In situ nucleophilic substitution reaction ofN,N-dialkylaminoethyl-2-chlorides monitored by gas chromatography/mass spectrometry

2006 ◽  
Vol 20 (14) ◽  
pp. 2209-2214 ◽  
Author(s):  
V. V. S. Lakshmi ◽  
T. Jagadeshwar Reddy ◽  
M. R. V. S. Murty ◽  
S. Prabhakar ◽  
M. Vairamani
Keyword(s):  
Mass Spectrometry ◽  
Gas Chromatography ◽  
Nucleophilic Substitution ◽  
Substitution Reaction ◽  
Nucleophilic Substitution Reaction ◽  
Gas Chromatography Mass Spectrometry ◽  
Chromatography Mass Spectrometry

Comparison of hydrogenolysis with thioacidolysis for lignin structural analysis

Holzforschung ◽  
2014 ◽  
Vol 68 (2) ◽  
pp. 151-155 ◽  
Author(s):  
Daniel J. van de Pas ◽  
Bernadette Nanayakkara ◽  
Ian D. Suckling ◽  
Kirk M. Torr
Keyword(s):  
Mass Spectrometry ◽  
Nuclear Magnetic Resonance ◽  
Gas Chromatography ◽  
Nmr Spectroscopy ◽  
Structural Analysis ◽  
Magnetic Resonance ◽  
Gas Chromatography Mass Spectrometry ◽  
Aryl Ether ◽  
Chromatography Mass Spectrometry

Abstract Mild hydrogenolysis has been compared with thioacidolysis as a method for degrading lignins in situ and in isolated form before analysis by gas chromatography/mass spectrometry and quantitative 31P nuclear magnetic resonance (NMR) spectroscopy. Both degradation methods gave similar levels of β-aryl ether-linked phenylpropane units that were released as monomers. Degradation by hydrogenolysis generally gave lower levels of total phenylpropane units when analyzed by 31P NMR, especially in the case of lignins with high levels of condensed units. Overall, these results indicate that mild hydrogenolysis could offer an alternative to thioacidolysis for probing lignin structure.

Sign in / Sign up

Export Citation Format

Share Document