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

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

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dc.contributor.author Royo Calvo, Santiago es_ES
dc.contributor.author Gotor Candel, Raul Jesús es_ES
dc.contributor.author Costero Nieto, Ana María es_ES
dc.contributor.author Parra Álvarez, Margarita es_ES
dc.contributor.author Gil Grau, Salvador es_ES
dc.contributor.author Martínez Mañez, Ramón es_ES
dc.contributor.author Sancenón Galarza, Félix es_ES
dc.date.accessioned 2014-05-09T13:54:27Z
dc.date.issued 2012-04-13
dc.identifier.issn 1144-0546
dc.identifier.uri http://hdl.handle.net/10251/37360
dc.description.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. es_ES
dc.description.sponsorship Financial support from the Spanish Government (project MAT2009-14564-C04-01) and the Generalitat Valencia (project PROMETEO/2009/016) is gratefully acknowledged. R. G. is grateful to the Spanish Ministry of Education and S. R. to Generalitat Valencia for their grants. en_EN
dc.language Inglés es_ES
dc.publisher Royal Society of Chemistry es_ES
dc.relation.ispartof New Journal of Chemistry es_ES
dc.rights Reserva de todos los derechos es_ES
dc.subject Acetonitrile es_ES
dc.subject Chemical warfare agent es_ES
dc.subject Methanol derivative es_ES
dc.subject Chemical reaction es_ES
dc.subject Elimination reaction es_ES
dc.subject Molecular probe es_ES
dc.subject Phosphorylation es_ES
dc.subject.classification QUIMICA INORGANICA es_ES
dc.subject.classification QUIMICA ORGANICA es_ES
dc.title Aryl carbinols as nerve agent probes. Influence of the conjugation on the sensing properties es_ES
dc.type Artículo es_ES
dc.embargo.lift 10000-01-01
dc.embargo.terms forever es_ES
dc.identifier.doi 10.1039/c2nj40104e
dc.relation.projectID info:eu-repo/grantAgreement/MICINN//MAT2009-14564-C04-01/ES/Nanomateriales Hibridos Para El Desarrollo De "Puertas Moleculares" De Aplicacion En Procesos De Reconocimiento Y Terapeutica Y Para La Deteccion De Explosivos./ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/Generalitat Valenciana//PROMETEO09%2F2009%2F016/ES/Ayuda prometeo 2009 para el grupo de diseño y desarrollo de sensores/ es_ES
dc.rights.accessRights Abierto es_ES
dc.contributor.affiliation Universitat Politècnica de València. Instituto de Reconocimiento Molecular y Desarrollo Tecnológico - Institut de Reconeixement Molecular i Desenvolupament Tecnològic es_ES
dc.contributor.affiliation Universitat Politècnica de València. Departamento de Química - Departament de Química es_ES
dc.description.bibliographicCitation Royo Calvo, S.; Gotor Candel, RJ.; Costero Nieto, AM.; Parra Álvarez, M.; Gil Grau, S.; Martínez Mañez, R.; Sancenón Galarza, F. (2012). Aryl carbinols as nerve agent probes. Influence of the conjugation on the sensing properties. New Journal of Chemistry. 36(12):1485-1489. https://doi.org/10.1039/c2nj40104e es_ES
dc.description.accrualMethod S es_ES
dc.relation.publisherversion http://dx.doi.org/10.1039/c2nj40104e es_ES
dc.description.upvformatpinicio 1485 es_ES
dc.description.upvformatpfin 1489 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion es_ES
dc.description.volume 36 es_ES
dc.description.issue 12 es_ES
dc.relation.senia 230309
dc.contributor.funder Generalitat Valenciana es_ES
dc.contributor.funder Ministerio de Ciencia e Innovación es_ES
dc.contributor.funder Ministerio de Educación es_ES
