Nature Communications (Mar 2024)

Squeezing formaldehyde into C60 fullerene

  • Vijyesh K. Vyas,
  • George R. Bacanu,
  • Murari Soundararajan,
  • Elizabeth S. Marsden,
  • Tanzeeha Jafari,
  • Anna Shugai,
  • Mark E. Light,
  • Urmas Nagel,
  • Toomas Rõõm,
  • Malcolm H. Levitt,
  • Richard J. Whitby

DOI
https://doi.org/10.1038/s41467-024-46886-5
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 11

Abstract

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Abstract The cavity inside fullerene C60 provides a highly symmetric and inert environment for housing atoms and small molecules. Here we report the encapsulation of formaldehyde inside C60 by molecular surgery, yielding the supermolecular complex CH2O@C60, despite the 4.4 Å van der Waals length of CH2O exceeding the 3.7 Å internal diameter of C60. The presence of CH2O significantly reduces the cage HOMO-LUMO gap. Nuclear spin-spin couplings are observed between the fullerene host and the formaldehyde guest. The rapid spin-lattice relaxation of the formaldehyde 13C nuclei is attributed to a dominant spin-rotation mechanism. Despite being squeezed so tightly, the encapsulated formaldehyde molecules rotate freely about their long axes even at cryogenic temperatures, allowing observation of the ortho-to-para spin isomer conversion by infrared spectroscopy. The particle in a box nature of the system is demonstrated by the observation of two quantised translational modes in the cryogenic THz spectra.