BINOLated aminostyryl BODIPYs: a workable organic molecular platform for NIR circularly polarized luminescence
dc.contributor.author | Jiménez González, Josué | |
dc.contributor.author | Díaz Norambuena, Carolina | |
dc.contributor.author | Serrano Villar, Sergio | |
dc.contributor.author | Ma, Shing Cho | |
dc.contributor.author | Moreno Jiménez, Florencio | |
dc.contributor.author | Maroto, Beatriz Lora | |
dc.contributor.author | Bañuelos Prieto, Jorge | |
dc.contributor.author | Muller, Gilles | |
dc.contributor.author | Moya Cerero, Santiago de la | |
dc.date.accessioned | 2023-06-17T09:21:47Z | |
dc.date.available | 2023-06-17T09:21:47Z | |
dc.date.issued | 2021-06-14 | |
dc.description | Submitted: 08 Mar 2021; Accepted: 10 May 2021; First published: 11 May 2021 | |
dc.description.abstract | The accessible at-boron-BINOLated 3,5-bis(4-aminostyryl)ated BODIPY scaffold is highlighted as a workable platform for developing enantiopure small organic molecules exhibiting CPL in the NIR region, even in water solution, the latter being key for CPL-based bioapplications. Synthetic simplicity, noticeable chiroptical efficiency in the NIR and the possibility to access water-soluble emitters pave the way for advancing CPL tools based on organic emitters and NI radiation. | |
dc.description.department | Depto. de Química Orgánica | |
dc.description.department | Sección Deptal. de Química Orgánica (Óptica y Optometría) | |
dc.description.faculty | Fac. de Ciencias Químicas | |
dc.description.faculty | Fac. de Óptica y Optometría | |
dc.description.refereed | TRUE | |
dc.description.sponsorship | Ministerio de Ciencia e Innovación (MICINN) | |
dc.description.sponsorship | Gobierno Vasco | |
dc.description.status | pub | |
dc.eprint.id | https://eprints.ucm.es/id/eprint/69688 | |
dc.identifier.doi | 10.1039/d1cc01255j | |
dc.identifier.issn | 1359-7345, ESSN: 1364-548X | |
dc.identifier.officialurl | http://dx.doi.org/10.1039/d1cc01255j | |
dc.identifier.relatedurl | https://pubs.rsc.org/en/content/articlelanding/2021/cc/d1cc01255j/unauth | |
dc.identifier.uri | https://hdl.handle.net/20.500.14352/8658 | |
dc.issue.number | 47 | |
dc.journal.title | Chemical Communications | |
dc.language.iso | eng | |
dc.page.final | 5753 | |
dc.page.initial | 5750 | |
dc.publisher | Royal Society of Chemistry | |
dc.relation.projectID | MAT2017-83856-C3-2-P y -3-P; PID2020-114755GB-C3 | |
dc.relation.projectID | IT912-16 | |
dc.rights.accessRights | restricted access | |
dc.subject.cdu | 66.085.1 | |
dc.subject.cdu | 543.426 | |
dc.subject.cdu | 535.37 | |
dc.subject.cdu | 534.544 | |
dc.subject.keyword | polarized luminescence | |
dc.subject.keyword | BODIPY | |
dc.subject.keyword | NIR region | |
dc.subject.ucm | Biología molecular (Química) | |
dc.subject.ucm | Optica (Química) | |
dc.subject.ucm | Química física (Química) | |
dc.title | BINOLated aminostyryl BODIPYs: a workable organic molecular platform for NIR circularly polarized luminescence | |
dc.type | journal article | |
dc.volume.number | 57 | |
dspace.entity.type | Publication | |
relation.isAuthorOfPublication | 09111c59-3829-4b92-a9d2-ee099b545e9e | |
relation.isAuthorOfPublication | 7940c6e8-25c3-4083-b533-0c34e155dfa8 | |
relation.isAuthorOfPublication.latestForDiscovery | 09111c59-3829-4b92-a9d2-ee099b545e9e |
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