Solubilization and Photostabilization in a Sodium Deoxycholate Hydrogel of a Neutral Conjugated Thiophene Oligomer and Polymer

05 March 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

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.

Keywords

Neutral polymer
Thiophene oligomer
Thiophene polymer
Sodium deoxycholate
Solubilization
Photostability
Fluorescence
Pyrene fluorescence
Rheology
Dynamic light scattering
Conjugated polymer

Supplementary materials

Title
Description
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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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