共查询到20条相似文献,搜索用时 78 毫秒
1.
G. Pelosi M. Belicchi Ferrari M. C. Rodríguez‐Argüelles S. Mosquera‐Vzquez J. Sanmartín 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(6):m241-m242
The title compound, Na+·C9H7N4O5S−·2H2O, presents a Z configuration around the imine C=N bond and an E configuration around the C(O)NH2 group, stabilized by two intramolecular hydrogen bonds. The packing is governed by ionic interactions between the Na+ cation and the surrounding O atoms. The ionic unit, Na+ and 2‐oxo‐3‐semicarbazono‐2,3‐dihydro‐1H‐indole‐5‐sulfonate, forms layers extending in the bc plane. The layers are connected by hydrogen bonds involving the water molecules. 相似文献
2.
G. Mazumder M. De S. K. Mazumder A. Mukhopadhyay 《Acta Crystallographica. Section C, Structural Chemistry》2001,57(5):562-563
In the title compound, oxonium 5‐amino‐2,6‐dioxo‐1,2,3,6‐tetrahydropyrimidine‐4‐sulfonate hydrate, H3O+·C4H4N3O5S?·H2O, the sulfonate group is in the anionic form and charge balance is provided by an oxonium cation, H3O+. Screw‐related molecules overlap significantly and are hydrogen bonded to form a zigzag chain of the uracil skeleton along the direction of the c screw axis. The partially stacked bases and their glide‐related equivalents run parallel to the a axis to form hydrophobic zones separated by hydrophilic zones built up by a network of hydrogen bonds. 相似文献
3.
Zun‐Ting Zhang Xin‐Li Cheng Yun He 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(10):m484-m487
In methylaminium 4′,7‐dihydroxyisoflavone‐3′‐sulfonate dihydrate, CH6N+·C15H9O7S−·2H2O, 11 hydrogen bonds exist between the methylaminium cations, the isoflavone‐3′‐sulfonate anions and the solvent water molecules. In hexaaquairon(II) bis(4′,7‐diethoxyisoflavone‐3′‐sulfonate) tetrahydrate, [Fe(H2O)6](C19H17O7S)2·4H2O, 12 hydrogen bonds exist between the centrosymmetric [Fe(H2O)6]2+ cation, the isoflavone‐3′‐sulfonate anions and the solvent water molecules. Additional π–π stacking interactions generate three‐dimensional supramolecular structures in both compounds. 相似文献
4.
From the reduction of heptamolybdate, a polyoxomolybdate was obtained with the formula [Na(H2O)16(NH2CH2COO)]4+·{Na+[H9MoMoO56(NH2CH2COO)]5?}4?·20H2O, i.e. heptasodium nonahydrogen tetracarbamate hexadecaaquahexapentacontaoxaoctadecamolybdate(V,VI) icosahydrate. The 18 Mo atoms are connected by bridging O atoms to form a centrosymmetric girdle‐like structure, in which MoV–MoV units are found. An Na+ cation occupies the central hole of the girdle, while four Na+ cations are bonded to the O atoms on the girdle edge. The girdles are linked into a one‐dimensional chain by the other Na+ cations. 相似文献
5.
