Aryl carbinols as nerve agent probes. Influence of the conjugation on the sensing properties

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Abstract

Two new aryl carbinols (1 and 3) have been synthesised and characterised and their ability as OFF-ON probes for the chromogenic detection of the nerve agent simulant in acetonitrile has been tested. In addition compound 2 has been also studied. The carbinols suffered a phosphorylation reaction followed by an elimination process giving rise to the corresponding carbocations. This transformation of the carbinol into the carbocation is responsible for a significant color change. © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2012.

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Royo, S., Gotor, R., Costero, A. M., Parra, M., Gil, S., Martínez-Máñez, R., & Sancenón, F. (2012). Aryl carbinols as nerve agent probes. Influence of the conjugation on the sensing properties. New Journal of Chemistry, 36(7), 1485–1489. https://doi.org/10.1039/c2nj40104e

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