dc.description.references Sadik, O. A., Land, W. H., & Wang, J. (2003). Targeting Chemical and Biological Warfare Agents at the Molecular Level. Electroanalysis, 15(14), 1149-1159. doi:10.1002/elan.200390140 es_ES
dc.description.references Russell, A. J., Berberich, J. A., Drevon, G. F., & Koepsel, R. R. (2003). Biomaterials for Mediation of Chemical and Biological Warfare Agents. Annual Review of Biomedical Engineering, 5(1), 1-27. doi:10.1146/annurev.bioeng.5.121202.125602 es_ES
dc.description.references Wang, H., Wang, J., Choi, D., Tang, Z., Wu, H., & Lin, Y. (2009). EQCM immunoassay for phosphorylated acetylcholinesterase as a biomarker for organophosphate exposures based on selective zirconia adsorption and enzyme-catalytic precipitation. Biosensors and Bioelectronics, 24(8), 2377-2383. doi:10.1016/j.bios.2008.12.013 es_ES
dc.description.references Im, H.-J., & Song, K. (2009). Applications of Prompt Gamma Ray Neutron Activation Analysis: Detection of Illicit Materials. Applied Spectroscopy Reviews, 44(4), 317-334. doi:10.1080/05704920902852125 es_ES
dc.description.references Sohn, H., Létant, S., Sailor, M. J., & Trogler, W. C. (2000). Detection of Fluorophosphonate Chemical Warfare Agents by Catalytic Hydrolysis with a Porous Silicon Interferometer. Journal of the American Chemical Society, 122(22), 5399-5400. doi:10.1021/ja0006200 es_ES
dc.description.references Steiner, W. E., Klopsch, S. J., English, W. A., Clowers, B. H., & Hill, H. H. (2005). Detection of a Chemical Warfare Agent Simulant in Various Aerosol Matrixes by Ion Mobility Time-of-Flight Mass Spectrometry. Analytical Chemistry, 77(15), 4792-4799. doi:10.1021/ac050278f es_ES
dc.description.references Burnworth, M., Rowan, S. J., & Weder, C. (2007). Fluorescent Sensors for the Detection of Chemical Warfare Agents. Chemistry - A European Journal, 13(28), 7828-7836. doi:10.1002/chem.200700720 es_ES
dc.description.references Thomas, S. W., Joly, G. D., & Swager, T. M. (2007). Chemical Sensors Based on Amplifying Fluorescent Conjugated Polymers. Chemical Reviews, 107(4), 1339-1386. doi:10.1021/cr0501339 es_ES
dc.description.references Royo, S., Martínez-Máñez, R., Sancenón, F., Costero, A. M., Parra, M., & Gil, S. (2007). Chromogenic and fluorogenic reagents for chemical warfare nerve agents’ detection. Chemical Communications, (46), 4839. doi:10.1039/b707063b es_ES
dc.description.references Giordano, B., & Collins, G. (2007). Synthetic Methods Applied to the Detection of Chemical Warfare Nerve Agents. Current Organic Chemistry, 11(3), 255-265. doi:10.2174/138527207779940883 es_ES
dc.description.references Kang, S., Kim, S., Yang, Y.-K., Bae, S., & Tae, J. (2009). Fluorescent and colorimetric detection of acid vapors by using solid-supported rhodamine hydrazides. Tetrahedron Letters, 50(17), 2010-2012. doi:10.1016/j.tetlet.2009.02.087 es_ES
dc.description.references Costero, A. M., Parra, M., Gil, S., Gotor, R., Mancini, P. M. E., Martínez-Máñez, R., … Royo, S. (2010). Chromo-Fluorogenic Detection of Nerve-Agent Mimics Using Triggered Cyclization Reactions in Push-Pull Dyes. Chemistry - An Asian Journal, 5(7), 1573-1585. doi:10.1002/asia.201000058 es_ES
dc.description.references Costero, A. M., Gil, S., Parra, M., Mancini, P. M. E., Martínez-Máñez, R., Sancenón, F., & Royo, S. (2008). Chromogenic detection of nerve agent mimics. Chemical Communications, (45), 6002. doi:10.1039/b811247a es_ES
