Consequences of Dispersity on the Self-Assembly of ABA-Type Amphiphilic Block Co-Oligomers
Author(s) -
Anindita Das,
Katja PetkauMilroy,
Gilian Klerks,
Bas van Genabeek,
René P. M. Lafleur,
Anja R. A. Palmans,
E. W. Meijer
Publication year - 2018
Publication title -
acs macro letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.966
H-Index - 92
ISSN - 2161-1653
DOI - 10.1021/acsmacrolett.8b00168
Subject(s) - dispersity , amphiphile , oligomer , ethylene glycol , materials science , polymer chemistry , crystallization , copolymer , crystallinity , tacticity , aqueous solution , self assembly , chemical engineering , polymerization , chemistry , organic chemistry , nanotechnology , polymer , engineering , composite material
Intriguingly, little is known about the impact of dispersity on the crystallization driven self-assembly (CDSA) of amphiphilic block copolymers in aqueous media. Here, we investigate the influence of dispersity on the CDSA of ABA-type amphiphilic block co-oligomers (ABCOs). Two pairs of ABCOs are synthesized comprising discrete ( Đ = 1.00) or disperse ( Đ = 1.20) isotactic l-lactic acid 16-mers as the semicrystalline hydrophobic block and either oligo(ethylene glycol) methyl ether (MeOoEG) or oligo(tetraethylene glycol succinate) (oTEGSuc) as the discrete hydrophilic block. Self-assembly studies in water with 10% THF reveal uniform nanofibers/2D sheets for the discrete oligomers, but such structural regularity is largely compromised in the disperse oligomers. The results are corroborated by sharp melting transitions in both solution and bulk for the discrete ABCOs, unlike their disperse analogues that show a lack of crystallization. Interestingly, the discrete MeOoEG-LLA oligomer reveals crystallization driven gelation, illustrating the contrasting differences between the discrete oligomers and their disperse counterparts.
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