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US5008422A Expired / Lapsed US ⏱️ 0.0 years remaining

Polysilazanes and related compositions, processes and uses

Assignee: SRI International Inc
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Filing: 1986-10-24
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Granted: 1991-04-16
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Expires: 2006-10-24
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Abstract

Abstract PCT No. PCT/US86/02266 Sec. 371 Date Dec. 1, 1986 Sec. 102(e) Date Dec. 1, 1986 PCT Filed Oct. 24, 1986.Silazanes and related compounds are prepared by (a) providing a precursor containing at least one Si-N bond, cleaving an Si-N bond in the precursor in the presence of hydrogen or a hydrogen donor, and reacting the cleavage product with a second cleavage product or with a compound containing an Si-H bond, an N-H bond, or both, to produce an initial silazane product having at least one newly formed Si-N bond or (b) providing one or more reactants which contain an Si-H bond and an N-H bond, and causing reaction to occur between the two bonds in the presence of a transition metal catalyst to form an initial silazane product having newly formed Si-N bonds. Further products may result from additional reaction of either type. Novel compounds, including siloxazanes and high molecular weight polysilazanes, are provided. The compounds may be pyroloyzed to yield ceramic materials such as silicon nitride, silicon carbide and silicon oxynitride. In a preferred embodiment, substantially pure silicon nitride and articles prepared therefrom are provided. Fibers coatings, binders, and the like may be prepared from the novel materials.

Inventors

  • 👤 Yigal D. Blum
  • 👤 Richard M. Laine

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-02 02:53
CPC Classifications
C; C04; C04B; C04B35/00; C04B35/515; C04B35/58; C04B35/584; C04B35/589; C04B35/01; C04B35/16; C04B35/18; C04B35/185; C04B35/56; C04B35/565; C04B35/571; C04B35/622; C04B35/626; C04B35/63; C04B35/6303; C04B35/6316; C04B41/00; C04B41/45; C04B41/4505; C04B41/455; C04B41/4554; C07; C07F; C07F7/00; C07F7/02; C07F7/08; C07F7/10; C07F7/21; C08; C08G; C08G77/00; C08G77/04; C08G77/38; C08G77/382; C08G77/398; C08G77/48; C08G77/54; C08G77/60; C08G77/62; C08G79/00

