The usual approaches to chiral electroactive molecular materials, relying on attaching chiral pendants to an electroactive polyconjugated backbone, generally result in modest chirality manifestations; other approaches, such as chiral templating agents, chiral counteranions, etc. actually imply the chirality source to be external to the electroactive material. Very recently, our research group has unveiled by electrochemical experiments the unprecedented enantioselectivity properties of molecular films based on a new family of "inherently chiral" polyheterocycles, where chirality is not external to the electroactive backbone, but inherent to it, resulting from a tailored torsion produced by the periodical presence of atropoisomeric, conjugatively active biheteroaromatic scaffolds [1]. The electroactive films obtained by electrooligomerization mostly consist of cyclic electroactive oligomers, constituted by several fully conjugated thiophene units. These ringlets, which can also be obtained by chemical oligomerization are endowed with an outstanding pool of attractive properties both as racemates and as enantiopure antipodes [1,2]. The neat peak separation for two enantiomers of electroactive chiral probes together with the linearity of the peak currents with enantiomer concentration affords estimation of the enantiomeric excess when both enantiomers are present. The new electrodes have been tested with very good results towards several chiral probes, quite different in molecular structure and of applicative interest, on different supports, and in different media. Moreover, we have verified that the same spectacular enantioselectivity is obtained on surfaces prepared starting from monomers designed according to the same structural concept but chemically different, which demonstrates the general validity of the new strategy. Albeit preliminary, such unprecedented outstanding results open the way to chiral voltammetry. Considering the outstanding enantioselectivity obtained with inherently chiral surfaces, our research group has been started to investigate whether the "inherently chiral" concept can also yield enantioselectivity when implemented in ionic liquids or supporting electrolytes. This study is still in its early stage, but preliminary tests seem to indicate that, also in this case, significant enantioselectivity could be achieved by applying the inherent chirality concept. [1] F. Sannicolò, S. Arnaboldi, T. Benincori, V. Bonometti, R. Cirilli, L. Dunsch, W. Kutner, G. Longhi, P. R. Mussini1, M. Panigati, M. Pierini and S. Rizzo, Angew. Chem. Int. Ed. 53 (2014) 2623-2327. [2] F. Sannicolò, P. R. Mussini, T. Benincori, R. Cirilli, S. Abbate, S. Arnaboldi, S. Casolo, E. Castiglioni, G. Longhi, R. Martinaz

Versatile inherently chiral materials for electrochemistry / S. Arnaboldi, P.R. Mussini, F. Sannicolò, T. Benincori - In: Sigma-Aldrich Young Chemists Symposium / [a cura di] F. Bella, D. Spinelli. - Roma : Società Chimica Italiana, 2015 Oct. - ISBN 9788886208949. - pp. 61-61 (( convegno Sygma Aldrich Young Chemists tenutosi a Rimini nel 2015.

Versatile inherently chiral materials for electrochemistry

S. Arnaboldi
;
P.R. Mussini
Secondo
;
F. Sannicolò
Penultimo
;
2015

Abstract

The usual approaches to chiral electroactive molecular materials, relying on attaching chiral pendants to an electroactive polyconjugated backbone, generally result in modest chirality manifestations; other approaches, such as chiral templating agents, chiral counteranions, etc. actually imply the chirality source to be external to the electroactive material. Very recently, our research group has unveiled by electrochemical experiments the unprecedented enantioselectivity properties of molecular films based on a new family of "inherently chiral" polyheterocycles, where chirality is not external to the electroactive backbone, but inherent to it, resulting from a tailored torsion produced by the periodical presence of atropoisomeric, conjugatively active biheteroaromatic scaffolds [1]. The electroactive films obtained by electrooligomerization mostly consist of cyclic electroactive oligomers, constituted by several fully conjugated thiophene units. These ringlets, which can also be obtained by chemical oligomerization are endowed with an outstanding pool of attractive properties both as racemates and as enantiopure antipodes [1,2]. The neat peak separation for two enantiomers of electroactive chiral probes together with the linearity of the peak currents with enantiomer concentration affords estimation of the enantiomeric excess when both enantiomers are present. The new electrodes have been tested with very good results towards several chiral probes, quite different in molecular structure and of applicative interest, on different supports, and in different media. Moreover, we have verified that the same spectacular enantioselectivity is obtained on surfaces prepared starting from monomers designed according to the same structural concept but chemically different, which demonstrates the general validity of the new strategy. Albeit preliminary, such unprecedented outstanding results open the way to chiral voltammetry. Considering the outstanding enantioselectivity obtained with inherently chiral surfaces, our research group has been started to investigate whether the "inherently chiral" concept can also yield enantioselectivity when implemented in ionic liquids or supporting electrolytes. This study is still in its early stage, but preliminary tests seem to indicate that, also in this case, significant enantioselectivity could be achieved by applying the inherent chirality concept. [1] F. Sannicolò, S. Arnaboldi, T. Benincori, V. Bonometti, R. Cirilli, L. Dunsch, W. Kutner, G. Longhi, P. R. Mussini1, M. Panigati, M. Pierini and S. Rizzo, Angew. Chem. Int. Ed. 53 (2014) 2623-2327. [2] F. Sannicolò, P. R. Mussini, T. Benincori, R. Cirilli, S. Abbate, S. Arnaboldi, S. Casolo, E. Castiglioni, G. Longhi, R. Martinaz
Settore CHIM/01 - Chimica Analitica
Settore CHIM/02 - Chimica Fisica
Settore CHIM/06 - Chimica Organica
ott-2015
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/388133
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