Chemical Shifts and Spin-Spin Coupling Interactions in the Nuclear Magnetic Resonance Spectra of endo- and exo-Norbornene Derivatives

1965 ◽  
Vol 87 (17) ◽  
pp. 3900-3905 ◽  
Author(s):  
Jeff C. Davis ◽  
Thomas V. Van Auken

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.



1991 ◽  
Vol 69 (6) ◽  
pp. 972-977 ◽  
Author(s):  
Gottfried Heinisch ◽  
Wolfgang Holzer

The 13C nuclear magnetic resonance spectra of 17 3,6-disubstituted pyridazine derivatives have been systematically analyzed. Chemical shifts and various 13C, 1H coupling constants are reported. Attempts were made to correlate these data with results obtained from semiempirical molecular orbital calculations as well as with substituent electronegativities and Taft's substituent constants σI and σR0. Key words: 3,6-disubstituted pyridazines, 13C NMR spectroscopy, 13C, 1H spin coupling constants.





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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