Visible-Light-Reactive Single-Chain Nanoparticles

被引:14
|
作者
Mundsinger, Kai [1 ,2 ]
Tuten, Bryan T. [1 ,2 ]
Wang, Lily [3 ]
Neubauer, Kira [4 ]
Kropf, Christian [4 ]
O'Mara, Megan L. [3 ,5 ]
Barner-Kowollik, Christopher [1 ,2 ,6 ]
机构
[1] Queensland Univ Technol QUT, Sch Chem & Phys, Brisbane, Qld 4000, Australia
[2] Queensland Univ Technol QUT, Ctr Mat Sci, Brisbane, Qld 4000, Australia
[3] Australian Natl Univ, Coll Sci, Res Sch Chem, Canberra, ACT 2601, Australia
[4] Henkel AG & Co KGaA, Henkelstr 67, D-40589 Dusseldorf, Germany
[5] Univ Queensland, Australian Inst Bioengn & Nanotechnol, St Lucia, Qld 4072, Australia
[6] Karlsruhe Inst Technol KIT, Inst Nanotechnol INT, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
基金
澳大利亚研究理事会;
关键词
Molecular Dynamics; Polymers; Reaction Confinement; Single-Chain Nanoparticle; Singlet Oxygen; OXYGEN;
D O I
10.1002/anie.202302995
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We introduce a single-chain nanoparticle (SCNP) system capable of catalyzing the photooxidation of nonpolar alkenes up to three times more efficiently than an equivalent small-molecule photosensitizer at an identical concentration. Specifically, we construct a polymer chain constituted of poly(ethylene glycol) methyl ether methacrylate and glycidyl methacrylate which we compact via multifunctional thiol-epoxide ligation and functionalize with Rose Bengal (RB) in a one pot reaction, affording SCNPs with a hydrophilic shell and hydrophobic photocatalytic regions. Photooxidation of the internal alkene in oleic acid proceeds under green light. RB confined within the SCNP is three times more effective for nonpolar alkenes than free RB in solution, which we hypothesize is due to the spatial proximity of the photosensitizing units to the substrate in the hydrophobic region. Our approach demonstrates that SCNP based catalysts can afford enhanced photocatalysis via confinement effects in a homogeneous reaction environment.
引用
收藏
页数:6
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