Reversible photoactivation of 4-methylumbelliferone in carboxymethyl cellulose self-standing films under LED irradiation

IF 6.5 Q1 CHEMISTRY, APPLIED
V. Andrews , R. Montecinos , E. Ortega , O. Ramirez , S. Bonardd , Caterina Quezada , D. Diaz Diaz , A. Leiva , C. Saldias
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引用次数: 0

Abstract

Cellulose-derived materials capable of reversible optical responses are attractive for sustainable light-responsive technologies. Here, we demonstrate the reversible photoactivation of carboxymethyl cellulose (CMC) films containing 4-methylumbelliferone (4MU) under alternating UV-A/UV-C LED irradiation. The films show robust switching of absorbance through reversible [2+2] cycloaddition, maintaining performance over multiple cycles without fatigue. Molecular dynamics simulations reveal that CMC provides a highly connected free-volume network and strong 4MU–polymer interactions that promote efficient photodimerization, in contrast to cellulose acetate (CA), whose weaker supramolecular environment results in slower kinetics and reduced reversibility. Complementary thermal and AFM analyses confirm light-induced structural reorganization in CMC/4MU films, while a preliminary life cycle assessment highlights their lower environmental footprint. Overall, CMC/4MU emerges as a promising sustainable platform for reversible light-responsive materials.
LED照射下4-甲基伞形酮在羧甲基纤维素自立膜中的可逆光活化
具有可逆光响应能力的纤维素衍生材料对于可持续光响应技术具有吸引力。在UV-A/UV-C LED交替照射下,我们展示了含有4-甲基伞形酮(4MU)的羧甲基纤维素(CMC)薄膜的可逆光活化。通过可逆的[2+2]环加成,薄膜显示出强大的吸光度开关,在多个循环中保持性能而不会疲劳。分子动力学模拟表明,CMC提供了一个高度连接的自由体积网络和强的4mu -聚合物相互作用,促进了有效的光二聚化,而醋酸纤维素(CA)的超分子环境较弱,导致动力学较慢,可逆性降低。互补的热分析和原子力显微镜分析证实了CMC/4MU薄膜的光诱导结构重组,而初步的生命周期评估强调了其较低的环境足迹。总的来说,CMC/4MU是一个有前途的可持续的可逆光响应材料平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
8.70
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