One- and two-dimensional CdIIcoordination polymers constructed from 2-(2-methyl-1H-benzimidazol-1-yl)acetate ligands

2014 ◽  
Vol 70 (10) ◽  
pp. 992-997 ◽  
Author(s):  
Qiang Li ◽  
Hui-Ting Wang ◽  
Qiong Ye

The one- and two-dimensional polymorphic cadmium polycarboxylate coordination polymers,catena-poly[bis[μ2-2-(2-methyl-1H-benzimidazol-1-yl)acetato-κ3N3:O,O′]cadmium(II)], [Cd(C10H9N2O2)2]n, and poly[bis[μ2-2-(2-methyl-1H-benzimidazol-1-yl)acetato-κ3N3:O,O′]cadmium(II)], also [Cd(C10H9N2O2)2]n, were prepared under solvothermal conditions. In each structure, each CdIIatom is coordinated by four O atoms and two N atoms from four different ligands. In the former structure, two crystallographically independent CdIIatoms are located on twofold symmetry axes and doubly bridged in a μ2-N:O,O′-mode by the ligands into correspondingly independent chains that run in the [100] and [010] directions. Chains containing crystallographically related CdIIatoms are linked into sheetsviaπ–π stacking interactions. Sheets containing one of the distinct types of CdIIatom are stacked perpendicular to [001] and alternate with sheets containing the other type of CdIIatom. The second complex is a two-dimensional homometallic CdII(4,4) net structure in which each CdIIatom is singly bridged to four neighbouring CdIIatoms by four ligands also acting in a μ2-N:O,O′-mode. A square-grid network results and the three-dimensional supramolecular framework is completed by π–π stacking interactions between the aromatic ring systems.

Author(s):  
Hua Cai ◽  
Ying Guo ◽  
Jian-Gang Li

The mixed-ligand metal–organic complex poly[(μ3-phthalato)[μ2-3-(pyridin-2-yl)-1H-pyrazol-1-ido]dicopper(II)], [Cu2(C8H4O4)(C8H6N3)2]n, has been synthesized by the reaction of copper(II) acetate with 2-(1H-pyrazol-3-yl)pyridine (HL) and phthalic acid. The binuclear chelating–bridgingLunits are further linked by bridging phthalate ligands into a two-dimensional network parallel to the (010) plane. The two-dimensional networks are extended into a three-dimensional supramolecular architectureviaπ–π stacking interactions.


2010 ◽  
Vol 63 (3) ◽  
pp. 463 ◽  
Author(s):  
Chun-Sen Liu ◽  
Min Hu ◽  
Song-Tao Ma ◽  
Qiang Zhang ◽  
Li-Ming Zhou ◽  
...  

To explore the coordination possibilities of perylene-based ligands with a larger conjugated π-system, four ZnII, MnII, and CoII coordination polymers with perylene-3,4,9,10-tetracarboxylate (ptc) and the chelating 1,10-phenanthroline (phen) ligands were synthesized and characterized: {[Zn2(ptc)(phen)2](H2O)10}∞ (1), {[Zn3(ptc)(OH)2(phen)2](H2O)3}∞ (2), {[Mn(ptc)0.5(phen)(H2O)2](H2O)1.5}∞ (3), and {[Co(ptc)0.5(phen)(H2O)2](H2O)2.5}∞ (4). Structural analysis reveals that complexes 1 and 2 both take one-dimensional polymeric chain structures with dinuclear and trinuclear units as nodes, respectively, which are further extended via the accessorial secondary interchain interactions, such as C–H···O H-bonding or aromatic π···π stacking interactions, to give rise to the relevant higher-dimensional frameworks. Compound 3 has a two-dimensional sheet structure that is further assembled to form a three-dimensional framework by interlayer π···π stacking interactions. Complex 4 is a one-dimensional ribbon-like array structure that is interlinked by the co-effects of intermolecular π···π stacking and C–H···π supramolecular interactions, resulting in a higher-dimensional framework from the different crystallographic directions. Moreover, complexes 1–4 exhibit strong solid-state luminescence emissions at room temperature, which mainly originate from intraligand π→π* transitions of ptc.


2014 ◽  
Vol 70 (7) ◽  
pp. 718-721
Author(s):  
Zhengliang Lu ◽  
Yuanchao Zhao ◽  
Baolian Chen ◽  
Ximing Huang ◽  
Chunhua Fan

The title compound, [MnCl2(C24H20N6)], has been synthesized and characterized based on the multifunctional ligand 2,5-bis(2,2′-bipyridyl-6-yl)-3,4-diazahexa-2,4-diene (L). The MnIIcentre is five-coordinate with an approximately square-pyramidal geometry. TheLligand acts as a tridendate chelating ligand. The mononuclear molecules are bridged into a one-dimensional chain by two C—H...Cl hydrogen bonds. These chains are assembled into a two-dimensional layer through π–π stacking interactions between adjacent uncoordinated bipyridyl groups. Furthermore, a three-dimensional supramolecular framework is attained through π–π stacking interactions between adjacent coordinated bipyridyl groups.


