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Directing the self-assembly and clic...

Kim, Tae-Dong.

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Directing the self-assembly and click chemistry of organic photonics materials for exceptional electro-optic properties.

Record Type:	Language materials, printed : Monograph/item
Title/Author:	Directing the self-assembly and click chemistry of organic photonics materials for exceptional electro-optic properties./
Author:	Kim, Tae-Dong.
Description:	122 p.
Notes:	Adviser: Alex K-Y Jen.
Contained By:	Dissertation Abstracts International68-05B.
Subject:	Chemistry, Polymer. -
Online resource:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3265359
ISBN:	9780549025702

Directing the self-assembly and click chemistry of organic photonics materials for exceptional electro-optic properties.
Kim, Tae-Dong.

Directing the self-assembly and click chemistry of organic photonics materials for exceptional electro-optic properties. - 122 p.

Adviser: Alex K-Y Jen.

Thesis (Ph.D.)--University of Washington, 2007.

A major breakthrough in the area of organic EO materials has been recently achieved. To go beyond the oriented gas model limit for organic EO materials, new approaches of using nanoscale architecture control and supramolecular self-assembly have been proved as a very effective method to create a new paradigm for materials with very exciting properties. High-performance EO polymers were demonstrated by a facile and reliable Diels-Alder "click" reaction for postfunctionalization and lattice hardening to improve EO activity (r 33) and thermal stability. This type of "click" chemistry paves the way to systematically study the relationship among EO activity, chromophore shape, and number density of the chromophores. Reversible supramolecular interactions were also introduced to a new generation of EO dendrimers and polymers to create self-assembled nano-objects, overcome strong intermolecular electrostatic interaction, and improve their poling efficiency and stability. These self-organized EO materials were used as hosts in a binary chromophore system to further improve chromophore number density and r33 value. With these novel approaches, we succeeded in enlarging the full potential of organic NLO materials by a factor of 3&sim;5 and developing a variety of nano-structured organic EO materials with ultrahigh r33 values (>300 pm/V at the wavelengths of 1310 and 1550 nm, more than 10 times that of LiNbO3) and excellent auxiliary property, such as thermal stability and optical transparency. The success of these material developments has inspired the exploration of new device concepts to take full advantage of organic EO materials with ultrahigh r33 values.

ISBN: 9780549025702Subjects--Topical Terms:

1018428
Chemistry, Polymer.

Directing the self-assembly and click chemistry of organic photonics materials for exceptional electro-optic properties.
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020 $a 9780549025702
035 $a (UMI)AAI3265359
035 $a AAI3265359
040 $a UMI $c UMI
100 1 $a Kim, Tae-Dong. $3 1280709
245 1 0 $a Directing the self-assembly and click chemistry of organic photonics materials for exceptional electro-optic properties.
300 $a 122 p.
500 $a Adviser: Alex K-Y Jen.
500 $a Source: Dissertation Abstracts International, Volume: 68-05, Section: B, page: 3326.
502 $a Thesis (Ph.D.)--University of Washington, 2007.
520 $a A major breakthrough in the area of organic EO materials has been recently achieved. To go beyond the oriented gas model limit for organic EO materials, new approaches of using nanoscale architecture control and supramolecular self-assembly have been proved as a very effective method to create a new paradigm for materials with very exciting properties. High-performance EO polymers were demonstrated by a facile and reliable Diels-Alder "click" reaction for postfunctionalization and lattice hardening to improve EO activity (r 33) and thermal stability. This type of "click" chemistry paves the way to systematically study the relationship among EO activity, chromophore shape, and number density of the chromophores. Reversible supramolecular interactions were also introduced to a new generation of EO dendrimers and polymers to create self-assembled nano-objects, overcome strong intermolecular electrostatic interaction, and improve their poling efficiency and stability. These self-organized EO materials were used as hosts in a binary chromophore system to further improve chromophore number density and r33 value. With these novel approaches, we succeeded in enlarging the full potential of organic NLO materials by a factor of 3&sim;5 and developing a variety of nano-structured organic EO materials with ultrahigh r33 values (>300 pm/V at the wavelengths of 1310 and 1550 nm, more than 10 times that of LiNbO3) and excellent auxiliary property, such as thermal stability and optical transparency. The success of these material developments has inspired the exploration of new device concepts to take full advantage of organic EO materials with ultrahigh r33 values.
590 $a School code: 0250.
650 4 $a Chemistry, Polymer. $3 1018428
650 4 $a Engineering, Materials Science. $3 1017759
690 $a 0495
690 $a 0794
710 2 $a University of Washington. $3 545923
773 0 $t Dissertation Abstracts International $g 68-05B.
790 $a 0250
790 1 0 $a Jen, Alex K-Y, $e advisor
791 $a Ph.D.
792 $a 2007
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3265359