The Experts below are selected from a list of 231 Experts worldwide ranked by ideXlab platform

Willy Malaisse - One of the best experts on this subject based on the ideXlab platform.

François Kayser - One of the best experts on this subject based on the ideXlab platform.

Brad Bendiak - One of the best experts on this subject based on the ideXlab platform.

  • Direct evidence for the ring opening of monosaccharide anions in the gas phase: photodissociation of Aldohexoses and Aldohexoses derived from disaccharides using variable-wavelength infrared irradiation in the carbonyl stretch region
    Carbohydrate Research, 2011
    Co-Authors: Darin J. Brown, Sarah E. Stefan, Giel Berden, Jeffrey D. Steill, Jos Oomens, John R. Eyler, Brad Bendiak
    Abstract:

    All eight D-Aldohexoses and Aldohexoses derived from the non-reducing end of disaccharides were investigated by variable-wavelength infrared multiple-photon dissociation (IRMPD) as anions in the negative-ion mode. Spectroscopic evidence supports the existence of a relatively abundant open-chain configuration of the anions in the gas phase, based on the observation of a significant carbonyl absorption band near 1710 cm(-1). The abundance of the open-chain configuration of the Aldohexose anions was approximately 1000-fold or greater than that of the neutral sugars in aqueous solution. This provides an explanation as to why it has not been possible to discriminate the anomeric configuration of Aldohexose anions in the gas phase when derived from the non-reducing sugar of a disaccharide. Evidence from photodissociation spectra also indicates that the different Aldohexoses yield product ions with maximal abundances at different wavelengths, and that the carbonyl stretch region is useful for differentiation of sugar stereochemistries. Quantum-chemical calculations indicate relatively low energy barriers to intramolecular proton transfer between hydroxyl groups and adjacent alkoxy sites located on open-chain sugar anions, suggesting that an ensemble of alkoxy charge locations contributes to their observed photodissociation spectra. Ring opening of monosaccharide anions and interconversion among configurations is an inherent property of the ions themselves and occurs in vacuo independent of solvent participation. (C) 2011 Elsevier Ltd. All rights reserved.

  • end group determination of oligosaccharides a gas chromatography mass spectrometry mass spectrometry method for distinguishing between all d Aldohexoses and d ketohexoses
    Carbohydrate Research, 2000
    Co-Authors: Brad Bendiak, Tammy T. Fang
    Abstract:

    Abstract A method for end-group determination of oligosaccharides is described, which involves conversion of the reducing monosaccharide into a 1-deoxy-1-hydrazinohexitol heptaacetate (Aldohexoses) or an epimeric pair of 2-deoxy-2-hydrazinohexitol heptaacetates (2-ketohexoses). Products are linear and unique to each Aldohexose or ketohexose. Methods are reported for separation of all stereoisomers of the derivatives on single columns by gas chromatography. Gas chromatography–mass spectrometry/mass spectrometry with electron-impact ionization enabled the 1-deoxy-1-hydrazinohexitol heptaacetates and 2-deoxy-2-hydrazinohexitol heptaacetates to be independently identified in each others presence. Chemical-ionization mass spectrometry/mass spectrometry permitted derivatives to be identified in subpicomolar quantities. The non-acetylated compounds could also be identified as their hydrochlorides by 1H NMR spectroscopy.

  • End-group determination of oligosaccharides: a gas chromatography-mass spectrometry/mass spectrometry method for distinguishing between all D-Aldohexoses and D-ketohexoses.
    Carbohydrate Research, 2000
    Co-Authors: Brad Bendiak, Tammy T. Fang
    Abstract:

    Abstract A method for end-group determination of oligosaccharides is described, which involves conversion of the reducing monosaccharide into a 1-deoxy-1-hydrazinohexitol heptaacetate (Aldohexoses) or an epimeric pair of 2-deoxy-2-hydrazinohexitol heptaacetates (2-ketohexoses). Products are linear and unique to each Aldohexose or ketohexose. Methods are reported for separation of all stereoisomers of the derivatives on single columns by gas chromatography. Gas chromatography–mass spectrometry/mass spectrometry with electron-impact ionization enabled the 1-deoxy-1-hydrazinohexitol heptaacetates and 2-deoxy-2-hydrazinohexitol heptaacetates to be independently identified in each others presence. Chemical-ionization mass spectrometry/mass spectrometry permitted derivatives to be identified in subpicomolar quantities. The non-acetylated compounds could also be identified as their hydrochlorides by 1H NMR spectroscopy.

Takeo Ohsaka - One of the best experts on this subject based on the ideXlab platform.

  • enhanced oxidation of Aldohexose and aldopentose on hg adatom modified au electrode in alkaline aqueous solution
    Electroanalysis, 2005
    Co-Authors: Futoshi Matsumoto, Masahiro Harada, Nobuyuki Koura, Takeyoshi Okajima, Takeo Ohsaka
    Abstract:

    The electrochemical behavior of Aldohexose and aldopentose monosaccharides was examined on Hg adatom-modified and bare Au electrodes in alkaline aqueous solution using cyclic voltammetry. For the bare Au electrode, the oxidation peak currents are dependent on hydroxyl group configuration on the monosaccharides. On the other hand, for the Hg adatom-modified Au electrode, the actual oxidation peak currents were similar for all monosaccharides other than glucose. Dispersion of Hg adatoms on the Au surface led to diminishment of configurational differences between monosaccharides as well as enhancement of oxidation peak current.

  • Enhanced Oxidation of Aldohexose and Aldopentose on Hg Adatom‐Modified Au Electrode in Alkaline Aqueous Solution
    Electroanalysis, 2005
    Co-Authors: Futoshi Matsumoto, Masahiro Harada, Nobuyuki Koura, Takeyoshi Okajima, Takeo Ohsaka
    Abstract:

    The electrochemical behavior of Aldohexose and aldopentose monosaccharides was examined on Hg adatom-modified and bare Au electrodes in alkaline aqueous solution using cyclic voltammetry. For the bare Au electrode, the oxidation peak currents are dependent on hydroxyl group configuration on the monosaccharides. On the other hand, for the Hg adatom-modified Au electrode, the actual oxidation peak currents were similar for all monosaccharides other than glucose. Dispersion of Hg adatoms on the Au surface led to diminishment of configurational differences between monosaccharides as well as enhancement of oxidation peak current.

Rudolph Willem - One of the best experts on this subject based on the ideXlab platform.