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1.
Abstract The crystal structure of 4,4′-bipyridin-1-ium perchlorate dihydrate, [C10H9N2](ClO4) · 2H2O, is determined by room temperature X-ray diffraction. The compound crystallizes in the triclinic space group P-1 with a = 8.122(3) ?, b = 9.726(3) ?, c = 17.648(6) ?, α = 78.181(4)°, β = 82.797(5)°, γ = 67.439(4)°, Z = 2, V = 1258.4(7) ?3. In the compound, monoprotonated 4,4′-bipyridin-1-ium cations are self-assembled into supramolecular chains along the a-axis through N–H···N hydrogen bonds in a head-to-tail fashion. The chains are stacked via π–π stacking interactions to create two-dimensional sheets. The interlayer space is occupied by the hydrogen-bonded water chains that are linked to the organic sheets via C–H···O interactions and the perchlorate anions that are linked to the water chains and the organic sheets via O–H···O and C–H···O hydrogen bonds, respectively, thus generating a three-dimensional supramolecular architecture. Index Abstract Supramolecular Network via Hydrogen Bonding and π–π Stacking in 4,4′-Bipyridin-1-ium perchlorate dihydrate Jian-Yong Zhang, Ai-Ling Cheng and En-Qing Gao* Monoprotonated 4,4′-bipyridin-1-ium cations are self-assembled into supramolecular chains along the a-axis through N–H···N hydrogen bonds, and these chains are stacked via π–π stacking and hydrogen bond interactions involving water molecules and perchlorate anions.   相似文献   

2.
Abstract Metronidazole (MET-OH), widely used as an antibacterial agent, is found to have some side effects on human bodies. Due to these disadvantages, people have been looking for its modification compounds for substituents. In this article, four MET-OH derivatives were designed, prepared, and structurally characterized by single crystal X-ray diffraction. These compounds are MET-OTs (1), MET-Br (2), MET-Cl (3), and MET-I (4). X-ray structure analyses revealed that, 1 crystallized in the monoclinic system with space group P2 1 /c, with a = 16.1178, b = 7.5473, c = 13.4161 ?, V = 1520.3 ?3, β = 111.3210o and Z = 4. 2 crystallized in the monoclinic system with space group P2 1 /c, with a = 12.079, b = 11.089, c = 6.380 ?, V = 847.1 ?3, β = 97.57o and Z = 4. 3 crystallized in the monoclinic system with space group P2 1 /c, with a = 12.098, b = 11.007, c = 6.295 ?, V = 830.3 ?3, β = 97.886o and Z = 4. 4 crystallized in the triclinic system with space group P1, with a = 6.192, b = 7.740, c = 10.001 ?, V = 457.9 ?3, α = 89.073, β = 86.903, γ = 73.097o and Z = 2. Index Abstract In this article, metronidazole-derived compounds were prepared and structurally characterized by single crystal X-ray diffraction   相似文献   

3.
Abstract 7,4′-bis-(hydroxyl)-8,3′,5′-tris-(hydroxymethyl)isoflavone (I) and its ester were synthesized and examined by IR, element analysis and 1H NMR. The crystal of 7,4′-bis-(acetyl oxide)-8,3′,5′-tris-(acetoxymethyl)isoflavone (II) was studied by X-ray diffraction. (II) crystallizes in the monoclinic with space group P2 1 /c. a = 17.987(3) ?, b = 17.972(3) ?, c = 8.4087(11) ?, β = 97.703(3)°, V = 2693.7(6) ?3 and Z = 4. The molecular structure of the ester consists of a benzopyranone moiety, a phenyl moiety, two acetyl oxides and three acetoxymethyl groups. Hydrogen bonds and aromatic stacking interactions link the ester into a two-dimensional structure. Index Abstract 7,4′-bis-(hydroxyl)-8,3′,5′-tris-(hydroxymethyl)isoflavone and its ester were synthesized and examined by IR, element analysis and 1H NMR. The result of the ester’s crystal structure showed that hydrogen bonding and aromatic π–π stacking assemble the ester into a two-dimensional networking structure.   相似文献   

