Siloxane nitrones and use thereof

1. Polymers, each comprising:

silicon; and

at least one nitrone group.

2. The polymers according to claim 1 ;

wherein the polymers are siloxanes.

3. The polymers according to claim 1 ;

wherein the polymers are siloxane nitrones of formula (I):

M 1 a1 M 2 a2 M 3 a3 D 1 b1 D 2 b2 D 3 b3 T c Q d   (I):

where:

M 1 =[R 1 3 SiO 1/2 ];

M 2 =[R 2 R 1 2 SiO 1/2 ];

M 3 =[R 3 R 1 2 SiO 1/2 ];

D 1 =[R 1 2 SiO 2/2 ];

D 2 =[R 1 R 2 SiO 2/2 ];

D 3 =[R 1 R 3 SiO 2/2 ];

T=[R 1 SiO 3/2 ]; and

Q=[SiO 4/2 ];

where:

a1 from 0 to 50;

a2 from 0 to 50;

a3 from 0 to 50;

b1 from 10 to 5000;

b2 from 0 to 50;

b3 from 0 to 50;

c from 0 to 50;

d from 0 to 50;

with the proviso that at least one of the indices a3 and b3 is greater than 0;

where R 1 represents independently in each occurrence identical or different linear or branched, saturated or unsaturated hydrocarbon radicals of 1 to 30 carbon atoms or aromatic hydrocarbon radicals of 6 to 30 carbon atoms;

where R 2 represents independently in each occurrence identical or different, linear or branched, saturated or unsaturated radical selected from the group consisting of

hydrocarbon radicals which may be substituted with:

one or more hydroxyl functions and/or nitrogen-bearing groups, wherein the nitrogen-bearing groups may be in the quaternary form of ammonium groups;

an epoxide group; and/or

one or more carboxyl, amino acid, betaine and/or ester groups;

aryl radicals of 6 to 30 carbon atoms;

polyoxyalkylene radicals of formula (IV):

where e is from 1 to 150;

where R 7 , R 8 , R 9 , R 10 in each occurrence are the same or different and independently represent hydrogen, monovalent alkyl radicals of 1 to 12 carbon atoms, and/or aryl radicals of 6 to 12 carbon atoms, which may optionally also be further substituted with hydroxyl, methoxy, ethoxy, methyl, and/or ethyl groups;

where R 7 and R 9 may alternatively combine to form a ring which includes the atoms to which R 7 and R 9 are bonded;

where R 8 and R 10 may alternatively combine to form a ring which includes the atoms to which R 8 and R 10 are bonded;

where R 7 and R 8 may alternatively combine to form a ring which includes the atoms to which R 7 and R 8 are bonded,

where R 9 and R 10 may combine to form a ring which includes the atoms to which R 9 and R 10 are bonded;

wherein any ring formed by R 7 and R 9 , R 8 and R 10 , R 7 and R 8 , and R 9 and R 10 may optionally also be further substituted with hydroxyl, methoxy, ethoxy, methyl, and/or ethyl groups, and/or be saturated or unsaturated,

wherein the individual fragments with the index e may differ from each other within the polyoxyalkylene radical of formula (IV) while forming a random distribution;

where R″ in each occurrence independently represents a hydrogen radical, substituted or unsubstituted C 1 -C 4 -alkyl, —C(O)NH—R I , —C(O)O—R I , or —C(O)—R III , where:

 R III represents substituted or unsubstituted C 1 -C 12 -alkyl, —CH 2 —O—R I , or substituted or unsubstituted C 6 -C 12 -aryl; and

 R I in each occurrence independently represents substituted or unsubstituted C 1 -C 12 -alkyl, substituted or unsubstituted C 6 -C 12 -aryl, or substituted or unsubstituted C 6 -C 30 -alkaryl; and

where R 3 represents independently in each occurrence identical or different radicals of formula (II):

where R 4 represents a divalent discretional organic radical bonded to the siloxane;

where R 5 represents:

hydrogen, substituted or unsubstituted C 1 -C 30 -alkyl, substituted or unsubstituted C 6 -C 30 -aryl, substituted or unsubstituted C 6 -C 30 -heteroaryl, substituted or unsubstituted C 1 -C 12 -alk-C 6 -C 12 -aryl, substituted or unsubstituted C 1 -C 30 -alkyloxy, or substituted or unsubstituted cyclic C 3 -C 30 -alkyl; or

a radical as set forth for R 4 , in which case the compositions of R 5 and R 4 need not be identical;

where R 6 represents substituted or unsubstituted C 1 -C 30 -alkyl, substituted or unsubstituted C 6 -C 30 -aryl, substituted or unsubstituted C 6 -C 30 -heteroaryl, substituted or unsubstituted C 1 -C 12 -alk-C 6 -C 12 -aryl, substituted or unsubstituted C 1 -C 30 -alkyloxy, or substituted or unsubstituted cyclic C 3 -C 30 -alkyl.

4. The polymer according to claim 3 ;

wherein:

a3=2; and

b3=0.

5. The polymer according to claim 3 ;

wherein:

a1=0,

a2=0;

a3=2;

b1=10 to 500;

b2=0;

b3=0;

c=0; and

d=0;

wherein R 1 represents a methyl group; and

wherein R 4 represents a para-substituted radical of formula (IIIa):

wherein R 5 represents a hydrogen atom and

wherein R 6 represents a methyl group.

6. A process for preparing polymers comprising silicon and at least one nitrone group, the process comprising:

reacting a polymer comprising silicon and one or more aldehyde or keto groups, with a nitrogen-monosubstituted hydroxylamine.

