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Electric dipole moment and hyperfine properties of bromoacetylene in the ground and first excited C-H stretching vibrational states
Molecular beam electric resonance spectroscopy, combined with color center laser excitation, has been used to measure the electric dipole moment and Br hyperfine properties of bromoacetylene in its ground and first excited C–H stretching vibrational states. For the HCC79Br, v=0: μ=0.229 62(1) D, eQq...
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Published in: | The Journal of chemical physics 1990, Vol.92 (1), p.71-75 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Molecular beam electric resonance spectroscopy, combined with color center laser excitation, has been used to measure the electric dipole moment and Br hyperfine properties of bromoacetylene in its ground and first excited C–H stretching vibrational states. For the HCC79Br, v=0: μ=0.229 62(1) D, eQq=648.113(3) MHz, CBr=6.4(3) kHz, and B=4000.07 MHz. For the HCC79Br, v=1: μ=0.248 82(1) D, eQq=648.160(2) MHz, CBr=7.0(3) kHz, and B=3992.79 MHz. For the HCC81Br, v=0: μ=0.229 56(1) D, eQq=541.430(1) MHz, CBr=7.4(1) kHz, and B=3978.46 MHz. For the HCC81Br, v=1: μ=0.248 61(1) D, eQq=541.464(3) MHz, CBr=7.6(4) kHz, and B=3971.34 MHz. The vibrational band origin for the C–H stretching vibration is 3367.7(2) cm−1. |
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ISSN: | 0021-9606 1089-7690 |
DOI: | 10.1063/1.458425 |