2008
DOI: 10.1002/adma.200702455
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Reversible and Amplified Fluorescence Quenching of a Photochromic Polythiophene

Abstract: Amplification of fluorescence quenching of a polythiophene is optically triggered by converting pendant dithienylethene (DTE) photoswitches to their ring‐ closed isomers using UV light. The effect can be reversed with visible light, which regenerates the original DTE isomer. Amplification attributed to the high mobility of electronic excited states in conjugated polymers, which facilitates energy transfer to a ring‐closed DTE.

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Cited by 57 publications
(39 citation statements)
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“…9c). Similar amplification of fluorescence photoswitching can be observed in other photoswitchable assembled systems such as silica NPs combined with DAEs 45 , P-dots containing DAEs 69 , and polymer systems [70][71][72] , but the quenching efficiency has been greatly enhanced by several orders of magnitude. Such a fascinating "giant amplification of fluorescence photoswitching" can be ascribed to a very efficient intermolecular FRET process between the fluorescent units and the closed-ring isomer of the DAE units within the NPs prepared exclusively from 9a (Fig.…”
Section: Nps Based On Organic Moleculessupporting
confidence: 68%
“…9c). Similar amplification of fluorescence photoswitching can be observed in other photoswitchable assembled systems such as silica NPs combined with DAEs 45 , P-dots containing DAEs 69 , and polymer systems [70][71][72] , but the quenching efficiency has been greatly enhanced by several orders of magnitude. Such a fascinating "giant amplification of fluorescence photoswitching" can be ascribed to a very efficient intermolecular FRET process between the fluorescent units and the closed-ring isomer of the DAE units within the NPs prepared exclusively from 9a (Fig.…”
Section: Nps Based On Organic Moleculessupporting
confidence: 68%
“…[77,78] Alternatively, independent fluorescent and photochromic components can be integrated within [79][80][81] or appended to [82] the main chain of a polymer backbone. Similarly, several photochromes can be attached to a single fluorescent polymer [83,84] or a fluorophore can first be connected to a photochrome and then multiple copies of the resulting dyad can be attached to a macromolecular chain. [85] For example, the co-polymer 16a ( Figure 13) bears pendant fluorophore-photochrome dyads along its macromolecular backbone in addition to hydrophilic polyethylene glycol chains.…”
Section: Polymersmentioning
confidence: 99%
“…The design of an effective light-triggered fluorescence switch is not trivial, and a zoology of diarylethene molecules [35,[134][135][136][137][138][139][140][141][142][143][144][145] and polymers [35,36,[146][147][148] have been reported so far. The main issue deals with the enhancement of the quantum yield of fluorescence of the emissive state, but maintaining overall good photochromism.…”
Section: Modulation Of Emission Propertiesmentioning
confidence: 99%