Dynamic adjustment of emission from both singlets and triplets: the role of excited state conformation relaxation and charge transfer in phenothiazine derivates

Luminescence behaviors in organic emitters are influenced greatly by the molecular conformation. However, the current research on room-temperature phosphorescence (RTP) mainly focuses on fixed molecular conformation, such as that in single crystals and rigid hosts. Herein, by linking the phenothiazi...

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Published inJournal of materials chemistry. C, Materials for optical and electronic devices Vol. 9; no. 4; pp. 1378 - 1386
Main Authors Qiu, Weidong, Cai, Xinyi, Li, Mengke, Wang, Liangying, He, Yanmei, Xie, Wentao, Chen, Zijian, Liu, Ming, Su, Shi-Jian
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 01.01.2021
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Abstract Luminescence behaviors in organic emitters are influenced greatly by the molecular conformation. However, the current research on room-temperature phosphorescence (RTP) mainly focuses on fixed molecular conformation, such as that in single crystals and rigid hosts. Herein, by linking the phenothiazine moiety with nitrogen heterocycles, we constructed four phenothiazine derivates having planar structure in the ground state. In the excited state, a large conformation relaxation occurs to give a dynamically tunable fluorescence and phosphorescence by the extent of the intramolecular charge transfer (ICT). In systems with a reduced ICT character, multiple emissions consisting of fluorescence and phosphorescence were observed and a white light emission was obtained in the amorphous film state. When increasing the ICT, strong spin mixing between the singlet and triplet occurs in the twisted intramolecular charge transfer (TICT) state, which is favorable for a short triplet lifetime. The emission of the thermally activated delayed fluorescence (TADF) or short RTP depends on the allowance or forbidden of fluorescence in the twisted excited state conformation. This work demonstrates the adjustment of the singlet and triplet emission behaviors through controlling the extent of TICT and provides an insight into the relationship between the molecular conformation and triplet exciton dynamics for future applications. Dynamic adjustment of emission behaviours by controlling the extent of twisted intramolecular charge transfer character in excited state.
AbstractList Luminescence behaviors in organic emitters are influenced greatly by the molecular conformation. However, the current research on room-temperature phosphorescence (RTP) mainly focuses on fixed molecular conformation, such as that in single crystals and rigid hosts. Herein, by linking the phenothiazine moiety with nitrogen heterocycles, we constructed four phenothiazine derivates having planar structure in the ground state. In the excited state, a large conformation relaxation occurs to give a dynamically tunable fluorescence and phosphorescence by the extent of the intramolecular charge transfer (ICT). In systems with a reduced ICT character, multiple emissions consisting of fluorescence and phosphorescence were observed and a white light emission was obtained in the amorphous film state. When increasing the ICT, strong spin mixing between the singlet and triplet occurs in the twisted intramolecular charge transfer (TICT) state, which is favorable for a short triplet lifetime. The emission of the thermally activated delayed fluorescence (TADF) or short RTP depends on the allowance or forbidden of fluorescence in the twisted excited state conformation. This work demonstrates the adjustment of the singlet and triplet emission behaviors through controlling the extent of TICT and provides an insight into the relationship between the molecular conformation and triplet exciton dynamics for future applications.
Luminescence behaviors in organic emitters are influenced greatly by the molecular conformation. However, the current research on room-temperature phosphorescence (RTP) mainly focuses on fixed molecular conformation, such as that in single crystals and rigid hosts. Herein, by linking the phenothiazine moiety with nitrogen heterocycles, we constructed four phenothiazine derivates having planar structure in the ground state. In the excited state, a large conformation relaxation occurs to give a dynamically tunable fluorescence and phosphorescence by the extent of the intramolecular charge transfer (ICT). In systems with a reduced ICT character, multiple emissions consisting of fluorescence and phosphorescence were observed and a white light emission was obtained in the amorphous film state. When increasing the ICT, strong spin mixing between the singlet and triplet occurs in the twisted intramolecular charge transfer (TICT) state, which is favorable for a short triplet lifetime. The emission of the thermally activated delayed fluorescence (TADF) or short RTP depends on the allowance or forbidden of fluorescence in the twisted excited state conformation. This work demonstrates the adjustment of the singlet and triplet emission behaviors through controlling the extent of TICT and provides an insight into the relationship between the molecular conformation and triplet exciton dynamics for future applications. Dynamic adjustment of emission behaviours by controlling the extent of twisted intramolecular charge transfer character in excited state.
Author Wang, Liangying
He, Yanmei
Liu, Ming
Qiu, Weidong
Su, Shi-Jian
Cai, Xinyi
Xie, Wentao
Chen, Zijian
Li, Mengke
AuthorAffiliation South China Institute of Collaborative Innovation
State Key Laboratory of Luminescent Materials and Devices and Institute of Polymer Optoelectronic Materials and Devices
South China University of Technology
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Snippet Luminescence behaviors in organic emitters are influenced greatly by the molecular conformation. However, the current research on room-temperature...
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SubjectTerms Charge transfer
Crystallography
Emissions control
Emitters
Excitation
Excitons
Fluorescence
Light emission
Molecular conformation
Phosphorescence
Planar structures
Room temperature
Single crystals
White light
Title Dynamic adjustment of emission from both singlets and triplets: the role of excited state conformation relaxation and charge transfer in phenothiazine derivates
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