1D heteronuclear coordination polymers of hexacyanocobaltate(III) with 2-hydroxymethylpyridine

被引:0
|
作者
Kekec, Seray [1 ]
Kurkcuoglu, Gunes Suheyla [1 ]
Yesilel, Okan Zafer [2 ]
Sahin, Onur [3 ]
机构
[1] Eskisehir Osmangazi Univ, Fac Sci, Dept Phys, TR-26040 Eskisehir, Turkiye
[2] Eskisehir Osmangazi Univ, Fac Sci, Dept Chem, TR-26040 Eskisehir, Turkiye
[3] Sinop Univ, Fac Hlth Sci, Dept Occupat Hlth & Safety, TR-57000 Sinop, Turkiye
关键词
Hexacyanocobaltate(III); 1D coordination polymer; 2-(hydroxymethyl)pyridine complexes; Cyanide complexes; METAL-ORGANIC FRAMEWORKS; CRYSTAL-STRUCTURE; CARBON-DIOXIDE; CHEMISTRY; COMPLEXES; HEXACYANOFERRATE(III);
D O I
10.1016/j.poly.2024.117096
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Three new hexacyanocobaltate(III) complexes, {[M 2 (hmpy) 4 Co( mu- CN) 4 (CN) 2 ] center dot 2H 2 O} n (M = Cu(II) ( 1 ), Zn(II) ( 2 ) and Cd(II) ( 3 )) were synthesized with 2-hydroxymethylpyridine (hmpy) ligand, and characterized by vibration (FT - IR and Raman) spectral, single crystal X-ray diffraction (SC-XRD) and powder X-ray diffraction (PXRD), thermal and elemental analyses techniques. The crystallographic analyses revealed that cyanide complexes 1 - 3 are infinite one-dimensional coordination polymers. Each M ion is coordinated by two nitrogen and two oxygen atoms from the hmpy ligands and two nitrogen atoms from the cyanide ligands, displaying a distorted octahedral coordination geometry. Similarly, each Co(III) ion is coordinated by six carbon atoms from cyanide ligands to form a distorted octahedral coordination geometry. These complexes form 3D supramolecular networks through O - H & sdot;& sdot;& sdot; O hydrogen bonds and C - H & sdot;& sdot;& sdot; N interactions. Additionally, structural analyses such as metal salts, pH values of the compounds obtained under different conditions were evaluated. A synthesis -structural analyses relation was made from these data.
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页数:6
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