Aminoferrocene:Determination of the acidity of unstable compounds
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F19%3A00110349" target="_blank" >RIV/00216224:14310/19:00110349 - isvavai.cz</a>
Výsledek na webu
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DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Aminoferrocene:Determination of the acidity of unstable compounds
Popis výsledku v původním jazyce
Ferrocenes are quite popular in electrochemistry, due to the simplicity of redox reactions of iron core. While ferrocene is nonpolar and thus of limited use, its cyclopentadienyl ring opens way for many interesting modifications. One of which is aminoferrocene (FcNH2), the -NH2 group increases solubility in polar solvents, introduces chemical reactivity and most importantly pH sensitivity to the ferrocene complex. Due to the proximity of NH2 group and Fe2+ ion in FcNH2, the redox potential of FcNH2 is influenced by protonation and vice versa the Fe3+ ion changes acidity of the complex upon oxidation. Electrochemical observation of this interplay can be used to deduce the acidity of the Fe3+ complex. Such approach is useful for complexes that are unstable in their oxidized form. pKa constants determined using electrochemical methods are obtained through kinetic processes, therefore great care needs to be taken when interpreting these results. While the limiting redox potential for FcNH2 is easily obtained from electrochemical results (Figure), the limiting potential for FcNH3+ strongly varies depending on the type of electrode used. This is anomalous from other ferrocene derivates, namely ferroceneboronic acid [1] and ferrocenecarboxylic acid [2], where both limiting redox potentials are easily obtainable. In our contribution, we tried to uncover the correct pKa value of aminoferrocene through different electrochemical methods both in buffered and unbuffered solutions. Spectrophotometry was used along to validate our findings.
Název v anglickém jazyce
Aminoferrocene:Determination of the acidity of unstable compounds
Popis výsledku anglicky
Ferrocenes are quite popular in electrochemistry, due to the simplicity of redox reactions of iron core. While ferrocene is nonpolar and thus of limited use, its cyclopentadienyl ring opens way for many interesting modifications. One of which is aminoferrocene (FcNH2), the -NH2 group increases solubility in polar solvents, introduces chemical reactivity and most importantly pH sensitivity to the ferrocene complex. Due to the proximity of NH2 group and Fe2+ ion in FcNH2, the redox potential of FcNH2 is influenced by protonation and vice versa the Fe3+ ion changes acidity of the complex upon oxidation. Electrochemical observation of this interplay can be used to deduce the acidity of the Fe3+ complex. Such approach is useful for complexes that are unstable in their oxidized form. pKa constants determined using electrochemical methods are obtained through kinetic processes, therefore great care needs to be taken when interpreting these results. While the limiting redox potential for FcNH2 is easily obtained from electrochemical results (Figure), the limiting potential for FcNH3+ strongly varies depending on the type of electrode used. This is anomalous from other ferrocene derivates, namely ferroceneboronic acid [1] and ferrocenecarboxylic acid [2], where both limiting redox potentials are easily obtainable. In our contribution, we tried to uncover the correct pKa value of aminoferrocene through different electrochemical methods both in buffered and unbuffered solutions. Spectrophotometry was used along to validate our findings.
Klasifikace
Druh
D - Stať ve sborníku
CEP obor
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OECD FORD obor
10405 - Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)
Návaznosti výsledku
Projekt
<a href="/cs/project/LQ1601" target="_blank" >LQ1601: CEITEC 2020</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach
Ostatní
Rok uplatnění
2019
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název statě ve sborníku
XIX. Workshop of Biophysical Chemists and Electrochemists
ISBN
9788021093096
ISSN
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e-ISSN
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Počet stran výsledku
2
Strana od-do
34-35
Název nakladatele
Masarykova univerzita
Místo vydání
Brno
Místo konání akce
Brno
Datum konání akce
14. 6. 2019
Typ akce podle státní příslušnosti
EUR - Evropská akce
Kód UT WoS článku
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