Mechanochemical Synthesis of Corannulene-Based Curved Nanographenes

Gábor Báti, Dániel Csókás, Teoh Yong, Si Man Tam, Raymond R.S. Shi, Richard D. Webster, Imre Pápai, Felipe García*, Mihaiela C. Stuparu*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

55 Citations (Scopus)

Abstract

It is shown that corannulene-based strained π-surfaces can be obtained through the use of mechanochemical Suzuki and Scholl reactions. Besides being solvent-free, the mechanochemical synthesis is high-yielding, fast, and scalable. Therefore, gram-scale preparation can be carried out in a facile and sustainable manner. The synthesized nanographene structure carries positive (bowl-like) and negative (saddle-like) Gaussian curvatures and adopts an overall quasi-monkey saddle-type of geometry. In terms of properties, the non-planar surface exhibits a high electron affinity that was measured by cyclic voltammetry, with electrolysis and in situ UV/vis spectroscopy experiments indicating that the one-electron reduced state displays a long lifetime in solution. Overall, these results indicate the future potential of mechanochemistry in accessing synthetically challenging and functional curved π-systems.

Original languageEnglish
Pages (from-to)21620-21626
Number of pages7
JournalAngewandte Chemie - International Edition
Volume59
Issue number48
DOIs
Publication statusPublished - Nov 23 2020
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2020 Wiley-VCH GmbH

ASJC Scopus Subject Areas

  • Catalysis
  • General Chemistry

Keywords

  • ball milling
  • fused-ring systems
  • mechanochemistry
  • solventless reactions
  • sustainable chemistry

Fingerprint

Dive into the research topics of 'Mechanochemical Synthesis of Corannulene-Based Curved Nanographenes'. Together they form a unique fingerprint.

Cite this