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US4145507A Expired / Lapsed US ⏱️ 0.0 years remaining

Reaction mixtures, processes for their preparation and their use as polymerization initiators

Assignee: Bayer AG
•
Filing: 1977-07-13
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Granted: 1979-03-20
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Expires: 1997-07-13
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Abstract

Abstract Mixtures obtained by reaction of an α-arylketone or of an arylaldehyde and the equivalent amount of a base metal in an inert aprotic solvent with a di-, tri- or tetrachlorosilane or a chlorinated polyorganosilane or -siloxane work as initiators for free radical-initiated polymerization reactions.

Inventors

  • 👤 Heinrich Wolfers
  • 👤 Hans Rudolph
  • 👤 Hans J. Rosenkranz

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-02 08:31
CPC Classifications
C; C08; C08G; C08G77/00; C08G77/42; C08G77/46; C07; C07F; C07F7/00; C07F7/02; C07F7/08; C07F7/0834; C07F7/0838; C07F7/0872; C07F7/0874; C07F7/18; C07F7/1804; C08F; C08F299/00; C08F299/02; C08F299/04; C08F299/0442; C08F299/0471; C08F4/00; C08F4/42; C08G77/04; C08G77/38

Claims Analysis

Total Claims: 5
Claim 1
Independent Claim 242 words
A process for the preparation of a reaction mixture suitable as an initiator for free radical-initiated polymerisation reactions, which comprises reacting 1 mol of an α-arylketone or of an arylaldehyde of the general formula V or VI respectively ##STR11## wherein R 4 represents an aryl radical optionally substituted by C 1 -C 4 alkyl, methoxy, chlorine or fluorine, and R 6 represents an aryl radical optionally substituted by C 1 -C 4 alkyl, methoxy, chlorine or fluorine, or a C 1 -C 6 -alkyl radical optionally substituted by C 1 -C 4 alkyl, methoxy, chlorine or fluorine, or a C 5 -C 7 -cycloalkyl radical or hydrogen, and approximately the equivalent amount of a base metal in an inert aprotic solvent at -10 to +70° C. with 0.4 to 0.8 mol of a dichloro-organosilane of the general formula VII r.sup.1 r.sup.2' siCl.sub.2 (VII) or with 0.25 to 0.6 mol of a trichloro-organosilane of the general formula VIII r.sup.1 siCl.sub.3 (VIII) wherein R 1 represents a methyl, ethyl, phenyl, benzyl or chloromethyl radical, and R 2 represents a chlorine atom, a hydroxyl, methoxy, or ethoxy radical, or one of the substituents R 1 or with 0.1 to 0.7 mol of tetrachlorosilane, chlorinated polyorganosilanes or -siloxanes having a molecular weight of 150 to 3.000 until the exothermic reaction has ended, hydrolysing the reaction product, separating off the organic phase and stripping off the solvent under a pressure of between 2 and 6 mm Hg.
Claim 2
Dependent Claim 242 words
A process for the preparation of a reaction mixture suitable as an initiator for free radical-initiated polymerisation reactions, which comprises reacting 1 mol of an α-arylketone or of an arylaldehyde of the general formula V or VI respectively ##STR11## wherein R 4 represents an aryl radical optionally substituted by C 1 -C 4 alkyl, methoxy, chlorine or fluorine, and R 6 represents an aryl radical optionally substituted by C 1 -C 4 alkyl, methoxy, chlorine or fluorine, or a C 1 -C 6 -alkyl radical optionally substituted by C 1 -C 4 alkyl, methoxy, chlorine or fluorine, or a C 5 -C 7 -cycloalkyl radical or hydrogen, and approximately the equivalent amount of a base metal in an inert aprotic solvent at -10 to +70° C. with 0.4 to 0.8 mol of a dichloro-organosilane of the general formula VII r.sup.1 r.sup.2' siCl.sub.2 (VII) or with 0.25 to 0.6 mol of a trichloro-organosilane of the general formula VIII r.sup.1 siCl.sub.3 (VIII) wherein R 1 represents a methyl, ethyl, phenyl, benzyl or chloromethyl radical, and R 2 represents a chlorine atom, a hydroxyl, methoxy, or ethoxy radical, or one of the substituents R 1 or with 0.1 to 0.7 mol of tetrachlorosilane, chlorinated polyorganosilanes or -siloxanes having a molecular weight of 150 to 3.000 until the exothermic reaction has ended, hydrolysing the reaction product, separating off the organic phase and stripping off the solvent under a pressure of between 2 and 6 mm Hg.
Claim 3
Dependent Claim 11 words
Reaction mixtures producible by a process as claimed in claim 1.
Claim 4
Dependent Claim 166 words
Oligomeric silyl ethers with a molecular weight, determined as a number-average, of 500 to 5,000 of the general formula I ##STR12## wherein R 1 denotes a methyl, ethyl, phenyl, benzyl or chloromethyl radical, R 2 denotes a chlorine atom, a hydroxyl, methoxy or ethoxy radical, R 1 or A, R 3 denotes a chlorine atom, a hydroxyl radical or A, R 4 and R 5 each denote an aryl radical optionally substituted by C 1 -C 4 -alkyl, methoxy, chlorine or fluorine, R 6 and R 7 each denote either R 4 or R 5 or an alkyl radical with 1-6 C-atoms which is optionally substituted by C 1 -C 4 -alkyl, methoxy, chlorine or fluorine, or a cycloalkyl radical with 5-7 C. atoms or hydrogen, R 8 denotes hydrogen or a silyl radical of the general formula II ##STR13## and a denotes a radical of the general formula III ##STR14## the compounds of the general formula I containing one to twenty partial structures IV ##STR15##
Claim 5
Dependent Claim 166 words
Oligomeric silyl ethers with a molecular weight, determined as a number-average, of 500 to 5,000 of the general formula I ##STR12## wherein R 1 denotes a methyl, ethyl, phenyl, benzyl or chloromethyl radical, R 2 denotes a chlorine atom, a hydroxyl, methoxy or ethoxy radical, R 1 or A, R 3 denotes a chlorine atom, a hydroxyl radical or A, R 4 and R 5 each denote an aryl radical optionally substituted by C 1 -C 4 -alkyl, methoxy, chlorine or fluorine, R 6 and R 7 each denote either R 4 or R 5 or an alkyl radical with 1-6 C-atoms which is optionally substituted by C 1 -C 4 -alkyl, methoxy, chlorine or fluorine, or a cycloalkyl radical with 5-7 C. atoms or hydrogen, R 8 denotes hydrogen or a silyl radical of the general formula II ##STR13## and a denotes a radical of the general formula III ##STR14## the compounds of the general formula I containing one to twenty partial structures IV ##STR15##

References Cited (Backward Citations)

US2559342A Cited
US3048499A Cited
US3078184A Cited
US3287291A Cited
US3981898A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1982-03-19 1982-09-18 1983-03-20 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1986-03-19 1986-09-18 1987-03-20 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1990-03-19 1990-09-18 1991-03-20 $7700.00 Window Closed / Lapsed

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