A highly selective colorimetric chemosensor for detection of iodide ions in aqueous solution
We synthesized a new iodide ion (I-) chemosensor (CS) based on a hydrazone derivative obtained from the condensation of 2-hydroxy-1-naphthaldehyde and 2,4-dinitrophenylhydrazine. The CS showed selective colorimetric recognition of I-
Synthesis, binding ability, and cell cytotoxicity of fluorescent probes for l-arginine detection based on naphthalene derivatives: Experiment and theory
Inspired by biological related parts, Schiff base derivatives and functional groups of chemical modification can provide efficient detection method of amino acids. Therefore, we have designed and prepared 4 compounds based on Schiff base derivatives invol
Orthometallation in bidentate Schiff base ligands via C-H activation: Synthesis of ruthenium(III) organometallic complexes
Schiff bases obtained by the reactions of substituted aromatic aldehydes with phenyl hydrazine or 2,4-dinitrophenyl hydrazine were synthesized and characterized by spectroscopic methods. Cyclometalated Ru(III) complexes of general formula, namely [Ru(L)(PPh3)2Cl], were synthesized from the Schiff bases via C-H bond activation and characterized by spectroscopic and electrochemical studies. In addition, one molecular structure of one of the complexes was determined by X-ray crystallography. The redox behavior of the complexes was examined by electrochemical studies, and one mechanism of orthometallation was investigated.
Ghosh, Kaushik,Kumar, Rajan,Kumar, Sushil,Bala, Manju,Singh, Udai P.
p. 831 - 837
(2015/10/28)
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