The odd-number cyclo[13]carbon and its dimer, cyclo[26]carbon

Author:

Albrecht Florian1ORCID,Rončević Igor2ORCID,Gao Yueze2ORCID,Paschke Fabian1ORCID,Baiardi Alberto3,Tavernelli Ivano3ORCID,Mishra Shantanu1ORCID,Anderson Harry L.2ORCID,Gross Leo1ORCID

Affiliation:

1. IBM Research Europe – Zürich, 8803 Rüschlikon, Switzerland.

2. Department of Chemistry, Oxford University, Chemistry Research Laboratory, Oxford, UK.

3. IBM Quantum, IBM Research Europe – Zürich, 8803 Rüschlikon, Switzerland.

Abstract

Molecular rings of N carbon atoms (cyclo[ N ]carbons, or C N ) 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, C 13 , by manipulation of decachlorofluorene with a scanning probe microscope tip. We elucidated the properties of C 13 by experiment and theoretical modeling. C 13 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 C 13 dimer, cyclo[26]carbon, demonstrating the potential of cyclocarbons and their precursors as building blocks for carbon allotropes.

Publisher

American Association for the Advancement of Science (AAAS)

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