TY - JOUR
T1 - On-demand acid-gated fluorescence switch-on in photo-generated nanospheres
AU - Hooker, Jordan P.
AU - Feist, Florian
AU - Delafresnaye, Laura
AU - Cavalli, Federica
AU - Barner, Leonie
AU - Barner-Kowollik, Christopher
N1 - Funding Information:
C. B.-K. acknowledges the Australian Research Council (ARC) for funding in the form of a Laureate Fellowship underpinning his photochemical research program as well as the Queensland University of Technology (QUT) for key continued support. C. B.-K. and L. B. acknowledge additional funding in the context of an ARC Linkage grant on advanced particle synthesis. The authors acknowledge the facilities and the scientific and technical assistance from the Australian Microscopy & Microanalysis Research Facility (AMMRF) at the Central Analytical Research Facility (CARF) operated by the Institute for Future Environments (IFE).
Publisher Copyright:
© The Royal Society of Chemistry 2020.
PY - 2020/5/7
Y1 - 2020/5/7
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/85084379276
U2 - 10.1039/d0cc01557a
DO - 10.1039/d0cc01557a
M3 - Article
C2 - 32297609
AN - SCOPUS:85084379276
SN - 1359-7345
VL - 56
SP - 4986
EP - 4989
JO - Chemical Communications
JF - Chemical Communications
IS - 37
ER -