Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/93304
Title: Dynamic chiral self-recognition in aromatic dimers of styrene oxide revealed by rotational spectroscopy
Authors: Domingos, Sérgio R. 
Pérez, Cristóbal 
Kreienborg, Nora M.
Merten, Christian
Schnell, Melanie
Issue Date: 2021
Project: Projekt DEAL 
Serial title, monograph or event: Communications Chemistry
Volume: 4
Issue: 1
Abstract: Chiral molecular recognition is a pivotal phenomenon in biomolecular science, governed by subtle balances of intermolecular forces that are difficult to quantify. Non-covalent interactions involving aromatic moieties are particularly important in this realm, as recurring motifs in biomolecular aggregation. In this work, we use high-resolution broadband rotational spectroscopy to probe the dynamic conformational landscape enclosing the self-pairing topologies of styrene oxide, a chiral aromatic system. We reach a definite assignment of four homochiral and two heterochiral dimers using auxiliary quantum chemistry calculations as well as structure-solving methods based on experimental isotopic information. A complete picture of the dimer conformational space is obtained, and plausible routes for conformational relaxation are derived. Molecular structures are discussed in terms of conformational flexibility, the concerted effort of weak intermolecular interactions, and their role in the expression of the molecular fit.
URI: http://hdl.handle.net/10316/93304
ISSN: 2399-3669
DOI: 10.1038/s42004-021-00468-4
Rights: openAccess
Appears in Collections:I&D CFis - Artigos em Revistas Internacionais

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