Paper
11 October 2011 Novel ene-yne compounds as quadratic nonlinear optical materials
Daniel Lumpi, Ernst Horkel, Berthold Stoeger, Christian Hametner, Frank Kubel, Georg A. Reider, Johannes Froehlich
Author Affiliations +
Proceedings Volume 8306, Photonics, Devices, and Systems V; 830615 (2011) https://doi.org/10.1117/12.912457
Event: Photonics Prague 2011, 2011, Prague, Czech Republic
Abstract
We present a reliable strategy towards title compounds as a novel scaffold for highly nonlinear optical chromophores, using the selective ring fragmentation of thiophenes as a key step. This methodology selectively leads to the Z-isomer of ene-yne substrates, which are subsequently modified by a Huisgen-type cycloaddition yielding the target compounds. To prove the reliability of the developed synthetic route, one target compound was successfully prepared. This material crystallizes in an enantiomorphic space group, despite of being a flexible non-chiral molecule. A detailed discussion regarding the synthetic approach towards title compounds, a determination of material characteristics, including the investigation of the second order nonlinear susceptibility as well as a systematic variation of substituents in order to examine the resulting effects on NLO properties are subject of this presentation.
© (2011) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Daniel Lumpi, Ernst Horkel, Berthold Stoeger, Christian Hametner, Frank Kubel, Georg A. Reider, and Johannes Froehlich "Novel ene-yne compounds as quadratic nonlinear optical materials", Proc. SPIE 8306, Photonics, Devices, and Systems V, 830615 (11 October 2011); https://doi.org/10.1117/12.912457
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Cited by 3 scholarly publications.
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KEYWORDS
Nonlinear optics

Crystals

Nonlinear crystals

Molecules

Chromophores

Electrons

Nonlinear optical materials

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