2018
Voltammetric and adsorption study of 4-nitrophenyl-triazole-labeled 2 '-deoxycytidine and 7-deazaadenosine nucleosides at boron-doped diamond electrode
VOSAHLOVA, J.; L. KOLACNA; A. DANHEL; J. FISCHER; J. BALINTOVA et al.Základní údaje
Originální název
Voltammetric and adsorption study of 4-nitrophenyl-triazole-labeled 2 '-deoxycytidine and 7-deazaadenosine nucleosides at boron-doped diamond electrode
Autoři
VOSAHLOVA, J.; L. KOLACNA; A. DANHEL; J. FISCHER; J. BALINTOVA; M. HOCEK; K. SCHWARZOVA-PECKOVA a Miroslav FOJTA
Vydání
Journal of Electroanalytical Chemistry, Lausanne, Elsevier, 2018, 1572-6657
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10405 Electrochemistry
Stát vydavatele
Švýcarsko
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 3.218
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14740/18:00101395
Organizační jednotka
Středoevropský technologický institut
UT WoS
EID Scopus
Klíčová slova anglicky
Adsorption; Boron-doped diamond; Nitro compounds; Nucleoside labeling; Voltammetry
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 13. 3. 2019 17:28, Mgr. Pavla Foltynová, Ph.D.
Anotace
V originále
Electrochemical properties of 4-nitrophenyl triazole labeled 2'-deoxycytidine (dCTRN 2) and 7-deazaadenosine (dA(TRNO2)) were studied using alumina-polished boron doped diamond (BDD) electrode in acetate buffer pH 5.0. Cyclic voltammetry revealed peak-shaped signals for reduction of the nitro group at the potentials of ca -0.6 V (vs. AllAgCl13 mol L-1 KCl reference electrode) and for the hydroxylamine/nitroso pair exhibiting quasireversible electron transfer at potentials comparable with redox processes of other nitro aromatic compounds at BDD electrodes. All electrochemical processes are directed by adsorption. Moreover, ex situ adsorption of dA(TRNO2) and transfer to supporting electrolyte enables its quantitation using square wave voltammetry in small (several microliter) sample volumes after optimization of parameters for the hydroxylamine/nitroso redox couple. Competitive adsorption/desorption at the BDD surface was further studied by cyclic voltammetry with dA(TRNO2) in the presence of electrochemically inactive phenyl triazole 7-deazaadenosine conjugate (dA(TR)), revealing mutual displacement of both compounds at BDD surface. Further, the redox processes of simpler aromatic nitro compounds (4-nitrophenyl acetylene and 2-nitronaphthalene) are strongly affected when the BDD surface is covered by dA(TR).
Návaznosti
| GBP206/12/G151, projekt VaV |
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