Anion-dependent self-assembly of copper coordination polymers based on pyrazole-3,5-dicarboxylate and 1,2-di(4-pyridyl)ethylene

2017 ◽  
Vol 46 (14) ◽  
pp. 4806-4815 ◽  
Author(s):  
Fatima Klongdee ◽  
Jaursup Boonmak ◽  
Sujittra Youngme

Anion-dependent self-assembly of new ternary copper coordination networks containing pyrazole-3,5-dicarboxylate and 1,2-di(4-pyridyl)ethylene with anion exchange studies.

1999 ◽  
Vol 54 (12) ◽  
pp. 1510-1516 ◽  
Author(s):  
B. Roßenbeck ◽  
W. S. Sheldrick

The discrete complex [(Cul)2 (pyzCN)4] (1) and the coordination polymers 1∞ [CuI(pyzCN)] (2) and 3∞ [(CuX)3 (pyzCN)2] (3, 4; X = Br, Cl) may be prepared from the respective copper(I) halide CuX and 2-cyanopyrazine (pyzCN) by self-assembly in acetonitrile solution at 100- 120°C. Whereas 2 exhibits 1 [Cul] staircase double chains as its characteristic substructure, the three-dimensional networks of 3 and 4 contain single zigzag CuX strings. The influence of the copper(I) halide on both the connectivity pattern and the dimensionality of a resulting coordination network is particularly apparent for the 1:1 complexes 1∞ [CuI(pymMe)] (5), 3∞ [(CuBr)3(pymMe)3] (6) and 2∞ [CuCl(pymMe)] (7), which were generated by reaction of CuX with 4-methylpyrimidine (pymMe) under reaction conditions similar to those above.


2007 ◽  
Vol 13 (29) ◽  
pp. 8131-8138 ◽  
Author(s):  
Ying Wang ◽  
Peng Cheng ◽  
You Song ◽  
Dai-Zheng Liao ◽  
Shi-Ping Yan

2020 ◽  
Vol 8 (1) ◽  
pp. 149-166
Author(s):  
Rasel Mukred ◽  
Samir Osman Mohammed

Three new homobinuclear nanosized supramolecular copper coordination polymers are hydrothermally synthesized by self-assembly reaction of L-tyrosine (Tyr), terephthalic acid (H2bdc), pyromellitic acid (H4btec) and benzimidazole (Hbzim) with copper chloride salt to generate with formula [[Cu2(tyr)2(bzim)2(Cl)2(H2O)2]]n 1, [[Cu2(bdc)2(bzim)2(H2O)6].3H2O]n 2 and [Cu2(H2btec)(bzim)(H2O)6].2H2O]n 3, which have been investigated by elemental analysis, molar conductivity and magnetic measurements, FT-IR and UV-Vis spectroscopy, (TGA/DTA) thermal analysis and X-ray powder diffraction(XRPD) analysis as well as MM2 theoretical calculations. The magnetic moment and electronic spectra of the complexes are certainly indicating the octahedral geometries. Thermal analysis of the complexes confirms the suggested structures and thermal stability. The results of the XRPD analysis and the average nanosized values of the complexes have nanosized supramolecular polymers in the triclinic system. The MM2 theoretical calculations are supported by the proposed structures.


CrystEngComm ◽  
2019 ◽  
Vol 21 (47) ◽  
pp. 7249-7259 ◽  
Author(s):  
Li-Na Zhu ◽  
Zhao-Peng Deng ◽  
Li-Hua Huo ◽  
Shan Gao

The self-assembly of d10 metal salts and two racemic bis(pyridyl) diamine ligands generates ten complexes, showing diverse helical and wavelike chains, (4,4) layers, as well as 3D sqc and uog nets.


CrystEngComm ◽  
2015 ◽  
Vol 17 (38) ◽  
pp. 7363-7371 ◽  
Author(s):  
Suryabhan Singh ◽  
Rajendran Karthik

Cu(i)/Ag(i) sulfonate CPs have been synthesized and characterized. One of the CPs exhibits a reversible anion exchange for perchlorate and permanganate.


2021 ◽  
Author(s):  
Haeri Lee ◽  
Jihun Han ◽  
Dongwon Kim ◽  
Ok-Sang Jung

Systematic interconversion between trigonal prisms [Pd3X6L2] (X- = Cl-, Br-, and I-) and cubic cages [Pd6L8]12+(X-)12 (X- = BF4- with CF3SO3-) via anion exchange was established. Self-assembly of K2PdX4 (X-...


2009 ◽  
Vol 65 (3) ◽  
pp. m139-m142 ◽  
Author(s):  
Rajesh Koner ◽  
Israel Goldberg

The title compound, (5,10,15,20-tetra-4-pyridylporphyrinato)zinc(II) 1,2-dichlorobenzene disolvate, [Zn(C40H24N8)]·2C6H4Cl2, contains a clathrate-type structure. It is composed of two-dimensional square-grid coordination networks of the self-assembled porphyrin moiety, which are stacked one on top of the other in a parallel manner. The interporphyrin cavities of the overlapping networks combine into channel voids accommodated by the dichlorobenzene solvent. Molecules of the porphyrin complex are located on crystallographic inversion centres. The observed two-dimensional assembly mode of the porphyrin units represents a supramolecular isomer of the unique three-dimensional coordination frameworks of the same porphyrin building block observed earlier. The significance of this study lies in the discovery of an additional supramolecular isomer of the rarely observed structures of metalloporphyrins self-assembled directly into extended coordination polymers without the use of external ligand or metal ion auxiliaries.


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