The interest in the chemistry and development of strontium precursors for atomic layer deposition (ALD) or chemical vapor deposition (CVD) were driven by several applications such as, SrTiO 3 for dynamic random access memories (DRAM), 1 ferroelectrics such as Ba In the synthesis and application of ALD precursor, it is important that the compound should have a good volatile character, stability, and chemical reactivity to allow formation of the target films. In common, the requirements for precursor were achieved by introducing functionalities to the ligands of the homoleptic compounds. But due to the uniformity of the ligands, it is difficult for homoleptic metal precursor to adopt a selective dissociation of one of the ligands. In heteroleptic metal precursors, the difference in reactivity of the ligands leads to a selective dissociation of one of the ligands over the other. On a substrate surface this ability of heteroleptic metal precursors may give more precise selflimiting character which results in formation of high quality films.The most common volatile precursors of strontium were synthesized using β-diketonates like 2,2,6,6-tetramethyl-3,5-heptanedione 7,8 and highly substituted cyclopentadienes.
9The studies 10 show that the significant carbon contamination exists on the films in ALD process using strontium β-diketonate complexes, due to the stronger metal-ligand bond and weaker bonds within the ligands, as a result, the ligand bonds breaks before metal-ligand bond. In substituted cyclopentadienyl strontium complexes, the metal-ligand bond dissociation occurs much easier due to the comparatively weaker nature of the bond and stronger intraligand interactions. We expect the combination of β-diketonate ligands with substituted cyclopentadienyl ligands can bring stability, and significantly lower the ligand dissociation energy and the carbon contamination. We selected the substituted cyclopentadiene and 2,2,6,6-tetramethyl-3,5-heptanedione (tmhdH) as ligands for synthesizing heteroleptic strontium precursors. Herein, we report synthesis of strontium complexes containing tri-isopropylcyclopentadienyl and 2,2,6,6-tetramethyl-3,5-heptanedionate as well as 1,3-di-t-butylcyclopentadienyl and 2,2,6,6-tetramethyl-3,5-heptanedionate.It has been well known that the stability of strontium complexes depends on the steric effects of the ligands and its ability to shield the central metal atom as well as metalligand bond strength. Among them, the ligand's steric factor is very important in precursor chemistry to prevent the complexes from forming the oligomers that ultimately lead to low volatility. So the use of substituted cyclopentadienyl ligands with sterically bulky 2,2,6,6-tetramethyl-3,5-heptanedionate (tmhd) should provide the much needed "encapsulation" to larger alkaline earth metal. To get the desired products the reactions were carried out by substitution of iodide ions from strontium iodide (SrI 2 ) one by one, first with substituted cyclopentadienyl potassium salt and then with sodium salt of 2,2,6,6-te...