1993
DOI: 10.1016/0022-0728(93)80486-2
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Solvent effects on the redox characteristics of different hydrazyls in nonaqueous media

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Cited by 10 publications
(13 citation statements)
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“…As can be seen in Table 1 DE 1/2 for all the investigated thiadiazoles (1a ±d, 2b ±d) decreased when the solvent changed from 1,2-dichloroethane to acetonitrile; i.e., the sum of the solvation energies increased which is in full agreement with that found in the literature [11]. This is in accordance with Gutmann×s donor model [15].…”
Section: Cpdssupporting
confidence: 81%
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“…As can be seen in Table 1 DE 1/2 for all the investigated thiadiazoles (1a ±d, 2b ±d) decreased when the solvent changed from 1,2-dichloroethane to acetonitrile; i.e., the sum of the solvation energies increased which is in full agreement with that found in the literature [11]. This is in accordance with Gutmann×s donor model [15].…”
Section: Cpdssupporting
confidence: 81%
“…This behavior can be attributed to a solvent effect, as already reported by many workers [11,16,17].…”
Section: Cpdssupporting
confidence: 63%
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“…All the purified solvents were stored under argon in the dark. Purification of different solvents was carried out according to the literature [7,11,12].…”
Section: Materials and Methodologymentioning
confidence: 99%
“…The electrochemistry of heterocyclic compounds with nitrogen heteroatom has been extensively studied [1][2][3][4][5][6][7][8][9]. In spite of great importance and wide uses of the heterocyclic aromatic compounds with oxygen or sulphur atoms, it is rare to find an attempt to study their electrochemical redox characteristics.…”
Section: Introductionmentioning
confidence: 99%