Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Vavilova Street 28, 119991 Moscow, Russia.
National Research Centre "Kurchatov Institute", Akademika Kurchatova pl. 1, 123182 Moscow, Russia.
Molecules. 2023 May 23;28(11):4275. doi: 10.3390/molecules28114275.
Two coordination polymers, Fe(L)(CHCOO)(CHCN)]•nCHCN and [Fe(L)AgNOBF•CHOH]•1.75nCHOH•nHO (L = 3,3'-(4-(4-cyanophenyl)pyridine-2,6-diyl)bis(1-(2,6-dichlorophenyl)-1H-pyrazol-5-olate)), were obtained via a PCET-assisted process that uses the hydroxy-pyrazolyl moiety of the ligand and the iron(II) ion as sources of proton and electron, respectively. Our attempts to produce heterometallic compounds under mild conditions of reactant diffusion resulted in the first coordination polymer of 2,6-bis(pyrazol-3-yl)pyridines to retain the core N(L)MN(L). Under harsh solvothermal conditions, a hydrogen atom transfer to the tetrafluoroborate anion caused the transformation of the hydroxyl groups into OBF in the third coordination polymer of 2,6-bis(pyrazol-3-yl)pyridines. This PCET-assisted approach may be applicable to produce coordination polymers and metal-organic frameworks with the SCO-active core N(L)MN(L) formed by pyrazolone- and other hydroxy-pyridine-based ligands.
通过使用配体的羟基吡唑部分和铁(II)离子分别作为质子和电子的来源的质子-电子转移(PCET)辅助过程,得到了两个配位聚合物,[Fe(L)(CHCOO)(CHCN)]·nCHCN 和 [Fe(L)AgNOBF·CHOH]·1.75nCHOH·nHO(L = 3,3'-(4-(4-氰基苯基)吡啶-2,6-二基)双(1-(2,6-二氯苯基)-1H-吡唑-5-醇))。我们试图在反应物扩散的温和条件下制备杂金属化合物,导致第一个 2,6-双(吡唑-3-基)吡啶的配位聚合物保留核心 N(L)MN(L)。在苛刻的溶剂热条件下,氢原子转移到四氟硼酸根阴离子导致第三个 2,6-双(吡唑-3-基)吡啶的配位聚合物中羟基转化为 OBF。这种 PCET 辅助方法可能适用于制备具有由吡唑啉酮和其他基于羟基吡啶的配体形成的 SCO 活性核心 N(L)MN(L)的配位聚合物和金属有机骨架。