Organoaminosilanes and methods for making same
US-2015246937-A1 · Sep 3, 2015 · US
US11780859B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11780859-B2 |
| Application number | US-202217665282-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 4, 2022 |
| Priority date | Sep 27, 2013 |
| Publication date | Oct 10, 2023 |
| Grant date | Oct 10, 2023 |
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Compounds and method of preparation of Si—X and Ge—X compounds (X═N, P, As and Sb) via dehydrogenative coupling between the corresponding unsubstituted silanes and amines (including ammonia) or phosphines catalyzed by metallic catalysts is described. This new approach is based on the catalytic dehydrogenative coupling of a Si—H and a X—H moiety to form a Si—X containing compound and hydrogen gas (X═N, P, As and Sb). The process can be catalyzed by transition metal heterogenous catalysts such as Ru(0) on carbon, Pd(0) on MgO) as well as transition metal organometallic complexes that act as homogeneous catalysts. The —Si—X products produced by dehydrogenative coupling are inherently halogen free. Said compounds can be useful for the deposition of thin films by chemical vapor deposition or atomic layer deposition of Si-containing films.
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We claim: 1. A method for the synthesis of diisopropylaminodisilane comprising the steps of: a) contacting diisopropylamine and disilane in the presence of a transition metal catalyst forming a reaction mixture; b) maintaining the reaction mixture at a temperature between about 0° C. to about 300° C.; c) allowing the reaction to proceed to form diisopropylaminodisilane; and d) separating the diisopropylaminodisilane from the reaction mixture. 2. The method of claim 1 , further comprising a step of adding a solvent to the reaction mixture. 3. The method of claim 1 , wherein the transition metal catalyst is selected from the group consisting of Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Hg, Yb, U, and combinations thereof. 4. The method of claim 3 , wherein the transition metal catalyst is selected from the group consisting of Ru, Pd, Rh, Ir, Fe, Ni, Pt, Cr, Cu, Au, and combinations thereof. 5. The method of claim 4 , wherein the transition metal catalyst is selected from the group consisting of Rh, Pd, Ru, Pt, and combinations thereof. 6. The method of claim 5 , wherein the transition metal catalyst comprises Ru, Pd, Ru on a carbon support, or Pd on a MgO support. 7. The method of claim 1 , wherein the transition metal catalyst is affixed to a support comprising alumina, MgO, zeolites, carbon, Monolith cordierite, diatomaceous earth, silica gel, silica/alumina, ZrO and/or TiO2. 8. The method of claim 1 , further comprising a step of adding a catalyst promoter to the reaction. 9. The method of claim 2 , wherein the solvent comprises a solvent component selected from the group consisting of C5 to C20 linear, branched or cyclic alkanes; alkenes; chloroalkanes; arenes; heterocycles; and mixtures thereof. 10. The method of claim 2 , wherein the solvent comprises n-octadecane.
the compound comprising silicon and nitrogen · CPC title
of semiconductor materials · CPC title
deposition by cyclic CVD, e.g. ALD, ALE or pulsed CVD · CPC title
the precursor containing a compound comprising Si · CPC title
without C-silicon linkages · CPC title
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