VS4 with a chain crystal structure used as an intercalation cathode for aqueous Zn-ion batteries

2020 ◽  
Vol 8 (21) ◽  
pp. 10761-10766 ◽  
Author(s):  
Qiancheng Zhu ◽  
Qin Xiao ◽  
Bowen Zhang ◽  
Zhengcong Yan ◽  
Xi Liu ◽  
...  

Vanadium tetrasulfide (VS4) with a beneficial one-dimensional atomic-chain structure is reported to be able to serve as a favorable intercalation cathode material for a high-performance Zn-ion battery.

2008 ◽  
Vol 47 (21) ◽  
pp. 10062-10066 ◽  
Author(s):  
Stanislav Ferdov ◽  
Mario S. Reis ◽  
Zhi Lin ◽  
Rute A. Sá Ferreira

2011 ◽  
Vol 322 ◽  
pp. 369-372
Author(s):  
Zhi Xiang Ji

A chain Ni (II) coordination polymer material was prepared and characterized by elemental analysis and single-crystal X-ray diffraction. It crystallizes in monoclinic, space group C2/c with a = 1.24348(13) nm, b = 1.29477(12) nm, c = 1.51480(17) nm and Dc = 1.401 g•cm-3. The results of structural analysis indicated that each Ni (II) ion forms six-coordinated with nitrogen atoms of pyridine and thiocyanate, and the Ni (II) coordination polymer material formed one dimensional chain structure by the interaction of pyridine rings.


1995 ◽  
Vol 50 (7) ◽  
pp. 993-996 ◽  
Author(s):  
Joachim Pickardt ◽  
Gill-Taik Gong ◽  
Isabella Hoffmeister

The reaction of [2.2.2]cryptand, 4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo- [8 .8 .8 ]hexacosane, with mercuric thiocyanate yields crystals of [Hg(cryptand 222 )][{Hg(SCN )3 }2]. The compound crystallizes monoclinically, space group C2/c, Z = 4, a = 2478.3(12), b = 1540.4(4), c = 1049.4(3) pm, β = 108.77(3)°. In the cation the mercury atom is 8 -coordinated by six oxygen and two nitrogen atoms with distances Hg -N 220(2) pm and Hg -O 268.8(9) pm (mean value). The polymeric anion consists of infinite chains -Hg -SCN -Hg - with bond distances Hg-S 254.2(4) and Hg-N 257(2) pm. Each Hg atom carries two additional terminal SCN ligands, with a mean Hg-S distance o f 244( 1) pm; the distance from Hg to the N atom of an SCN ligand of a neighbouring Hg atom is 300(2) pm, probably indicating an additional, although weak bonding.


1974 ◽  
Vol 29 (1-2) ◽  
pp. 10-12 ◽  
Author(s):  
Horst Sabrowsky ◽  
Welf Bronger ◽  
Dieter Schmitz

The ternary oxide K2PdO2 has been prepared by a reaction between K2O and PdO. X-ray investigations suggest a chain-structure-type which corresponds to that of K2PtS2. The planar oxygen coordinations of the palladium atoms are connected laterally in one dimension. The orthorhombic unit cell (a = 8.523, b = 6.089, c = 3.119 Å) contains two formula units.


2013 ◽  
Vol 830 ◽  
pp. 185-188
Author(s):  
Li Hua Wang ◽  
Zhi Xiang Ji

A new Na (I) complex, [Na (H2O)5(DMF)]·(L) (L=1,5-naphthalenedisulfonate) has been obtained in the CH3CH2OH and a little DMF solution. The complex was characterized by X-ray single crystal diffraction analysis. The results showed that the local geometry around central Na (I) ion can be described a distorted octahedral environment which connected by five water molecules and one DMF molecule. The complex formed one dimensional chain structure through intramolecule and intermolecule hydrogen bonds and π-π stacking.


