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Qin-Hui Luo

Publications and source records attributed to Qin-Hui Luo.

7 recordsLinked to original sources
PubMed2006

Incorporation of triazacyclononane into the metal phosphonate backbones.

This paper reports the syntheses and crystal structures of a manganese and a uranyl phosphonate based on 1,4,7-triazacyclononane-1,4,7-triyl-tris(methylenephosphonic acid), namely, Mn3{C9N3H18(PO3)3}(H2O)6 x 1.5 H2O (1) and UO2{C9N3H19(PO3H)3} x H2O (2). Compound 1 shows a unique layer structure where the hydrophobic triazacyclononane moieties all reside on one side of the inorganic backbone of the manganese phosphonate layer while the hydrophilic coordinated water molecules reside on the other side. In compound 2, the triazacyclononane moieties are immobilized on the inorganic backbone of the uranyl phosphonate chains. The magnetic properties of compound 1 and the ion exchange properties of compound 2 have been studied.

Journal Article↗
PubMed2004

A study on the mimics of Cu-Zn superoxide dismutase with high activity and stability: two copper(II) complexes of 1,4,7-triazacyclononane with benzimidazole groups.

Two copper(II) complexes [CuL(1)Cl]ClO(4) and [CuL(2)MeCN](ClO(4))(2)xH(2)O were synthesized (L(1)= 1-(benzimidazole-2-ylmethyl)-1,4,7-triazacyclononane, L(2)= 1,4-bis(benzimidazole-2-ylmethyl)-1,4,7-triazacyclonone). The benzimidazole groups were N-substituents of tacn, and the complexes are more stable than their parents. They are able to catalyse the dismutation of superoxide anion in aqueous solutions at physiological pH and in bovine serum albumin solution (0.5 mg ml(-1)). X-ray structure analysis and EPR and electronic spectra show that the structure of complex is more similar to the Cu(II) centre of Cu(2)Zn(2)SOD than that. Comparing with other Cu(II) complexes, the complex possesses both high SOD activity and highly thermodynamic stability.

Benzimidazoles↗
PubMed2004

A study on oxygen insertion in dinuclear silver cryptates.

Two novel silver(I) cryptates are reported in this paper. [Ag(2)(L(1)O)](ClO(4))(2).H(2)O and [Ag(2)L(1)](ClO(4))(2).1.5H(2)O were synthesized by the condensation of tris (3-aminopropyl) amine with m-phthalaldehyde in the presence of silver(i) ion, under aerobic and anaerobic conditions, respectively. (The ligand L(1)O represents the oxygen insertion product of L(1).) Cryptates 1, 2 and their hydrogenated ligand H(12)(L(1)O) 3 and H(12)L(1) 4 (obtained by reduction of the cryptates) were investigated by electrospray mass spectroscopy (ES-MS). 1 and 2 were also decomposed by HCl treatment and their products were separated and identified by HPLC and ES-MS. Our experiments show that cryptate 2 is able to activate dioxygen that results in quantitative aliphatic hydroxylation of L(1) on one of its HC=N bonds. Crystal structure analysis shows an interesting difference between 1 and 2 in that 1 is an oxygenated and 2 is a non-oxygenated cryptate. Up to date, ligand hydroxylation has not been achieved in silver(I) complex-O(2) systems.

Journal Article↗
PubMed2002

Heterodinuclear cryptates [EuML(dmf)](ClO(4))(2)(M=Ca, Cd, Ni, Zn): tuning the luminescence of europium(III) through the selection of the second metal ion.

Four heterodinuclear cryptates [EuML(dmf)](ClO(4))(2) (M=Ca, Cd, Ni, Zn) were synthesized by a two-step method (L denotes deprotonated anionic cryptand synthesized by condensation of tris(2-aminoethyl)amine with 2,6-diformyl-4-chlorophenol). The ES-MS spectra of the four cryptates and the crystal structure of [EuNiL(dmf)](ClO(4))(2) x MeCN confirm that a strict dinuclear Eu(III)-M(II) entity exits in the cryptates. The cyclic voltammetry and luminescence spectral investigations indicate that the introduction of second metal ions into the mononuclear Eu(III) cryptate result in a negative shift of the redox potential of Eu(III) and a change in luminescence intensity of Eu(III). The cryptate [EuML(dmf)](ClO(4))(2) was shown to quench the emission of Eu(III) when M=Ni and to enhance the emission of Eu(III) when M=Ca, Cd, and Zn in the sequence: mononuclear<Eu-Ca<Eu-Cd<Eu-Zn.

Europium↗
PubMed2002

A study on Cu2Co2SOD and Co2Co2SOD by voltammetry and thin-layer spectroelectrochemistry.

The electrochemistry of Co(2)Co(2)SOD and Cu(2)Co(2)SOD on a pyrolytic graphite electrode (PGE) without using mediators was investigated by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The reversible and quasi-reversible voltammetric responses were observed for Co(2)Co(2)SOD and Cu(2)Co(2)SOD, respectively. Their formal redox potentials and electron numbers involved in electrode reactions were obtained, and are in agreement with those by spectroelectrochemistry (SEC).

Carbon↗