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1.
Fen Sun Yan‐Tuan Li Zhi‐Yong Wu Yu‐Lan Song Man Jiang 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(12):m584-m586
The structure of the title compound, [Cu2(C12H24N4O2)(C3H4N2)2(CH4O)2](ClO4)2 or [Cu2(dmoxpn)(HIm)2(CH3OH)2](ClO4)2, where dmoxpn is the dianion of N,N′‐bis[3‐(dimethylamino)propyl]oxamide and HIm is imidazole, consists of a centrosymmetric trans‐oxamidate‐bridged copper(II) binuclear cation, having an inversion centre at the mid‐point of the central C—C bond, and two perchlorate anions. The CuII atom has square‐pyramidal coordination geometry involving two N atoms and an O atom from the dmoxpn ligand, an N atom from an imidazole ring, and an O atom from a methanol molecule. The crystal structure is stabilized by O—H⋯O, N—H⋯O and C—H⋯O hydrogen bonds and imidazole π–π stacking interactions to form a three‐dimensional supramolecular array. 相似文献
2.
Yao‐Cheng Shi Bei‐Bei Zhu Xiao‐Bi Jing 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(11):m559-m562
The molecules of N,N′‐bis(2‐pyridylmethyl)ferrocene‐1,1′‐diyldicarboxamide, [Fe(C12H11N2O)2], contain intramolecular N—H⋯N hydrogen bonds and are linked into sheets by three independent C—H⋯O hydrogen bonds. The molecules of the isomeric compound N,N′‐bis(3‐pyridylmethyl)ferrocene‐1,1′‐diyldicarboxamide lie across inversion centres, and the molecules are linked into sheets by a combination of N—H⋯N hydrogen bonds and π–π stacking interactions between pyridyl groups. 相似文献
3.
Jason K. Vohs Duston O. Miller Dan R. Denomme Joseph W. Ziller Bradley D. Fahlman 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(6):m287-m288
In the title compound, [Ga(C12H18N2O2)Cl], the Ga atom is coordinated to a Cl atom and the two imine N and two enolate O atoms of the Schiff base ligand. The literature reveals few examples of a five‐coordinate GaO2N2Cl environment, and only two where both the N and the O atoms are contained within the same ligand. This configuration has the effect of constraining the complex into a square‐pyramidal geometry with less distortion than if formed by two or more ligands. The Ga—N and Ga—O distances are within the ranges expected for Ga–Schiff base derivatives. This compound is also the first group 13 complex containing the N,N′‐ethylenebis(acetylacetoneimine) (acacen) ligand. 相似文献
4.
Jaromír Marek Pavel Kopel Zdenk Trvní
ek 《Acta Crystallographica. Section C, Structural Chemistry》2003,59(12):m558-m560
In the crystal structure of the title compound, [N,N′‐bis(3‐aminopropyl)ethylenediamine‐κ4N,N′,N′′,N′′′][1,3,5‐triazine‐2,4,6(1H,3H,5H)‐trithionato(2−)‐κ2N,S]zinc(II) ethanol solvate, [Zn(C8H22N4)2(C3HN3S3)]·C2H6O, the ZnII atom is octahedrally coordinated by four N atoms [Zn—N = 2.104 (2)–2.203 (2) Å] of a tetradentate N‐donor N,N′‐bis(3‐aminopropyl)ethylenediamine (bapen) ligand and by two S and N atoms [Zn—S = 2.5700 (7) Å and Zn—N = 2.313 (2) Å] of a trithiocyanurate(2−) (ttcH2−) dianion bonded as a bidentate ligand in a cis configuration. The crystal structure of the compound is stabilized by a network of hydrogen bonds. 相似文献
5.
Amen Allah Hajem Basma Trojette Ahmed Driss Tahar Jouini 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(7):793-794
The title compound, N,N,N′,N′‐tetramethylethylenediammonium diaqua(arsenate)(hydrogen arsenate)dizinc(II), (C6H18N2)0.5[Zn2(AsO4)(HAsO4)(H2O)2], is a new zincoarsenate obtained by hydrothermal synthesis. The structure consists of infinite two‐dimensional anionic layers alternating with planes containing centrosymmetric organic diprotonated template N,N,N′,N′‐tetramethylethylenediammonium cations, [H3NC6H12NH3]2+. The latter are interconnected to the framework through hydrogen bonds. 相似文献
6.
Giuseppe Bruno Santo Lanza Francesco Nicol Giuseppe Tresoldi Giuseppe Rosace 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(10):o608-o609
The title compound, alternatively known as N,N′‐dibenzylethanedithioamide, C16H16N2S2, lies about an inversion centre and contains a planar trans‐dithiooxamide fragment characterized by a strong intramolecular hydrogen bond between the S atom and the adjacent amide H atom in the solid state, with an S?N distance of 2.926 (1) Å. The aryl substituent is oriented orthogonal to the mean plane of the trans‐dithiooxamide fragment due to steric hindrance and this effect is discussed. 相似文献
7.
