Polymer globule with fractal properties caused by intramolecular nanostructuring and spatial constrains

Abstract

By means of computer simulation, we studied macromolecules composed of N dumbbell amphiphilic monomer units with attractive pendant groups. In poor solvents, these macromolecules form spherical globules that are dense in the case of short chains (the gyration radius R_G ∼ N^1/3), or hollow inside and obey the R_G ∼ N^1/2 law when the macromolecules are sufficiently long. Due to the specific intramolecular nanostructuring, the vesicle-like globules of long amphiphilic macromolecules posses some properties of fractal globules, by which they (i) could demonstrate the same scaling statistics for the entire macromolecule and for short subchains with m monomer units and (ii) possess a specific territorial structure. Within a narrow slit, the globule loses its inner cavity, takes a disk-like shape and scales as N^1/2 for much shorter macromolecules. However, the field of end-to-end distance r(m) ∼ m^1/2 dependence for subchains becomes visibly smaller. The results obtained were compared with the homopolymer case.