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将脒基锰和β-酮亚胺配合物作为锰基薄膜沉积前驱体的研究

Targeting Manganese Amidinate and ß-Ketoiminate Complexes as Precursors for Mn-Based Thin Film Deposition.

作者信息

Wilken Martin, Muriqi Arbresha, Krusenbaum Annika, Nolan Michael, Devi Anjana

机构信息

Inorganic Materials Chemistry, Ruhr University Bochum, Universitätsstr. 150, 44801, Bochum, Germany.

Tyndall National Institute, University College Cork, Lee Maltings, Cork, T12 R5CP, Ireland.

出版信息

Chemistry. 2024 Aug 12;30(45):e202401275. doi: 10.1002/chem.202401275. Epub 2024 Jul 4.

Abstract

With a focus on Mn based organometallic compounds with suitable physico-chemical properties to serve as precursors for chemical vapor deposition (CVD) and atomic layer deposition (ALD) of Mn-containing materials, systematic synthetic approaches with ligand variation, detailed characterization, and theoretical input from density functional theory (DFT) studies are presented. A series of new homoleptic all-nitrogen and mixed oxygen/nitrogen-coordinated Mn(II) complexes bearing the acetamidinate, formamidinate, guanidinate and ß-ketoiminate ligands have been successfully synthesized for the first time. The specific choice of these ligand classes with changes in structure and coordination sphere and side chain variations result in significant structural differences whereby mononuclear and dinuclear complexes are formed. This was supported by density functional theory (DFT) studies. The compounds were thoroughly characterized by single crystal X-ray diffraction, magnetic measurements, mass spectrometry and elemental analysis. To evaluate their suitability as precursors for deposition of Mn-based materials, the thermal properties were investigated in detail. Mn(II) complexes possessing the most promising thermal properties, namely Bis(N,N'-ditertbutylformamidinato)manganese(II) (IV) and Bis(4-(isopropylamino)pent-3-en-2-onato)manganese(II) (ßIII) were used in reactivity studies with DFT to explore their interaction with oxidizing co-reactants such as oxygen and water which will guide future CVD and ALD process development.

摘要

本文聚焦于具有合适物理化学性质的锰基金属有机化合物,它们可作为含锰材料化学气相沉积(CVD)和原子层沉积(ALD)的前驱体,介绍了通过配体变化的系统合成方法、详细表征以及密度泛函理论(DFT)研究的理论输入。首次成功合成了一系列带有脒基、甲脒基、胍基和β-酮亚胺基配体的新型全氮和氧/氮混合配位的Mn(II)配合物。这些配体类别的特定选择,随着结构、配位球和侧链变化,导致形成单核和双核配合物的显著结构差异。这得到了密度泛函理论(DFT)研究的支持。通过单晶X射线衍射、磁性测量、质谱和元素分析对这些化合物进行了全面表征。为了评估它们作为锰基材料沉积前驱体的适用性,详细研究了其热性质。具有最有前景热性质的Mn(II)配合物,即双(N,N'-二叔丁基甲脒基)锰(II)(IV)和双(4-(异丙基氨基)戊-3-烯-2-酮基)锰(II)(βIII),用于与DFT的反应性研究,以探索它们与氧气和水等氧化共反应物的相互作用,这将指导未来CVD和ALD工艺的发展。

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