Concepedia

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].

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

2018 - 2024