Symmetry‐Broken Charge Transfer Excited‐State in Homoleptic ZincII Imidazo[1,2‐a]pyridine Complexes

نویسندگان

چکیده

A series of four homoleptic cationic ZnII complexes (Zn1–Zn4) coordinated by two substituted bis-imidazo[1,2-a]pyridine (ImPy) ligands (L1–L4) is herein presented. The are functionalized with either electron acceptor or donor functional groups at the C6 positions ImPy moieties. In DMF solution, all display intense near-UV to blue emission (λem = 379–450 nm) high photoluminescence quantum yield (PLQY) up 0.50 and short-lived excited state. Additionally, complex Zn4 displays an interesting solvatochromic behavior. absorption spectrum characterized electronic transitions mainly ligand-centered (1LC) intraligand charge-transfer (1ILCT) character, which involves a symmetric density redistribution Franck-Condon (FC). stark contrast, subsequent excited-state dynamics relaxes molecular symmetry allows symmetry-breaking hole-electron pair on bichromophoric system. As consequence, efficient radiative deexcitation process takes place that ascribed singlet-manifold state symmetry-broken charge transfer (1SBCT) as supported in-depth photophysical, electrochemical time-dependent theory (TD-DFT) investigation. Remarkably, 1SBCT nature provides structureless green in solid 520 nm for Zn4), rather uncommon complexes.

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ژورنال

عنوان ژورنال: ChemPhotoChem

سال: 2023

ISSN: ['2367-0932']

DOI: https://doi.org/10.1002/cptc.202300092