The use of labelled analogues for the determination of mass spectrometric fragmentation mechanisms of cannabinoids. A re-investigation of the formation of the most abundant fragment ion [C15,H19,O2]+ in Δ1(6)tetrahydrocannabinol

1976 ◽  
Vol 11 (6) ◽  
pp. 659-663 ◽  
Author(s):  
Edward G. Boeren ◽  
Wigger Heerma ◽  
Johan K. Terlouw
2021 ◽  
Vol 19 (10) ◽  
pp. 2224-2232
Author(s):  
Geng Li ◽  
Yue-Wei Guo ◽  
Jeroen S. Dickschat

The EI-MS fragmentation mechanisms of three diterpenes from Catenulispora acidiphila and two semisynthetic derivatives were studied in extensive 13C-labelling experiments.


2017 ◽  
Author(s):  
Xueming Dong

Catalytic deoxygenation of coal enhances the stability and combustion performance of coal-derived liquids. However, determination of the selectivity of removal of oxygen atoms incorporated in or residing outside of aromatic rings is challenging. This limits the ability to evaluate the success of catalytic deoxygenation processes. A mass spectrometric method, in-source collision-activated dissociation (ISCAD), combined with high resolution product ion detection, is demonstrated to allow the determination of whether the oxygen atoms in aromatic compounds reside outside of aromatic rings or are part of the aromatic system, because alkyl chains can be removed from aromatic cores via ISCAD. Application of this method for the analysis of a subbituminous coal treated using a supported catalyst revealed that the catalytic treatment reduced the number of oxygen-containing heteroaromatic rings but not the number of oxygen atoms residing outside the aromatic rings.<br>


2017 ◽  
Author(s):  
Xueming Dong

Catalytic deoxygenation of coal enhances the stability and combustion performance of coal-derived liquids. However, determination of the selectivity of removal of oxygen atoms incorporated in or residing outside of aromatic rings is challenging. This limits the ability to evaluate the success of catalytic deoxygenation processes. A mass spectrometric method, in-source collision-activated dissociation (ISCAD), combined with high resolution product ion detection, is demonstrated to allow the determination of whether the oxygen atoms in aromatic compounds reside outside of aromatic rings or are part of the aromatic system, because alkyl chains can be removed from aromatic cores via ISCAD. Application of this method for the analysis of a subbituminous coal treated using a supported catalyst revealed that the catalytic treatment reduced the number of oxygen-containing heteroaromatic rings but not the number of oxygen atoms residing outside the aromatic rings.<br>


2015 ◽  
pp. 40-43 ◽  
Author(s):  
Andreas G. Degenhardt

The isotope ratios of water, organic matter and micronutrients from food are dependent on the circumstances and sites of their origin and production. Analytical methods, based on mass spectrometry, are established for routine determination of isotopes. Differentiation between metabolic pathways of C3 and C4 plants is realizable by determination 13C/12C ratios which can distinguish and identify sucrose from pure beet (Beta vulgaris) and pure cane (Saccharum officinarum). Influenced by the worldwide hydrological cycle the isotope ratios of 2H/1H and 18O/16O vary systematically, the variations give information about geographical origin. The exemplarily determination of authenticity is demonstrated by using mass spectrometric isotope ratio evaluation for identification of plant source and geographical origin with the help of selected sugar samples with known origin.


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