Anion recognition and sensing of ruthenium(II) and cobalt(II) sulfonamido complexes.

A series of artificial receptors, based on a sulfonamido system, have been designed and synthesized. The interaction of these receptors with biologically important anions was determined by UV-vis, (1)H NMR titration and electrochemical experiments. Results indicate that these receptors show high recognition abilities for fluoride (F(-)) or acetate (AcO(-)), moderate affinities for dihydrogen phosphate (H(2)PO(4)(-)) or hydroxyl (OH(-)) and almost no affinities for chloride (Cl(-)), bromide (Br(-)) or iodide (I(-)).

A highly selective naked-eye colorimetric sensor for acetate ion based on 1,10-phenanthroline-2,9-dicarboxyaldehyde-di-(p-substitutedphenyl-hydrazone).

A new and simple colorimetric sensor with high selectivity for acetate ion based on 1,10-phenanthroline-2,9-dicarboxyaldehyde-di-(p-substitutedphenylhydrazone) receptor 2 has been synthesized. The selectively binding ability of receptor 2 to acetate ion over other anions tested was demonstrated by UV-vis absorption spectroscopy in DMSO. Comparing with other anions studied, the UV-vis absorption spectrum in dimethyl sulfoxide shows significant response toward acetate ion with high selectivity, and meanwhile dramatic color change is observed from yellow to green in the presence of acetate ion (5 x 10(-6)mol/L).

A simple and efficient colorimetric anion sensor based on a thiourea group in DMSO and DMSO-water and its real-life application.

An efficient colorimetric sensor with a thiourea moiety as binding sites and p-nitrophenylhydrazine as a signaling unit has been synthesized by only one single-step procedure. Selectivity for anions with the distinct geometry (tetrahedral, trigonal planar and spherical) has been investigated in dry DMSO and even in DMSO/H(2)O (95:5, v/v) solutions through the naked-eye experiment, UV-vis titration and (1)H NMR titration techniques. In particular, the fluoride of toothpaste can be detected qualitatively by the sensor 1.

A phenylhydrazone-based indole receptor for sensing acetate.

A novel phenylhydrazone-based indole anion receptor is synthesized by a simple method, and the receptor binds acetate anions with good selectivity in DMSO solution, which is related to the structure of the receptor matching with the anion. The binding properties of the host are examined by UV-vis changes. The color changes of the host upon the addition of a variety of structurally different anions were also utilized as nake-eyed recognization (from orange to purple, first figure), The hydrogen bonds between recognization sites (phenylhydrazone and indole N-H) and anions were determined on the basis of (1)H NMR experiments.

A simple and efficient colorimetric anion receptor for H(2)PO(4)(-).

A novel and neutral anion sensor bearing a urea group as binding sites and 2,4-di nitrophenylhydrazine unit as a molecular architecture and a chromophore was synthesized and the visible color changes, the UV-vis and (1)H NMR spectral responses toward anions were assessed.

Effects of the receptors bearing phenol group and copper(II) on the anion recognition and their analytical application.

Two novel artificial receptors based on diamide and bearing phenol group and copper(II) have been synthesized. Their anion-binding properties are evaluated for F(-), Cl(-), Br(-), I(-), AcO(-), H(2)PO(4)(-) and OH(-) by UV-vis and (1)H NMR titration experiments to further elucidate the impact of phenol group and copper(II) on the chemistry of anion-recognition. Results indicate that the interacted model of fluoride anion with receptor 1 is different from other anions and the (1)H NMR signals of receptor 2 occur changes after the addition of fluoride anion.

Studies on synthesis and anion recognition properties of (3'-nitrobenzo)[2,3-d]-(3''-nitrobenzo)[9,10-d]-1,4,8,11-tetraazacyclotetradecane-5,7,12,14-tetraone.

