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Stapled helical o-OPE foldamers as new circularly polarized luminescence emitters based on carbophilic interactions with Ag(i)-sensitivity†‡
Sara P. Morcillo,Delia Miguel,Luis Álvarez de Cienfuegos,José Justicia,Sergio Abbate,Ettore Castiglioni,Christophe Bour,María Ribagorda,Diego J. Cárdenas,José Manuel Paredes,Luis Crovetto,Duane Choquesillo-Lazarte,Antonio J. Mota,M. Carmen Carreño,Giovanna Longhi,Juan M. Cuerva
Chemical Science Pub Date : 05/17/2016 00:00:00 , DOI:10.1039/C6SC01808D
Abstract

ortho-Oligo(phenylene)ethynylenes (o-OPEs) stapled with enantiopure 2,3-dihydroxybutane diethers have highly intense circular dichroism (CD) spectra and excellent circular polarized luminescence (CPL) responses (glum values up to 1.1 × 10−2), which are consistent with homochiral helically folded structures. In the presence of Ag(I), a change in the CPL emission is observed, representing the first example of CPL active small organic molecular emitters, which can be modulated by carbophilic interactions in a reversible manner.

Graphical abstract: Stapled helical o-OPE foldamers as new circularly polarized luminescence emitters based on carbophilic interactions with Ag(i)-sensitivity
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