scholarly journals The Nuclear Magnetic Resonance Spectra of Olefinic Protons and the Substituent Effects. V. Spin-spin Coupling intrans1,2-Disubstituted Ethylenes

1967 ◽  
Vol 40 (9) ◽  
pp. 2192-2194 ◽  
Author(s):  
Jun Niwa
1966 ◽  
Vol 44 (7) ◽  
pp. 759-769 ◽  
Author(s):  
Emil J. Moriconi ◽  
John P. St. George ◽  
W. F. Forbes

Infrared, ultraviolet, and nuclear magnetic resonance spectra of the following compounds are reported: 2-indanone (I), trans- and cis-hexahydro-2-indanone (V and XI), 1-chloro-2-indanone-1,3,3-d3 (III), 1-bromo-2-indanone-1,3,3-d3 (IV), 1-chloro-trans-hexahydro-2-indanone (VII), 1-bromo-trans-hexahydro-2-indanone (VIII), some deuterated forms of these compounds, 2-chlorocyclohexanone-2,6,6-d3, and 2-bromocyclohexanone-2,6,6-d3.2-Indanone and trans-hexahydro-2-indanone each display two peaks in the carbonyl infrared region with intensity ratios of approximately 40:1. The origin of these doublets is discussed.Nuclear magnetic resonance spectra were determined to indicate the presence or absence of ring mobility, and spin–spin coupling data were used to support some of the conclusions deduced from the infrared data for some of the compounds.


1971 ◽  
Vol 49 (18) ◽  
pp. 3071-3073 ◽  
Author(s):  
John S. Martin ◽  
Fred Y. Fujiwara

The high resolution 1H and 19F nuclear magnetic resonance (n.m.r.) spectra of the four bihalide ions have been observed in aprotic solvents. The 1H shielding is, in every case, 14 p.p.m. less than that in the related molecule. The spin–spin coupling in FHF− is 120.5 ± 0.3 Hz.


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