共查询到20条相似文献,搜索用时 15 毫秒
1.
Paul D. Robinson Kevin R. Smith Lori A. Vermeulen 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(10):o632-o634
The structure of the title compound, C14H16N2O6S2·2C6H6O2, consists of 2,2′‐(4,4′‐bipyridinium‐1,1′‐diyl)di(ethanesulfonate) molecules (with crystallographically imposed twofold symmetry) that are hydrogen bonded to each other, as well as to hydroquinone molecules, in a complex three‐dimensional motif. The orange color of the crystals is indicative of the donor–acceptor interaction between the electron‐rich hydroquinone π‐donor and the electron‐deficient bipyridinium π‐acceptor. The dihedral angle between the bipyridyl planes is 38.31 (11)°. The distance from the centroid of one of the hydroquinone molecules to the center of the bipyridinium group is 3.653 (3) Å, which is within the range typically observed for molecular complexes exhibiting charge‐transfer characteristics. 相似文献
2.
Ruizhan Tong Bin Liu Ganglin Xue Prof. Dr. Huaiming Hu Feng Fu Jiwu Wang 《无机化学与普通化学杂志》2010,636(8):1601-1605
A new polynuclear copper‐complex‐substituted dimeric tungstoarsenate(V), H2[{Cu(2,2′‐bpy)}8(H2O)2(AsW9O34)2] · 12H2O ( 1 ) (2,2′‐bpy = 2,2′‐bipydine), was synthesized hydrothermally and its structure was determined by single‐crystal X‐ray diffraction. The title compound has Ci symmetry and consists of two trilacunary Keggin anions [α‐AsW9O34]9– supported by eight copper complex cations. The compound was also characterized by IR and fluorescence spectroscopy, TG analysis, and magnetic measurements. The emission spectrum of the compound in solid‐state exhibits a redshift relative to those of Na8[A‐HAsW9O34] · 11H2O and the free ligand 2,2′‐bpy. Magnetic measurements of the compound indicate competing ferro‐ and antiferromagnetic intramolecular coupling among the CuII atoms in the cluster anion. 相似文献
3.
Guibin Ma Andrey Ilyukhin Julius Glaser 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(12):1473-1475
The title compound, [H2bipy](ClO4)2 or C10H10N22+·2ClO4?, was obtained at the interface between an organic (2,2′‐bipyridine in methanol) and an aqueous phase (perchloric acid in water). The compound crystallizes in space group P and comprises discrete diprotonated trans‐bipyridinium cations, [H2bipy]2+, and ClO4? anions. The cations and anions are connected through N—H?O and C—H?O hydrogen bonds [distances N?O 2.817 (4) and 2.852 (4) Å, and C?O 3.225 (6)–3.412 (5)Å]. The C—C bond distance between the two rings is 1.452 (5) Å. The bipyridinium cation has a trans conformation and the N—C—C—N torsion angle is 152.0 (3)°. 相似文献
4.
H. G. von Schnering R. Türck W. Hnle K. Peters E.‐M. Peters R. Kremer J.‐H. Chang 《无机化学与普通化学杂志》2002,628(12):2772-2777
CsMn2P2, a Manganese(II, III) Phosphide with BaZn2P2 Structure. With a Contribution to the BaAl4 Structure Type CsMn2P22is formed by the reaction of Cs4P6 with Mn and red phosphorus (Nb ampoule; 1073 K) as black platelets. The compound is paramagnetic following the Curie‐Weiss law above 110 K (μ = 4.81 B.M. / CsMn2P2; θ = —79 K) and orders antiferromagnetically below 110 K. The magnetic moment corresponds with the ratio MnII : MnIII = 1:1. CsMn2P2 is isotypic with BaZn2P2 (tI10; I4/mmm; a = 4.098(1) Å, c = 14.215(4) Å, d(Mn—P) = 2.387(1) Å (4×), d(Cs—P) = 3.718(2) Å (8×)), and shows, therefore, no P—P‐bonds. The different regions of the BaAl4 (ThCr2Si2) structure type are analysed and parameterized once more. 相似文献
5.