Claims Analysis

Total Claims: 13
Claim 1
Independent Claim 130 words
A method of producing polysilazanes useful as preceramic polymers and containing at least one newly formed Si--N bond which comprises: (a) providing a precursor containing at least one Si--N bond, catalytically cleaving an Si--N bond in the precursor in the presence of a transition metal catalyst effective to activate Si--N bonds, such cleavage being carried out in the presence of hydrogen or a hydrogen donor, and reacting the cleavage product to produce an initial polysilazane product; or (b) providing one or more reactants which contain an Si--H bond and an N--H bond, and causing reaction to occur between such Si--H and N--H bonds in the presence of a transition metal catalyst effective to activate Si--H and N--H bonds, to produce an initial polysilazane product having at least two Si--N bonds.
Claim 2
Independent Claim 130 words
A method of producing polysilazanes useful as preceramic polymers and containing at least one newly formed Si--N bond which comprises: (a) providing a precursor containing at least one Si--N bond, catalytically cleaving an Si--N bond in the precursor in the presence of a transition metal catalyst effective to activate Si--N bonds, such cleavage being carried out in the presence of hydrogen or a hydrogen donor, and reacting the cleavage product to produce an initial polysilazane product; or (b) providing one or more reactants which contain an Si--H bond and an N--H bond, and causing reaction to occur between such Si--H and N--H bonds in the presence of a transition metal catalyst effective to activate Si--H and N--H bonds, to produce an initial polysilazane product having at least two Si--N bonds.
Claim 3
Dependent Claim 43 words
The method of claim 1, wherein in said type (a) reaction, said initial polysilazane product results from reaction of said cleavage product is reacted with a second such cleavage product or with a compound containing an Si--H bond, an N--H bond, or both.
Claim 4
Dependent Claim 46 words
The method of claim 1, wherein a compound having an M--H bond reacts with either the cleavage product in said type (a) reaction or with a reactant in said type (b) reaction or both, wherein M is B, Al, Ga, In, Ge, Pb, Sn or S.
Claim 5
Dependent Claim 183 words
The method of claim 1, wherein the transition metal catalyst is a homogeneous catalyst selected from the group consisting of H 4 Ru 4 (CO) 12 , Fe(CO) 5 , Rh 6 (CO) 16 , Co 2 (CO) 8 , (Ph 3 P) 2 Rh(CO)H, H 2 PtCl 6 , nickel cyclooctadiene, Os 3 (CO) 12 , Ir 4 (CO) 12 , (Ph 3 P) 2 Ir(CO)H, NiCl 2 , Ni(OAc) 2 , Cp 2 TiCl 2 , (Ph 3 P) 3 RhCl, H 2 Os 3 (CO) 10 , Pd(Ph 3 P) 4 , Fe 3 (CO) 12 , Ru 3 (CO) 12 , ZnCl 2 , RuCl 3 , NaHRu 3 (CO) 11 , PdCl 2 , Pd(OAc) 2 , (φCH) 2 PdCl 2 , and mixtures thereof, or a heterogeneous catalyst selected from the group consisting of Pt/C, Pt/BaSO 4 , Cr, Pd/C, Co/C, Pt black, Co black, Ru black, Ra--Ni, Pd black, Ir/Al 2 O 3 , Pt/SiO 2 , Ru/TiO 2 , Rh/La 2 O 3 , Pd/Ag alloy, LaNi 5 , PtO 2 , and mixtures thereof.
Claim 6
Dependent Claim 14 words
The method of claim 1, wherein said transition metal catalyst is a palladium catalyst.
Claim 7
Dependent Claim 18 words
The method of claim 1, wherein the reaction temperature is between about -78° C. and about 250° C.
Claim 8
Dependent Claim 54 words
The method of claim 1, wherein the polysilazanes produced are in a tractable preceramic polymer composition having either an Mn greater than about 10,000 D, an Mw greater than about 16,000 D, an Mz greater than about 40,000 D, a polysilazane species having a molecular weight higher than about 50,000 D, or combinations thereof.
Claim 9
Independent Claim 252 words
A method of preparing silazanes and siloxazanes suitable as preceramic polymers, comprising the steps of: (a) providing a linear, branched or cyclic starting material having the structure --R' 2 Si--A-- in its molecule, in which A is hydrogen, NR, or Si and wherein said starting material is oligomeric, polymeric or copolymeric; (b) providing a transition metal catalyst effective to activate Si--N, Si--Si and/or Si--H bonds; and (c) reacting the starting material in the presence of such catalyst with (1) hydrogen or a hydrogen donor where A is NR and the starting material is part of a silazane or (2) H--X--R where A is hydrogen or Si, wherein: the R groups are independently selected from the group consisting of: hydrogen; boryl; hydrocarbyl including lower alkyl, alkenyl, alkynyl, aryl, lower alkyl substituted aryl, cycloaliphatic; silyl or polysilyl; said hydrocarbyl or silyl optionally substituted with amino, hydroxyl, an ether moiety or an ester moiety, lower alkoxy, a fused aromatic radical of 8 to 20 carbon atoms, or an organometallic radical; the R' moieties are independently selected from the group consisting of: hydrogen; amino; hydrocarbyl including lower alkyl, alkoxy, alkenyl, alkynyl, aryl, lower alkyl substituted aryl, cycloaliphatic; silyl or polysilyl; said hydrocarbyl or silyl optionally substituted with amino, hydroxyl, an ether moiety or an ester moiety, lower alkoxy, or a fused aromatic radical of 8 to 20 carbon atoms, and wherein R and R' may be part of an oligomeric or polymeric structure; and X is selected from the group consisting of NR, NR--NR, and NR--R--NR.
Claim 10
Independent Claim 252 words
A method of preparing silazanes and siloxazanes suitable as preceramic polymers, comprising the steps of: (a) providing a linear, branched or cyclic starting material having the structure --R' 2 Si--A-- in its molecule, in which A is hydrogen, NR, or Si and wherein said starting material is oligomeric, polymeric or copolymeric; (b) providing a transition metal catalyst effective to activate Si--N, Si--Si and/or Si--H bonds; and (c) reacting the starting material in the presence of such catalyst with (1) hydrogen or a hydrogen donor where A is NR and the starting material is part of a silazane or (2) H--X--R where A is hydrogen or Si, wherein: the R groups are independently selected from the group consisting of: hydrogen; boryl; hydrocarbyl including lower alkyl, alkenyl, alkynyl, aryl, lower alkyl substituted aryl, cycloaliphatic; silyl or polysilyl; said hydrocarbyl or silyl optionally substituted with amino, hydroxyl, an ether moiety or an ester moiety, lower alkoxy, a fused aromatic radical of 8 to 20 carbon atoms, or an organometallic radical; the R' moieties are independently selected from the group consisting of: hydrogen; amino; hydrocarbyl including lower alkyl, alkoxy, alkenyl, alkynyl, aryl, lower alkyl substituted aryl, cycloaliphatic; silyl or polysilyl; said hydrocarbyl or silyl optionally substituted with amino, hydroxyl, an ether moiety or an ester moiety, lower alkoxy, or a fused aromatic radical of 8 to 20 carbon atoms, and wherein R and R' may be part of an oligomeric or polymeric structure; and X is selected from the group consisting of NR, NR--NR, and NR--R--NR.
Claim 11
Dependent Claim 87 words
The method of claim 8, wherein the starting material is of the following structures, where x is an integer from 0 to 4 inclusive, y is an integer from 0 to 4 inclusive, z is an integer from 0 to 2 inclusive, the sum of x, y and z is 4, a and b are integers from 0 to 2 inclusive, the sum of a and b is 2, and m is an integer defining the number of monomer units in the oligomer, polymer or copolymer. ##STR37##
Claim 12
Dependent Claim 45 words
The method of claim 8, wherein the starting material is of the formula R' a SiH b wherein a is an integer from 0 to 2 inclusive, b is an integer from 2 to 4 inclusive, and the sum of a and b is 4.
Claim 13
Dependent Claim 26 words
The method of claim 1, wherein said reaction is of type (b), said one or more reactants includes a siloxane, and said silazane products include siloxazanes.

References Cited (Backward Citations)

US4540803A Cited
US4482689A Cited
US4668642A Cited
US4666872A Cited
US4689382A Cited
US4656300A Cited
US4675424A Cited

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