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Wavelength-Orthogonal Stiffening of Hydrogel Networks with Visible Light.
Truong, Vinh X; Bachmann, Julian; Unterreiner, Andreas-Neil; Blinco, James P; Barner-Kowollik, Christopher.
Afiliação
  • Truong VX; Centre for Materials Science, Queensland University of Technology (QUT), 2 George St., Brisbane, QLD 4000, Australia.
  • Bachmann J; School of Chemistry and Physics, Queensland University of Technology (QUT), 2 George St., Brisbane, QLD 4000, Australia.
  • Unterreiner AN; Centre for Materials Science, Queensland University of Technology (QUT), 2 George St., Brisbane, QLD 4000, Australia.
  • Blinco JP; School of Chemistry and Physics, Queensland University of Technology (QUT), 2 George St., Brisbane, QLD 4000, Australia.
  • Barner-Kowollik C; Institute of Physical Chemistry, Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 2, 76131, Karlsruhe, Germany.
Angew Chem Int Ed Engl ; 61(15): e202113076, 2022 Apr 04.
Article em En | MEDLINE | ID: mdl-35029002
Herein, we introduce the wavelength-orthogonal crosslinking of hydrogel networks using two red-shifted chromophores, i.e. acrylpyerene (AP, λactivation =410-490 nm) and styrylpyrido[2,3-b]pyrazine (SPP, λactivation =400-550 nm), able to undergo [2+2] photocycloaddition in the visible-light regime. The photoreactivity of the SPP moiety is pH-dependent, whereby an acidic environment inhibits the cycloaddition. By employing a spiropyran-based photoacid generator with suitable absorption wavelength, we are able to restrict the activation wavelength of the SPP moiety to the green light region (λactivation =520-550 nm), enabling wavelength-orthogonal activation of the AP group. Our wavelength-orthogonal photochemical system was successfully applied in the design of hydrogels whose stiffness can be tuned independently by either green or blue light.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article