The Rotational Spectrum of Monothioformic Acid IV. cis- and trans-H13C(:O)SH and HC(:18O)SH

1977 ◽  
Vol 32 (10) ◽  
pp. 1108-1118 ◽  
Author(s):  
William H. Hocking ◽  
Gisbert Winnewisser

The microwave and millimeter wave spectra of two isotopically substituted species of monothioformic acid, H13COSH and HC18OSH. have been investigated. Over 60 rotational transitions in the ground vibrational state have been assigned and measured for both the eis and trans thiol rotamers. HC(:O)SH. of each isotopic species. Rotational constants and quartic centrifugal distortion comstants of H13COSH and HC18OSH have been determined from the observed spectra. These data have been combined with previously published results on HCOSH, DCOSH. HCOSD and HCO34SH to obtain complete substitutions structures for the planar eis and trans rotamers of HC(:O)SH. All of the in-plane bond angles as well as the SH distance are significantly different for the two rotamers. For the eis rotamer the HSC and HCS angles increase by more than 2°, the OCS angle decreases by more than 3°, and the SH bond shortens compared to the trans rotamer geometry. The eis structure is: r(C-H) = 1.104 ± 0.003 Å, r(C = O) 1.203 ± 0.003 Å. r(C-S) = 1.771 ± 0.003 Å, r(S-H) = 1.335 ± 0.002 Å, ∢(OCS) = 122.5° ± 0.3°, ∢(HSC) = 94.9° ± 0.2° and ∢(HCS) = 114.4° ± 0.2°; whereas the trans structure is: r(C-S) = 1.104 ± 0.003 Å. r(C = O) = 1.205 ± 0.003 Å, r(C-S) = 1.768 ± 0.003 Å, r(S-H) = 1.354 ± 0.002 Å. ∢(OCS) = 125.9° ± 0.3°, (HSC) = 92.5° ± 0.2° and ∢(HCS) = 111.0° ± 0.2°

1995 ◽  
Vol 50 (12) ◽  
pp. 1179-1181 ◽  
Author(s):  
K. M. T. Yamada ◽  
A. Moravec ◽  
G. Winnewisser

Abstract Sixteen new rotational transitions of cyanoacetylene in the ground vibrational state have been measured in the frequency region from 570 GHz to 710 GHz by the Cologne sub-millimeter wave spectrometer. The observed transition frequencies were analyzed together with unpublished millimeter wave data of our group and with the data available in the literature. Precise rota­ tional constant and the quartic and sextic centrifugal distortion constants have been determined; B = 4549.058224(37) MHz, D = 0.544110(19) kHz, and H = 0.0345(21) mHz.


2003 ◽  
Vol 58 (5-6) ◽  
pp. 275-279 ◽  
Author(s):  
A. Guarnieri ◽  
A. Huckaufa

The pure rotational spectra of [18O]ketene, H2C=C18O, [1-13C]ketene, H2C=13CO, and [2-13C]ketene, H213C=CO, have been revisited in the frequency region 200 - 350 GHz in the ground vibrational state.From more than 100 R-branch transitions for each isotopomer a set of rotational and centrifugal distortion constants could be derived using the Watson S-reduction formalism. The values obtained for the rotational constants B and C agree very well with results of former investigations. The agreement is worse with respect to the A constants, but our newly determined A values agree well with the corresponding values of the main species and the 17O isotopomer.


1975 ◽  
Vol 30 (5) ◽  
pp. 672-689 ◽  
Author(s):  
Koichi Yamada ◽  
Manfred Winnewisser

Abstract The pure rotational spectrum of vinyl isocyanide in the ground vibrational state has been as-signed in the frequency region from 8 GHz to 180 GHz. The measured absorption lines encompass 157 a-type transitions from the qRK , qQ1, qQ2,qQ3, qQ4 and qQ5 branches and 48 b-type transitions from the rP0 , rP1, rP2, rP3 , rP4 , rP5, rQ0 , and rQ1 branches for values of J up to 54. The rotational constants have been refined and all quartic and sextic centrifugal distortion constants have been determined using Watson's reduced Hamiltonian. No quadrupole hyperfine splitting was observed.


