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US5008423A Expired / Lapsed US ⏱️ 0.0 years remaining

Polymeric hydridochlorosilazanes and processes for their preparation

Assignee: Hoechst AG
•
Filing: 1988-09-22
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Granted: 1991-04-16
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Expires: 2008-09-22
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Abstract

Abstract The invention relates to novel polymeric hydridochlorosilazanes and a process for their preparation. The compounds according to the invention can be converted into polyhydridosilaznes by reaction with ammonia, and these can in turn be pyrolyzed to ceramic material containing silicon nitride. To prepare the polymeric hydridochlorosilazanes, oligohydridoalkylsilazanes (R 1 SiHNH) n are reacted with a dichlorohydridoalkylsilane R 2 SiHCl 2 .

Inventors

  • 👤 Thomas Gerdau
  • 👤 Hans-Jerg Kleiner
  • 👤 Marcellus Peuckert
  • 👤 Martin Bruck
  • 👤 Fritz Aldinger

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-03 13:06
CPC Classifications
C; C07; C07F; C07F7/00; C07F7/02; C07F7/08; C07F7/10; C04; C04B; C04B35/00; C04B35/515; C04B35/58; C04B35/584; C04B35/589; C08; C08G; C08G77/00; C08G77/60; C08G77/62

Claims Analysis

Total Claims: 16
Claim 1
Independent Claim 72 words
A process for the preparation of a polymeric hydridochlorosilazane, which comprises reacting an oligohydridoalkylsilazane of the formula (R 1 SiHNH) n , in which n is 3 to 12 and R 1 denotes an alkyl group with 1 to 6 carbon atoms, with a dichlorohydridoalkylsilane of the formula R 2 SiHCL 2 , in which R 2 denotes an alkyl group having 1 to 6 carbon atoms, at 30° to 300° C.
Claim 2
Dependent Claim 72 words
A process for the preparation of a polymeric hydridochlorosilazane, which comprises reacting an oligohydridoalkylsilazane of the formula (R 1 SiHNH) n , in which n is 3 to 12 and R 1 denotes an alkyl group with 1 to 6 carbon atoms, with a dichlorohydridoalkylsilane of the formula R 2 SiHCL 2 , in which R 2 denotes an alkyl group having 1 to 6 carbon atoms, at 30° to 300° C.
Claim 3
Dependent Claim 58 words
A process for the preparation of a polymeric hydridochlorosilazane, which comprises reacting an oligohydridoalkylsilazane which has been obtained by reacting a dichlorohydridoalkylsilane R 1 SiHCL 2 with NH 3 with a dichlorohydridoalkylsilane of the formula R 2 SiHCL 2 at 30° to 300° C., R 1 and R 2 denoting alkyl groups having 1 to 6 carbon atoms.
Claim 4
Dependent Claim 58 words
A process for the preparation of a polymeric hydridochlorosilazane, which comprises reacting an oligohydridoalkylsilazane which has been obtained by reacting a dichlorohydridoalkylsilane R 1 SiHCL 2 with NH 3 with a dichlorohydridoalkylsilane of the formula R 2 SiHCL 2 at 30° to 300° C., R 1 and R 2 denoting alkyl groups having 1 to 6 carbon atoms.
Claim 5
Dependent Claim 22 words
The process as claimed in claim 1, wherein R 1 and R 2 denote alkyl groups having 1 to 3 carbon atoms.
Claim 6
Dependent Claim 15 words
The process as claimed in claim 1, wherein R 1 =R 2 =CH 3 .
Claim 7
Dependent Claim 34 words
The process as claimed in claim 1, wherein the molar ratio of dichlorohydridoalkylsilane R 2 SiHCL 2 to an R 1 SiHNH unit of the oligohydridoalkylsilazane is 0.2 : 1 to 1.5 : 1.
Claim 8
Dependent Claim 34 words
The process as claimed in claim 1, wherein a temperature of 30° to 50° C. is maintained when the reactants are brought together and the mixture is then heated to 100° to 300° C.
Claim 9
Dependent Claim 66 words
A polymeric hydridochlorosilazane of the formula ##STR3## in which the free valencies of the nitrogen atoms are saturated with H atoms or silyl radicals R*SiXN<(X=H,Cl or N<) and in which R, R', R" and R* denote alkyl groups having 1 to 6 carbon atoms and a, b and c have values ranging from 0.1 to 0.8 and denote the molar fractions of the particular structural units.
Claim 10
Dependent Claim 66 words
A polymeric hydridochlorosilazane of the formula ##STR3## in which the free valencies of the nitrogen atoms are saturated with H atoms or silyl radicals R*SiXN<(X=H,Cl or N<) and in which R, R', R" and R* denote alkyl groups having 1 to 6 carbon atoms and a, b and c have values ranging from 0.1 to 0.8 and denote the molar fractions of the particular structural units.
Claim 11
Dependent Claim 23 words
A polymeric hydridochlorosilazane as claimed in claim 7, wherein R, R', R" and R* are alkyl groups having 1 to 3 carbon atoms.
Claim 12
Dependent Claim 14 words
A polymeric hydridochlorosilazane as claimed in claim 7, wherein R =R'=R"=R* =CH 3 .
Claim 13
Dependent Claim 12 words
A polymeric hydridochlorosilazane obtainable by the process as claimed in claim 1.
Claim 14
Dependent Claim 12 words
A polymeric hydridochlorosilazane obtainable by the process as claimed in claim 2.
Claim 15
Dependent Claim 12 words
A polymeric hydridochlorosilazane obtainable by the process as claimed in claim 3.
Claim 16
Dependent Claim 12 words
A polymeric hydridochlorosilazane obtainable by the process as claimed in claim 4.

References Cited (Backward Citations)

FR1453660A Cited
US3408379A Cited
AU568050B2 Cited
US4482689A Cited
US4535007A Cited
EP0235486A1 Cited
US4806666A Cited
US4745205A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1994-04-15 1994-10-15 1995-04-16 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1998-04-15 1998-10-15 1999-04-16 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2002-04-15 2002-10-15 2003-04-16 $7700.00 Window Closed / Lapsed

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