Organopolymer with dual chromophores and fast charge-transfer properties for sustainable photocatalysis.
Justin D SmithAbdelqader M JamhawiJacek B JasinskiFabrice GallouJin GeRigoberto AdvinculaJinjun LiuSachin HandaPublished in: Nature communications (2019)
Photocatalytic polymers offer an alternative to prevailing organometallics and nanomaterials, and they may benefit from polymer-mediated catalytic and material enhancements. MPC-1, a polymer photoredox catalyst reported herein, exhibits enhanced catalytic activity arising from charge transfer states (CTSs) between its two chromophores. Oligomeric and polymeric MPC-1 preparations both promote efficient hydrodehalogenation of α-halocarbonyl compounds while exhibiting different solubility properties. The polymer is readily recovered by filtration. MPC-1-coated vessels enable batch and flow photocatalysis, even with opaque reaction mixtures, via "backside irradiation." Ultrafast transient absorption spectroscopy indicates a fast charge-transfer process within 20 ps of photoexcitation. Time-resolved photoluminescence measurements reveal an approximate 10 ns lifetime for bright valence states. Ultrafast measurements suggest a long CTS lifetime. Empirical catalytic activities of small-molecule models of MPC-1 subunits support the CTS hypothesis. Density functional theory (DFT) and time-dependent DFT calculations are in good agreement with experimental spectra, spectral peak assignment, and proposed underlying energetics.
Keyphrases
- density functional theory
- visible light
- molecular dynamics
- small molecule
- energy transfer
- ionic liquid
- quantum dots
- reduced graphene oxide
- single molecule
- high resolution
- electron transfer
- genome wide
- magnetic resonance
- magnetic resonance imaging
- single cell
- cancer therapy
- room temperature
- protein protein
- dna methylation
- carbon dioxide
- molecular docking