Protonation-Induced Room-Temperature Phosphorescence in Fluorescent Polyurethane

The Journal of Physical Chemistry. a
Wei SunGuoqing Zhang

Abstract

Room-temperature phosphorescence (RTP) from purely organic systems is of practical importance in biological imaging, oxygen sensing and displaying technologies. The key step to obtaining RTP from organic molecules is efficient intersystem crossing (ISC), which is usually low compared to inorganic materials. Here we show that protonation of a dye molecule, a thioflavin derivative, in strongly polar polyurethane can be used to effectively harness RTP. Prior to protonation, the predominant transition is π-π* for the polymer, which has nearly undetectable RTP due to the large singlet-triplet energy splitting (0.87 eV); when Brønsted acids are gradually added to the system, increasingly strong RTP is observed due to the presence of a new intramolecular charge-transfer state (ICT). The ICT state serves to lower the singlet-triplet energy gap (0.46 eV). The smaller gap results in more efficient ISC and thus strong RTP under deoxygenated conditions. The thioflavin-polyurethane system can be tuned via proton concentration and counterions and opens new doors for RTP-based polymeric sensors and stimuli-responsive materials.

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Citations

May 3, 2019·Chemistry, an Asian Journal·Khemnath Patir, Sonit Kumar Gogoi
Oct 22, 2020·The Journal of Physical Chemistry. B·Akitsu HironoTaku Hasobe

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