Molecular and structural analysis via hydrodynamic methods: Cationic poly(2-aminoethyl-methacrylate)s

Pharmaceutically relevant cationic linear poly(2-aminoethyl-methacrylate)s were synthesized by reversible addition-fragmentation chain transfer polymerization resulting in a homologous series of the homopolymers in a wide range of molar masses (10,000

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Veröffentlicht in:Polymer (Guilford) 2017-11, Vol.131, p.252-262
Hauptverfasser: Perevyazko, Igor, Trützschler, Anne-K., Gubarev, Alexander, Lebedeva, Elena, Traeger, Anja, Schubert, Ulrich S., Tsvetkov, Nikolay
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container_issue
container_start_page 252
container_title Polymer (Guilford)
container_volume 131
creator Perevyazko, Igor
Trützschler, Anne-K.
Gubarev, Alexander
Lebedeva, Elena
Traeger, Anja
Schubert, Ulrich S.
Tsvetkov, Nikolay
description Pharmaceutically relevant cationic linear poly(2-aminoethyl-methacrylate)s were synthesized by reversible addition-fragmentation chain transfer polymerization resulting in a homologous series of the homopolymers in a wide range of molar masses (10,000
doi_str_mv 10.1016/j.polymer.2017.10.032
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The polymers were studied in 0.2MNaCl and 0.2MNaOH in water, applying combined analytical approach comprising of complementary hydrodynamic and optical methods such as analytical ultracentrifugation, intrinsic viscosity, translation diffusion, flow birefringence and asymmetric flow field-flow fractionation (AF4) as well as standard characterization technique (SEC). The efforts were focused on the evaluation of solution (solvation), molecular (absolute molar masses), conformational (equilibrium rigidity, diameter of the polymer chain) and optical (anisotropy of optical polarizability of the monomer unit) characteristics of the polymers. Consequently the absolute values of the molar masses were determined by the sedimentation-diffusion analysis and AF4 resulting in well consistent results. The corresponding scaling relationships in 0.2MNaCl water ([η]=0.0031×M0.83; s0=0.0324×M0.39; D0=3,909×M−0.64) show linear trends in whole range of molar masses revealing random coil conformation of the macromolecules. Conformational characteristics were determined in 0.2MNaCl (equilibrium rigidity A=5.3±1.5nm) and 0.2MNaOH (A=1.3±0.1nm) revealing an influence of uncompensated charges on the polymer conformation. [Display omitted] •Combination of hydrodynamic and optical methods is used to study cationic polymers.•The absolute molar masses are determined by AUC and AF4 techniques.•The influence of the polymer α-end group on the solvation properties is shown.•The conformation is established via the scaling relationships.•The conformational characteristics are determined for different solvent systems.</description><identifier>ISSN: 0032-3861</identifier><identifier>EISSN: 1873-2291</identifier><identifier>DOI: 10.1016/j.polymer.2017.10.032</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Addition polymerization ; Analytical ultracentrifugation ; Anisotropy ; Asymmetric flow field-flow fractionation ; Birefringence ; Cationic polymers ; Cations ; Chain transfer ; Chains (polymeric) ; Characterization ; Chemical compounds ; Chemical synthesis ; Coils ; Conformation ; Diffusion ; Fluid mechanics ; Fractionation ; Homology ; Macromolecules ; Optics ; Polarizability ; Poly(2-aminoethyl-methacrylate) ; Polymerization ; Polymers ; Random coil ; Rigidity ; Scaling ; Sedimentation ; Sodium chloride ; Solution properties ; Solvation ; Structural analysis ; Ultracentrifugation ; Viscosity</subject><ispartof>Polymer (Guilford), 2017-11, Vol.131, p.252-262</ispartof><rights>2017 Elsevier Ltd</rights><rights>Copyright Elsevier BV Nov 22, 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c289t-ea75f4e29c88ad87987178de94bd29d5582161cbb9a8f85d17012354765d968a3</citedby><cites>FETCH-LOGICAL-c289t-ea75f4e29c88ad87987178de94bd29d5582161cbb9a8f85d17012354765d968a3</cites><orcidid>0000-0003-4978-4670</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.polymer.2017.10.032$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids></links><search><creatorcontrib>Perevyazko, Igor</creatorcontrib><creatorcontrib>Trützschler, Anne-K.</creatorcontrib><creatorcontrib>Gubarev, Alexander</creatorcontrib><creatorcontrib>Lebedeva, Elena</creatorcontrib><creatorcontrib>Traeger, Anja</creatorcontrib><creatorcontrib>Schubert, Ulrich S.