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dc.contributor.author | Fedeli S. | |
dc.contributor.author | Paoli P. | |
dc.contributor.author | Brandi A. | |
dc.contributor.author | Venturini L. | |
dc.contributor.author | Giambastiani G. | |
dc.contributor.author | Tuci G. | |
dc.contributor.author | Cicchi S. | |
dc.date.accessioned | 2018-09-18T20:11:09Z | |
dc.date.available | 2018-09-18T20:11:09Z | |
dc.date.issued | 2015 | |
dc.identifier.issn | 0947-6539 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/137365 | |
dc.description.abstract | © 2015 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. A series of azido-dyes were synthesized through Knoevenagel reactions of an azido-BODIPY with aromatic aldehydes. The nature of the substituents allowed the fine tuning of their spectroscopic properties. The dyes were used to decorate oxidized multiwalled carbon nanotubes (ox-MWCNTs), bearing terminal triple bond groups, by CuAAC reactions, affording fluorescent materials. This decoration allowed the efficient determination of the internalization of the ox-MWCNT derivatives by different model cancer cells, such as MCF7. | |
dc.relation.ispartofseries | Chemistry - A European Journal | |
dc.subject | BODIPY | |
dc.subject | carbon nanotubes | |
dc.subject | click reaction | |
dc.subject | fluorescent probes | |
dc.title | Azido-Substituted BODIPY Dyes for the Production of Fluorescent Carbon Nanotubes | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 43 | |
dc.relation.ispartofseries-volume | 21 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 15349 | |
dc.source.id | SCOPUS09476539-2015-21-43-SID84945473580 |