4.8 Article

Facile Preparation of Full-Color Tunable Room Temperature Phosphorescence Cellulose via Click Chemistry

Journal

SMALL
Volume -, Issue -, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202309131

Keywords

cellulose; click chemistry; directed redox; full-color tunable afterglow; room temperature phosphorescence

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A sustainable and long-lived room temperature phosphorescent cellulose material with color-tunable afterglows is synthesized via click chemistry. This environmentally friendly material can be used for nontoxic afterglow inks, delay lighting, and afterglow display.
Sustainable long-lived room temperature phosphorescence (RTP) materials with color-tunable afterglows are attractive but rarely reported. Here, cellulose is reconstructed by directed redox to afford ample active hydroxyl groups and water-solubility; arylboronic acids with various pi conjugations can be facilely anchored to reconstructed cellulose via click chemistry within 1 min in pure water, resulting in full-color tunable RTP cellulose. The rigid environment provided by the BO covalent bonds and hydrogen bonds can stabilize the triplet excitons, thus the target cellulose displays outstanding RTP performances with the lifetime of 2.67 s, phosphorescence quantum yield of 9.37%, and absolute afterglow luminance of 348 mcd m-2. Furthermore, due to the formation of various emissive species, the smart RTP cellulose shows excitation- and time-dependent afterglows. Taking advantages of sustainability, ultralong lifetime, and full-color tunable afterglows, et al, the environmentally friendly RTP cellulose is successfully used for nontoxic afterglow inks, delay lighting, and afterglow display. An ingenious design strategy is developed to rapidly prepare room temperature phosphorescence (RTP) cellulose with long-lived and full-color tunable afterglows via click chemistry within 1 min in pure water. Specifically, cellulose is reconstructed by directed redox to afford water-solubility and ample active primary hydroxyl groups and further to anchor arylboronic acid chromophores with various pi conjugations by BO click reaction.image

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