scholarly journals Crystal structure of the one-dimensional coordination polymer formed by the macrocyclic [Ni(cyclam)]2+ cation and the dianion of diphenylsilanediylbis(4-benzoic acid)

2020 ◽  
Vol 76 (6) ◽  
pp. 929-932
Author(s):  
Sergey P. Gavrish ◽  
Sergiu Shova ◽  
Maria Cazacu ◽  
Yaroslaw D. Lampeka
Keyword(s):  
Crystal Structure ◽  
Macrocyclic Ligand ◽  
Three Dimensional ◽  
Polymeric Chain ◽  
Water Molecules ◽  
Supramolecular Network ◽  
Asymmetric Unit ◽  
One Dimensional ◽  
Polymeric Chains ◽  
The One

The asymmetric unit of the title compound, catena-poly[[[(1,4,8,11-tetraazacyclotetradecane-κ4 N 1,N 4,N 8,N 11)nickel(II)]-μ-4,4′-(diphenylsilanediyl)dibenzoato-κ2 O:O′] sesquihydrate], {[Ni(C26H18O4Si)(C10H24N4)]·1.5H2O} n , consists of the halves of the centrosymmetric macrocyclic cation and the C 2-symmetric dicarboxylate dianion and of the water molecule of crystallization. The Ni2+ ion is coordinated by the four secondary N atoms of the macrocyclic ligand characterized by the most energetically favourable trans-III conformation and two mutually trans O atoms of the carboxylate, forming a slightly tetragonally elongated trans-N4O2 octahedron. The crystals are composed of parallel polymeric chains of the macrocyclic cations linked by the anions of the acid running along the [101] direction. Each polymeric chain is bonded to four neighbouring ones via water molecules providing O—H...O hydrogen bonds to the non-coordinated carboxyl O atoms to form a three-dimensional supramolecular network.

scholarly journals Syntheses and crystal structures of the one-dimensional coordination polymers formed by [Ni(cyclam)]2+ cations and 1,3-bis(3-carboxypropyl)tetramethyldisiloxane anions in different degrees of deprotonation

2020 ◽  
Vol 76 (3) ◽  
pp. 446-451 ◽  
Author(s):  
Sergey P. Gavrish ◽  
Sergiu Shova ◽  
Maria Cazacu ◽  
Mihaela Dascalu ◽  
Yaroslaw D. Lampeka
Keyword(s):  
Metal Ion ◽  
Macrocyclic Ligand ◽  
Three Dimensional ◽  
Polymeric Chain ◽  
Supramolecular Network ◽  
One Dimensional ◽  
Polymeric Chains ◽  
Carboxylic Groups ◽  
The One ◽  
Oriented Parallel

The asymmetric units of the title compounds, namely, catena-poly[[(1,4,8,11-tetraazacyclotetradecane-κ4 N 1,N 4,N 8,N 11)nickel(II)]-μ-1,3-bis(3-carboxylatopropyl)tetramethyldisiloxane-κ2 O:O′], [Ni(C10H24O5Si2)(C12H24N4)] n (I), and catena-poly[[[(1,4,8,11-tetraazacyclotetradecane-κ4 N 1,N 4,N 8,N 11)nickel(II)]-μ-4-({[(3-carboxypropyl)dimethylsilyl]oxy}dimethylsilyl)butanoato-κ2 O:O′] perchlorate], {[Ni(C10H25O5Si2)(C12H24N4)]ClO4} n (II), consist of one (in I) or two crystallographically non-equivalent (in II) centrosymmetric macrocyclic cations and one centrosymmetric dianion (in I) or two centrosymmetric monoanions (in II). In each compound, the metal ion is coordinated by the four secondary N atoms of the macrocyclic ligand, which adopts the most energetically stable trans-III conformation, and the mutually trans O atoms of the carboxylate in a slightly tetragonally distorted trans-NiN4O2 octahedral coordination geometry. The crystals of both types of compounds are composed of parallel polymeric chains of the macrocyclic cations linked by the anions of the acid running along the [101] and [110] directions in I and II, respectively. In I, each polymeric chain is linked to four neighbouring ones by hydrogen bonding between the NH groups of the macrocycle and the carboxylate O atoms, thus forming a three-dimensional supramolecular network. In II, each polymeric chain contacts with only two neighbours, forming hydrogen bonds between the partially protonated carboxylic groups of the bridging ligand. As a result, a lamellar structure is formed with the layers oriented parallel to the (1\overline{1}1) plane.

