Synthesis and Crystal Structure of the Lead(II) Complex with 5-Hydroxyisophthalic Acid

2013 ◽  
Vol 634-638 ◽  
pp. 451-455
Author(s):  
Yan Yang ◽  
Liu Ting Yan ◽  
Rong Huan Qin ◽  
Wen Gui Duan

The lead(II) Complex constructed with 5-hydroxyisophthalic acid, [Pb3(5-hipa)2]n•4H2O(1), (5-hipa = 5-hydro- xyisophthalic acid) has been synthesized by hydrothermal methods and structurally characterized by elemental analysis, IR and X-ray single crystal diffraction. In trinuclear symmetrical complex 1, Pb1 is four-coordinated, Pb2 and Pb3 are three-coordinated by 5-nitroisophthalic acid groups, respectively, which is further connected through intermolecular hydrogen bonds resulting in a three-dimensional (3D) network.

2011 ◽  
Vol 418-420 ◽  
pp. 59-62
Author(s):  
Yan Yang ◽  
Liu Ting Yan ◽  
Xiao Li ◽  
Rong Huan Qin ◽  
Wen Gui Duan

The Cobalt (Ⅱ) Complex constructed with 5-nitroisophthalic acid and 2,2’-bibenzimidazole, [Co(H2bibim)2( 5-nipa)] (1), (H2bibim =2,2’-bibenzimidazole, 5-nipa=5-nitroisophthalic acid) have been synthesized by hydrothermal methods and structurally characterized by elemental analysis, IR and X-ray single crystal diffraction. Complex 1 has six coordinated by two H2bibim ligands and one 5-nitroisophthalic acid groups that is further connected though intermolecular hydrogen bonds and resulting in a three-dimensional (3D) network.


2011 ◽  
Vol 396-398 ◽  
pp. 959-962
Author(s):  
Yan Yang ◽  
Liu Ting Yan ◽  
Xiao Li ◽  
Rong Huan Qin ◽  
Wen Gui Duan

The Cobalt (II) Complex constructed with 5-nitroisophthalic acid and 2,2’-bibenzimidazole, [Co(H2bibim)3](5-nipa)•H2O (1), (H2bibim =2,2’-bibenzimidazole, 5-nipa=5-nitroisophthalic acid) have been synthesized by hydrothermal methods and structurally characterized by elemental analysis, IR and X-ray single crystal diffraction. Complex 1 possesses distorted CoN6 octahedrals linked by the H2bibim ligands in a bidentate chelating mode and the 5-nitroisophthalic acid groups act as counterions, and there exists a 2D supramolecular network linked by intermolecular O−H•••O and N−H•••O hydrogen-bonding interactions.


Author(s):  
Dohyun Moon ◽  
Jong-Ha Choi

The crystal structure of the hydrated title salt, C22H48N4 4+·4Cl−·4H2O (C22H48N4 = H4 L = 3,14-diethyl-2,6,13,17-tetraazoniatricyclo[16.4.0.07,12]docosane), has been determined using synchrotron radiation at 220 K. The structure determination reveals that protonation has occurred at all four amine N atoms. The asymmetric unit comprises one half of the macrocyclic cation (completed by crystallographic inversion symmetry), two chloride anions and two water molecules. The macrocyclic ring of the tetracation adopts an exodentate (3,4,3,4)-D conformation. The crystal structure is stabilized by intermolecular hydrogen bonds involving the macrocycle N—H groups and water O—H groups as donors, and the O atoms of the water molecules and chloride anions as acceptors, giving rise to a three-dimensional network.


2013 ◽  
Vol 454 ◽  
pp. 276-279
Author(s):  
Li Hua Wang ◽  
Zhi Xiang Ji

The crystals of one-dimensional chained polymer constructed by 3-indolepropionic acid and 2,2-bipyridinium have been synthesized by evaporation from ethanol solution. The crystal structure of one-dimensional chained polymer was determined by X-ray single crystal diffraction analysis. The results shows that the polymer belongs to monoclinic, space group P2(1)/c, a = 5.2557(11) Å, b = 12.249(2) Å, c = 21.467(4) Å, V = 1380.1(5) Å3, Z = 2, Mr = 531.58, De = 1.279 g/cm3, T = 293(2) K, F (000) = 558, R = 0.1136 and wR = 0.3376. The compound forms one-dimensional chained polymer through hydrogen bonds. 3D network structure was constructed by the interaction of the one-dimensional chained polymer.


2020 ◽  
Vol 76 (10) ◽  
pp. 1675-1678
Author(s):  
Xuan Tu Nguyen ◽  
Thuy Quynh Le ◽  
Tra My Bui Thi ◽  
Dinh Hung Mac ◽  
Thai Thanh Thu Bui

The synthesis and crystal structure of peptide 6,6′-dimethyl biphenyl hybrid are described. The title compound was synthesized by reaction between 6,6′-dimethyl-[1,1′-biphenyl]-2,2′-dicarbonyl dichloride in CH2Cl2, amine HN–proline–phenylalanine–alanine–COOMe and Et3N at 273 K under N2 atmosphere and characterized by single-crystal X-ray diffraction. The asymmetric unit contains one peptide molecule and a quarter of a water molecule. A disorder of a methyl and methoxycarbonyl group of one alanine residue is observed with occupancy ratio 0.502 (6):0.498 (6). The structure is consolidated by intra- and intermolecular hydrogen bonds.


