Correlation of dative bond length and donor proton affinity in adducts of SO3: A good predictor for HCCCN-SO3

S. W. Hunt, D. L. Fiacco, M. Craddock, K. R. Leopold

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

The rotational spectrum of HCCCN-SO3 has been observed using Fourier transform microwave spectroscopy. The vibrationally averaged structure is that of a symmetric top, with the HCCCN axis along the C3 axis of the SO3, and the nitrogen end near the sulfur. The N-S bond length is 2.567(13) Å, which is slightly shorter than the sum of the van der Waals radii. The NSO angle is 91.7(4)°, indicating a small but distinct distortion of the SO3 from planarity, and the N-S interaction can be described as a chemical bond in an early stage of its formation. The N-S bond lengths in a series of SO3 adducts with amines, nitriles, and pyridine are shown to correlate well with the proton affinities of the bases. In addition, for the bases considered here, the proton affinities vary in a regular manner with the ionization energies corresponding to removal of a lone pair electron. Thus, the trend in proton affinities follows the variation in energy gap between donor and acceptor orbitals in these complexes, accounting for the utility of the proton affinity in correlating aspects of structure and bonding across the series.

Original languageEnglish (US)
Pages (from-to)213-218
Number of pages6
JournalJournal of molecular spectroscopy
Volume212
Issue number2
DOIs
StatePublished - Jan 1 2002

Keywords

  • Cyanoacetylene
  • HCCCN
  • Lewis acid-base adduct
  • Partially bound complex
  • Proton affinity
  • SO

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