1987•The Knowledge Bank (The Ohio State University)Requires access

VIBRATIONAL SPECTRA AND CONFORMATIONS OF (CHLOROMETHYL) THIIRANE

Charles J. Wurrey, VICTOR F. KALASINSKY, Yueh-Han Chien, Fred G. Rojas, P. M. Green

Open publisher page 0 citations

Abstract

The infrared spectra of (chioromethyl) thiirane in all three phases have been recorded, along with the Raman spectra of this compound in the condensed phases. Since both the liquid phase infrared and Raman spectra exhibit several "doublets" in which one member disappears upon crystallization, it has been concluded that (chloramethyl) thiirane exists in the liquid phase as an equilibrium mixture of two conformers, namely the gauche-1 and gauche-2 rotameric forms. From the temperature behavior of the Raman intensities of three liquid phase doublets, measured over the range 233 k - 293 k, an enthalpy difference between these two confarmers has been determined to be $1.1 \\pm 0.2 cal/mole$. In addition, a vibrational assignment of the fundamental modes of this molecule has been proposed, and it is in excellent agreement with assignments proposed for similar compounds.

About this research paper

What this paper is about

The infrared spectra of (chioromethyl) thiirane in all three phases have been recorded, along with the Raman spectra of this compound in the condensed phases. Since both the liquid phase infrared and Raman spectra exhibit several "doublets" in which one member disappears upon crystallization, it has been concluded that (chloramethyl) thiirane exists in the liquid phase as an equilibrium mixture of two conformers, namely the gauche-1 and gauche-2 rotameric forms. From the temperature behavior of the Raman intensities of three liquid phase doublets, measured over the range 233 k - 293 k, an enthalpy difference between these two confarmers has been determined to be $1.1 \\pm 0.2 cal/mole$. In addition, a vibrational assignment of the fundamental modes of this molecule has been proposed, and it is in excellent agreement with assignments proposed for similar compounds.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

The infrared spectra of (chioromethyl) thiirane in all three phases have been recorded, along with the Raman spectra of this compound in the condensed phases. Since both the liquid phase infrared and Raman spectra exhibit several "doublets" in which one member disappears upon crystallization, it has been concluded that (chloramethyl) thiirane exists in the liquid phase as an equilibrium mixture of two conformers, namely the gauche-1 and gauche-2 rotameric forms. From the temperature behavior of the Raman intensities of three liquid phase doublets, measured over the range 233 k - 293 k, an enthalpy difference between these two confarmers has been determined to be $1.1 \\pm 0.2 cal/mole$. In addition, a vibrational assignment of the fundamental modes of this molecule has been proposed, and it is in excellent agreement with assignments proposed for similar compounds.

Key concepts: Thiirane, Spectral line, Chemistry, Physics, Organic chemistry, Ring (chemistry), Astronomy

Related papers

Back to paper searchBrowse research topicsOriginal source
VIBRATIONAL SPECTRA AND CONFORMATIONS OF (CHLOROMETHYL) THIIRANE — Research Paper | ScholarLens