Combination of X-ray photoelectron and solid-state 13C nuclear magnetic resonance spectroscopy in the structural characterisation of humic acids

2000 ◽  
Vol 424 (2) ◽  
pp. 243-255 ◽  
Author(s):  
Fanny Monteil-Rivera ◽  
Eric B. Brouwer ◽  
Sonia Masset ◽  
Yves Deslandes ◽  
Jacques Dumonceau
1987 ◽  
Vol 65 (9) ◽  
pp. 2217-2222 ◽  
Author(s):  
Pierre Brouant ◽  
Jacques Barbe ◽  
Alain Marsura ◽  
Catherine Soula ◽  
Cuong Luu-Duc

The solid state structures of three compounds belonging to the Δ-2 imidazoline series have been compared. X-ray data and molecular parameters are given. It is noteworthy to point out that substituents are trans to one another in these structures. Moreover, the spatial orientation of the carbonyl group attached to C(4) depends on the nature of the substituent attached to nitrogen N(3). In addition, results are in close agreement with those of nuclear magnetic resonance spectroscopy.


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