Unraveling the Substituent-Controlled Fluorescence Modulation in One-Dimensional Cd-Based Coordination Polymers: A Structure-Property Relationship Study
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Updated: Oct 31, 2026

Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
Published on: September 26, 2016
Shuyu Wang1,2, Qianhong Fan1,2, Lei Wang1,2
1Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education and Yunnan Province, School of Chemical Science and Technology, Yunnan University, Kunming 650500, P.R. China.
Abstract:
The substituent engineering strategy has emerged as a powerful tool for precise modulation of the structure-property relationships in coordination polymers (CPs), yet the rational design of isostructural CPs with tunable dual-channel fluorescence and integrated stimulus-responsive behaviors remains a compelling challenge. Herein, three isostructural, one-dimensional Cd-based CPs (1-3) were rationally designed and hydrothermally synthesized via systematic substituent modification. Notably, the solid-state fluorescence of 1-3 is precisely regulated by the electronic and steric effects of substituents, enabling dual-channel emission encompassing ligand-centered monomer fluorescence and excimer-derived fluorescence. Furthermore, systematic investigations reveal that these CPs exhibit distinct thermoresponsive and mechanoresponsive fluorescence behaviors, which are closely correlated with substituent-induced structural subtlety. This work not only demonstrates the efficacy of substituent engineering in tailoring dual-channel fluorescence within isostructural CPs but also provides insights into the design of multifunctional, stimulus-responsive fluorescent materials for potential applications in sensors and optoelectronics.
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