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On-demand acid-gated fluorescence switch-on in photo-generated nanospheres

  • Jordan P. Hooker
  • , Florian Feist
  • , Laura Delafresnaye
  • , Federica Cavalli
  • , Leonie Barner
  • , Christopher Barner-Kowollik

Research output: Contribution to journalArticleResearchpeer-review

Abstract

Herein, we introduce a fast, additive-free, ambient temperature photochemical approach - utilising the novel Diels-Alder cycloaddition of a photo-activeortho-methylbenzaldehyde (oMBA) with a terminal alkyne - for preparing functional acid-sensitive profluorescent nano-/microspheres in one step. Not previously reported, the possibility of applying such a reaction in the context of particle synthesis provides new possibilities for particle design, where multi-step reactivity can be gated into distinct steps. First, a photochemically-gated particle formation step yields a material possessing a reactive, spring-loaded intermediate at every cross-linking point. A second, on-demand step to initiate fluorescence generation subsequently imparts the properties of the chemical transformation to the material itself. The synthesised particles are narrow-disperse with an average diameter ranging from 170-380 nm.

Original languageEnglish
Pages (from-to)4986-4989
Number of pages4
JournalChemical Communications
Volume56
Issue number37
DOIs
Publication statusPublished - 7 May 2020
Externally publishedYes

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