Luminescent zinc(II) and cadmium(II) complexes based on 2-(4,5-dimethyl-1H-imidazol-2-yl)pyridine and 2-(1-hydroxy-4,5-dimethyl-1H-imidazol-2-yl)pyridine
摘要:
Complexes (ZnLCl2)-Cl-1, (CdLCl2)-Cl-1, ZnL (2) (1) Cl-2 (center dot)1.5H(2)O, CdL (2) (1) Cl-2 (center dot)2H(2)O, CdL (2) (1) Cl-2 (MeOH)-Me-center dot center dot H2O [L-1 = 2-(4,5-dimethyl-1H-imidazol-2-yl)pyridine] and inner-complex compounds ZnL (2) (2) center dot 2H(2)O, CdL (2) (2) [HL2 = 2-(1-hydroxy-4,5-dimethyl-1H-imidazol-2-yl)pyridine] were synthesized. The complexes exhibit bright photoluminescence in the blue region of the spectrum, with the intensity exceeding this characteristic of the compounds L-1 and HL2. Compound L-1 in aqueous solution is a potential chemosensor for the determination of zinc and cadmium.
Luminescent zinc(II) and cadmium(II) complexes based on 2-(4,5-dimethyl-1H-imidazol-2-yl)pyridine and 2-(1-hydroxy-4,5-dimethyl-1H-imidazol-2-yl)pyridine
摘要:
Complexes (ZnLCl2)-Cl-1, (CdLCl2)-Cl-1, ZnL (2) (1) Cl-2 (center dot)1.5H(2)O, CdL (2) (1) Cl-2 (center dot)2H(2)O, CdL (2) (1) Cl-2 (MeOH)-Me-center dot center dot H2O [L-1 = 2-(4,5-dimethyl-1H-imidazol-2-yl)pyridine] and inner-complex compounds ZnL (2) (2) center dot 2H(2)O, CdL (2) (2) [HL2 = 2-(1-hydroxy-4,5-dimethyl-1H-imidazol-2-yl)pyridine] were synthesized. The complexes exhibit bright photoluminescence in the blue region of the spectrum, with the intensity exceeding this characteristic of the compounds L-1 and HL2. Compound L-1 in aqueous solution is a potential chemosensor for the determination of zinc and cadmium.
Synthesis of 2-aryl(hetaryl)-1-hydroxyimidazoles by the reaction of aliphatic 1,2-hydroxylamino oximes with aromatic and heteroaromatic aldehydes
作者:B. A. Selivanov、A. Ya. Tikhonov
DOI:10.1007/s11172-013-0169-z
日期:2013.5
A reaction of aliphatic 1,2-hydroxylamino oximes bearing the hydroxylamino group at the secondary carbon atom with aromatic and heteroaromatic aldehydes in acetic acid leads to the corresponding 1-hydroxy-2-aryl(hetaryl)-4,5-dialkylimidazoles in high yields. α-Aryl(hetaryl)-nitrones initially formed by the condensation of 1,2-hydroxylamino oximes with aldehydes are quantitatively converted to the corresponding imidazoles.
Cu(II) and Zn(II) complexes of N-hydroxyimidazoles were synthesised by reacting simple metal perchlorate salts with the imidazole ligand in alcohol and formulated with a metal:ligand ratio of 1:2. The X-ray crystal structures of five complexes (four Cu(II) and one Zn(II)) were obtained and each showed the two trans, N-hydroxyimidazole ligands forming six-membered, chelate rings with the metal. Both of the NO chelating, neutral N-hydroxyimidazole ligands are in the zwitterion form, with the uncoordinated imidazole imine N atom being protonated and the oxime O atom deprotonated. In the solid state the complexes form hydrogen-bonded supramolecular structures. (c) 2007 Elsevier Ltd. All rights reserved.
Zinc(II) complexes with an imidazolylpyridine ligand: luminescence and hydrogen bonding
作者:Mark B. Bushuev、Boris A. Selivanov、Natalia V. Pervukhina、Dmitrii Yu. Naumov、Lilia A. Sheludyakova、Marianna I. Rakhmanova、Alexsei Ya. Tikhonov、Stanislav V. Larionov
DOI:10.1080/00958972.2014.892589
日期:2014.2.16
ZnLCl and [H2L](2)[ZnCl4], based on 2-(1-hydroxy-4,5-dimethyl-1H-imidazol-2-yl)pyridine (HL), have been synthesized. There is a short intraionic O-H center dot center dot center dot N hydrogen bond between the hydroxyimidazolyl and pyridyl of H2L+ cations (N center dot center dot center dot O 2.608(2) angstrom) in the structure of [H2L](2)[ZnCl4]. The formation of this rather strong hydrogen bond is confirmed by IR spectroscopy through a broad band at 3200-2200 cm(-1) and a band at 1655 cm(-1). HL crystallizes in the form of a hemihydrate, HL center dot 0.5H(2)O. HL assemble into infinite helical chains due to N-H center dot center dot center dot O intermolecular hydrogen bonds between the NH of imidazole and O of the N-oxide (O center dot center dot center dot N 2.623(2) angstrom). An unusual mid-IR pattern with three broad bands at 3373, 2530, and 1850 cm(-1) is typical for strong hydrogen bonds, explained by resonance-assisted hydrogen bonding occurring in the helical chains. On cooling to 5 K, noticeable changes in the IR spectra of [H2L](2)[ZnCl4] and HL center dot 0.5H(2)O were observed. ZnLCl and [H2L](2)[ZnCl4] exhibit bright photoluminescence with maxima of emission at 458 nm (for ZnLCl) and 490 nm (for [H2L](2)[ZnCl4]).
Luminescent zinc(II) and cadmium(II) complexes based on 2-(4,5-dimethyl-1H-imidazol-2-yl)pyridine and 2-(1-hydroxy-4,5-dimethyl-1H-imidazol-2-yl)pyridine
作者:M. B. Bushuev、B. A. Selivanov、N. V. Pervukhina、D. Yu. Naumov、M. I. Rakhmanova、L. A. Sheludyakova、A. Ya. Tikhonov、S. V. Larionov
DOI:10.1134/s1070363212110230
日期:2012.11
Complexes (ZnLCl2)-Cl-1, (CdLCl2)-Cl-1, ZnL (2) (1) Cl-2 (center dot)1.5H(2)O, CdL (2) (1) Cl-2 (center dot)2H(2)O, CdL (2) (1) Cl-2 (MeOH)-Me-center dot center dot H2O [L-1 = 2-(4,5-dimethyl-1H-imidazol-2-yl)pyridine] and inner-complex compounds ZnL (2) (2) center dot 2H(2)O, CdL (2) (2) [HL2 = 2-(1-hydroxy-4,5-dimethyl-1H-imidazol-2-yl)pyridine] were synthesized. The complexes exhibit bright photoluminescence in the blue region of the spectrum, with the intensity exceeding this characteristic of the compounds L-1 and HL2. Compound L-1 in aqueous solution is a potential chemosensor for the determination of zinc and cadmium.