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Wavelength‐Orthogonal Stiffening of Hydrogel Networks with Visible Light

Herein, we introduce the wavelength‐orthogonal crosslinking of hydrogel networks using two red‐shifted chromophores, i.e. acrylpyerene (AP, λ (activation)=410–490 nm) and styrylpyrido[2,3‐b]pyrazine (SPP, λ (activation)=400–550 nm), able to undergo [2+2] photocycloaddition in the visible‐light regim...

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Detalles Bibliográficos
Autores principales: Truong, Vinh X., Bachmann, Julian, Unterreiner, Andreas‐Neil, Blinco, James P., Barner‐Kowollik, Christopher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305448/
https://www.ncbi.nlm.nih.gov/pubmed/35029002
http://dx.doi.org/10.1002/anie.202113076
Descripción
Sumario:Herein, we introduce the wavelength‐orthogonal crosslinking of hydrogel networks using two red‐shifted chromophores, i.e. acrylpyerene (AP, λ (activation)=410–490 nm) and styrylpyrido[2,3‐b]pyrazine (SPP, λ (activation)=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 (λ (activation)=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.