scholarly journals Crystal structure ofcatena-poly[[diaquacobalt(II)]-bis[μ-5-(4-carboxyylatophenyl)picolinato]-κ3N,O2:O5;κ3O5:N,O2-[diaquacobalt(II)]-μ-1-[4-(1H-imidazol-1-yl)phenyl]-1H-imidazole-κ2N3:N3′]

2015 ◽  
Vol 71 (7) ◽  
pp. m145-m146
Author(s):  
Guo-Wang Xu ◽  
Ye-Nan Wang ◽  
Hai-Bing Wang ◽  
Zhong-Long Wang
Keyword(s):  
Crystal Structure ◽  
Three Dimensional ◽  
Polymeric Chain ◽  
Water Molecules ◽  
Coordination Geometry ◽  
Supramolecular Architecture ◽  
Asymmetric Unit ◽  
Polymeric Chains ◽  
Coordination Water ◽  
Binuclear Unit

The asymmetric unit of the title polymeric CoIIcomplex, [Co2(C13H7NO4)2(C12H10N4)(H2O)4]n, contains a CoIIcation, a 5-(4-carboxylatophenyl)picolinate dianion, two coordination water molecules and half of 1-[4-(1H-imidazol-1-yl)phenyl]-1H-imidazole ligand. The CoIIcation is coordinated by two picolinate dianions, two water molecules and one 1-[4-(1H-imidazol-1-yl)phenyl]-1H-imidazole molecule in a distorted N2O4octahedral coordination geometry. The two picolinate dianions are related by an inversion centre and link two CoIIcations, forming a binuclear unit, which is further bridged by the imidazole molecules, located about an inversion centre, into the polymeric chain propagating along the [-1-11] direction. In the crystal, the three-dimensional supramolecular architecture is constructed by O—H...O hydrogen bonds between the coordinating water molecules and the non-coordinating carboxylate O atoms of adjacent polymeric chains.

scholarly journals Synthesis and crystal structure of a 6-chloronicotinate salt of a one-dimensional cationic nickel(II) coordination polymer with 4,4′-bipyridine

2020 ◽  
Vol 76 (5) ◽  
pp. 599-604
Author(s):  
Nives Politeo ◽  
Mateja Pisačić ◽  
Marijana Đaković ◽  
Vesna Sokol ◽  
Boris-Marko Kukovec
Keyword(s):  
Molecular Structure ◽  
Coordination Polymer ◽  
Three Dimensional ◽  
Polymeric Chain ◽  
Water Molecules ◽  
Sulfate Heptahydrate ◽  
Synthesis And Crystal Structure ◽  
One Dimensional ◽  
Polymeric Chains ◽  
Hydrogen Bonded

A 6-chloronicotinate (6-Clnic) salt of a one-dimensional cationic nickel(II) coordination polymer with 4,4′-bipyridine (4,4′-bpy), namely, catena-poly[[[tetraaquanickel(II)]-μ-4,4′-bipyridine-κ2 N:N′] bis(6-chloronicotinate) tetrahydrate], {[Ni(C10H8N2)(H2O)4](C6H3ClNO2)2·4H2O} n or {[Ni(4,4′-bpy)(H2O)4](6-Clnic)2·4H2O} n , (1), was prepared by the reaction of nickel(II) sulfate heptahydrate, 6-chloronicotinic acid and 4,4′-bipyridine in a mixture of water and ethanol. The molecular structure of 1 comprises a one-dimensional polymeric {[Ni(4,4′-bpy)(H2O)4]2+} n cation, two 6-chloronicotinate anions and four water molecules of crystallization per repeating polymeric unit. The nickel(II) ion in the polymeric cation is octahedrally coordinated by four water molecule O atoms and by two 4,4′-bipyridine N atoms in the trans position. The 4,4′-bipyridine ligands act as bridges and, thus, connect the symmetry-related nickel(II) ions into an infinite one-dimensional polymeric chain extending along the b-axis direction. In the extended structure of 1, the polymeric chains of {[Ni(4,4′-bpy)(H2O)4]2+} n , the 6-chloronicotinate anions and the water molecules of crystallization are assembled into an infinite three-dimensional hydrogen-bonded network via strong O—H...O and O—H...N hydrogen bonds, leading to the formation of the representative hydrogen-bonded ring motifs: tetrameric R 2 4(8) and R 4 4(10) loops, a dimeric R 2 2(8) loop and a pentameric R 4 5(16) loop.

