LACINA, Karel, Jan NOVOTNÝ, Zdeněk MORAVEC and Petr SKLÁDAL. Interaction of ferroceneboronic acid with diols at aqueous and non-aqueous conditions - signalling and binding abilities of an electrochemical probe for saccharides. Electrochimica Acta. Oxford: PERGAMON-ELSEVIER SCIENCE LTD, 2015, vol. 153, january, p. 280-286. ISSN 0013-4686. Available from: https://dx.doi.org/10.1016/j.electacta.2014.12.009.
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Basic information
Original name Interaction of ferroceneboronic acid with diols at aqueous and non-aqueous conditions - signalling and binding abilities of an electrochemical probe for saccharides
Authors LACINA, Karel (203 Czech Republic, guarantor, belonging to the institution), Jan NOVOTNÝ (203 Czech Republic, belonging to the institution), Zdeněk MORAVEC (203 Czech Republic, belonging to the institution) and Petr SKLÁDAL (203 Czech Republic, belonging to the institution).
Edition Electrochimica Acta, Oxford, PERGAMON-ELSEVIER SCIENCE LTD, 2015, 0013-4686.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10405 Electrochemistry
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 4.803
RIV identification code RIV/00216224:14740/15:00082937
Organization unit Central European Institute of Technology
Doi http://dx.doi.org/10.1016/j.electacta.2014.12.009
UT WoS 000348450000036
Keywords in English Ferroceneboronic acid; Lewis acid; Non-aqueous environment; Binding properties; Detection of saccharides
Tags rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Eva Špillingová, učo 110713. Changed: 29/3/2016 16:34.
Abstract
Ferroceneboronic acid (FcBA) was employed as a model compound for clarification of binding and signalling properties of molecular probe for saccharides. As the simplest electrochemically active boronic acid, its interactions with diverse diols were studied in homogeneous phase under aqueous and non-aqueous conditions. The FcBA-diol system was examined by cyclic voltammetry resulting in two redox pairs corresponding to free and bound forms of FcBA. Redox potential of the bound form of FcBA was shifted in the cathodic direction in aqueous conditions due to coordination of the hydroxyl group to the boron atom. Oppositely, the anodic shift of the redox potential was observed upon the interaction of FcBA with diols in non-aqueous solvents. The binding properties and signalling mechanism of electrochemically active boronic acids were deduced and the assumptions resulting from the electrochemical behaviour were confirmed by 1H and 11B NMR spectroscopies. The binding constants of the tested diols in aqueous and non-aqueous media were determined and compared.
Links
ED1.1.00/02.0068, research and development projectName: CEITEC - central european institute of technology
EE2.3.30.0037, research and development projectName: Zaměstnáním nejlepších mladých vědců k rozvoji mezinárodní spolupráce
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