4.
The title compound has been synthesized by the reaction of 4 with 1,4-dimethoxybenzene. The yielded product 5 was investigated with X-ray crystallographic, NMR, EI-MS, and IR techniques. The crystal belongs to a monoclinic system, space group P21/c with unit cell parameters a = 12.7790(17) Å, b = 21.565(3) Å, c = 12.2544(16) Å, α = 90°, β = 107.014(2)°, γ = 90°, V = 3229.3(7) Å3, Z = 4, D= 1.661, Mr = 807.32, μ = 2.732 mm?1, F(000) = 1632, R= 0.0540 and wR2 = 0.0989.  相似文献   

5.
The title compound, 9,10-dihydro-8,8-dimethyl-2-oxo-2H,8H-benzo[1,2-b:3,4-b']dipyran-9-yl-2-methyl-2-butenoate, C19H20O5, was isolated from the roots of Selinum vaginatum. The compound crystallizes into monoclinic space group P2 1 with unit cell parameters: a = 12.830(2) Å, b = 9.041(1) Å, c = 14.983(1) Å, β = 95.09(1)°, Z = 4. The crystal structure has been determined using direct methods and refined by full-matrix least-squares to a final R value of 0.0529 for 3142 observed reflections. There are two independent molecules, A and B, per asymmetric unit. In both the molecules, the coumarin nucleus is planar. However pronounced differences are observed in the conformation of dihydropyran ring which has a half-chair conformation with an 8β-9α orientation in molecule A and is intermediate between half-chair and sofa in molecule B. Differences also occur in the conformation of the 2-methylbutenoyloxy side chain at C9 due to the different geometry of C–H···π interactions in molecules A and B. Molecules A and B are connected by π–π interactions between their coumarin fragments forming dimers. The dimers interact through C–H···O and C–H···πhydrogen bonds.  相似文献   

6.
7.

Abstract  

Two new antipyrine derivatives, 4-{[1-(5-bromo-2-methoxyphenyl)methylidene]amino}-1,5-dimethyl-2-phenyl-2,3-dihydro-1H-pyrazol-3-one (C19H18BrN3O2, 1) and 4-{[1-(2-hydroxy-3-ethoxyphenyl)methylidene]amino}-1,5-dimethyl-2-phenyl-2,3-dihydro-1H-pyrazol-3-one (C20H21N3O3, 2), were synthesized and structurally characterized by elemental analysis, IR and single crystal X-ray diffractions. Compound 1 crystallizes in the monoclinic space group P21/n with unit cell dimensions a = 6.987(1) ?, b = 27.930(2) ?, c = 9.483(1) ?, β = 109.36(2)°, V = 1745.9(4) ?3, Z = 4, R 1 = 0.0430, and wR 2 = 0.0870. Compound 2 crystallizes in the monoclinic space group P21/c with unit cell dimensions a = 19.523(2) ?, b = 7.466(1) ?, c = 12.954(2) ?, β = 108.797(1)°, V = 1787.5(4) ?3, Z = 4, R 1 = 0.0421, and wR 2 = 0.1032. X-ray structure determinations revealed that the molecules of both compounds display trans configurations about the C=N double bonds. In the crystal structures, molecules are linked together by intermolecular C–H···O hydrogen bonds. Both compounds show strong antibacterial activities.  相似文献   

8.
Abstract  The two 1-aryl-5-methyl-1,2,3-triazole derivatives were prepared by the 1-aryl-5-methyl-1,2,3-triazol-4-carboxylic acids 3. The yielded products 4a–b were confirmed by NMR, MS, IR spectra. We investigated the crystalline structure of compounds 4a and 4b. Compound 4a, C9H8BrN3, Mr = 238.09, crystallizes in the monoclinic space group P2(1)/n with unit cell parameters a = 11.660(2), b = 7.668(2), c = 11.818(2) ?, α = 90.00, β = 116.01(3), γ = 90.00o. V = 949.6(3) ?3, Z = 4, Dx = 1.665 Mg m−3. The final R was 0.0477. Compound 4b, C13H11N3, Mr = 209.25, crystallized in the orthorhombic space group Pbca with unit cell parameters a = 10.373(2) ?, b = 11.691(2) ?, c = 17.579(4) ?, α = 90.00o, β = 90.00o, γ = 90.00o, V = 2131.8(7) ?3, Z = 8, D m = 1.304 Mg m−3. The final R was 0.0565. Index Abstract  The two 1-aryl-5-methyl-1,2,3-triazole derivatives were prepared by the 1-aryl-5-methyl-1,2,3-triazol-4-carboxylic acids 3. The yielded products 4ab were confirmed by NMR, MS, IR spectra. We investigated the crystalline structure of compounds 4a and 4b. Compound 4a, C9H8BrN3, Mr = 238.09, crystallizes in the monoclinic space group P2(1)/n with unit cell parameters a = 11.660(2), b = 7.668(2), c = 11.818(2)  ?, α = 90.00, β = 116.01(3), γ =90.00o. V = 949.6(3) ?3, Z = 4, Dx = 1.665 Mg m−3. The final R was 0.0477. Compound 4b, C13H11N3, Mr = 209.25, crystallized in the orthorhombic space group Pbca with unit cell parameters a = 10.373(2) ?, b = 11.691(2) ?, c = 17.579(4) ?, α = 90.00o, β = 90.00o, γ = 90.00o, V = 2131.8(7) ?3, Z = 8, D m = 1.304 Mg m−3. The final R was 0.0565.   相似文献   