Two cobalt complexes, [Co3(L)2(CH3OH)2(μ3‐OH)2] ( 1 ) and [Co(L)(bpe)0.5] · H2O ( 2 ) [H2L = 5‐(4‐carboxyphenoxy)‐pyridine‐2‐carboxylic acid; bpe = 1, 2‐bis(4‐pyridyl)ethylene] were synthesized and fully characterized by elemental analyses, IR spectroscopy, single‐crystal X‐ray diffraction, thermogravimetric analysis (TGA), and magnetic analysis. Complex 1 has a two‐dimensional (2D) structure with puckered Co–O–Co chains, and 2 displays a three‐dimensional (3D) network containing one‐dimensional rectangular channels with dimensions of 9.24 × 13.84 Å. In complex 1 , variable‐temperature magnetic susceptibility measurements indicate antiferromagnetic interactions between cobalt magnetic centers. 相似文献
6.
Yasemin Yahsi 《Acta Crystallographica. Section C, Structural Chemistry》2016,72(7):585-592
The coordination chemistry of multinuclear metal compounds is important because of their relevance to the multi‐metal active sites of various metalloproteins and metalloenzymes. Multinuclear CuII and MnIII compounds are of interest due to their various properties in the fields of coordination chemistry, inorganic biochemistry, catalysis, and optical and magnetic materials. Oxygen‐bridged binuclear MnIII complexes generally exhibit antiferromagnetic interactions and a few examples of ferromagnetic interactions have also been reported. Binuclear CuII complexes are important due to the fact that they provide examples of the simplest case of magnetic interaction involving only two unpaired electrons. Two novel dioxygen‐bridged copper(II) and manganese(III) Schiff base complexes, namely bis(μ‐4‐bromo‐2‐{[(3‐oxidopropyl)imino]methyl}phenolato)dicopper(II), [Cu2(C10H10BrNO2)2], (1), and bis(diaqua{4,4′‐dichloro‐2,2′‐[(1,1‐dimethylethane‐1,2‐diyl)bis(nitrilomethanylylidene)]diphenolato}manganese(III)) bis{μ‐4,4′‐dichloro‐2,2′‐[(1,1‐dimethylethane‐1,2‐diyl)bis(nitrilomethanylylidene)]diphenolato}bis[aquamanganese(III)] tetrakis(perchlorate) ethanol disolvate, [Mn(C18H16Cl2N2O2)(H2O)2]2[Mn2(C18H16Cl2N2O2)2(H2O)2](ClO4)4·2C2H5OH, (2), have been synthesized and single‐crystal X‐ray diffraction has been used to analyze their crystal structures. The structure analyses of (1) and (2) show that each CuII atom is four‐coordinated, with long weak Cu…O interactions of 2.8631 (13) Å linking the dinuclear halves of the centrosymmetric tetranucelar molecules, while each MnIII atom is six‐coordinated. The shortest intra‐ and intermolecular nonbonding Mn…Mn separations are 3.3277 (16) and 5.1763 (19) Å for (2), while the Cu…Cu separations are 3.0237 (3) and 3.4846 (3) Å for (1). The magnetic susceptibilities of (1) and (2) in the solid state were measured in the temperature range 2–300 K and reveal the presence of antiferromagnetic spin‐exchange interactions between the transition metal ions. 相似文献
7.
Jin‐Kui Tang Li‐Na Zhu Xiao‐Zeng Li Wen Dong Dai‐Zheng Liao Zong‐Hui Jiang Shi‐Ping Yan Peng Cheng 《无机化学与普通化学杂志》2003,629(11):2000-2003
A novel coordination polymer {[Mn(azpy)(NCS)2(MeOH)2] · azpy}n( 1 ) (azpy = 4, 4'‐azopyridine), has been synthesized and characterized by X‐ray diffraction. It consists of a quasi two‐dimensional network structure constructed from 1‐D chains of [Mn(azpy)(NCS)2(MeOH)2]n connected by hydrogen bonds, which creates about 13.6 Å × 17.1 Å of channels. The coordination sphere of the manganese(II) ion is a distorted octahedron. The determination of the variable temperature magnetic susceptibilities (5—300 K) shows the existence of a very weak antiferromagnetic interaction with a J value of —0.03 cm—1. 相似文献
8.
