Structural diversification and single-crystal-to-single-crystal transformation of alkaline earth metal-based MOFs regulated by solvent effect

CrystEngComm ◽  
2016 ◽  
Vol 18 (16) ◽  
pp. 2864-2872 ◽  
Author(s):  
Xi Wang ◽  
Min Hu ◽  
Jia-Yue Tian ◽  
Chun-Sen Liu
1976 ◽  
Vol 31 (12) ◽  
pp. 1604-1606 ◽  
Author(s):  
Hk. Müller-Buschbaum ◽  
W. Schmachtel

Mixed crystals of the formulae CaGaAlO4 (1) and CaGa0.5Al1.5O4 (2) were investigated by X-ray single crystal work. 1 shows a tetrahedral orientation like that of CaGa2O4 (monokl.), 2 another one of CaAl2O4. A discussion of the different polyhedral arrangement of the stuffed tridymite structures is given.


2020 ◽  
Vol 235 (4-5) ◽  
pp. 137-141
Author(s):  
Maximilian K. Reimann ◽  
Rainer Pöttgen

AbstractThe copper-rich intermetallic compounds CaCu9Mg2 and SrCu9Mg2 were synthesized by induction melting of the elements and subsequent annealing in a muffle furnace. CaCu9Mg2 and SrCu9Mg2 crystallize with the TbCu9Mg2 type structure, space group P 63/mmc, which is a ternary ordered variant of CeNi3. The polycrystalline samples were characterized through their X-ray powder patterns. The CaCu9Mg2 structure was refined from single-crystal X-ray diffraction data. a = 504.13(9), c = 1622.5(3) pm, wR2 = 0.0635, 302 F2 values and 19 variables. The two striking coordination polyhedra in the CaCu9Mg2 structure are Ca@Cu18Mg2 and Mg@Cu12Mg3Ca. These polyhedra condense to layers which are stacked in ABA′B′ sequence. The X-ray data give no hint for Ca/Mg mixing.


2021 ◽  
Author(s):  
Omer Yurdakul ◽  
Dursun Ali Köse ◽  
Zarife Sibel Şahin ◽  
Onur Şahin

Abstract Mixed-ligand coordination compounds containing neutral nicotinamide and monoanionic diphenate organic molecules of alkaline earth metal cations, Mg2+ (I), Ca2+ (II), Sr2+ (III) and Ba2+ (IV) were synthesised. Chemical composition analysis, single crystal XRD, spectroscopic and thermal analysis methods were used to determine the structural properties of the compounds obtained. According to the data obtained from single-crystal XRD analysis of the Mg2+ complex, the coordination environment of the metal cation was surrounded by four aqua and two nicotinamide ligands to form a distorted octahedral geometry. The charge balance of the complex sphere was provided by two diphenate ligands placed mono-anionically outside the coordination sphere. The structure is a salt type complex. Since crystals suitable for single crystal structure analysis of other metal cations complexes (II, III and IV) could not be formed, the structural properties were tried to be explained by chemical composition analysis, spectroscopic and thermal analysis methods. Accordingly, it is thought that the coordination circles of metal cations are octal and all ligands (two aqua, two neutral nicotinamide and two monoanionic-double-toothed diphenate) coordinate with the metal in the coordination sphere. The geometries of the complexes are thought to be of distorted cubic structure.


2010 ◽  
Vol 65 (9) ◽  
pp. 1077-1083 ◽  
Author(s):  
Christine Walbaum ◽  
Ingo Pantenburg ◽  
Gerd Meyer

Salts of alkaline earth metal cations sequestered in dibenzo-18-crown-6 (Db18c6) and benzo-15- crown-5 (B15c5), respectively, with I5−, I7− and I82− as the anions, have been synthesized and their crystal structures determined by single-crystal X-ray diffraction. [Ca(Db18c6)(H2O)3](I5)2- (Db18c6)(H2O) (1): monoclinic, P21 (no. 4), a = 1322.1(2), b = 1849.1(2), c = 1344.0(2) pm, β = 114.70(1)◦, V = 2985.2(6) × 106 pm3, Z = 2; [Sr(B15c5)2](I7)2 (2): triclinic, P1 (no. 2), a = 973.9(5), b = 1244.0(5), c = 1293.3(5) pm, α = 115.28(1), β = 90.18(1), γ = 104.57(1)◦, V = 1360.2(10) × 106 pm3, Z = 2; [Ba(Db18c6)2]I8 (3): orthorhombic, Pbcn (no. 60), a = 1452.0(2), b = 1924.6(2), c = 1912.1(2) pm, V = 5343.3(10) × 106 pm3, Z = 4. Compound 1 contains two crystallographically independent V-shaped pentaiodide anions, I5 −, which are linked to dimers by weak interionic contacts. The unusual heptaiodide anion, I7−, in 2 can be described as a V-shaped pentaiodide unit, which is connected to a slightly widened iodine molecule to give the rare Z form. Secondary bonding distances lead to almost planar ten-membered iodine rings, which are connected through common edges to form ribbons with staircase-like folding. 3 is built of sandwich-like cations and centrosymmetric octaiodide anions, I82−. An inspection for secondary contacts reveals that the iodine substructure of 3 consists of essentially isolated octaiodide units.


2019 ◽  
Author(s):  
Nga Phung ◽  
Hans Köbler ◽  
Diego Di Girolamo ◽  
Thi Tuyen Ngo ◽  
Gabrielle Sousa e Silva ◽  
...  

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