2014 ◽  
Vol 70 (11) ◽  
pp. m365-m366 ◽  
Author(s):  
Junshan Sun

In the title compound, [Cu2(C7HF4O2)4(C12H8N2)2]·2H2O, the CuIIion has a square-pyramidal coordination sphere. The basal plane consists of two N atoms [Cu—N = 2.008 (3) and 2.032 (3) Å] from the phenanthroline ligand, and of two carboxylate O atoms [Cu—O = 1.942 (3) and 1.948 (3) Å] from two 2,3,4,5-tetrafluorobenzoate anions. Another 2,3,4,5-tetrafluorobenzoate anion provides the apical carboxylate O atom [Cu—O = 2.262 (3) Å] and bridges two CuIIions into a binuclear centrosymmetric dimer. Intramolecular π–π interactions between one of the tetrafluorobenzene rings and the middle of the phenenanthroline rings [3.617 (3) Å] stabilize the molecular configuration. O—H...O hydrogen bonds between the lattice water molecules and the unbound carboxylate O atoms of the metal complexes leads to the formation of a chain structure parallel to [100].


2011 ◽  
Vol 282-283 ◽  
pp. 96-99
Author(s):  
Xi Shi Tai

1D chain Ca(II) coordination polymer was synthesized and characterized by elemental analysis, molar conductance, IR and single-crystal X-ray diffraction, The results of crystal structure show that each Ca(II) ion forms eight-coordinated and the complex formed one dimensional chain structure by the oxygen atoms of carboxylate and water bridged. The antibacterial activity of the Ca(II) coordination polymer and the ligand were tested, the results show that the complex show considerable antibacterial activity against escherichia coli, bacillus subtilis and staphylococcus white.


2000 ◽  
Vol 57 (1) ◽  
pp. m25-m27 ◽  
Author(s):  
Miao Du ◽  
Xian-He Bu ◽  
Lin-Hong Weng ◽  
Xue-Bing Leng ◽  
Ya-Mei Guo

In the crystal structure of the title complex, [Cu(C10H9N3)2](ClO4)2, the CuIIcenter is four-coordinated by the nitrogen donors of the pyridine rings of the ligand, bis(2-pyridyl)amine. The crystal structure reveals that the CuN4coordination sphere has a distorted tetrahedral coordination geometry with a crystallographicC2axis through the CuIIcenter. The perchlorate anions link the complex cations to form a chain structure through C—H...O close contacts and N—H...O hydrogen bonds.


Author(s):  
Chen Zhao ◽  
Yi Li ◽  
Jin-Sheng Xiao ◽  
Peng-Dan Zhang ◽  
Xue-Qian Wu ◽  
...  

The asymmetric unit of the title coordination polymer, [Co(C9H4N2O4)(C2H4N4)] n or [Co(L 1)(L 2)] n , consists of one crystallographically independent Co2+ centre, one L 1 2− ligand and one L 2 ligand (L 1 = 1H-benzimidazole-5,6-dicarboxylic acid, L 2 = 3-amino-1,2,4-triazole). The Co2+ centre is coordinated by two carboxylato-O atoms from two independent L 1 2− ligands and two nitrogen atoms from L 2 and another L 1 ligand. Thus, the metal center adopts a four-coordinate mode, forming a tetrahedral geometry. Interestingly, through the combination of two L 1 2−, two L 2 ligands and two Co2+ ions, a basic repeating unit is constructed, resulting in the formation of a one-dimensional straight chain structure. These chains are further expanded to the final three-dimensional framework via N—H...O hydrogen-bonding interactions.


1990 ◽  
Vol 45 (8) ◽  
pp. 1193-1196 ◽  
Author(s):  
Klaus Brodersen ◽  
Axel Knörr

[Hg2(p-SC6H4NO2)]NO3 is formed by the reaction of p-nitrothiophenol with dimercury(I)-dinitrate in methanol. It crystallizes in the monoclinic space group P21/n with a = 1175.5(9) pm, b = 1079.8(8) pm, c = 876.2(8) pm, β = 110.74(4)° and Z = 4. The crystal structure has been determined by X-ray diffraction and refined to an R-value of 0.052. The results show that the compound exists as a chain structure of [—®S(C6H4NO2)— Hg— Hg—]n with nitrate ions connecting the chains.


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