EP2150577A1

EP2150577A1 - Cross-linkable masses comprising phosphorus compounds

Info

Publication number: EP2150577A1
Application number: EP08750220A
Authority: EP
Inventors: Marko Prasse
Original assignee: Wacker Chemie AG
Current assignee: Wacker Chemie AG
Priority date: 2007-05-23
Filing date: 2008-05-09
Publication date: 2010-02-10
Also published as: JP2010528138A; KR20100024941A; DE102007023932A1; US20100305263A1; WO2008141951A1; CN101679679A

Abstract

The invention relates to masses that can be cross-linked by a condensation reaction, comprising an organic polymer having at least one organyloxysilyl radical (A) and compounds (B) of the formula (I) [R4P+]s X5-, wherein X is equal to a group of the formula (II) O=PR1n (0-) m (OR2) 3-n-m, and/or the condensates thereof having one or more P-O-P bonds or a group of the formula (III) -OC (=0) R1', and the remaining radicals and indices have the meanings listed in claim 1, to a method for the production thereof, and to the use thereof.

Description

Crosslinkable compounds comprising phosphorus compounds

The invention relates to crosslinkable compositions by condensation reaction, which have phosphorus compounds, processes for their preparation and their use.

In the absence of water storable, on access of water at room temperature to elastomers vulcanizing Einkomponen- th sealing compounds are known. These products are used in large quantities, for example, in the construction industry. The basis of these blends are polymers terminated by silyl groups bearing reactive substituents such as OH groups or hydrolyzable groups such as alkoxy groups. Such compositions usually contain curing catalysts, such as tin compounds with amines and, if appropriate, acids of

phosphorus; Titanate or zirconate. Furthermore, compounds of zinc, bismuth and vanadium are mentioned. All of these catalysts have certain disadvantages. Thus, the labeling of dibutyltin compounds sharply tightened, which generally raises the demand for a substitution of tin compounds. The other known alternatives often tend to yellow, hindering the production of transparent, colorless masses. In addition, the storage stability of masses with other metals is often unsatisfactory.

The invention relates to crosslinkable compositions by condensation reaction, the organic polymer having at least one organyloxysilyl radical (A) and

Compounds (B) of the formula

, +

[R ₄ P ⁺ I ₃ X ^E : D where s is 1, 2 or 3,

R may be the same or different and is optionally substituted hydrocarbon radicals having from 1 to 40 carbon atoms,

X is a group of the formula

O = PR ¹ _n (O ^" ) _m (OR ² ) ₃ -n- _m (II)

and / or their condensates having one or more P-O-P bonds or a group of the formula

^" OC C = O) R ^{1 '} (III)

is, where

R ^{1 may be} identical or different and optionally substituted hydrocarbon radicals which may be interrupted by oxygen atoms, R ¹ may be identical or different and optionally substituted hydrocarbon radicals which may be interrupted by oxygen atoms, n is 0, 1 or 2 is m is 1, 2 or 3 and m + n is 1, 2 or 3, R ^{2 may be the} same or different and represents hydrogen atom or optionally substituted hydrocarbon radicals which may be interrupted by oxygen atoms.

Examples of R are alkyl radicals, such as the methyl, ethyl, n-propyl, iso-propyl, 1-n-butyl, 2-n-butyl, iso-butyl, tert. Butyl, n-pentyl, iso-pentyl, neo-pentyl, tert-pentyl; Hexyl radicals, such as the n-hexyl radical; Heptyl radicals, such as the n-heptyl radical; Octyl radicals, such as the n-octyl radical and iso-Oc- tyl radicals, such as the 2, 2, 4-trimethylpentyl radical; Nonyl radicals, such as the n-nonyl radical; Decyl radicals, such as the n-decyl radical; Dodecyl radicals, such as the n-dodecyl radical; Octadecyl radicals, such as the n-octadecyl radical; Cycloalkyl radicals, such as the cyclopentyl, cyclohexyl, cyclohephenyl radical and methylcyclohexyl radicals; Alkenyl radicals, such as the vinyl, 1-propenyl and the 2-propenyl radical; Aryl radicals, such as the phenyl, naphthyl, anthryl and phenanthryl radicals; Alkaryl radicals, such as o-, m-, p-tolyl radicals; Xylyl radicals and ethylphenyl radicals; and aralkyl radicals, such as the benzyl radical, the CC and the .beta.-phenylethyl radical.

Examples of halogenated radicals R are haloalkyl radicals, such as the 3, 3, 3-trifluoro-n-propyl radical, the 2, 2, 2, 2 ', 2', 2'-hexafluoroisopropyl radical, the heptafluoroisopropyl radical and haloaryl radicals, such as the o-, m- and p-chlorophenyl.

Radicals R are preferably optionally substituted hydrocarbon radicals having 1 to 20 carbon atoms, particularly preferably hydrocarbon radicals having 1 to 16 carbon atoms, in particular hydrocarbon radicals having 1 to 8 carbon atoms.

Examples of radicals R ¹ are the examples of hydrocarbon radicals given for radical R which have halogen atoms, amino groups, ether groups, ester groups, epoxy groups, mercapto groups, cyano groups, (poly) glycol radicals, groups -C (O) O ^' , - P (O) (R ') 0 ^~, -P (0) (oR') 0 ^~, -C (O) OH, -C (O) oR ', -P (O) (R') OH or - P (O) (OR ') OH may be substituted and / or which may be interrupted by oxygen atoms, where R' may each be identical or different and has a meaning given for R. Examples of radicals R ¹ are the examples given for the radical R hydrocarbon radicals, the groups by halogen atoms, amino groups, ether groups, Estergruppen, epoxy groups, mercapto groups, cyano groups, ^'(poly) glycol radicals, -C (0) 0 ^~, -P (O) (R ') 0 ^~, -P (0) (oR') 0 ^~, -C (O) OH, -C (O) oR ', -P (0) (R') OH, or -P (O) (OR ') OH may be substituted and / or which may be interrupted by oxygen atoms, where R' in each case identical or different and has a meaning given for R, such as the 4-Carbonsäurecyclohexyl-, Cyclohe- xyl-4-carbonate, O-ethylcyclohexyl-4-carbonate, 11-carboxylic acid undecyl, 11-undecanoate, O-isooctyl-11-undecanoate, lauryldiethyleneglycolate-methyl, 4-nonylphenylpentaethyleneglycolatemethyl- , Oleyletherhexaethylenglykolatmethyl- or 4-tert-butylphenyletheroligoethylenglykolatmethylrest.

Radicals R ¹ are optionally halogen atoms, amino groups, ether groups, ester groups, epoxy groups, mercapto groups, cyano groups, (poly) glycol radicals, groups -C (O) O ^" , -P (O) (R ') O ^" , -P (O) (OR ') O ^" , -C (O) OH, -C (O) OR', -P (O) (R ') OH or -P (O) (OR') OH substituted Hydrocarbon radicals having 1 to 50 carbon atoms, which may be interrupted by oxygen atoms, particularly preferably hydrocarbon radicals having 1 to 30 carbon atoms, in particular hydrocarbon radicals having 1 to 20 carbon atoms, wherein R 'may each be identical or different and has a meaning given for R meaning.

