Concept
responsive polymers
Variants
Stimuli-responsive Polymers, Smart Polymers
Parents
42.6K
Publications
2.3M
Citations
105.7K
Authors
7.5K
Institutions
Glass Transition Driven Thermodynamics
1958 - 1964
During 1958-1964, polymer science advanced a unified thermo-statistical perspective, merging statistical thermodynamics and solution theory with chain statistics to predict dilute polymer solution properties such as intrinsic viscosity and second virial behavior. Parallel efforts mapped molecular motion and segmental dynamics via spectroscopy, linking microdynamics to macroscopic mechanical and thermal behavior. Investigations into structure, dimensions, and architecture clarified how unperturbed dimensions, linear versus branched topology, and stereo- sequence or bond-angle effects shape elasticity, while crosslinking and solid-state polymerization revealed kinetic pathways and network formation distinct from solution behavior. Electrical and dielectric studies highlighted temperature-dependent conduction in conducting polymers and differentiated dielectric loss mechanisms, underscoring a cohesive thermo-mechanical paradigm across phases of polymer organization.
• Statistical thermodynamics and solution theory unify chain statistics, excluded volume, and solvent quality to predict solution properties (intrinsic viscosity, second virial behavior) of dilute polymers [6], [3], [7].
• Molecular motion and dynamics in polymers: spectroscopy-based mapping (NMR, dielectric) of segmental and local motions across temperatures, linking microdynamics to mechanical and thermal behavior [4], [15], [17], [18].
• Structure, dimensions, and architecture shaping polymer properties: methods to estimate unperturbed dimensions, study chain dimensions in linear vs branched polymers, and assess stereo-sequence and bond-angle effects on elasticity [1], [11], [19], [2], [9].
• Crosslinking and solid-state polymerization: UV and gamma-induced crosslinking, grafting, and solid-state polymerization reveal alternative kinetic pathways and network formation distinct from solution behavior [5], [13], [16], [20].
• Electrical and dielectric properties illuminate charge transport in polymers: semiconducting behavior and temperature-dependent conduction in conducting polymers, contrasting with dielectric loss mechanisms across temperatures [14], [18].
Popular Keywords
Electric-Field Responsive Polymers
1965 - 1988
Stimuli-Responsive Polymer Networks
1989 - 1995
Stimuli-Responsive Polymer Architectures
1996 - 2003
RAFT-Driven Stimuli-Responsive Polymers
2004 - 2010
Light-Driven Photoresponsive Polymers
2011 - 2017
Hierarchical Supramolecular Hydrogels
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