2012 ◽  
Vol 68 (8) ◽  
pp. m229-m232
Author(s):  
Di Sun ◽  
Zhi-Hao Yan

A novel infinite one-dimensional silver cylinder, namely poly[μ-ethylenediamine-μ5-(2-sulfanidylbenzoato)-μ4-(2-sulfanidylbenzoato)-tetrasilver(I)], [Ag4(C7H4O2S)2(C2H8N2)]n, has been synthesized by one-pot reaction of equivalent molar silver nitrate and 2-mercaptobenzoic acid (H2mba) in the presence of ethylenediamine (eda). One Ag atom is located in an AgS2NO four-coordinated tetrahedral geometry, two other Ag atoms are in an AgS2O three-coordinated T-shaped geometry and the fourth Ag atom is in an AgSNO coordination environment. The two mba ligands show two different binding modes. The μ2-N:N′-eda ligand, acting as a bridge, combines with mba ligands to extend the AgIions into a one-dimensional silver cylinder incorporating abundant Ag...Ag interactions ranging from 2.9298 (11) to 3.2165 (13) Å. Interchain N—H...O hydrogen bonds extend the one-dimensional cylinder into an undulating two-dimensional sheet, which is further packed into a three-dimensional supramolecular framework by van der Waals interactions; no π–π interactions were observed in the crystal structure.


1999 ◽  
Vol 55 (4) ◽  
pp. 573-590 ◽  
Author(s):  
George Ferguson ◽  
Christopher Glidewell ◽  
Richard M. Gregson ◽  
Emma S. Lavender

The structures of six hydrogen-bonded adducts of 4,4′-sulfonyldiphenol with heteroaromatic amines have been determined. In 4,4′-sulfonyldiphenol–pyrazine (2/1) the pyrazine molecules lie across centres of inversion. The bisphenol molecules are linked into C(8) chains parallel to [100] by means of O—H...O=S hydrogen bonds, and antiparallel pairs of these chains are cross-linked by the pyrazine molecules, via O—H...N hydrogen bonds, to form molecular ladders containing R_6^6(50) rings between the rungs of the ladders. Each ladder is interwoven with two neighbouring ladders, thus producing a continuous two-dimensional sheet. The structure of 4,4′-sulfonyldiphenol–4,4′-bipyridyl (1/1) consists of spiral C_2^2(21) chains parallel to [010] containing alternating bisphenol and bipyridyl molecules linked by O—H...N hydrogen bonds: these chains are linked by two types of C—H...O hydrogen bonds which form C(5) chains along [001] and C_2^2(10) chains along [101], thus generating two interconnected nets characterized in the one case by a chequerboard pattern of R_6^6(44) and R_6^6(52) rings, and in the other by a single type of R_6^6(46) ring. 4,4′-Sulfonyldiphenol–trans-1,2-bis(4-pyridyl)ethene (1/1) [systematic name: 4,4′-sulfonyldiphenol–trans-4,4′-vinylenedipyridine (1/1)] and 4,4′-sulfonyldiphenol–1,2-bis(4-pyridyl)ethane (1/1) [systematic name: 4,4′-sulfonyldiphenol–trans-4,4′-ethylenedipyridine (1/1)] are isomorphous: the 1,2-bis(4-pyridyl)ethene component exhibits orientational disorder, corresponding approximately to a 180° rotation of ca 23% of the molecules about the N...N vector; in each compound the structure is built from C_2^2(23) chains of alternating bisphenol and bis(pyridyl) molecules connected by O—H...N hydrogen bonds, running parallel to [112] and generated by translation. The [112] chains are linked by C—H...O hydrogen bonds which generate C_2^2(12) chains parallel to [101], so forming a two-dimensional net built from R_6^6(50) rings. The structure of 4,4′-sulfonyldiphenol–4,4′-trimethylenedipyridine (1/1) consists of C_2^2(24) chains parallel to [100] generated by translation and consisting of alternating bisphenol and bis(pyridyl) molecules linked by O—H...N hydrogen bonds. Pairs of such chains are coiled together to form double helices, and pairs of such double helices, of opposite hand, are linked together by paired C—H...O hydrogen bonds in R_2^2(10) rings to form pairs of interwoven ladders in which the C_2^2(24) chains form the uprights and the R_2^2(10) rings form the rungs, between which are R_6^6(50) rings: an R_2^2(10) ring belonging to one ladder lies at the centre of an R_6^6(50) ring belonging to the other. 4,4′-Sulfonyldiphenol–4,4′-trimethylenedipiperidine–water (2/2/1) is a salt, 2C13H27N_2^+·2C12H9O4S−·H2O, containing two independent singly protonated diamine cations, two independent bisphenolate anions, and neutral water molecules. The two independent diamine cations are linked by N—H...N hydrogen bonds into C_2^2(24) chains running parallel to [001] and generated by translation, and each type of bisphenolate anion forms an independent spiral C(12) chain, also parallel to [001]. The three types of chain are linked by the water molecules: the two types of bisphenolate chain are linked by water molecules acting as double donors in O—H...O− hydrogen bonds in a C_6^4(32) chain parallel to [100], thus generating a two-dimensional net built from R_8^6(56) rings; the diamine chains are linked to these nets by means of N—H...O hydrogen bonds in which the water molecules act as acceptors and further hydrogen bonds, of N—H...O− and N—H...O=S types, link these two-dimensional nets into a continuous three-dimensional framework.


