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Tubular All-Benzene Nanocarbon with Evolving Excited-State Chirality

  • Gaolei Li
  • , Xueli Wang
  • , Liang Liang Mao
  • , Jia Nan Gao
  • , Xueliang Shi
  • , Hongwei Li
  • , Zi Tong Li
  • , Zi Ye Huo
  • , Yiming Chen
  • , Hai Bo Yang
  • , Jinquan Chen*
  • , Chen Ho Tung
  • , Li Zhu Wu
  • , Huan Cong*
  • *Corresponding author for this work
  • CAS - Technical Institute of Physics and Chemistry
  • East China Normal University
  • Peking University

Research output: Contribution to journalArticlepeer-review

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 languageEnglish
Article numbere202518587
JournalAngewandte Chemie - International Edition
Volume64
Issue number49
DOIs
StatePublished - 1 Dec 2025

Keywords

  • All-benzene scaffold
  • Circularly polarized luminescence
  • Excited-state chirality
  • Time-resolved spectroscopy
  • Tubular nanocarbons

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