Аннотация:
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.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
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
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3973
https://www.mathnet.ru/rus/mendc/v13/i3/p97
Эта публикация цитируется в следующих 4 статьяx:
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
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
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
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