Molecular Recognition, Transient Chirality and Sulfur Hydrogen Bonding in the Benzyl Mercaptan Dimer

The homodimers of transiently chiral molecules offer physical insight into the process of molecular recognition, the preference for homo or heterochiral aggregation and the nature of the non-covalent interactions stabilizing the adducts. We report the observation of the benzyl mercaptan dimer in the...

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Veröffentlicht in:	Symmetry (Basel) 2021-11, Vol.13 (11), p.2022
Hauptverfasser:	Saragi, Rizalina Tama, Juanes, Marcos, Pinacho, Ruth, Rubio, José Emiliano, Fernández, José A., Lesarri, Alberto
Format:	Artikel
Sprache:	eng
Schlagworte:	Adducts Alcohol Approximation Benzyl alcohol Broadband chiral recognition Chirality Dimers Hydrogen bonding Hydrogen bonds jet spectroscopy non-covalent interactions Recognition rotational spectroscopy Spectrum analysis Sulfur sulfur hydrogen bonding transient chirality
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