7. The process according to claim 6 ;

wherein the polymer is a siloxane.

8. The process according to claim 6 ;

wherein the polymer is an aldehyde-functional polysiloxane.

9. The process according to claim 8 ;

wherein the aldehyde-functional siloxane obtained by hydrosilylating an SiH-functional siloxane with a terminally olefinic aldehyde.

10. The process according to claim 6 ;

wherein the polymer is obtained by a first step comprising reacting an SiH-functional polysiloxane with an aliphatic terminally olefinic aldehyde at temperatures of 20 to 200° C. by hydrosilylation in the presence of a Karstedt catalyst; and

wherein the polymer obtained by the first step is then reacted with the nitrogen-monosubstituted hydroxylamine at temperatures of 20 to 200° C.

11. A process for preparing polymers according to claim 1 , the process comprising:

reacting a polymer comprising silicon and one or more aldehyde or keto groups, with a nitrogen-monosubstituted hydroxylamine.

12. A method of manufacturing a preparation, comprising:

adding polymers according to claim 1 in the manufacture of the preparation.

13. The method according to claim 12 ;

wherein the polymers according to claim 1 are present in the preparation in an amount of from 0.1 to 99% (w/w of, based on the preparation; and

wherein the preparation includes at least one further polymer containing double bonds and/or further functional groups.

14. The method according to claim 12 ;

wherein the preparation includes further additives selected from the group consisting essentially of:

siccatives, flow control agents, colours and/or colour pigments, wetting agents, binders, reactive diluents, surfactants, thermally activatable initiators, photoinitiators, catalysts, emollients, emulsifiers, antioxidants, hydrotropes (or polyols), solid and filler materials, pearl lustre additives, insect repellents, anti-foulants, nucleators, preservatives, optical brighteners, flame retardants, antistats, blowing agents, plasticizers/softeners, perfumes, active ingredients, care additives, superfatting agents, solvents; and viscosity modulators.

15. A preparation comprising:

the polymers according to claim 1 in an amount of from 0.1 to 99 wt % based on the preparation; and

at least one further polymer which contains double bonds and/or further functional groups.

16. The preparation according to claim 15 ;

wherein the viscosity of the preparation is below 5000 mPa·s.

17. The preparation according to claim 15 ;

wherein the preparation is a coating or a printing ink.

18. The polymers according to claim 3 ;

wherein R 2 is selected from the group consisting of:

—CH 2 —CH 2 —CH 2 —O—(CH 2 —CH 2 O—) x —(CH 2 —CH(R I )O—) y —R II ;

—CH 2 —CH 2 —O—(CH 2 —CH 2 O—) x —(CH 2 —CH(R I )O—) y —R II ;

—CH 2 —CH 2 —CH 2 —O—CH 2 —CH(OH)—CH 2 OH;

—CH 2 —CH 2 —(O) x′ —CH 2 —R IV , —CH 2 —R IV ; and

—CH 2 —CH 2 —CH 2 —O—CH 2 —C(CH 2 OH) 2 —CH 2 —CH 3 ;

where:

x is from 0 to 100;

x′ is 0 or 1;

y is from 0 to 100;

R I , R II and R III are each as defined above; and

R IV represents C 1 -C 50 -alkyl, cyclic C 1 -C 50 -alkyl.

19. The polymers according to claim 3 ;

where R 4 represents a substituted or unsubstituted, branched or unbranched C 1 -C 30 -alkylene which may also be interrupted by heteroatoms and in the case of interruption by nitrogen this nitrogen may also be quaternized, cyclic C 3 -C 30 -alkylene, substituted or unsubstituted C 1 -C 30 -alkyleneoxy, substituted or unsubstituted C 6 -C 30 -arylene, substituted or unsubstituted C 6 -C 30 -aryleneoxy, substituted or unsubstituted C 1 -C 12 -alkene-C 6 -C 12 -arylene, which may also be interrupted by heteroatoms and in the case of interruption by nitrogen this nitrogen may also be quaternized, and bear sulphates, chlorides and carboxylates, especially citrates, lactates, stearates and acetates as counter-ions.

20. The polymers according to claim 3 ;

where R 4 represents a radical of formulae IIIa to IIIi:

where nitrone is a radical of formula (II); and

where Si represents the siloxane.

21. A method of manufacturing a preparation, comprising:

adding polymers obtained according to claim 6 in the manufacture of the preparation.

22. The method according to claim 21 ;

wherein the polymers obtained according to claim 6 are present in the preparation in an amount of from 0.1 to 99% (w/w of, based on the preparation; and

wherein the preparation includes at least one further polymer containing double bonds and/or further functional groups.

23. The method according to claim 21 ;

wherein the preparation includes further additives selected from the group consisting essentially of:

siccatives, flow control agents, colours and/or colour pigments, wetting agents, binders, reactive diluents, surfactants, thermally activatable initiators, photoinitiators, catalysts, emollients, emulsifiers, antioxidants, hydrotropes (or polyols), solid and filler materials, pearl lustre additives, insect repellents, anti-foulants, nucleators, preservatives, optical brighteners, flame retardants, antistats, blowing agents, plasticizers/softeners, perfumes, active ingredients, care additives, superfatting agents, solvents; and viscosity modulators.

24. A preparation comprising:

polymers obtained according to claim 6 in an amount of from 0.1 to 99 wt % based on the preparation; and

at least one further polymer which contains double bonds and/or further functional groups.

25. The preparation according to claim 24 ;

wherein the viscosity of the preparation is below 5000 mPa·s.

26. The preparation according to claim 24 ;

wherein the preparation is a coating or a printing ink.