A novel artificial receptor, (3'-nitrobenzo)[2,3-d]-(3''-nitrobenzo)[9,10-d]-1,4,8,11-tetraazacyclotetradecane-5,7,12,14-tetraone, was designed and synthesized. The interactions of this receptor with different anions were determined by UV-vis and (1)H NMR titration experiments, and their affinity constants to different anions were compared with those of other similar/different systems. The results indicated that this receptor showed a high selective and recognitive ability for F(-) among F(-), Cl(-), Br(-), I(-), AcO(-), OH(-), and H(2)PO(4)(-).

Synthesis, characterization and biological activity of lanthanum(III) complexes containing 2-methylene-1,10-phenanthroline units bridged by aliphatic diamines.

Two novel lanthanum(III) complexes containing 2-methylene-1,10-phenanthroline units bridged by aliphatic diamines were synthesized and characterized by elemental analysis, IR, NMR, thermal analysis and conductance measurements. They have been assayed for anticancer activity in vitro against HL-60 (human leukocytoma) cells, PC-3MIE8 (human prostate carcinoma) cells, BGC-823 (human stomach carcinoma) cells, MDA-MB-435 (human galactophore carcinoma) cells, Bel-7402 (human liver carcinoma) cells, and Hela (human cervix carcinoma) cells. The results show that the two complexes exhibit good cytotoxic activities against different cell lines in general, especially more effective than cisplatin against Bel-7402, BGC-823 and MDA-MB-435 cell lines.

Spectroscopic properties, catalytic activities and mechanism studies of [(TpPh)Co(X)(CH3OH)m] . nCH3OH: bicarbonate dehydration in the presence of inhibitors.

Two inhibitor-containing 'half-sandwich' cobalt(II) complexes [(TpPh)Co(X)(CH3OH)m] x nCH3OH ((TpPh) = hydrotris (3-phenylpyrazolyl)borate; 1: X- = N3-, m = 1, n = 2; 2: X- = NCS-, m = 0, n = 0) have been synthesized and used as the catalysts in the bicarbonate dehydration reaction. The structures of 1 and 2 were determined by X-ray diffraction analysis, which shows that N3- and NCS- coordinate to the Co(II) ions of 1 and 2, respectively, with the Co-N bond lengths of 1.992(6) A and 1.

The different roles of metal ions and water molecules in the recognition and catalyzed hydrolysis of ATP by phenanthroline-containing polyamines.

The phenanthroline bridging polyaza ligands L1, L2 and L3 can selectively and strongly bind nucleotides at physiological pH, and hence accelerate the hydrolysis rate of the bound ATP. It is interesting that a phosphoramidate intermediate at 2.88 ppm (should be added 5.

Kinetic study of the effects of inhibitors on the catalyzed dehydration of HCO3- by copper(II) complexes [TpPh]CuX (X- = OH-, N3-, NCS-).

A series of half-sandwich copper(II) complexes [TpPh]CuX ([TpPh] = hydrotris(3-phenyl-pyrazolyl)borate; X- = OH- (1), N3- (2), NCS- (3)) have been synthesized as models for carbonic anhydrase. The structure of 3 was determined by X-ray diffraction analysis. Crystals of 3 (C37H30BCuN9S) are triclinic, space group P1 with a = 11.

Spectroscopy, cytotoxicity and DNA-binding of the lanthanum(III) complex of an L-valine derivative of 1,10-phenanthroline.

The interaction of the lanthanum(III) La(III)-L (L=N,N'-bis-(1-carboxy-2-methylpropyl)-1,10-phenanthroline-2,9-dimethanamine) complex with calf thymus DNA was studied by electronic spectra, fluorescence spectra and circular dichroic spectra. The La(III)-L complex was assayed for antitumor activity in vitro against the HL-60 (the human leucocytoma) cells, HCT-8 (the human coloadenocarcinoma) cells, BGC-823 (the human carcinoma of stomach) cells, Bel-7402 (the human liver carcinoma) cells and KB (the human nasopharyngeal carcinoma) cells. The results show that the La(III)-L complex has activity against HL-60 cells, Bel-7402 cells and KB cells.