The radicals R ^{1 are} preferably halogen atoms, amino groups, ether groups, ester groups, epoxy groups, mercapto groups, cyano groups, (poly) glycol radicals, groups -C (O) O ^" , -P (O) (R ') CT, -P (O) (OR ') O ^" , -C (O) OH, -C (O) OR', -P (O) (R ') OH or -P (O) (OR') OH substituted hydrocarbon radicals having from 1 to 50 carbon atoms represented by oxygen atoms may be interrupted, particularly preferably hydrocarbon radicals having 3 to 50 carbon atoms, which may be interrupted by oxygen atoms and / or substituted by the group -C (O) OR ', -C (O) O ^" or -C (O) OH substituted in particular, hydrocarbon radicals having from 3 to 20 carbon atoms which may be interrupted by oxygen atoms and / or those containing the group -C (O) OR ', -C (O) O ^" or -C (O) OH, may be substituted, wherein R 'may be the same or different and has a meaning given for R.

Examples of radicals R ² are the examples given for radical R and the lauryl diethylene glycol ethyl, 4-nonylphenyl pentaethylene glycol ethyl, Oleyletherhexaethy- lenglykolatethyl- or 4-tert-Butylphenyletheroligo- ethylenglykolatethylrest.

Radical R ² is preferably hydrogen and optionally substituted hydrocarbon radicals having from 1 to 50 carbon atoms which may be interrupted by oxygen atoms, more preferably hydrogen, hydrocarbon radicals having from 2 to 20 carbon atoms or hydrocarbon radicals having from 1 to 40 carbon atoms are interrupted by oxygen atoms, in particular by hydrogen atom or by hydrocarbon radicals having 4 to 16 carbon atoms.

Preferably s is equal to 1 or 2, more preferably s is equal to 1.

Anion X is preferably acylate groups having 4 to 31 carbon atoms, phosphate groups having 4 to 30 carbon atoms, hydrogen phosphate groups having 2 to 15 carbon atoms, and phosphonate groups having 2 to 15 carbon atoms. to hydrogenphosphonate groups having 2 to 15 carbon atoms or to phosphinate groups having 4 to 30 carbon atoms.

More preferably, anion X is acylate groups of 6 to 25 carbon atoms, phosphate groups of 6 to 20 carbon atoms, hydrogen phosphate groups of 4 to 10 carbon atoms, phosphonate groups of 2 to 12 carbon atoms, hydrogenphosphonate groups of 2 to 12 carbon atoms, and to phosphinate groups with 6 to 24 carbon atoms.

In particular, anion X is acylate groups having 6 to 25 carbon atoms, phosphonate groups having 2 to 10 carbon atoms, hydrogenphosphonate groups having 2 to 10 carbon atoms, or phosphinate groups having 8 to 20 carbon atoms.

With very particular preference, anion X is acylate groups or phosphinate groups.

Examples of compound (B) are

Tetra-n-butylphosphonium bis (2,4,4-trimethylpentyl) phosphinate, tri-n-butylmethylphosphonium bis (2,4,4-trimethylpentyl) phosphinate, tri-n-hexyltetradecylphosphonium bis (2,4,4-trimethylpentyl ) - phosphinate,

Tetra-n-butylphosphonium octyl hydrogenphosphonate, bis (tetra-n-butylphosphonium) octylphosphonate, tetra-n-butylphosphonium vinylhydrogenphosphonate, bis (tetra-n-butylphosphonium) vinylphosphonate,

Tetra-n-butylphosphonium lauryl hydrogenphosphonate, bis (tetra-n-butylphosphonium) lauryl phosphonate, tri-n-butylmethylphosphonium octyl hydrogen phosphonate, Bis (tri-n-butylmethylphosphonium) octylphosphonate, tri-n-hexyl-n-tetradecylphosphonium octyl hydrogenphosphonate, bis (tri-n-hexyl-n-tetradecylphosphonium) octylphosphonate, tetra-n-butylphosphonium bis (2-ethylhexyl) phosphate, tetra -n-butylphosphonium dioctyl phosphate,

Tri-n-butylmethylphosphonium dibutyl phosphate, triethylmethylphosphonium dibutyl phosphate, tetraphenylphosphonium dibutyl phosphate, tetra-n-butylphosphonium di (ethylethoxylate-lauryl ether) -phosphate,

Di-n-butyldimetylphosphonium dimethyl phosphate, dicyclohexyldimethylphosphonium dimethyl phosphate, diisobutyldimethylphosphonium dimethyl phosphate, tri-n-butylmethylphosphonium bis (2-ethylhexyl) phosphate, tri-n-hexyl-n-tetradecylphosphonium dioctyl phosphate, tetra-n-butylphosphonium octyl hydrogenphosphate, bis (tetra-n -butylphosphonium) octyl phosphate, tetra-n-butylphosphonium (2-ethylhexyl) hydrogen phosphate, bis (tetra-n-butylphosphonium) 2-ethylhexyl phosphate, tetra-n-butylphosphonium butyl hydrogen phosphate, bis (tetra-n-butylphosphonium) butyl phosphate, tetra-n butylphosphonium lauryl hydrogenphosphate, bis (tetra-n-butylphosphonium) lauryl phosphate, tri-n-butylmethylphosphonium octyl hydrogenphosphate, bis (tri-n-butylmethylphosphonium) octyl phosphate,

Tri-n-hexyltetradecylphosphonium octyl hydrogenphosphate, bis (tri-n-hexyltetradecylphosphonium) octylphosphate, tetra-n-butylphosphonium n-octoate, tetra-n-butylphosphonium 2-ethyl-hexanoate, tetra-n-butylphosphonium neodecanoate,

Tetra-n-butylphosphonium monomethyl-adipate, tetra-n-butylphosphonium monoisobutyl-succinate, triphenylvinylphosphonium neodecanoate, Tetraphenylphosphonium neodecanoate, tetra-n-butylphosphonium acetate,

Tetra-n-butylphosphonium glycolate ethoxylate lauryl ether, bis (tetra-n-butylphosphonium) cyclohexyl dicarbonate, tetra-n-butylphosphonium cyclohexylhydrogencarbonate, bis (tetra-n-butylphosphonium) dodecanedionate, tetra-n-butylphosphonium hydrogendodecanoate, tri-n-butylmethylphosphonium n-octoate, tetramethylphosphonium n-octoate, triethylmethylphosphonium n-octoate,

Tri-n-butylmethylphosphonium n-octoate, tri-n-hexyl-n-tetradecylphosphonium n-octoate and tri-n-hexyl-n-tetradecylphosphonium decanoate.

