钴
咪唑
机制(生物学)
降水
化学
共沉淀
锰
无机化学
组合化学
材料科学
有机化学
认识论
物理
哲学
气象学
作者
Anna-Caroline Lavergne-Bril,David Peralta,Pascale Maldivi,J. Colin
标识
DOI:10.1021/acssuschemeng.5c00842
摘要
Imidazolate linkers selectively precipitate in pure cobalt-based hybrid materials [zeolitic-imidazolate-frameworks (ZIFs)] when they are directly added in solutions containing nickel, manganese, and cobalt. The favored reactivity of imidazole against cobalt versus other cations is deeply studied, and selectivity mechanisms are explained, thanks to experimental data supported by DFT calculations. The preferential coordination of imidazole with cobalt instead of nickel cations is explained, thanks to the tetrahedral Co(Im)4 cluster formation, which is the main building block of ZIF structures. On the other hand, the cobalt/manganese selectivity is kinetically driven. Different ligands from the imidazole family have been compared, and a direct correlation between cobalt/manganese selectivity and pKa of molecules has been highlighted.
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