TY - JOUR
T1 - More insight into tandem ROMP and ADMET polymerization for yielding reactive long-chain highly branched polymers and their transformation to functional polymer nanoparticles
AU - Ding, Liang
AU - Yang, Guangda
AU - Xie, Meiran
AU - Gao, Danyi
AU - Yu, Jiahui
AU - Zhang, Yiqun
PY - 2012/1/24
Y1 - 2012/1/24
N2 - Tandem chain transfer ring-opening metathesis polymerization (ROMP-CT) and acyclic diene metathesis (ADMET) polymerization were carried out in a controlled one-pot procedure, and behaved noticeable differences in polymerization of monomers by different ruthenium catalysts, whereas there indeed had been two distinctly polymerization stages. In the first one, ROMP-CT of functional monomers was conducted in the presence of a symmetrical multi-olefin as chain transfer agent within various reaction time scales, yielding linear telechelic polymers. Next, ADMET polymerization of telechelic polymers was performed and generated a series of reactive long-chain highly branched polymers (LCHBPs) with acrylate and/or azobenzene groups having molecular weights of 8.5-47.9 kDa under varied conditions. LCHBPs were fully characterized by several techniques, and interestingly, UV-vis analysis displayed the specific peak at 278 nm, which offered a new evidence for the existence of internal acrylate structure on the LCHBP backbone, and supported the highly branched architecture of polymers. LCHBP containing a number of pendent acrylate groups was readily converted, by thiol-Michael addition click reaction, to novel thiol-functionalized intra-molecular crosslinked unimolecular polymer nanoparticles with diameter of 40-60 nm, which provided a facile method for post-functionalization of branched polymers.
AB - Tandem chain transfer ring-opening metathesis polymerization (ROMP-CT) and acyclic diene metathesis (ADMET) polymerization were carried out in a controlled one-pot procedure, and behaved noticeable differences in polymerization of monomers by different ruthenium catalysts, whereas there indeed had been two distinctly polymerization stages. In the first one, ROMP-CT of functional monomers was conducted in the presence of a symmetrical multi-olefin as chain transfer agent within various reaction time scales, yielding linear telechelic polymers. Next, ADMET polymerization of telechelic polymers was performed and generated a series of reactive long-chain highly branched polymers (LCHBPs) with acrylate and/or azobenzene groups having molecular weights of 8.5-47.9 kDa under varied conditions. LCHBPs were fully characterized by several techniques, and interestingly, UV-vis analysis displayed the specific peak at 278 nm, which offered a new evidence for the existence of internal acrylate structure on the LCHBP backbone, and supported the highly branched architecture of polymers. LCHBP containing a number of pendent acrylate groups was readily converted, by thiol-Michael addition click reaction, to novel thiol-functionalized intra-molecular crosslinked unimolecular polymer nanoparticles with diameter of 40-60 nm, which provided a facile method for post-functionalization of branched polymers.
KW - Long-chain highly branched polymers
KW - Metathesis polymerization
KW - Polymer nanoparticles
UR - https://www.scopus.com/pages/publications/84855835073
U2 - 10.1016/j.polymer.2011.12.022
DO - 10.1016/j.polymer.2011.12.022
M3 - 文章
AN - SCOPUS:84855835073
SN - 0032-3861
VL - 53
SP - 333
EP - 341
JO - Polymer
JF - Polymer
IS - 2
ER -