Samii Rouzbeh, Zanders David, Buttera Sydney C, Kessler Vadim, Ojamäe Lars, Pedersen Henrik, O'Brien Nathan J
Department of Physics, Chemistry and Biology, Linköping University, SE-581 83 Linköping, Sweden.
Faculty of Chemistry and Biochemistry, Ruhr University Bochum, Universitätsstraße 150, 44801 Bochum, Germany.
Inorg Chem. 2021 Apr 5;60(7):4578-4587. doi: 10.1021/acs.inorgchem.0c03496. Epub 2021 Mar 12.
Amidinate and guanidinate ligands have been used extensively to produce volatile and thermally stable precursors for atomic layer deposition. The triazenide ligand is relatively unexplored as an alternative ligand system. Herein, we present six new Al(III) complexes bearing three sets of a 1,3-dialkyltriazenide ligand. These complexes volatilize quantitatively in a single step with onset volatilization temperatures of ∼150 °C and 1 Torr vapor pressures of ∼134 °C. Differential scanning calorimetry revealed that these Al(III) complexes exhibited exothermic events that overlapped with the temperatures of their mass loss events in thermogravimetric analysis. Using quantum chemical density functional theory computations, we found a decomposition pathway that transforms the relatively large hexacoordinated Al(III) precursor into a smaller dicoordinated complex. The pathway relies on previously unexplored interligand proton migrations. These new Al(III) triazenides provide a series of alternative precursors with unique thermal properties that could be highly advantageous for vapor deposition processes of Al containing materials.
脒基和胍基配体已被广泛用于制备用于原子层沉积的挥发性和热稳定前驱体。三氮烯配体作为一种替代配体系统相对未被充分探索。在此,我们展示了六种带有三组1,3 - 二烷基三氮烯配体的新型Al(III)配合物。这些配合物在一步中定量挥发,起始挥发温度约为150°C,1托蒸气压下的温度约为134°C。差示扫描量热法表明,这些Al(III)配合物在热重分析中表现出与质量损失事件温度重叠的放热事件。使用量子化学密度泛函理论计算,我们发现了一条将相对较大的六配位Al(III)前驱体转化为较小的二配位配合物的分解途径。该途径依赖于先前未探索的配体间质子迁移。这些新型Al(III)三氮烯提供了一系列具有独特热性质的替代前驱体,这对于含铝材料的气相沉积过程可能非常有利。