AMINOSILANES AND METHODS FOR MAKING SAME
Aminosilanes, such as diisopropylaminosilane (DIPAS), are precursors for the deposition of silicon containing films such as silicon-oxide and silicon-nitride films. Described herein are methods to make these aminosilanes as well as intermediate compounds such as haloaminosilane compounds having the following formula: X 4-n H n-1 SiN(CH(CH 3 ) 2 ) 2 wherein n is a number selected from 1, 2 and 3; and X is a halogen selected from Cl, Br, or a mixture of Cl and Br provided that when X is Cl, n is not 1.
1 . A haloaminosilane compound having the following formula:
X 4-n H n-1 SiN(CH(CH 3 ) 2 ) 2
wherein n is a number selected from 1, 2 and 3; and X is a halogen selected from Cl, Br, or a mixture of Cl and Br, provided that when X is Cl, n is not 1 or 2,
wherein the haloaminosilane compound is used as an intermediate for the preparation of an aminosilane compound having the following formula:
H 3 SiNR 1 R 2
wherein R 1 and R 2 are each independently selected from C 1 -C 10 linear, branched or cyclic, saturated or unsaturated, aromatic, heterocyclic, substituted or unsubstituted alkyl groups wherein R 1 and R 2 are linked to form a cyclic group or wherein R 1 and R 2 are not linked to form a cyclic group.
2 . The haloaminosilane of claim 1 wherein X is Cl.
3 . The haloaminosilane of claim 2 wherein X is Br.
4 . The haloaminosilane of claim 1 wherein X is Cl and Br.
5 . A method for making a haloaminosilane compound having the following formula:
X 4-n H n-1 SiN(CH(CH 3 ) 2 ) 2
wherein n is a number selected from 1, 2 and 3; and X is a halogen selected from Cl, Br, or a mixture of Cl and Br, provided that when X is Cl, n is not 1 or 2, the method comprising the steps of:
reacting a halosilane having the formula H n SiX 4-n wherein n is 0, 1, or 2 and X is Cl, Br, or a mixture of Cl and Br, and an amine to provide the haloaminosilane compound.
6 . The method of claim 5 wherein the reacting is conducted in the presence of a solvent.
7 . The method of claim 6 wherein the solvent is an anhydrous solvent.
8 . The method of claim 5 wherein the reacting is conducted in the absence of a solvent.
9 . A method for making an aminosilane compound having the following formula:
X 4-n H n-1 SiN(CH(CH 3 ) 2 ) 2
wherein X is a halogen selected from Cl, Br, or a mixture of Cl and Br, provided that when X is Cl, n is not 1 or 2; R 1 and R 2 are each independently selected from C 1 -C 10 linear, branched or cyclic, saturated or unsaturated, aromatic, heterocyclic, substituted or unsubstituted alkyl groups, and n is a number selected from 1, 2 and 3, the method comprising the steps of:
reacting a halosilane having the formula H n SiX 4-n wherein n is 0, 1, or 2 and X is Cl, Br, or a mixture of Cl and Br, and an amine to provide a slurry comprising a haloaminosilane compound X 4-n H n-1 SiN(CH(CH 3 ) 2 ) 2 wherein n is a number selected from 1, 2 and 3; and X is a halogen selected from Cl, Br, or a mixture of Cl and Br, provided that when X is Cl, n is not 1 or 2 and a amine-hydrohalide byproduct; and
introducing into the slurry a reducing agent wherein at least a portion of the reducing agent reacts with the haloaminosilane compound and provides an end product mixture comprising the aminosilane compound and optionally reducing agent.
10 . The method of claim 9 wherein at least a portion of the amine-hydrohalide byproduct is removed prior to the introducing step.
11 . The method of claim 10 wherein the amino-hydrohalide byproduct is removed by at least one process selected from distillation, evaporation, membrane separation, filtration, vapor phase transfer, extraction, fractional distillation, and combinations thereof.
12 . The method of claim 9 wherein the reducing agent is at least one selected from the group consisting of alkali aluminum hydride, alkali borohydride, alkali germanium hydride, alkali hydride, alkaline earth hydride, and combinations thereof.
13 . The method of claim 9 further comprising: adding a neutralizing agent to the end product mixture to remove at least a portion of reducing agent comprised therein.
14 . The method of claim 9 further comprising: removing the aminosilane compound from the end product mixture.
15 . A method for making an aminosilane compound having the following formula:
H 3 SiNR 1 R 2
wherein R 1 and R 2 are each independently selected from C 1 -C 10 linear, branched or cyclic, saturated or unsaturated, aromatic, heterocyclic, substituted or unsubstituted alkyl groups wherein R 1 and R 2 are linked to form a cyclic group or wherein R 1 and R 2 are not linked to form a cyclic group, the method comprising the steps of:
reacting a halosilane having the formula H n SiX 4-n wherein n is 0, 1, or 2 and X is Cl, Br, or a mixture of Cl and Br, and an amine to provide a slurry comprising a haloaminosilane compound X 4-n H n-1 SiN(CH(CH 3 ) 2 ) 2 wherein n is a number selected from 1, 2 and 3; and X is a halogen selected from Cl, Br, or a mixture of Cl and Br, provided that when X is Cl, n is not 1 or 2 and a amine-hydrohalide byproduct;
introducing into the slurry a reducing agent wherein at least a portion of the reducing agent reacts with the haloaminosilane compound and provides an end product mixture comprising the aminosilane compound and optionally reducing agent; and
optionally adding a neutralizing agent to the end product mixture to remove at least a portion of reducing agent comprised therein.
16 . A haloaminosilane compound having the following formula:
X 4-n H n-1 SiN(CH(CH 3 ) 2 ) 2
wherein n is a number selected from 1, 2 and 3; and X is a halogen selected from Cl, Br, or a mixture of Cl and Br, provided that when X is Cl, n is not 1 or 2.
17 . A method for making an aminosilane compound having the following formula:
H 3 SiNR 1 R 2
wherein R 1 and R 2 are each independently selected from C 1 -C 10 linear, branched or cyclic, saturated or unsaturated, aromatic, heterocyclic, substituted or unsubstituted alkyl groups wherein R 1 and R 2 are linked to form a cyclic group or wherein R 1 and R 2 are not linked to form a cyclic group, the method comprising the steps of:
reacting a halosilane comprising SiX 4 , where X═Cl, Br, or combinations thereof and an amine to provide a slurry comprising a haloaminosilane compound X 4-n H n-1 SiN(CH(CH 3 ) 2 ) 2 wherein n is a number selected from 1, 2 and 3; and X is a halogen selected from Cl, Br, or a mixture of Cl and Br, provided that when X is Cl, n is not 1 and a amine-hydrohalide byproduct; and
introducing into the slurry a reducing agent wherein at least a portion of the reducing agent reacts with the haloaminosilane compound and provides an end product mixture comprising the aminosilane compound and optionally reducing agent.
18 . The method of claim 17 wherein the molar ratio of halosilane to the amine in the reaction mixture is selected from the group consisting of 1 to 1, 1 to 2, and 1 to 2.2.
19 . The method of claim 17 wherein the amine comprises diisopropylamine.