《无机化学与普通化学杂志》2018,644(2):109-113
The 2D CuII metal‐organic framework [Cu2(bptc)(H2O)4]n · 4nH2O ( 1 ) (H4bptc = biphenyl‐2,2′,4,4′‐tetracarboxylic acid) was hydrothermally synthesized and characterized by single‐crystal X‐ray diffraction and magnetic measurements. In the structure, bptc4– serves as a twisted Π‐shaped organic building block to connect paddlewheel [Cu2(COO)4] dinuclear units and mononuclear units through 2‐/2′‐carboxylate and 4‐/4′‐carboxylate, respectively. According to the magnetic analysis using a dimer‐plus‐monomer model, strong antiferromagnetic coupling is operative within the dinuclear unit (J = –311 cm–1 based on H = –J S 1 S 2), and the compound behaves like a mononuclear molecule at low temperature. 相似文献
9.
Kazumasa Ueda Toyonari Sugimoto Toshiji Tada Kei‐ichiro Nishimura Tomoyuki Mochida 《Acta Crystallographica. Section C, Structural Chemistry》2001,57(4):400-402
In the tetramethylarsonium salt of 2,5‐dichloro‐7,7,8,8‐tetracyanoquinodimethanide [systematic name: tetramethylarsonium 2,2′‐(2,5‐dichlorocyclohexa‐2,5‐diene‐1,4‐diylidene)bis(propanedinitrile)], C4H12As+·C12H2Cl2N4? or [As(CH3)4](C12H2Cl2N4), the cation lies disordered about a twofold axis and the radical ion lies about an inversion center forming a uniform [interplanar distance 3.35 (2) Å] and one‐dimensional stacking without any slip. The electrical conductivity of the single crystal at room temperature was less than 10?9 S cm?1, and the temperature dependence of paramagnetic susceptibility obeyed a one‐dimensional antiferromagnetic Heisenberg model with a spin‐exchange integral of 83 K in the temperature range 1.8–320.0 K. 相似文献
10.
Sebastin Suarez Fabio Doctorovich Miguel Angel Harvey Ricardo Baggio 《Acta Crystallographica. Section C, Structural Chemistry》2013,69(4):351-355
The title ionic compound, [Ni(C12H12N2)(H2O)4]SO4·H2O, is composed of an NiII cation coordinated by a chelating 4,4′‐dimethyl‐2,2′‐bipyridine ligand via its two N atoms [mean Ni—N = 2.056 (2) Å] and by four aqua ligands [mean Ni—O = 2.073 (9) Å], the net charge being balanced by an external sulfate anion. The whole structure is stabilized by a solvent water molecule. Even though the individual constituents are rather featureless, they generate an extremely complex supramolecular structure consisting of a central hydrogen‐bonded two‐dimensional hydrophilic nucleus made up of complex cations, sulfate anions and coordinated and solvent water molecules, with pendant hydrophobic 4,4′‐dimethyl‐2,2′‐bipyridine ligands which interact laterally with their neighbours viaπ–π interactions. The structure is compared with closely related analogues in the literature. 相似文献
11.
Wen‐Tong Chen Xi‐Rui Zeng Xiao‐Niu Fang Xin‐Fa Li Han‐Mao Kuang 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(12):m571-m573
The title compound, (C10H10N2)[CdBr4], was synthesized via a hydrothermal reaction. Its structure features discrete 4,4′‐bipyridinium cations and tetrahedral [CdBr4]2− anions linked into ion pairs by single N—H⋯Br hydrogen bonds. Photoluminescent investigation reveals that the title compound displays a strong emission in the blue region, which may originate from π→π* charge‐transfer interactions of the 4,4′‐bipyridinium cations. 相似文献
12.
