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Mendeleev Communications, 2003, Volume 13, Issue 3, Pages 97–99
DOI: https://doi.org/10.1070/MC2003v013n03ABEH001801
(Mi mendc3973)
 

This article is cited in 4 scientific papers (total in 4 papers)

Pasteur-like resolution of quasi-racemates in solid and gas phases

R. G. Kostyanovskya, E. N. Nikolaevb, O. N. Kharybinb, G. K. Kadorkinaa, V. R. Kostyanovskya

a N.N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation
b Institute for Energy Problems of Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (151 kB) Citations (4)
Abstract: Isotopomeric quasi-racemates (IQR), i.e., 1:1 mixtures of enantiomers one of which contains an isotopic label, can undergo crystallisation as conglomerates or true quasi-racemates. In the former case, each single crystal contains, predominantly or exclusively, either labelled or non-labelled enantiomers, whereas in the latter case, it contains both enantiomers (1:1). If solution sputtering is used to ionise quasi-racemates, the formation of homochiral protonated and metallated enantiomers and their homochiral oligomers in the gas phase is detected in ion cyclotron resonance (ICR) mass spectra; these compounds differ in their m/z values; hence, Pasteur-like ‘manual sorting’ can be employed to catch them successively in the ion trap of the spectrometer.
Document Type: Article
Language: English


Citation: R. G. Kostyanovsky, E. N. Nikolaev, O. N. Kharybin, G. K. Kadorkina, V. R. Kostyanovsky, “Pasteur-like resolution of quasi-racemates in solid and gas phases”, Mendeleev Commun., 13:3 (2003), 97–99
Linking options:
  • https://www.mathnet.ru/eng/mendc3973
  • https://www.mathnet.ru/eng/mendc/v13/i3/p97
  • This publication is cited in the following 4 articles:
    1. Emily N. Pinter, Lee S. Cantrell, Graeme M. Day, Kraig A. Wheeler, “Pasteur's tartaramide/malamide quasiracemates: new entries and departures from near inversion symmetry”, CrystEngComm, 20:30 (2018), 4213  crossref
    2. Nicola Castellucci, Giuseppe Falini, Lorenzo Milli, Magda Monari, Sergio Abbate, Giovanna Longhi, Ettore Castiglioni, Giuseppe Mazzeo, Claudia Tomasini, “Solid‐State Properties and Vibrational Circular Dichroism Spectroscopy in Solution of Hybrid Foldamers Stereoisomeric Mixtures”, ChemPlusChem, 79:1 (2014), 114  crossref
    3. Joseph Gal, “The Discovery of Stereoselectivity at Biological Receptors: Arnaldo Piutti and the Taste of the Asparagine Enantiomers—History and Analysis on the 125th Anniversary”, Chirality, 24:12 (2012), 959  crossref
    4. Eugene N. Nikolaev, Igor A. Popov, Oleg N. Kharybin, Alexey S. Kononikhin, Marina I. Nikolaeva, Yurij V. Borisov, “In situ recognition of molecular chirality by mass spectrometry”, International Journal of Mass Spectrometry, 265:2-3 (2007), 347  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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