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Nonlinear optical properties polymers

Simoni F 1997 Nonlinear Optical Properties of Liquid Crystals and Polymer-Dispersed Liquid Crystals (Singapore World Scientific)... [Pg.2571]

There have been some attempts to compute nonlinear optical properties in solution. These studies have shown that very small variations in the solvent cavity can give very large deviations in the computed hyperpolarizability. The valence bond charge transfer (VB-CT) method created by Goddard and coworkers has had some success in reproducing solvent effect trends and polymer results (the VB-CT-S and VB-CTE forms, respectively). [Pg.259]

The polysdanes are normally electrical insulators, but on doping with AsF or SbF they exhibit electrical conductivity up to the levels of good semiconductors (qv) (98,124). Conductivities up to 0.5 (H-cm) have been measured. However, the doped polymers are sensitive to air and moisture thereby making them unattractive for practical use. In addition to semiconducting behavior, polysilanes exhibit photoconductivity and appear suitable for electrophotography (qv) (125—127). Polysdanes have also been found to exhibit nonlinear optical properties (94,128). [Pg.263]

Liquid crystal polymers are also used in electrooptic displays. Side-chain polymers are quite suitable for this purpose, but usually involve much larger elastic and viscous constants, which slow the response of the device (33). The chiral smectic C phase is perhaps best suited for a polymer field effect device. The abiHty to attach dichroic or fluorescent dyes as a proportion of the side groups opens the door to appHcations not easily achieved with low molecular weight Hquid crystals. Polymers with smectic phases have also been used to create laser writable devices (30). The laser can address areas a few micrometers wide, changing a clear state to a strong scattering state or vice versa. Future uses of Hquid crystal polymers may include data storage devices. Polymers with nonlinear optical properties may also become important for device appHcations. [Pg.202]

Optical properties of cyanines can be usefiil for both chiral substituents/environments and also third-order nonlinear optical properties in polymer films. Methine-chain substituted die arbo cyanines have been prepared from a chiral dialdehyde (S)-(+)-2-j -butylmalonaldehyde [127473-57-8] (79), where the chiral properties are introduced via the chiral j -butyl group on the central methine carbon of the pentamethine (die arbo cyanine) chromophore. For a nonchiral oxadicarbocyanine, the dimeric aggregate form of the dye shows circular dichroism when trapped in y-cyclodextrin (80). Attempts to prepare polymers with carbocyanine repeat units (linked by flexible chains) gave oligomers with only two or three repeat units (81). However, these materials... [Pg.400]

In the field of polymer chemistry the regio- and stereoselectivity of the Diels-Alder reaction is used for the concerted synthesis of structurally homogeneous double-stranded ladder polymers [39], which are useful materials with nonlinear optical properties and high electrical conductivity. It has turned out that the repeated Diels-Alder method is superior to an alternative two-step process, in which first an open chain precursor is formed followed by polymer ring closure as structural defects can occur [40]. [Pg.21]

Chiang, W. Thompson, M. E. Van Engen, D. Synthesis and Nonlinear Optical Properties of Inorganic Co-ordination Polymers. In Organic Materials for Nonlinear Optics II Hann, R. A., Bloor, D., Eds. Royal Society of Chemistry London, 1991 pp 210-216. [Pg.681]

The linear and nonlinear optical properties of one-dimensional conjugated polymers contain a wealth of information closely related to the structure and dynamics of the ir-electron distribution and to their interaction with the lattice distorsions. The existing values of the nonlinear susceptibilities indicate that these materials are strong candidates for nonlinear optical devices in different applications. However their time response may be limited by the diffusion time of intrinsic conjugation defects and the electron-phonon coupling. Since these defects arise from competition of resonant chemical structures the possible remedy is to control this competition without affecting the delocalization. The understanding of the polymerisation process is consequently essential. [Pg.183]

This paper will review the linear and nonlinear optical properties of polydiacetylenes with an emphasis on our work with the nBCMU polymers. The following section will discuss material... [Pg.188]

Agrawal, G. P. Cojan, C. Flytzanis, C. "Nonlinear Optical Properties of One-Dimensional Semiconductors and Conjugated Polymers," Phys. Rev. 1978, B17, 776. [Pg.228]

Binaphthyl molecules (chiral 2,2/-dihydroxy-l,T-binaphthyl) have been studied by Hicks et al., who reported the first experimental observation of CD-SHG on surfaces.4,29,43 In this section, we investigate the nonlinear optical properties of a chiral 1,1-binaphthyl-based helical polymer. [Pg.557]

The Suzuki coupling has been utilized to craft (Toctasubstituted tetramesitylporphyrins using various arylboronic acids [62], and Schluter has adopted this reaction to prepare phenyl-pyrrole mixed polymers 75 [63]. The BOC group is easily removed by heating [64] and polymers with molecular weights of up to 23,000 were synthesized. These polymers are potentiaEy interesting for their electrical and nonlinear optical properties [65]. [Pg.47]

Oligomerization and polymerization of terminal alkynes may provide materials with interesting conductivity and (nonlinear) optical properties. Phenylacetylene and 4-ethynyltoluene were polymerized in water/methanol homogeneous solutions and in water/chloroform biphasic systems using [RhCl(CO)(TPPTS)2] and [IrCl(CO)(TPPTS)2] as catalysts [37], The complexes themselves were rather inefficient, however, the catalytic activity could be substantially increased by addition of MesNO in order to remove the carbonyl ligand from the coordination sphere of the metals. The polymers obtained had an average molecular mass of = 3150-16300. The rhodium catalyst worked at room temperature providing polymers with cis-transoid structure, while [IrCl(CO)(TPPTS)2] required 80 °C and led to the formation of frani -polymers. [Pg.202]

Ramasesha, S., Pati, S.K., Krishnamurthy, H.R., Shuai, Z., Bredas, J.L. Low-lying electronic excitations and nonlinear optic properties of polymers via symmetrized density matrix renormalization group method. Synth. Met. 1997, 85(1-3), 1019. [Pg.161]

The driving force in polymer synthesis is the search for new polymers with improved properties to replace other materials of construction. Polymers are lightweight and can be processed easily and economically into a wide range of shapes and forms. The major synthetic efforts at present are aimed at polymers with high temperature, liquid crystal, conducting, and nonlinear optical properties [Maier et al., 2001 Sillion, 1999]. There is an interrelationship between these efforts as will become apparent. [Pg.144]

Nonlinear Optical Properties of Polymers Heeger, A. J. Orenstein, J. Ulrich, D. R., Eds. Materials Research Society Symposium Proceedings Pittsburgh, 1987 Vol. 109. [Pg.71]

The nonlinear optical properties of thin films of the polymers were investigated through measurement of second-harmonic generation, and exhibit second-harmonic coefficients, d33, in the range 4.1-34 pm/V. [Pg.261]

Model Polymers with Distyrylbenzene Segments for Third-Order Nonlinear Optical Properties... [Pg.497]


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