Abstract:Mononuclear and coordination polymer compounds of 2,2 0 -dimethyl-4,4 0 -bithiazole (dm4bt) ligand have been prepared by metallation of dm4bt with Cd(NO 3 ) 2 Á 4H 2 O and CdCl 2 Á H 2 O. The compounds were characterized by IR, 1 H NMR, UV-Vis spectroscopy, and X-ray crystallography. The structural study of [Cd(dm4bt) 2 (NO 3 ) 2 ] Á H 2 O (1) shows that the complex is a monomeric seven-coordinate (CdN 4 O 3 ) cadmium(II)-bithiazole system with two bidentate dm4bt and mono and bidentate nitrates. The structure… Show more
“…We have previously reported the synthesis and crystal structure of dm4bt and also its zinc, mercury, cadmium, thallium, and copper complexes resulting from ZnCl 2 , HgCl 2 , [28][29][30][31]. In all of these cases, we obtained monomeric compounds with [Zn(dm4bt)Cl 2 ], and [{Cu(dm4bt) 2 (NO 3 )}NO 3 ].…”
Copper complexes, [Cu(dm4bt)Cl 2 (DMSO)] (1) and [{Cu(dm4bt)(H 2 O)(tpht)} Á H 2 O] n (2) (dm4bt, 2,2 0 -dimethyl-4,4 0 -bithiazole; tpht, terephthalate), have been synthesized and their crystal structures were determined by X-ray crystallography. Complex 1 was prepared from a reaction of CuCl 2 Á 2H 2 O with dm4bt and terephthalic acid in a mixture of methanol, water, and DMSO. Complex 2 was prepared from a reaction of CuCl 2 Á 2H 2 O with dm4bt, terephthalic acid, and ethylene diamine in a mixture of methanol and water. The two complexes were characterized by IR, UV-Vis spectroscopy, and single-crystal structure. Complex 2 was also characterized by electron paramagnetic resonance spectra. Complex 1 is a monomer while 2 is a coordination polymer. This copper tpht polymer has a cis-configuration of tpht rings opposed to zigzag chains with anti-configuration usually reported in the literature.
“…We have previously reported the synthesis and crystal structure of dm4bt and also its zinc, mercury, cadmium, thallium, and copper complexes resulting from ZnCl 2 , HgCl 2 , [28][29][30][31]. In all of these cases, we obtained monomeric compounds with [Zn(dm4bt)Cl 2 ], and [{Cu(dm4bt) 2 (NO 3 )}NO 3 ].…”
Copper complexes, [Cu(dm4bt)Cl 2 (DMSO)] (1) and [{Cu(dm4bt)(H 2 O)(tpht)} Á H 2 O] n (2) (dm4bt, 2,2 0 -dimethyl-4,4 0 -bithiazole; tpht, terephthalate), have been synthesized and their crystal structures were determined by X-ray crystallography. Complex 1 was prepared from a reaction of CuCl 2 Á 2H 2 O with dm4bt and terephthalic acid in a mixture of methanol, water, and DMSO. Complex 2 was prepared from a reaction of CuCl 2 Á 2H 2 O with dm4bt, terephthalic acid, and ethylene diamine in a mixture of methanol and water. The two complexes were characterized by IR, UV-Vis spectroscopy, and single-crystal structure. Complex 2 was also characterized by electron paramagnetic resonance spectra. Complex 1 is a monomer while 2 is a coordination polymer. This copper tpht polymer has a cis-configuration of tpht rings opposed to zigzag chains with anti-configuration usually reported in the literature.
“…We also obtained . We were not able to make complexes bearing two dm4bt ligands for chloride salts of Zn, Cd, Hg, and Cu, but in complexes from nitrate salts two dm4bt ligands coordinated to Cd [14], Tl [15], and Cu.…”
Section: Crystal Structure Determination and Refinementmentioning
confidence: 89%
“…We recently introduced the coordination chemistry of 2,2 0 -dimethyl-4,4 0 -bithiazole (dm4bt) with Zn(II), Hg(II) [13], Cd(II) [14] and Tl(III) [15], in addition to the nickel bithiazole reported previously [16]. We report here the synthesis and characterization of two copper complexes with dm4bt.…”
{CuCl(dm4bt)} 2 -Cl) 2 ] (1) (dm4bt ¼ 2,2 0 -dimethyl-4,4 0 -bithiazole) was prepared from the reaction of CuCl 2 Á 2H 2 O with 2,2 0 -dimethyl-4,4 0 -bithiazole in methanol; [Cu(dm4bt) 2 NO 3 ](NO 3 ) (2) was prepared from the reaction of Cu(NO 3 ) 2 Á 3H 2 O with 2,2 0 -dimethyl-4,4 0 -bithiazole in methanol. Both complexes were characterized by IR, UV-Vis spectroscopy, and single-crystal structure. The structure of 1 consists of centrosymmetric dimeric [{CuCl(dm4bt)}(-Cl)], in which two chloro ligands bridge the coppers forming a fourmembered ring; a terminal chloride and a bidentate chelating bithiazole complete five coordination at each Cu(II) in a highly distorted trigonal-bipyramidal geometry. The mononuclear structure 2 consists of a Cu(II), two 2,2 0 -dimethyl-4,4 0 -bithiazoles, one monodentate nitrate and one uncoordinated nitrate in a highly distorted square pyramid.
“…For example, a Co(II) complex and a Ni(II) complex with 2,2 0 -diamino-4,4 0 -bithiazole (DABT) have both been found to be effective inhibitors of DNA synthesis in tumor cells [9,10], and multinuclear Fe(II) and Cu(II) complexes with a DABT Schiff base have been found to be excellent soft magnetic materials [11][12][13][14]. We have also introduced the coordination chemistry of 2,2 0 -dimethyl-4,4 0 -bithiazole (dm4bt) with Zn(II), Hg(II) [19], Cd(II) [20], Tl(III) [21], and Cu(II) [22].…”
The complex [Fe(C 6 H 4 N 2 S 2 ) 3 ] 2? (NO 3 -) 2 was prepared from the reaction of 4,4 0 -bithiazole with Fe(NO 3 ) 3 Á9H 2 O in methanol. It was characterized by IR, UV-Vis, luminescence, 1 H NMR and 13 C NMR spectroscopy, and X ray crystallography. The structure was solved in the orthorhombic space group P2 1 2 1 2 1 with a = 12.1500(5), b = 12.8434(6), c = 16.2222(7) Å , V = 2531.43(19) Å 3 , Z = 4, and with wR 2 = 0.0897.
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