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“CinNapht” dyes: a new cinnoline/naphthalimide fused hybrid fluorophore. Synthesis, photo-physical study and use for bio-imaging
Six-membered-diaza ring of cinnoline has been fused on naphthalimide dye to give a donor–acceptor system called CinNapht. This red shifted fluorophore, that can be synthesised in gram scale, exhibits a large Stoke shift and a fluorescence quantum yield up to 0.33. It is also characterized by a stron...
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Royal Society of Chemistry
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9041350/ https://www.ncbi.nlm.nih.gov/pubmed/35493990 http://dx.doi.org/10.1039/d1ra05110e |
| _version_ | 1784694527199543296 |
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| author | Hoang, Minh-Duc Bodin, Jean-Baptiste Savina, Farah Steinmetz, Vincent Bignon, Jérôme Durand, Philippe Clavier, Gilles Méallet-Renault, Rachel Chevalier, Arnaud |
| author_facet | Hoang, Minh-Duc Bodin, Jean-Baptiste Savina, Farah Steinmetz, Vincent Bignon, Jérôme Durand, Philippe Clavier, Gilles Méallet-Renault, Rachel Chevalier, Arnaud |
| author_sort | Hoang, Minh-Duc |
| collection | PubMed |
| description | Six-membered-diaza ring of cinnoline has been fused on naphthalimide dye to give a donor–acceptor system called CinNapht. This red shifted fluorophore, that can be synthesised in gram scale, exhibits a large Stoke shift and a fluorescence quantum yield up to 0.33. It is also characterized by a strong solvatochromic effect from green to red emission as well and can be used for bio-imaging. |
| format | Online Article Text |
| id | pubmed-9041350 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2021 |
| publisher | The Royal Society of Chemistry |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-90413502022-04-28 “CinNapht” dyes: a new cinnoline/naphthalimide fused hybrid fluorophore. Synthesis, photo-physical study and use for bio-imaging Hoang, Minh-Duc Bodin, Jean-Baptiste Savina, Farah Steinmetz, Vincent Bignon, Jérôme Durand, Philippe Clavier, Gilles Méallet-Renault, Rachel Chevalier, Arnaud RSC Adv Chemistry Six-membered-diaza ring of cinnoline has been fused on naphthalimide dye to give a donor–acceptor system called CinNapht. This red shifted fluorophore, that can be synthesised in gram scale, exhibits a large Stoke shift and a fluorescence quantum yield up to 0.33. It is also characterized by a strong solvatochromic effect from green to red emission as well and can be used for bio-imaging. The Royal Society of Chemistry 2021-09-08 /pmc/articles/PMC9041350/ /pubmed/35493990 http://dx.doi.org/10.1039/d1ra05110e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
| spellingShingle | Chemistry Hoang, Minh-Duc Bodin, Jean-Baptiste Savina, Farah Steinmetz, Vincent Bignon, Jérôme Durand, Philippe Clavier, Gilles Méallet-Renault, Rachel Chevalier, Arnaud “CinNapht” dyes: a new cinnoline/naphthalimide fused hybrid fluorophore. Synthesis, photo-physical study and use for bio-imaging |
| title | “CinNapht” dyes: a new cinnoline/naphthalimide fused hybrid fluorophore. Synthesis, photo-physical study and use for bio-imaging |
| title_full | “CinNapht” dyes: a new cinnoline/naphthalimide fused hybrid fluorophore. Synthesis, photo-physical study and use for bio-imaging |
| title_fullStr | “CinNapht” dyes: a new cinnoline/naphthalimide fused hybrid fluorophore. Synthesis, photo-physical study and use for bio-imaging |
| title_full_unstemmed | “CinNapht” dyes: a new cinnoline/naphthalimide fused hybrid fluorophore. Synthesis, photo-physical study and use for bio-imaging |
| title_short | “CinNapht” dyes: a new cinnoline/naphthalimide fused hybrid fluorophore. Synthesis, photo-physical study and use for bio-imaging |
| title_sort | “cinnapht” dyes: a new cinnoline/naphthalimide fused hybrid fluorophore. synthesis, photo-physical study and use for bio-imaging |
| topic | Chemistry |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9041350/ https://www.ncbi.nlm.nih.gov/pubmed/35493990 http://dx.doi.org/10.1039/d1ra05110e |
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