Zoran tefani Anton Meden Martin Lutz Antoine M. M. Schreurs Biserka Koji‐Prodi 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(10):o754-o756
The title compound, rac‐(R,R)‐N,N′‐bis(1‐hydroxy‐3‐methyl‐2‐butyl)oxalamide, C12H24N2O4, crystallizes as a non‐merohedral twin in the triclinic space group . The twin is generated by a twofold rotation about c*. The terminal hydroxy groups of molecules related by an inversion center form hydrogen‐bonded dimers. This hydrogen‐bonding pattern is further extended into a one‐dimensional chain by N—H⋯O hydrogen bonds. 相似文献
8.
Wei Sun Yan‐Tuan Li Zhi‐Yong Wu Ning‐Yu Xiao 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(3):m111-m113
In the crystal structure of the title complex, [Ni2(C10H20N4O2)(C12H12N2)2](ClO4)2 or [Ni(dmaeoxd)Ni(dmbp)2](ClO4)2 {H2dmaeoxd is N,N′‐bis[2‐(dimethylamino)ethyl]oxamide and dmbp is 4,4′‐dimethyl‐2,2′‐bipyridine}, the deprotonated dmaeoxd2− ligand is in a cis conformation and bridges two NiII atoms, one of which is located in a slightly distorted square‐planar environment, while the other is in an irregular octahedral environment. The cation is located on a twofold symmetry axis running through both Ni atoms. The dmaeoxd2− ligands interact with each other via C—H⋯O hydrogen bonds and π–π interactions, which results in an extended chain along the c axis. 相似文献
9.
From extracts of Oncinotis tenuiloba STAPF , two novel polyamine alkaloids, oncinotin-11-one ( 5 ) and oncinotin-12-one ( 6 ), were isolated. Peracetylation of 6 provided the N-acetyl derivative 11 as well as N,N′-diacetylinandenin-10-en-12-one ( 12 ) due to a β-elimination-type side reaction resulting in ring enlargement of 11 (Scheme 1). Deuteration of 12 yielded 13 , showing the same retention time as N,N′-diacetylinandenin-12-one ( 14 ), when co-HPLC was performed together with different keto-isomeric N,N′-diacetylinandeninones. Structure elucidation was extended by Schmidt degradation of 6 and N,N′-diacetyl(10,11-2H2)inandenin-12-one ( 13 ); the degradation products were identified by GC and ESI-MS. The structure of 5 was proposed on the basis of spectroscopic means. Comparison of the spectroscopic data of 5 with those obtained from synthetic material as well as co-HPLC of the N-acetyl derivative 20 together with the corresponding synthetic compound revealed the identity of the substances and confirmed the structure of 5 . Additionally, oncinotine ( 2 ) and neooncinotine ( 3 ) were isolated, separated, and identified with authentic samples by co-HPLC of their N-acetyl derivatives 8 and 9 , respectively. 相似文献
10.
Hydrogen‐bonding network of N,N′‐bis[2‐(tert‐butyldimethylsiloxy)ethyl]ethylenediammonium dichloride
Mei‐Feng Wen Bi‐Ting Lin Chang‐Shuai He Jian‐Zhong Wu 《Acta Crystallographica. Section C, Structural Chemistry》2013,69(7):787-789
The title salt, C18H46N2O2Si22+·2Cl−, has been synthesized by reaction of N,N′‐bis(2‐hydroxyethyl)ethylenediamine with tert‐butyldimethylsilyl chloride. The zigzag backbone dication is located across an inversion centre and the two chloride anions are related by inversion symmetry. The ionic components form a supramolecular two‐dimensional network via N—H...Cl hydrogen bonding, which is responsible for the high melting point compared with the oily compound N,N′‐bis[2‐(tert‐butyldimethylsiloxy)ethyl]ethylenediamine. 相似文献
11.
Guohong Zhang Yongge Wei Ping Wang Hongyou Guo 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(12):m605-m607
The title compound, [Co(C12H6N2O4)(H2O)2]n, has been hydrothermally synthesized and structurally characterized. It consists of polymeric chains of [Co{μ‐(2,2′‐bipyridyl‐3,3′‐dicarboxylato‐κ4N,N′:O,O′)}(H2O)2] units, in which each CoII cation is octahedrally coordinated by two chelating pyridyl N atoms, two chelating carboxyl O atoms from different carboxylate groups of another bipyridyl ligand, and two water molecules as terminal ligands. A crystallographic twofold axis parallel to the chain axis, passes through the Co atom. 相似文献
12.