9.
10.
Abstract  The structure of the benznenehexacarboxylic acid (mellitic acid, MA)––phenanthroline (PL) complex (MA−2   2PL+1) consisting of infinite stacks of phenanthroline separated for optimum π–π interactions and sandwiched between MA ribbons suggested a design of models with more significant π–π interactions to produce conducting materials. Phenazine (9,10-diazaanthracene) was considered as a promising choice. The X-ray structure of the complex (MA1–PZ4) from MA−2 and neutral PZ was a major surprise since the complex was not only radically different from MA–PL but also the MA exhibited the rare direct interaction with the base PZ. In a novel arrangement, a continuous chain formed by the linking of the peri carboxylic groups of MA−2 mediated with hydronium ions, H3O+, supports a 4-fold arrangement of four phenazine molecules where four carboxylic groups are engaged in hydrogen bond formation with one of the nitrogens of each PZ. The running chain of MA−2 supports the formation of stacks of phenazine molecules which are separated by ~3.39–3.60 ?, well suited for π–π overlap. The proximal placement of such threaded modules enables their transformation to layered stacks thus possibly enhancing their π–π interactions. Crystal structure parameters are: sp. gr. C2/c, a = 13.2819(23) ?, b = 11.3669(20) ?, c = 33.3757(57) ?, β = 96.515(3), R 1 = 0.0521 for 4,198 data (I > 2σ(I)) and wR 2 = 0.0828 for all 6,194 data. Graphical Abstract  Dark brown thick crystals from MA and phenazine form the sandwiched module (PZ2–MA−2–PZ2) that assembles vertically to produce infinite π–π stacks of PZ. Isabella L. Karle (Senior Scientist) is responsible for the structure analysis and discussion. Subramania Ranganathan (Professor) is responsible for design of molecule and synthesis.  相似文献   

11.
12.
The title compound, cis-[Rh(biq)2Cl2]Cl·3H2O (biq = 2,2′-biquinoline) crystallized in the monoclinic space group P2 1 /n with a = 11.231(2) Å, b = 20.895(4) Å, c = 14.081(3) Å, β = 94.76(3)°, V = 3293.0(11) Å3, D c = 1.565 g cm−3, μ = 0.806 mm−1, F(000) = 1576 and Z = 4. It contains a monomeric [Rh(biq)2Cl2]+ cation, a chloride ion and three molecules of H2O. The rhodium(III) ion is hexa coordinated forming a distorted octahedral arrangement. The mean Rh(III)–N distance for the four Rh(III)–N bonds is 2.0625 Å. The two chloride atoms are bonded in a cis configuration [Rh(III)–Cl bond distances are 2.329(3) and 2.341(4) Å]. The structure shows a curling stacks of cationic complexes interacting via offset-face-to-face (OFF) π–π aryl interaction motif. Water molecules and chloride ions are hydrogen bonded (H2O···H–OH and Cl···H–OH) and links the curling stacks by hydrogen bonding via Rh–Cl···H–OH interactions.  相似文献   

