The DOI matches its Crossref record; 35 of the 35 references it cites were found in a registry or an index.
Multistimuli Responsive Organogels Based on a New Gelator Featuring Tetrathiafulvalene and Azobenzene Groups: Reversible Tuning of the Gel−Sol Transition by Redox Reactions and Light Irradiation
Abstract
For the development of multistimuli responsive organogels, the new organic gelator LMWG 1, featuring electroactive TTF and photoresponsive azobenzene groups, was designed and studied. By manipulating the redox state of the TTF group in LMWG 1, the gel-sol transition for organogels with the LMWG 1 can be reversibly tuned by either chemical or electrochemical oxidation/reduction reactions. Alternatively, the photoisomerization of the azobenzene group in LMWG 1 can also trigger the gel-sol transition. Therefore, organogels with LMWG 1 respond not only to thermal stimuli but also to redox reactions and light irradiation.
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Cites
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Cited by
Using the dynamic bond to access macroscopically responsive structurally dynamic polymers
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Characterization of supramolecular gels
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Metadata
- Authors
- Wang, C., Chen, Q., Sun, F., Zhang, D., Zhang, G., Huang, Y., Zhao, R., & Zhu, D.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2010-02-16
- Volume
- 132
- Issue
- 9
- Pages
- 3092-3096
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W2053048760
- Cited by
- 278
- References
- 35
- FWCI
- 11.60
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Multistimuli Responsive Organogels Based on a New Gelator Featuring Tetrathiafulvalene and Azobenzene Groups: Reversible Tuning of the Gel−Sol Transition by Redox Reactions and Light Irradiation. https://app.cochat.ai/papers/10.1021/ja910721s
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- Wang, C., Chen, Q., Sun, F., Zhang, D., Zhang, G., Huang, Y., Zhao, R., & Zhu, D. (2010). Multistimuli Responsive Organogels Based on a New Gelator Featuring Tetrathiafulvalene and Azobenzene Groups: Reversible Tuning of the Gel−Sol Transition by Redox Reactions and Light Irradiation. Journal of the American Chemical Society. https://doi.org/10.1021/ja910721s
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