversion‐symmetric tetranuclear copper framework, with each CuII atom displaying a square‐pyramidal geometry and one additional long Cu...O contact. The four piperidine ligands are terminal, one at each CuII atom, and the two hydroxide ligands are triply bridging. The six acetate ligands exhibit two distinct coordination modes, namely as two monodentate acetates and four bridging acetates that bridge the two inequivalent copper centres. The noncoordinating acetate O atom is involved in intramolecular hydrogen bonding with H atoms from the hydroxide and one piperidine ligand. In addition, extensive intermolecular hydrogen bonding involving the solvent water molecules is observed. 相似文献
7.
Tetrakis(2,2′‐bipyridine‐κ2N,N′)tetrakis(μ‐salicylato‐κ3O,O′:O′′)‐quadro‐tetrazinc(II) decahydrate
Yue Wang Mamiko Odoko Nobuo Okabe 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(10):m479-m481
The title compound, [Zn4(C7H4O3)4(C10H8N2)4]·10H2O, crystallizes as a centrosymmetric tetranuclear cyclic complex containing four ZnII atoms bridged by four carboxylate groups from salicylate ligands, with a syn–anti configuration. Each ZnII atom has a distorted trigonal–bipyramidal coordination geometry, formed by two N atoms of a 2,2′‐bipyridine ligand and three O atoms from two salicylate ligands. The complex is stabilized by intramolecular π–π interactions between pairs of bipyridine rings and a 16‐membered gear‐wheel‐shaped cyclic framework. The hydrogen‐bonding network is formed via the water molecules. 相似文献
8.
Yun‐Liang Jiang Qing‐Yan Liu Yu‐Ling Wang 《Acta Crystallographica. Section C, Structural Chemistry》2011,67(9):m297-m300
The title compound, [Zn2(C9H4O6)2(C6H6N4)2], consists of two ZnII ions, two 5‐carboxybenzene‐1,3‐dicarboxylate (Hbtc2−) dianions and two 2,2′‐bi‐1H‐imidazole (bimz) molecules. The ZnII centre is coordinated by two carboxylate O atoms from two Hbtc2− ligands and by two imidazole N atoms of a bimz ligand, in a distorted tetrahedral coordination geometry. Two neighbouring ZnII ions are bridged by a pair of Hbtc2− ligands, forming a discrete binuclear [Zn2(Hbtc)2(bimz)2] structure lying across an inversion centre. Hydrogen bonds between carboxyl H atoms and carboxylate O atoms and between imidazole H atoms and carboxylate O atoms link the binuclear units. These binuclear units are further extended into a three‐dimensional supramolecular structure through extensive O—H...O and N—H...O hydrogen bonds. Moreover, the three‐dimensional nature of the crystal packing is reinforced by the π–π stacking. The title compound exhibits photoluminescence in the solid state, with an emission maximum at 415 nm. 相似文献
9.
Meng Wen Zu‐Ping Xiao Chun‐Ya Wang Xi‐He Huang 《Acta Crystallographica. Section C, Structural Chemistry》2015,71(2):136-139
The title compound, {[Zn4(C8H4O4)3(OH)2(C12H6N2O2)2]·2H2O}n, has been prepared hydrothermally by the reaction of Zn(NO3)2·6H2O with benzene‐1,4‐dicarboxylic acid (H2bdc) and 1,10‐phenanthroline‐5,6‐dione (pdon) in H2O. In the crystal structure, a tetranuclear Zn4(OH)2 fragment is located on a crystallographic inversion centre which relates two subunits, each containing a [ZnN2O4] octahedron and a [ZnO4] tetrahedron bridged by a μ3‐OH group. The pdon ligand chelates to zinc through its two N atoms to form part of the [ZnN2O4] octahedron. The two crystallographically independent bdc2− ligands are fully deprotonated and adopt μ3‐κO:κO′:κO′′ and μ4‐κO:κO′:κO′′:κO′′′ coordination modes, bridging three or four ZnII cations, respectively, from two Zn4(OH)2 units. The Zn4(OH)2 fragment connects six neighbouring tetranuclear units through four μ3‐bdc2− and two μ4‐bdc2− ligands, forming a three‐dimensional framework with uninodal 6‐connected α‐Po topology, in which the tetranuclear Zn4(OH)2 units are considered as 6‐connected nodes and the bdc2− ligands act as linkers. The uncoordinated water molecules are located on opposite sides of the Zn4(OH)2 unit and are connected to it through hydrogen‐bonding interactions involving hydroxide and carboxylate groups. The structure is further stabilized by extensive π–π interactions between the pdon and μ4‐bdc2− ligands. 相似文献
10.
