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Dyes and Pigments
Article . 2016 . Peer-reviewed
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Rhodamine analogs for molecular ruler applications

descriptionPublicationkeyboard_double_arrow_right Article 01 Mar 2016 United States English Publisher:Elsevier BVJournal:Dyes and Pigments, volume 126, pages 46-53 (issn: 0143-7208, Copyright policy )
Authors: Yu-Hsuan Chu; Jorge O. Escobedo; Meiyan Jiang; Peter S. Steyger; Robert M. Strongin;

doi: 10.1016/j.dyepig.2015.11.015

pmid: 26752798

pmc: PMC4702047

Rhodamine analogs for molecular ruler applications

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.

Country
United States
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Keywords

Chemistry

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    		 5
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    		 Average
    influence
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
5
Average
Average
Average
bronze