Lei Zhang Zhi‐Liang Liu Lin‐Hong Weng Dai‐Zheng Liao Zong‐Hui Jiang Shi‐Ping Yan Pan‐Wen Shen Martin Baumgarten 《Helvetica chimica acta》2001,84(4):834-841
The structure of a novel oxido‐aminoxyl (=`nitronyl nitroxide') biradical, 2,2′‐(1‐oxidopyridine‐2,6‐diyl)bis[4,5‐dihydro‐4,4,5,5‐tetramethyl‐3‐oxido‐1H‐imidazol‐1‐oxyl] hydrate ( 1 ⋅H2O) was established by X‐ray analysis in the solid state: monoclinic, space group P21/c, Z=4 with a=12.621(4), b=15.704(5), and c=13.001(4) Å, and β=115.202(6)°. Variable‐temperature magnetic susceptibilities show a weak antiferromagnetic interaction between the two oxido‐substituted aminoxyl moieties of 1 , indicative of a singlet ground state. AM1 Calculations located minima for the possible structure based on the X‐ray crystal structure. A hybride density‐functional‐theory calculation with the UB3LYP method from the X‐ray crystal structure establishes the same spin sign in the two aminoxyl moieties and shows that a small spin density is localized at the C‐atoms of the pyridine moiety. These theoretic results are in good agreement with the determined weak antiferromagnetic interaction of 1 . 相似文献
13.
吡啶修饰的线性五核金属化合物[Ni5(μ-dmpzda)4(NCS)2][ dmpzda-H2=N,N’-Di(4-methyl pyrydin-2-yl)pyrazine-2,6-diamine]被合成并表征,其电化学和磁性被报告。 化合物含有接近180º的 Ni-Ni-Ni角,末端含有两个轴配体的Ni5 线性链。这个五核线性金属链被四个顺式的dmpzda2-配体螺旋包裹。化合物中存在两种类型的Ni-Ni键长:末端连接有轴配体的Ni-Ni键长被配体影响,其键长为2.3821 Å;内部的Ni-Ni距离比较短,为2.2959 Å。两末端的Ni(II)离子由于连接轴配体构成四方锥形(NiN4NCS)并存在较长的Ni-N 键长(2.103 Å),这个键长符合高自旋Ni(II)构型。内部的三个Ni-N 距离为1.886-1.906 Å,这样构成正方形平面(NiN4)并呈低自旋的顺磁构型。化合物显示了同[Ni5(μ-tpda)4(NCS)2]类似的磁性,即在化合物中两末端Ni(II)仍存在反铁磁性的作用。 相似文献
14.
Chun‐Yuan Liao Chi‐Wang Chen Hsin‐Huang Lin Sung‐Chung Cheng Chin‐Jhan Lee Ho‐Hsiang Wei 《中国化学会会志》2005,52(4):707-716
Four new complexes of [Cu(bpm)(ox)(H2O)] ( 1 ), [Cu(tpd)(dca)(H2O)] ( 2 ), [Cu(bppz)(N3)2] ( 3 ), and [Cu(bpm)2(μ1,3‐N3)(N3)] ( 4 ) (bpm = 2,2′‐bipyrimidine, bppz = 2,3‐bis(2‐pyridyl)pyrazine, tpd = 4‐terpyridone, dca = dicyanamide, ox = oxalate) have been prepared and characterized by X‐ray single‐crystal analysis and variable‐temperature magnetic measurements. Compounds 1–4 are essentially mononuclear Cu(II) complexes. However, in complex 1 , Cu(II) it was found that intermolecular hydrogen bonding through between H2O and ox formed 1‐D chain structure. In complex 2 it was found that the hydrogen bonding between H2O and tpd of the next molecule led to for a binuclear Cu(II) complex. In complex 3 , two nitrogen atoms, one of the pyridyl group of bppz and one of N3? ligands, are weakly coordinated to neighbor Cu(II) ion thus leading to formation of a 1‐D chain structure. In complex 4 , one nitrogen atom of terminated N3? is weakly coordinated to the neighbor Cu(II) site to form a 1‐D polymeric structure. The magnetic susceptibility measurements indicate that complex 1 and 4 exhibit a weak antiferromagnetic interaction whereas a ferromagnetic coupling has been established for complexes 2 and 3 . 相似文献
15.