scholarly journals Crystal structure ofcatena-poly[[[tetraaquairon(II)]-trans-μ-1,2-bis(pyridin-4-yl)ethene-κ2N:N′] bis(p-toluenesulfonate) methanol disolvate]

2017 ◽  
Vol 73 (12) ◽  
pp. 1977-1980
Author(s):  
Volodymyr M. Hiiuk ◽  
Diana D. Barakhty ◽  
Sergiu Shova ◽  
Ruslan A. Polunin ◽  
Il'ya A. Gural'skiy
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Three Dimensional ◽  
Distorted Octahedral Geometry ◽  
Water Molecules ◽  
Supramolecular Network ◽  
Polymeric Complex ◽  
Distorted Octahedral ◽  
Polymeric Chains ◽  
Coordinated Water

In the title polymeric complex, {[Fe(C12H10N2)2(H2O)4](CH3C6H4SO3)2·2CH3OH}n, the FeIIcation, located on an inversion centre, is coordinated by four water molecules in the equatorial positions and two 1,2-bis(pyridin-4-yl)ethene molecules in the axial positions. This results in a distorted octahedral geometry for the [N2O4] coordination polyhedron. The 1,2-bis(pyridin-4-yl)ethene molecules bridge the FeIIcations, forming polymeric chains running along thea-axis direction. Stabilization of the crystal structure is provided by O—H...O hydrogen bonds; these are formed by coordinated water molecules as donors towards the O atoms of the methanol molecules and tosylate anions as acceptors of protons, leading to the formation of a three-dimensional supramolecular network. Weak C—H...O hydrogen bonds are also observed in the crystal.

A novel one-dimensional CoIIcoordination polymer:catena-poly[[hexaaquacobalt(II)] [[diaquabis(sulfato-κO)cobalt(II)]-μ-4,4′-bipyridine-κ2N:N′] [[triaqua(sulfato-κO)cobalt(II)]-μ-4,4′-bipyridine-κ2N:N′]]

2012 ◽  
Vol 68 (9) ◽  
pp. m265-m268 ◽  
Author(s):  
Kai-Long Zhong ◽  
Ming-Yi Qian
Keyword(s):  
Crystal Structure ◽  
Three Dimensional ◽  
The Other ◽  
Water Molecules ◽  
Supramolecular Network ◽  
Sulfate Ion ◽  
Sulfate Ions ◽  
One Dimensional ◽  
The Third ◽  
Hydrogen Bonding Interactions

The title compound, {[Co(H2O)6][Co(SO4)(C10H8N2)(H2O)3][Co(SO4)2(C10H8N2)(H2O)2]}n, contains three crystallographically unique CoIIcentres, all of which are in six-coordinated environments. One CoIIcentre is coordinated by two bridging 4,4′-bipyridine (4,4′-bipy) ligands, one sulfate ion and three aqua ligands. The second CoIIcentre is surrounded by two N atoms of two 4,4′-bipy ligands and four O atoms,i.e.two O atoms from two monodentate sulfate ions and two from water molecules. The third CoIIcentre forms part of a hexaaquacobalt(II) ion. In the crystal structure, there are two different one-dimensional chains, one being anionic and the other neutral, and adjacent chains are arranged in a cross-like fashion around the mid-point of the 4,4′-bipy ligands. The structure features O—H...O hydrogen-bonding interactions between sulfate anions and water molecules, resulting in a three-dimensional supramolecular network.

scholarly journals catena-Poly[[diaquabis[1,4-bis(pyridin-4-yl)buta-1,3-diyne-κN]iron(II)]-μ-cyanido-κ2N:C-[dicyanido-κ2C-platinum(II)]-μ-cyanido-κ2C:N]

IUCrData ◽  
2017 ◽  
Vol 2 (10) ◽  
Author(s):  
Lucia Piñeiro-López ◽  
Francisco Javier Valverde-Muñoz ◽  
Maksym Seredyuk ◽  
Kateryna Znovjyak
Keyword(s):  
Molecular Structure ◽  
Hydrogen Bonds ◽  
Bond Length ◽  
Title Compound ◽  
Three Dimensional ◽  
Water Molecules ◽  
Stacking Interactions ◽  
One Dimensional ◽  
Polymeric Chains ◽  
The One

