WO1994009011A1 - Siloxane derivatives containing quaternary ammonium groups, process for their production and their use - Google Patents

Siloxane derivatives containing quaternary ammonium groups, process for their production and their use Download PDF

Info

Publication number
WO1994009011A1
WO1994009011A1 PCT/DE1993/000955 DE9300955W WO9409011A1 WO 1994009011 A1 WO1994009011 A1 WO 1994009011A1 DE 9300955 W DE9300955 W DE 9300955W WO 9409011 A1 WO9409011 A1 WO 9409011A1
Authority
WO
WIPO (PCT)
Prior art keywords
groups
quaternary ammonium
formula
production
mutually independently
Prior art date
Application number
PCT/DE1993/000955
Other languages
German (de)
French (fr)
Inventor
Gerd Schmaucks
Andrea JÄNICKE
Original Assignee
MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. filed Critical MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V.
Publication of WO1994009011A1 publication Critical patent/WO1994009011A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04Polysiloxanes
    • C08G77/38Polysiloxanes modified by chemical after-treatment
    • C08G77/382Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
    • C08G77/392Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing sulfur
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic System
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/0834Compounds having one or more O-Si linkage
    • C07F7/0838Compounds with one or more Si-O-Si sequences
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04Polysiloxanes
    • C08G77/38Polysiloxanes modified by chemical after-treatment
    • C08G77/382Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
    • C08G77/388Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing nitrogen
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/40Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen or sulfur, e.g. silicon, metals
    • C09K19/406Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen or sulfur, e.g. silicon, metals containing silicon
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/40Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen or sulfur, e.g. silicon, metals
    • C09K19/406Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen or sulfur, e.g. silicon, metals containing silicon
    • C09K19/408Polysiloxanes

Abstract

The description relates to siloxane derivatives containing quaternary ammonium groups of general formula (I) in which Y represents mutually independently C1-C6 alkyl groups, C1-C6 alkoxy groups or phenyl groups, Z is mutually independently C1-C6 alkyl groups, C1-C6 alkoxy groups, phenyl groups or groups of formula (Y)3SiO-, in which Y has the above meanings, A and B are mutually independently quaternary ammonium groups of formula (a) in which R is mutually independently C1-C6 alkyl groups or C1-C6 alkenyl groups and Hal is Cl, Br or J, or A and B together are a quaternary ammonium group of formula (b) in which R?1 and R2¿ are mutually independently C¿1?-C6 alkyl groups or C1-C6 alkenyl groups or R?1 and R2¿ together are a group of formula (c) and Hal has the above meanings, or A and B together are a quaternary ammonium group of formula (d) in which R1 has the meanings given above and p is a number from 2 to 6, m is a number from 0 to 200, n is a number from 1 to 50 and m:n is a number from 0 to 10. Process for their production and their use as tensides and siloxane derivatives containing tertiary amino groups suitable for their production.
PCT/DE1993/000955 1992-10-09 1993-10-07 Siloxane derivatives containing quaternary ammonium groups, process for their production and their use WO1994009011A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEP4234105.1 1992-10-09
DE4234105A DE4234105C1 (en) 1992-10-09 1992-10-09 Quaternary ammonium group-containing siloxane derivatives, process for their preparation and their use

Publications (1)

Publication Number Publication Date
WO1994009011A1 true WO1994009011A1 (en) 1994-04-28

Family

ID=6470100

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/DE1993/000955 WO1994009011A1 (en) 1992-10-09 1993-10-07 Siloxane derivatives containing quaternary ammonium groups, process for their production and their use

Country Status (2)

Country Link
DE (1) DE4234105C1 (en)
WO (1) WO1994009011A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20150073069A1 (en) * 2013-09-11 2015-03-12 Evonik Industries Ag Coating composition comprising polysiloxane quats

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112592478B (en) * 2020-11-24 2022-03-25 华南农业大学 Non-permeable random copolymer containing polysiloxane, preparation method and application thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2140062A1 (en) * 1971-05-28 1973-01-12 Gen Electric
EP0276114A2 (en) * 1987-01-20 1988-07-27 Dow Corning Corporation Zwitteronic polysiloxane compositions
EP0436359A2 (en) * 1990-01-04 1991-07-10 Dow Corning Corporation Quaternary ammonium functional siloxane surfactants

