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140122 ||| eng |
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|a 9781461309536
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| 100 |
1 |
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|a Prasad, Paras N.
|e [editor]
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| 245 |
0 |
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|a Nonlinear Optical and Electroactive Polymers
|h Elektronische Ressource
|c edited by Paras N. Prasad, D.R. Ulrich
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| 250 |
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|a 1st ed. 1988
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| 260 |
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|a New York, NY
|b Springer US
|c 1988, 1988
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| 300 |
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|a 448 p
|b online resource
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| 505 |
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|a Poled Copoly(Vinylidene Flouride-Triflouroethylene) As A Host for Guest Nonlinear Optical Molecules -- Electroactive Polymers -- Electroactive Polymers:Consequences of Electron Delocalization -- Optical Properties of Poly(p-Phenylene Vinylene) -- Holes,Electrons,Polarons, and Bibpolarons and the Thermodynamics of electrically Active Dopants in Conduting Polymers -- Transient Current Spectroscopy in Polymeric Films -- Electrochemistry of Polyaniline:Consderation of a Dimer Model -- Theory -- A PPP Variational-Perturbation Calculating of Hyperplarizabilities of Conjudated Chains -- Optical Spectra of Flexible Conjugated Polymers -- Excitation in Conjugated Polymers -- Synthesis -- Towards New Electronic Structures in Crytallographically Ordered Conjugated Polymers -- Side Chain Liquid Crystalline Copolymers for NLO Response -- Synthesis of Certain Specific Electroactive Polymers --
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| 505 |
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|a Rigid Aromatic Heterocyclic Polymers:Synthesis of Ploymers and Oligomers Containing Benzazole Units for Electrooptic Application -- Devices -- Nonlinear and Electro-Optic Organic Devices -- Nonlinear and Optical processes in Optical Fibers -- Nonlinear Optical Processes and Application in the Infrared with Nematic Liquid Crystals
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| 505 |
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|a Nonlinear Optical and Electroactive Polymers: An Overview -- Nonlinear Optical Polymers -- Microscopic Origin of Second Order Nonlinear Optical Properties of Organic Structures -- Design, Ultrastructure, and Dynamics of Nonlinear Optical Effects in Polymeric Thin Films -- New Nonlinear Organic Crystals for Ultrafast Infra-Red Optical Processing -- Electric-Field Poling of Nonlinear Optical Polymers -- Frequency and Temperature Variations of Cubic Susceptibility in Polydiacetylesnes -- Femtosecond Studies of Dephasing and Conjugation with Incoherent Light -- Studies of Monomer and Polymer Monolayers Using Optical Second and Third Harmonic Generation -- Development of Polymer Nonlinear Optical Materials -- Orientationally Ordered Electro-Optic Materials -- Conformation Transition in Polydiacetylene Solution -- Molecular Engineering Approaches to Molecular and Macromolecular Nonlinear Optical Materials: Recent Theoretical and Exprimental Result --
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| 653 |
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|a Chemistry, Organic
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| 653 |
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|a Organic Chemistry
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| 700 |
1 |
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|a Ulrich, D.R.
|e [editor]
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| 041 |
0 |
7 |
|a eng
|2 ISO 639-2
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| 989 |
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|b SBA
|a Springer Book Archives -2004
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| 028 |
5 |
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|a 10.1007/978-1-4613-0953-6
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| 856 |
4 |
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|u https://doi.org/10.1007/978-1-4613-0953-6?nosfx=y
|x Verlag
|3 Volltext
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| 082 |
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|a 547
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| 520 |
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|a This treatise is a compendium of papers based on invited talks presented at the American Chemical Society Symposium on Electroactive Polymers which covered nonlinear optical polymers and conducting polymers, the common denominator being the correlated pi-electron structures. The improved understanding of the consequences of pi-electron delocalization upon nonlinear optical properties and charge carrier dynamics has laid the foundation for the rapid development and application of the electroresponse of conjugated polymers. As a result, the area of electroactive and nonlinear optical polymers is emerging as a frontier of sCience and technology. It is a multidisciplinary field that is bringing together scientists and engineers of varied background to interface their expertise. The recent explosion of interest in this area stems from the prospect of utilizing nonlinear optical effects for optical switching and logic operations in optical computing, optical signal processing, optical sensing and optical fiber communications. Polymers and organic are rapidly becoming one of the major material classes for nonlinear optical applications along with multiple quantum wells, ferroelectrics and other oxides, and direct band-gap semiconductors. The reasons for this lie in the unique molecular structures of polymers and organics and the ability to molecularly engineer the architecture of these structures through chemical synthesis
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