Area selective carbon-based film deposition
US-2024234127-A1 · Jul 11, 2024 · US
US10092927B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10092927-B2 |
| Application number | US-51383107-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 13, 2007 |
| Priority date | Nov 13, 2006 |
| Publication date | Oct 9, 2018 |
| Grant date | Oct 9, 2018 |
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Ultrathin layers of organic polymers or organic-inorganic hybrid polymers are deposited onto a substrate using molecular layer deposition methods. The process uses vapor phase materials which contain a first functional group and react only monofunctionally at the surface to add a unit to the polymer chain. The vapor phase reactant in addition has a second functional group, which is different from the first functional group, or a blocked, masked or protected functional group, or else has a precursor to such a functional group.
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What is claimed is: 1. A molecular layer deposition process for forming, under appropriate reaction conditions, a layer of an organic polymer or organic-inorganic polymer onto a first hydroxyl-functionalized surface while preventing chain termination and cross-linking, comprising: reacting a cyclic azasilane comprising 2,2-dimethoxy-1,6-diaza-2-silacyclooctane with a surface hydroxyl on the first hydroxyl-functionalized surface; allowing a ring of the 2,2-dimethoxy-1,6-diaza-2-silacyclooctane to open and form a silicon-oxygen bond to the first hydroxyl-functionalized surface; allowing the opened ring of the 2,2-dimethoxy-1,6-diaza-2-silacyclooctane to unfold, thereby leaving a primary amine surface species; allowing ethylene carbonate to react with the primary amine surface species to generate a urethane linkage to the primary amine surface species, and unfold, thereby forming the layer of the organic polymer or organic-inorganic polymer having a second hydroxyl-functionalized surface. 2. The molecular layer deposition process of claim 1 , wherein the first hydroxyl-functionalized surface and the second hydroxyl-functionalized surface comprise silica. 3. A molecular layer deposition process for forming a layer of an organic polymer or organic-inorganic polymer onto a first hydroxyl-functionalized surface while preventing chain termination, comprising, under appropriate reaction conditions the steps of: allowing trimethylaluminum in the vapor phase to react with hydroxyl surface groups on the first hydroxyl-functionalized surface, thereby forming an Al—CH 3 surface species; allowing ethanolamine in the vapor phase to react with the Al—CH 3 surface species, thereby forming an Al—O—CH 2 CH 2 —NH 2 surface species; and allowing maleic anhydride in the vapor phase to react with the amine, —NH 2 , groups on the Al—O—CH 2 CH 2 —NH 2 surface species, thereby forming the layer of the organic polymer or organic-inorganic polymer having a second hydroxyl-functionalized surface. 4. A molecular layer deposition process for forming a layer of an organic polymer or organic-inorganic polymer onto a first hydroxyl-functionalized surface while preventing chain termination and cross-linking, comprising, under appropriate reaction conditions the steps of: contacting the first hydroxyl-functionalized surface with 3(1,3-dimethylbutylidene)aminopropyltriethoxysilane (PS) wherein a protecting group hides the —NH 2 functionality; allowing the PS to form a siloxane linkage to the hydroxylated surface; contacting the PS surface with water; allowing the water to react with the imine moiety on the PS, thereby removing the protecting group, releasing 4-methyl-2-pentanone, and forming a surface terminated with primary amine groups; exposing the surface to an acid chloride or an acid chloride precursor, which bonds to the surface with an amide linkage, the amide linkage producing a nitrobenzyl-protected surface wherein the surface nitrobenzyl-protection group hides an underlying hydroxyl group; and exposing the surface nitrobenzyl-protection group to ultra-violet light at an appropriate wavelength and for a sufficient period of time to remove the nitrobenzyl-protection group and unmask the underlying hydroxyl group, thereby forming the layer of an organic polymer or organic-inorganic polymer having a second hydroxyl-functionalized surface.
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