2005
DOI: 10.1016/j.ica.2004.12.050
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Molecular sensing behavior of the first Mn(I)-compound of di-2-pyridylketone-p-nitrophenylhydrazone (dpknph), fac-[Mn(CO)3(dpknph)Br]

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Cited by 17 publications
(10 citation statements)
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“…Mixed ligand metal complexes of hydrazones, have proved to be useful catalysts in reactions such as hydrogenation, oxidation, carbonylation and hydroformylation [2]. The applications of rhenium-carbonyl compounds as electrochemical sensors and the optosensing behavior of ruthenium(II), manganese(I) compounds of di-2-pyridyl ketone have been reported [3,4]. The use of these systems as molecular sensors is due to their high values of extinction coefficients and low values for their activation parameters.…”
Section: Introductionmentioning
confidence: 99%
“…Mixed ligand metal complexes of hydrazones, have proved to be useful catalysts in reactions such as hydrogenation, oxidation, carbonylation and hydroformylation [2]. The applications of rhenium-carbonyl compounds as electrochemical sensors and the optosensing behavior of ruthenium(II), manganese(I) compounds of di-2-pyridyl ketone have been reported [3,4]. The use of these systems as molecular sensors is due to their high values of extinction coefficients and low values for their activation parameters.…”
Section: Introductionmentioning
confidence: 99%
“…All non-hydrogen atoms were refined with anisotropic thermal parameters. (2) 1294 (4) 153 (3) 3424 (2) 35(1) C (11) 3167 (5) 1266 (4) 5642 (3) 50(1) C (12) 4700 (5) 1354 (4) 5833 (3) 63(1) C (13) 5631 (5) 1647 (4) 5210 (3) 62(1) C (14) 5016 (5) 1848 (4) 4415 (3) 49(1) C (15) 3468 (4) 1768 (3) 4275 (3) 39 (1) The appearance of broad O-H stretching vibration at 3425 cm À1 signifies intensive intermolecular hydrogen bonding in the solid state as the free hydroxyl stretching band appears sharp between 3700-3580 cm À1 [22]. The 1 H-NMR spectra measured in d 6 -dmso confirmed the symmetrical coordination of 3 -dpkO,OH as evident by the appearance of four peaks with the same intensity.…”
Section: X-ray Crystallographymentioning
confidence: 99%
“…We have been interested in the chemistry of di-2-pyridyl ketone (dpk) and its oxime and hydrazone derivatives (see scheme 1), and reported on the synthesis, characterization and structures of a series of low-valent metal compounds of di-2-pyridyl ketone derivatives, and their applications as molecular sensors for metal ions and biomolecules that include monosaccharide [8][9][10][11][12][13][14][15][16][17][18][19]. The electrochemical reactions of fac-[Re(CO) 3 3 (dpk)Cl] as an electrochemical sensor for electrophiles [8,9].…”
Section: Introductionmentioning
confidence: 99%
“…In continuation of our efforts to explore the chemistry of di-2-pyridyl ketone derivatives, this report will describe the synthesis and physico-chemical properties of the first rhenium compound di-2-pyridyl ketone semicarbazone (see Scheme 1). In previous reports, we described the synthesis, spectroscopic, electrochemical, and solid state structures of a variety of metal compounds that contain di-2-pyridyl ketone derivatives [30][31][32][33][34][35][36][37]. Electrochemical reactions of CO 2 with fac-[Re(CO) 3 (dpk)Cl] measured on non-aqueous solvents showed strong solvent dependence and revealed metal-based and ligandbased reactivity [30].…”
Section: Introductionmentioning
confidence: 99%
“…Electrochemical reactions of CO 2 with fac-[Re(CO) 3 (dpk)Cl] measured on non-aqueous solvents showed strong solvent dependence and revealed metal-based and ligandbased reactivity [30]. Spectroscopic measurements done on nonaqueous solutions of di-2-pyridyl ketone hydrazones and their metal complexes show high sensitivity of these compounds to changes in their surroundings [32][33][34][35][36][37]. Solid state structures of a variety of di-2-pyridyl ketone derivatives and their metal compounds show strong solvent dependence due to solvent complex interaction and the presence of extensive network of hydrogen bond [33][34][35][36][37].…”
Section: Introductionmentioning
confidence: 99%