Microwave spectrum and conformational composition of 2-chloroethylisocyanide.

Harald Møllendal, Svein Samdal, Jean-Claude Guillemin

Index: J. Phys. Chem. A 115(46) , 13474-81, (2011)

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Abstract

2-Chloroethylisocyanide (ClCH(2)CH(2)N≡C) has been synthesized, and its microwave spectrum has been investigated in the 20-97 GHz spectral region. The spectra of (35)Cl and (37)Cl isotopologues of two conformers have been assigned. The Cl-C-C-N chain of atoms is antiperiplanar in one of these rotamers and synclinal in the second. The energy difference between the two forms has been obtained from relative intensity measurements. It was found that the antiperiplanar conformer is favored over the synclinal form by 4.3(8) kJ/mol. Quantum chemical calculations at the CCSD/cc-pVTZ and B3LYP/cc-pVTZ levels of theory have been performed. Most, but not all, of the spectroscopic constants predicted in these calculations are in good agreement with their experimental counterparts. The theoretical calculations correctly predict that the 2-chloroethylisocyanide exists as a mixture of an antiperiplanar and a synclinal conformer, with the former about 3.5 kJ/mol more stable than the latter. Both methods of calculations find that the antiperiplanar rotamer has a symmetry plane. The dihedral angle formed by the Cl-C-C-N link of atoms of the synclinal form is 67° according to the CCSD calculations. It is estimated from a comparison with the experimental rotational constants that this dihedral angle is uncertain by ±3°.