Ayhan Elmali C. Tugrul Zeyrek YalcÛn Elerman Ingrid Svoboda 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(11):1302-1304
The title compounds, {4,4′‐dibromo‐2,2′‐[1,3‐propanediylbis(nitrilomethylidyne‐N)]diphenolato‐O,O′}nickel(II), [Ni(C17H14Br2N2O2)], and {4,4′‐dichloro‐2,2′‐[1,3‐propanediylbis(nitrilomethylidyne‐N)]diphenolato‐O,O′}copper(II), [Cu(C17H14Cl2N2O2)], lie on crystallographic twofold axes. In both structures, the metal coordination sphere is a tetrahedrally distorted square plane formed by the four‐coordinate N2O2 donor set of the Schiff base imine–phenol ligands. In the Ni compound, the Ni—O and Ni—N distances are 1.908 (3) and 1.959 (4) Å, respectively, while in the Cu compound, the Cu—O and Cu—N distances are 1.907 (2) and 1.960 (2) Å, respectively. The two Schiff base moieties, which themselves are nearly planar, are inclined at an angle of 29.26 (7)° for the Ni compound and 29.26 (5)° for the Cu compound. 相似文献
16.
A. Castieiras M. C. F. Vidal J. Romero R. Sez A. Matilla J. Nicls J. M. Tercero 《无机化学与普通化学杂志》2001,627(7):1553-1559
New dinuclear complexes of the types [Ni2(L)(H2O)2] and [Ni2(L)(H2O)6] [H4L = N,N′‐bis(carboxymethyl) dithiooxamide (H4GLYDTO), N,N′‐bis(1‐carboxyethyl) dithiooxamide (H4ALADTO), N,N′‐bis(1‐carboxy‐2‐methylpropyl) dithiooxamide (H4VALDTO) and N,N′‐bis(1‐carboxy‐3‐methylbutyl) dithiooxamide (H4LEUDTO)] have been prepared and characterized by IR and electronic absorption spectroscopy, and the structure of [Ni2(ALADTO)(H2O)6] crystals has been determined by single crystal X‐ray analysis. This compound is composed of discrete dinuclear units in which two NiII atoms with NO4S kernels are linked by a single [ALADTO]4– group that coordinates through its carboxylato oxygen, amino nitrogen and thiolato sulphur atoms. In each dimer unit the two nickel(II) ions in distorted octahedral coordination are separated by 5.863(2) Å The temperature dependence of the magnetic susceptibility of the new compounds was measured over the range 2 to 300 K. In the complexes of [GLYDTO]4– and [ALADTO]4– the two Ni atoms are antiferromagnetically coupled, with J = –23.51(4) and –20.95(8) cm–1, respectively. By constrast, [Ni2(VALDTO)(H2O)2], [Ni2(VALDTO)(H2O)6] and [Ni2(LEUDTO)(H2O)2] remain paramagnetic down to 2 K, with magnetic moment values between 2.8 and 3.3 M.B. 相似文献
17.
Ganna A. Senchyk Andrey B. Lysenko Eduard B. Rusanov Alexander N. Chernega Konstantin V. Domasevitch 《Acta Crystallographica. Section C, Structural Chemistry》2010,66(7):m180-m183
In the structures of the CdII pseudohalide coordination polymer poly[[diaquabis[μ2‐3,3′‐bis(1,2,4‐triazol‐4‐yl)‐1,1′‐biadamantane‐κ2N1:N1′]cadmium(II)] dithiocyanate dihydrate], {[Cd(C24H32N6)2(H2O)2](NCS)2·2H2O}n, (I), and the isomorphous selenocyanate analogue, {[Cd(C24H32N6)2(H2O)2](NCSe)2·2H2O}n, (II), the CdII cations occupy inversion centres and have octahedral CdN4O2 environments, completed by four N atoms of the organic ligands [Cd—N = 2.316 (2) and 2.361 (2) Å for (I), and 2.313 (3) and 2.372 (3) Å for (II)] and two trans‐coordinated aqua ligands [Cd—O = 2.3189 (15) Å for (I) and 2.323 (2) Å for (II)]. In each compound, the ligand displays a bidentate N1:N1′‐bridging mode, connecting the metal centres at a distance of 14.66 Å into two‐dimensional nets of (4,4)‐topology, while the uncoordinated thio(seleno)cyanate anions reside inside the net cavities. Hydrogen bonding between the water molecules, anions and 1,2,4‐triazole N atoms supports the tight packing, with an interlayer distance of 6.09 Å. 相似文献
18.
