http://www.cnr.it/ontology/cnr/individuo/prodotto/ID33909
Photoionization Spectroscopy and Mass Spectrometry of Some Molecular and Supramolecular Asymmetric Systems in the Isolated State (Articolo in rivista)
- Type
- Label
- Photoionization Spectroscopy and Mass Spectrometry of Some Molecular and Supramolecular Asymmetric Systems in the Isolated State (Articolo in rivista) (literal)
- Anno
- 2006-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1002/chir.20274 (literal)
- Alternative label
A.Giardini, A. Paladini, D. Catone, S. Piccirillo, F. Rondino, M. Satta, A. Filippi, M. Speranza, S. Turchini, N. Zema (2006)
Photoionization Spectroscopy and Mass Spectrometry of Some Molecular and Supramolecular Asymmetric Systems in the Isolated State
in Chirality (N.Y., N.Y. Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- A.Giardini, A. Paladini, D. Catone, S. Piccirillo, F. Rondino, M. Satta, A. Filippi, M. Speranza, S. Turchini, N. Zema (literal)
- Pagina inizio
- Pagina fine
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- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Dipartimento di Chimica, Università degli Studi di Roma \"La Sapienza\", Rome, Italy
CNR-IMIP, Tito Scalo (Pz), Italy
CNR-ISM, Monterotondo Stazione (RM), Italy
Dipartimento di Scienze e Tecnologie Chimiche, Università di Roma \"Tor Vergata\", Rome, Italy
CNR-IMC, via dei Taurini, 00185 Rome, Italy
Dipartimento di Studi di Chimica e Tecnologia delle Sostanze Biologicamente Attive, Facoltà di Farmacia, Università di Roma \"La Sapienza\", Roma, Italy (literal)
- Titolo
- Photoionization Spectroscopy and Mass Spectrometry of Some Molecular and Supramolecular Asymmetric Systems in the Isolated State (literal)
- Abstract
- Asymmetric molecular and supramolecular systems are characterized by: i. the circular dicroism in the angular distribution of valence photoelectrons emitted from randomly oriented chiral molecules by their interaction with circularly polarized VUV light; ii. the different stability and reactivity of diastereomeric aggregates. Both these aspects may have some relationship with the \"chiral enrichment mechanism\" of chirogenesis, based on the preferential destruction of one enantiomer of a racemate by interaction with a chiral agent, whether a massive species or a circularly polarized photon. The most recent spectroscopic and mass spectrometric studies on this topic are reported in the present mini-review. (literal)
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- Autore CNR
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