Electrochemistry of parent and exo-skeletally substituted
icosahedral monocarba and dicarbaboranes and their derivatives
at the graphite carbon electrode in aqueous phosphate buffers

J 2014

Electrochemistry of parent and exo-skeletally substituted icosahedral monocarba and dicarbaboranes and their derivatives at the graphite carbon electrode in aqueous phosphate buffers

FOJT, Lukáš, Miroslav FOJTA, Bohumír GRUNER a Radim VESPALEC

Základní údaje

Originální název

Electrochemistry of parent and exo-skeletally substituted icosahedral monocarba and dicarbaboranes and their derivatives at the graphite carbon electrode in aqueous phosphate buffers

Autoři

FOJT, Lukáš (203 Česká republika), Miroslav FOJTA (203 Česká republika, garant, domácí), Bohumír GRUNER (203 Česká republika) a Radim VESPALEC (203 Česká republika)

Vydání

Journal of Electroanalytical Chemistry, Lausanne, Elsevier, 2014, 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: 2.729

Kód RIV

RIV/00216224:14740/14:00074407

Organizační jednotka

Středoevropský technologický institut

DOI

http://dx.doi.org/10.1016/j.jelechem.2014.07.023

UT WoS

000342955900003

Klíčová slova anglicky

Boranes; Carboranes; Glassy carbon electrode; DPV

Štítky

kontrola MP, MP, rivok

Příznaky

Mezinárodní význam, Recenzováno

Změněno: 23. 2. 2015 14:56, Martina Prášilová

Anotace

V originále

Electrochemistry of eight different boron clusters based on 12-vertex icosahedral framework has been studied in water-based electrolytes. This study revealed dependence of the electrochemical behavior on particular exo-skeletal substitution as well as on differences between previously studied divalent clos-o-dodecaborate anion and monovalent [CB11H12](-) anion. Electrochemical response of the latter ion retains the potential of that of the dodecaborate anion, but its relative intensity is considerably lower. Presence of two carbon atoms in parent neutral closo-1,2- and 1,7-dicarbaborane (ortho- and metacarborane) and their respective hydroxyderivative caused a shift of the electrochemical potential to lower values and higher peak sizes than for [CB11H12](-) anion. Most promising behavior for analytical determination in water-based interfaces was found for clusters substituted by OH group. (C) 2014 Elsevier B.V. All rights reserved.

Návaznosti

GBP206/12/G151, projekt VaV

Název: Centrum nových přístupů k bioanalýze a molekulární diagnostice

Citovat

FOJT, Lukáš, Miroslav FOJTA, Bohumír GRUNER a Radim VESPALEC. Electrochemistry of parent and exo-skeletally substituted icosahedral monocarba and dicarbaboranes and their derivatives at the graphite carbon electrode in aqueous phosphate buffers. Journal of Electroanalytical Chemistry. Lausanne: Elsevier, 2014, roč. 730, September, s. 16-19. ISSN 1572-6657. Dostupné z: https://dx.doi.org/10.1016/j.jelechem.2014.07.023.

@article{1227616,
   author = {Fojt, Lukáš and Fojta, Miroslav and Gruner, Bohumír and Vespalec, Radim},
   article_location = {Lausanne},
   article_number = {September},
   doi = {http://dx.doi.org/10.1016/j.jelechem.2014.07.023},
   keywords = {Boranes; Carboranes; Glassy carbon electrode; DPV},
   language = {eng},
   issn = {1572-6657},
   journal = {Journal of Electroanalytical Chemistry},
   title = {Electrochemistry of parent and exo-skeletally substituted icosahedral monocarba and dicarbaboranes and their derivatives at the graphite carbon electrode in aqueous phosphate buffers},
   volume = {730},
   year = {2014}
}

TY  - JOUR
ID  - 1227616
AU  - Fojt, Lukáš - Fojta, Miroslav - Gruner, Bohumír - Vespalec, Radim
PY  - 2014
TI  - Electrochemistry of parent and exo-skeletally substituted icosahedral monocarba and dicarbaboranes and their derivatives at the graphite carbon electrode in aqueous phosphate buffers
JF  - Journal of Electroanalytical Chemistry
VL  - 730
IS  - September
SP  - 16-19
EP  - 16-19
PB  - Elsevier
SN  - 15726657
KW  - Boranes
KW  - Carboranes
KW  - Glassy carbon electrode
KW  - DPV
N2  - Electrochemistry of eight different boron clusters based on 12-vertex icosahedral framework has been studied in water-based electrolytes. This study revealed dependence of the electrochemical behavior on particular exo-skeletal substitution as well as on differences between previously studied divalent clos-o-dodecaborate anion and monovalent [CB11H12](-) anion. Electrochemical response of the latter ion retains the potential of that of the dodecaborate anion, but its relative intensity is considerably lower. Presence of two carbon atoms in parent neutral closo-1,2- and 1,7-dicarbaborane (ortho- and metacarborane) and their respective hydroxyderivative caused a shift of the electrochemical potential to lower values and higher peak sizes than for [CB11H12](-) anion. Most promising behavior for analytical determination in water-based interfaces was found for clusters substituted by OH group. (C) 2014 Elsevier B.V. All rights reserved.
ER  -

FOJT, Lukáš, Miroslav FOJTA, Bohumír GRUNER a Radim VESPALEC. Electrochemistry of parent and exo-skeletally substituted icosahedral monocarba and dicarbaboranes and their derivatives at the graphite carbon electrode in aqueous phosphate buffers. \textit{Journal of Electroanalytical Chemistry}. Lausanne: Elsevier, 2014, roč.~730, September, s.~16-19. ISSN~1572-6657. Dostupné z: https://dx.doi.org/10.1016/j.jelechem.2014.07.023.

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