Preferably, compound (B) is

Tetra-n-butylphosphonium bis (2,4, 4-trimethylpentyl) phosphinate, tri-n-butylmethylphosphonium bis (2,4,4-trimethylpentyl) phosphinate, tetra-n-butylphosphonium octyl hydrogenphosphonate, bis (tetra-n-butylphosphonium ) octyl phosphonate,

Tetra-n-butylphosphonium vinylhydrogenphosphonate, bis (tetra-n-butylphosphonium) vinylphosphonate, tetra-n-butylphosphonium laurylhydrogenphosphonat, bis (tetra-n-butylphosphonium) laurylphosphonat, tri-n-butylmethylphosphonium octylhydrogenphosphonat, bis (tri-n-butylmethylphosphonium) octylphosphonat , Tetra-n-butylphosphonium bis (2-ethylhexyl) phosphate, tetra-n-butylphosphonium dioctyl phosphate, tri-n-butylmethylphosphonium dibutyl phosphate, triethylmethylphosphonium dibutyl phosphate,

Tri-n-butylmethylphosphonium bis (2-ethylhexyl) phosphate, tetra-n-butylphosphonium octyl hydrogen phosphate, bis (tetra-n-butylphosphonium) octyl phosphate, Tetra-n-butylphosphonium (2-ethylhexyl) -hydrogenphosphate, bis (tetra-n-butylphosphonium) 2-ethylhexylphosphate, tetra-n-butylphosphonium butylhydrogenphosphate, bis (tetra-n-butylphosphonium) butylphosphate, tetra-n-butylphosphonium laurylhydrogenphosphate, bis (tetra-n-butylphosphonium) lauryl phosphate, tri-n-butylmethylphosphonium octyl hydrogenphosphate, bis (tri-n-butylmethylphosphonium) octyl phosphate, tetra-n-butylphosphonium n-octoate, tetra-n-butylphosphonium 2-ethyl-hexanoate, tetra-n- butylphosphonium neodecanoate, tetra-n-butyl phosphonium monomethyl adipate, tetra-n-butyl phosphonium monoisobutyl succinate, tetra-n-butyl phosphonium glycol ethoxylate lauryl ether, bis (tetra-n-butyl phosphonium) cyclohexyl dicarbonate, tetra-n-butyl phosphonium cyclohexyl hydrogen carbonate, bis (tetra-n-butylphosphonium) dodecanedionate, tetra-n-butylphosphonium hydrogendodecanoate, tri-n-butylmethylphosphonium n-octoate, tetramethylphosphonium n-octoate,

Triethylmethylphosphonium n-octoate and

Tri-n-butylmethylphosphonium n-octoate, more preferably

Tetra-n-butylphosphonium bis (2,4,4-trimethylpentyl) phosphinate, tri-n-butylmethylphosphonium bis (2,4,4-trimethylpentyl) phosphinate,

Tetra-n-butylphosphonium octyl hydrogenphosphonate, bis (tetra-n-butylphosphonium) octylphosphonate, tri-n-butylmethylphosphonium octyl hydrogenphosphonate, bis (tri-n-butylmethylphosphonium) octylphosphonate,

Tetra-n-butylphosphonium bis (2-ethylhexyl) phosphate, tetra-n-butylphosphonium dioctyl phosphate, tri-n-butylmethylphosphonium dibutyl phosphate, Triethylmethylphosphonium dibutyl phosphate, tri-n-butylmethylphosphonium bis (2-ethylhexyl) phosphate, tetra-n-butylphosphonium octyl hydrogenphosphate, bis (tetra-n-butylphosphonium) octylphosphate, tetra-n-butylphosphonium (2-ethylhexyl) hydrogenphosphate, bis (tetra -n-butylphosphonium) 2-ethylhexyl phosphate, tetra-n-butylphosphonium butyl hydrogen phosphate, bis (tetra-n-butylphosphonium) butyl phosphate, tetra-n-butylphosphonium lauryl hydrogen phosphate, bis (tetra-n-butylphosphonium) lauryl phosphate,

Tri-n-butylmethylphosphonium octyl hydrogenphosphate, bis (tri-n-butylmethylphosphonium) octylphosphate, tetra-n-butylphosphonium n-octoate, tetra-n-butylphosphonium 2-ethylhexanoate, tetra-n-butylphosphonium neodecanoate,

Tetra-n-butylphosphonium glycolate ethoxylate lauryl ether, bis (tetra-n-butylphosphonium) cyclohexyl dicarbonate, tetra-n-butylphosphonium cyclohexylhydrogencarbonate, bis (tetra-n-butylphosphonium) dodecanedionate, tetra-n-butylphosphonium hydrogendodecanoate, tri-n-butylmethylphosphonium n octoate, tetramethylphosphonium n-octoate, triethylmethylphosphonium n-octoate and tri-n-butylmethylphosphonium n-octoate, especially

Tetra-n-butylphosphonium bis (2,4,4-trimethylpentyl) phosphinate, tri-n-butylmethylphosphonium bis (2,4,4-trimethylpentyl) phosphinate, tetra-n-butylphosphonium n-octoate, tetra-n-butylphosphonium 2-ethylhexanoate, tetra-n-butylphosphonium neodecanoate,

Tetra-n-butylphosphonium glycolate ethoxylate lauryl ether, tri-n-butylmethylphosphonium n-octoate, Tetramethylphosphonium n-octoate, triethylmethylphosphonium n-octoate and tri-n-butylmethylphosphonium n-octoate.

The component (B) used according to the invention are commercially available products or can be prepared by conventional methods in chemistry.

In the context of the present invention, organic polymers (A) are to be understood as meaning all polymers in which at least 50%, preferably at least 70%, particularly preferably at least 90%, of all bonds in the main chain are carbon-carbon, carbon-nitrogen or carbon Oxygen bonds are.

The compositions of the invention comprise component (B) in amounts of preferably 0.005 to 5 parts by weight, more preferably 0.01 to 3 parts by weight, in particular 0.05 to 2 parts by weight, in each case based on 100 parts by weight of component (A).

In addition to the components (A) and (B), the compositions according to the invention can now contain all substances which have hitherto been used in compositions crosslinkable by condensation reaction.

Preferably, the compositions according to the invention are those containing

(A) organic polymer containing at least one group of formula

have, wherein R ^{3 may be} identical or different and optionally substituted hydrocarbon radicals which may be interrupted by oxygen atoms means

R ^{4 may be} identical or different and is hydrogen or optionally substituted hydrocarbon radicals and a is 0, 1 or 2, (B) compound of formula (I), optionally (C) crosslinker, optionally

(D) plasticizer, if appropriate

(E) fillers, optionally

(F) adhesion promoter and, where appropriate

(G) additives.

Radical R ³ is preferably monovalent hydrocarbon radicals having 1 to 18 carbon atoms which are optionally substituted by halogen atoms, amino groups, ether groups, ester groups, epoxy groups, mercapto groups, cyano groups or (poly) glycol radicals, the latter being selected from oxyethylene and / or Oxypropylene units are constructed, particularly preferably to alkyl radicals having 1 to 12 carbon atoms, in particular the methyl radical. However, radical R can also be divalent radicals which, for example, link together two silyl groups.

Examples of radical R are the examples given for radical R. Examples of radicals R ⁴ are the radicals specified for R.

Radical R ⁴ is preferably hydrogen or alkyl radicals having 1 to 12 carbon atoms, particularly preferably hydrogen or alkyl radicals having 1 to 4 carbon atoms, in particular hydrogen or the methyl and ethyl radical.

Examples of component (A) are organyloxysilyl-group-containing organic polymers, such as polyacrylates, vinyl polymers, polyurethanes and polyglycols, which may be linear or branched. The preparation of these polymers can be accomplished by known methods, such as addition reactions, e.g. hydrosilylation, Michael addition, Diels-Alder addition, the addition of isocyanate to active hydrogen-reactive groups, such as amines, amides, hydroxyl or mercapto groups, as well as the addition of epoxides with amines or the copolymerization of vinyl silanes with organic Double bond monomers or the grafting of vinyl silanes to vinyl polymers. The preparation methods can optionally be combined with each other.

As component (A), however, it is also possible to use copolymers of siloxane blocks and organic polymers, such as e.g. in EP-Bl 1 370 602, which is to be included in the disclosure of the present application.

