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  4. AGET and SARA ATRP of styrene and methyl methacrylate mediated by pyridyl-imine based copper complexes
 
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AGET and SARA ATRP of styrene and methyl methacrylate mediated by pyridyl-imine based copper complexes

Journal
European Polymer Journal
Journal Volume
51
Journal Issue
1
Pages
12-20
Date Issued
2014
Author(s)
Hsiao C.-Y.
Han H.-A.
Lee G.-H.
CHI-HOW PENG  
DOI
10.1016/j.eurpolymj.2013.11.013
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84890515807&doi=10.1016%2fj.eurpolymj.2013.11.013&partnerID=40&md5=1c793b5684b944d5ca0c841e5921cfcb
https://scholars.lib.ntu.edu.tw/handle/123456789/624022
Abstract
Two pyridyl-imine ligands, N,N-dimethyl-N′-((pyridin-2-yl)methylene)- ethane-1,2-diamine (paenMe2) and N,N-diethyl-N′-((pyridin-2-yl) methylene)-ethane-1,2-diamine (paenEt2), have been applied to AGET and SARA ATRP of styrene and methyl methacrylate. The polymeric products showed a narrow molecular weight distribution (Mw/Mn = 1.16-1.28) and a molecular weight that not only increased linearly with monomer conversion (>70%) but also matched to the theoretical value. The performance of Cu II(paenMe2)Br2 and CuII(paenEt 2)Br2 in AGET ATRP was almost the same and thus the steric effect between these two complexes was not significant. The activation rate constant (kact) of CuI(paenMe2)Br with PEBr was measured as 7.96 × 10-3 M-1 s-1 and the deactivation rate constant (kdeact) was estimated as 2.8 × 105 M-1 s-1. This kinetic measurement indicated that the improved control efficiency of pyridyl-imine based catalysts in AGET and SARA ATRP should be attributed to the high deactivator/activator (Cu II species/CuI species) ratio that relatively enhanced the deactivation rate and lowered the radical concentration to minimize the influence of radical termination and other side reactions.
Subjects
AGET ATRP;Cu(0);Pyridyl-imine;SARA ATRP
Other Subjects
Activation rate constants;AGET ATRP;Kinetic measurement;Methyl methacrylates;Monomer conversions;Narrow molecular weight distributions;Pyridyl-imine;Radical concentration;Amines;Catalyst deactivation;Esters;Ethane;Molecular weight distribution;Rate constants;Styrene;Copper compounds
Type
journal article

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