| Literature DB >> 28813152 |
Brittany L Cannon1, Donald L Kellis1, Lance K Patten1, Paul H Davis1, Jeunghoon Lee1, Elton Graugnard1, Bernard Yurke1, William B Knowlton1.
Abstract
Coherent exciton delocalization in dye aggregate systems gives rise to a variety of intriguing optical phenomena, including J- and H-aggregate behavior and Davydov splitting. Systems that exhibit coherent exciton delocalization at room temperature are of interest for the development of artificial light-harvesting devices, colorimetric detection schemes, and quantum computers. Here, we report on a simple dye system templated by DNA that exhibits tunable optical properties. At low salt and DNA concentrations, a DNA duplex with two internally functionalized Cy5 dyes (i.e., dimer) persists and displays predominantly J-aggregate behavior. Increasing the salt and/or DNA concentrations was found to promote coupling between two of the DNA duplexes via branch migration, thus forming a four-armed junction (i.e., tetramer) with H-aggregate behavior. This H-tetramer aggregate exhibits a surprisingly large Davydov splitting in its absorbance spectrum that produces a visible color change of the solution from cyan to violet and gives clear evidence of coherent exciton delocalization.Entities:
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Year: 2017 PMID: 28813152 PMCID: PMC6705113 DOI: 10.1021/acs.jpca.7b04344
Source DB: PubMed Journal: J Phys Chem A ISSN: 1089-5639 Impact factor: 2.781