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 ( e ATRP). 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 e ATRP. 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. 
                        more » 
                        « less   
                    
                            
                            Electrochemically Mediated Atom Transfer Radical Polymerization Driven by Alternating Current
                        
                    
    
            Abstract Alternating current (AC) and pulsed electrolysis are gaining traction in electro(organic) synthesis due to their advantageous characteristics. We employed AC electrolysis in electrochemically mediated Atom Transfer Radical Polymerization (eATRP) to facilitate the regeneration of the activator CuIcomplex on Cu0electrodes. Additionally, Cu0served as a slow supplemental activator and reducing agent (SARA ATRP), enabling the activation of alkyl halides and the regeneration of the CuIactivator through a comproportionation reaction. We harnessed the distinct properties of Cu0dual regeneration, both chemical and electrochemical, by employing sinusoidal, triangular, and square‐wave AC electrolysis alongside some of the most active ATRP catalysts available. Compared to linear waveform (DC electrolysis) or SARA ATRP (without electrolysis), pulsed and AC electrolysis facilitated slightly faster and more controlled polymerizations of acrylates. The same AC electrolysis conditions could successfully polymerize eleven different monomers across different mediums, from water to bulk. Moreover, it proved effective across a spectrum of catalyst activity, from low‐activity Cu/2,2‐bipyridine to highly active Cu complexes with substituted tripodal amine ligands. Chain extension experiments confirmed the high chain‐end fidelity of the produced polymers, yielding functional and high molecular‐weight block copolymers. SEM analysis indicated the robustness of the Cu0electrodes, sustaining at least 15 consecutive polymerizations. 
        more » 
        « less   
        
    
                            - Award ID(s):
- 2401112
- PAR ID:
- 10597613
- Publisher / Repository:
- Wiley VCH
- Date Published:
- Journal Name:
- Angewandte Chemie International Edition
- Volume:
- 63
- Issue:
- 29
- ISSN:
- 1433-7851
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
- 
            
- 
            ABSTRACT Electrochemically mediated atom transfer radical polymerizations (ATRPs) provide well‐defined polymers with designed dispersity as well as under external temporal and spatial control. In this study, 1‐cyano‐1‐methylethyl diethyldithiocarbamate, typically used as chain‐transfer agent (CTA) in reversible addition–fragmentation chain transfer (RAFT) polymerization, was electrochemically activated by the ATRP catalyst CuI/2,2′‐bipyridine (bpy) to control the polymerization of methyl methacrylate. Mechanistic study showed that this polymerization was mainly controlled by the ATRP equilibrium. The effect of applied potential, catalyst counterion, catalyst concentration, and targeted degree of polymerization were investigated. The chain‐end functionality was preserved as demonstrated by chain extension of poly(methyl methacrylate) withn‐butyl methacrylate and styrene. This electrochemical ATRP procedure confirms that RAFT CTAs can be activated by an electrochemical stimulus. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem.2019,57, 376–381more » « less
- 
            Abstract A facile and efficient two‐step synthesis ofp‐substituted tris(2‐pyridylmethyl)amine (TPMA) ligands to form Cu complexes with the highest activity to date in atom transfer radical polymerization (ATRP) is presented. In the divergent synthesis,p‐Cl substituents in tris(4‐chloro‐2‐pyridylmethyl)amine (TPMA3Cl) were replaced in one step and high yield by electron‐donating cyclic amines (pyrrolidine (TPMAPYR), piperidine (TPMAPIP), and morpholine (TPMAMOR)) by nucleophilic aromatic substitution. The [CuII(TPMANR2)Br]+complexes exhibited larger energy gaps between frontier molecular orbitals and >0.2 V more negative reduction potentials than [CuII(TPMA)Br]+, indicating >3 orders of magnitude higher ATRP activity. [CuI(TPMAPYR)]+exhibited the highest reported activity for Br‐capped acrylate chain ends in DMF, and moderate activity toward C−F bonds at room temperature. ATRP ofn‐butyl acrylate using only 10–25 part per million loadings of [CuII(TPMANR2)Br]+exhibited excellent control.more » « less
- 
            Abstract Photoinduced initiators for continuous activator regeneration atom transfer radical polymerization (PICAR ATRP) using sodium pyruvate and blue light (λmax = 456 nm) is reported. Water‐soluble oligo(ethylene oxide) methyl ether methacrylate (OEOMA500) was polymerized under biologically relevant conditions. Polymerizations were conducted with 1000 ppm (with respect to the monomer) concentrations of CuBr2, tris(2‐pyridylmethyl)amine, and 1000 ppm or less FeCl3as a cocatalyst in water. Well‐defined polymers with up to 90% monomer conversion, high molecular weights (Mn > 190,000), and low dispersity (1.14 < Ð < 1.19) were synthesized in less than 60 min. The polymerization rate and dispersity were tuned by varying the concentration of sodium pyruvate (SP), iron, and supporting halide, as well as light intensity. The Cu/Fe dual catalysis provided oxygen tolerance enabling rapid, well‐controlled, aqueous PICAR ATRP of OEOMA500without deoxygenation.more » « less
- 
            Abstract Atom transfer radical polymerization (ATRP) is one of the most powerful methods to prepare well‐defined (co)polymers. Cu‐catalyzed ATRP methods are most commonly used because of the excellent control and tunable catalytic activities via ligand functionalization. This minireview summarizes the development of Cu‐catalyzed ATRP in the presence of cocatalysts, which are used to regenerate CuIcomplex activators during polymerizations. Fundamentals of Cu‐based ATRP catalysts are first introduced, followed by the discussion of different types of cocatalysts in different Cu‐catalyzed ATRP methods. Recent developments of photochemical cocatalysts for oxygen‐tolerant ATRP and ATRP using long‐wavelength irradiation are highlighted, which significantly expand the applications of Cu‐catalyzed ATRP. Methods to study the properties of cocatalysts and their roles in Cu‐catalyzed ATRP are discussed, with an outlook for the future development of cocatalysts.more » « less
 An official website of the United States government
An official website of the United States government 
				
			 
					 
					
 
                                    