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Bond Rotations and Heteroatom Effects in Donor-Acceptor-Donor Molecules: Implications for Thermally Activated Delayed Fluorescence and Room Temperature Phosphorescence

Ward, Jonathan S.; Nobuyasu, Roberto S.; Fox, Mark A.; Batsanov, Andrei S.; Santos, Jose; Dias, Fernando B.; Bryce, Martin R.

Bond Rotations and Heteroatom Effects in Donor-Acceptor-Donor Molecules: Implications for Thermally Activated Delayed Fluorescence and Room Temperature Phosphorescence Thumbnail


Authors

Jonathan S. Ward

Roberto S. Nobuyasu

Andrei S. Batsanov

Jose Santos



Abstract

The synthesis of 1-methylphenoxazine via CO2-directed lithiation chemistry is reported. This electron donor was coupled with 2,8-dibenzothiophene-S,S-dioxide with Buchwald–Hartwig chemistry to give a new D–A–D charge-transfer fluorescent molecule 1b. X-ray crystal structures and calculations show that the phenoxazinyl groups are coplanar and equatorial (eq) to the acceptor plane in non-methylated 1a, but are pyramidal and axial (ax) in 1b. The bond rotation energy barriers between donor and acceptor groups for 1a and 1b are only 0.13 and 0.19 eV respectively from hybrid-DFT computations at the CAM-B3LYP/6-31G(d) level. Many possible conformers are present in solutions and in zeonex. In zeonex, the methyl groups in 1b shift the emission band 0.13 eV higher in energy compared to 1a. Excited state eq-eq and ax-ax geometries were identified with DFT calculations, with charge transfer (CT) emission assigned as 1CT(eq) and 1CT(ax) dominating. The lower energy 1CT(eq) contributes to thermally activated delayed fluorescence (TADF), whereas the higher energy 1CT(ax) does not. Phenothiazine analogs 2a and 2b, also have major fluorescence emissions assigned as 1CT(eq) and 1CT(ax) respectively. 2a-b have substantial room temperature phosphorescence (RTP) whereas 1a-b do not, highlighting the importance of the sulfur atom in 2a-b to obtain RTP emission.

Citation

Ward, J. S., Nobuyasu, R. S., Fox, M. A., Batsanov, A. S., Santos, J., Dias, F. B., & Bryce, M. R. (2018). Bond Rotations and Heteroatom Effects in Donor-Acceptor-Donor Molecules: Implications for Thermally Activated Delayed Fluorescence and Room Temperature Phosphorescence. Journal of Organic Chemistry, 83(23), 14431-14442. https://doi.org/10.1021/acs.joc.8b02187

Journal Article Type Article
Acceptance Date Oct 30, 2018
Online Publication Date Oct 31, 2018
Publication Date Oct 31, 2018
Deposit Date Oct 31, 2018
Publicly Available Date Oct 31, 2019
Journal Journal of Organic Chemistry
Print ISSN 0022-3263
Electronic ISSN 1520-6904
Publisher American Chemical Society
Peer Reviewed Peer Reviewed
Volume 83
Issue 23
Pages 14431-14442
DOI https://doi.org/10.1021/acs.joc.8b02187
Public URL https://durham-repository.worktribe.com/output/1314466

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Copyright Statement
This document is the Accepted Manuscript version of a Published Work that appeared in final form in the Journal of organic chemistry copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.joc.8b02187






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