Coassembly of Poly(N-isopropylacrylamide) with Dodecyl and Carboxyl Terminal Groups with Cationic Surfactant: Critical Comparison of Experimental and Simulation Data

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F18%3A10386102" target="_blank" >RIV/00216208:11310/18:10386102 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/61389013:_____/18:00493880

Výsledek na webu

<a href="https://doi.org/10.1021/acs.macromol.8b01161" target="_blank" >https://doi.org/10.1021/acs.macromol.8b01161</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1021/acs.macromol.8b01161" target="_blank" >10.1021/acs.macromol.8b01161</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Coassembly of Poly(N-isopropylacrylamide) with Dodecyl and Carboxyl Terminal Groups with Cationic Surfactant: Critical Comparison of Experimental and Simulation Data

Popis výsledku v původním jazyce

Comicellization of poly(N-isopropylacrylamide) with dodecyl and carboxyl terminal groups (mPNIPAm) with cationic surfactant N-dodecylpyridinium chloride was studied by scattering techniques (light scattering, SAXS), isothermal titration calorimetry, fluorescence spectroscopy, and coarse-grained simulations using dissipative particle dynamics (DPD) as a function of charge ratio of N-dodecylpyridinium (DP+) ions to mPNIPAm terminal carboxylate groups, Z = [DP+]/[COO-]. While both experimental results and DPD data indicate that up to Z = 2 tails of the surfactant enter and swell the dodecyl core of mPNIPAm micelles, the further increase in the size of the core for Z &gt; 2 caused by the dehydration and collapse of inner parts of PNIPAm chains observed by SAXS is not reproduced by DPD simulations. Nevertheless, the study demonstrates that the simplified coarse-grained model can account for hydrogen bonding and elucidate the mechanism of comicellization. The study shows that the electrostatic interactions modify appreciably the behavior of mPNIPAm, but the assembly with cationic surfactant is governed by hydrophobic interactions.

Název v anglickém jazyce

Coassembly of Poly(N-isopropylacrylamide) with Dodecyl and Carboxyl Terminal Groups with Cationic Surfactant: Critical Comparison of Experimental and Simulation Data

Popis výsledku anglicky

Comicellization of poly(N-isopropylacrylamide) with dodecyl and carboxyl terminal groups (mPNIPAm) with cationic surfactant N-dodecylpyridinium chloride was studied by scattering techniques (light scattering, SAXS), isothermal titration calorimetry, fluorescence spectroscopy, and coarse-grained simulations using dissipative particle dynamics (DPD) as a function of charge ratio of N-dodecylpyridinium (DP+) ions to mPNIPAm terminal carboxylate groups, Z = [DP+]/[COO-]. While both experimental results and DPD data indicate that up to Z = 2 tails of the surfactant enter and swell the dodecyl core of mPNIPAm micelles, the further increase in the size of the core for Z &gt; 2 caused by the dehydration and collapse of inner parts of PNIPAm chains observed by SAXS is not reproduced by DPD simulations. Nevertheless, the study demonstrates that the simplified coarse-grained model can account for hydrogen bonding and elucidate the mechanism of comicellization. The study shows that the electrostatic interactions modify appreciably the behavior of mPNIPAm, but the assembly with cationic surfactant is governed by hydrophobic interactions.

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

18

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

14

Strana od-do

7295-7308

Kód UT WoS článku

000445971800031

EID výsledku v databázi Scopus

2-s2.0-85053612699