TY - JOUR
T1 - Acid-Enhanced Photoiniferter Polymerization under Visible Light
AU - Antonopoulou, Maria Nefeli
AU - Truong, Nghia P.
AU - Egger, Timon
AU - Kroeger, Asja A.
AU - Coote, Michelle L.
AU - Anastasaki, Athina
PY - 2025/2/24
Y1 - 2025/2/24
N2 - Photoiniferter (PI) is a promising polymerization methodology, often used to overcome restrictions posed by thermal reversible addition-fragmentation chain-transfer (RAFT) polymerization. However, in the overwhelming majority of reports, high energy UV irradiation is required to effectively trigger photolysis of RAFT agents and facilitate the polymerization, significantly limiting its potential, scope, and applicability. Although visible light PI has emerged as a highly attractive alternative, most current approaches are limited to the synthesis of lower molecular weight polymers (i.e. 10,000 g/mol), and typically suffer from prolonged reaction times, extended induction periods, and higher dispersities when high activity CTAs (photoiniferters), such as trithiocarbonates, are employed. Herein, an acid-enhanced PI polymerization is introduced that efficiently operates under visible light irradiation. The presence of small amounts of biocompatible citric acid fully eliminates the lengthy induction period (21 hours) by enhancing photolysis, rapidly consuming the CTA, and accelerating the reaction rate, yielding polymers with narrow molar mass distributions (Ð ~1.1), near-quantitative conversions (>97 %), and high end-group fidelity in just two hours. A particularly noteworthy aspect of this work is the possibility to target very high degrees of polymerization (i.e. DP=3,000) within short timescales (i.e. less than five hours) without compromising the control over the dispersity (Ð ~1.1). The versatility of the technique is further demonstrated through the synthesis of well-defined diblock copolymers and its compatibility to various polymer classes (i.e. acrylamides, acrylates, methacrylates), thus establishing visible-light PI as a robust tool for polymer synthesis.
AB - Photoiniferter (PI) is a promising polymerization methodology, often used to overcome restrictions posed by thermal reversible addition-fragmentation chain-transfer (RAFT) polymerization. However, in the overwhelming majority of reports, high energy UV irradiation is required to effectively trigger photolysis of RAFT agents and facilitate the polymerization, significantly limiting its potential, scope, and applicability. Although visible light PI has emerged as a highly attractive alternative, most current approaches are limited to the synthesis of lower molecular weight polymers (i.e. 10,000 g/mol), and typically suffer from prolonged reaction times, extended induction periods, and higher dispersities when high activity CTAs (photoiniferters), such as trithiocarbonates, are employed. Herein, an acid-enhanced PI polymerization is introduced that efficiently operates under visible light irradiation. The presence of small amounts of biocompatible citric acid fully eliminates the lengthy induction period (21 hours) by enhancing photolysis, rapidly consuming the CTA, and accelerating the reaction rate, yielding polymers with narrow molar mass distributions (Ð ~1.1), near-quantitative conversions (>97 %), and high end-group fidelity in just two hours. A particularly noteworthy aspect of this work is the possibility to target very high degrees of polymerization (i.e. DP=3,000) within short timescales (i.e. less than five hours) without compromising the control over the dispersity (Ð ~1.1). The versatility of the technique is further demonstrated through the synthesis of well-defined diblock copolymers and its compatibility to various polymer classes (i.e. acrylamides, acrylates, methacrylates), thus establishing visible-light PI as a robust tool for polymer synthesis.
KW - acid catalysis
KW - controlled radical polymerization
KW - photoiniferter
KW - RAFT
UR - http://www.scopus.com/inward/record.url?scp=85214702954&partnerID=8YFLogxK
UR - http://purl.org/au-research/grants/ARC/CE23010002
U2 - 10.1002/anie.202420733
DO - 10.1002/anie.202420733
M3 - Article
AN - SCOPUS:85214702954
SN - 1433-7851
VL - 64
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 9
M1 - e202420733
ER -