AI Article Synopsis

  • A gas-phase study explored how d-fructose dehydrates in the presence of various bases using mass spectrometry and theoretical calculations.
  • Electrospray ionization produced protonated d-fructose addition products, allowing the investigation of intermediates and reaction pathways.
  • The study concluded that the final product, protonated 5-hydroxymethyl-2-furaldehyde (5-HMF), forms more effectively with specific bases that remain clustered throughout the dehydration process.

Article Abstract

A gas-phase investigation of the d-fructose dehydration reaction in the presence of base has been performed by the joint application of mass spectrometric techniques and theoretical calculations. Protonated addition products of d-fructose and base were generated in the gas phase by electrospray ionization using several bases of different proton affinity. The intermediates, products and decomposition channels were investigated by ion trap mass spectrometry. Electronic structure calculations allowed the identification of the ionic intermediates and products of a selected system containing NH, helping to rationalize the observed reaction pathways. The obtained results show that the final product, the protonated 5-hydroxymethyl-2-furaldheyde [5-HMF]H, is better formed using selected bases and only if these remain clustered until the end of the dehydration process.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6723769PMC
http://dx.doi.org/10.1002/open.201900173DOI Listing

Publication Analysis

Top Keywords

intermediates products
8
base-assisted conversion
4
conversion protonated
4
protonated d-fructose
4
d-fructose 5-hmf
4
5-hmf searching
4
searching gas-phase
4
gas-phase green
4
green models
4
models gas-phase
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!