Compositions and related methods of alkyltintrihalides
US-2023391803-A1 · Dec 7, 2023 · US
US2022153763A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2022153763-A1 |
| Application number | US-202217591007-A |
| Country | US |
| Kind code | A1 |
| Filing date | Feb 2, 2022 |
| Priority date | Jul 3, 2020 |
| Publication date | May 19, 2022 |
| Grant date | — |
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Provided is an efficient and effective process for preparing certain organotin compounds having alkyl and alkylamino substituents. The process provides the organotin compounds in a highly pure crystalline form which are particularly useful as precursors in the deposition of high-purity tin oxide films in, for example, extreme ultraviolet light (EUV) lithography techniques used in the manufacture of certain microelectronic devices.
Opening claim text (preview).
What is claimed is: 1 - 18 . (canceled) 19 . A compound of Formula (I): wherein each R is the same or different and is a C 1 -C 4 alkyl group and R 1 is a substituted or unsubstituted saturated or unsaturated linear or branched C 1 -C 5 group. 20 . The compound of claim 19 , wherein each R is independently a methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, or sec-butyl group. 21 . The compound of claim 19 , wherein each R is a methyl group. 22 . The compound of claim 19 , wherein R 1 is a methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, sec-butyl, n-pentyl, iso-pentyl, or neopentyl group. 23 . The compound of claim 19 , wherein R 1 is a vinyl group or an acetylenyl group. 24 . The compound of claim 19 , wherein R 1 is substituted with one or more halogen groups. 25 . The compound of claim 19 , wherein R 1 is an alkylether group. 26 . The compound of claim 19 , wherein each R is a methyl group and R 1 is an isopropyl group. 27 . The compound of claim 19 , wherein the compound is dissolved in a non-polar solvent. 28 . A compound of Formula (I): wherein each R is the same or different and is a C 2 -C 4 alkyl group and R 1 is a substituted or unsubstituted saturated or unsaturated linear, branched, or cyclic C 1 -C 5 group. 29 . The compound of claim 28 , wherein R 1 is a cyclic C 1 -C 5 group. 30 . The compound of claim 28 , wherein R 1 is a cyclic C 5 group. 31 . The compound of claim 28 , wherein each R is the same. 32 . The compound of claim 28 , wherein at least one R is an ethyl group. 33 . A compound of the Formula (II): wherein each R is the same or different and is a C 1 -C 4 alkyl group and X is iodo, bromo, and chloro, provided that wherein X is chloro, at least one R is other than a methyl group. 34 . The compound of claim 33 , wherein X is selected from the group consisting of iodo and bromo. 35 . The compound of claim 33 , wherein X is iodo. 36 . The compound of claim 33 , wherein each R is a methyl group and X is iodo. 37 . The compound of claim 33 , wherein each R is the same. 38 . The compound of claim 33 , wherein at least one R is a methyl group and X is chloro.
Crystalline forms, e.g. polymorphs · CPC title
Compounds with one or more Sn-N linkages · CPC title
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