Francisco J. Martínez‐Martínez Rodrigo E. Rojas‐Prez Efrn V. García‐Bez Herbert Hpfl Itzia I. Padilla‐Martínez 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(9):o699-o701
The ethyl oxamate group, N–C(O)–C(O)–OEt, in the title compound, alternatively called diethyl N,N′:N,N′‐bis(ethylene)dioxamate, C12H18N2O6, can be considered as being composed of two singly bonded amide and ester functionalities. The ethyl oxamate group is not planar. The two carbonyl groups are almost perpendicular, with an oxalyl O=C—C=O torsion angle of −111.34 (17)°. The molecule is located on an inversion centre. Infinite supramolecular tapes, propagating along the b axis, are formed through soft C—H⋯O interactions which form a centrosymmetric R(12) motif. 相似文献
13.
Anne‐Christine Chamayou Chaitali Biswas Ashutosh Ghosh Christoph Janiak 《Acta Crystallographica. Section C, Structural Chemistry》2009,65(8):m311-m313
The crystal structure of the title compound, [Cu(C6H4NO2)(C2H3O2)(C3H4N2)(H2O)]·0.87H2O, has a square‐pyramidal‐coordinated CuII centre (the imidazole is trans to the picolinate N atom, the acetate is trans to the picolinate –CO2 group and the aqua ligand is in a Jahn–Teller‐elongated apical position) and has two symmetry‐independent molecules in the unit cell (Z′ = 2), which are connected through complementary imidazole–picolinate N—H...O hydrogen bonding. The two partially occupied solvent water molecules are each disordered over two positions. The disordered solvent water molecules, together with pseudosymmetry elements, support the notion that a crystal structure with multiple identical chemical formula units in the structural asymmetric unit (Z′ > 1) can represent a crystal `on the way', that is, a kinetic intermediate form which has not yet reached its thermodynamic minimum. Neighbouring molecules form π–π stacks between their imidazole and picolinate N‐heterocycles, with centroid–centroid distances in the range 3.582 (2)–3.764 (2) Å. 相似文献
14.
Ligia R. Gomes John Nicolson Low Ana S. M. C. Rodrigues James L. Wardell Camillo H. da Silva Lima Marcus V. N. de Souza 《Acta Crystallographica. Section C, Structural Chemistry》2013,69(5):549-555
The compounds N′‐benzylidene‐N‐methylpyrazine‐2‐carbohydrazide, C13H12N4O, (IIa), N′‐(2‐methoxybenzylidene)‐N‐methylpyrazine‐2‐carbohydrazide, C14H14N4O2, (IIb), N′‐(4‐cyanobenzylidene)‐N‐methylpyrazine‐2‐carbohydrazide dihydrate, C14H11N5O·2H2O, (IIc), N‐methyl‐N′‐(2‐nitrobenzylidene)pyrazine‐2‐carbohydrazide, C13H11N5O3, (IId), and N‐methyl‐N′‐(4‐nitrobenzylidene)pyrazine‐2‐carbohydrazide, C13H11N5O3, (IIe), have dihedral angles between the pyrazine rings and the benzene rings in the range 55–78°. These methylated pyrazine‐2‐carbohydrazides have supramolecular structures which are formed by weak C—H...O/N hydrogen bonds, with the exception of (IIc) which is hydrated. There are π–π stacking interactions in all five compounds. Three of these structures are compared with their nonmethylated counterparts, which have dihedral angles between the pyrazine rings and the benzene rings in the range 0–6°. 相似文献
15.
In the title compound, catena‐poly[[[N,N′‐bis(pyridin‐3‐ylmethyl)‐[1,1′‐biphenyl]‐4,4′‐dicarboxamide]chloridozinc(II)]‐μ‐[1,1′‐biphenyl]‐4,4′‐dicarboxylato‐[[N,N′‐bis(pyridin‐3‐ylmethyl)‐[1,1′‐biphenyl]‐4,4′‐dicarboxamide]chloridozinc(II)]‐μ‐[N,N′‐bis(pyridin‐3‐ylmethyl)‐[1,1′‐biphenyl]‐4,4′‐dicarboxamide]], [Zn2(C14H8O4)Cl2(C26H22N4O2)3]n, the ZnII centre is four‐coordinate and approximately tetrahedral, bonding to one carboxylate O atom from a bidentate bridging dianionic [1,1′‐biphenyl]‐4,4′‐dicarboxylate ligand, to two pyridine N atoms from two N,N′‐bis(pyridin‐3‐ylmethyl)‐[1,1′‐biphenyl]‐4,4′‐dicarboxamide ligands and to one chloride ligand. The pyridyl ligands exhibit bidentate bridging and monodentate terminal coordination modes. The bidentate bridging pyridyl ligand and the bridging [1,1′‐biphenyl]‐4,4′‐dicarboxylate ligand both lie on special positions, with inversion centres at the mid‐points of their central C—C bonds. These bridging groups link the ZnII centres into a one‐dimensional tape structure that propagates along the crystallographic b direction. The tapes are interlinked into a two‐dimensional layer in the ab plane through N—H...O hydrogen bonds between the monodentate ligands. In addition, the thermal stability and solid‐state photoluminescence properties of the title compound are reported. 相似文献
16.
