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Microwave spectrum and conformation of thiomorpholine

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TLDR
In this paper, the microwave spectrum of normal thiomorpholine (CH 2 ) was investigated within the region 8-40 GHz, and that of N -deuterothiomorphic (ND) within the range 26.5 -40 GHz.
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This article is published in Journal of Molecular Spectroscopy.The article was published on 1980-12-01. It has received 4 citations till now. The article focuses on the topics: Thiomorpholine & Dipole.

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Citations
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Journal ArticleDOI

Energetics and Reactivity of Morpholine and Thiomorpholine: A Joint Experimental and Computational Study

TL;DR: In this article, the influence of the heteroatoms in the conformational, energetic, and reactivity trends exhibited by morpholine and thiomorpholine isosteres was obtained from computational and experimental thermochemical studies.
Journal ArticleDOI

Synthesis, spectroscopic characterization, DFT studies, and preliminary antimicrobial evaluation of new antimony(III) and bismuth(III) complexes derived from 1,3,5-triazine

TL;DR: In this article, the synthesis and characterizations of 2,4,6-tris(thiomorpholine)-1,3,5-triazine, 2, 4,6 tris(piperazine) and 1, 3,5 triazine and their new Sb(III and Bi(III) complexes are described.
Journal ArticleDOI

Equatorial and axial hydrogens in heterocyclic six-membered rings: the rotational spectrum of piperazine

TL;DR: In this article, the rotational spectrum of piperazine has been investigated by free jet absorption millimeter wave spectroscopy, and the spectrum of the polar conformer with axial-equatorial orientations of the two amino hydrogens was only observed.
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Centrifugal Distortion Effects in The Microwave Spectrum of Thiomorpholine

TL;DR: In this article, a first order distortion analysis was carried out on the equatorial form of normal thiomorpholine (CH2-CH 2-S-CH2 -S, CH2-NH) and the obtained frequencies combined with the low J transitions were used to determine the Watson's distortion constants.
References
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Journal ArticleDOI

The vibrational spectra of piperidine and morpholine and their N-deuterated analogs

TL;DR: The i.r. spectra of piperidine (pentamethylene imine) and morpholine (diethyleneimide oxide) as vapours, liquids and as amorphous and crystalline solids at −180°C were recorded between 4000 and 200 cm−1.
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Low-resolution microwave spectroscopy: A new band type

TL;DR: Curl et al. as mentioned in this paper, T. Ikeda, and R, Kewley, J. M. Pickett, and J. F. Curl.
Journal ArticleDOI

Microwave spectrum of morpholine

TL;DR: In this paper, the microwave spectra of morpholine and N-deuteromorpholine have been investigated within the 8 to 40 GHz region, and strong a-type spectra which are due to the chair conformer with an equatorial imino group were recorded.

The microwave spectrum of morpholine.

J. J. Sloan, +1 more
TL;DR: In this article, the authors proposed a method to solve the problem of protein synthesis in the context of chemistry, which is similar to our work in terms of chemistry education and research.
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The conformational analysis of saturated heterocycles. Part XVIII. The orientation of NH-groups in piperidines and morpholines from infrared spectroscopy

TL;DR: Piperidine, morpholine, and cis-2,6-dimethylpiperidine in carbon tetrachlorid egives ΔH 0·6 ± 0·2 kcal/mole preference for NH-equatorial as discussed by the authors.
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