TY - JOUR
T1 - Molecular Photothermal Conversion Catalyst Promotes Photocontrolled Atom Transfer Radical Polymerization
AU - Preston-Herrera, Cristina
AU - Dadashi-Silab, Sajjad
AU - Oblinsky, Daniel G.
AU - Scholes, Gregory D.
AU - Stache, Erin E.
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/4/3
Y1 - 2024/4/3
N2 - Photothermal conversion is a growing research area that promotes thermal transformations with visible light irradiation. However, few examples of dual photothermal conversion and catalysis limit the power of this phenomenon. Here, we take inspiration from nature’s ability to use porphyrinic compounds for nonradiative relaxation to convert light into heat to facilitate thermal polymerization catalysis. We identify the photothermal conversion catalytic activity of a vitamin B12 derivative, heptamethyl ester cobyrinate (HME-Cob), to perform atom transfer radical polymerization (ATRP) under irradiation. Rapid polymerization are obtained under photothermal activation while maintaining good control over polymerization with the aid of a photoinitiator to enable light-induced catalyst regeneration. The catalyst exhibits exquisite temporal control in photocontrolled thermal polymerization. Ultimately, the activation of this complex is accessed across a broad range of wavelengths, including near-IR light, with excellent temporal control. This work showcases the potential of developing photothermal conversion catalysts.
AB - Photothermal conversion is a growing research area that promotes thermal transformations with visible light irradiation. However, few examples of dual photothermal conversion and catalysis limit the power of this phenomenon. Here, we take inspiration from nature’s ability to use porphyrinic compounds for nonradiative relaxation to convert light into heat to facilitate thermal polymerization catalysis. We identify the photothermal conversion catalytic activity of a vitamin B12 derivative, heptamethyl ester cobyrinate (HME-Cob), to perform atom transfer radical polymerization (ATRP) under irradiation. Rapid polymerization are obtained under photothermal activation while maintaining good control over polymerization with the aid of a photoinitiator to enable light-induced catalyst regeneration. The catalyst exhibits exquisite temporal control in photocontrolled thermal polymerization. Ultimately, the activation of this complex is accessed across a broad range of wavelengths, including near-IR light, with excellent temporal control. This work showcases the potential of developing photothermal conversion catalysts.
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U2 - 10.1021/jacs.4c00562
DO - 10.1021/jacs.4c00562
M3 - Article
C2 - 38507569
AN - SCOPUS:85188430200
SN - 0002-7863
VL - 146
SP - 8852
EP - 8857
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 13
ER -