Xiao‐Hua Chen Qiong‐Jie Wu Zhi‐Yu Liang Chun‐Rong Zhan Jian‐Bin Liu 《Acta Crystallographica. Section C, Structural Chemistry》2009,65(5):m190-m194
In the complex (morpholine)[2‐hydroxy‐N′‐(5‐nitro‐2‐oxidobenzylidene)benzohydrazidato]nickel(II), [Ni(C14H9N3O5)(C4H9NO)], (I), the NiII center is in a square‐planar N2O2 coordination geometry. The complex bis[μ‐2‐hydroxy‐N′‐(2‐oxidobenzylidene)benzohydrazidato]bis[(morpholine)zinc(II)], [Zn2(C14H10N2O3)2(C4H9NO)2], (II), consists of a neutral centrosymmetric dimer with a coplanar Zn2(μ2‐O)2 core. The two ZnII centers are bridged by phenolate O atoms. Each ZnII center exhibits a distorted square‐pyramidal stereochemistry, in which the four in‐plane donors come from the O,N,O′‐tridentate 2‐hydroxy‐N′‐(2‐oxidobenzylidene)benzohydrazidate(2−) ligand and a symmetry‐related phenolate O atom, and the axial position is coordinated to the N atom from the morpholine molecule. There are intramolecular phenol–hydrazide O—H...N hydrogen bonds present in both (I) and (II). In (I), square‐planar nickel complexes are linked by intermolecular morpholine–morpholine N—H...O hydrogen bonds, leading to a one‐dimensional chain, while in (II) an infinite two‐dimensional network is formed via intermolecular hydrogen bonds between the coordinated morpholine NH groups and the uncoordinated phenolate O atoms. 相似文献
11.
Li-Juan Zhou Chang-Bao Han Yu-Ling Wang 《Acta Crystallographica. Section C, Structural Chemistry》2016,72(2):133-138
Coordination polymers constructed from metal ions and organic ligands have attracted considerable attention owing to their diverse structural topologies and potential applications. Ligands containing carboxylate groups are among the most extensively studied because of their versatile coordination modes. Reactions of benzene‐1,4‐dicarboxylic acid (H2BDC) and pyridine (py) with ZnII or CoII yielded two new coordination polymers, namely, poly[(μ4‐benzene‐1,4‐dicarboxylato‐κ4O:O′:O′′:O′′′)(pyridine‐κN)zinc(II)], [Zn(C8H4O2)(C5H5N)]n, (I), and catena‐poly[aqua(μ3‐benzene‐1,4‐dicarboxylato‐κ3O:O′:O′′)bis(pyridine‐κN)cobalt(II)], [Co(C8H4O2)(C5H5N)2(H2O)]n, (II). In compound (I), the ZnII cation is five‐coordinated by four carboxylate O atoms from four BDC2− ligands and one pyridine N atom in a distorted square‐pyramidal coordination geometry. Four carboxylate groups bridge two ZnII ions to form centrosymmetric paddle‐wheel‐like Zn2(μ2‐COO)4 units, which are linked by the benzene rings of the BDC2− ligands to generate a two‐dimensional layered structure. The two‐dimensional layer is extended into a three‐dimensional supramolecular structure with the help of π–π stacking interactions between the aromatic rings. Compound (II) has a one‐dimensional double‐chain structure based on Co2(μ2‐COO)2 units. The CoII cations are bridged by BDC2− ligands and are octahedrally coordinated by three carboxylate O atoms from three BDC2− ligands, one water O atom and two pyridine N atoms. Interchain O—H…O hydrogen‐bonding interactions link these chains to form a three‐dimensional supramolecular architecture. 相似文献
12.
Pronay Kumar Biswas Abir Goswami Suchismita Saha Prof. Dr. Michael Schmittel 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(62):14095-14099
The dynamics of hydrogen bonding do not only play an important role in many biochemical processes but also in Nature's multicomponent machines. Here, a three-component nanorotor is presented where both the self-assembly and rotational dynamics are guided by hydrogen bonding. In the rate-limiting step of the rotational exchange, two phenolic O-H–N,N(phenanthroline) hydrogen bonds are cleaved, a process that was followed by variable-temperature 1H NMR spectroscopy. Activation data (ΔG≠298=46.7 kJ mol−1 at 298 K, ΔH≠=55.3 kJ mol−1, and ΔS≠=28.8 J mol−1 K−1) were determined, furnishing a rotational exchange frequency of k298=40.0 kHz. Fully reversible disassembly/assembly of the nanorotor was achieved by addition of 5.0 equivalents of trifluoroacetic acid (TFA)/1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) over three cycles. 相似文献
13.
