Atom transfer radical polymerization (ATRP) enables the precise synthesis of polymers with well-defined architectures, controlled molecular weights, and low dispersity. However, the halogen end-groups inherent to ATRP polymers can pose challenges due to their chemical reactivity and thermal instability. To address these issues, various strategies, including chemical and photochemical methods, have been developed for chain-end modification. This study introduces an electrochemical approach to selectively reduce halogen end-groups in ATRP polymers. Using glassy carbon (GC) and silver electrodes, the reductive cleavage of C-Br in bromine-capped polystyrene was investigated. Cyclic voltammetry revealed that polystyrene-bromide undergoes electron transfer accompanied by the concerted removal of the C-Br functionality. The Ag electrode facilitated electrocatalysis with enhanced activity. Controlled-potential electrolysis demonstrated that reaction conditions, particularly the choice of proto...
Polystyrene−Br End-Group Modification via Electrolysis: Adjusting Hydrogenation vs Coupling Selectivity
	
	
	
		
		
		
		
		
	
	
	
	
	
	
	
	
		
		
		
		
		
			
			
			
		
		
		
		
			
			
				
				
					
					
					
					
						
						
							
							
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
						
							
							
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
						
							
							
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
							
						
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
							
						
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
						
							
							
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
							
						
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
							
						
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
		
		
		
	
Giovanni Lissandrini;Marco Fantin
;Christian Durante;Abdirisak A. Isse
	
		
		
	
			2025
Abstract
Atom transfer radical polymerization (ATRP) enables the precise synthesis of polymers with well-defined architectures, controlled molecular weights, and low dispersity. However, the halogen end-groups inherent to ATRP polymers can pose challenges due to their chemical reactivity and thermal instability. To address these issues, various strategies, including chemical and photochemical methods, have been developed for chain-end modification. This study introduces an electrochemical approach to selectively reduce halogen end-groups in ATRP polymers. Using glassy carbon (GC) and silver electrodes, the reductive cleavage of C-Br in bromine-capped polystyrene was investigated. Cyclic voltammetry revealed that polystyrene-bromide undergoes electron transfer accompanied by the concerted removal of the C-Br functionality. The Ag electrode facilitated electrocatalysis with enhanced activity. Controlled-potential electrolysis demonstrated that reaction conditions, particularly the choice of proto...| File | Dimensione | Formato | |
|---|---|---|---|
| zampieri-et-al-2025-polystyrene-br-end-group-modification-via-electrolysis-adjusting-hydrogenation-vs-coupling.pdf accesso aperto 
											Tipologia:
											Published (Publisher's Version of Record)
										 
											Licenza:
											
											
												Creative commons
												
												
													
													
													
												
												
											
										 
										Dimensione
										2 MB
									 
										Formato
										Adobe PDF
									 | 2 MB | Adobe PDF | Visualizza/Apri | 
Pubblicazioni consigliate
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.




