6533b7defe1ef96bd1275ec3

RESEARCH PRODUCT

3D Conformations of Thick Synthetic Polymer Chains Observed by Cryogenic Electron Microscopy.

Hao YuAvraham HalperinKurt BinderA. Dieter SchlüterMartin KrögerChristoph BöttcherDaniel Messmer

subject

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceScatteringGeneral EngineeringGeneral Physics and Astronomy02 engineering and technologyPolymerElectron010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceslaw.inventionCondensed Matter::Soft Condensed MatterchemistryChemical physicslawPolymer physicsGeneral Materials ScienceElectron microscope0210 nano-technologyScalingSelf-avoiding walkMacromolecule

description

The backbone conformations of individual, unperturbed synthetic macromolecules have so far not been observed directly in spite of their fundamental importance to polymer physics. Here we report the dilute solution conformations of two types of linear dendronized polymers, obtained by cryogenic transmission electron stereography and tomography. The three-dimensional trajectories show that the wormlike chain model fails to adequately describe the scaling of these thick macromolecules already beyond a few nanometers in chain length, in spite of large apparent persistence lengths and long before a signature of self-avoidance appears. This insight is essential for understanding the limitations of polymer physical models, and it motivated us to discuss the advantages and disadvantages of this approach in comparison to the commonly applied scattering techniques.

10.1021/acsnano.8b09621https://pubmed.ncbi.nlm.nih.gov/30835993