2011
DOI: 10.1007/s11270-011-1055-7
|View full text |Cite
|
Sign up to set email alerts
|

Formation of Tebuconazole Complexes with Cadmium(II) Investigated by Electrospray Ionization Mass Spectrometry

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
5
0

Year Published

2015
2015
2023
2023

Publication Types

Select...
9

Relationship

1
8

Authors

Journals

citations
Cited by 18 publications
(5 citation statements)
references
References 17 publications
0
5
0
Order By: Relevance
“…Concerning the triazole moiety, it is not electrochemically active unless the utilization of complexation reaction with metal ions. 55 The piperazine ring is thus a clear target of electrooxidation of itraconazole, as this heterocyclic possesses lone electron pairs on N atoms and its oxidation was described for other compounds possessing this moiety at different electrode materials [14][15][16][17][18][56][57][58][59] Although, comparison of electrochemical oxidation mechanism of piperazine ring itself in different compounds is not reasonable, because the various groups attached to the two piperazine nitrogens significantly change their basicity and redox behavior, but some comparisons could be benefit to through the light on the oxidation mechanism of itraconazole drug under investigation.…”
Section: Resultsmentioning
confidence: 99%
“…Concerning the triazole moiety, it is not electrochemically active unless the utilization of complexation reaction with metal ions. 55 The piperazine ring is thus a clear target of electrooxidation of itraconazole, as this heterocyclic possesses lone electron pairs on N atoms and its oxidation was described for other compounds possessing this moiety at different electrode materials [14][15][16][17][18][56][57][58][59] Although, comparison of electrochemical oxidation mechanism of piperazine ring itself in different compounds is not reasonable, because the various groups attached to the two piperazine nitrogens significantly change their basicity and redox behavior, but some comparisons could be benefit to through the light on the oxidation mechanism of itraconazole drug under investigation.…”
Section: Resultsmentioning
confidence: 99%
“…In soil, tebuconazole has a half-life ranging from 49 to 610 days under aerobic conditions [6]. Regular use of tebuconazole in agriculture leads to its accumulation in soils and, subsequently, can cause risks for surface water, groundwater, and soil ecosystems [7]. According to the United States Environmental Protection Agency (US EPA), tebuconazole is listed as a possible carcinogen with a rating of C, and it has the potential to affect the endocrine system of different species by interacting with the steroidogenesis pathway [8].…”
Section: Introductionmentioning
confidence: 99%
“…Concerning the electrochemistry of triazole and imidazole agents, literature data are rather scarce. Since the triazole moiety is not electrochemically active, a universal approach could be the utilization of complexation reactions with metal ions [10], i.e., enhancement of voltammetric signals assigned to oxidation of a metallic electrode in the presence of the triazolic compound due to its complexation reaction [11,12]. The direct redox activity of triazoles relies on other moieties, e.g., electrochemical oxidation of the amino group in amitrole [13,14] or reduction of azomethine moiety (e.g., in propiconazole).…”
Section: Introductionmentioning
confidence: 99%