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Dynamic polystyrene (d-PS) and poly n-butyl acrylate) (d-poly n-butyl acrylateazone linkage at each chain center were synthesized by atom transfer radical polymerization (ATRP) of corresponding monomers using a bis-bromoisobutyrate initiator bearing one acylhydrazone bond.
However, this is indeed expected as the maximal range of gyration can only be large if the maximal distance possible between C-alpha and side chain center is large and vice versa.
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Each residue is represented by the Cα and the side-chain center of mass (the CAS model [ 20]).
Each residue in TOUCHSTONE-II is represented by its Cα, Cβ, and the side-chain center of mass (the CABS model [ 12]).
The side-chain center of mass is determined by a two-rotamer approximation that depends on whether the local backbone configuration is extended or compact.
Another approach which leads to similar results is to use an anisotropic weighting function that takes into account not only the distance between the reference site and its neighbors but also its relative orientation with respect to a unit vector directed from the site's C α to its C β or side-chain center of mass.
We investigated the linear viscoelastic properties in the melt of a series of nearly monodisperse poly n-butyl acrylate) (poly n-butyl center-functionacrylateith a bis-urea sticker grouPnBAble to self-assochainsby quadruple hydrogen bonding.
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