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The odd-number cyclo[13]carbon and its dimer, cyclo[26]carbon.
Albrecht, Florian; Roncevic, Igor; Gao, Yueze; Paschke, Fabian; Baiardi, Alberto; Tavernelli, Ivano; Mishra, Shantanu; Anderson, Harry L; Gross, Leo.
Affiliation
  • Albrecht F; IBM Research Europe - Zürich, 8803 Rüschlikon, Switzerland.
  • Roncevic I; Department of Chemistry, Oxford University, Chemistry Research Laboratory, Oxford, UK.
  • Gao Y; Department of Chemistry, Oxford University, Chemistry Research Laboratory, Oxford, UK.
  • Paschke F; IBM Research Europe - Zürich, 8803 Rüschlikon, Switzerland.
  • Baiardi A; IBM Quantum, IBM Research Europe - Zürich, 8803 Rüschlikon, Switzerland.
  • Tavernelli I; IBM Quantum, IBM Research Europe - Zürich, 8803 Rüschlikon, Switzerland.
  • Mishra S; IBM Research Europe - Zürich, 8803 Rüschlikon, Switzerland.
  • Anderson HL; Department of Chemistry, Oxford University, Chemistry Research Laboratory, Oxford, UK.
  • Gross L; IBM Research Europe - Zürich, 8803 Rüschlikon, Switzerland.
Science ; 384(6696): 677-682, 2024 May 10.
Article in En | MEDLINE | ID: mdl-38723091
ABSTRACT
Molecular rings of N carbon atoms (cyclo[N]carbons, or CN) are excellent benchmarking systems for testing quantum chemical theoretical methods and valuable precursors to other carbon-rich materials. Odd-N cyclocarbons, which have been elusive to date, are predicted to be even less stable than even-N cyclocarbons. We report the on-surface synthesis of cyclo[13]carbon, C13, by manipulation of decachlorofluorene with a scanning probe microscope tip. We elucidated the properties of C13 by experiment and theoretical modeling. C13 adopts an open-shell configuration with a triplet ground state and a kinked geometry, which shows different extents of distortion and carbene localization depending on the molecular environment. Moreover, we prepared and characterized the C13 dimer, cyclo[26]carbon, demonstrating the potential of cyclocarbons and their precursors as building blocks for carbon allotropes.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Science Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Science Year: 2024 Document type: Article Affiliation country:
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