Linear and cyclic siloxanes and cosmetic compositions made thereof
US-9221952-B2 · Dec 29, 2015 · US
US2025034181A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2025034181-A1 |
| Application number | US-202418784513-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jul 25, 2024 |
| Priority date | Jul 26, 2023 |
| Publication date | Jan 30, 2025 |
| Grant date | — |
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Disclosed are Metal-containing film forming compositions comprising metal precursors having the formula M[N(R1)A(R2)(R3)(NR4R5)]a(L1)b(L2)c(L3)d. These precursors are useful as single-source precursors for depositing metal silicate via vapor deposition processes.
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What is claimed is: 1 . A chemical suitable for use as a vapor phase deposition precursor, the chemical have a formula wherein: M=a transition metal, a rare earth element (lanthanide elements, Y, Sc), an alkali metal, or an alkaline earth metal; a+b+2c=the oxidation state of the metal M; and a, b, c, d are each ≥0; A=C, Si, Ge R 1 , R 2 , R 3 , R 4 , R 5 are each independently selected from H, C 1 -C 10 branched or linear alkyl or fluoroalkyl chain; L 1 is/are −1 anionic ligands, that are typically selected from halides, —OR a , —NR a R b , amidinate group, beta diketonate, non-fluorinated dienyl group, alkyl group; with each of R a and R b being independently selected from the group consisting of H and —(CX 2 ) p CY 3 ; each X is independently H or F, each Y is independently H or F, p=0-10; L 2 is/are −2 anionic ligands, that are typically selected from imido groups ═N—R c (R c ═C 1 -C 6 linear, cyclic, or branched), diamines (e.g. R c —N—C 2 H 4 —N—R c ) or Cp linkaged amine (Cp-C x H y —N—R c ); and L 3 is/are neutral ligands or adducts, selected from 1) Oxygen based ligands: Aliphatic and aromatic—alcohols, diols, ethers, epoxides, aldehydes, ketones, carboxylic acids, enols, esters, anhydrides, phenols, substituted phenols; 2) Nitrogen based ligands: Aliphatic and aromatic—amines, imines, imides, amides, azides, cyanates, nitrile, nitrate, nitrite, nitrogen containing heterocycles; 3) Sulfur based ligands: aliphatic and aromatic—thiols, sulfides, disulfide, sulfoxide, sulfone, thiocyanates, isothiocyanates, thioesters; 4) Phosphorus based ligands: aliphatic and aromatic phosphines, phosphonic acid, phosphodiesters; 5) Boron based ligands: aliphatic and aromatic—boronic acid, boronic ester, borinic esters; 6) carbon based ligands: aliphatic-alkenes, alkynes and benzene derivatives. 7) Halide containing organic molecules, inorganic halide, e.g. 12, H 2 O vapor, H 2 gas, CO gas, CS gas, NOx gas, any radical form of gases at RT. 2 . The chemical of claim 1 , having at least one of L 1 or L 2 and at least one of L 3 . 3 . The chemical of claim 2 , wherein the least one of L 3 is covalently linked to the at least one of L 1 or L 2 . 4 . The chemical of claim 1 , wherein A is selected from Ge or Si. 5 . The chemical of claim 1 , wherein A is Si. 6 . The chemical of claim 1 , wherein the chemical is Zr[N(iPr)SiMe 2 (NMe 2 )](NMe 2 ) 3 . 7 . A composition, comprising a vapor phase of the chemical of claim 1 . 8 . The composition of claim 7 , further comprising a carrier gas, preferably comprising an inert gas selected from Helium, Nitrogen, Argon, Neon, Xenon and combinations thereof. 9 . A method of vapor phase depositing a metal silicate or a metal-germanium containing material on a surface, the method comprising: a. providing a substrate having a surface, and b. exposing the substrate to a vapor phase of the chemical of claim 1 , under conditions suitable to form a deposited material, comprising M and A, on the surface. 10 . The method of claim 9 , wherein the deposited material is a contiguous and conformal film or layer on the surface of the substrate. 11 . The method of claim 9 , further comprising exposing the surface of the substrate to a gaseous co-reactant capable of acting as a reducing agent, contemporaneously with, or subsequent to claim 14 , step b). 12 . The method of claim 11 , wherein the gaseous co-reactant is ammonia or hydrogen. 13 . The vapor phase method of claim 9 , wherein the vapor phase method is a chemical vapor phase deposition or an atomic layer deposition.
Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides · CPC title
Metallocenes · CPC title
from metallo-organic compounds · CPC title
characterized by the use of precursors specially adapted for ALD · CPC title
Cyclic compounds having at least one ring containing silicon, but no carbon in the ring · CPC title
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