Ming Sun Alasdair C. Macculloch Thomas A. Hamor Richard T. Walker 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(1):116-117
The pyrimidine ring of the title compound, C11H16N2O5S·H2O, is planar to within 0.026 (1) Å and makes an angle of 77.73 (8)° with the mean plane of the thiosugar ring. In terms of standard nucleoside nomenclature, this ring has a C1′‐exo,C2′‐endo conformation. The O5′—C5′—C4′—C3′ torsion angle is ?167.4 (2)° and the glycosidic S4′—C1′—N1—C2 torsion angle is ?101.8 (2)° (anti). 相似文献
19.
En Tang Yu‐Mei Dai Shen Lin 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(9):m433-m434
The title compound, [Zn(C8H5O4)2(C10H8N2)2], was obtained by the hydrothermal reaction of ZnSO4·7H2O with phthalic acid (H2pht) and 4,4′‐bipyridine (4,4′‐bipy). Crystallographic analysis shows that it has a one‐dimensional double‐chain structure via hydrogen‐bonding interactions. Each ZnII atom, adopting a distorted tetrahedral geometry, is coordinated by two N atoms from two 4,4′‐bipy ligands, with Zn—N distances of 2.054 (4) and 2.104 (4) Å, and by two O atoms from symmetry‐related Hpht− ligands, with Zn—O distances of 1.921 (4) and 2.019 (4) Å. 相似文献
20.
Stefan Steinhauser Uwe Heinz Jürgen Sander Kaspar Hegetschweiler 《无机化学与普通化学杂志》2004,630(12):1829-1838
Complex formation of 2, 6‐bis(2′‐hydroxyphenyl)pyridine (H2Li) with Fe3+ and Cu2+ was investigated in a H2O/DMSO medium (mole fraction xDMSO = 0.2) by potentiometric and spectrophotometric methods. The pKa values of [H3Li]+ are 2.25, 10.51 and 14.0 (25 °C, 0.1 M KCl). The formation constants of [FeIII(Li)]+ and [CuII(Li)] (25 °C, 0.1 M KCl) are log β1 = 21.5 for Fe3+ and log β1 = 18.5 for Cu2+. The crystal structures of [Al(Li)2Na(EtOH)3], [Fe(Li)2Na(EtOH)3], and [Cu(Li)(py)]2 were investigated by single‐crystal X‐ray diffraction analyses. The FeIII and the AlIII compound are isotypic and crystallize in the monoclinic space group P21/n. Al‐compound (215 K): a = 12.599(3) Å, b = 16.653(3) Å, c = 17.525(4) Å, β = 100.27(3)°, Z = 4 for C40H40AlN2NaO7; Fe‐compound (293 K): a = 12.753(3) Å, b = 16.715(3) Å, c = 17.493(3) Å, β = 99.68(3)°, Z = 4 for C40H40FeN2NaO7. Both compounds contain a homoleptic, anionic bis‐complex [M(Li)2]‐ of approximate D2 symmetry. The Cu compound crystallized as an uncharged, dinuclear and centrosymmetric [Cu(Li)(py)]2 complex in the monoclinic space group P21/n with (293 K) a = 13.386(3) Å, b = 9.368(2) Å, c = 14.656(3) Å, β = 100.65(3)°, Z = 2 for C44H32Cu2N4O4. The structural properties and in particular the possible influence of the ligand geometry on the stability of the metal complexes is discussed. 相似文献