You have requested a machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Neither SPIE nor the owners and publishers of the content make, and they explicitly disclaim, any express or implied representations or warranties of any kind, including, without limitation, representations and warranties as to the functionality of the translation feature or the accuracy or completeness of the translations.
Translations are not retained in our system. Your use of this feature and the translations is subject to all use restrictions contained in the Terms and Conditions of Use of the SPIE website.
1 April 1992Substituent effects in the design of new organic NLO materials
Several approaches have been suggested during the past few years for increasing third order nonlinearity in organic compounds. In general, these have focused on manipulation of the effective conjugation length of the pi-electron framework to maximize orbital overlap. It has only recently become apparent that substituent effects, which affect the overall electron density distribution, may be an extremely effective way of enhancing nonlinearity. In this study we review known substituent effects on nonlinearity, and suggest how donor-donor, acceptor- acceptor, and donor-acceptor interaction can be utilized in the design of molecules and polymers with enhanced nonlinearity.
The alert did not successfully save. Please try again later.
Charles W. Spangler, Pei-Kang Liu, Tracy Ann Kelleher, Eric G. Nickel, "Substituent effects in the design of new organic NLO materials," Proc. SPIE 1626, Nonlinear Optics III, (1 April 1992); https://doi.org/10.1117/12.58114