Graham Smith Urs D. Wermuth Jonathan M. White 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(8):o575-o581
The crystal structures of quinolinium 3‐carboxy‐4‐hydroxybenzenesulfonate trihydrate, C9H8N+·C7H5O6S−·3H2O, (I), 8‐hydroxyquinolinium 3‐carboxy‐4‐hydroxybenzenesulfonate monohydrate, C9H8NO+·C7H5O6S−·H2O, (II), 8‐aminoquinolinium 3‐carboxy‐4‐hydroxybenzenesulfonate dihydrate, C9H9N2+·C7H5O6S−·2H2O, (III), and 2‐carboxyquinolinium 3‐carboxy‐4‐hydroxybenzenesulfonate quinolinium‐2‐carboxylate, C10H8NO2+·C7H5O6S−·C10H7NO2, (IV), four proton‐transfer compounds of 5‐sulfosalicylic acid with bicyclic heteroaromatic Lewis bases, reveal in each the presence of variously hydrogen‐bonded polymers. In only one of these compounds, viz. (II), is the protonated quinolinium group involved in a direct primary N+—H⋯O(sulfonate) hydrogen‐bonding interaction, while in the other hydrates, viz. (I) and (III), the water molecules participate in the primary intermediate interaction. The quinaldic acid (quinoline‐2‐carboxylic acid) adduct, (IV), exhibits cation–cation and anion–adduct hydrogen bonding but no direct formal heteromolecular interaction other than a number of weak cation–anion and cation–adduct π–π stacking associations. In all other compounds, secondary interactions give rise to network polymer structures. 相似文献
6.
Samuel Sakwa Kraig A. Wheeler 《Acta Crystallographica. Section C, Structural Chemistry》2003,59(6):o332-o334
The title compounds, bis(ammonium) naphthalene‐1,5‐disulfonate, 2NH4+·C10H6O6S22−, and bis[1‐(hydroxymethyl)‐3,5,7‐triaza‐1‐azoniatricyclo[3.3.1.13,7]decane] 1,5‐naphthalenedisulfonate, 2C7H15N4O+·C10H6O6S22−, were prepared from the acid‐promoted reaction of hexamethylenetetramine. In both structures, the disulfonate anion is positioned on an inversion center, with each sulfonate group contributing to the supramolecular assemblies via hydrogen bonds. The ammonium cations are linked to sulfonate groups by four distinct N+—H⃛−O—S contacts [N⃛O = 2.846 (2)–2.898 (2) Å and N—H⃛O = 160 (2)–175 (2)°], whereas the 1‐(hydroxymethyl)‐3,5,7‐triaza‐1‐azoniatricyclo[3.3.1.13,7]decane cations form one O—H⃛−O—S [O⃛O = 2.628 (2) Å and O—H⃛O = 176°] and three C—H⃛−O—S [C⃛O = 3.359 (2)–3.380 (2) Å and C—H⃛O = 148–155°] interactions to neighboring sulfonate groups. 相似文献
7.
Madhukar Hemamalini Packianathan Thomas Muthiah Gabriele Bocelli Andrea Cantoni 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(4):o284-o286
In the title compound, C10H9N2+·C9H5INO4S−·2H2O, the 4,4′‐bipyridine molecule is protonated at one of the pyridine N atoms. These moieties self‐assemble into a supramolecular chain along the a axis through N—H⋯N hydrogen bonds. The quinolinol OH group acts as a donor with respect to a sulfonate O atom [O—H⋯O(sulfonate)] and acts as an acceptor with respect to a C—H group of ferron [C—H⋯O(hydroxy)], forming a supramolecular chain along the b axis. These two types of supramolecular chains (one type made up of bipyridine motifs and the other made up of sulfoxine motifs) interact viaπ–π stacking, generating a three‐dimensional framework. These chains are further crosslinked by C—H⋯O hydrogen bonds and O—H⋯O hydrogen bonds involving water molecules. 相似文献
8.
Elizabeth George Subramania Vivekanandan Kandasamy Sivakumar 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(10):1208-1209
In the title compound, sodium N‐chlorobenzenesulfonamide sesquihydrate, Na+·C6H5ClNO2S?·1.5H2O, the sodium ion exhibits octahedral coordination by O atoms from three water molecules and by three sulfonyl O atoms of three different N‐chlorobenzenesulfonamide anions. A two‐dimensional polymeric layer consists of units, each comprising two face‐sharing octahedra which share four corners with four other such units, the layer running parallel to the ab plane. The water molecules participate in hydrogen bonds of the types O—H?O, O—H?N and O—H?Cl. 相似文献
9.
