New electrocatalytic reactions at a mercury electrode in the presence of homocysteine or cysteine and cobalt or nickel ions

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F09%3A00008402" target="_blank" >RIV/00216275:25310/09:00008402 - isvavai.cz</a>

Výsledek na webu

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DOI - Digital Object Identifier

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Jazyk výsledku

angličtina

Název v původním jazyce

New electrocatalytic reactions at a mercury electrode in the presence of homocysteine or cysteine and cobalt or nickel ions

Popis výsledku v původním jazyce

Homocysteine (Hcy) and cysteine (Cys) mercury thiolate layers were prepared by anodic polarization of a mercury electrode in amino acid containing solutions and then investigated in the cathodic regime in the presence of Ni or Co ions. Mercury thiolate undergoes a slow disintegration resulting in surface-attached mercury sulfide. Hg substitution by Ni or Co yields minute amounts of the relevant metal sulfide. Such a species catalyzes hydrogen evolution at -1.3 V vs. Ag/AgCl. Hcy experiences a faster decomposition and displays a stronger catalytic effect. Each compound catalyzes the reduction of Ni or Co, but only Cys induces typical catalytic evolution processes as the Brdička reaction or the catalytic hydrogen prewave. HCy catalyzes the hydrogen evolution in the presence of Co at -1.5 V in the same way than sulfur derivatives with no amine function do. Correlation between the physical state of the metal sulfide and its catalytic properties are discussed and possible analytical applica

Název v anglickém jazyce

New electrocatalytic reactions at a mercury electrode in the presence of homocysteine or cysteine and cobalt or nickel ions

Popis výsledku anglicky

Homocysteine (Hcy) and cysteine (Cys) mercury thiolate layers were prepared by anodic polarization of a mercury electrode in amino acid containing solutions and then investigated in the cathodic regime in the presence of Ni or Co ions. Mercury thiolate undergoes a slow disintegration resulting in surface-attached mercury sulfide. Hg substitution by Ni or Co yields minute amounts of the relevant metal sulfide. Such a species catalyzes hydrogen evolution at -1.3 V vs. Ag/AgCl. Hcy experiences a faster decomposition and displays a stronger catalytic effect. Each compound catalyzes the reduction of Ni or Co, but only Cys induces typical catalytic evolution processes as the Brdička reaction or the catalytic hydrogen prewave. HCy catalyzes the hydrogen evolution in the presence of Co at -1.5 V in the same way than sulfur derivatives with no amine function do. Correlation between the physical state of the metal sulfide and its catalytic properties are discussed and possible analytical applica

Druh

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

CEP obor

CG - Elektrochemie

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)

Rok uplatnění

2009

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

21

Číslo periodika v rámci svazku

2

Stát vydavatele periodika

DE - Spolková republika Německo

Počet stran výsledku

8

Strana od-do

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Kód UT WoS článku

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EID výsledku v databázi Scopus

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