Publication: Benzotriazole-based multidonor-acceptor systems as attractive two-photon absorption dye platforms
dc.contributor.author | Benitez-Martin, Carlos | |
dc.contributor.author | Donoso, Beatriz | |
dc.contributor.author | Torres-Moya, Ivan | |
dc.contributor.author | Herrera, Jesus | |
dc.contributor.author | Diaz-Ortiz, Angel | |
dc.contributor.author | Najera, Francisco | |
dc.contributor.author | Prieto, Pilar | |
dc.contributor.author | Perez-Inestrosa, Ezequiel | |
dc.contributor.authoraffiliation | [Benitez-Martin, Carlos] Univ Malaga, Dept Quim Organ, IBIMA, Malaga 29071, Spain | |
dc.contributor.authoraffiliation | [Najera, Francisco] Univ Malaga, Dept Quim Organ, IBIMA, Malaga 29071, Spain | |
dc.contributor.authoraffiliation | [Perez-Inestrosa, Ezequiel] Univ Malaga, Dept Quim Organ, IBIMA, Malaga 29071, Spain | |
dc.contributor.authoraffiliation | [Benitez-Martin, Carlos] Ctr Andaluz Nanomed & Biotecnol BIONAND, Parque Tecnol Andalucia, Malaga 29590, Spain | |
dc.contributor.authoraffiliation | [Perez-Inestrosa, Ezequiel] Ctr Andaluz Nanomed & Biotecnol BIONAND, Parque Tecnol Andalucia, Malaga 29590, Spain | |
dc.contributor.authoraffiliation | [Donoso, Beatriz] Univ Castilla La Mancha, Fac Chem & Technol Sci IRICA, Dept Organ Inorgan Chem & Biochem, Ciudad Real 13071, Spain | |
dc.contributor.authoraffiliation | [Torres-Moya, Ivan] Univ Castilla La Mancha, Fac Chem & Technol Sci IRICA, Dept Organ Inorgan Chem & Biochem, Ciudad Real 13071, Spain | |
dc.contributor.authoraffiliation | [Herrera, Jesus] Univ Castilla La Mancha, Fac Chem & Technol Sci IRICA, Dept Organ Inorgan Chem & Biochem, Ciudad Real 13071, Spain | |
dc.contributor.authoraffiliation | [Diaz-Ortiz, Angel] Univ Castilla La Mancha, Fac Chem & Technol Sci IRICA, Dept Organ Inorgan Chem & Biochem, Ciudad Real 13071, Spain | |
dc.contributor.authoraffiliation | [Prieto, Pilar] Univ Castilla La Mancha, Fac Chem & Technol Sci IRICA, Dept Organ Inorgan Chem & Biochem, Ciudad Real 13071, Spain | |
dc.contributor.funder | Spanish Ministry for Science, Innovation, and Universities | |
dc.contributor.funder | Institute of Health Carlos III (ISCIII) | |
dc.contributor.funder | Junta de Andalucia | |
dc.contributor.funder | MCIN/AEI | |
dc.contributor.funder | MCIN | |
dc.contributor.funder | FEDER | |
dc.contributor.funder | Junta de Comunidades de Castilla-La Mancha | |
dc.contributor.funder | Universidad de Malaga / CBUA | |
dc.date.accessioned | 2023-05-03T14:54:38Z | |
dc.date.available | 2023-05-03T14:54:38Z | |
dc.date.issued | 2022-02-09 | |
dc.description.abstract | Pyrazine-decorated benzotriazole cores allow the orthogonal combination of two dipolar systems within a single molecule. A series of this type of derivatives was synthesized and their photophysical features were studied. The properties of these compounds showed remarkable differences in function depending on the substitution in the pyrazine ring of the benzotriazole core. Furthermore, the two-photon absorption property (2PA) was studied to determine the structure-properties relationship for the reported compounds. The best dye achieved a crosssection of 1532 GM, which was higher than values previously obtained for similar D-pi-A-pi-D benzotriazole derivatives. TD-DFT calculations, which supported the experimental observations, indicating the interaction between the two dipolar systems was responsible for enhancing the 2 PA properties and favoring bathochromic shifts. | |
dc.description.version | Si | |
dc.identifier.citation | Benitez-Martin C, Donoso B, Torres-Moya I, Herrera J, Díaz-Ortiz Á, Najera F, et al. Benzotriazole-based multidonor-acceptor systems as attractive twophoton absorption dye platforms. Dyes and Pigments. 2022, (200). 110149 | |
dc.identifier.doi | 10.1016/j.dyepig.2022.110149 | |
dc.identifier.essn | 1873-3743 | |
dc.identifier.issn | 0143-7208 | |
dc.identifier.unpaywallURL | https://doi.org/10.1016/j.dyepig.2022.110149 | |
dc.identifier.uri | http://hdl.handle.net/10668/22157 | |
dc.identifier.wosID | 783214000009 | |
dc.journal.title | Dyes and pigments | |
dc.journal.titleabbreviation | Dyes pigment. | |
dc.language.iso | en | |
dc.organization | Centro Andaluz de Nanomedicina y Biotecnología-BIONAND | |
dc.organization | Instituto de Investigación Biomédica de Málaga-IBIMA | |
dc.publisher | Elsevier | |
dc.relation.projectID | PCI2019-111825-2 | |
dc.relation.projectID | PID2019-104293GB-I00 | |
dc.relation.projectID | RD16/0006/0012 | |
dc.relation.projectID | UMA18-FEDERJA007 | |
dc.relation.projectID | PID2020-119636GB-I00 | |
dc.relation.projectID | MCIN/ AEI /10.13039/501100011033 | |
dc.relation.projectID | RED2018-102331-T | |
dc.relation.projectID | CTQ2017-84825-R | |
dc.relation.projectID | MCIN/ AEI /10.13039/501100011033/ | |
dc.relation.projectID | SBPLY/17/180501/000189 | |
dc.relation.projectID | FPU16/05099 | |
dc.relation.projectID | SBPLY/19/180501/000346 | |
dc.relation.publisherversion | https://www.sciencedirect.com/science/article/pii/S0143720822000717 | |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International | |
dc.rights.accessRights | open access | |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.subject | Two-photon absorption | |
dc.subject | Fluorescence | |
dc.subject | DFT calculations | |
dc.subject | Benzotriazole dyes | |
dc.subject | Optical-data storage | |
dc.subject | Absorbing chromophores | |
dc.subject | Fluorescent-probe | |
dc.subject | Red-fluorescent | |
dc.subject | Wave-guide | |
dc.subject | Design | |
dc.subject | Benzothiadiazole | |
dc.subject | Emission | |
dc.subject | Thiadiazoloquinoxaline | |
dc.subject | Initiators | |
dc.subject.decs | Fenómenos químicos | |
dc.subject.decs | Fotones | |
dc.subject.decs | Teoría funcional de la densidad | |
dc.subject.mesh | Density functional theory | |
dc.subject.mesh | Benzotriazole | |
dc.subject.mesh | Chemical phenomena | |
dc.subject.mesh | Photons | |
dc.subject.mesh | Triazoles | |
dc.title | Benzotriazole-based multidonor-acceptor systems as attractive two-photon absorption dye platforms | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 200 | |
dc.wostype | Article | |
dspace.entity.type | Publication |
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