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 |
|