Thermally responsive polymers and their applications

This thesis focuses on development of polymeric materials that can alter their functions according to temperature changes. We chose poly(N-isopropylacrylamide) (polyNIPA) as a platform, which phase-separates from water upon heating. The thermally responsive properties and applications of polyNIPA are introduced in Chapter One. In Chapter Two, we described the synthesis of polyNIPA gels with an imidazole comomoer and examined copper ion adsorption by the swollen (room temperature) and shrunken gels (60⁰C). The data analysis using a Langmuir adsorption isotherm indicates that the imidazole groups form 2:1 and 4:1 complexes with a copper ion in the swollen and shrunken gels, respectively, which suggests that thermal gel swelling and shrinking control the formation of multivalent Cu complexes by changing the distance among imidazole groups. In Chapters Three to Six, the synthesis of polyNIPA-conjugated polymer block copolymers and their applications are described. Non-ionic water-soluble poly(phenylene-ethynylene)s (PPEs) (Chapter Three) were used as conjugated polymer segments in the block copolymers. In a route to synthesis of the block copolymers, atom transfer radical polymerization (ATRP) and nitroxide-mediated radical polymerization (NMRP) of NIPA were developed. Incorporation of ATRP or NMRP initiators to the polymer ends of PPEs and the following polymerizations of NIPA were expected to provide tri-block copolymers with precise structures. The ATRP method produced pure polyNIPA with monodisperse and defined molecular weights (Chapter Four). However, endcapping of PPEs with an ATRP initiator ((α-chloroamide) was not successful due to its instability to PPE polymerization conditions (Chapter Five).

Department dc:contributor.department

Massachusetts Institute of Technology. Dept. of Chemistry.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2003

Author dc:creator

• Kuroda, Kenichi, 1972-

Advisor dc:contributor.advisor

• Timothy M. Swager.

• Chemistry.

Statement dc:rights

• M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/29641

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/29641