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE666745A (en) * 1964-07-14 1966-01-12
US4059581A (en) * 1969-12-22 1977-11-22 Union Carbide Corporation Heterocyclic nitrogen containing siloxanes
US3658867A (en) * 1969-12-22 1972-04-25 Union Carbide Corp Ammonium and tertiary amino bis(trimethylsiloxy) siloxanes
DE3417912C1 (en) * 1984-05-15 1985-07-25 Goldschmidt Ag Th Siloxanes containing betaine groups, their production and use in cosmetic preparations
DE3422268C1 (en) * 1984-06-15 1985-07-25 Goldschmidt Ag Th Siloxanes containing betaine groups, their production and use in hair care products

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2140062A1 (en) * 1971-05-28 1973-01-12 Gen Electric
EP0276114A2 (en) * 1987-01-20 1988-07-27 Dow Corning Corporation Zwitteronic polysiloxane compositions
EP0436359A2 (en) * 1990-01-04 1991-07-10 Dow Corning Corporation Quaternary ammonium functional siloxane surfactants

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20150073069A1 (en) * 2013-09-11 2015-03-12 Evonik Industries Ag Coating composition comprising polysiloxane quats
US9353289B2 (en) * 2013-09-11 2016-05-31 Evonik Degussa Gmbh Coating composition comprising polysiloxane quats

Also Published As

Publication number Publication date
DE4234105C1 (en) 1993-10-21

Similar Documents

Publication Publication Date Title
CA2051224A1 (en) Carbamate silicon compounds as latent coupling agents and process for preparation and use
MY118065A (en) Cleaning compositions
CA2143636A1 (en) Derivatives of valproic and 2-valproenoic acid amides and use as anticonvulsants
PL344012A1 (en) Novel substituted cyclic compounds, preparation method and pharmaceutical compositions containing them
AU8017591A (en) Anionic compounds
FI922561A (en) DERIVATIVES AV 1-METHYLKARBAPENEM, DERAS FRMASTAELLNING OCH ANVAENDNING SOM ANTIBIOTIKA
EP0602254A4 (en) Polymerizable monomer, polymer thereof, and process for producing the same.
EP0340754A3 (en) Monopersulfates of amino-(poly) percarboxylic acids
EP0467662A3 (en) Liquid crystal racemic mixture, liquid crystal composition and liquid crystal element, process for manufacturing and uses thereof
EP0262806A3 (en) Organosilicon compound
EP0530369A4 (en) Crystal comprising indolinospirobenzothiopyran derivative and ring-opening isomer thereof
PL315052A1 (en) Condensed dihydropyridines, method of obtaining them, their application in producing pharmaceutic preparations and pharmaceutic preparations containing such compounds
EP0757988A4 (en) Imidazole derivative and process for producing the same
WO1994009011A1 (en) Siloxane derivatives containing quaternary ammonium groups, process for their production and their use
EP0267970A4 (en) Novel biphenyl derivatives, process for their preparation, and their use.
IL119297A (en) 2,3-Dihydroxypropyl-2-(1-oxoalkyl) amino-2-deoxyglucopyranosides a process for their preparation and compositions containing them
FR2672603B1 (en) PHOSPHINITE-BORANES CHIRAUX, THEIR PREPARATION AND APPLICATIONS.
IN186092B (en)
EP0709358A4 (en) Novel clathrate compound, process for producing the same, and antifouling agent
MY106839A (en) Carboxylate compounds, liquid crystal compositions containing said compounds and liquid crystal elements.
YU25699A (en) Novel erythromycin derivatives, method for preparing them and their use
EP0508623A3 (en) Peroxyacids
YU222490A (en) BENZOXAZINE PAINTS
IL91806A0 (en) Pyrazolines,compositions containing them and their use for controlling arthropods
DE69411783T2 (en) Process for the preparation of sulfonylurea derivatives

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): JP US

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LU MC NL PT SE

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
121 Ep: the epo has been informed by wipo that ep was designated in this application
122 Ep: pct application non-entry in european phase