The polymers (A) used according to the invention may be homopolymers as well as copolymers, which may each be linear or branched.

Component (A) preferably has at least two groups of the formula (IV). Component (A) can be the organyloxy groups have any locations in the polymer, such as chain and / or terminal. Furthermore, the organylsiloxy groups can also be bonded to the organic polymer via one or more diorganosiloxy groups.

Component (A) is preferably organyloxysilyl-containing organic polymers which contain, as polymer chain, polyoxyalkylenes, such as polyoxyethylene, polyoxypropylene, polyoxybutylene, polyoxytetramethylene, polyoxyethylene-polyoxypropylene copolymer and polyoxypropylene-polyoxybutylene copolymer; Hydrocarbon polymers, such as polyisobutylene and copolymers of polyisobutylene with isoprene; polychloroprene; polyisoprene; polyurethanes; Polyester; polyamides; polyacrylates; Polymetacrytal; Vinyl polymer and polycarbonates included.

Component (A) is particularly preferably polyoxyalkylenes and polyacrylates, in particular polyoxyalkylenes.

If the component (A) used according to the invention is polyoxyalkylenes (Al), these preferably contain repeat units of the formula

-R-O- (V),

in which

R ^{7 may be the} same or different and is an optionally substituted divalent hydrocarbon radical having 1 to 12 carbon atoms, which may be linear or branched.

The polyoxyalkylenes (Al) used according to the invention preferably contain at least 50%, particularly preferably at least 70%, Repeating units of the formula (V), in each case based on the total number of repeating units.

In addition to the repeat units of the formula (V), the polyoxyalkylenes (Al) used according to the invention may contain further units, such as e.g. Amide, urea, urethane, thioure-, alkylene, arylene, ester, carbonate, imide or imine units.

Radical R ⁷ is preferably a divalent, optionally substituted hydrocarbon radical having 1 to 4 carbon atoms, more preferably a divalent hydrocarbon radical having 1 to 4 carbon atoms, in particular the propylene radical.

Examples of R ⁷ are -CH ₂ -, -CH ₂ -CH ₂ -, -CH ₂ -CH (CH ₃ ) -, -CH ₂ - CH ₂ -CH ₂ -, -CH ₂ -CH (-CH ₂ -CH ₃ ) -, -CH (CH ₃ ) -CH (CH ₃ ) -, -CH ₂ -CH ₂ -CH ₂ -CH ₂ - and -CH ₂ -C (CH ₃ ) ₂ -, wherein -CH ₂ -CH ₂ - and -CH ₂ -CH (CH ₃ ) - are particularly preferred, in particular -CH ₂ -CH (CH ₃ ) -.

If the organic polymers (A) used according to the invention are polyacrylates (A2), these preferably contain repeat units of the formula

-CH ₂ -C (R ⁸ ) (COOR ⁹ ) - (VI),

in which

R may be the same or different and is hydrogen or methyl and R ^{9 may be the} same or different and represents optionally substituted monovalent hydrocarbon radicals. The polyacrylates (A2) used according to the invention preferably contain at least 50%, particularly preferably at least 70%, of repeating units of the formula (VI), in each case based on the total number of repeating units.

In addition to the repeating units of the formula (VI), the polyacrylates (A2) used according to the invention may also contain further groups, such as e.g. Styrene, perfluoroethylene, maleic acid or their mono- or diester or derivatives thereof, such as maleimides, fumaric acid or their mono- or diester-,

Nitrile, vinyl ester, such as vinyl acetate or vinyl laurate, alkene, such as ethylene, propylene or octylene, conjugated Die- n-, such as butadiene or isoprene, vinyl chloride, vinyl chloride, allyl chloride or Allyl alcohol units. Following the language customary in polymer chemistry, these units are named in part according to the monomers used in the polymerization process, which is known to the person skilled in the art.

Radicals R ⁹ are preferably unsubstituted hydrocarbon radicals having 1 to 30 carbon atoms, particularly preferably 1 to 20 carbon atoms.

Examples of the repeating unit according to formula (VI) are: -CH ₂ -C (CH ₃ ) (COOCH ₃ ) -, -CH ₂ -C (CH ₃ ) (COOCH ₂ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COOCH ₂ CH ₂ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COOCH ₂ CH ₂ CH ₂ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COOCH (CH ₃ ) ₂ ) -, CH ₂ -C (H) (COOCH ₂ CH (CH ₃ ) ₂ ) -, -CH ₂ -C (H) (COOC (CH ₃ ) ₃ ) -, -CH ₂ -C (CH ₃ ) ( COO (CH ₂ ) ₄ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COO (CH ₂ ) ₅ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COO -cyclohexyl) -, -CH ₂ -C (CH ₃ ) (COO (CH ₂ ) ₆ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COO (CH ₂ ) ₇ CH ₃ ) -, -CH ₂ -C (CH ₃ ) ( COOCH ₂ CH (CH ₂ CH ₃ ) CH ₂ CH ₂ CH ₂ CH ₃ ) -,

-CH ₂ -C (CH ₃ ) (COOCH ₂ CH (CH ₃ ) CH ₂ C (CH ₃ ) ₃ ) -, -CH ₂ -C (CH ₃ ) (COO (CH ₂ ) ₈ CH ₃ ) -, - CH ₂ -C (CH ₃ ) (COO (CH ₂ ) 9 CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COO (CH ₂ ) _n CH ₃ ) -, -CH ₂ -C (CH ₃ ) ( COO (CH ₂ ) ₁₃ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COO (CH ₂ ) ₁₅ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COO (CH ₂ ) I ₇ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COOPh) -, -CH ₂ -C (CH ₃ ) (COO (CH ₂ Ph) -, -CH ₂ -C (CH ₃ ) (COOCH ₂ CH ₂ OCH ₃ ) -, -CH ₂ -C (CH ₃ ) (COOCH ₂ CH ₂ OH) -, -CH ₂ -C (CH ₃ ) (COOCH ₂ CH ₂ CH (OCH ₃ ) CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COOCH ₂ CH (OH) CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COO-glycidyl) -, CH ₂ -C (CH ₃ ) (COO-CH ₂ CH ₂ CH ₂ Si (OCH ₃ ) ₃ ) -,

-CH ₂ -C (CH ₃ ) (COO-CH ₂ CH ₂ CH ₂ Si (OCH ₃ ) ₂ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COO- (CH ₂ CH ₂ O) _x H ) -, -CH ₂ -C (CH ₃ ) (COOCF ₃ ) -,

-CH ₂ -C (CH ₃ ) (COOCH ₂ CH ₂ CF ₃ ) - and -CH ₂ -C (CH ₃ ) (COOCH ₂ CH ₂ CF ₂ CF ₃ ) -; and -CH ₂ -C (H) (COOCH ₃ ) -, -CH ₂ -C (H) (COOCH ₂ CH ₃ ) -, -CH ₂ -C (H) (COOCH ₂ CH ₂ CH ₃ ) -, - CH ₂ -C (H) (COOCH ₂ CH ₂ CH ₂ CH ₃ ) -, -CH ₂ -C (H) (COOCH (CH ₃ ) ₂ ) -, -CH ₂ -C (H) (COOCH ₂ CH ( CH ₃ ) ₂ ) -, -CH ₂ -C (H) (COOC (CH ₃ ) ₃ ) -, -CH ₂ -C (H) (COO (CH ₂ ) ₄ CH ₃ ) -, -CH ₂ -C (H) (COO (CH ₂ ) ₅ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COOCH ₂ CH ₂ OCH ₃ ) -, -CH ₂ -C (CH ₃ ) (COOCH ₂ CH ₂ OCH ₂ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COOCH ₂ CH ₂ CH (OCH ₃ ) CH ₃ ) - and -CH ₂ -C (H) (COOCH ₂ CH (CH ₂ CH ₃ ) CH ₂ CH ₂ CH ₂ CH ₃ ) -.

