TY - JOUR
T1 - Polyion complex nanomaterials from block polyelectrolyte micelles and linear polyelectrolytes of opposite charge
T2 - 1. Solution behavior
AU - Chelushkin, Pavel S.
AU - Lysenko, Evgeny A.
AU - Bronich, Tatiana K.
AU - Eisenberg, Adi
AU - Kabanov, Victor A.
AU - Kabanov, Alexander V.
PY - 2007/7/26
Y1 - 2007/7/26
N2 - The present study investigates whether block polyelectrolyte micelles can form soluble complexes upon interaction with oppositely charged linear polyelectrolytes. The phase behavior and molecular characteristics of the complexes were examined by turbidimetry, phase analysis, dynamic light scattering, and sedimentation velocity techniques. At an excess of polyelectrolyte micelles, soluble complexes were formed either independently on the route of preparation or, for select linear polyelectrolytes, through routes that avoided macrophase separation. Such soluble complexes are in a thermodynamic equilibrium state for all polyion pairs. The hydrodynamic sizes and sedimentation coefficients did not depend on the chemical nature of the linear polyelectrolyte, but were determined by the charge ratios and the hydrodynamic properties of the initial micelles. At an excess of linear polyelectrolyte, complex solubility and molecular characteristics depended on the chemical nature of the linear polyelectrolyte. In this region, linear polyelectrolytes formed soluble complexes with micelles if soluble complexes could be formed with the corresponding linear analogues of the block polyelectrolyte.
AB - The present study investigates whether block polyelectrolyte micelles can form soluble complexes upon interaction with oppositely charged linear polyelectrolytes. The phase behavior and molecular characteristics of the complexes were examined by turbidimetry, phase analysis, dynamic light scattering, and sedimentation velocity techniques. At an excess of polyelectrolyte micelles, soluble complexes were formed either independently on the route of preparation or, for select linear polyelectrolytes, through routes that avoided macrophase separation. Such soluble complexes are in a thermodynamic equilibrium state for all polyion pairs. The hydrodynamic sizes and sedimentation coefficients did not depend on the chemical nature of the linear polyelectrolyte, but were determined by the charge ratios and the hydrodynamic properties of the initial micelles. At an excess of linear polyelectrolyte, complex solubility and molecular characteristics depended on the chemical nature of the linear polyelectrolyte. In this region, linear polyelectrolytes formed soluble complexes with micelles if soluble complexes could be formed with the corresponding linear analogues of the block polyelectrolyte.
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U2 - 10.1021/jp0674221
DO - 10.1021/jp0674221
M3 - Article
C2 - 17441751
AN - SCOPUS:34547691034
SN - 1520-6106
VL - 111
SP - 8419
EP - 8425
JO - Journal of Physical Chemistry B
JF - Journal of Physical Chemistry B
IS - 29
ER -