Marina S. Fonari Yurii A. Simonov Mark Botoshansky Eduard V. Ganin Arkadii A. Yavolovskii 《Acta Crystallographica. Section C, Structural Chemistry》2003,59(2):o88-o90
In the title hydrated adduct, 1,4,10,13‐tetraoxa‐7,16‐diazoniacyclooctadecane bis(4‐aminobenzenesulfonate) dihydrate, C12H28N2O42+·2C6H6NO3S−·2H2O, formed between 7,16‐diaza‐18‐crown‐6 and the dihydrate of 4‐aminobenzenesulfonic acid, the macrocyclic cations lie across centres of inversion in the orthorhombic space group Pbca. The anions alone form zigzag chains, and the cations and anions together form sheets that are linked via water molecules and anions to form a three‐dimensional grid. 相似文献
10.
Graeme J. Gainsford Tim Kemmitt 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(3):m136-m138
In the title compound, [Na4(C8H16BO4)4(C4H10O2)]n, there are two coordination types for the four independent Na+ cations: two Na+ cations bond to six diolate O atoms [Na—O = 2.305 (2)–2.609 (2) Å], while the other two are five‐coordinate via one 1,4‐butanediol [2.289 (2) and 2.349 (3) Å] and four diolate O atoms [2.295 (2)–2.408 (2) Å]. Corresponding to this, there are three‐ and four‐coordinate diolate O atoms, the latter bridging Na atoms. The 1,4‐butanediol molecules lie on inversion centres. The boron stereochemistry shows minor local perturbations from its usual tetrahedral state [B—O = 1.457 (4)–1.503 (4) Å]. The resulting polymer packs as sheets parallel to the (10) plane crosslinked by the butanediol molecules. The structure was solved using data from a multiple crystal. 相似文献
11.
Emiliana Damian Lars Eriksson Magnus Sandstrm 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(9):m419-m420
Sodium trichloromethanesulfonate monohydrate, Na+·CCl3SO3−·H2O, crystallizes in P21/a with all the atoms located in general positions. The trichloromethanesulfonate (trichlate) anion consists of pyramidal SO3 and CCl3 groups connected via an S—C bond in a staggered conformation with approximate C3v symmetry. The water molecule is hydrogen bonded to the sulfonate O atoms, with one water H atom forming weak bifurcated O—H⋯O hydrogen bonds to two different trichlate ions. Two water O atoms and three O atoms from different SO3 groups form a square‐pyramidal arrangement around the sodium ion. 相似文献
12.
John N. Low Paloma Arranz Justo Cobo M. Angeles Fontecha M. Luz Godino Rafael Lpez Christopher Glidewell 《Acta Crystallographica. Section C, Structural Chemistry》2001,57(5):534-537
In the title compound, polymeric potassium N‐(6‐amino‐3,4‐dihydro‐3‐methyl‐5‐nitroso‐4‐oxopyrimidin‐2‐yl)glycylglycinate hydrate, (K+·C9H11N6O5?·H2O)n, the hexacoordinate K+ cation is linked to five different anions as well as to the water molecule, with K—O distances in the range 2.617 (2)–2.850 (2) Å. Four of the O atoms in each anion coordinate to K centres, one of them acting as a bridging ligand, leading to the formation of nearly square centrosymmetric K2O2 rings. The structure is analysed in terms of (010) metal–ligand sheets linked by [010] chains of fused rings. 相似文献
13.
