Two-Dimensional Sheets of Tetragonal Copper(II) Lattices: X-Ray Crystal Structure and Magnetic Properties of[Cu(C6O4Cl2)(C4H4N2)]n

1994 ◽  
Vol 33 (17) ◽  
pp. 1759-1761 ◽  
Author(s):  
Satoshi Kawata ◽  
Susumu Kitagawa ◽  
Mitsuru Kondo ◽  
Isamu Furuchi ◽  
Megumu Munakata
Polyhedron ◽  
2010 ◽  
Vol 29 (1) ◽  
pp. 188-195 ◽  
Author(s):  
Laura Cañadillas-Delgado ◽  
Oscar Fabelo ◽  
Jorge Pasán ◽  
Miguel Julve ◽  
Francesc Lloret ◽  
...  

2015 ◽  
Vol 72 (1) ◽  
pp. 21-27 ◽  
Author(s):  
Ying-Lian Qin ◽  
Chen-Zhong Yao ◽  
Bin-Wu Yang ◽  
Jian-Fang Qin ◽  
Qiao-Juan Gong

Cyanide as a bridge can be used to construct homo- and heterometallic complexes with intriguing structures and interesting magnetic properties. These ligands can generate diverse structures, including clusters, one-dimensional chains, two-dimensional layers and three-dimensional frameworks. The title cyanide-bridged CuII–CoIIIheterometallic compound, [CuIICoIII(CN)6(C4H11N2)(H2O)]n, has been synthesized and characterized by single-crystal X-ray diffraction analysis, magnetic measurement, thermal study, vibrational spectroscopy (FT–IR) and scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM–EDS). The crystal structure analysis revealed that it has a two-dimensional grid-like structure built up of [Cu(Hpip)(H2O)]3+cations (Hpip is piperazinium) and [Co(CN)6]3−anions that are linked through bridging cyanide ligands. The overall three-dimensional supramolecular network is expanded by a combination of interlayer O—H...N and N—H...O hydrogen bonds involving the coordinated water molecules and the N atoms of the nonbridging cyanide groups and monodentate cationic piperazinium ligands. A magnetic investigation shows that antiferromagnetic interactions exist in the title compound.


2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Runmei Ding ◽  
Zixin He ◽  
Meilin Wang ◽  
Danian Tian ◽  
Peipei Cen

AbstractBased on 2-(4-pyridyl)-terephthalate (H2pta) and oxalate ligands, two new lanthanide-containing coordination polymers (CPs), [Tb(pta)(C2O4)0.5(H2O)2)]·2H2O (1) and [Sm(pta)(C2O4)0.5(H2O)2)]·2H2O (2), have been synthesized under solvothermal conditions. The structures of both 1 and 2 have been determined by single-crystal X-ray diffraction. Infrared, elemental analysis, powder X-ray diffraction and thermogravimetric analysis data are also presented. The crystals of 1 and 2 exhibit isostructural layer-like networks, crystallizing in the triclinic space group P$‾{1}$. The layers are further stabilized and associated into 3D architectures through hydrogen bonding. Remarkably, the CPs 1 and 2 exhibit excellent water stability and remarkable thermostability with thermal decomposition temperatures of more than 420 °C.


2013 ◽  
Vol 52 (12) ◽  
pp. 7087-7093 ◽  
Author(s):  
Miguel Cortijo ◽  
Santiago Herrero ◽  
Reyes Jiménez-Aparicio ◽  
Emilio Matesanz

2003 ◽  
Vol 58 (10) ◽  
pp. 971-974 ◽  
Author(s):  
U. Ch. Rodewald ◽  
R.-D. Hoffmann ◽  
R. Pöttgen ◽  
E.V. Sampathkumaran

Single crystals of Eu2PdSi3 were obtained from an arc-melted sample that was further annealed at 1020 K for seven days in a silica tube. The structure of Eu2PdSi3 was refined from single crystal X-ray diffractometer data: P6/mmm, a = 831.88(12), c = 435.88(9) pm, wR2 = 0.1175, 265 F2 values, and 13 variable parameters. It crystallizes with the U2RuSi3 structure, a superstructure of the AlB2 type. The palladium and silicon atoms form a planar two-dimensional [PdSi3] network. The two crystallographically different europium atoms have hexagonal prismatic coordinations Eu1Si12 and Eu2Pd4Si8. The Pd-Si and Si-Si distances within the [PdSi3] network are 244 and 236 pm, respectively.


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