Synthesis and characterization of uniform OCL-OEG block cooligomers
Block copolymers are an interesting class of materials, offering the opportunity to form nanostructured morphologies, making them suitable for a broad range of applications in nanotechnology, medicine, or biotechnology. Especially for the pharmaceutical sector, a uniform structure and a distinct str...
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Veröffentlicht in: | Polymer chemistry 2023-10, Vol.14 (41), p.4765-4773 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Block copolymers are an interesting class of materials, offering the opportunity to form nanostructured morphologies, making them suitable for a broad range of applications in nanotechnology, medicine, or biotechnology. Especially for the pharmaceutical sector, a uniform structure and a distinct structure-property relationship is desirable to manufacture highly reproducible and tailor-made materials. Herein, we report the synthesis and characterization of uniform (
= 1.01) oligo( -caprolactone)-oligo(ethylene glycol) (OCL-OEG) block co-oligomers (BCOs). Three different BCOs, varying in the length of the hydrophobic caprolactone segment, were obtained
via
Steglich esterification of the corresponding homo oligomers. A clear dispersity and composition dependent structure-property relationship based on the thermal properties is observed, compared to identical structures similar in
M
n
and dispersities of
= 1.06, obtained
via
ring-opening polymerization (ROP) of -caprolactone. In addition, increased long-range-order distances
L
0
with increasing dispersity of the BCOs are found for the formed morphologies after solvent vapor annealing (SVA). These results highlight the importance of uniform structures for a better understanding of the structure-property relationship of block copolymers.
OCL-OEG block cooligomers were prepared
via
an iterative exponential growth strategy (
= 1.01) and their thermal properties and self-assembly behavior were investigated and compared with narrowly distributed analogues obtained from ROP. |
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ISSN: | 1759-9954 1759-9962 |
DOI: | 10.1039/d3py01052j |