Probing the Nonlinear Chiroptical Activity of Multiturn Aromatic Helices Using Linearly Polarized Light
Abstract
Abstract Four quinoline‐based oligoamide foldamers of varying lengths, from 6 to 28 Å, were synthesized in both of their enantiomeric forms, exhibiting between 1.6 and 6 helical turns. The helically chiral structures were analyzed using hyper‐Rayleigh scattering (HRS) in solution to evaluate their chiroptical nonlinear activity in second‐harmonic generation, exclusively employing linear polarization of the incident light. To achieve this, we completely overhauled our homemade equipment setup. By applying a nonlinear chiroptical model developed by us, we were able to distinguish between the achiral and chiral contributions to the nonlinear response of the samples. Surprisingly, the effect of helix elongation on the chiral response, as monitored by HRS, exhibited a nonmonotonic trend, which contrasts with the behavior observed with classical linear optical techniques. A detailed investigation revealed that the number of helical turns in the foldamers governs the magnitude of the nonlinear optical (NLO) response, exhibiting a periodic evolution rather than a linear increase with length.
Article Details
Authors (7)
Rita Borges‐Anastácio
Institut des Sciences Moléculaires Université de Bordeaux 351 cours de la Libération Talence 33400 France
Eric Merlet
CBMN, UMR, Univ. Bordeaux CNRS, Bordeaux INP Pessac F‐33600 France
Frederic Adamietz
Brice Kauffmann
UAR 3033, US1, Univ. Bordeaux CNRS, Inserm Pessac F‐33600 France
Yann Ferrand
CBMN, UMR, Univ. Bordeaux CNRS, Bordeaux INP Pessac F‐33600 France
Céline Olivier
Institut des Sciences Moléculaires Université de Bordeaux 351 cours de la Libération Talence 33400 France
Vincent Rodriguez
Institut des Sciences Moléculaires Université de Bordeaux 351 cours de la Libération Talence 33400 France