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Updated: Jan 10, 2026

Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes
Published on: November 21, 2017
Mechanochemistry unlocking stoichiometric control in alkali metal carboxylate coordination polymers
Michał K Leszczyński1,2, Iwona Justyniak1, Janusz Lewiński1,2
1Institute of Physical Chemistry Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland. leszczynski.m@hotmail.com.
Abstract:
Alkali metal-based coordination polymers represent a promising alternative to transition metal systems, yet their development remains limited due to the inherent challenges in controlling and predicting the assembly of structures based on alkali cations. In this report we demonstrate a comprehensive study on the preparation of Na, K and Rb 1,3,5-benzenetricarboxylates using both self-assembly in an aqueous solution and the solid-state mechanochemical methods, revealing a remarkable degree of structural diversity in these seemingly simple systems. Notably, the developed mechanochemical procedures enabled excellent control over the metal-to-linker stoichiometry, as demonstrated by the selective formation of two M2HBTC-type phases (M = K, Rb; BTC = 1,3,5-benzenetricarboxylate), which were not readily accessible by solution-based synthesis. These results demonstrate the unique advantages of mechanochemistry in enabling stoichiometric control and accessing coordination polymers that remain out of reach for conventional solution-based methods.
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