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Metal-centered polymers: Using contr...

Johnson, Robert Matthew.

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Metal-centered polymers: Using controlled polymerization methodologies for the generation of responsive materials.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Metal-centered polymers: Using controlled polymerization methodologies for the generation of responsive materials./
作者:	Johnson, Robert Matthew.
面頁冊數:	225 p.
附註:	Source: Dissertation Abstracts International, Volume: 64-10, Section: B, page: 4967.
Contained By:	Dissertation Abstracts International64-10B.
標題:	Chemistry, Polymer. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3108795

Metal-centered polymers: Using controlled polymerization methodologies for the generation of responsive materials.
Johnson, Robert Matthew.

Metal-centered polymers: Using controlled polymerization methodologies for the generation of responsive materials. - 225 p.

Source: Dissertation Abstracts International, Volume: 64-10, Section: B, page: 4967.

Thesis (Ph.D.)--University of Virginia, 2004.

Controlled polymerization methods were used to prepare highly modular polymeric metal complexes via convergent and divergent strategies. In these materials, the metal center provides a versatile hub for preparing diverse architectures through coordinative bonds. Moreover, the metal complex introduces various properties to the polymer such as luminescence, magnetism, or electroactivity. Suitably functionalized metal complexes have been used for the atom transfer radical polymerization of acrylate and methacrylate monomers by metalloinitiation to generate luminescent biocompatible materials through a divergent synthesis. By cleaving the tert-butyl groups from poly(tert -butyl acrylate), water soluble [Ru(bpyPAA2)3] 2+ has been prepared as well as the amphiphilic star block copolymer [Ru{bpy(PLA-PAA)2}3]2+ (PLA = poly(lactic acid), PAA = poly(acrylic acid)Subjects--Topical Terms:

1018428
Chemistry, Polymer.

Metal-centered polymers: Using controlled polymerization methodologies for the generation of responsive materials.
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245 1 0 $a Metal-centered polymers: Using controlled polymerization methodologies for the generation of responsive materials.
300 $a 225 p.
500 $a Source: Dissertation Abstracts International, Volume: 64-10, Section: B, page: 4967.
500 $a Adviser: Cassandra L. Fraser.
502 $a Thesis (Ph.D.)--University of Virginia, 2004.
520 $a Controlled polymerization methods were used to prepare highly modular polymeric metal complexes via convergent and divergent strategies. In these materials, the metal center provides a versatile hub for preparing diverse architectures through coordinative bonds. Moreover, the metal complex introduces various properties to the polymer such as luminescence, magnetism, or electroactivity. Suitably functionalized metal complexes have been used for the atom transfer radical polymerization of acrylate and methacrylate monomers by metalloinitiation to generate luminescent biocompatible materials through a divergent synthesis. By cleaving the tert-butyl groups from poly(tert -butyl acrylate), water soluble [Ru(bpyPAA2)3] 2+ has been prepared as well as the amphiphilic star block copolymer [Ru{bpy(PLA-PAA)2}3]2+ (PLA = poly(lactic acid), PAA = poly(acrylic acid)
520 $a Bipyridine-centered polymeric macroligands may be chelated to a variety of metal salts. The polymer size greatly influences the formation of [Fe(bpy) 3]2+ centered polymers. As the molecular weight increases (> &sim;25 kDa) tris complex formation decreases. Tris(bpy) synthesis is also impacted by chemical composition. BpyPtBA2 (PtBA = poly(tert-butyl acrylate) generates an iron mono(bpy) complex before giving rise to the bis(bpy) iron complex; no tris complex is observed. In contrast, the combination of bpyPEG2 (3 equiv) (PEG = (poly(ethylene glycol)) results in the formation of some iron tris(bpy) compound; however, complete tris(bpy) product formation is suppressed, presumably because of the chelating ability of the PEG chains. These examples contrast with other polymeric macroligands such as bpyPS2, bpyPMMA2, bpyPCL2 and bpyPLA 2 (PS = polystyrene; PMMA = poly(methyl methacrylate); PCL = poly(epsilon-caprolactone); PLA = poly(DL-lactic acid)) for which chelation reactions are facile for low molecular weight macroligands (<15 kDa), with chelation efficiencies (defined as (epsilonPMC/epsilonbpy) x 100%) only declining with increased molecular weight.
520 $a Finally, a series of bipyridine (bpy)-centered triblock copolymers, BA-bpy-AB, were generated by ring opening polymerization (ROP) and atom transfer radical polymerization (ATRP) mechanisms. Hydroxyl chain ends of poly(epsilon-caprolactone) (PCL) and poly(lactic acid) (PLA) precursors, bpyPCL2 and bpyPLA 2 respectively, were converted to alpha-bromoesters for use as macroinitiators for the subsequent addition of second blocks, poly(methyl methacrylate) (PMMA) or poly(t-butyl acrylate) (PtBA). Materials formed by sequential ATRP reactions, bpy(PMMA-PS)2 and bpy(PS-PMMA)2, were also produced. New [Fe(bpy(AB)2)3]2+ analogues were formed by combination of triblock macroligands with [Fe(OH2) 6](BF4)s in 3:1 CH2Cl2:MeOH solutions. For bpy(PCL-PtBA)2 and bpy(PLA-PtBA)2 macroligands, only bis(bpy) materials resulted. These synthetic studies lay the foundation for future investigations of how polymer composition and film morphology affect nanocluster formation in metal-centered star block copolymer templates.
590 $a School code: 0246.
650 4 $a Chemistry, Polymer. $3 1018428
650 4 $a Engineering, Materials Science. $3 1017759
690 $a 0495
690 $a 0794
710 2 0 $a University of Virginia. $3 645578
773 0 $t Dissertation Abstracts International $g 64-10B.
790 1 0 $a Fraser, Cassandra L., $e advisor
790 $a 0246
791 $a Ph.D.
792 $a 2004
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3108795