1991
DOI: 10.1515/zna-1991-0714
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The Microwave Spectrum of 4-Methylisothiazole

Abstract: The microwave spectrum of 4-methylisothiazole was assigned by means of a pulsed molecular beam microwave Fourier transform spectrometer. Analysis of the spectrum yielded the rotational constants A = 7370.642 (

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Cited by 18 publications
(7 citation statements)
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“…Some results obtained for 2MP are compared with those of other five-membered heterocycles in Figure 3. The V3 potential varies in a wide range from 34 cm 1 for 2-methylthiazole ( 6) [1], 106 cm 1 for 4-methylisothiazole ( 8) [2], 252 cm 1 for 2-methyloxazole ( 7) [21] to 280 cm 1 for 2MP (5).…”
Section: Discussionmentioning
confidence: 99%
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“…Some results obtained for 2MP are compared with those of other five-membered heterocycles in Figure 3. The V3 potential varies in a wide range from 34 cm 1 for 2-methylthiazole ( 6) [1], 106 cm 1 for 4-methylisothiazole ( 8) [2], 252 cm 1 for 2-methyloxazole ( 7) [21] to 280 cm 1 for 2MP (5).…”
Section: Discussionmentioning
confidence: 99%
“…Many investigations have been carried out on such aromatic systems, especially heterocyclic five-membered rings, to determine the methyl barrier heights, i.a. 2-methylthiazole (34.9 cm 1 ) [1], 4-methylisothiazole (105.8 cm 1 ) [2], 2,5dimethylthiophene (248.0 cm 1 ) [3], 2-acetyl-5-methylfuran (369.8 cm 1 for the trans conformer and 356.5 cm 1 for the cis conformer) [4], and 2,5-dimethylfuran (439.2 cm 1 ) [5]. From those studies it is obvious that the torsional potentials of methyl groups attached to planar aromatic rings vary in a wide range in both, shape and height.…”
Section: Introductionmentioning
confidence: 99%
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“…The program BELGI has been extended in its hyperfine versions BELGI-Cs-hyperfine and BELGI-C 1 -hyperfine, which can treat molecules with one internal rotor and one weakly coupling nucleus like 14 N. Its predictive power has been proven for several molecules containing one methyl rotor and a nitrogen nucleus such as Ntert-butylacetamide (Cs), 11 N-ethylacetamide (C 1 ), 11 3-nitrotoluene (Cs), 12 and 2-methylpyrrole (Cs). 13 Monomethyl derivatives of aromatic heterocyclic five-membered rings containing a nitrogen nucleus are ideally suited to test the Hamiltonian model because the V 3 potential value of the methyl group covers a wide range from low barriers like those in 2-methylthiazole (34.9 cm −1 ) 14 and 4-methylisothiazole (105.8 cm −1 ) 15 to intermediate barriers such as in 4-and 5-methylthiazole (357.6 cm −1 and 332.0 cm −1 , respectively), 16,17 as well as in 2-, 4-, and 5-methyloxazole (252.0 cm −1 , 428.3 cm −1 , and 478.2 cm −1 , respectively). 18 The first molecule mentioned above, 2-methylthiazole (2MTA), has been studied by Grabow et al in the frequency range from 7 GHz to 13 GHz.…”
Section: Introductionmentioning
confidence: 99%
“…This is due to the coupling of internal methyl and overall rotation yielding first-order contributions from off-diagonal elements of the tensor for lines with E symmetry. Although this effect has been described earlier (10), it has been exploited only in a few cases when analyzing the nuclear quadrupole hyperfine structures of rotational lines of molecules with internal rotation of methyl groups (11)(12)(13).…”
Section: Introductionmentioning
confidence: 99%