The molecular structure of the title compound, [FePt(CN)4(C14H8N2)2(H2O)2]n, consists of one-dimensional polymeric [–Fe–NC–Pt(CN)2–CN–]∞chains. Two water molecules and two monodentate 1,4-bis(pyridin-4-yl)buta-1,3-diyne (bpb) ligand molecules complete the octahedral coordination sphere of the FeIIatoms. The Fe—N(py) bond length (py is pyridine) is 2.2700 (15) Å, Fe—N(cyanide) is 2.1185 (16) Å and the Fe—O distance is 2.1275 (14) Å. The water molecules are hydrogen bonded to either bpb ligands or cyanide groups of the planar [Pt(CN)4]2−anion of adjacent polymeric chains. These O—H...N hydrogen bonds, in conjunction with offset and tilted π–π stacking interactions between bpb ligands and cyanide groups, extend the one-dimensional chains into a three-dimensional assembly.

scholarly journals A one-dimensional HgIIcoordination polymer based on bis(pyridin-3-ylmethyl)sulfane

2017 ◽  
Vol 73 (12) ◽  
pp. 1871-1874
Author(s):  
Suk-Hee Moon ◽  
Youngjin Kang ◽  
Ki-Min Park
Keyword(s):  
Hydrogen Bonds ◽  
Central Atom ◽  
Three Dimensional ◽  
Supramolecular Network ◽  
Zigzag Chain ◽  
Asymmetric Unit ◽  
Tetrahedral Geometry ◽  
One Dimensional ◽  
Centroid Distance ◽  
The One

The reaction of mercury(II) chloride with bis(pyridin-3-ylmethyl)sulfane (L, C12H12N2S) in methanol afforded the title crystalline coordination polymercatena-poly[[dichloridomercury(II)]-μ-bis(pyridin-3-ylmethyl)sulfane-κ2N:N′], [HgCl2L]n. The asymmetric unit consists of one HgIIcation, oneLligand and two chloride anions. Each HgIIion is coordinated by two pyridine N atoms from separateLligands and two chloride anions. The metal adopts a highly distorted tetrahedral geometry, with bond angles about the central atom in the range 97.69 (12)–153.86 (7)°. EachLligand bridges two HgIIions, forming an infinite –(Hg–L)n– zigzag chain along thebaxis, with an Hg...Hg separation of 10.3997 (8) Å. In the crystal, adjacent chains are connected by intermolecular C—H...Cl hydrogen bonds, together with Hg—Cl...π interactions [chloride-to-centroid distance = 3.902 (3) Å], that form between a chloride anion and the one of the pyridine rings ofL, generating a two-dimensional layer extending parallel to (101). These layers are further linked by intermolecular C—H...π hydrogen bonds, forming a three-dimensional supramolecular network.

scholarly journals A one-dimensional polymeric cobalt(III)–potassium complex with 18-crown-6, cyanide and porphyrinate ligands

2014 ◽  
Vol 70 (3) ◽  
pp. m104-m105 ◽  
Author(s):  
Yassine Belghith ◽  
Hamza Toumi ◽  
Jean-Claude Daran ◽  
Habib Nasri
Keyword(s):  
Three Dimensional ◽  
Water Molecules ◽  
Inversion Center ◽  
Asymmetric Unit ◽  
One Dimensional ◽  
Lattice Water ◽  
Porphyrin Ligand ◽  
Polymeric Chains ◽  
Potassium Complex ◽  
Cyanide Ligands

The reaction of CoII(TpivPP) {TpivPP is the dianion of 5,10,15,20-tetrakis[2-(2,2-dimethylpropanamido)phenyl]porphyrin} with an excess of KCN salts and an excess of the 18-crown-6 in chlorobenzene leads to the polymeric title compoundcatena-poly[[dicyanido-2κ2C-(1,4,7,10,13,16-hexaoxacyclooctadecane-1κ6O){μ3-(2α,2β)-5,10,15,20-tetrakis[2-(2,2-dimethylpropanamido)phenyl]porphyrinato-1κO5:2κ4N,N′,N′′,N′′′:1′κO15}cobalt(III)potassium] dihydrate], {[CoK(CN)2(C12H24O6)(C64H64N8O4]·2H2O}n. The CoIIIion lies on an inversion center, and the asymmetric unit contains one half of a [CoIII(2α,2β-TpivPP)(CN)2]−ion complex and one half of a [K(18-C-6]+counter-ion (18-C-6 is 1,4,7,10,13,16-hexaoxacyclooctadecane), where the KIion lies on an inversion center. The CoIIIion is hexacoordinated by two C-bonded axial cyanide ligands and the four pyrrole N atoms of the porphyrin ligand. The KIion is chelated by the six O atoms of the 18-crown-6 molecule and is further coordinated by two O atoms of pivalamido groups of the porphyrin ligands, leading to the formation of polymeric chains running along [011]. In the crystal, the polymeric chains and the lattice water molecules are linked by N—H...O and O—H...N hydrogen bonds, as well as weak C—H...O, O—H...π and C—H...π interactions into a three-dimensional supramolecular architecture.

