Article
Rhodamine Analogues for Molecular Ruler Applications
Dyes and Pigments
Sponsor
This work was supported by the National Institute on Deafness and Other Communication Disorders at the National Institutes of Health (R21 DC010231; R01 DC012588).
Document Type
Citation
Publication Date
3-1-2016
Disciplines
Abstract
A series of geometrically well-defined cationic fluorophores were designed based on molecular mechanics. They contain biaryl linkers to impart rigidity preventing intramolecular folding between a conjugated biomolecule and fluorophore. All probes have absorption and emission maxima within 20 nm from Texas Red, as predicted by TDDFT calculations and validated experimentally.
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DOI
10.1016/j.dyepig.2015.11.015
Persistent Identifier
http://archives.pdx.edu/ds/psu/18852
Citation Information
Yu-Hsuan Chu, Jorge O. Escobedo, Meiyan Jiang, Peter S. Steyger, Robert M. Strongin. (2016). Rhodamine analogs for molecular ruler applications, Dyes and Pigments, Volume 126, Pages 46-53.