As a unique class of modular nanomaterials, metal–organic
framework (MOF) nanoparticles have attracted widespread interest for
use in various fields because of their diverse chemical functionalities,
intrinsic microporosity, and three-dimensional (3D) nanoarchitectures.
However, endowing MOF nanomaterials with precisely controlled structural
symmetries and hierarchical macro/mesoporosities remains a formidable
challenge for the researchers. Herein, we report a facile noncentrosymmetric
pore-induced anisotropic assembly strategy to prepare a series of
3D dendritic MOF (UiO-66) nanomaterials with highly controllable structural
symmetries and hierarchical macro/meso/microporosities. The synthetic
route of these nanomaterials depends on the anisotropic nucleation
of MOF spherical nanocones with noncentrosymmetric center-radial channels
and their oriented growth to isotropic nanospheres through a continuous
increase in radius and solid angle. This strategy enables the controllable
fabrication of asymmetric MOF nanostructures with abundant geometries
and porous structures by regulating the concentration of amphiphilic
triblock copolymer templates. Furthermore, the average pore diameter
of the resultant MOF nanospheres can be systematically manipulated
in a wide range from 35 to 130 nm by finely tuning the reaction temperature.
Meanwhile, the strategy can also be extended to synthesize other MOF
nanoparticles with similar architectures. Compared with microporous
UiO-66 nanocrystals, the MOF nanoparticles with controllable structural
symmetries and macro/meso/microporosities show enhanced catalytic
activity in the CO2 cycloaddition reaction. The methodology
provides new insights into the rational construction of sophisticated
asymmetric open nanostructures of hierarchically porous MOFs for many
potential applications.