1994 ◽  
Vol 72 (11-12) ◽  
pp. 1043-1050 ◽  
Author(s):  
Masaharu Fujitake ◽  
Eizi Hirota

The rotational spectrum of the ClS2 free radical in the gaseous phase has been observed in the millimetre- and submillimetre-wave regions. The ClS2 radical was generated by a dc glow discharge in either S2Cl2 or SCl2. Both a- and b-type R-branch transitions, most of which were split into two fine structure components, were detected for both of the 35Cl and 37Cl isotopic species in the ground vibronic state. As expected from the small hyperfine interaction constants reported by an electron spin resonance (ESR) study, the hyperfine structure was resolved for none of the transitions observed in the present study. Analysis of the observed transition frequencies yielded rotational and centrifugal distortion constants and also spin–rotation interaction constants with their centrifugal corrections. The spin–rotation interaction constants obtained in the present study were consistent with g values of the ESR study. The rotational constants of the two isotopic species led to the structure parameters r(S—S) = 1.906 (7) Å, r(S—Cl) = 2.071 (5) Å, and θ(SSCl) = 110.3 (4)°. A harmonic force field was derived from the observed centrifugal distortion constants and inertial defects combined with the ν1 frequency reported in literature on electronic spectroscopy. This harmonic force field yielded the ν2 and ν3 frequencies (445 (21) and 213.0 (2) cm−1, respectively, for 35ClS2), which differed considerably from the values reported previously.


1976 ◽  
Vol 31 (5) ◽  
pp. 422-437
Author(s):  
William H. Hocking ◽  
Gisbert Winnewisser

Abstract The rotational spectra of the two abundant isomers of monothioformic acid, cis- and trans- HC(:O)SH, have been assigned in the frequency region 8 -250 GHz. Over 90 a-type transitions and over 60 b-type transitions have been measured for each rotamer. The a-type transitions belong to the qRK , qQ1, qQ2, qQ3 and qQ4 branches and the b-type absorption lines encompass the Ka = 1 - 0, 2 - 1, 3 - 2, 4 - 3 and 5 - 4 rotational sub-bands. The rotational constants and all quartic and sextic centrifugal distortion constants have been determined for each rotamer using Watson's reduced Hamiltonian. In addition to the measured line positions the frequencies of some selected low-J transitions, not observed in this work but of potential astrophysical interest, have been listed as an aid in the interstellar search for monothioformic acid.


1974 ◽  
Vol 29 (8) ◽  
pp. 1213-1215 ◽  
Author(s):  
N. W. Larsen ◽  
B. P. Winnewisser

Rotational transitions of 16012C32S and 16013C32S in the ground vibrational state and of 16012C32S in several excited states have been accurately measured in the millimeter wave region for a minimum of four different J values. The analysis of the measured frequencies leads to rotational constants for the following vibrational states: 0 00 0 of 16O13C32S and 0 00 0, 0 1 1c 0, 0 1 1d 0, 0 20 0, 0 22c 0, 0 22d 0, 0 00 1 of 16O12C32S. Since the two components of the 0 22 0 transitions were resolved, an analysis of the l-type resonance was carried out and the interval 0 22 0 - 0 20 0 has been determined to be -4.63(10) cm-1. The result is in good agreement with the presently available determination of this level from vibrational spectra.


1987 ◽  
Vol 42 (11) ◽  
pp. 1275-1278
Author(s):  
H. Zerbe ◽  
A. Guarnieri

The microwave and millimeterwave spectrum of 15N-fluoracetonitrile(CH2FC15N) in the ground vibrational state are investigated in the region between 8 and 150 GHz. The measured transitions are fitted to a Hamiltonian with three rotational constants, five quartic and seven sextic centrifugal distortion constants in the symmetric top limit of van Eijck-Typke and in the s-reduction of Watson. The rotational constants are used to improve the calculated r0 -restructure of the fluoracetonitrile molecule.


Sign in / Sign up

Export Citation Format

Share Document