Particularly preferred are the repeating units -CH ₂ -

C (CH ₃ ) (COOCH ₃ ) -, -CH ₂ -C (CH ₃ ) (COOCH ₂ CH ₃ ) -,

-CH ₂ -C (CH ₃ ) (COOCH ₂ CH ₂ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COOCH ₂ CH ₂ CH ₂ CH ₃ ) -, -CH ₂ -C (CH ₃ ) ( COOCH (CH ₃ ) ₂ ) -, -CH ₂ -C (H) (COOCH ₂ CH (CH ₃ ) ₂ ) -, -CH ₂ -C (H) (COOC (CH ₃ ) ₃ ) -, -CH ₂ -C (CH ₃ ) (COO (CH ₂ ) ₄ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COO (CH ₂ ) ₅ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COO -CycloHexyl) -, -CH ₂ -C (CH ₃ ) (COO (CH ₂ ) ₆ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COO (CH ₂ ) ₇ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COOCH ₂ CH (CH ₂ CH ₃ ) CH ₂ CH ₂ CH ₂ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COOCH ₂ CH (CH ₃ ) CH ₂ C (CH ₃ ) ₃ ) -, -CH ₂ -C (CH ₃ ) (COO (CH ₂ ) ₈ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COO (CH ₂ ) 9 CH ₃ ) -, -CH ₂ - C (CH ₃ ) (COO (CH ₂ ) ₁₁ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COO (CH ₂ ) ₁₃ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COO (CH ₂ ) ₁₅ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COO (CH ₂ ) ₁₇ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COOCH ₂ CH ₂ OCH ₃ ) - and -CH ₂ -C (CH ₃ ) (COOCH ₂ CH ₂ CH (OCH ₃ ) CH ₃ ) -; and -CH ₂ -C (H) (COOCH ₃ ) -, -CH ₂ -C (H) (COOCH ₂ CH ₃ ) -, -CH ₂ -C (H) (COOCH ₂ CH ₂ CH ₃ ) -,

-CH ₂ -C (H) (COOCH ₂ CH ₂ CH ₂ CH ₃ ) -, -CH ₂ -C (H) (COOCH (CH ₃ ) ₂ ) -, -CH ₂ -C (H) (COOCH ₂ CH (CH ₃ ) ₂ ) -, -CH ₂ -C (H) (COOC (CH ₃ ) ₃ ) -, -CH ₂ -C (H) (COO (CH ₂ ) ₄ CH ₃ ) -, -CH ₂ - C (H) (COO (CH ₂ ) ₅ CH ₃ ) -, -CH ₂ -C (CH ₃ ) (COOCH ₂ CH ₂ OCH ₃ ) -, -CH ₂ -C (CH ₃ ) (COOCH ₂ CH ₂ OCH ₂ CH ₃ ) -, -CH ₂ -C (CH ₃ ) ( COOCH ₂ CH ₂ CH (OCH ₃ ) CH ₃ ) - and -CH ₂ -C (H) (COOCH ₂ CH (CH ₂ CH ₃ ) CH ₂ CH ₂ CH ₂ CH ₃ ) -.

The polymers (A) used according to the invention, more preferably the polyoxyalkylenes (Al), preferably contain units of the formula

-NR ¹⁰ -C (= O) - (VII),

in which

R ^{10 may be} identical or different and represents hydrogen atom or optionally substituted, monovalent hydrocarbon radical.

Radical R ¹⁰ is preferably hydrogen or optionally substituted hydrocarbon radicals having 1 to 12 carbon atoms, particularly preferably hydrogen or hydrocarbon radicals having 1 to 6 carbon atoms.

Component (A) has a viscosity of preferably 100 to 1,000,000 mPas, more preferably 1000 to 350,000 mPas, in each case at 25 ° C.

Organic polymers (A) are commercially available products or can be prepared by conventional methods in chemistry.

The crosslinkers (C) optionally used in the compositions according to the invention may be any known crosslinkers having at least two condensable radicals, for example silanes or siloxanes having at least two organyloxy groups. The crosslinkers (C) optionally used in the compositions according to the invention are preferably organosilicon compounds of the formula

(R ⁵ O) _b SiR ⁶ ₍₄ -b) (VIII),

in which

R ^{5 may be the} same or different and is hydrogen or a monovalent, optionally substituted hydrocarbon radical,

R ^{6 may be the} same or different and monovalent, optionally substituted hydrocarbon radicals which may be interrupted by oxygen atoms, and b is 2, 3 or 4, and their Teilhydrolysate.

The partial hydrolysates may be partial homohydrolates, i. Partial hydrolysates of one type of organosilicon compound of the formula (VIII), as well as partial cohydrolysates, i. Partial hydrolysates of at least two different types of organosilicon compounds of the formula (VIII).

If the crosslinkers (C) optionally used in the compositions according to the invention are partial hydrolyzates of organosilicon compounds of the formula (VIII), those having up to 6 silicon atoms are preferred.

Examples of radical R ⁵ are the examples mentioned above for radical R ⁴ .

Due to the often inevitable in practice contact with atmospheric moisture during the preparation and storage of the organosilicon compounds of the formula (VIII) silanol groups can arise, so R ⁵ is then the same hydrogen atom. These Si nol groups are usually not specifically produced, but will generally be detectable in practice.

Radicals R ⁵ are preferably alkyl radicals having 1 to 12 carbon atoms, particularly preferably alkyl radicals having 1 to 4 carbon atoms, in particular the methyl and ethyl radical.

Examples of radical R are the monovalent examples mentioned above for radical R, preference being given to optionally substituted hydrocarbon radicals having 1 to 12 carbon atoms and the methyl, N-cyclohexylaminomethyl, O-methyl-N-carbamatomethyl and the vinyl radical in particular are preferred.

Crosslinkers (C) which are optionally used in the compositions of the invention are particularly preferably tetramethoxysilane, tetraethoxysilane, tetrapropoxysilane, tetrabutoxysilane, methyltrimethoxysilane, methyltriethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, 3-cyanopropyltrimethoxysilane, 3-cyanoproxy pyltriethoxysilane, 3- (glycidoxy) propyltriethoxysilane, 1,2-bis (trimethoxysilyl) ethane, 1,2-bis (triethoxysilyl) ethane, (N-cyclohexylaminomethyl) methyldiethoxysilane, (N-cyclohexylaminomethyl) triethoxysilane, (N-phenylaminomethyl) methyldimethoxysilane , (Methacryloxymethyl) methyldimethoxysilane, (methacryloxymethyl) -methyldiethoxysilane, N- (trimethoxysilylmethyl) -O-methylcarbamate, methyltris (methylethylketoximo) silane, vinyltris (methylethylketoximo) silane, tetrakis- (methylethylketoximo) silane and also partial hydrolysates of said organosilicon compounds, such as Hexamethoxydisiloxane, octamethoxytrisiloxane or hexa-ethoxydisiloxane.

