2022
DOI: 10.1016/j.mtchem.2022.100954
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Cucurbit[8]uril-induced diarylethene thermally activated delay fluorescence supramolecular switch for sequential energy transfer

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Cited by 5 publications
(3 citation statements)
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“…To this end, the multivalent supramolecular assembly of SC4A/TPA provides a good platform for constructing light-controllable luminescence assembly. Dicationic diarylethene derivative (DE) [25] was selected as the photo-switch unit, which exhibited good reversible photoisomerization performance (Figure S16, Supporting Information) and could co-assemble with the SC4A/TPA to form the photo-stimulus supramolecular assembly. First, we investigated the absorption band of DE to evaluate the potential of which acts as a switch of the NIR emitting system.…”
Section: Resultsmentioning
confidence: 99%
“…To this end, the multivalent supramolecular assembly of SC4A/TPA provides a good platform for constructing light-controllable luminescence assembly. Dicationic diarylethene derivative (DE) [25] was selected as the photo-switch unit, which exhibited good reversible photoisomerization performance (Figure S16, Supporting Information) and could co-assemble with the SC4A/TPA to form the photo-stimulus supramolecular assembly. First, we investigated the absorption band of DE to evaluate the potential of which acts as a switch of the NIR emitting system.…”
Section: Resultsmentioning
confidence: 99%
“…So far, only one example of TADF-based photochromic switching has been reported. 32 Therefore, developing efficient visible light-controlled DTE systems with multi-mode TADF characteristics is highly desirable for photoelectric applications, but remains a severe challenge.…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, it is very significant but greatly challenging to develop a visible-light-induced DAE molecular switch in both directions. Among adoptive strategies in previous works, such as energy transfer, multiphoton absorption, electron transfer, , intramolecular proton transfer, and host–guest complexation to realize visible or near-infrared (NIR)-light photochromism, the simplest one involves modifying aromatic groups on the central hexatriene skeleton to expand π-conjugation systems for shifting the absorption bands of the open form of DAEs in visible or NIR regions . Nevertheless, for a majority of diarylethene derivatives with aromatic dyes at the side location, their visible-light reactive activation was apparently restrained because the extension of π-conjugation did not effectively enhance the contribution of the excited singlet state of the central hexatriene section. , It is imperative to seek a universal method for constructing dual visible-light-switched DAEs through simple chemical modifications.…”
mentioning
confidence: 99%