Dual electrochemical and chemical control in atom transfer radical polymerization with copper electrodes

被引:7
作者
De Bon, Francesco [1 ]
Lorandi, Francesca [2 ,3 ]
Coelho, Jorge F. J. [1 ]
Serra, Armenio C. [1 ]
Matyjaszewski, Krzysztof [3 ]
Isse, Abdirisak A. [2 ]
机构
[1] Univ Coimbra, Dept Chem Engn, Ctr Mech Engn Mat & Proc CEMMPRE, Rua Silvio Lima,Polo 2, P-3030790 Coimbra, Portugal
[2] Univ Padua, Dept Chem Sci, Via Marzolo 1, I-35131 Padua, Italy
[3] Carnegie Mellon Univ, Dept Chem, 4400 Fifth Ave, Pittsburgh, PA 15213 USA
基金
美国国家科学基金会;
关键词
N-BUTYL ACRYLATE; SARA ATRP; METHYL-METHACRYLATE; MEDIATED ATRP; ACTIVATION; STYRENE; HEXAFLUOROPHOSPHATE; COPOLYMER; CATALYST; LIGAND;
D O I
10.1039/d2sc01982e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In Atom Transfer Radical Polymerization (ATRP), Cu-0 acts as a supplemental activator and reducing agent (SARA ATRP) by activating alkyl halides and (re)generating the Cu-I activator through a comproportionation reaction, respectively. Cu-0 is also an unexplored, exciting metal that can act as a cathode in electrochemically mediated ATRP (eATRP). Contrary to conventional inert electrodes, a Cu cathode can trigger a dual catalyst regeneration, simultaneously driven by electrochemistry and comproportionation, if a free ligand is present in solution. The dual regeneration explored herein allowed for introducing the concept of pulsed galvanostatic electrolysis (PGE) in eATRP. During a PGE, the process alternates between a period of constant current electrolysis and a period with no applied current in which polymerization continues via SARA ATRP. The introduction of no electrolysis periods without compromising the overall polymerization rate and control is very attractive, if large current densities are needed. Moreover, it permits a drastic charge saving, which is of unique value for a future scale-up, as electrochemistry coupled to SARA ATRP saves energy, and shortens the equipment usage.
引用
收藏
页码:6008 / 6018
页数:11
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