This is a copy of the slides presented at the meeting but not formally written up for the volume.

Current large scale atomistic simulations remain too computationally demanding to be generally applicable to industrial and bioengineering materials. It is desirable to develop multiscale modeling algorithms to perform efficient and informative mesoscopic simulations. Here we present a multipolar expansion method to construct coarse grained force fields (CGFF) for polymer nanostructures and nanocomposites. This model can effectively capture the stereochemical response to anisotropic long-range interactions and can be systematically improved upon adding higher order terms. The coarse-graining procedure forms the basis to perform a hierarchy of multiscale simulations starting with the quantum chemistry calculations to coarse grained molecular dynamics, hopefully toward continuum modeling. We have applied this procedure to molecular clusters such as alkane, benzene, and fullerene. For liquid alkane, molecular dynamics simulations using the CGFF can reproduce the pair distribution functions using atomistic force fields. Molecular mechanics simulations using the CGFF can well reproduce the energetics of benzene clusters from quantum chemistry electronic structure calculations. Subtle anisotropy in the interaction potentials of the fullerene dimer using the Brenner force field can also be well represented by the model. It is promising this procedure can be standardized and further extended.