Abstract
Molecular nanocarbons with precisely defined conjugated scaffolds can provide an ideal platform for investigating mechanistic insights into photophysical properties. Here, we report the synthesis and time-resolved spectroscopic characterization of two isomeric tubular all-benzene nanocarbon (TANC) molecules, named meso- and chiral-TANC, respectively. Structurally, they feature triple covalent linkages, with different connectivity, between coaxially stacked cycloparaphenylene units. While meso-TANC maintains conformational rigidity, chiral-TANC shows photo-induced dynamic helicity. Femtosecond transient absorption (TA) and time-resolved circularly polarized luminescence (TRCPL) spectroscopy demonstrate that chiral-TANC undergoes ultrafast relaxation accompanied by untwisting motions within 8 ps upon photoexcitation, establishing the direct correlation between photo-induced conformational evolution and chiroptical dynamics in heteroatom-free, fully conjugated molecules.
| Original language | English |
|---|---|
| Article number | e202518587 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 64 |
| Issue number | 49 |
| DOIs | |
| State | Published - 1 Dec 2025 |
Keywords
- All-benzene scaffold
- Circularly polarized luminescence
- Excited-state chirality
- Time-resolved spectroscopy
- Tubular nanocarbons
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