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Updated: Jul 5, 2026

A Microwave-Assisted Direct Heteroarylation of Ketones Using Transition Metal Catalysis
Published on: February 16, 2020
A microwave and quantum chemical study of cyclopropanethiol
Rajmund Mokso1, Harald Møllendal, Jean-Claude Guillemin
1Centre for Theoretical and Computational Chemistry (CTCC), Department of Chemistry, University of Oslo, P.O. Box 1033 Blindern, NO-0315 Oslo, Norway.
Abstract:
The microwave spectra of cyclopropanethiol, C(3)H(5)SH, and one deuterated species C(3)H(5)SD, have been investigated in the 20 - 80 GHz frequency range. The spectra of the ground vibrational state and of three vibrationally excited states of the parent species of a conformer which has a synclinal ("gauche") arrangement for the H-C-S-H chain of atoms, was assigned. The H-C-S-H dihedral angle is 76(5)° from synperiplanar (0°). The b-type transitions of the ground and of the vibrationally excited states of the parent species were split into two components, which is assumed to arise from tunneling of the proton of the thiol group between two equivalent synclinal potential wells. No splitting was resolved in the spectrum of C(3)H(5)SD. The tunneling frequency of the ground vibrational state of C(3)H(5)SH is 1.664(22) MHz. The tunneling frequency of the first excited-state of the C-S torsion is 52.330(44) MHz, whereas this frequency is 26.43(13) and 3.286(61) MHz, respectively, for the first excited states of the two lowest bending vibrations. The dipole moment of the ground vibrational state of the parent species is μ(a) = 4.09(5), μ(b) = 2.83(11), μ(c) = 0.89(32), and μ(tot) = 5.06(16) × 10(-30) C m. The microwave study has been augmented by high-level density functional and ab initio quantum chemical calculations.
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