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The influence of molecular geometry on the efficiency of thermally activated delayed fluorescence

DOI: 10.1039/C9TC00720B DOI Help

Authors: Roberto S. Nobuyasu (Durham University) , Jonathan S. Ward (Durham University) , Jamie Gibson (Newcastle University) , Beth A. Laidlaw (Newcastle University) , Zhongjie Ren (Durham University; Beijing University of Chemical Technology) , Przemyslaw Data (Durham University; Silesian University of Technology) , Andrei S. Batsanov (Durham University) , Thomas J. Penfold (Newcastle University) , Martin R. Bryce (Durham University) , Fernando B. Dias (Durham University)
Co-authored by industrial partner: No

Type: Journal Paper
Journal: Journal Of Materials Chemistry C , VOL 7 , PAGES 6672-6684

State: Published (Approved)
Published: May 2019
Diamond Proposal Number(s): 11145

Open Access Open Access

Abstract: In this work we successfully developed a strategy for positively influencing the conformation of thermally activated delayed fluorescence (TADF) molecules containing phenothiazine as the electron donor (D) unit, and dibenzothiophene-S,S-dioxide as the acceptor (A), linked in D–A and D–A–D structures. In this strategy the effect of restricted molecular geometry is explored to maximize TADF emission. The presence of bulky substituents in different positions on the donor unit forces the molecules to adopt an axial conformer where the singlet charge transfer state is shifted to higher energy, resulting in the oscillator strength and luminescence efficiency decreasing. With bulky substituents on the acceptor unit, the molecules adopt an equatorial geometry, where the donor and acceptor units are locked in relative near-orthogonal geometry. In this case the individual signatures of the donor and acceptor units are evident in the absorption spectra, demonstrating that the substituent in the acceptor uncouples the electronic linkage between the donor and acceptor more effectively than with donor substitution. In contrast with the axial conformers that show very weak TADF, even with a small singlet triplet gap, molecules with equatorial geometry show stronger oscillator strength and luminescence efficiency and are excellent TADF emitters. Acceptor-substituted molecules 6 and 7 in particular show extremely high TADF efficiency in solution and solid film, even with a singlet–triplet energy gap around 0.2 eV. This extensive study provides important criteria for the design of novel TADF and room temperature phosphorescence (RTP) emitters with optimized geometry.

Subject Areas: Chemistry


Instruments: I19-Small Molecule Single Crystal Diffraction

Added On: 20/06/2019 10:23

Documents:
c9tc00720b.pdf

Discipline Tags:

Organic Chemistry Physical Chemistry Chemistry

Technical Tags:

Diffraction Single Crystal X-ray Diffraction (SXRD)