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A Symmetric and Rigid Tetrahydropentalene Derivative as an Ideal Acceptor for Efficient Triplet-Triplet Annihilation-Assisted Photon Upconversion.

PubMed
Authors: Nagaoka T, Matsui Y, Ogaki T, Ikeda H

Year

2026

Paper ID

60161

Status

Peer-reviewed

Abstract Read

~2 min

Abstract Words

135

Citations

0

Abstract

The triplet-triplet annihilation (TTA)-assisted photon upconversion (PUC) properties of a solution system containing the newly developed acceptor di(-anisyl)tetrahydropentalene , containing a rigidly constrained planar diene subunit, were elucidated. Due to its symmetric and rigid structure, undergoes rapid fluorescence emission and slow nonradiative processes, respectively, resulting in its unity fluorescence quantum yield and its short singlet excited state lifetime of 1.13 ns in degassed toluene. Its rigidity also affords a long triplet excited state lifetime of 654 μs, essential for efficient TTA-PUC. Moreover, the experimentally determined singlet (, 3.22 eV) and triplet (, 1.62-1.79 eV) excited state energy levels of meet the requirements for exergonic TTA ( ≲ 2). Analysis of the green-to-purple TTA-PUC behavior (anti-Stokes shift: 0.89 eV) reveals that a toluene solution of and platinum octaethylporphyrin displays a quite low threshold excitation intensity (10 mW cm) and high PUC quantum yield (ca 23%).

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  • The triplet-triplet annihilation (TTA)-assisted photon upconversion (PUC) properties of a solution system containing the newly developed acceptor di(-anisyl)tetrahydropentalene...

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Current Paper #60161 #68465 Bounding Eigenstate Overlap fro... #68440 Classical State Preparation for... #68437 Transition-state lattice modes ... #68423 Selective Fermi-Level Pinning: ...

External citation index: OpenAlex citation signal • updated 2026-06-10 07:42:10

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