Chemoenzymatic synthesis of novel N-(2-hydroxyethyl)-β-peptoid oligomer derivatives and application to porous polycaprolactone films

The biocatalytic synthesis of a novel peptoid oligomer is reported. The oligomer is acetylated and a copolymer with polycaprolactone is prepared. These derivatives are employed for the preparation of nanoporous films. Poly[N-(2-hydroxyethyl)-β-propylamide] oligomer is synthesized using a simple enzy...

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Autor principal: Monsalve, L.N
Otros Autores: Petroselli, G., Erra-Ballsells, R., Vázquez, A., Baldessari, A.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2013
Acceso en línea:Registro en Scopus
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Registro en la Biblioteca Digital
Aporte de:Registro referencial: Solicitar el recurso aquí
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100 1 |a Monsalve, L.N. 
245 1 0 |a Chemoenzymatic synthesis of novel N-(2-hydroxyethyl)-β-peptoid oligomer derivatives and application to porous polycaprolactone films 
260 |c 2013 
270 1 0 |m Monsalve, L.N.; Laboratorio de Polímeros y Materiales Compuestos Instituto de Tecnología en Poli&acuteemail: lmonsalve@fi.uba.ar 
506 |2 openaire  |e Política editorial 
520 3 |a The biocatalytic synthesis of a novel peptoid oligomer is reported. The oligomer is acetylated and a copolymer with polycaprolactone is prepared. These derivatives are employed for the preparation of nanoporous films. Poly[N-(2-hydroxyethyl)-β-propylamide] oligomer is synthesized using a simple enzymatic procedure involving Candida antarctica lipase B. This novel compound is obtained by a green and chemoselective method from economic reactants in good yield. The β-peptoid oligomer is characterized by spectroscopic methods showing low molecular weight and low dispersity. Two derivatives of the β-peptoid oligomer are prepared by acetylation and by grafting polycaprolactone by ring opening polymerization from the pendant hydroxyl groups. These products are blended with polycaprolactone to make films by solvent casting. The inclusion of the acyl derivatives of the β-peptoid to polycaprolactone affects the morphology of the film yielding microstructured and nanostructured patterns. © 2013 Society of Chemical Industry.  |l eng 
536 |a Article in Press 
593 |a Laboratorio de Polímeros y Materiales Compuestos Instituto de Tecnología en Polímeros y Nanotecnología (ITPN), Facultad de Ingeniería, UBA - CONICET Las Heras 2214 (C1127AAR) Buenos Aires Argentina 
593 |a Departamento de Química Orgánica y CIHIDECAR, Facultad de Ciencias Exactas y Naturales Universidad de Buenos Aires, Ciudad Universitaria Pabellón 2, Piso 3 (C1428EGA) Buenos Aires Argentina 
593 |a INTI - Centro de Micro y Nanoelectrónica del Bicentenario Parque tecnológico Miguelete Av. General Paz 5445 (B1650WAB) San Martín Buenos Aires Argentina 
593 |a Laboratorio de Biocatálisis, Departamento de Química Orgánica y UMYMFOR, Facultad de Ciencias Exactas y Naturales Universidad de Buenos Aires, Ciudad Universitaria Pabellón 2, Piso 3 (C1428EGA) Buenos Aires Argentina 
690 1 0 |a Β-PEPTOID 
690 1 0 |a FILMS 
690 1 0 |a LIPASE 
690 1 0 |a POLYCAPROLACTONE 
690 1 0 |a SURFACE PROPERTIES 
700 1 |a Petroselli, G. 
700 1 |a Erra-Ballsells, R. 
700 1 |a Vázquez, A. 
700 1 |a Baldessari, A. 
773 0 |d 2013  |p Polym. Int.  |x 09598103  |t Polymer International 
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