A Synergistic Enhancement Strategy for Realizing Ultralong and Efficient Room‐Temperature Phosphorescence

An enhancement strategy is realized for ultralong bright room‐temperature phosphorescence (RTP), involving polymerization between phosphor monomers and acrylamide and host–guest complexation interaction between phosphors and cucurbit[6,7,8]urils (CB[6,7,8]). The non‐phosphorescent monomers exhibit 2...

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Veröffentlicht in:Angewandte Chemie International Edition 2020-10, Vol.59 (42), p.18748-18754
Hauptverfasser: Zhang, Zhi‐Yuan, Xu, Wen‐Wen, Xu, Wen‐Shi, Niu, Jie, Sun, Xiao‐Han, Liu, Yu
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container_issue 42
container_start_page 18748
container_title Angewandte Chemie International Edition
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creator Zhang, Zhi‐Yuan
Xu, Wen‐Wen
Xu, Wen‐Shi
Niu, Jie
Sun, Xiao‐Han
Liu, Yu
description An enhancement strategy is realized for ultralong bright room‐temperature phosphorescence (RTP), involving polymerization between phosphor monomers and acrylamide and host–guest complexation interaction between phosphors and cucurbit[6,7,8]urils (CB[6,7,8]). The non‐phosphorescent monomers exhibit 2.46 s ultralong lifetime after copolymerizing with acrylamide. The improvement is due to the rich hydrogen bond and carbonyl within the polymers which promote intersystem crossing, suppress nonradiative relaxation and shield quenchers effectively. By tuning the ratio of chromophores, a series of phosphorescent copolymers with different lifetimes and quantum yields are prepared. The complexation of macrocyclic hosts CB[6,7,8] promote the RTP of polymers by blocking aggregation‐caused quenching, and offsetting the losses of aforementioned interaction provided by polymer. Multiple lifetime‐encoding for digit and character encryption are achieved by utilizing the difference of their lifetimes. A synergistic enhancement strategy is realized for ultralong bright RTP, involving polymerization between phosphor monomers and acrylamide and host–guest complexation interaction between phosphors and cucurbit[6, 7, 8]urils (CB[6, 7, 8]). The phosphorescence lifetime and efficiency is up to 2.81 s and 76 %. Multiple lifetime‐encoding for digit and character encryption are achieved.
doi_str_mv 10.1002/anie.202008516
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The non‐phosphorescent monomers exhibit 2.46 s ultralong lifetime after copolymerizing with acrylamide. The improvement is due to the rich hydrogen bond and carbonyl within the polymers which promote intersystem crossing, suppress nonradiative relaxation and shield quenchers effectively. By tuning the ratio of chromophores, a series of phosphorescent copolymers with different lifetimes and quantum yields are prepared. The complexation of macrocyclic hosts CB[6,7,8] promote the RTP of polymers by blocking aggregation‐caused quenching, and offsetting the losses of aforementioned interaction provided by polymer. Multiple lifetime‐encoding for digit and character encryption are achieved by utilizing the difference of their lifetimes. A synergistic enhancement strategy is realized for ultralong bright RTP, involving polymerization between phosphor monomers and acrylamide and host–guest complexation interaction between phosphors and cucurbit[6, 7, 8]urils (CB[6, 7, 8]). The phosphorescence lifetime and efficiency is up to 2.81 s and 76 %. 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subjects Acrylamide
anti-counterfeiting
Carbonyl compounds
Carbonyls
Chromophores
Complexation
Copolymerization
Copolymers
cucurbiturils
Encryption
host–guest interactions
Hydrogen bonds
Monomers
Phosphorescence
Phosphors
Polymers
RTP
Temperature
title A Synergistic Enhancement Strategy for Realizing Ultralong and Efficient Room‐Temperature Phosphorescence
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