Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractThe fate of environmental contaminants in the food chain    Next AbstractMaternal age and spine development in a rotifer: ecological implications and evolution »

J Am Soc Mass Spectrom


Title:Ion/ion reactions with 'onium' reagents: an approach for the gas-phase transfer of organic cations to multiply-charged anions
Author(s):Gilbert JD; Prentice BM; McLuckey SA;
Address:"Department of Chemistry, Purdue University, West Lafayette, IN, 4907-2084, USA"
Journal Title:J Am Soc Mass Spectrom
Year:2015
Volume:20150205
Issue:5
Page Number:818 - 825
DOI: 10.1007/s13361-015-1077-2
ISSN/ISBN:1879-1123 (Electronic) 1044-0305 (Print) 1044-0305 (Linking)
Abstract:"The use of ion/ion reactions to effect gas-phase alkylation is demonstrated. Commonly used fixed-charge 'onium' cations are well-suited for ion/ion reactions with multiply deprotonated analytes because of their tendency to form long-lived electrostatic complexes. Activation of these complexes results in an SN2 reaction that yields an alkylated anion with the loss of a neutral remnant of the reagent. This alkylation process forms the basis of a general method for alkylation of deprotonated analytes generated via electrospray, and is demonstrated on a variety of anionic sites. SN2 reactions of this nature are demonstrated empirically and characterized using density functional theory (DFT). This method for modification in the gas phase is extended to the transfer of larger and more complex R groups that can be used in later gas-phase synthesis steps. For example, N-cyclohexyl-N'-(2-morpholinoethyl)carbodiimide (CMC) is used to transfer a carbodiimide functionality to a peptide anion containing a carboxylic acid. Subsequent activation yields a selective reaction between the transferred carbodiimide group and a carboxylic acid, suggesting the carbodiimide functionality is retained through the transfer process. Many different R groups are transferable using this method, allowing for new possibilities for charge manipulation and derivatization in the gas phase"
Keywords:Alkylation/drug effects CME-Carbodiimide/analogs & derivatives/chemistry/pharmacology Catalysis Chelating Agents/chemistry/pharmacology Cross-Linking Reagents/chemistry/pharmacology Edetic Acid/chemistry/pharmacology Energy Transfer Hot Temperature Indica;
Notes:"MedlineGilbert, Joshua D Prentice, Boone M McLuckey, Scott A eng R01 GM045372/GM/NIGMS NIH HHS/ R37 GM045372/GM/NIGMS NIH HHS/ GM 45372/GM/NIGMS NIH HHS/ Comparative Study Research Support, N.I.H., Extramural 2015/02/06 J Am Soc Mass Spectrom. 2015 May; 26(5):818-25. doi: 10.1007/s13361-015-1077-2. Epub 2015 Feb 5"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 26-12-2024