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Exact mass analysis of sulfur clusters upon encapsulation by a polyaromatic capsular matrix

Structural determination of inorganic clusters relies heavily on mass spectrometry because of, in most cases, their poor responsivities toward nuclear magnetic resonance, ultraviolet/visible, and infrared analyses. Nevertheless, mass spectrometry analysis of oligosulfurs (S(n)), which are unique clu...

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Detalles Bibliográficos
Autores principales: Matsuno, Sho, Yamashina, Masahiro, Sei, Yoshihisa, Akita, Munetaka, Kuzume, Akiyoshi, Yamamoto, Kimihisa, Yoshizawa, Michito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5622087/
https://www.ncbi.nlm.nih.gov/pubmed/28963533
http://dx.doi.org/10.1038/s41467-017-00605-5
Descripción
Sumario:Structural determination of inorganic clusters relies heavily on mass spectrometry because of, in most cases, their poor responsivities toward nuclear magnetic resonance, ultraviolet/visible, and infrared analyses. Nevertheless, mass spectrometry analysis of oligosulfurs (S(n)), which are unique clusters with copious allotropic forms, usually displays their fragment peaks. Here we report that a polyaromatic capsule acts as a supramolecular matrix for the mass determination of the neutral sulfur clusters. Upon encapsulation, molecular ion peaks derived from the host–guest complexes including cyclic S(6) and S(8) clusters are exclusively detected by common electrospray ionization time-of-flight mass spectrometry analysis. Furthermore, mass spectrometry analysis of a cyclic S(12) cluster, which is in situ prepared from two S(6) clusters within the matrix upon light irradiation, is achieved by the same way. The present matrix can remarkably stabilize the otherwise labile S(6) and S(12) clusters in the polyaromatic shell not only under mass spectrometry conditions but also in an ambient solution state.