Large Molecular Third-Order Optical Nonlinearities in Polarized Carotenoids
- 23 May 1997
- journal article
- other
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 276 (5316), 1233-1236
- https://doi.org/10.1126/science.276.5316.1233
Abstract
Garito and co-workers have suggested a mechanism to dramatically increase the second hyperpolarizability, γ, in linear π-electron–conjugated molecules. Polarization is introduced that leads to a difference between the dipole moments of the molecule’s ground state and excited state. Here a series of carotenoids was examined that had increasing intramolecular charge transfer (ICT) from the polyenic chain to the acceptor moiety in the ground state, and γ was measured for these compounds as a function of wavelength by third-harmonic generation. The compound with the greatest ICT exhibited a 35-fold enhancement of γ max (the γ measured at the peak of the three-photon resonance) relative to the symmetric molecule β-carotene, which itself has one of the largest third-order nonlinearities known. Stark spectroscopic measurements revealed the existence of a large difference dipole moment, Δμ, between the ground and excited state. Quantum-chemical calculations underline the importance of interactions involving states with large Δμ.Keywords
This publication has 13 references indexed in Scilit:
- Higher-Order Stark Spectroscopy: Polarizability of Photosynthetic PigmentsThe Journal of Physical Chemistry, 1995
- Second-harmonic generation in absorptive mediaOptics Letters, 1994
- Electric Field Modulated Nonlinear Optical Properties of Donor-Acceptor Polyenes: Sum-Over-States Investigation of the Relationship between Molecular Polarizabilities (.alpha., .beta., and .gamma.) and Bond Length AlternationJournal of the American Chemical Society, 1994
- Coupled quantum well semiconductors with giant electric field tunable nonlinear optical properties in the infraredIEEE Journal of Quantum Electronics, 1994
- Chain-length dependence of the third-order polarizability of disubstituted polyenes: effects of end groups and conjugation lengthThe Journal of Physical Chemistry, 1993
- Donor-acceptor diphenylacetylenes: geometric structure, electronic structure, and second-order nonlinear optical propertiesJournal of the American Chemical Society, 1993
- Synthesis and first hyperpolarizabilities of acceptor-substituted β-apo-8′-carotenal derived compoundsJournal of the Chemical Society, Chemical Communications, 1993
- A simplified three‐level model describing the molecular third‐order nonlinear optical susceptibilityInternational Journal of Quantum Chemistry, 1992
- Tunable third harmonic generation of trans-β-caroteneOptics Communications, 1991
- Observation of extremely large quadratic susceptibility at 9.6–10.8μm in electric-field-biased AlGaAs quantum wellsPhysical Review Letters, 1989