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Updated: Feb 16, 2026

Synthesis of pH Dependent Pyrazole, Imidazole, and Isoindolone Dipyrrinone Fluorophores using a Claisen-Schmidt Condensation Approach
Published on: June 10, 2021
Pyrazole and Triazole Fused Perylene Bisimides: Synthesis and Photophysical Properties
Wenshu Feng1,2, Andrey A Sukhanov3, Xue Zhang1
1State Key Laboratory of Fine Chemicals, Frontier Science Center for Smart Materials, School of Chemical Engineering, Dalian University of Technology, Dalian, P.R. China.
Abstract:
We studied the intersystem crossing (ISC) of neutral, monoanion, and dianion of a series of phenyl, pyrazole, and triazole fused perylene bisimides (PBI) derivatives. The neutral compounds exhibit high fluorescence quantum yields (ΦF = 66.5%-91.9%) and low singlet oxygen quantum yields (ΦΔ < 7.8%), with no triplet state signals detected via femtosecond transient absorption (fs-TA) or nanosecond transient absorption (ns-TA) spectral measurements. Time-resolved electron paramagnetic resonance (TREPR) revealed an e,e,e,a,a,a electron spin polarization (ESP) for the T1 state of these PBIs. Calculations of spin-orbit coupling matrix elements (SOCMEs) and g-tensor anisotropy both confirm the weak spin-orbit coupling (SOC) of the molecules, accounting for their low ISC efficiency. Pulse electron paramagnetic resonance (pulse EPR) measurements of radical anions showed that PBI derivatives lacking pyrazole/triazole moieties have much longer transverse relaxation times (Tm = 2.5-2.6 µs) than the other compounds. Additionally, ns-TA spectra confirmed ISC in PBI dianions, which possess long-lived triplet states (213-558 µs). These species can be used as super strong reductants in photocatalytic redox organic reactions.
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