TY - JOUR
T1 - N-[Salicylidene-1,2-ethanediaminoethyl]-2-bromoisobutyramide as initiator for atom transfer radical polymerization and surface-initiated ATRP of methyl methacrylate on copper
AU - Lu, Gang
AU - Li, Yi Min
AU - Lu, Chun Hua
AU - Xu, Zhong Zi
PY - 2010/8
Y1 - 2010/8
N2 - N-[Salicylidene-1,2-ethanediaminoethyl]-2-bromoisobutyramide (SEB) was synthesized and characterized by elemental analysis, FT-IR and1H NMR. It had been successfully used as a bidentate initiator for the atom transfer radical polymerization (ATRP) of methyl methacrylate with CuBr/2,2'-bipyridine as the catalyst and N,N-dimethylformamide as the solvent at 70 °C. The kinetics was first order in monomer and the number-average molecular weight of the polymer increased linearly with monomer conversion, indicating the 'living'/controlled nature of the polymerization. The polymerization reached high conversions producing polymers with a low molecular weight distribution (Mw/Mn - 1.34). The obtained poly(methylmethacrylate) (PMMA) functionalized with salicylidene-1,2-ethanediaminoethyl and ω-Br as the end groups were characterized by FT-IR spectroscopy. They can be used as macroinitiators for chain-extension reaction. Then, PMMA coatings were grafted from copper substrates by surface-initiated ATRP from a surface-bound SEB initiator. The electrochemical impedance spectroscopy measurements and potentiodynamic electrochemical experiments confirmed the successful grafting of the polymer coatings. Greatly improved short-term anticorrosive properties for PMMA modified electrodes were demonstrated by substantially increased resistance of the film for a period of 24 h as compared to bare copper.
AB - N-[Salicylidene-1,2-ethanediaminoethyl]-2-bromoisobutyramide (SEB) was synthesized and characterized by elemental analysis, FT-IR and1H NMR. It had been successfully used as a bidentate initiator for the atom transfer radical polymerization (ATRP) of methyl methacrylate with CuBr/2,2'-bipyridine as the catalyst and N,N-dimethylformamide as the solvent at 70 °C. The kinetics was first order in monomer and the number-average molecular weight of the polymer increased linearly with monomer conversion, indicating the 'living'/controlled nature of the polymerization. The polymerization reached high conversions producing polymers with a low molecular weight distribution (Mw/Mn - 1.34). The obtained poly(methylmethacrylate) (PMMA) functionalized with salicylidene-1,2-ethanediaminoethyl and ω-Br as the end groups were characterized by FT-IR spectroscopy. They can be used as macroinitiators for chain-extension reaction. Then, PMMA coatings were grafted from copper substrates by surface-initiated ATRP from a surface-bound SEB initiator. The electrochemical impedance spectroscopy measurements and potentiodynamic electrochemical experiments confirmed the successful grafting of the polymer coatings. Greatly improved short-term anticorrosive properties for PMMA modified electrodes were demonstrated by substantially increased resistance of the film for a period of 24 h as compared to bare copper.
KW - Atom transfer radical polymerization
KW - Electrochemical impedance spectroscopy
KW - N-Salicylidene-diethylenetriamine
KW - Pmma-covered copper electrodes
KW - Potentiodynamic polarization
KW - Surface-initiated ATRP
UR - http://www.scopus.com/inward/record.url?scp=77954951442&partnerID=8YFLogxK
U2 - 10.1007/s00289-010-0260-7
DO - 10.1007/s00289-010-0260-7
M3 - 文章
AN - SCOPUS:77954951442
SN - 0170-0839
VL - 65
SP - 377
EP - 394
JO - Polymer Bulletin
JF - Polymer Bulletin
IS - 4
ER -