Graphene quantum
dots (GQDs) are the harbingers of a paradigm shift
that revitalize self-assembly of the colloidal puzzle by adding shape
and size to the material-design palette. Although self-assembly is
ubiquitous in nature, the extent to which these molecular legos can
be engineered reminds us that we are still apprenticing polymer carpenters.
In this quest to unlock exotic nanostructures ascending from eventual
anisotropy, we have utilized different concentrations of GQDs as a
filler in free-radical-mediated aqueous copolymerization. Extensive
polymer grafting over the geometrically confined landscape of GQDs
(0.05%) bolsters crystallization instilling a loom which steers interaction
of polymeric cilia into interlaced equilateral triangles with high
sophistication. Such two-dimensional (2D) assemblies epitomizing the
planar tiling of “Star of David” forming a molecular
kagome lattice (KL) without metal templation evoke petrichor. Interestingly,
a higher percentage (0.3%) of GQDs allow selective tuning of the interfacial
property of copolymers breaking symmetry due to surface energy incongruity,
producing exotic Janus nanomicelles (JNMs). Herein, with the help
of a suite of characterizations, we delineate the mechanism behind
the formation of the KL and JNMs which forms a depot of heightened
drug accretion with targeted delivery of 5-fluorouracil in the colon
as validated by gamma scintigraphy studies.