Abstract
A novel polyviologen-based molecular architecture was developed via the step-growth polymerization of a hydroxyl-substituted aryl dihydrazide with a water soluble viologen-dialdehyde in water under acidic conditions. When polymerized in the presence of π-electron rich aromatic templates, the reaction mixture underwent hydrogelation. The templates were found to facilitate monomer-monomer as well as monomer-polymer preorganization during polymerization via donor-acceptor charge transfer interactions. Following polymerization, the templates effectively served as post-synthetic non-covalent cross linkers connecting the hydrogel network. The chemical structures of the polymers and molecular recognition between the reacting species were investigated in solution using 1H NMR, while donor-acceptor charge transfer interactions were investigated using UV-vis absorption spectroscopy. We also report the hydrochromic behavior of the templated and non-templated polymers. The surface morphology of the polymers was characterized using scanning electron microscopy, which revealed the formation of sheet-like structures. The new hydrogels developed in this work represents an interesting example of materials comprised of reversible dynamic covalent bonds and reversible non-covalent crosslinking interactions occurring between the electron-rich aryl templates and the electron-deficient bipyridinium units.
Original language | English (US) |
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Article number | 100289 |
Journal | Materials Today Chemistry |
Volume | 17 |
DOIs | |
State | Published - Sep 2020 |
Externally published | Yes |
Keywords
- Bipyridinium
- Charge transfer
- Hydrochromism
- Polymer
- Rheology
ASJC Scopus subject areas
- Catalysis
- Electronic, Optical and Magnetic Materials
- Biomaterials
- Polymers and Plastics
- Colloid and Surface Chemistry
- Materials Chemistry