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Azadioxatriangulenium: Synthesis and Photophysical Properties of Reactive Dyes for Bioconjugation
Author(s) -
Bora Ilkay,
Bogh Sidsel A.,
Santella Marco,
Rosenberg Martin,
Sørensen Thomas Just,
Laursen Bo W.
Publication year - 2015
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201500888
Subject(s) - maleimide , chemistry , chromophore , bioconjugation , photochemistry , fluorescence , nucleophile , fluorescence anisotropy , thiol , tetrafluoroborate , amine gas treating , combinatorial chemistry , polymer chemistry , organic chemistry , membrane , ionic liquid , biochemistry , physics , quantum mechanics , catalysis
Azadioxatriangulenium (ADOTA) is a fluorescent triangulenium dye with a long fluorescence lifetime, highly polarized transitions and emission in the red part of the visible spectrum. These properties make the chromophore suited for application in fluorescence polarization/anisotropy assays. To be useful for these applications, reactive forms of the dyes must be available in significant quantities. Here, the synthesis and photophysical properties of amine‐reactive N ‐hydroxysuccinimide (NHS) esters and a thiol‐reactive maleimide derivative of ADOTA are reported. The synthesis involves two steps of nucleophilic bridge‐forming reactions starting from tris(2,6‐dimethoxyphenyl)methylium tetrafluoroborate, which can readily be prepared on a 100 g scale. In the third and final step the reactive NHS or maleimide groups are formed. The beneficial photophysical properties of the ADOTA chromophore are maintained in these derivatives, and we conclude that these systems are ideal to study protein motion and protein–protein interactions for systems of up to 1000 kDa.