2012 ◽  
Vol 68 (7) ◽  
pp. m177-m180 ◽  
Author(s):  
Xia Yin ◽  
Song-Liang Cai ◽  
Sheng-Run Zheng ◽  
Jun Fan ◽  
Wei-Guang Zhang

The title compound, poly[aqua(μ2-1H-imidazole-4-carboxylato-κ3N3,O:O′)hemi(μ2-oxalato-κ4O1,O2:O1′,O2′)cadmium(II)], [Cd(C4H3N2O2)(C2O4)0.5(H2O)]n, exhibits a two-dimensional network. The CdIIcation is coordinated to one N atom and two carboxylate O atoms from two 1H-imidazole-4-carboxylate (Himc) ligands, two carboxylate O atoms from the bridging oxalate anion and one ligated water molecule; these six donor atoms form a distorted octahedral configuration. The oxalate anion lies on a centre of inversion. The Himc ligands connect the CdIIcations to form –Cd–Himc–Cd–Himc–Cd– zigzag chains, with a Cd...Cd separation of 5.8206 (6) Å along thebdirection, which are further linked by tetradentate oxalate anions to generate a two-dimensional herringbone architecture in theabplane. These layers are extended to form a three-dimensional supramolecular frameworkviaO—H...O and N—H...O hydrogen bonds and π–π stacking interactions. The solid-state photoluminscent behaviour of the title compound has been investigated at room temperature.


2008 ◽  
Vol 64 (1) ◽  
pp. 84-100 ◽  
Author(s):  
Solange M. S. V. Wardell ◽  
Marcus V. N. de Souza ◽  
Thatyana R. A. Vasconcelos ◽  
Marcelle de L. Ferreira ◽  
James L. Wardell ◽  
...  

The molecular and supramolecular structures of 18 N-arylpyrazinecarboxamides, Ar NHCO(C4H3N2), have been determined, including the stoichiometric monohydrate of N-(3-methoxyphenyl)pyrazinecarboxamide, and two polymorphs of N-(4-fluorophenyl)pyrazinecarboxamide having Z′ values of 1 and 4, respectively. The aryl groups were selected to include the geometric isomers for a compact range of substituents, namely methyl, trifluoromethyl, fluoro, chloro, methoxy and nitro groups, which exhibit markedly varied electronic properties and markedly varied behaviour as hydrogen-bond donors and acceptors. However, not all isomers in each group could be structurally investigated. A small number of derivatives containing disubstituted aryl groups have also been included in this study. The crystal structures of the solvent-free carboxamides reported here exhibit a wide range of direction-specific intermolecular forces, including N—H...N, N—H...O, C—H...N and C—H...O hydrogen bonds, and π...π stacking interactions, while the structure of N-(3-methoxyphenyl)pyrazinecarboxamide monohydrate also contains O—H...N and O—H...O hydrogen bonds. The resulting supramolecular structures can be zero-, one- or two-dimensional, although no three-dimensional supramolecular aggregation has been observed. In the finite, zero-dimensional structures, pairs of molecules are linked by hydrogen bonds to form cyclic centrosymmetric dimers. The one-dimensional structures include chains formed by the π-stacking of otherwise isolated molecules, simple chains generated by either C—H...O or C—H...N hydrogen bonds, and hydrogen-bonded chains of rings. The two-dimensional structures include examples of both π-stacked hydrogen-bonded chains and hydrogen-bonded sheets.


2015 ◽  
Vol 70 (7) ◽  
pp. 467-473 ◽  
Author(s):  
Yan-Jing Wang ◽  
Ai-Quan Jia ◽  
Xing-Shun Chen ◽  
Hua-Tian Shi ◽  
Qian-Feng Zhang

AbstractTwo new organically templated borates, [(1,10-phen)(H3BO3)2] (1) and [2-EtpyH][(B5O6(OH)4] (2), were synthesized under mild solvothermal conditions and characterized by single-crystal X-ray diffraction, FT-IR, elemental analyses and thermogravimetry. Complex 1 is a co-crystal component in which B(OH)3 molecules form crinkled tapes via hydrogen bonds, which in turn are packed in a two-dimensional framework with 1,10-phen molecules sandwiched between the framework of crinkled chains. The structure of complex 2 is composed of 2-ethylpyridinium cations [2-EtpyH]+ and pentaborate anions [B5O6(OH)4]– which are linked together with hydrogen bonds to form a three-dimensional supramolecular framework. The templating [2-EtpyH]+ cations are situated in the cavities arising from the supramolecular pentaborate framework and interact also with the inorganic framework through hydrogen bonds.


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