The Crystal Structure of Cesium Dodecachlorotrirhenate-(III), a Compound with a New Type of Metal Atom Cluster

1963 ◽  
Vol 2 (6) ◽  
pp. 1166-1171 ◽  
Author(s):  
J. A. Bertrand ◽  
F. A. Cotton ◽  
W. A. Dollase
ChemInform ◽  
2010 ◽  
Vol 24 (29) ◽  
pp. no-no
Author(s):  
F. A. COTTON ◽  
X. FENG ◽  
M. SHANG ◽  
Z. S. SUN
Keyword(s):  

1993 ◽  
Vol 32 (8) ◽  
pp. 1321-1326 ◽  
Author(s):  
F. Albert Cotton ◽  
Xuejun Feng ◽  
Maoyu Shang ◽  
Zhong Sheng Sun
Keyword(s):  

Author(s):  
Süheyla Özbey ◽  
F. B. Kaynak ◽  
M. Toğrul ◽  
N. Demirel ◽  
H. Hoşgören

AbstractA new type of inclusion complex, S(–)-1 phenyl ethyl ammonium percholorate complex of R-(–)-2-ethyl - N - benzyl - 4, 7, 10, 13 - tetraoxa -1- azacyclopentadecane, has been prepared and studied by NMR, IR and single crystal X-ray diffraction techniques. The compound crystallizes in space group


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Xinzhao Xia ◽  
Lixian Xia ◽  
Geng Zhang ◽  
Yuxuan Jiang ◽  
Fugang Sun ◽  
...  

Abstract In this work, a new type of zinc(II) coordination polymer {[Zn(HIDC)(BBM)0.5]·H2O} n (Zn-CP) was synthesized using 4,5-imidazoledicarboxylic acid (H3IDC) and 2,2-(1,4-butanediyl)bis-1,3-benzimidazole (BBM) under hydrothermal conditions. Its structure has been characterized by infrared spectroscopy, elemental analysis and single crystal X-ray diffraction analysis. The Zn(II) ion is linked by the HIDC2− ligand to form a zigzag chain by chelating and bridging, and then linked by BBM to form a layered network structure. Adjacent layers are further connected by hydrogen bond interaction to form a 3-D supramolecular framework. The solid-state fluorescence performance of Zn-CP shows that compared with free H3IDC ligand, its fluorescence intensity is significantly enhanced.


1989 ◽  
Vol 156 ◽  
Author(s):  
E. Takayama-Muromachi

ABSTRACTSince the discovery of the high-Tc superconductor in the La-Ba-Cu-O system [1], a great deal of experimental and theoretical effort have been made to clarify the nature of the Cu-based oxides. In order to elucidate mechanism of the high-Tc superconductivity, discovery of a new type of superconductor is no doubt of great importance. Recently, Akimitsu et al. found a new oxide superconductor in the Nd-Ce-Sr-Cu-O system [2]. Soon after their discovery, the superconducting phase was isolated and identified [3]. It has a tetragonal cell with space group P4/nmm and has a structure closely related to but different from the K2NiF4− or T'-Nd2CuO4− -type structure. Although, Tc of the Nd-Ce-Sr-Cu oxide is not so high (ca. 20 K) compared with the 1–2–3 or Bi(Tl)-based superconductors, it has aroused interest widely due to a very simple crystal structure. In this article, I will discuss superconductivity and crystal chemistry of the Nd-Ce-Sr-Cu oxide. Also, various compounds isostructural to it will be presented.


2015 ◽  
Vol 71 (5) ◽  
pp. m104-m105
Author(s):  
Sowmianarayanan Parimala ◽  
Parasuraman Selvam

In the unsymmetrical title vanadyl complex, [V(C9H9NO2)(C7H5O2)O], one of the ligands (2-formylphenol) is disordered over two sets of sites, with an occupancy ratio of 0.55 (2):0.45 (2). The metal atom is hexacoordinated, with a distorted octahedral geometry. The vanadyl O atom (which subtends the shortest V—O bond) occupies one of the apical positions and the remaining axial bond (the longest in the polyhedron) is provided by the (disordered) formyl O atoms. The basal plane is defined by the two phenoxide O atoms, the iminoalcoholic O and the imino N atom. The planes of the two benzene rings are almost perpendicular to each other, subtending an interplanar angle of 84.1 (2)° between the major parts. The crystal structure features weak C—H...O and C—H...π interactions, forming a lateral arrangement of adjacent molecules.


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