TY  - JOUR
A1  - Kyriakos, Konstantinos
A1  - Philipp, Martine
A1  - Lin, Che-Hung
A1  - Dyakonova, Margarita
A1  - Vishnevetskaya, Natalya
A1  - Grillo, Isabelle
A1  - Zaccone, Alessio
A1  - Miasnikova, Anna
A1  - Laschewsky, Andre
A1  - Müller-Buschbaum, Peter
A1  - Papadakis, Christine M.
T1  - Quantifying the Interactions in the Aggregation of Thermoresponsive Polymers: The Effect of Cononsolvency
JF  - Macromolecular rapid communications
N2  - The aggregation kinetics of thermoresponsive core-shell micelles with a poly(N-isopropyl acrylamide) shell in pure water or in mixtures of water with the cosolvents methanol or ethanol at mole fractions of 5% is investigated during a temperature jump across the respective cloud point. Characteristically, these mixtures give rise to cononsolvency behavior. At the cloud point, aggregates are formed, and their growth is followed with time-resolved small-angle neutron scattering. Using the reversible association model, the interaction potential between the aggregates is determined from their growth rate in dependence on the cosolvents. The effect of the cosolvent is attributed to the interaction potential on the structured layer of hydration water around the aggregates. It is surmised that the latter is perturbed by the cosolvent and thus the residual repulsive hydration force between the aggregates is reduced. The larger the molar volume of the cosolvent, the more pronounced is the effect. This framework provides a molecular-level understanding of solvent-mediated effective interactions in polymer solutions and new opportunities for the rational control of self-assembly in complex soft matter systems.
KW  - colloidal aggregation
KW  - cononsolvency
KW  - interaction potential
KW  - polymer solutions
KW  - self-assembled micelles
KW  - thermoresponsive polymers
Y1  - 2016
U6  - https://doi.org/10.1002/marc.201500583
SN  - 1022-1336
SN  - 1521-3927
VL  - 37
SP  - 420
EP  - 425
PB  - Wiley-VCH
CY  - Weinheim
ER  - 
TY  - JOUR
A1  - Vishnevetskaya, Natalya S.
A1  - Hildebrand, Viet
A1  - Niebuur, Bart-Jan
A1  - Grillo, Isabelle
A1  - Filippov, Sergey K.
A1  - Laschewsky, Andre
A1  - Müller-Buschbaum, Peter
A1  - Papadakis, Christine M.
T1  - Aggregation Behavior of Doubly Thermoresponsive Polysulfobetaine-b-poly(N-isopropylacrylamide) Diblock Copolymers
JF  - Macromolecules : a publication of the American Chemical Society
N2  - A 2-fold thermoresponsive diblock copolymer PSPP430-b-PNIPAM(200) consisting of a zwitterionic polysulfobetaine (PSPP) block and a nonionic poly(N-isopropylacrylamide) (PNIPAM) block is prepared by successive RAFT polymerizations. In aqueous solution, the corresponding homopolymers PSPP and PNIPAM feature both upper and lower critical solution temperature (UCST and LCST) behavior, respectively. The diblock copolymer exhibits thermally induced "schizophrenic" aggregation behavior in aqueous solutions. Moreover, the ion sensitivity of the, cloud point of the zwitterionic PSPP block to both the ionic strength and the nature of the salt offers the possibility to create switchable systems which respond sensitively to changes of the temperature and of the electrolyte type and concentration. The diblock copolymer solutions in D2O are investigated by means of turbidimetry and small-angle neutron scattering (SANS) with respect to the phase behavior and the self-assembled structures in dependence on temperature and electrolyte content. Marked, differences of the aggregation below the UCST-type and above the LCST-type transition are observed. The addition of a small amount of NaBr (0.004 M) does not affect the overall behavior, and only the UCST-type transition and aggregate structures are slightly altered, reflecting the well-known ion sensitivity of the zwitterionic PSPP block.
Y1  - 2016
U6  - https://doi.org/10.1021/acs.macromol.6b01186
SN  - 0024-9297
SN  - 1520-5835
VL  - 49
SP  - 6655
EP  - 6668
PB  - American Chemical Society
CY  - Washington
ER  -