In: JBIC Journal of Biological Inorganic Chemistry, 2014, vol. 19, no. 2, p. 145-159
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In: Dyes and Pigments, 2019, vol. 165, p. 157–163
In order to meet the need for NMR reference compounds in the study of tautomeric azo dyes, two series of azo dyes, derived from 3-methyl-1-phenyl-4- (phenyldiazenyl)-1H-pyrazol-5-amine and 5-methyl-2-phenyl-4-(2- phenylhydrazono)-2,4-dihydro-3H-pyrazol-3-one, have been studied by using molecular spectroscopy (UV–Vis and NMR) and quantum-chemical calculations (M06- 2X/TZVP) in solution. The...
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In: Tribology Letters, 2010, vol. 40, no. 3, p. 375-394
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In: Monatshefte für Chemie / Chemical Monthly, 2005, vol. 136, no. 7, p. 1205-1219
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In: JBIC Journal of Biological Inorganic Chemistry, 2007, vol. 12, no. 1, p. 118-125
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In: Amino Acids, 2010, vol. 39, no. 5, p. 1131-1137
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In: Journal of Low Temperature Physics, 2006, vol. 142, no. 3-4, p. 461-464
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In: Monatshefte für Chemie - Chemical Monthly, 2007, vol. 138, no. 2, p. 121-129
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In: The Journal of Organic Chemistry, 2017, vol. 82, no. 12, p. 6133–6141
A kinetic study of the hydrogen atom transfer (HAT) reactions from a series of organic compounds to the quinolinimide-N-oxyl radical (QINO) was performed in CH3CN. The HAT rate constants are significantly higher than those observed with the phthalimide- N-oxyl radical (PINO) as a result of enthalpic and polar effects due to the presence of the N-heteroaromatic ring in QINO. The relevance of...
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In: Radiochimica Acta, 1997, vol. 79, no. 4, p. 217-220
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