The crosslinkers (C) optionally used in the compositions according to the invention are commercially available products or can be prepared by processes known in silicon chemistry. If the compositions according to the invention contain crosslinkers (C), these are amounts of preferably 0.01 to 20 parts by weight, more preferably 0.5 to 10 parts by weight, in particular 1.0 to 5.0 parts by weight, based in each case on 100 parts by weight of component ( A).

Examples of plasticizers (D) are dimethylpolysiloxanes which are liquid at room temperature and endblocked by trimethylsiloxy groups, in particular having viscosities at 25 ° C. in the range from 50 to 1000 mPas, and high-boiling hydrocarbons, for example paraffin oils, dialkylbenzenes, dialkylnaphthalenes or mineral oils consisting of naphthenic and paraffinic units, polyglycols, especially polypropylene glycols, which may optionally be substituted, high-boiling esters, such as. B phthalates, citric acid esters or diesters of dicarboxylic acids, liquid polyesters, polyacrylates or polymethacrylates and alkylsulfonic acid esters.

The compositions of the invention comprise plasticizers (D) in amounts of preferably 0 to 300 parts by weight, more preferably 10 to 200 parts by weight, in particular 20 to 100 parts by weight, based in each case on 100 parts by weight of component (A).

Examples of fillers (E) are non-reinforcing fillers, ie fillers with a BET surface area of up to 50 m ² / g, such as quartz, diatomaceous earth, calcium silicate, zirconium silicate, zeolites, metal oxide powder, such as aluminum, titanium, iron or Zinc oxides or their mixed oxides, barium sulfate, calcium carbonate, gypsum, silicon nitride, silicon carbide, boron nitride, glass and plastic powders, such as polyacrylonitrile powder; reinforcing fillers, ie fillers having a BET surface area of more than 50 m ² / g, such as fumed silica, precipitated Silica, precipitated chalk, carbon black, such as furnace and acetylene black, and large BET surface area silicon-aluminum mixed oxides; fibrous fillers such as asbestos as well as plastic fibers. The fillers mentioned may be rendered hydrophobic, for example by treatment with organosilanes or siloxanes or with stearic acid or by etherification of hydroxyl groups to alkoxy groups. If fillers (E) are used, it is preferably hydrophobic fumed silica and precipitated or ground calcium carbonate.

The compositions of the invention contain fillers (E) in amounts of preferably 0 to 300 parts by weight, more preferably 1 to 200 parts by weight, in particular 5 to 200 parts by weight, based in each case on 100 parts by weight of component (A).

Examples of the adhesion promoters (F) used in the compositions according to the invention are silanes and organopolysiloxanes having functional groups, such as those having glycidoxypropyl, amino or methacryloyloxypropyl radicals, and siloxanes containing tetraalkoxysilanes and T or Q groups, which may be Alkoxgruppen may have. If, however, another component, such as component (A) or crosslinker (C), already has the said functional groups, it is possible to dispense with the addition of adhesion promoters.

The compositions of the invention comprise adhesion promoters (F) in amounts of preferably 0 to 50 parts by weight, more preferably 1 to 20 parts by weight, in particular 1 to 10 parts by weight, based in each case on 100 parts by weight of component (A).

Examples of additives (G) are pigments, dyes, fragrances, oxidation inhibitors, such as sterically hindered phenols, eg 2, 6-di-tert-butyl-4-methylphenol (BHT), products available under the trade name Irganox® 1076, Irganox® 1010, Ir- ganox® 245 or Irganox® 1135 from Ciba, Switzerland or vitamin E, fungicides, such as isothiazolinones, in particular n-2-octyl-2H-isothiazolin-3-one, n-butyl-1,2-benzisothiazolin-3 -on or 4, 5-dichloro-2-octyl-3 (2H) -isothiazolin-3-one, 3-iodo-2-propynylbutylcarbamate, thiabendazole, carbendazim, 3-benzo [b] thien-2-yl 5, 6-dihydro-l, 4, 2-oxathiazine, 4-oxides, benzothiophene-2-cyclohexylcarboxamide-S, S-dioxide, 2-thiazol-4-yl-lH-benzoimidazole, silver-containing carriers or nano-silver , Triazole derivatives, such as tebuconazole or combinations of two or three active agents, agents for influencing the electrical properties, such as conductive carbon black, flame retardants, light stabilizers, such as UV absorbers, eg benzotriazole derivatives (products available under the trade name Tinuvin® P, Tinu - vin® 213, Tinuvin® 234, Tinuvin® 327, Tinuvin® 328 or Tinuvin® 571 from Ciba, Switzerland or Uvinul® 3026, Uvinul® 3027, Uvinul® 3028, Uvinul® 3029, Uvinul ® 3033P or Uvinul® 3034 from BASF AG, Germany), nanometal oxides, for example of titanium or zinc, cyanoacrylates, for example Uvinul® 3030, Uvinul® 3035 or Uvinul® 3039 from BASF AG, Germany, benzophenones, for example Uvinul® 3008, such as radical scavengers , eg sterically hindered amines (HALS, eg Tinuvin® 622, Tinuvin® 765, Tinuvin® 770 or Tinuvin® 123 from Ciba, Switzerland or Uvinul® 4050H, Uvinul® 4077H, Uvinul® 4092H, Uvinul® 5050H, or Uvinul® 5062H from BASF AG, Germany), agents for prolonging the skin formation time, such as silanes with an SiC-bonded mercaptoalkyl radical, cell-forming agents, for example azodicarbonamide, heat stabilizers, scavengers, such as silanes or silylamides containing Si-N, cocatalysts, such as Lewis and Brönsted acids, for example sulfonic acids, organic acids, phosphoric acids, phosphonic acids and phosphonic acid monoesters and thixotropic agents, for example amide waxes, hydrogenated castor oil or polyglycols, and organic solvents, such as A Alkylaromatics, n-methylpyrrolidone, dipropylene glycol dimethyl ether or triethyl phosphate. The compositions of the invention comprise additives (G) in amounts of preferably 0.01 to 100 parts by weight, more preferably 0.05 to 30 parts by weight, in particular 0.1 to 10 parts by weight, in each case based on 100 parts by weight of component (A).

The inventive compositions are particularly preferably preparable using

(A) organic polymers containing at least one unit of the formula (IV),

(B) Compound of formula (I), optionally

(C) crosslinker of the formula (VIII), optionally (D) plasticizer, if appropriate

(E) fillers, optionally

(F) adhesion promoters, (G) additives selected from the group consisting of antioxidants, UV absorbers, sterically hindered amines and cocatalysts.

In particular, the compositions according to the invention contain no further constituents apart from the components (A) to (G).

The compositions according to the invention are preferably viscous to pasty masses.

To prepare the compositions of the invention, all components can be mixed together in any order. This mixing can be carried out at room temperature and the pressure of the surrounding atmosphere, that is about 900 to 1100 hPa. If desired, this mixing can also take place at higher temperatures, for example at temperatures in the range of 35 up to 135 ° C. Furthermore, it is possible to mix temporarily or constantly under reduced pressure, such as at 30 to 500 hPa absolute pressure, to remove volatile compounds and / or air.

The individual constituents of the compositions according to the invention may each be one type of such constituent as well as a mixture of at least two different types of such constituents.

