The ability to monitor mechanical stresses and strains in polymers an optical signal enables the investigation of deformation processes in such materials and is technologically useful for sensing damage and failure in critical components. We show here that this can be achieved by simply blending polymers of interest with a small amount of a mechanochromic luminescent additive (Py-PEB) that can be accessed in one step by end-functionalizing a telechelic poly(ethylene--butylene) (PEB) with excimer-forming pyrenes. Py-PEB is poorly miscible with polar polymers, such as poly(ε-caprolactone) and poly(urethane), so that blends undergo microphase separation even at low additive concentrations (0.1-1 wt%), and the emission is excimer-dominated. Upon deformation, the ratio of excimer-to-monomer emission intensity decreases in response to the applied stress or strain. The approach appears to be generalizable, although experiments with poly(isoprene) show that it is not universal and that the (in)solubility of the additive in the polymer must be carefully tuned.
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http://dx.doi.org/10.1039/d3sm01489d | DOI Listing |
ACS Appl Mater Interfaces
January 2025
Supramolecular Chemistry Group, Centre of Macromolecular Chemistry (CMaC), Department of Organic and Macromolecular Chemistry, Faculty of Sciences, Ghent University, Krijgslaan 281, S4-bis, B-9000 Ghent, Belgium.
Physical understanding and determination of different analytes without the need for advanced and additional equipment are highly important, which can be achieved by using stimuli-induced chromic materials. Physical and chemical incorporation of responsive chromophores into different polymers results in the fabrication of chromic polymers. Chromic electrospun nanofibers are prepared using the electrospinning technique, and their stimuli-responsivity is improved due to their high surface-to-volume ratio.
View Article and Find Full Text PDFMacromol Rapid Commun
December 2024
Department of Chemistry "Giacomo Ciamician", University of Bologna, Via Selmi 2, Bologna, 40126, Italy.
Mechanofluorescent polymers represent a promising class of materials exhibiting fluorescence changes in response to mechanical stimuli. One approach to fabricating these polymers involves incorporating aggregachromic dyes, whose emission properties are governed by the intermolecular distance, which can, in turn, be readily altered by microstructural changes in the surrounding polymer matrix during mechanical deformation. In this study, a mechanofluorescent additive featuring excimer-forming oligo(p-phenylene vinylene) dyes (tOPV) is incorporated into electrospun polyurethane fibers, producing mats of fibers with diameters ranging from 300 to 700 nm.
View Article and Find Full Text PDFACS Sens
December 2024
Institute of Industrial Science, The University of Tokyo, 4-6-1 Komaba Meguro-ku, Tokyo 153-8505, Japan.
We demonstrated a mechanochromic chameleon packaging that quantitatively visualizes damage based on the polydiacetylene blue-to-red color transition. The applied pressures on the damage can be conveniently read by taking a photograph via a homemade mobile app called the "Pressure Analysis App". The key aspects of the development were 1) the adjustment of the sensitivity by adding guest molecules into the PDA matrix, 2) quantitative calibration, and 3) the accurate reading of the pressure from RGB images based on the calibration.
View Article and Find Full Text PDFMacromol Rapid Commun
December 2024
Department of Chemical Science and Engineering, Institute of Science Tokyo, 2-12-1 Ookayama, Meguro-ku, Tokyo, 152-8550, Japan.
Mechanochromic polymers can be used to visualize mechanical stimuli applied to materials. However, many of these polymers exhibit single-color mechanochromism, i.e.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2024
Julius-Maximilians-Universität Würzburg, Institute of Inorganic Chemistry and Institute for Sustainable Chemistry & Catalysis with Boron (ICB), Am Hubland, 97074, Würzburg, Germany.
Incorporation of BN units into π-conjugated organic compounds, as substitutes for specific CC couples, often leads to new hybrid materials with modified physical and chemical properties. Poly(p-phenylene iminoborane)s are derived from well-known poly(p-phenylene vinylene) (PPV) by replacement of the vinylene groups by B=N linking units. Herein, an unprecedented poly(p-phenylene iminoborane) is presented that features a strictly alternating sequence of BN units along the main chain.
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