TY - JOUR
T1 - Sequence-Controlled Polymers via Simultaneous Living Anionic Copolymerization of Competing Monomers
AU - Rieger, Elisabeth
AU - Alkan, Arda
AU - Manhart, Angelika
AU - Wagner, Manfred
AU - Wurm, Frederik R.
PY - 2016/5/1
Y1 - 2016/5/1
N2 - Natural macromolecules, i.e., sequence-controlled polymers, build the basis for life. In synthetic macromolecular chemistry, reliable tools for the formation of sequence-controlled macromolecules are rare. A robust and efficient chain-growth approach based on the simultaneous living anionic polymerization of sulfonamide-activated aziridines for sequence control of up to five competing monomers resulting in gradient copolymers is presented. The simultaneous azaanionic copolymerization is monitored by real-time (1) H NMR spectroscopy for each monomer at any time during the reaction. The monomer sequence can be adjusted by the monomer reactivity, depending on the electron-withdrawing effect by the sulfonamide (nosyl-, brosyl-, tosyl-, mesyl-, busyl) groups. This method offers unique opportunities for sequence control by competing copolymerization: a step forward to well-engineered synthetic polymers with defined microstructures.
AB - Natural macromolecules, i.e., sequence-controlled polymers, build the basis for life. In synthetic macromolecular chemistry, reliable tools for the formation of sequence-controlled macromolecules are rare. A robust and efficient chain-growth approach based on the simultaneous living anionic polymerization of sulfonamide-activated aziridines for sequence control of up to five competing monomers resulting in gradient copolymers is presented. The simultaneous azaanionic copolymerization is monitored by real-time (1) H NMR spectroscopy for each monomer at any time during the reaction. The monomer sequence can be adjusted by the monomer reactivity, depending on the electron-withdrawing effect by the sulfonamide (nosyl-, brosyl-, tosyl-, mesyl-, busyl) groups. This method offers unique opportunities for sequence control by competing copolymerization: a step forward to well-engineered synthetic polymers with defined microstructures.
KW - anionic polymerization
KW - aziridines
KW - copolymerization
KW - ring-opening polymerization
KW - sequence-controlled polymers
UR - http://www.scopus.com/inward/record.url?scp=85027942702&partnerID=8YFLogxK
U2 - 10.1002/marc.201600092
DO - 10.1002/marc.201600092
M3 - Article
C2 - 27071917
AN - SCOPUS:85027942702
SN - 1022-1336
VL - 37
SP - 833
EP - 839
JO - Macromolecular rapid communications
JF - Macromolecular rapid communications
IS - 10
ER -