Data di Pubblicazione:
2015
Citazione:
Enantiorecognition towards L- and D-DOPA on easy-to-prepare inherently chiral film electrodes / S. Arnaboldi, P.R. Mussini, F. Sannicolò, T. Benincori, A. Penoni. ((Intervento presentato al convegno Sensori e biosensori: stato dell'arte e nuove prospettive tenutosi a Parma nel 2015.
Abstract:
We have recently shown1,2 that oligomers endowed with “inherent chirality” display high chirality manifestations plus a pool of unprecedented properties. In particular, in the very last months we have
demonstrated that electrooligomerization (especially in ionic liquids) of our inherently chiral monomers on screen‐printed electrodes and on glassy carbon tip electrodes affords inherently chiral electroactive films of outstanding enantiodiscrimination ability towards a series of chiral probes of quite different bulkiness and chemical nature (also of pharmaceutical interest like DOPA, common antibiotics and FANS)3. The general validity of the "inherent chirality" concept has been confirmed by characterizing monomers and related films based on different atropisomeric biheteroaromatic scaffolds (i.e. bis‐benzothiophene, bis‐indole, and “all thiophene” core). In this work the enantiorecognition ability of our smart films towards L‐ and D‐DOPA will be presented focusing on the variation in voltammetric peak separation of the probe enantiomers when changing i) the medium (e.g. increasing pH), ii) the nature of electrode material and iii) the probe carboxylic unit (i.e. DOPA
methyl ester). The impressive enantiomer peak potential separation combined with the peak current linear dynamic ranges enables to estimate enantiomeric excesses in probe enantiomeric mixtures. Such synthetic electrode surfaces able to neatly discriminate the antipodes of chiral probes as separate peaks are unprecedented in literature, opening the way to the development of efficient chiral voltammetric sensors.
Figure. Effect of the variation in the pH medium on the enantiorecognition ability of our bithianaphthene‐based (BT2‐T4)n inherently chiral electrodes with L‐ and D‐DOPA probes, superimposed on a speciation plot of DOPA.
This work was supported by Fondazione Cariplo (Grant no. 2011‐0417)
References
[1] F. Sannicolò, S. Arnaboldi, T. Benincori, V. Bonometti, R. Cirilli, L. Dunsch, W. Kutner, G. Longhi, P. R. Mussini, M.
Panigati, M. Pierini and S. Rizzo, Angewandte Chemie Int. Ed., 53 (2014), 2623
[2] F. Sannicolò, P. R. Mussini, T. Benincori, R. Cirilli, S. Abbate, S. Arnaboldi, S. Casolo, E. Castiglioni, G. Longhi, R.
Martinazzo, M. Panigati, M. Pappini, E. Quartapelle Procopio, S. Rizzo, Chemistry‐A European Journal 10, (2014), 15261
[3] S. Arnaboldi, P. Mussini, M. Magni, F. Sannicolò, T. Benincori, R. Cirilli, K. Noworyta and W. Kutner, Chemical
Science, 6 (2015), 1706
Tipologia IRIS:
14 - Intervento a convegno non pubblicato
Elenco autori:
S. Arnaboldi, P.R. Mussini, F. Sannicolò, T. Benincori, A. Penoni
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