13.
3-(2,4-Dimethylphenyloxymethyl)-3,4-dihydroisocoumarin (C18H18O3) was prepared by the alkylation of o-lithio N-methyl benzamide with 2-(2,4-dimethylphenoxy)methyl oxirane, followed by alkaline hydrolysis. The compound crystallizes in the orthorhombic space group Pbca with unit cell parameters : a = 8.239(2) Å, b = 14.918(5) Å, c = 24.831(9) Å, Z = 8. The crystal structure was solved by direct methods and refined to R = 0.0514 for 1564 observed reflections. The heterocyclic ring adopts a distorted half-chair conformation. Molecules are connected by π–π interactions between phenyl rings of the isocoumarin nucleus forming dimers. Dimers are connected via C–H...O hydrogen bonds forming chains. Further intermolecular C–H...π hydrogen bonds link the dimer chains to form supramolecular structure.  相似文献   

14.
Abstract   N-(1,3-Diphenyl-4-benzal-5-pyrazolone)-salicylidene hydrazone(H2L 1 ) and its zinc complex Zn(HL 1 )2 · 2CH3OH (1) have been synthesized and characterized by elemental analyses, IR spectra, thermal analyses and single-crystal X-ray diffraction studies. The X-ray diffraction analyses of the complex Zn(HL 1 )2 · 2CH3OH (1) and the known compound Zn4(L 2 )4 (2) (H2L 2  = N-(1,3-diphenyl-4-phenylethylene-5-pyrazolone)-salicylidene hydrazone) show that different acyl groups in position 4 of pyrazolones may lead to the different coordination mode of the ligands and distinctive structures of the same central metal Zn(II) complexes, of which 1 is a mononuclear complex while 2 is a tetranuclear complex. Meanwhile, two Zn(II) complexes have different thermal stabilities and fluorescence properties. Graphical Abstract     相似文献   

15.
Syntheses and X-ray structural characterizations of two new luminescent imidazopyridinium derivatives, 2-(phenyl)-N(3)-(4(methyl)phenyl)-imidazo[1,5a] pyridinium perchlorate (1) and 2-(pyridyl)-N(3)-(4-(chloro)phenyl)-imidazo[1,5a] pyridinium perchlorate (2) are reported. The compounds are prepared in one step from N-(4-(methyl)phenyl) pyridine-2-aldimine and N-(4-(chloro)phenyl) pyridine-2-aldimine respectively in a transformation mediated by Mn(OAc)2-KMnO4 mixture. It is found that the molecular structures of the two compounds are similar. In the solid state, 1 forms a three-dimensional network through a series of hydrogen bonds between the cations and anions in the lattice while 2 forms a similar but less extensively linked network. The substitution of hydrogen at the 2-position of the imidazopyridinium ring by phenyl or 2-(pyridyl) affects the nature of their first excited states as detected by changes in their emission and absorption spectra.  相似文献   

16.
Abstract  Two novel benzothiazoles 2-chloro-N-(benzothiazol-2-yl)benzamide (1) and 2-chloro-N-(6-cyanobenzothiazol-2-yl)benzamide (2) were obtained in multistep synthesis. They were characterised by means of IR, 1H- and 13C-NMR spectroscopy and also by single-crystal X-ray diffraction. The compound 1 crystallises with triclinic space group P , a = 9.5923(8) ?, b = 9.8583(8) ?, c = 13.8962(10) ?, α = 89.162(6)°, β = 77.741(7)°, γ = 80.064(7)°, V = 1264.5(2) ?3, Z = 4 and compound 2 crystallises as methanol solvate with monoclinic space group P 21/n, a = 7.5093(9) ?, b = 13.0211(14) ?, c = 16.032(2) ?, β = 92.717(10)°, V = 1565.9(3) ?3, Z = 4. Both crystal structures consist of discrete dimers connected into a three-dimensional network by intermolecular C–H···O and C–H···X (X = Cl or S) hydrogen bonds and by face-to-face π–π stacking interactions. Index Abstract  The synthesis and structure of two novel N-(benzothiazol-2-yl)benzamides. Irena Ćaleta, Dominik Cinčić, GraceKarminski-Zamola and Branko Kaitner. Hydrogen bonds and π–π interactions in N-(benzothiazol-2-yl)benzamides N-(benzothiazol-2-yl)benzamides.   相似文献   

