Mechanoluminescent units, when integrated into polymer matrices, undergo structural transformations in response to mechanical force, resulting in changes in fluorescence. This phenomenon holds considerable promise for the development of stress-sensing materials. Despite the high demand for robust, tunable mechanoluminescent mechanophores for force assessment and smart force-responsive materials, strategies for their design and synthesis remain underdeveloped. In an attempt to address this challenge, we have introduced a novel dual-pathway responsive mechanophore, bis(2-(2-(-butyldimethylsilanyloxy)benzylidene)amino)aryl disulfides (), which, when incorporated into polymer chains, exhibits fluorescence upon the combined application of force and chemical stimulus, irrespective of their sequence. This property is facilitated by the disulfide bond's sensitivity to mechanical force and the fluoride anion-induced desilylation and deprotonation. Notably, the force-responsive threshold of the mechanophore can be finely tuned by TBAF treatment, as supported by both experimental and computational studies, providing a simple, yet effective means, to regulate polymer force responsiveness on demand. We believe that the strategy developed in this investigation will shed light on the design of mechanophores for the fabrication of intelligent luminescent polymer materials and advance the development of smart force-reporting systems.
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http://dx.doi.org/10.1021/jacs.4c15655 | DOI Listing |
J Am Chem Soc
January 2025
Stoddart Institute of Molecular Science, Department of Chemistry, Zhejiang University, Hangzhou 310058, PR China.
Mechanoluminescent units, when integrated into polymer matrices, undergo structural transformations in response to mechanical force, resulting in changes in fluorescence. This phenomenon holds considerable promise for the development of stress-sensing materials. Despite the high demand for robust, tunable mechanoluminescent mechanophores for force assessment and smart force-responsive materials, strategies for their design and synthesis remain underdeveloped.
View Article and Find Full Text PDFAnal Chem
January 2025
The Institute for Advanced Studies, Wuhan University, Wuhan, Hubei 430072, China.
The position and configuration of the C═C bond have a significant impact on the spatial conformation of unsaturated lipids, which subsequently affects their biological functions. Double bond isomerization of lipids is an important mechanism of bacterial stress response, but its in-depth mechanistic study still lacks effective analytical tools. Here, we developed a visible-light-activated dual-pathway reaction system that enables simultaneous [2 + 2] cycloaddition and catalytic - isomerization of the C═C bond of unsaturated lipids via directly excited anthraquinone radicals.
View Article and Find Full Text PDFFront Chem
September 2024
Department of Radiology, The Second Hospital of Jilin University, Changchun, China.
Biochim Biophys Acta Mol Basis Dis
January 2025
Endocrinology Division, CSIR-Central Drug Research Institute, Lucknow 226031, India; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India. Electronic address:
Mutations in SOST can lead to various monogenic bone diseases. Its paralog, SOSTDC1, shares 55 % protein sequence homology and belongs to the BMP antagonist class. Sostdc1-/- mice exhibit distinct effects on cortical and trabecular bone.
View Article and Find Full Text PDFActa Biomater
October 2024
Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Xuzhou Medical University, Xuzhou, Jiangsu 221004, China. Electronic address:
The regulation of intracellular ionic homeostasis to trigger antigen-specific immune responses has attracted extensive interest in tumor therapy. In this study, we developed a dual-pathway nanoreactor, Au-CuSe@ZIF-8@P18 NPs (ACS-Z-P NPs), which targets danger-associated molecular patterns (DAMPs) and releases Zn and reactive oxygen species (ROS) within the tumor microenvironment (TME). Zn released from the metal-organic frameworks (MOFs) was deposited in the cytoplasm, leading to aberrant transcription levels of intracellular zinc-regulated proteins and DNA damage, thereby inducing pyroptosis and immunogenic cell death (ICD) dependent on caspase1/gasdermin D (GSDMD) pathway.
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