</creatorcontrib><creatorcontrib>Tsvetkov, Nikolay</creatorcontrib><title>Molecular and structural analysis via hydrodynamic methods: Cationic poly(2-aminoethyl-methacrylate)s</title><title>Polymer (Guilford)</title><description>Pharmaceutically relevant cationic linear poly(2-aminoethyl-methacrylate)s were synthesized by reversible addition-fragmentation chain transfer polymerization resulting in a homologous series of the homopolymers in a wide range of molar masses (10,000&lt;M&lt;130,000gmol−1) and relatively narrow dispersities (Ð:1.3±0.4). The polymers were studied in 0.2MNaCl and 0.2MNaOH in water, applying combined analytical approach comprising of complementary hydrodynamic and optical methods such as analytical ultracentrifugation, intrinsic viscosity, translation diffusion, flow birefringence and asymmetric flow field-flow fractionation (AF4) as well as standard characterization technique (SEC). The efforts were focused on the evaluation of solution (solvation), molecular (absolute molar masses), conformational (equilibrium rigidity, diameter of the polymer chain) and optical (anisotropy of optical polarizability of the monomer unit) characteristics of the polymers. Consequently the absolute values of the molar masses were determined by the sedimentation-diffusion analysis and AF4 resulting in well consistent results. The corresponding scaling relationships in 0.2MNaCl water ([η]=0.0031×M0.83; s0=0.0324×M0.39; D0=3,909×M−0.64) show linear trends in whole range of molar masses revealing random coil conformation of the macromolecules. Conformational characteristics were determined in 0.2MNaCl (equilibrium rigidity A=5.3±1.5nm) and 0.2MNaOH (A=1.3±0.1nm) revealing an influence of uncompensated charges on the polymer conformation. 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The polymers were studied in 0.2MNaCl and 0.2MNaOH in water, applying combined analytical approach comprising of complementary hydrodynamic and optical methods such as analytical ultracentrifugation, intrinsic viscosity, translation diffusion, flow birefringence and asymmetric flow field-flow fractionation (AF4) as well as standard characterization technique (SEC). The efforts were focused on the evaluation of solution (solvation), molecular (absolute molar masses), conformational (equilibrium rigidity, diameter of the polymer chain) and optical (anisotropy of optical polarizability of the monomer unit) characteristics of the polymers. Consequently the absolute values of the molar masses were determined by the sedimentation-diffusion analysis and AF4 resulting in well consistent results. The corresponding scaling relationships in 0.2MNaCl water ([η]=0.0031×M0.83; s0=0.0324×M0.39; D0=3,909×M−0.64) show linear trends in whole range of molar masses revealing random coil conformation of the macromolecules. Conformational characteristics were determined in 0.2MNaCl (equilibrium rigidity A=5.3±1.5nm) and 0.2MNaOH (A=1.3±0.1nm) revealing an influence of uncompensated charges on the polymer conformation. [Display omitted] •Combination of hydrodynamic and optical methods is used to study cationic polymers.•The absolute molar masses are determined by AUC and AF4 techniques.•The influence of the polymer α-end group on the solvation properties is shown.•The conformation is established via the scaling relationships.•The conformational characteristics are determined for different solvent systems.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.polymer.2017.10.032</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-4978-4670</orcidid></addata></record>
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source ScienceDirect Journals (5 years ago - present)
subjects Addition polymerization
Analytical ultracentrifugation
Anisotropy
Asymmetric flow field-flow fractionation
Birefringence
Cationic polymers
Cations
Chain transfer
Chains (polymeric)
Characterization
Chemical compounds
Chemical synthesis
Coils
Conformation
Diffusion
Fluid mechanics
Fractionation
Homology
Macromolecules
Optics
Polarizability
Poly(2-aminoethyl-methacrylate)
Polymerization
Polymers
Random coil
Rigidity
Scaling
Sedimentation
Sodium chloride
Solution properties
Solvation
Structural analysis
Ultracentrifugation
Viscosity
title Molecular and structural analysis via hydrodynamic methods: Cationic poly(2-aminoethyl-methacrylate)s
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