Guided by theoretical predictions, the rotational spectrum of fluoroiodomethane, CH(2)FI, has been recorded and assigned. Accurate values are reported for the ground-state rotational constants, all quartic, sextic, and two octic centrifugal-distortion constants. The hyperfine structure of the rotational spectrum was thoroughly investigated using a Fourier-transform microwave spectrometer and the Lamb-dip technique in the millimeter-/submillimeter-wave region, thus allowing the accurate determination of the complete iodine quadrupole-coupling tensor and of the diagonal elements of the iodine spin-rotation tensor. Relativistic effects turned out to be essential for the accurate theoretical prediction of the dipole moment and quadrupole-coupling constants and were accounted for by direct perturbation theory and a spin-free four-component treatment based on the Dirac-Coulomb Hamiltonian. The relativistic corrections to the dipole moment amount to up to 34% and to the iodine quadrupole-coupling tensor to about 15-16% of the total values.
Guided by theoretical predictions, the rotational spectra of the mono- and bideuterated species of bromofluoromethane, CDH(79)BrF, CDH(81)BrF, CD(2) (79)BrF, and CD(2) (81)BrF, have been recorded for the first time. Assignment of a few hundred rotational transitions led to the accurate determination of the ground-state rotational constants, all of the quartic and most of the sextic centrifugal distortion constants, as well as the full bromine quadrupole-coupling tensor for both (79)Br and (81)Br, in good agreement with corresponding theoretical predictions based on high-level coupled-cluster calculations. The rotational spectra of the (13)C containing species (13)CH(2) (79)BrF and (13)CH(2) (81)BrF have been observed in natural abundance and have been assigned, thus allowing the determination of the rotational and centrifugal distortion constants as well as the bromine quadrupole-coupling tensor. Furthermore, empirical equilibrium structures have been obtained within a least-squares fit procedure using the available experimental ground-state rotational constants for various isotopic species. Vibrational effects have been accounted for in the analysis using vibration-rotation interaction constants derived from anharmonic force fields computed at the second-order Moller-Plesset perturbation theory as well as coupled-cluster (CC) levels. The empirical equilibrium geometries obtained in this way agree well with the corresponding theoretical predictions obtained from CC calculations [at the CCSD(T) level] after extrapolation to the complete basis set limit and inclusion of core-valence correlation corrections and relativistic effects.
A combined microwave, infrared, and computational investigation of CHBrF(2) is reported. For the vibrational ground state, measurements in the millimeter- and sub-millimeter-wave regions for CH(79)BrF(2) and CH(81)BrF(2) provided rotational and centrifugal-distortion constants up to the sextic terms as well as the hyperfine parameters (quadrupole-coupling and spin-rotation interaction constants) of the bromine nucleus. The determination of the latter was made possible by recording of spectra at sub-Doppler resolution, achieved by means of the Lamb-dip technique, and supporting the spectra analysis by high-level quantum chemical calculations at the coupled-cluster level. In this context, the importance of relativistic effects, which are of the order of 6.5% and included in the present work using second-order direct perturbation theory, needs to be emphasized for accurate predictions of the bromine quadrupole-coupling constants. The infrared measurements focused on the ν(4) fundamental band of CH(79)BrF(2). Fourier transform investigations using a synchrotron radiation source provided the necessary resolution for the observation and analysis of the rotational structure. The spectroscopic parameters of the v(4) = 1 state were found to be close to those of the vibrational ground state, indicating that the ν(4) band is essentially unaffected by perturbations.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.