Abstract
Oligo(3-hexylthiophene-co-1,4-phenylene) and poly(3-hexylthiophene) were solubilized in sodium deoxycholate self-assemblies in water solutions and hydrogels. The oligomer and polymer were incorporated as monomers into the self-assemblies with sodium deoxycholate aggregates, leading to the photoprotection of these neutral conjugated and water insoluble molecules. Dynamic light scattering, rheology and fluorescence experiments established that the deoxycholate aggregation and gel formation properties were not altered with the incorporation of the oligomer or polymer into the deoxycholate self-assemblies, showing that this adaptable host system with some molecular recognition elements is a viable strategy to incorporate neutral conjugated molecules into hydrogels.
Supplementary materials
Title
Supporting Information for "Solubilization and Photostabilization in a Sodium Deoxycholate Hydrogel of a Neutral Conjugated Thiophene Oligomer and Polymer"
Description
Synthesis of OTPh, absorption, fluorescence, and photostability studies for OTPh and P3TH in NaDC solutions and NaDC gels, photophysics of pyrene in OTPh/NaDC gels (pdf).
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Title
Video for "Solubilization and Photostabilization in a Sodium Deoxycholate Hydrogel of a Neutral Conjugated Thiophene Oligomer and Polymer"
Description
Video showing the transfer of the sodium deoxycholate gel to the plate on the rheometer.
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