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Single Fluorophore Blinking

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dc.contributor.author Pati, Avik K.
dc.date.accessioned 2024-08-08T07:12:07Z
dc.date.available 2024-08-08T07:12:07Z
dc.date.issued 2018-04
dc.identifier.uri https://link.springer.com/referenceworkentry/10.1007/978-3-642-35943-9_483-1
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15156
dc.description.abstract Light-emitting species, including organic dye molecules, fluorescent proteins, and semiconductor particles, are prone to enter transient dark states. At the ensemble scale, reversibly entry and exit from dark states, referred to as “blinking” events, lower fluorophore brightness and thus effective quantum yield and typically result in photo-induced reactions with solvent. Depending on the nature of the fluorophore species, the illumination source, and intensity, as well as the environmental conditions, blinking events can range from rare to frequent and last from microseconds to minutes. Blinking events are distinguished from photobleaching, the irreversible loss of fluorescence, by their temporary nature. Temporary dark states can arise for a variety of reasons. In the case of organic fluorophores, transient dark states may occur due to reversible isomerization of the conjugated π orbital system, resulting in. en_US
dc.language.iso en en_US
dc.publisher Springer en_US
dc.subject Chemical Engineering en_US
dc.subject Organic Dye molecules en_US
dc.subject Fluorescent proteins en_US
dc.title Single Fluorophore Blinking en_US
dc.type Article en_US


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