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  4. Synthesis of j-aggregating dibenz[a,j]anthracene-based macrocycles

Synthesis of j-aggregating dibenz[a,j]anthracene-based macrocycles

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Author(s)
Chan, Julian M. W.
•
Tischler, Jonathan R.
•
Bulovic, Vladimir
•
Swager, Timothy M
•
Kooi, Steven E
Date Issued
March 2009
Journal
Journal of the American Chemical Society
Publisher
American Chemical Society (ACS)
Citation
Chan, Julian M. W. et al. “Synthesis of j-aggregating dibenz[a,j]anthracene-based macrocycles.” Journal of the American Chemical Society 131.15 (2009): 5659–5666.
Version
Author's final manuscript
Abstract
Several fluorescent macrocycles based on 1,3-butadiyne-bridged dibenz[a,j]anthracene subunits have been synthesized via a multistep route. The synthetic strategy involved the initial construction of a functionalized dibenz[a,j]anthracene building block, subsequent installation of free alkyne groups on one side of the polycyclic aromatic framework, and a final cyclization based on a modified Glaser coupling under high-dilution conditions. Photophysical studies on three conjugated macrocycles revealed the formation of J-aggregates in thin films, as well as in concentrated solid solutions (polyisobutylene matrix), with peak absorption and emission wavelength in the range of λ = 460−480 nm. The characteristic red-shifting of the J-aggregate features as compared to the monomer spectra, enhancement in absorption intensities, narrowed linewidths, and minimal Stokes shift values, were all observed. We demonstrate that improvements in spectral features can be brought about by annealing the films under a solvent-saturated atmosphere, where for the best films the luminescence quantum efficiency as high as 92% was measured. This class of macrocycles represents a new category of J-aggregates that due to their high peak oscillator strength and high luminescence efficiency have the potential to be utilized in a variety of optoelectronic devices.
MIT Department
Massachusetts Institute of Technology. Institute for Soldier Nanotechnologies
Massachusetts Institute of Technology. Department of Chemistry
Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science
Massachusetts Institute of Technology. Microsystems Technology Laboratories
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Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
Persistent DSpace Link
http://hdl.handle.net/1721.1/74239
DOI of Published Version
https://doi.org/10.1021/ja900382r
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