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Fig. 1 Illustration of open-shell ZTGMs and the synthetic strategy to π-extended [5]triangulene. Illustration of open-shell ZTGMs and the synthetic strategy.

Published byAlf Gustafsson Modified over 5 years ago

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Presentation on theme: "Fig. 1 Illustration of open-shell ZTGMs and the synthetic strategy to π-extended [5]triangulene. Illustration of open-shell ZTGMs and the synthetic strategy."— Presentation transcript:

1 Fig. 1 Illustration of open-shell ZTGMs and the synthetic strategy to π-extended [5]triangulene.
Illustration of open-shell ZTGMs and the synthetic strategy to π-extended [5]triangulene. (A) Open-shell ZTGMs with different numbers of zigzag carbon atom (N) and predicted spin multiplicity (S). Yellow, monoradical phenalenyl (N= 2); red, biradical triangulene (N= 3); violet, π-extended triradical [4]triangulene (N= 4); blue, tetraradical [5]triangulene (N= 5). (B) Schematic illustration of the surface-assisted transformation of rationally designed precursor (compound 1) to [5]triangulene. The two yellow spots indicate the sites where the on-surface dehydrogenation initiated, and the six red spots represent the methyl groups that undergo the cyclodehydrogenation process. Jie Su et al. Sci Adv 2019;5:eaav7717 Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).

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