Acid-Base Equilibrium of 6-Benzylaminopurine and Its 4-Chloro and 4-Methoxy Derivatives in Water-Ethanol Solutions Studied by Voltammetry and Spectrophotometry

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F11%3A00053590" target="_blank" >RIV/00216224:14310/11:00053590 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1002/elan.201100282" target="_blank" >http://dx.doi.org/10.1002/elan.201100282</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1002/elan.201100282" target="_blank" >10.1002/elan.201100282</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Acid-Base Equilibrium of 6-Benzylaminopurine and Its 4-Chloro and 4-Methoxy Derivatives in Water-Ethanol Solutions Studied by Voltammetry and Spectrophotometry

Popis výsledku v původním jazyce

The apparent pK(a) values of 6-benzylaminopurine (BAP) and its 4-chloro-6-benzylaminopurine and 4-methoxy-6-benzylaminopurine derivatives were determined in good agreement with voltammetric approaches and with spectrophotometry. Whereas at acidic pH values two overlapped reduction peaks on the mercury electrode were obtained, at more slightly alkaline solutions one reduction signal was measured not only for BAP but also for its derivatives. Furthermore, high scan rates, low ionic strength concentrationand a high percentage of the organic solvent cause the best splitting of signals. For the detailed study of such a phenomenon, elimination voltammetry with linear scan (EVLS) was used concluding that the reasons of the peak splitting seem to be related to two different reduction mechanisms that take place on the electrode mainly controlled by adsorption.

Název v anglickém jazyce

Acid-Base Equilibrium of 6-Benzylaminopurine and Its 4-Chloro and 4-Methoxy Derivatives in Water-Ethanol Solutions Studied by Voltammetry and Spectrophotometry

Popis výsledku anglicky

The apparent pK(a) values of 6-benzylaminopurine (BAP) and its 4-chloro-6-benzylaminopurine and 4-methoxy-6-benzylaminopurine derivatives were determined in good agreement with voltammetric approaches and with spectrophotometry. Whereas at acidic pH values two overlapped reduction peaks on the mercury electrode were obtained, at more slightly alkaline solutions one reduction signal was measured not only for BAP but also for its derivatives. Furthermore, high scan rates, low ionic strength concentrationand a high percentage of the organic solvent cause the best splitting of signals. For the detailed study of such a phenomenon, elimination voltammetry with linear scan (EVLS) was used concluding that the reasons of the peak splitting seem to be related to two different reduction mechanisms that take place on the electrode mainly controlled by adsorption.

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

CF - Fyzikální chemie a teoretická chemie

OECD FORD obor

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Projekt

<a href="/cs/project/LC06035" target="_blank" >LC06035: Centrum biofyzikální chemie, bioelektrochemie a bioanalýzy. Nové nástroje pro genomiku, proteomiku a biomedicínu.</a><br>

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)<br>S - Specificky vyzkum na vysokych skolach

Rok uplatnění

2011

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Electroanalysis

ISSN

1040-0397

e-ISSN

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Svazek periodika

23

Číslo periodika v rámci svazku

9

Stát vydavatele periodika

CZ - Česká republika

Počet stran výsledku

9

Strana od-do

2217-2225

Kód UT WoS článku

000295143900031

EID výsledku v databázi Scopus

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