Jing‐lin Wang Bin Liu Bin‐sheng Yang 《Acta Crystallographica. Section C, Structural Chemistry》2010,66(10):m280-m282
Centrosymmetric dimers of ZnII with singly deprotonated 2‐[(2‐carbamoylhydrazin‐1‐ylidene)methyl]phenolate, [Zn2(C8H8N3O2)Cl2]·2CH3OH, form an infinite one‐dimensional hydrogen‐bonded chain which is further aggregated by non‐aromatic–aromatic π–π stacking and nonclassical N—H...Cl hydrogen bonding. 相似文献
14.
Shakir Mohammad Parveen Shama Begum Nishat Chingsubam Poonam 《Transition Metal Chemistry》2004,29(2):196-199
Complexes of the type [M(tren)(abpt)](NO3)2(H2O)n
(1–6) [M = MnII, FeII, CoII, CuII, ZnII (n = 2), NiII (n = 2.25), tren = tris(2-aminoethyl)amine, and abpt = 4-amino-3,5-bis(pyridin-2yl)-1,2,4 triazole] have been prepared. The bonding mode and overall geometry of the complexes have been deduced by elemental analyses, molar conductance values, spectral studies (obtained from FT-IR), 1H-n.m.r., electronic spectral analyses and magnetic susceptibility measurements. A detailed molecular structure of complex (4) has been determined by single X-ray crystallography. 相似文献
15.
Sorption Behavior and Magnetic Properties of A Heterometallic Organic Framework with Octahedral Cages and One‐Dimensional Channels 下载免费PDF全文
The ZnII‐CoII organic framework [Me2NH2][Zn2Co(μ3‐OH)(BTC)2(H2O)] · 2H2O ( FJI‐6 ) (H3BTC = 1, 3,5‐benzenetricarboxylic acid and DMA = N.N′‐dimethyl acetamide), was synthesized and structurally characterized. FJI‐6 shows a three‐dimensional heterometallic microporous framework with coexisting octahedral cages and one‐dimensional channels assembled by Zn2Co(μ3‐OH)(CO2)6 secondary building units. In addition, the sorption behavior and magnetic properties of FJI‐6 were investigated. 相似文献
16.
Huaze Dong Xia Liu Juan Yang Zhaolian Chu Wei Huang Shaohua Gou 《Transition Metal Chemistry》2007,32(4):518-522
Reactions of sodium 4-pyridin-2-yl-pyrimidine-2-sulfonate (NaL) with CuII and MnII ions in water produced a zig-zag chain polymer, [CuL(NCS)]
n
(1), and a dinuclear complex, [Mn2L2Cl2(H2O)2] (2), respectively. It is observed that counteranions and hydrogen bonds play basic roles in the resulting structure in which
3D networks were formed through intermolecular hydrogen bonding. 相似文献
17.
Levon A. Tavadyan Gegham Z. Sedrakyan Seyran H. Minasyan Frederick T. Greenaway John R.J. Sorenson 《Transition Metal Chemistry》2004,29(6):684-696
Bioactive copper(II), iron(III), and manganese(II) 3,5-di-i-propylsalicylate (3,5-DIPS) chelates were investigated in order to determine their ability to inhibit the free radical initiated chain reactions leading to the peroxidation of isopropylbenzene (i-PrPh) and ethylbenzene (EtPh). Quantitative kinetic studies of these chelates established the following order of anti-oxidant reactivities: manganese(II)-(3,5-DIPS)2>iron(III)(3,5-DIPS)3>copper(II)2(3,5-DIPS)4> > 3,5-DIPS acid. The mechanism of anti-oxidant reactivity of these three chelates is established as being due, in part, to their chain-breaking capacity resulting from the chemical reduction of the generated peroxyl radical to yield alkybenzenelhydroperoxides via reaction of the 3,5-DIPS ligand with the peroxyl radical. In the case of manganese(II)3,5-di-i-propylsalicylate, the central metalloelement also interacts with the peroxyl radical. The manganese(II)-(3,5-DIPS)2 and copper(II)2(3,5-DIPS)4 chelates were also found to exhibit alkylhydroperoxide pro-oxidative reactivity leading to the formation of the alkylbenzeneperoxyl radical. In addition, the manganese(II) atom underwent oxidation to manganese(III) with the formation of the alkylbenzenehydroperoxide or superoxide with air oxygen oxidation. Amyl acetate and dipropylamine (n-Pr2NH) were added to the reaction mixture to model the biochemical presence of ester or amine cellular components. Addition of amyl acetate to the reaction mixture increased the anti-oxidant reactivity of manganese(II)-(3,5-DIPS)2 while decreasing its pro-oxidant reactivity. The weaker anti-oxidant reactivites of iron(III)(3,5-DIPS)3 and copper(II)2(3,5-DIPS)4 were less affected by the addition of amyl acetate and the pro-oxidant reactivity of copper(II)2(3,5-DIPS)4 was not changed by the addition of amyl acetate, while the pro-oxidant property of iron(III)(3,5-DIPS)3 was eliminated. In contrast to 2,6-di-t-butyl-4-methylphenol, butylated hydroxy toluene (BHT), anti-oxidant reactivities of copper(II), iron(III), and manganese(II) 3,5-DIPS chelates were dramatically enhanced by the addition of n-Pr2NH to the reaction mixture. It is concluded that all three metalloelement chelates react with and remove alkylbenzeneperoxyl radicals and the hydroperoxyl radical. The manganese(II)-(3,5-DIPS)2 and copper(II)2(3,5-DIPS)4 chelates may also be useful in removing hydroperoxides in vivo. These reactivities, in addition to their established superoxide dismutase (SOD)-mimetic and catalase-mimetic reactivities, are suggested to possibly permit anti-oxidant and pro-oxidant reactivities in aqueous and organic cellular compartments. 相似文献
18.
