Detailed Information on Publication Record
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 and Radim VESPALECBasic information
Original name
Electrochemistry of parent and exo-skeletally substituted icosahedral monocarba and dicarbaboranes and their derivatives at the graphite carbon electrode in aqueous phosphate buffers
Authors
FOJT, Lukáš (203 Czech Republic), Miroslav FOJTA (203 Czech Republic, guarantor, belonging to the institution), Bohumír GRUNER (203 Czech Republic) and Radim VESPALEC (203 Czech Republic)
Edition
Journal of Electroanalytical Chemistry, Lausanne, Elsevier, 2014, 1572-6657
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10405 Electrochemistry
Country of publisher
Switzerland
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 2.729
RIV identification code
RIV/00216224:14740/14:00074407
Organization unit
Central European Institute of Technology
UT WoS
000342955900003
Keywords in English
Boranes; Carboranes; Glassy carbon electrode; DPV
Tags
Tags
International impact, Reviewed
Změněno: 23/2/2015 14:56, Martina Prášilová
Abstract
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.
Links
GBP206/12/G151, research and development project |
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