Co-ordination of alkali metals to sulfur-based organometallic ligands:133Cs and19F nuclear magnetic resonance studies of Cs[Mo(SC6F5)4(η5-C5H5)], the first example of caesium–fluorine spin–spin coupling

1992 ◽  
pp. 2531-2532 ◽  
Author(s):  
Alan S. F. Boyd ◽  
Jack L. Davidson ◽  
Calum H. McIntosh ◽  
Pascal C. Leverd ◽  
W. Edward Lindsell ◽  
...  
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Alkali Metals ◽  
Spin Coupling ◽  
Magnetic Resonance Studies ◽  
Spin Spin Coupling ◽  
Nuclear Magnetic

ORGANIC AND BIOLOGICAL SPECTROCHEMICAL STUDIES: XXII. THE INFRARED, ULTRAVIOLET, AND NUCLEAR MAGNETIC RESONANCE SPECTRA OF SOME SUBSTITUTED 2-INDANONES AND REFERENCE COMPOUNDS

1966 ◽  
Vol 44 (7) ◽  
pp. 759-769 ◽  
Author(s):  
Emil J. Moriconi ◽  
John P. St. George ◽  
W. F. Forbes
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Infrared Region ◽  
Spin Coupling ◽  
Nuclear Magnetic Resonance Spectra ◽  
Two Peaks ◽  
Spin Spin Coupling ◽  
Infrared Data ◽  
Magnetic Resonance Spectra ◽  
Nuclear Magnetic

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.

Sign in / Sign up

Export Citation Format

Share Document