Structure–property studies of P-triarylamine-substituted dithieno[3, 2-b:2′, 3′-d]phospholes. Issue 114 (3rd November 2015)

• Record Type: Journal Article
• Authors: Puntscher, Hannes; Kautny, Paul; Stöger, Berthold; Tissot, Antoine; Hametner, Christian; Hagemann, Hans R.; Fröhlich, Johannes; Baumgartner, Thomas; Lumpi, Daniel
• Is Part Of: RSC advances. Volume 5:Issue 114(2015)
• Page Start: 93797
• Page End: 93807
• Publication Date: 2015-11-03
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c5ra13651b
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : The photo-physical and theoretical investigation of 10 novel donor–acceptor materials sheds new light on charge transfer in dithienophosphole oxide derivatives. Abstract : The synthesis of 10 novel P -substituted dithienophosphole oxide compounds applying phenylcarbazole and indolocarbazole donors is presented. Based on photo-physical and theoretical investigations, the study reveals that the pyramidal geometry of the phosphorus allows for the synthesis of charge transfer materials by introducing strong exocyclic donor groups but suppresses intramolecular charge transfer below a certain donor strength threshold, which is an appealing structural feature for the design of donor–acceptor materials. The triplet energies of the phenylcarbazole based compounds are in the range of 2.49–2.65 eV, sufficiently high for potential applications as host materials in PhOLEDs. By contrast, the introduction of indolocarbazole, the weakest employed donor, yields materials exhibiting a significantly higher triplet energy of up to 2.87 eV and a remarkably low singlet–triplet splitting (0.18 eV). In addition an interesting example of an intramolecular electronic through-space interaction has been observed for the ortho -linked phenylcarbazole derivative.