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Bonding, Structure, and Stability of [(Na) n(Phe) m] n+ Clusters: Some Surprising Results from an Experimental and Theoretical Investigation in Gas Phase
Author(s) -
Melissa S. Caetano,
Teodorico C. Ramalho,
Tales Giuliano Vieira,
Arlan da Silva Gonçalves,
Daiana T. Mancini,
Elaine F. F. da Cunha
Publication year - 2013
Publication title -
journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.436
H-Index - 50
eISSN - 2090-9063
pISSN - 2090-9071
DOI - 10.1155/2013/362894
Subject(s) - chemistry , gas phase , dipole , stability (learning theory) , chemical physics , symmetry (geometry) , planar , ground state , moment (physics) , molecule , phase (matter) , computational chemistry , charge (physics) , molecular physics , atomic physics , classical mechanics , quantum mechanics , organic chemistry , geometry , physics , mathematics , computer graphics (images) , machine learning , computer science
Structure and stability of clusters in the ground state were analyzed at the theoretical and experimental levels. Our experimental and theoretical findings showed that the clusters in gas phase tend to form mainly planar rings of four members. The symmetry and the small dipole moment in these specific configurations suggested that their stability could be associated with an alignment of the water molecules, maximizing attractive electrostatic interactions caused by changes in the charge distribution of the clusters

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