Interplay of thermosensitivity and pH sensitivity of amphiphilic block-gradient copolymers of dimethylaminoethyl acrylate and styrene

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389013%3A_____%2F18%3A00491337" target="_blank" >RIV/61389013:_____/18:00491337 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1021/acs.macromol.8b00621" target="_blank" >http://dx.doi.org/10.1021/acs.macromol.8b00621</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1021/acs.macromol.8b00621" target="_blank" >10.1021/acs.macromol.8b00621</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Interplay of thermosensitivity and pH sensitivity of amphiphilic block-gradient copolymers of dimethylaminoethyl acrylate and styrene

Popis výsledku v původním jazyce

Novel pH- and thermoresponsive amphiphilic diblock copolymer, comprising hydrophilic poly(2-dimethylaminoethyl acrylate) (PDMAEA) and amphiphilic poly(styrene-grad-2-dimethylaminoethyl acrylate) (P(S-grad-DMAEA)) blocks, was synthesized by nitroxide-mediated radical polymerization. A series of copolymers (PS-grad-PDMAEA) with controlled molar masses and low dispersities over a wide range of monomer feed ratios (0 < fS,0 < 1) were synthesized. Both conventional linearization and nonlinear least-squares methods were applied to estimate reliable values of the reactivity ratios for S and DMAEA radical polymerization. The calculated values of the reactivity ratios (rDMAEA = 0.25 and rS = 1.15) perfectly fitted the drift in monomer feed ratio versus conversion, showing a gradient distribution along the copolymer chains. The self-assembling behavior of the copolymers in the aqueous medium was investigated by dynamic light scattering and small-angle neutron scattering over a wide range of pH, temperature, and salt concentration. These block-gradient copolymers show reversible self-association into micelle-like structure (Dh ∼ 20 nm) in aqueous solutions triggered by both pH and temperature.

Název v anglickém jazyce

Interplay of thermosensitivity and pH sensitivity of amphiphilic block-gradient copolymers of dimethylaminoethyl acrylate and styrene

Popis výsledku anglicky

Novel pH- and thermoresponsive amphiphilic diblock copolymer, comprising hydrophilic poly(2-dimethylaminoethyl acrylate) (PDMAEA) and amphiphilic poly(styrene-grad-2-dimethylaminoethyl acrylate) (P(S-grad-DMAEA)) blocks, was synthesized by nitroxide-mediated radical polymerization. A series of copolymers (PS-grad-PDMAEA) with controlled molar masses and low dispersities over a wide range of monomer feed ratios (0 < fS,0 < 1) were synthesized. Both conventional linearization and nonlinear least-squares methods were applied to estimate reliable values of the reactivity ratios for S and DMAEA radical polymerization. The calculated values of the reactivity ratios (rDMAEA = 0.25 and rS = 1.15) perfectly fitted the drift in monomer feed ratio versus conversion, showing a gradient distribution along the copolymer chains. The self-assembling behavior of the copolymers in the aqueous medium was investigated by dynamic light scattering and small-angle neutron scattering over a wide range of pH, temperature, and salt concentration. These block-gradient copolymers show reversible self-association into micelle-like structure (Dh ∼ 20 nm) in aqueous solutions triggered by both pH and temperature.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10404 - Polymer science

Projekt

Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2018

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Macromolecules

ISSN

0024-9297

e-ISSN

—

Svazek periodika

51

Číslo periodika v rámci svazku

14

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

15

Strana od-do

5219-5233

Kód UT WoS článku

000440105200022

EID výsledku v databázi Scopus

2-s2.0-85050688894