Yu‐Ling Wang 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(11):m522-m524
In the title compound, {[Zn(C10H8N2)(H2O)4](C6H5O4S)2·3H2O}n, the Zn atom, the bipyridine ligand and one of water molecules are located on twofold rotation axes. The Zn atom is coordinated by four O atoms from four water molecules and two N atoms from two 4,4′‐bipyridine molecules in a distorted octahedral geometry. The Zn2+ ions are linked by the 4,4′‐bipyridine molecules to form a one‐dimensional straight chain propagating along the c axis. The 4‐hydroxybenzenesulfonate counter‐ions are bridged by the solvent water molecules through hydrogen bonds to generate a two‐dimensional layer featuring large pores. In the crystal packing, the intralayer pores form one‐dimensional channels along the c axis, in which the one‐dimensional [Zn(C10H8N2)(H2O)4]2+ chains are encapsulated. Electrostatic interactions between cations and anions and extensive hydrogen bonds result in a three‐dimensional supramolecular structure. 相似文献
14.
Craig M. Forsyth Douglas R. MacFarlane Pamela M. Dean 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(4):m169-m170
The title compound, also known as sodium nicotinate, Na+·C6H4NO2−, consists of two unique Na atoms coordinated to two unique pyridine‐3‐carboxylate ligands through the N atoms and carboxylate groups. One Na atom and one pyridine‐3‐carboxylate ligand lie on a twofold axis. Extensive Na coordination results in a three‐dimensional array comprising infinite NaO2CR chains linked by intrachain Na—N bonds. 相似文献
15.
Robert J. Hinkle Robert McDonald 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(2):o117-o121
The crystal structures of [(Z)‐2‐methylbut‐1‐en‐1‐yl][4‐(trifluoromethyl)phenyl]iodonium trifluoromethanesulfonate, C12H13F3I+·CF3O3S?, (I), (3,5‐dichlorophenyl)[(Z)‐2‐methylbut‐1‐en‐1‐yl]iodonium trifluoromethanesulfonate, C11H12Cl2I+·CF3O3S?, (II), and bis{[3,5‐bis(trifluoromethyl)phenyl][(Z)‐2‐methylbut‐1‐en‐1‐yl]iodonium} bis(trifluoromethanesulfonate) dichloromethane solvate, 2C13H12F6I+·2CF3O3S?·CH2Cl2, (III), are described. Neither simple acyclic β,β‐dialkyl‐substituted alkenyl(aryl)idonium salts nor a series containing electron‐deficient aryl rings have been described prior to this work. Compounds (I)–(III) were found to have distorted square‐planar geometries, with each I atom interacting with two trifluoromethanesulfonate counter‐ions. 相似文献
16.
Graham Smith Urs D. Wermuth Peter C. Healy 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(9):o555-o558
The crystal structures of two proton‐transfer compounds of 3‐carboxy‐4‐hydroxybenzenesulfonic acid (5‐sulfosalicylic acid) with the aromatic polyamines 2,6‐diaminopyridine [namely 2,6‐diaminopyridinium 3‐carboxy‐4‐hydroxybenzenesulfonate monohydrate, C5H8N3+·C7H5O6S−·H2O, (I)] and 1,4‐phenylenediamine [namely 1,4‐phenylenediaminium 3‐carboxylato‐4‐hydroxybenzenesulfonate, C6H10N22+·C7H4O6S2−, (II)] have been determined. Both compounds feature extensively hydrogen‐bonded three‐dimensional layered polymer structures having significant interlayer π–π interactions between the cation and anion species. In (I), the pyridine N atom of the Lewis base is protonated and forms a direct hydrogen‐bonding interaction with the water molecule, which together with the two amine groups of the cation and the carboxylic acid group of the anion also give additional interactions with O‐atom acceptors of the sulfonate group. In (II), a dianionic species results from deprotonation of both the sulfonic and the carboxylic acid groups, and all available O‐atom acceptors interact with all dication donors, which lie about inversion centres. 相似文献
17.
Zhong‐Lu You Hai‐Liang Zhu Wei‐Sheng Liu 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(12):m620-m622
The title compound, {[Ag2(C4H4N2)3](CF3SO3)2·2H2O}n, is a polymeric pyrazine–silver(I) complex. Each AgI ion is three‐coordinated by N atoms of three different pyrazine ligands, forming a T‐shaped coordination configuration. In the crystal structure, uncoordinated water molecules are linked to trifluoromethanesulfonate anions through intermolecular O—H⋯O hydrogen bonds. There are weaker Ag⋯O interactions involving the water and sulfonate O atoms. 相似文献
18.
