Dipole moment and hyperfine properties of the ground state and the C–H excited vibrational state of HCN
- 1 May 1984
- journal article
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 80 (9) , 3989-3991
- https://doi.org/10.1063/1.447269
Abstract
Radio frequency transitions have been measured in the J=1 rotational level of HCN for both the ground vibrational state and the first excited state of the C–H stretching mode using molecular beam electric resonance spectroscopy. The vibrationally excited state was populated with an infrared laser. The dipole moment and hyperfine properties for the ground and excited states are 〈μ〉000=2.985 188(3)D, 〈μ〉001=3.017 408(4)D, 〈eQq〉000=−4707.83(6) kHz, 〈eQq〉001=−4661.39(8) kHz, 〈CN〉000=10.13(2) kHz, 〈CN〉001=10.06(3) kHz, 〈CH〉000=−4.35(5) kHz, 〈CH〉=−4.21(3) kHz.This publication has 9 references indexed in Scilit:
- Sub-Doppler resolution infrared molecular-beam spectroscopy. Stark effect measurement of the dipole moment of hydrogen fluoride and hydrogen cyanide in excited vibrational statesFaraday Discussions of the Chemical Society, 1981
- Millimeterwave spectroscopy of active laser plasmas; the excited vibrational states of HCNThe Journal of Chemical Physics, 1977
- Molecular beam electric resonance study of formaldehyde, thioformaldehyde, and keteneThe Journal of Chemical Physics, 1977
- The 1973 Least-Squares Adjustment of the Fundamental ConstantsJournal of Physical and Chemical Reference Data, 1973
- Polarizability Anisotropy of Hydrogen FluorideThe Journal of Chemical Physics, 1972
- Dipole Moment and Hyperfine Parameters of H35Cl and D35ClThe Journal of Chemical Physics, 1970
- Hyperfine Structure Constants of HF and DFThe Journal of Chemical Physics, 1970
- Electric Dipole Moment of Carbonyl SulfideThe Journal of Chemical Physics, 1968
- Rotational Dependency of the Stark Effect of a Polar Diatomic MoleculeThe Journal of Chemical Physics, 1963