The reversible isomerization behavior of molecular switches in liquid crystal elastomers (LCEs) usually only can be monotonically repeated, because the molecular motion environment is the same for each isomerization cycle in a permanently cross-linked polymer network. Therefore, achieving a tunable photostationary state (PSS) in the same LCE material system is a significant challenge. Herein, a spiropyran-based material (SPBM) as the molecular switch is introduced into a LCE system, which constructed a typical photo-responsive material with reversible isomerization behavior. Furthermore, dynamic cross-linked polymer networks via diselenide bonds endow the SPBM in this system with a tunable molecular motion environment, which switches freely or restrictedly depending on the size of the free volume. Thus, the molecular switch can endow the LCE with programmable photo-response, and a program locking or unlocking is enabled by tuning the free volume. This post-programming locking (PPL) strategy may offer a new sight for promoting the higher controllability of the stimulus-responsive behavior of the smart materials.
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http://dx.doi.org/10.1002/smll.202500899 | DOI Listing |
Sci Rep
March 2025
Faculty of Biology, Shenzhen MSU-BIT University, Shenzhen, 518172, China.
Cancer treatment remains a pressing challenge, with paclitaxel playing a pivotal role in chemotherapy by disrupting mitotic spindle dynamics through microtubule stabilization. However, the molecular details of paclitaxel interaction with β-tubulin, its target, remain elusive, impeding efforts to overcome drug resistance and optimize efficacy. Here, we employ extensive molecular dynamics simulations to probe the binding modes of paclitaxel within tubulin protofilaments.
View Article and Find Full Text PDFBMC Chem
March 2025
College of Chemical and Material Engineering, Quzhou University, Quzhou, Zhejiang Province, 324000, China.
The light-modulated isomerization and aggregation behavior of ionic liquids (ILs) in aqueous solutions holds fundamental and technological significance. Although several azobenzene-based photoresponsive ILs have been synthesized, there is still a lack of understanding regarding the aggregation mechanism, regularity of the alkyl chain length, and the position of the azobenzene (cis- and trans-) in these photoresponsive ILs. To elucidate the structure-property relationship of photoresponsive ILs, four types of azobenzene groups photosensitive ILs ([AzoCDMEA]Br, n = 2,4,6,10) in both trans- and cis- configurations were investigated by density functional theory (DFT) calculations.
View Article and Find Full Text PDFChemistry
March 2025
Wroclaw University of Science and Technology Faculty of Chemistry, Chemistry, Wybrzeże Stanisława Wyspiańskiego 27, 50-370 Wrocław, 50-370, Wrocław, POLAND.
During transcription, replication, and DNA repair, DNA unwinds to reveal guanine-rich sequences that form stable G-quadruplexes. In cancer cells, increased transcription and replication promote G4 formation, making them attractive therapeutic targets. G4s block DNA and RNA polymerases, inducing replication stress and causing toxic single- and double-strand breaks.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
March 2025
University of Bristol, School of Chemistry, Cantock's Close, BS8 1TS, Bristol, UNITED KINGDOM OF GREAT BRITAIN AND NORTHERN IRELAND.
Colour vision relies on selective, reversible isomerisation by visible light of a mixture of retinyl chromophores in photoreceptor cells. Synthetic molecular mimics of this wavelength-dependent induction of function are rare, despite the attractiveness of controlling chemical processes solely by the wavelength of incident light. Here, we report a colour-responsive chemical system composed of a cationic receptor complex, two competing chiral anionic ligands and two metastable photoacids with contrasting absorption properties.
View Article and Find Full Text PDFSmall
March 2025
School of Materials Science and Engineering, Peking University, Beijing, 100871, PR China.
The reversible isomerization behavior of molecular switches in liquid crystal elastomers (LCEs) usually only can be monotonically repeated, because the molecular motion environment is the same for each isomerization cycle in a permanently cross-linked polymer network. Therefore, achieving a tunable photostationary state (PSS) in the same LCE material system is a significant challenge. Herein, a spiropyran-based material (SPBM) as the molecular switch is introduced into a LCE system, which constructed a typical photo-responsive material with reversible isomerization behavior.
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