Turan K. Yazicilar Omer Andac Yunus Bekdemir Halil Kutuk Veysel T. Yilmaz William T. A. Harrison 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(1):m21-m22
The title compound, alternatively named sodium 6‐nitro‐3H‐1,2,3‐benzoxathiazole 2,2‐dioxide monohydrate, Na+·C6H3N2O5S?·H2O, consists of chains of NaO7 units, with the seven donor‐O atoms coming from two water molecules and five p‐nitrobenzoxasulfamate anions. The seven‐coordinate geometry around the Na+ ion is described as monocapped trigonal prismatic, but with a large distortion from ideal geometry. Each triangular face is defined by one O atom each from a water molecule, a nitro group and a sulfonyl group. An O atom from a sulfonyl group caps one of the square faces of the trigonal prism in an unsymmetrical fashion. The water molecules and one sulfonyl O atom are involved in bridging adjacent units, as is the nitro group of the anion. The sulfamate ions adopt an antiparallel alignment between the NaO7 units and are connected to each other by C—H?O and π–π interactions. The three‐dimensional crystal structure is stabilized by a network of strong O—H?N hydrogen bonds. 相似文献
19.
Miroslav Bo
a Duan Valigura Ingrid Svoboda Hartmut Fuess Wolfgang Linert 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(7):838-839
The title compound, C19H14N5+·ClO4?·H2O, contains planar C19H14N5+ cations, perchlorate anions and water molecules. The two closest parallel cations (plane‐to‐plane distance of 3.41 Å), together with two neighbouring perchlorate anions and two water molecules, form an electrically neutral quasi‐dimeric unit. Two acidic H atoms of the cation, both H atoms of the water molecule, the N atoms of the imidazole rings and three of the four O atoms of the perchlorate anion are involved in the hydrogen‐bonding network within the dimeric unit. The remaining third acidic H atom of the imidazole rings and the water molecules complete a two‐dimensional network of hydrogen bonds, thus forming puckered layers of dimers. The angle between the planes of two neighbouring dimeric units in the same layer is 33.25 (3)°. 相似文献
20.
Eric P. Kelson Proma P. Phengsy Atta M. Arif 《Acta Crystallographica. Section C, Structural Chemistry》2001,57(5):517-519
The aldehyde moiety in the title complex, chloro(2‐pyridinecarboxaldehyde‐N,O)(2,2′:6′,2′′‐terpyridine‐κ3N)ruthenium(II)–chloro(2‐pyridinecarboxylic acid‐N,O)(2,2′:6′,2′′‐terpyridine‐κ3N)ruthenium(II)–perchlorate–chloroform–water (1.8/0.2/2/1/1), [RuCl(C6H5NO)(C15H11N3)]1.8[RuCl(C6H5NO2)(C15H11N3)]0.2(ClO4)2·CHCl3·H2O, is a structural model of substrate coordination to a transfer hydrogenation catalyst. The title complex features two independent RuII complex cations that display very similar distorted octahedral coordination provided by the three N atoms of the 2,2′:6′,2′′‐terpyridine ligand, the N and O atoms of the 2‐pyridinecarboxaldehyde (pyCHO) ligand and a chloride ligand. One of the cation sites is disordered such that the aldehyde group is replaced by a 20 (1)% contribution from a carboxylic acid group (aldehyde H replaced by carboxyl O—H). Notable dimensions in the non‐disordered complex cation are Ru—N 2.034 (2) Å and Ru—O 2.079 (2) Å to the pyCHO ligand and O—C 1.239 (4) Å for the pyCHO carbonyl group. 相似文献