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Design and Precise Synthesis of Thermoresponsive Polyacrylamides

In this thesis, the author describes versatile and easy-to-use methods to control the properties of thermoresponsive polyacrylamides by developing novel synthetic methods for end-functionalized poly(N-isopropylacrylamide) (PNIPAM) and block copolymers of poly(N,N-diethylacrylamide) (PDEAA). The synt...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Fuchise, Keita (Autor)
Autor Corporativo: SpringerLink (Online service)
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Tokyo : Springer Japan : Imprint: Springer, 2014.
Edición:1st ed. 2014.
Colección:Springer Theses, Recognizing Outstanding Ph.D. Research,
Temas:
Acceso en línea:Texto Completo

MARC

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100 1 |a Fuchise, Keita.  |e author.  |4 aut  |4 http://id.loc.gov/vocabulary/relators/aut 
245 1 0 |a Design and Precise Synthesis of Thermoresponsive Polyacrylamides  |h [electronic resource] /  |c by Keita Fuchise. 
250 |a 1st ed. 2014. 
264 1 |a Tokyo :  |b Springer Japan :  |b Imprint: Springer,  |c 2014. 
300 |a XVIII, 81 p. 60 illus., 6 illus. in color.  |b online resource. 
336 |a text  |b txt  |2 rdacontent 
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490 1 |a Springer Theses, Recognizing Outstanding Ph.D. Research,  |x 2190-5061 
505 0 |a General introduction -- Control of Thermoresponsive Properties of Urea End-Functionalized Poly(N-isopropylacrylamide) Based on the Hydrogen Bond Assisted Self-Assembly in Water -- Precise Synthesis of Poly(N,N-Dimethylacrylamide) by Group Transfer Polymerization Using a Strong Brønsted Acid and an Amino Silyl Enolate -- Facile Synthesis of Thermoresponsive Block Copolymers Bearing Poly(N,N-diethylacrylamide) Segment through Group Transfer Polymerization -- Conclusions. 
520 |a In this thesis, the author describes versatile and easy-to-use methods to control the properties of thermoresponsive polyacrylamides by developing novel synthetic methods for end-functionalized poly(N-isopropylacrylamide) (PNIPAM) and block copolymers of poly(N,N-diethylacrylamide) (PDEAA). The synthesis of various urea end-functionalized PNIPAMs was achieved by the atom transfer radical polymerization (ATRP) and the click reaction. The phase transition temperature of PNIPAM in water was controlled depending on the strength of the hydrogen bonding of the urea groups introduced at the chain end of the polymer. Novel living polymerization methods for N,N-dimethylacrylamide and N,N-diethylacrylamide were developed by group transfer polymerization (GTP) using a strong Brønsted acid as a precatalyst and an amino silyl enolate as an initiator. This process enabled the precise synthesis of PDEAA and its block copolymers-namely, thermoresponsive amphiphilic block copolymers and double-hydrophilic block copolymers. 
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