Enantiopure double ortho-oligophenylethynylene-based helical structures with circularly polarized luminescence activity
Entity
UAM. Departamento de Química OrgánicaPublisher
WileyDate
2021-09-12Citation
10.1002/cptc.202100160
ChemPhotoChem 6.1 (2022): e202100160
ISSN
2367-0932DOI
10.1002/cptc.202100160Project
Gobierno de España. CTQ2017-85454-C2-1-P; Gobierno de España. CTQ2017-85454-C2-2-P; Gobierno de España. PID2020-113059GB-C21; Gobierno de España. PID2020-113059GB-C22Editor's Version
https://doi.org/10.1002/cptc.202100160Subjects
Chiroptical properties; Circularly polarized luminescence; Foldamers; Helical structures; Supramolecular metallofoldamers; QuímicaRights
© 2021 The AuthorsAbstract
In this paper, we describe the optical and chiroptical properties of an enantiopure multipodal ortho-oligophenylethynylene (S,S,S,S)-1 presenting four chiral sulfoxide groups at the extremes. The presence of these groups together with alkynes allows the coordination with carbophilic Ag(I), and/or oxophilic Zn(II) cations, yielding double helical structures in an enantiopure way. In this sense, different behaviors in absorption, fluorescence, ECD and CPL spectra have been found depending on the stoichiometry and nature of the metal. We have observed that Zn(II) coordination favors an intensity increase of the electronic circular dichroism (ECD) spectra of compound (S,S,S,S)-1 yielding an M-helicity in the ortho-oligophenylene ethynylene (o-OPE) backbone. On the other hand, ECD spectra of final Ag(I) complex shows two different bands with an opposite sign to the free ligand, thus giving the P-helical isomer. In addition, circularly polarized luminescence (CPL) exhibit an enhanced intensity and negative sign in both complexes. Computational studies were also carried out, supporting the experimental results
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Google Scholar:Reine, Pablo
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Ortuño, Ana M
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Resa, Sandra
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Álvarez de Cienfuegos, Luis
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Ribagorda Lobera, María
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Mota, Antonio J.
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Abbate, Sergio
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Longhi, Giovanna
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Miguel, Delia
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Cuerva, Juan M.
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