17.
Abstract  The synthesis, NMR and X-ray structure of 4-methyl-6H-pyrido[3,2,1-jk]carbazol-6-one—a potential DNA intercalator are reported. The compound crystallizes in the orthorhombic Pbca space group with unit cell parameters: a = 7.775(8), b = 15.113(7), c = 19.849(7) ?, V = 2332.8(3) ?3, Mr = 233.26 and Z = 8. In the three-dimensional arrangement of the molecules no classical hydrogen bonds were found; weak π···π and C–H···O interactions are responsible for the packing of the molecules in the crystal structure. Index Abstract  In the three-dimensional arrangement of the title compound no classical hydrogen bonds were found; weak π···π and C–H···O interactions are responsible for the packing of the molecules in the crystal structure.   相似文献   

18.
Abstract  The title compound, C18H18BrN3O3S, a derivative of 1,3,4-oxadiazole, crystallizes in the triclinic space group P-1 with unit cell parameters a = 6.8731(3), b = 8.9994(4), c = 15.7099(6) ?, α = 92.779(3)°, β = 130.575(3)°, γ = 107.868(4)°, Z = 2. The dihedral angle between the mean planes of the planar naphthyl and morpholine (chair) rings with the planar oxadiazol ring is 50.1(8) and 76.8(6)°, respectively. The planar naphthyl ring is twisted 52.2(5)° with the mean plane of the morpholine ring. A group of four intermolecular close contacts are observed between a bromine atom and hydrogen atoms from the closely packed naphthyl, morpholine and oxy–methyl groups in the unit cell. These molecular interactions in concert with an additional series of π–π stacking interactions that occur between the center of gravity of the two 6-membered rings of the naphthalene group influence the twist angles of each of these three groups. A MOPAC AM1 calculation of the conformation energy of the crystal structure [226.0128(9) kcal] compared to that of the minimum energy structure after geometry optimization [29.9744(1) kcal] reveals a significantly reduced value. The twist angles of the three groups above also change after the AM1 calculation giving support to the influence of both intermolecular C–H···Br short-range interactions and Cg π–π stacking interactions on these angles which therefore play a role in stabilizing crystal packing. Graphical Abstract  Crystal structure of 5-{[(6-bromonaphthalen-2-yl)oxy]methyl}-3-(morpholin-4-ylmethyl)-1,3,4-oxadiazole-2(3H)-thione, C18H18BrN3O3S, is reported and its geometric and packing parameters described and compared to a MOPAC computational calculation. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

19.
The bis(2-amino-5-methylpyridinium) tetrabromomercurate(II) (C6H9N2)2[HgBr4] salt is triclinic, P1, with the following cell parameters: a=8.060(8) ?, b=9.035(9) ?, c=14.964(10) ?, α=96.032(19)°, β=90.317(15)°, γ=113.32(2)°, V=993.8(15) ?3, with Z=2 formula units. The crystal structure consists of alternating stacks of inorganic HgBr4 2− anions and organic layers of 2-amino-5-methylpyridinium cations parallel to c-axis. The cohesion forces that connect molecules in the organic layers are N···HC hydrogen bonding and π–π stacking. The HgBr4 2− units in the inorganic stacks are attracted via Br···Br intermolecular interactions.Supplementary material CCDC 270395 contains the supplementary crystallographic data. These data can be obtained free of charge via www.ccdc.cam.ac.uk/data_request/cif, or by e-mailing at data_request@ccdc.cam.ac.uk, or by contacting the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; fax: + 44(0)1223-336033.  相似文献   

20.
The structure of the Meisenheimer complex 2′,4′,6′-trinitro-3′,5′-dihydrospiro(1,3-dioxolane-2,8′-cyclohexadienide) C8H6N3O8(?) 1? with tetra-n-butyl-ammonium C16H36 N(+) has been determined by X-ray crystallography. The compound 1 crystallizes in the space group P21 with two molecules (Z′ = 2) in the asymmetric unit. The unit cell parameters are a = 8.728(3) Å, b = 13.760(4) Å, c = 22.882(7) Å, β = 96.17(3)°. Interactions between the Meisenheimer complex and organic cation in 1 involve only a number of weak to moderate C–H?sO bonds. Thus, it has been concluded that the structure 1 represents the geometry of the Meisenheimer complex minimally influenced by the cation. Comparison the structure 1 and the compound 2 (1? K+?H2O) studied previously reveals an interesting structural effect attributed to coordination of potassium cations with the nitro groups of 1?. It leads to notable shortening of the C–N bond lengths of the nitro groups only, while changes of other bond lengths in the Meisenheimer complex are not significant.  相似文献   

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