dc.description.references Climent, E., Martínez-Máñez, R., Sancenón, F., Marcos, M. D., Soto, J., Maquieira, A., & Amorós, P. (2010). Controlled Delivery Using Oligonucleotide-Capped Mesoporous Silica Nanoparticles. Angewandte Chemie International Edition, 49(40), 7281-7283. doi:10.1002/anie.201001847 es_ES
dc.description.references Candel, I., Bernardos, A., Climent, E., Marcos, M. D., Martínez-Máñez, R., Sancenón, F., … Parra, M. (2011). Selective opening of nanoscopic capped mesoporous inorganic materials with nerve agent simulants; an application to design chromo-fluorogenic probes. Chemical Communications, 47(29), 8313. doi:10.1039/c1cc12727f es_ES
dc.description.references Royo, S., Costero, A. M., Parra, M., Gil, S., Martínez-Máñez, R., & Sancenón, F. (2011). Chromogenic, Specific Detection of the Nerve-Agent Mimic DCNP (a Tabun Mimic). Chemistry - A European Journal, 17(25), 6931-6934. doi:10.1002/chem.201100602 es_ES
dc.description.references Gotor, R., Costero, A. M., Gil, S., Parra, M., Martínez-Máñez, R., & Sancenón, F. (2011). A Molecular Probe for the Highly Selective Chromogenic Detection of DFP, a Mimic of Sarin and Soman Nerve Agents. Chemistry - A European Journal, 17(43), 11994-11997. doi:10.1002/chem.201102241 es_ES
dc.description.references Duxbury, D. F. (1993). The photochemistry and photophysics of triphenylmethane dyes in solid and liquid media. Chemical Reviews, 93(1), 381-433. doi:10.1021/cr00017a018 es_ES
dc.description.references Akiyama, S., Yoshida, K., Hayashida, M., Nakashima, K., Nakatsuji, S., & Iyoda, M. (1981). ETHYNOLOGS OF TRIPHENYLMETHANE DYES. SYNTHESES AND PROPERTIES OF ACETYLENIC ANALOGS OF MALACHITE GREEN, CRYSTAL VIOLET, AND THEIR RELATED COMPOUNDS. Chemistry Letters, 10(3), 311-314. doi:10.1246/cl.1981.311 es_ES
dc.description.references Dikusar, E. A. (2003). Tertiary Acetylenic Alcohols and Peroxides Derived from 4,4’-Bis(dimethylamino)benzophenone (Michler’s Ketone). Russian Journal of General Chemistry, 73(9), 1406-1409. doi:10.1023/b:rugc.0000015988.84852.9d es_ES
dc.description.references Gabbutt, C. D., Heron, B. M., Kilner, C., & Kolla, S. B. (2010). The influence of a 1,1-diarylvinyl moiety on the photochromism of naphthopyrans. Organic & Biomolecular Chemistry, 8(21), 4874. doi:10.1039/c0ob00141d es_ES
dc.description.references Akiyama, S., Nakatsuji, S., Nakashima, K., & Yamasaki, S. (1988). Diphenylmethane and triphenylmethane dye ethynovinylogues with absorption bands in the near-infrared11Ethynologues of Triphenylmethane Dyes V: Part IV.2,3. Dyes and Pigments, 9(6), 459-466. doi:10.1016/0143-7208(88)82005-9 es_ES
dc.description.references Gorman, S. A., Hepworth, J. D., & Mason, D. (2000). The effects of cyclic terminal groups in di- and tri-arylmethane dyes. Part 3. Consequences of unsymmetrical substitution in Malachite Green. Journal of the Chemical Society, Perkin Transactions 2, (9), 1889-1895. doi:10.1039/b003219k es_ES
dc.description.references Nakatsuji, S., Okamoto, N., Nakashima, K., & Akiyama, S. (1986). SYNTHESIS AND ELECTRONIC ABSORPTION SPECTRA OF MONOETHYNOLOGS OF MALACHITE GREEN WITH p-SUBSTITUENT ON PHENYL RING. Chemistry Letters, 15(3), 329-332. doi:10.1246/cl.1986.329 es_ES
dc.description.references Tachikawa, T., Handa, C., & Tokita, S. (2003). Synthesis and Radiation Sensitivity of Tris (4-N,N-dimethylaminophenyl)methanethiol. Journal of Photopolymer Science and Technology, 16(2), 187-190. doi:10.2494/photopolymer.16.187 es_ES


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