TY - JOUR
T1 - Alternating terpyridlne-endfunctionalized copolymers of styrene and dlphenylethylene via anionic polymerization techniques: A detailed characterization study
AU - Ott, C.
AU - Pavlov, G.M.
AU - Guerrero Sanchez, C.A.
AU - Schubert, U.S.
PY - 2009
Y1 - 2009
N2 - 1,1-Diphenylethylenene (DPE) was copolymerized anionically with styrene to yield well-defined alternating copolymers, which were terminated by reacting the "living" polymeric carbanion species with 4'-chloro-2,2': 6'2"-terpyridine. DPE containing polymers show improved long-term service temperatures due to the stiffening of the polymer main chain by the bulky phenyl-rings. In addition, the functionality provided by the terpyridine group allows the synthesis of attractive materials for various fields of application. The obtained polymers were fully characterized by means of nuclear magnetic resonance, gel permeations chromatography, elemental analysis, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, ultraviolet-visible spectroscopy, and macromolecular hydrodynamic methods (analytical ultracentrifugation, gel permeation chromatography, intrinsic viscosimetry). In the molar mass range of 2 <M <25 kg/mol, the scaling relationships between M and hydrodynamic characteristics are obtained. The values of the Kuhn segment length (or persistence length) and hydrodynamic diameters are evaluated and compared with those of linear polystyrene. © 2009 Wiley Periodicals, Inc.
AB - 1,1-Diphenylethylenene (DPE) was copolymerized anionically with styrene to yield well-defined alternating copolymers, which were terminated by reacting the "living" polymeric carbanion species with 4'-chloro-2,2': 6'2"-terpyridine. DPE containing polymers show improved long-term service temperatures due to the stiffening of the polymer main chain by the bulky phenyl-rings. In addition, the functionality provided by the terpyridine group allows the synthesis of attractive materials for various fields of application. The obtained polymers were fully characterized by means of nuclear magnetic resonance, gel permeations chromatography, elemental analysis, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, ultraviolet-visible spectroscopy, and macromolecular hydrodynamic methods (analytical ultracentrifugation, gel permeation chromatography, intrinsic viscosimetry). In the molar mass range of 2 <M <25 kg/mol, the scaling relationships between M and hydrodynamic characteristics are obtained. The values of the Kuhn segment length (or persistence length) and hydrodynamic diameters are evaluated and compared with those of linear polystyrene. © 2009 Wiley Periodicals, Inc.
U2 - 10.1002/pola.23407
DO - 10.1002/pola.23407
M3 - Article
SN - 0887-624X
VL - 47
SP - 3691
EP - 3701
JO - Journal of Polymer Science, Part A: Polymer Chemistry
JF - Journal of Polymer Science, Part A: Polymer Chemistry
IS - 14
ER -