Method of forming an MT-propyl siloxane resin
US-9221848-B2 · Dec 29, 2015 · US
US10329312B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10329312-B2 |
| Application number | US-201615092953-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 7, 2016 |
| Priority date | Jul 7, 2015 |
| Publication date | Jun 25, 2019 |
| Grant date | Jun 25, 2019 |
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A silicon-containing intermediate is synthesized by reacting a lanthanum tris[bis(trialkylsilyl)amide] complex with an alkylcyclopentadiene. A lanthanum compound is synthesized by reacting the silicon-containing intermediate with a dialkylamidine-based compound.
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What is claimed is: 1. A compound of the following Chemical Formula 1: wherein R 1 is a C1-C4 linear or branched alkyl group, and each R X is independently a C1-C2 alkyl group. 2. The compound as claimed in claim 1 , wherein the compound is pure. 3. A method of forming the compound as claimed in claim 1 , the method comprising: reacting a lanthanum tris(alkylsilylamide) complex with an alkylcyclopentadiene, wherein: in the lanthanum tris(alkylsilylamide) complex, the alkyl groups are each independently a C1-C2 alkyl group, and in the alkylcyclopentadiene, the alkyl group is a C1-C4 linear or branched alkyl group. 4. The method as claimed in claim 3 , further comprising purifying the resultant of the reaction of the lanthanum tris(alkylsilylamide) complex with the alkylcyclopentadiene. 5. The method as claimed in claim 4 , wherein the purifying includes sublimation of the compound represented by Chemical Formula 1. 6. A method of manufacturing an integrated circuit (IC) device using the compound as claimed in claim 1 , the method comprising: forming a lower structure on a substrate; and forming a lanthanum-containing film on the lower structure, the lanthanum-containing film being produced by deposition of lanthanum-containing species from a composition that includes the compound represented by Chemical Formula 1 and a compound represented by the following Chemical Formula 2: wherein, in Chemical Formula 2, R 1 is a C1-C4 linear or branched alkyl group, each of R 2 and R 3 is independently a C1-C4 linear or branched alkyl group, and R 4 is hydrogen or a methyl group. 7. A synthesis method, the method comprising: synthesizing a silicon-containing intermediate of Chemical Formula 1 by reacting a lanthanum tris[bis(trialkylsilyl)amide] complex with an alkylcyclopentadiene, wherein R 1 is a C1-C4 linear or branched alkyl group, and each R X is independently a C1-C2 alkyl group; and synthesizing a lanthanum compound of Chemical Formula 2 by reacting the silicon-containing intermediate of Chemical Formula 1 with a dialkylamidine-based compound, wherein R 1 is a C1-C4 linear or branched alkyl group, each of R 2 and R 3 is independently a C1-C4 linear or branched alkyl group, and R 4 is hydrogen atom or a methyl group. 8. The method as claimed in claim 7 , wherein in the silicon-containing intermediate of Chemical Formula 1, R X is a methyl group. 9. The method as claimed in claim 7 , wherein the lanthanum compound of Chemical Formula 2 is a liquid at room temperature. 10. The method as claimed in claim 7 , wherein the dialkylamidine-based compound is formed from diisopropyl acetamidine. 11. The method as claimed in claim 7 , wherein in the lanthanum compound of Chemical Formula 2, R 1 is an ethyl group, each of R 2 and R 3 is an isopropyl group, and R 4 is a methyl group. 12. The method as claimed in claim 7 , wherein in the lanthanum compound of Chemical Formula 2, each of R 1 , R 2 , and R 3 is an isopropyl group, and R 4 is a methyl group. 13. The method as claimed in claim 7 , wherein in the lanthanum compound of Chemical Formula 2, R 1 is an isopropyl group, each of R 2 and R 3 is a t-butyl group, and R 4 is a methyl group. 14. The method as claimed in claim 7 , further comprising, before the synthesizing of the silicon-containing intermediate, synthesizing the lanthanum tris[bis(trialkylsilyl)amide] complex by reacting a lanthanum halide with a bis(trialkylsilyl)amide alkali metal salt. 15. The method as claimed in claim 14 , wherein the lanthanum halide is LaCl 3 . 16. The method as claimed in claim 14 , wherein the bis(trialkylsilyl)amide alkali metal salt includes sodium (Na), lithium (Li), or potassium (K).
characterized by the use of precursors specially adapted for ALD · CPC title
containing nitrogen {having a Si-N linkage} · CPC title
Compounds containing elements of Groups 3 or 13 of the Periodic Table · CPC title
of refractory metals or yttrium · CPC title
Liquid deposition, e.g. spin-coating, sol-gel techniques or spray coating · CPC title
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