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HERO ID
7639328
Reference Type
Journal Article
Title
Copolymerization of Caprolactone Isomers to Obtain Nanoparticles with Constant Hydrophobicity and Tunable Crystallinity
Author(s)
Bandelli, D; Muljajew, I; Scheuer, K; Max, JB; Weber, C; Schacher, FH; Jandt, KD; Schubert, US; ,
Year
2020
Is Peer Reviewed?
1
Journal
Macromolecules
ISSN:
0024-9297
EISSN:
1520-5835
Publisher
AMER CHEMICAL SOC
Location
WASHINGTON
Volume
53
Issue
13
Page Numbers
5208-5217
Language
English
DOI
10.1021/acs.macromol.0c00486
Web of Science Id
WOS:000551424200020
URL
https://pubs.acs.org/doi/10.1021/acs.macromol.0c00486
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Abstract
To obtain a set of polycaprolactones (PCL) with varying crystallinity, the triazabicyclodecene-catalyzed co-polymerization of the two constitutional isomers epsilon-caprolactone (epsilon CL) and delta-caprolactone (delta CL) was carried out at room temperature in toluene. Variation of the feed fraction of epsilon CL from 50% to 80% and the detailed kinetic studies accompanied by application of terminal as well as nonterminal kinetic models suggested the formation of random copolymers. Differential scanning calorimetry and wideangle X-ray scattering investigations revealed the decrease of melting temperatures and degree of crystallinity with the epsilon CL fraction in the PCL. All copolymers were suited to obtain aqueous nanoparticle dispersions by means of nanoprecipitation. Encapsulation of the fluorescent probe pyrene confirmed a constant hydrophilic/hydrophobic balance of the nanoparticles.
Series
MACROMOLECULES
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