Spectroscopic studies of some substituted methyl formates. Part 1.—Microwave spectra and internal rotation barriers of methyl-fluoroformate, -propiolate, -cyanoformate, -acrylate and -acetate
- 1 January 1971
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Transactions of the Faraday Society
- Vol. 67, 922-949
- https://doi.org/10.1039/tf9716700922
Abstract
The stable molecular conformations of methyl-fluoroformate, -propiolate, -cyanoformate, -acrylate (cis) and -acetate have been shown to be planar, and for the latter four compounds the cis ester molecular skeleton has been established. Barriers to internal rotation of the methyl group were measured from splittings of the microwave lines for each compound. [XCOOCH3; X = F, V3= 1077; X = HCC, V3= 1266; X = CN, V3= 1172; X = CH3, V3= 1215; X = CH2CH, V3= 1220 (values of V3 in cal/mol).] For methyl acetate a value of 307 ± 50 cal/mol for the acetyl methyl group was calculated from internal rotation splittings in the spectrum of CD3COOCD3. The dipole moments of methyl-fluoroformate and cyanoformate were 2.83 and 4.23 D respectively.Keywords
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