Activation of Sulfur Dioxide by Bis[N,N′‐diisopropylbenzamidinato(−)]silicon(II): Synthesis of Neutral Six‐Coordinate Silicon(IV) Complexes with Chelating O,O′‐Sulfito or O,O′‐Dithionito Ligands
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Konstantin Junold Felix M. Mück Claudia Kupper Johannes A. Baus Dr. Christian Burschka Prof. Dr. Reinhold Tacke 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(40):12781-12785
The neutral six‐coordinate silicon(IV) complexes 2 and 3 (mixture of cis‐ 3 and trans‐ 3 ) were synthesized by reaction of the donor‐stabilized silylene bis[N,N′‐diisopropylbenzamidinato(?)]silicon(II) ( 1 ) with SO2. Compounds 2 and 3 are the first silicon(IV) complexes with chelating sulfito or dithionito ligands, and 3 is even the first molecular compound with a chelating dithionito ligand. Compounds 2 and 3 were structurally characterized by crystal structure analyses and multinuclear NMR spectroscopic studies in the solid state and in solution. 相似文献
17.
Gavin Blewett Catharine Esterhuysen Martin W. Bredenkamp Klaus R. Koch 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(12):o862-o864
The title compound, C14H16N2O4S2, is the first reported X‐ray crystallographic structure determination of a bipodal O‐alkyl N‐benzoylthiocarbamate. This compound crystallizes in a cis‐S,O orientation (Z,Z′ configuration), with the two S/O moieties anti relative to one another, as indicated by the twofold rotation axis located at the center of the benzene ring. 相似文献
18.
Sergio Baggio M. Enriqueta Díaz de Vivar Ricardo Baggio María Teresa Garland 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(5):m195-m198
The title compound, [Cd2(SO3)2(C18H12N6)2]·8H2O, is a dimer built up around a symmetry center, where the sulfite anion displays a so far unreported coordination mode in metal‐organic complexes; the anion binds as a μ2‐sulfite‐κ4O,O′:O′,O′′ ligand to two symmetry‐related seven‐coordinate CdII cations, binding through its three O atoms by way of two chelate bites with an O atom in common, which acts as a bridge. The cation coordination is completed by a 2,4,6‐tri‐2‐pyridyl‐1,3,5‐triazine ligand acting in its usual tridentate mode. 相似文献
19.
The Trihydrochloride Monohydrate of N -(Pyrid-2-ylmethyl)ethylenediamine- N , N′ , N′ -triacetic Acid and its Lanthanum(III) Complex We report the results of the investigation of N-(pyrid-2-ylmethyl)ethylenediamine-N,N′,N′-triacetic acid (H3pedta) and its complexes with rare earth metal ions. The X-ray crystal structures of H3pedta · 3 HCl · H2O and of the lanthanum(III) complex [La(pedta)(H2O)] · 2 H2O were determined. The complex forms a polymer, lanthanum(III) has coordination number 10, one water molecule is coordinated. The water degradation of H3pedta · 3 HCl · H2O and of the complex was investigated by thermoanalysis. Luminescence studies of the corresponding europium(III) complex in aqueous solution show three coordinated water molecules. 相似文献
20.
Vnia Denise Schwade Eliandro Faoro Ernesto Schulz Lang 《Acta Crystallographica. Section C, Structural Chemistry》2016,72(7):525-529
Aroylhydrazones of ortho‐hydroxy aldehydes are Schiff base ligands that typically coordinate as a chelate in an O,N,O′‐manner. Dinuclear complexes are normally observed, with the phenolate O atom acting as the bridging atom. The switchable protonation state of the tridentate N′‐(2‐hydroxybenzylidene)benzohydrazide (H2sabhz) ligand can lead to variations in the resulting supramolecular structure. The title compound, [Pb2(C14H10N2O2)2], was prepared by the reaction of [Pb(OAc)2]·3H2O (OAc is acetate) with the benzoylhydrazone derivative of salicylaldehyde, i.e. H2sabhz, in the presence of triethylamine in methanol. In the crystal structure, each PbII atom of the dimer has an NO3 coordination environment, with one sabhz ligand coordinating in an O,N,O′‐manner and with the second sabhz ligand coordinating via the bridging phenolate O atom, since the dimers are located on a centre of inversion. It has been found that the dimers are connected by Pb…N interactions, resulting in a two‐dimensional supramolecular network which shows the [32.52,3.53] net topology. The s2 electron pair of the PbII ion clearly influences the observed intermolecular interactions. 相似文献