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 and Radim VESPALEC

Basic 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

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
Name: Centrum nových přístupů k bioanalýze a molekulární diagnostice