scholarly journals Crystal structure of a one-dimensional coordination polymer of tin(IV) bromide with 1,4-dithiane

2015 ◽  
Vol 71 (12) ◽  
pp. m267-m268 ◽  
Author(s):  
Hans Reuter ◽  
Natalia Röwekamp-Krugley ◽  
Marius Imwalle ◽  
Simona Keil ◽  
Martin Reichelt
Keyword(s):  
Crystal Structure ◽  
Chair Conformation ◽  
Mean Value ◽  
Formula Unit ◽  
Asymmetric Unit ◽  
One Dimensional ◽  
Distorted Octahedral ◽  
Polymeric Chains ◽  
The One ◽  
Typical Range

The title compound, [SnBr4(C4H8S2)] {systematic name:catena-poly[[tetrabromidotin(IV)]-μ-1,4-dithiane-κ2S:S′]}, represents the first 1,4-dithiane complex with tin as coordination centre. The asymmetric unit consist of half a formula unit with the tin(IV) atom at the centre of symmetry at 0,0,1/2 (Wyckoff symbolb) and a centrosymmetric 1,4-dithiane molecule with the centre of symmetry in 1/2,0,1 (Wyckoff symbolc). The tin(IV) atom is coordinated in a distorted octahedral manner by the four bromine atoms and two sulfur atoms of two 1,4-dithiane molecules in atrans-position. Sn—Br [mean value: 2.561 (5) Å] and Sn—S distances [2.6546 (6) Å] are in the typical range for octahedrally coordinated tin(IV) atoms and the dithiane molecule adopts a chair conformation. The one-dimensional polymeric chains propagate along the [101] direction with weak intermolecular Br...Br [3.5724 (4) Å] between parallel chains and weak Br...H interactions [2.944–2.993 Å] within the chains.

scholarly journals The first coordination compound of 6-fluoronicotinate: the crystal structure of a one-dimensional nickel(II) coordination polymer containing the mixed ligands 6-fluoronicotinate and 4,4′-bipyridine

2020 ◽  
Vol 76 (4) ◽  
pp. 500-505 ◽  
Author(s):  
Nives Politeo ◽  
Mateja Pisačić ◽  
Marijana Đaković ◽  
Vesna Sokol ◽  
Boris-Marko Kukovec
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bond ◽  
Coordination Polymer ◽  
Three Dimensional ◽  
Water Molecules ◽  
Sulfate Heptahydrate ◽  
One Dimensional ◽  
Lattice Water ◽  
Mixed Ligands ◽  
Polymeric Chains

A one-dimensional nickel(II) coordination polymer with the mixed ligands 6-fluoronicotinate (6-Fnic) and 4,4′-bipyridine (4,4′-bpy), namely, catena-poly[[diaquabis(6-fluoropyridine-3-carboxylato-κO)nickel(II)]-μ-4,4′-bipyridine-κ2 N:N′] trihydrate], {[Ni(6-Fnic)2(4,4′-bpy)(H2O)2]·3H2O} n , (1), was prepared by the reaction of nickel(II) sulfate heptahydrate, 6-fluoronicotinic acid (C6H4FNO2) and 4,4′-bipyridine (C10H8N2) in a mixture of water and ethanol. The nickel(II) ion in 1 is octahedrally coordinated by the O atoms of two water molecules, two O atoms from O-monodentate 6-fluoronicotinate ligands and two N atoms from bridging 4,4′-bipyridine ligands, forming a trans isomer. The bridging 4,4′-bipyridine ligands connect symmetry-related nickel(II) ions into infinite one-dimensional polymeric chains running in the [1\overline{1}0] direction. In the extended structure of 1, the polymeric chains and lattice water molecules are connected into a three-dimensional hydrogen-bonded network via strong O—H...O and O—H...N hydrogen bonds, leading to the formation of distinct hydrogen-bond ring motifs: octameric R 8 8(24) and hexameric R 8 6(16) loops.

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