Eun-Hye Kang, In-Hwan Lee, and Tae-Lim Choi
http://pubs.acs.org/doi/pdf/10.1021/mz3002897
Conjugated backbone brush polymers were synthesized by first using a
1,6-heptadiyne with an alcohol group as an initiator to polymerize
L-lactide or E-caprolactone by ring opening polymerization. These
macromonomers were polymerized to brushes through cyclopolymerization
with the Grubbs-Hoveyda catalyst. The resulting brushes were
semiconducting with a bandgap of less than 2.0 eV as determined from
UV-vis spectra. Time-dependent Mark-Houwink-Sakurada plots from
SEC-viscometry suggested the brushes tend to extend over time. They also
characterized their polymers through GPC-MALS, differential scanning
calorimetry, and AFM.
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