For the crosslinking of the compositions of the invention, the usual water content of the air is sufficient. The crosslinking of the compositions of the invention is preferably carried out at room temperature. It can, if desired, also at higher or lower tempera- tures than room temperature, for example at -5 ° to 15 ° C or at 30 ° to 50 ⁰ C and / or increasing means in the moisture content of the air concentrations are carried out by water.

Preferably, the crosslinking is carried out at a pressure of 100 to 1100 hPa, in particular at the pressure of the surrounding atmosphere, that is about 900 to 1100 hPa.

Another object of the present invention are molded articles prepared by crosslinking of the inventive masses.

The compositions according to the invention can be used for all uses for which materials which are storable with the exclusion of water and can be crosslinked on admission of water at room temperature to give elastomers can be used.

The compositions according to the invention are thus excellently suitable, for example, as sealing compounds for joints, including vertically extending joints, and similar voids of, for example, 10 to 40 mm clear width, eg of buildings, land, water, and aircraft, or as adhesives or bonding compounds, for example in window construction or in the manufacture of showcases, and for example for the production of protective coatings, or slip-preventing coatings, or rubber-elastic moldings as well as for the isolation of electrical or electronic devices.

The compositions of the invention have the advantage that they are easy to prepare.

The condensation-crosslinkable compositions according to the invention have the advantage that they contain no or only extremely small amounts of heavy metal-containing compounds and are thus free of labeling and toxicologically harmless.

Furthermore, the compositions of the invention have the advantage that they do not yellow during storage and in the cured state and thus high-quality transparent products can be produced.

The crosslinkable compositions of the invention have the advantage that they are characterized by a very high storage stability and a high crosslinking rate.

In the examples described below, all viscosity data refer to a temperature of 25 ° C. Unless stated otherwise, the examples below are at a pressure of the surrounding atmosphere, ie at about 1000 hPa, and at room temperature, ie at about 23 ° C, or at a temperature, which is at room temperature without adding the reactants additional heating or cooling, and carried out at a relative humidity of about 50%. Furthermore, all parts and percentages are by weight unless otherwise indicated. Evaluation of the curing behavior Test 1:

To assess the curing behavior, the crosslinkable compositions obtained in the examples are applied to PE film in a 2 mm thick layer and stored under standard conditions (23 ° C. and 50% relative atmospheric humidity). During curing, the formation of a skin is tested every 5 min. For this purpose, a dry finger is carefully placed on the surface of the sample and pulled upwards. If the sample sticks to the finger, no skin has formed yet. If no sample sticks to the finger, a skin has formed and the time is noted. After 24 hours of curing under standard conditions (23 ° C and 50% relative humidity), the stickiness of the surface is tested. For evaluation, the dry palm is pressed onto the surface and pulled upwards. The value 1 means surface is hardly or not sticky (sample remains lying), 2 means surface is slightly sticky (sample is pulled a little bit), 3 means surface is sticky (sample is retouched and sticks).

Examples 1-7

A 40% aqueous solution of tetrabutylphosphonium hydroxide, called TBP solution (commercially available from Sigma-Aldrich, Germany) and the same molar amount of the acid shown in Table 1 were stirred and at 70 to 80 ⁰ C to a pressure distilled off the water from 15-20 mbar. It was then cooled and bottled the product. The water content of the products thus obtained, determined by means of Karl Fischer titration, was below 1.0%.

The prepared phosphorus compounds are summarized in Table 1.

Table 1

* 20% clear, colorless solution in methyltrimethoxysilane was used below.

444 g of a double-sided dimethoxymethylsily-terminated linear polypropylene glycol (commercially available under the name GENIOSIL® STP-E30 from Wacker Chemie AG, Germany), 6.0 g of a liquid stabilizer mixture consisting of about 50% of a sterically hindered amine, mainly consisting of bis (1, 2, 2, 6, 6-pentamethyl) 4-piperidyl) sebacate and methyl 1, 2, 2, 6, 6-pentamethyl-4-piperidyl sebacate, as free radical scavengers, about 35% of a benzotriazole type UV absorber, mainly consisting of 2- (2H-benzotriazole-2-) yl) 4-methyl-6-dodecylphenol and about 15% of a sterically hindered phenol, mainly consisting of C7-C9 branched alkyl [3- (3,5-di-tert-butyl-4-hydroxyphenyl)] propionate antioxidant (commercially available under the name Tinuvin B 75 from Bodo Möller Chemie GmbH, Germany), 150 g of a polypropylene glycol monohydroxy monobutyl ether having a viscosity at 50 ⁰ C of 240 mPa-s and a water content, determined by titration according to Karl Fischer, of 120 ppm and 24 g of N- (trimethoxysilylmethyl) -O-methylcarbamate (commercially available e available under the name GENIOSIL® XL 63 from Wacker Chemie AG, Germany) are mixed in a planetary mixer and stirred for 5 minutes. The mixture is then by homogeneous mixing of 80 g of fumed silica having a specific surface area of 200 m ² / g (commercially available under the name HDK® H18 from Wacker Chemie AG, Germany) and 150 g polypropylenglykol monohydroxy monobutylethers with a viscosity at 50 ⁰ C of 240 mPa-s and a water content, determined by means of Karl Fischer titration, of 120 ppm completed. Finally, the mixture is stirred for 5 minutes at about 100 mbar absolute pressure, filled airtight and stored.

In each case 50 g of the mass thus obtained was mixed with the amount of phosphorus compound given in Table 2 for a period of 1 minute at 3500 rpm in a mixer from Hauschild, Germany. Subsequently, test 1 is carried out. The results are shown in Table 2. Table 2

* as a 30% solution in methanol

Comparative Examples 1-3 (V1-V3)

A 40% aqueous solution of tetrabutylphosphonium hydroxide, called TBP solution (commercially available from Sigma-Aldrich, Germany) and the same molar amount of the acid shown in Table 3 were stirred and at 70 to 80 ⁰ C to a pressure distilled off the water from 15-20 mbar. Subsequently ^¬ ßend was cooled and the product is packaged. The Wasserge ^¬ content of the thus-obtained products, as determined by titration according to Karl-Fischer, was in each case below 1.0%. The phosphorus compounds prepared are summarized in Table 3.

Table 3

Identification of the production amount of acid amount appearance tes TBP-Lö ^¬ acid product solution [g] [g] Tetra-n-butylphosphonium 6, 9 dodecylben3, 26 yellow-braododecylbenzenesulfonate cosol- sulphonic oil

(P8) acid

Tetra-n-butyl-phosphoni- 6, 9 cyclohexylbo-1, 28 brown oil around cyclohexylhydrogenboronic acid ronate (P9)

The procedure described in Examples 1-7 is repeated with the modification that instead of the phosphorus compounds (Pl) to (P7), the compounds (P8), (P9) or tetrabutylphosphonium chloride was used.

The results are shown in Table 2.

