The vibrational spectra (100–1600 cm−1) and scaled a b i n i t i o STO-3G and 3-21G harmonic force fields for norbornane, norbornene, and norbornadiene

Abstract
The vibrational spectra in the region of 100–1600 cm1 of norbornane and norbornadiene are reinvestigated, and those of norbornene reported for the first time. On the basis of 3‐21G ab initio force fields, evaluated for each molecule and scaled using overlay refinements of 12 scaling factors, the spectra are assigned and the observed transition frequencies reproduced with an overall average error of 6.2 cm1. STO‐3G force constants, modified to correct for deficiencies in the stretch/bend interaction force constants but otherwise scaled analogously to 3‐21G, reproduce the final set of assignments to within 10.1 cm1 on average. The STO‐3G basis is shown to be suitable as a less costly alternative to split‐valence basis sets, particularly for describing the vibrational dynamics of low frequency ring bending and torsional modes.