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Self-assembly of ordered, conjugated...
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McCaughey, Byron.
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Self-assembly of ordered, conjugated polymer nanocomposites.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Self-assembly of ordered, conjugated polymer nanocomposites./
作者:
McCaughey, Byron.
面頁冊數:
184 p.
附註:
Source: Dissertation Abstracts International, Volume: 66-04, Section: B, page: 2262.
Contained By:
Dissertation Abstracts International66-04B.
標題:
Engineering, Materials Science. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3170374
ISBN:
0542066467
Self-assembly of ordered, conjugated polymer nanocomposites.
McCaughey, Byron.
Self-assembly of ordered, conjugated polymer nanocomposites.
- 184 p.
Source: Dissertation Abstracts International, Volume: 66-04, Section: B, page: 2262.
Thesis (Ph.D.)--Tulane University, 2005.
This research aims to control the configuration and properties of functional, conjugated polymer systems by tuning the composite nanostructure and molecular interactions. This is accomplished by self-assembly of specific organic and inorganic building blocks. New nanocomposite synthesis schemes are demonstrated for poly(2,5-thienylene ethynylene) (PTE) and polydiacetylene (PDA) that focus on the combination of amphiphiles with hydrophobic and hydrophilic components. The weak molecular interactions between these building blocks result in spontaneous organization into highly ordered amorphous and crystalline structures. Emulsion polymerization, simultaneous monomer incorporation during self-assembly, and PDA supramolecular assembly synthesis paradigms will be discussed. By controlling the interactions, synthesis conditions, and building blocks; this research tunes the structure, molecular conformation, and therefore the optical properties of the resultant composites. Notable results include control of PTE particle size; direction of PTE/silica nanocomposite mesostructure; synthesis of free-standing mesoporous PTE; completely reversible thermochromatic and structural transitions in PDA assemblies; chemical and solvent sensing with PDA; and tunable mechanochromatic response with PDA composites. The synthesis schemes developed in this dissertation research program provide a general route to prepare functional materials with beneficial properties such as thermally controlled optical adsorption, self-healing mesostructure, molecular recognition, and mechanically induced color changes for the detection of damage in plastic composites.
ISBN: 0542066467Subjects--Topical Terms:
1017759
Engineering, Materials Science.
Self-assembly of ordered, conjugated polymer nanocomposites.
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This research aims to control the configuration and properties of functional, conjugated polymer systems by tuning the composite nanostructure and molecular interactions. This is accomplished by self-assembly of specific organic and inorganic building blocks. New nanocomposite synthesis schemes are demonstrated for poly(2,5-thienylene ethynylene) (PTE) and polydiacetylene (PDA) that focus on the combination of amphiphiles with hydrophobic and hydrophilic components. The weak molecular interactions between these building blocks result in spontaneous organization into highly ordered amorphous and crystalline structures. Emulsion polymerization, simultaneous monomer incorporation during self-assembly, and PDA supramolecular assembly synthesis paradigms will be discussed. By controlling the interactions, synthesis conditions, and building blocks; this research tunes the structure, molecular conformation, and therefore the optical properties of the resultant composites. Notable results include control of PTE particle size; direction of PTE/silica nanocomposite mesostructure; synthesis of free-standing mesoporous PTE; completely reversible thermochromatic and structural transitions in PDA assemblies; chemical and solvent sensing with PDA; and tunable mechanochromatic response with PDA composites. The synthesis schemes developed in this dissertation research program provide a general route to prepare functional materials with beneficial properties such as thermally controlled optical adsorption, self-healing mesostructure, molecular recognition, and mechanically induced color changes for the detection of damage in plastic composites.
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