2015 ◽  
Vol 34 (1) ◽  
pp. 101
Author(s):  
Alparslan Karadogan ◽  
Ahmet Karadag ◽  
Veysel T. Yilmaz

A new nickel(II) saccharinate (sac) complex containing <em>N</em>,<em>N</em>′-bis(2-hydroxyethyl)ethylenediamine (bishydeten), [Ni(bishydeten)<sub>2</sub>](sac)<sub>2</sub>, has been synthesized and characterized by elemental analysis, FTIR and single crystal X-ray diffraction. The title complex consists of a [Ni(bishydeten)<sub>2</sub>]<sup>2+</sup> cation and two sac anions. In the complex cation, the nickel(II) ion is coordinated by two neutral bishydeten ligands, leading to a distorted octahedral NiN<sub>4</sub>O<sub>2</sub> coordination, while both sac anions remain outside the coordination sphere. In the crystal, the complex cations and sac anions are connected by an extensive network of N–H∙∙∙N, N–H∙∙∙O, O–H∙∙∙O and C–H∙∙∙O hydrogen bonds into a three-dimensional supramolecular lattice.


Author(s):  
Valeriia Zozulia ◽  
Vladimir Ovchynnikov ◽  
Tetiana Slyva ◽  
Julia Rusanova ◽  
Volodymyr Amirkhanov

The novel binuclear Zn(II) complex of general formula Zn2(L)4(CH3OH)2 where HL is N-[bis(benzylamino)phosphoryl]-2,2,2-trichloroacetamide has been synthesized from non-aqueous solution and characterized by elemental analysis, FTIR and NMR spectroscopy as well by X-ray single crystal diffraction. This complex represents the third example of binuclear complexes with this ligand within four known for today.


Author(s):  
Alagappa Rammohan ◽  
Amy A. Sarjeant ◽  
James A. Kaduk

The crystal structure of tricaesium citrate monohydrate, 3Cs+·C6H5O73−·H2O, has been solved and refined using laboratory X-ray single-crystal diffraction data, and optimized using density functional techniques. This compound is isostructural to the K+and Rb+compounds with the same formula. The three independent Cs cations are eight-, eight-, and seven-coordinate, with bond-valence sums of 0.91, 1.22, and 1.12 valence units. The coordination polyhedra link into a three-dimensional framework. The hydroxy group forms the usualS(5) hydrogen bond with the central carboxylate group, and the water molecule acts as a donor in two strong hydrogen bonds.


2014 ◽  
Vol 1025-1026 ◽  
pp. 717-722
Author(s):  
Hua Mei Guo ◽  
Qian Wu ◽  
Yu Feng Li

A malononitrile derivative, 6-Amino-5,5,7-tricyano-3,3a,4,5-tetrahydro-2H-indene-4- Spirocyclopentane was synthesized in ethanol with malononitrile and cyclopentanone as raw materials. It was characterized by X-ray single crystal diffraction analysis.The crystal of the title complex belongs to Triclinic, P21/c space group with a=6.4687(13)Å, b=8.9901(18)Å, c=12.004(2)Å, α=93.55(3) deg, β=91.86(3) deg, γ=92.25(3) deg. V=695.8(2)Å3, Z=2, F(000)=278 and final R1=0.0524,WR2=0.1497. X-ray analysis reveals that The cyclohexene ring has a distorted half-chair conformation and the cyclopentene and cyclopentane rings adopt envelope conformations. The dihedral angles between planar fragments of the cyclohexene and cyclopentene rings and of the cyclohexene and cyclopentane rings are 10.67 (7) and 87.33 (3)°, respectively. In the crystal, intermolecular N-HN hydrogen bonds link the molecules into infinite chains running in the [10] direction.


2014 ◽  
Vol 2014 ◽  
pp. 1-6 ◽  
Author(s):  
Ramadan M. El-mehdawi ◽  
Abdussalam N. EL-dewik ◽  
Mufida M. Ben-Younes ◽  
Fathia A. Treish ◽  
Ramadan G. Abuhmaiera ◽  
...  

The title complex was isolated as a red solid from the reaction of 4-(salicylaldiminato)antipyrine, HL, and cobalt (II) acetate in ethanol. The complex has been characterized by elemental analysis, FTIR, UV-Vis, and X-ray single crystal diffraction. Two crystallographically different cationic units, A and B, of the title complex are found. Both units are essentially isostructural; nevertheless, small differences exist between them. Both units contain four cobalt atoms arranged at the corners of distorted cubane-like core alternatively with phenoxy oxygen of the Schiff base. In both cases, one cobalt binds to three coordinated sites from the corresponding tridentate Schiff base ligand, and the fourth one was bonded by the acetate oxygen, and the fifth and the sixth donor sites come from the phenolate oxygen of another Schiff base ligand.


Sign in / Sign up

Export Citation Format

Share Document