Syntheses,Structures and Spectral Properties of Mononuclear CuII and Dimeric ZnII Complexes Based on an Asymmetric Salamo‐type N2O2 Ligand 下载免费PDF全文
Li Xu Li‐Chun Zhu Jian‐Chun Ma Yang Zhang Jing Zhang Wen‐Kui Dong 《无机化学与普通化学杂志》2015,641(14):2520-2524
The asymmetric Salamo‐type N2O2 ligand H2L and its corresponding CuII and ZnII complexes [CuL] and [{ZnL}2]·2CH3CN were synthesized and structurally characterized. Crystallographic data of the CuII complex revealed that the CuII ion is tetracoordinate with a slightly distorted square planar arrangement forming a 2D supramolecular plane structure by hydrogen bonding and π···π stacking interactions. In the ZnII complex, the ZnII ions are pentacoordinate in N2O2 tetradentate fashion and intermolecular contacts between ZnII and oxygen atoms result in a head‐to‐tail dimer. The ZnII ions were found to have slightly distorted square pyramidal and trigonal bipyramidal arrangements, respectively. Hydrogen bonding interactions stabilized the ZnII complex to facilitate self‐assembly to a 1D linear chain. The CuII and ZnII complexes show intense photoluminescence with maximum emissions at approx. 426 and 411 nm upon excitation at 360 and 350 nm, respectively. 相似文献
19.
Boris‐Marko Kukovec Zora Popovi Gordana Pavlovi 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(12):m615-m617
The title compound, [Co(C7H6NO2)2(H2O)4]·4H2O, contains a CoII ion lying on a crystallographic inversion centre. The CoII ion is octahedrally coordinated by two 6‐methylpyridine‐3‐carboxylate ligands in axial positions [Co—O = 2.0621 (9) Å] and by four water molecules in the equatorial plane [Co—O = 2.1169 (9) and 2.1223 (11) Å]. There are also four uncoordinated water molecules. The 6‐methylpyridine‐3‐carboxylate ligands are bound to the CoII ion in a monodentate manner through a carboxylate O atom. There is one strong intramolecular O—H...O hydrogen bond, and six strong intermolecular hydrogen bonds of type O—H...O and one of type O—H...N in the packing, resulting in a complex three‐dimensional supramolecular structure. 相似文献
20.
The reaction of 4-methyl-3,5-di(2-pyridyl)-4H-1,2,4-triazole (medpt) with Zn(ClO4)2·6H2O and NaSCN, NaN3 or NaNO2 in a 2:1:1 molar ratio in MeOH/H2O (9:1) affords the mononuclear complexes [ZnII(medpt)2(NCS)]ClO4, [ZnII(medpt)2(N3)]ClO4 and [ZnII(medpt)2(NO2)]ClO4, respectively. All three complexes have been structurally characterised and found to feature unusual coordination polyhedra
for 3,5-di(2-pyridyl)-4H-1,2,4-triazole complexes. In [ZnII(medpt)2(NCS)]ClO4 and [ZnII(medpt)2(N3)]ClO4, the zinc atom resides within a distorted square-pyramidal N5 coordination sphere [τ = 0.22 and 0.04, respectively] with two bidentate medpt ligands bound equatorially and the pseudohalide ion coordinating
as a unidentate co-ligand in the apical position. In contrast, the NO2
− ion in [ZnII(medpt)2(NO2)]ClO4 acts as a bidentate ligand, which leads to a strongly distorted N4O2 coordination environment about the metal centre. 相似文献