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  2. Consequences of Dispersity on the Self-Assembly of ABA-Type Amphiphilic Block Co-Oligomers

Consequences of Dispersity on the Self-Assembly of ABA-Type Amphiphilic Block Co-Oligomers

  • ACS Macro Lett. 2018 May 15;7(5):546-550. doi: 10.1021/acsmacrolett.8b00168.
Anindita Das 1 Katja Petkau-Milroy 1 Gilian Klerks 1 Bas van Genabeek 1 René P M Lafleur 1 Anja R A Palmans 1 E W Meijer 1
Affiliations

Affiliation

  • 1 Institute for Complex Molecular Systems and Laboratory of Macromolecular and Organic Chemistry, Eindhoven University of Technology, P.O. Box 513, 5600 MB Eindhoven, The Netherlands.
Abstract

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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