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Rotational Spectrum and Conformational Analysis of Perillartine: Insights into the Structure-Sweetness Relationship.


ABSTRACT: We used high-resolution rotational spectroscopy coupled to a laser ablation source to study the conformational panorama of perillartine, a solid synthetic sweetener. Four conformers were identified under the isolation conditions of the supersonic expansion, showing that all of them present an E configuration of the C=N group with respect to the double bond of the ring. The observed structures were verified against Shallenberger-Acree-Kier's sweetness theory to shed light on the structure-sweetness relationship for this particular oxime, highlighting a deluge of possibilities to bind the receptor.

SUBMITTER: Juarez G 

PROVIDER: S-EPMC8954681 | biostudies-literature | 2022 Mar

REPOSITORIES: biostudies-literature

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Rotational Spectrum and Conformational Analysis of Perillartine: Insights into the Structure-Sweetness Relationship.

Juárez Gabriela G   Sanz-Novo Miguel M   Alonso José L JL   Alonso Elena R ER   León Iker I  

Molecules (Basel, Switzerland) 20220316 6


We used high-resolution rotational spectroscopy coupled to a laser ablation source to study the conformational panorama of perillartine, a solid synthetic sweetener. Four conformers were identified under the isolation conditions of the supersonic expansion, showing that all of them present an <i>E</i> configuration of the C=N group with respect to the double bond of the ring. The observed structures were verified against Shallenberger-Acree-Kier's sweetness theory to shed light on the structure-  ...[more]

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