The static and dynamic properties of polymer-layered silicate nanocomp
osites are discussed in the context of polymers in confined media. Des
pite the topological constraints imposed by the host lattice, mass tra
nsport of the polymer into the silicate layers (at least in the case o
f essentially non-polar polystyrene) appears to be unhindered and exhi
bits mobility similar to that of the pure polymer. However, both the l
ocal and global dynamics of the polymer in the hybrids are dramaticall
y different from those in the bulk. On a local scale, intercalated pol
ymer chains exhibit higher flexibility along their backbone along with
a marked suppression (or even absence of cooperative dynamics typical
ly associated with the glass transition. On a global scale, relaxation
of polymer chains either tethered to or in close proximity (<1 nm as
in intercalated hybrids) to the host surface are dramatically alter ed
and parallel those of other intrinsically anisotropic materials such
as block copolymers and liquid crystals.