The results in Table 2 show that the phosphonium compound fertilize (Pl) to (P7) work very well as curing catalysts. The resulting vulcanizates are transparent, colorless and remain unchanged even after 14 days of storage under a xenon UV lamp. 5 Examples 8-11

300 g of a double-sided trimethoxymethylsilyl-terminated linear polypropylene glycol (commercially available under the name GENIOSIL® STP-E35 from Wacker Chemie AG, Germany), 5.0 g of a liquid stabilizer mixture consisting of about 50% of a sterically hindered amine, consisting mainly of Bis (1, 2, 2, 6, 6-pentamethyl-4-piperidyl) sebacate and methyl 1, 2, 2, 6, 6-pentamethyl-4-piperidyl sebacate, as radical scavenger, about 35% of a UV absorber from A benzotriazole type composed mainly of 2- (2H-benzotriazol-2-yl) 4-methyl-6-5-dodecylphenol and about 15% of a hindered phenol mainly consisting of C7-C9 branched alkyl- [3- (3, 5-di-tert-butyl-4-hydroxyphenyl)] propionate as an oxidation inhibitor (commercially available under the name Tinuvin B 75 from Bodo Möller Chemie GmbH, Germany), 100 g of polypropylene glycol monohydroxy monobutyl ether having a viscosity at 50 ⁰ C of 240 mPa-s and a water content, determined by titration according to Karl Fischer, from 120 ppm, 10 g (N-aminoethyl-aminopropyl) triethoxysilane (commercially available under the name GENIOSIL® GF 94 from Wacker Chemie AG, Germany), 15 g (N- (dimethoxymethylsilylmethyl) -O-methylcarbamate (commercially available available under the name GENIOSIL® XL 65 from Wacker Chemie AG, Germany) and 10 g (3-glycidoxypropyl) trimethoxysilane (commercially available under the name GENIOSIL® GF 80 from Wacker Chemie AG, Germany) are combined in a planetary mixer The mixture is stirred for 5 minutes and the mixture is then mixed by homogeneously mixing in 30 g of fumed silica having a specific surface area of 200 m ² / g (commercially available from Be HDK® H18 at Wacker Chemie AG, Germany), 530 g of a marble powder having a mean particle diameter (D50%) of 5 μm, a carbonate content of 98%, a surface of 1.0 m ² / g and an oil number of 16 g / 100g (ISO787 / 5) completed. Finally, the mixture is stirred for 5 minutes at about 100 mbar absolute pressure, filled airtight and stored.

In each case 70 g of the mass thus obtained were mixed with the amount of phosphorus compound indicated in Table 4 for a period of 1 minute at 3500 rpm in a mixer from Hauschild, Germany. Subsequently, test 1 is carried out. The results are shown in Table 4.

Table 4

The results in Table 4 show that the phosphonium compounds (P1), (P3), (P4) and (P7) function very well as curing catalysts.

Example 12

30 g of a double-sided trimethoxymethylsilyl-terminated linear polypropylene glycol (polymer 12) (commercially available under the name GENIOSIL® STP-E35 from Wacker Chemie AG, Germany) and 0.15 g of phosphorus compound (P7) are irradiated for 1 minute at 3500 Rpm in a mixer from Hauschild, Germany. Subsequently, test 1 is carried out. The results are shown in Table 5.

Example 13

30 g of a double-sided methoxysilyl-containing linear polyurethane (polymer 13) (commercially available under the name "Polymer ST 61" at Hanse Chemie AG, Germany) and 0.15 g of phosphorus compound (P7) are for a period of 1 minute at 3500 U / min in a mixer from Hauschild,

Germany, mixed. Subsequently, test 1 is carried out. The results are shown in Table 5.

Example 14 30 g of a methoxysilyl-containing polyurethane (polymer 14) (commercially available under the name "Polymer XP ST 75" from Hanse Chemie AG, Germany) and 0.15 g of phosphorus compound (P7) are used for a duration of 1 minute at 3500 Rpm in a mixer from Hauschild, Germany, mixed. Subsequently, test 1 is carried out. The results are shown in Table 5.

Table 5

The results in Table 5 show that the phosphonium compound (P7) functions very well as a cure catalyst for various silylated organic polymers.

Claims

claims

1. Compositions crosslinkable by condensation reaction, the organic polymer having at least one organyloxysilyl radical (A) and

Compounds (B) of the formula

[R ₄ P ⁺ J ₃ X ^{s "} (I)

where s is 1, 2 or 3,

R may be the same or different and is optionally substituted hydrocarbon radicals having 1 to 40 carbon atoms, X is a group of the formula

^" OC (= 0) R ¹ Uli)

where R ^{1 may be} identical or different and optionally substituted hydrocarbon radicals which may be interrupted by oxygen atoms,

R ^{1 may be} identical or different and optionally substituted hydrocarbon radicals which may be interrupted by oxygen atoms, n is 0, 1 or 2, m is 1, 2 or 3 and m + n is 1, 2 or 3, R ^{2 may be the} same or different and is hydrogen or optionally substituted hydrocarbon radicals which may be interrupted by oxygen atoms.

2. Crosslinkable compositions according to claim 1, characterized in that the radical R is hydrocarbon radicals having 1 to 16 carbon atoms.

3. Crosslinkable compositions according to claim 1 or 2, characterized in that radicals R ¹ are optionally halogen atoms, amino groups, ether groups, ester groups, epoxy groups, mercapto groups, cyano groups, (poly) glycol groups, groups -C ( O) O ^", -P (O) (R ') Cf, -P (0) (OR') 0 ^~, -C (O) OH, -C (O) OR ',

-P (O) (R ') OH or -P (O) (OR') OH are substituted hydrocarbon radicals having 1 to 50 carbon atoms which may be interrupted by oxygen atoms.

4. Crosslinkable compositions according to one or more of claims 1 to 3, characterized in that the radical R ¹ is optionally halogen atoms, amino groups, ether groups, ester groups, epoxy groups, mercapto groups, cyano groups, (poly-Iy) glycol residues, -C (0) 0 ^" , -P (O) (R ') CT, -P (0) (OR') O ^" , -C (O) OH, -C (O) OR ', -P ( O) (R ') OH or -P (O) (OR') OH is substituted hydrocarbon radicals having 1 to 50 carbon atoms.

5. Crosslinkable compositions according to one or more of Claims 1 to 4, characterized in that anion X is acylate groups or phosphinate groups.

6. Crosslinkable compositions according to one or more of claims 1 to 5, characterized in that they are those containing (A) organic polymer containing at least one group of formula

have, wherein

R may be the same or different and is an optionally substituted hydrocarbon radical which may be interrupted by oxygen atoms, R ^{4 may be the} same or different and is hydrogen or an optionally substituted hydrocarbon radical and a is 0, 1 or 2,

(B) Compound of formula (I), optionally

(C) crosslinker, optionally

(D) plasticizer optionally (E) fillers, optionally

(F) adhesion promoter and, where appropriate

(G) additives.

7. Crosslinkable compositions according to one or more of Claims 1 to 6, characterized in that polymer (A) comprises organyloxysilyl-containing organic polymers which, as polymer chain, comprise polyoxyalkylenes, hydrocarbon polymers, polychloroprenes, polyisoprene, polyurethanes, polyesters, polyamides, Polyacrylates, polymethacrylates, vinyl polymer and polycarbonates.

8. Crosslinkable compositions according to one or more of claims 1 to 7, characterized in that component (A) is polyoxyalkylenes (Al) containing repeating units of the formula

-R-O- (V)

is, where

9. Crosslinkable compositions according to one or more of claims 1 to 8, characterized in that component (A) is polyacrylate (A2) containing repeating units of the formula

-CH ₂ -C (R ⁸ ) (COOR ⁹ ) - (VI)

are, where

R ^{8 may be the} same or different and is hydrogen or

Methyl radical means and

R ^{9 may be the} same or different and is optionally substituted, monovalent hydrocarbon radicals.

10. Shaped body produced by crosslinking of the compositions according to one or more of claims 1 to 9.