Tuning Excited-State Properties in Pyrrolo[3,2-b]pyrrole-Based Donor–Acceptor Emitters via Molecular Conformation and Conjugation Control
Taotao Gan, Jie Su, Feiyang Li, Qiuxia Li, Chao Shi

TL;DR
This paper shows how adjusting molecular structure in nitrogen-based compounds can control their light-emitting properties for better optoelectronic applications.
Contribution
A strategy for tuning excited-state properties in PP-based emitters through molecular conformation and conjugation control is demonstrated.
Findings
PP-6F shows efficient π-electron delocalization and dominant local excitation emission.
PPA-3F exhibits a hybrid ICT/LE excited state due to increased dihedral angle and reduced conjugation.
Rigid anthracene in PPA-3F suppresses nonradiative decay and maintains high oscillator strength.
Abstract
Nitrogen-fused conjugated heterocycles have attracted growing interest owing to their tunable electronic properties and potential in organic optoelectronics. In this study, two centrosymmetric donor–acceptor-type emitters PP-6F and PPA-3F were designed by incorporating trifluorophenyl and anthracene acceptor units into a pyrrolo[3,2-b]pyrrole (PP) framework. The experimental and theoretical results reveal that subtle modulations in molecular conformation and π-conjugation pathways strongly affect the excited-state characteristics. PP-6F, featuring a nearly coplanar donor–acceptor configuration, exhibits efficient π-electron delocalization and a dominant local excitation (LE) emission with a large oscillator strength. In contrast, the bulky anthracene in PPA-3F increases the donor–acceptor dihedral angle, reduces conjugation coupling, and promotes orbital separation, leading to a hybrid…
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Taxonomy
TopicsSynthesis and Properties of Aromatic Compounds · Organic Light-Emitting Diodes Research · Organic Electronics and Photovoltaics
