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Updated: May 5, 2026

Synthesis and Characterization of Functionalized Metal-organic Frameworks
Published on: September 5, 2014
Dimension-Tunable Supramolecular Organic Frameworks with Chiral Pore Channels for Selective Guest Encapsulation and
Tiejun Li1,2,3, Dian Niu1, Jingdan Zhang1,2
1CAS Key Laboratory of Colloid, Interface and Thermodynamics, Institute of Chemistry, Chinese Academy of Sciences, No. 2 North First Street, Zhongguancun, Beijing 100190, China.
None:
Here, we report a dimension-tunable supramolecular organic framework (SOF) with chiral pore channels, which shows selective guest encapsulation and enhanced circularly polarized luminescence (CPL). SOFs from a chiral para-substituted bis-naphthalene bis-urea (PNU) are fabricated by both vapor diffusion crystallization and an antisolvent self-assembly approach, leading to the formation of one-dimensional (1D) micrometer-sized single crystal and two-dimensional (2D) plate-like and three-dimensional (3D) octahedral self-assembled microstructures, respectively. The similar permanent porosity of these dimension-tunable chiral SOFs is collectively proved by N2 adsorption-desorption experiments, single-crystal structure, high-resolution transmission electron microscopy (HR-TEM), and density functional theory (DFT) calculations. By soaking octahedral SOFs in aqueous dye solutions, the chiral porous channels effectively absorb size-matched guest dyes and impart their chirality, leading to enhanced CPL with a dissymmetry factor of 1.6 × 10-2. This work provides insights for the efficient synthesis of chiral SOFs with pore channels from a single component, which also deepens our understanding of size-selective adsorption and chirality transfer in confined space, as well as the enhancement of circularly polarized luminescence.

