Color-tunable upconversion emission from a twisted intramolecular charge-transfer state of anthracene dimers via triplet–triplet annihilation. Issue 5 (4th February 2019)

• Record Type: Journal Article
• Authors: Liu, Heyuan; Yan, Xinyu; Shen, Li; Tang, Zhaofeng; Liu, Shanshan; Li, Xiyou
• Is Part Of: Materials horizons. Volume 6:Issue 5(2019)
• Page Start: 990
• Page End: 995
• Publication Date: 2019-02-04
• Subjects: Materials -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c8mh01586d
• Languages: English
• ISSNs: 2051-6347

Abstract

Abstract : Color-tunable upconversion emission based on triplet–triplet annihilation was achieved for the first time in two anthracene dimers with twisted intramolecular charge-transfer states. Abstract : Two anthracene dimers, 9, 9′-BiAn and2, 9-BiAn, linked symmetrically or asymmetrically with a single bond were used as emitters in triplet–triplet annihilation upconversion (TTA-UC) for the first time. Upon photoexcitation, the localized excited states (LE) formed first and then twisted intramolecular charge-transfer (TICT) states were generated from these LE states in these two dimers. The generation of the TICT state in the symmetrical dimer, 9, 9′-BiAn, is faster than that in the asymmetrical one, 2, 9-BiAn . The TICT states of these two dimers are highly emissive, so they were tested as emitters in the TTA-UC process. The UC quantum yields could exceed 13% with PtOEP as a sensitizer. Notably, the color of the UC emission can be tuned from purple to cyan as the solvent polarity increases. This is the first example of color-tunable TTA-UC emission and also the first time that TICT molecules have been used as emitters in the TTA-UC process. As the interaction between the anthracene subunits is designable, this provides an opportunity to tune the emission properties of TTA-UC for different purposes of application without varying the excitation wavelength.