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Bidirectional switching of near IR emitting boradiazaindacene fluorophores
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Date
2008-08-21
Author
Deniz, Erhan
Isbasar, G. Ceyda
Bozdemir, Oe. Altan
YILDIRIM, LEYLA
Siemiarczuk, Aleksander
AKKAYA, Engin Umut
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Two novel distyryl-boradiazaindacene dyes with dimethylaminostyryl and pyridylethenyl substituents display opposite spectral shifts on protonation with TFA in organic solvents. This bidirectional switching of the dyes can be shown to be directly related to ICT donor and acceptor characteristics of the substituents attached to the BODIPY core. The observed spectral response of these dyes could be very useful in the design of novel NIR fluorescent ratiometric probes for pH.
Subject Keywords
Resonance energy-transfer
,
Fluorescent bodipy dyes
,
Distyryl-boradiazaindacenes
,
Borane complexes
,
Emission
,
Functionalization
,
Light
,
Boron
,
Chemosensor
,
Derivatives
URI
https://hdl.handle.net/11511/68355
Journal
ORGANIC LETTERS
DOI
https://doi.org/10.1021/ol801062h
Collections
Department of Chemistry, Article
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E. Deniz, G. C. Isbasar, O. A. Bozdemir, L. YILDIRIM, A. Siemiarczuk, and E. U. AKKAYA, “Bidirectional switching of near IR emitting boradiazaindacene fluorophores,”
ORGANIC LETTERS
, pp. 3401–3403, 2008, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/68355.