期刊
POLYMER CHEMISTRY
卷 2, 期 1, 页码 203-208出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c0py00264j
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资金
- Dutch Polymer Institute (DPI)
(Chiral) poly(2-oxazoline)s are regarded as pseudo-polypeptides, however, not much is known about their secondary structure formation. Recently we reported that chiral homopolymers based on R-and S-2-butyl-4-ethyl-2-oxazoline (BuEtOx) monomers form flexible dynamic helices in solution (Soft Matter, 2010, 6, 994-1003) and a chiral crystalline structure in the solid state (Macromolecules, 2010, 43, 4654-4659). In the current work we addressed the chiral structure formation of main-chain chiral copoly(2-oxazoline) s with controlled ratio of S-BuEtOx and R-BuEtOx. No chiral amplification was found in solution or in the solid state, clearly indicating that the polymers adopt a dynamic helical structure that is easily disrupted by incorporation of the second monomer. Nonetheless, the properties of these main-chain chiral copoly(2-oxazoline) s, such as the optical rotation, solubility and crystallinity, can be tuned by controlling the enantiomeric excess (ee).
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