From cyclic amines and acetonitrile to amidine zinc(ii) complexes

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Abstract

A seemingly simple combination of [Zn(quin)2(H2O)] (quin-= quinaldinate) and a selected secondary cyclic amine, piperidine (pipe), pyrrolidine (pyro) or morpholine (morph), afforded in acetonitrile a number of products: anionic homoleptic quinaldinate, neutral heteroleptic quinaldinate/amine and quinaldinate/amidine complexes. The piperidine and pyrrolidine systems underwent reaction with acetonitrile to give amidines. Thein situformed piperidinoacetamidine (pipeam) or pyrrolidinoacetamidine (pyroam) coordinated to zinc(ii). Reactions with piperidine led totrans-[Zn(quin)2(pipe)2]·2CH3CN (1), [Zn(quin)2(pipe)]·cis-[Zn(quin)2(pipe)2] (2), pipeH[Zn(quin)3]·CH3CN (3), [Zn(quin)2(pipeam)]·CH3CN (4a), [Zn(quin)2(pipeam)]·2CHCl3(4b), pipeamH[Zn(quin)3] (5) and pipeamH[Zn(quin)2(CH3COO)]·acetamide (6) (pipeH+and pipeamH+denote protonated amine or amidine). By analogy, [Zn(quin)2(pyro)2] (7), pyroH[Zn(quin)3]·CH3CN (8), pyroH[Zn(quin)2Cl] (9), [Zn(quin)2(pyroam)]·CH3CN·0.5pyroam·0.5H2O (10a), [Zn(quin)2(pyroam)]·2CHCl3(10b), [Zn(quin)2(pyroam)]·CH2Cl2(10c) and pyroamH[Zn(quin)3] (11) were obtained in the pyrrolidine reactions. The morpholine system allowed isolation of only two novel products,trans-[Zn(quin)2(morph)2] (12) and morphH[Zn(quin)3]·CH3CN (13). Importantly, no amidine could be isolated. Instead, in autoclaves at 105 °C morpholine degraded to ammonia, as confirmed by mass spectrometry of the gas phase. pyroamH[Zn(quin)3] exists in two polymorphs which differ in the binding modes of quinaldinate ligands. In11triclinic, the metal ion of [Zn(quin)3]-features a five-coordinate environment, whereas that in11monoclinicis surrounded by six donors. Stabilities of the [Zn(quin)3]-isomers were assessed with DFT calculations. The one with a six-coordinate zinc(ii) ion was found to be more stable than its five-coordinate counterpart. Favorable intermolecular interactions in the solid state stabilize both and reduce the energy difference between them. The calculations show the conversion of the five-coordinate [Zn(quin)3]-into its coordinatively saturated isomer to be an almost barrierless process.

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Podjed, N., Modec, B., Alcaide, M. M., & López-Serrano, J. (2020). From cyclic amines and acetonitrile to amidine zinc(ii) complexes. RSC Advances, 10(31), 18200–18221. https://doi.org/10.1039/d0ra03192e

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