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A Water-Soluble Organic Photocatalyst Discovered for Highly Efficient Additive-Free Visible-Light-Driven Grafting of Polymers from Proteins at Ambient and Aqueous Environments
被引:30
|作者:
Lee, Yungyeong
[1
]
Kwon, Yonghwan
[1
,2
]
Kim, Youngmu
[1
,2
]
Yu, Changhoon
[1
]
Feng, Siyang
[3
]
Park, Jeehun
[4
]
Doh, Junsang
[1
,4
]
Wannemacher, Reinhold
[3
]
Koo, Byungjin
[5
]
Gierschner, Johannes
[3
]
Kwon, Min Sang
[1
,4
]
机构:
[1] Seoul Natl Univ, Dept Mat Sci & Engn, Seoul 08826, South Korea
[2] Ulsan Natl Inst Sci & Technol UNIST, Dept Mat Sci & Engn, Ulsan 44919, South Korea
[3] IMDEA Nanosci, Madrid Inst Adv Studies, Calle Faraday 9,Campus Cantoblanco, Madrid 28049, Spain
[4] Seoul Natl Univ, Res Inst Adv Mat, Seoul 08826, South Korea
[5] Dankook Univ, Dept Polymer Sci & Engn, Gyeonggi Do 16890, South Korea
基金:
新加坡国家研究基金会;
关键词:
organic photocatalysts;
photocatalyzed RAFT;
photoredox catalysis;
protein-polymer conjugates;
reversible-deactivation radical polymerization;
CONTROLLED RADICAL POLYMERIZATION;
PET-RAFT;
OXYGEN TOLERANCE;
CONJUGATION;
SUPEROXIDE;
GENERATION;
DESIGN;
D O I:
10.1002/adma.202108446
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Since the pioneering discovery of a protein bound to poly(ethylene glycol), the utility of protein-polymer conjugates (PPCs) is rapidly expanding to currently emerging applications. Photoinduced energy/electron-transfer reversible addition-fragmentation chain-transfer (PET-RAFT) polymerization is a very promising method to prepare structurally well-defined PPCs, as it eliminates high-cost and time-consuming deoxygenation processes due to its oxygen tolerance. However, the oxygen-tolerance behavior of PET-RAFT polymerization is not well-investigated in aqueous environments, and thereby the preparation of PPCs using PET-RAFT polymerization needs a substantial amount of sacrificial reducing agents or inert-gas purging processes. Herein a novel water-soluble and biocompatible organic photocatalyst (PC) is reported, which enables visible-light-driven additive-free "grafting-from" polymerizations of a protein in ambient and aqueous environments. Interestingly, the developed PC shows unconventional "oxygen-acceleration" behavior for a variety of acrylic and acrylamide monomers in aqueous conditions without any additives, which are apparently distinct from previously reported systems. With such a PC, "grafting-from" polymerizations are successfully performed from protein in ambient buffer conditions under green light-emitting diode (LED) irradiation, which result in various PPCs that have neutral, anionic, cationic, and zwitterionic polyacrylates, and polyacrylamides. It is believed that this PC will be widely employed for a variety of photocatalysis processes in aqueous environments, including the living cell system.
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