Synthesis and Thermal Study of Hexacoordinated Aluminum(III) Triazenides for Use in Atomic Layer Deposition

被引:13
作者
Samii, Rouzbeh [1 ]
Zanders, David [2 ,3 ]
Buttera, Sydney C. [3 ]
Kessler, Vadim [4 ]
Ojamae, Lars [1 ]
Pedersen, Henrik [1 ]
O'Brien, Nathan J. [1 ]
机构
[1] Linkoping Univ, Dept Phys Chem & Biol, SE-58183 Linkoping, Sweden
[2] Ruhr Univ Bochum, Fac Chem & Biochem, D-44801 Bochum, Germany
[3] Carleton Univ, Dept Chem, Ottawa, ON K1S 5B6, Canada
[4] Swedish Univ Agr Sci, Dept Mol Sci, S-75007 Uppsala, Sweden
关键词
THIN-FILMS; LIGAND-EXCHANGE; CRYSTALLINE ALN; NITRIDE; TRIS(DIMETHYLAMIDO)ALUMINUM;
D O I
10.1021/acs.inorgchem.0c03496
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
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 similar to 150 degrees C and 1 Torr vapor pressures of similar to 134 degrees 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.
引用
收藏
页码:4578 / 4587
页数:10
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