Bottlebrush polymers, formed from
a linear backbone polymer with
a high density of grafted side chains, are functional macromolecules
useful in molecular assembly and responsive materials due to their
unique physical properties. Interactions between the side chains stiffen
the molecular backbone and imbue it with a molecular dimension beyond
simply the polymer length, drastically altering dynamic relaxation
and intrapolymer interactions. Simulation prediction of these material
properties remains a challenge, however, because they specifically
depend on side chain degrees of freedom that are computationally expensive
to model. In this work, we use the wormlike cylinder framework to
systematically map molecular features from a single-molecule hybrid
Brownian dynamics and Monte Carlo (BD/MC) simulation with explicit
side chains to a simple touched-bead polymer model. We use static
properties from the explicit side chain simulations such as end-to-end
distance and radius of gyration to parameterize the wormlike cylinder
model and consistently reproduce other single-chain properties such
as hydrodynamic radius and intrinsic viscosity. This parameterization
yields the stiffness parameter and equivalent diameter of a bottlebrush
and is compared to prior scaling theories and simulation results.
We find that the wormlike cylinder model, appropriately parameterized,
provides an accurate description of these quantities over a wide range
of side chain lengths and grafting densities. We demonstrate that
a coarse-grained representation is able to consistently reproduce
the bottlebrush structure and show that the wormlike cylinder model
can be useful for large-scale coarse-grained simulations of bottlebrush
suspensions.