Subtleties of catanionic surfactant reverse micelle assemblies revealed by a fluorescent molecular probe
In this work, the absorption and emission behavior of the cationic hemicyanine trans-4-[4(dimethylamino)styryl]-N-methylpyridinium iodide (HC) in reverse micelles (RMs) formed by the catanionic surfactants benzyl-n-hexadecyldimethylammonium-1,4-bis-2-ethylhexylsulfosuccinate (AOT-BHD) and cetyltrime...
| Autores: | , , , |
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| Tipo de documento: | artigo |
| Estado: | Versão publicada |
| Data de publicação: | 2017 |
| País: | Argentina |
| Recursos: | Consejo Nacional de Investigaciones Científicas y Técnicas |
| Repositório: | CONICET Digital (CONICET) |
| Idioma: | inglês |
| OAI Identifier: | oai:ri.conicet.gov.ar:11336/67636 |
| Acesso em linha: | http://hdl.handle.net/11336/67636 |
| Access Level: | Acceso aberto |
| Palavra-chave: | Catanionic Surfactant Hc Reverse Micelles Water Entrapped Supplementary Material For this Article Is Available Online https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
| Resumo: | In this work, the absorption and emission behavior of the cationic hemicyanine trans-4-[4(dimethylamino)styryl]-N-methylpyridinium iodide (HC) in reverse micelles (RMs) formed by the catanionic surfactants benzyl-n-hexadecyldimethylammonium-1,4-bis-2-ethylhexylsulfosuccinate (AOT-BHD) and cetyltrimethylammonium-1,4-bis-2-ethylhexylsulfosuccinate (AOT-CTA) have been investigated. Our results show that the spectroscopic behavior of HC changes when the dye is dissolved in AOT-BHD or in AOT-CTA RMs. While HC undergoes an intramolecular charge-transfer process upon excitation in AOT-CTA RMs, in AOT-BHD RMs this process is inhibited due to a specific interaction between HC and the polar head group of the BHD+ cation. This implies that the chemical structure of CTA+ and BHD+ cations has a large impact on the excited stated from which HC emission occurs. Additionally, the structural difference between the two cations impacts on the water–RM interface interaction, which provides a way of controlling the solvation process in these RMs. Furthermore, differences in the interfacial fluidity between the two catanionic RMs is observed, a result that is particularly interesting with regard to these systems being used as nanoreactors. |
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