Curable condensation compounds based on alkoxy-functional polysiloxanes

1. A curable condensation compound, obtained by a reaction of end-equilibrated acetoxy group-bearing siloxanes of formula (I) and/or formula (II)

with at least one alkoxy-functional polysiloxane of formula (III):

wherein R=an alkyl radical having 1 to 4 carbon atoms and/or phenyl radical,

and 1≤x≤500;

and/or

wherein R=an alkyl radical having 1 to 4 carbon atoms and/or phenyl radical,

and 0≤a≤100 and 1≤b≤10;

with

R 1 c Si(OR 2 ) d O (4-c-d)/2   Formula (III)

wherein c is not less than 0 to not more than 2, d is not less than 0 to not more than 4, and a sum total of c+d is less than 4,

R 1 is the same or different and is independently linear or branched, saturated or else mono- or polyunsaturated or aromatic hydrocarbon radicals, and

R 2 is an alkyl group comprising 1 to 8 carbon atoms; and

in the presence of a catalyst, wherein the end-equilibrated acetoxy group-bearing siloxanes of formula (I) and/or formula (II) have been neutralized,

said curable condensation compound is a liquid at ambient temperature, and said catalyst is a titanium alkoxide catalyst.

2. The condensation compound according to claim 1 , wherein the reaction includes at least one crosslinker of formula (IV):

R 3 c Si(OR 4 ) f   Formula (IV)

wherein e is not less than 0 to not more than 2, f is not less than 2 to not more than 4, and a sum total of e+f is 4,

R 3 =a saturated or unsaturated alkyl group comprising 1 to 8 carbon atoms or an aromatic moiety having 6 to 20 carbon atoms, and

R 4 =an alkyl or acyl group comprising 1 to 8 carbon atoms.

3. The condensation compound according to claim 1 , wherein the end-equilibrated acetoxy group-bearing siloxanes of formula (I) and/or formula (II) are α,ω-acetoxy group-bearing linear polydimethylsiloxanes.

4. The condensation compound according to claim 1 , wherein in the at least one alkoxy-functional polysiloxane of formula (III), R 1 =a methyl radical and/or a phenyl radical.

5. The condensation compound according to claim 1 , wherein a weight-average molecular weight of the at least one alkoxy-functional polysiloxane of formula (III) is 200 to 20,000 g/mol.

6. The condensation compound according to claim 1 , having 3 to 50% by weight of methyl and/or ethyl groups as R 2 radicals based on a total mass of compound of general formula (III).

7. The condensation compound according to claim 1 , wherein the catalyst is at least one selected from the group consisting of tetraethoxytitanium, tetra-n-propoxytitanium, tetraisopropoxytitanium, tetra-n-butoxytitanium, tetraisobutoxytitanium, tetrakis(2-ethylhexoxy)titanium, diisopropoxybis(ethylacetoacetato)titanium, dipropoxybis(acetylacetonato)titanium, diisopropoxybis(acetylacetonato)titanium, dibutoxybis(acetylacetonato)titanium, triisopropoxyallyltitanium acetate, and isopropoxyoctylene glycol-titanium oxide.

8. The condensation compound according to claim 2 , wherein the at least one crosslinker of formula (IV) is selected from the group consisting of methyltriacetoxysilane, ethyltriacetoxysilane, dimethyldiacetoxysilane, methyltrimethoxysilane, methyltriethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, tetramethoxysilane, tetraethoxysilane, phenyltriethoxysilane, phenyltrimethoxysilane, propyltrimethoxysilane, propyltriethoxysilane, dimethyldimethoxysilane, dimethyldiethoxysilane, dimethoxyphenylmethylsilane, and diethoxyphenylmethylsilane.

9. A process for preparing the condensation compound according to claim 1 , the process comprising:

reacting the end-equilibrated acetoxy group-bearing siloxanes of formula (I) and/or formula (II) with the at least one alkoxy-functional polysiloxane of formula (III), in the presence of the catalyst which is a titanium alkoxide catalyst.

10. The process according to claim 9 , wherein a weight ratio of the end-equilibrated acetoxy group-bearing siloxanes of formula (I) and/or formula (II) to the at least one alkoxy-functional polysiloxane of formula (III) is 1:99 to 99:1.

11. The process according to claim 9 , wherein the end-equilibrated acetoxy group-bearing siloxanes of formula (I) and/or formula (II) have been neutralized and optionally distilled.

12. The process according to claim 9 , wherein the end-equilibrated acetoxy group-bearing siloxanes of formula (I) and/or formula (II) are α,ω-acetoxy group-bearing linear polydimethylsiloxanes.

13. The process according to claim 9 , wherein in the at least one alkoxy-functional polysiloxane of formula (III), R 1 =a methyl radical and/or a phenyl radical.

14. The process according to claim 9 , having 3 to 50% by weight of methyl and/or ethyl groups as R 2 radicals based on a total mass of compound of general formula (III).

15. The process according to claim 9 , wherein the catalyst is at least one selected from the group consisting of tetraethoxytitanium, tetra-n-propoxytitanium, tetraisopropoxytitanium, tetra-n-butoxytitanium, tetraisobutoxytitanium, tetrakis(2-ethylhexoxy)titanium, diisopropoxybis(ethylacetoacetato)titanium, dipropoxybis(acetylacetonato)titanium, diisopropoxybis(acetylacetonato)titanium, dibutoxybis(acetylacetonato)titanium, triisopropoxyallyltitanium acetate, and isopropoxyoctylene glycol-titanium oxide.

16. The process according to claim 9 , wherein at least one crosslinker of formula (IV) is used in the reaction:

R 3 c Si(OR 4 ) f   Formula (IV)

wherein e is not less than 0 to not more than 2, f is not less than 2 to not more than 4, and a sum total of e+f is 4,

R 3 =a saturated or unsaturated alkyl group comprising 1 to 8 carbon atoms or an aromatic moiety having 6 to 20 carbon atoms, and

R 4 =an alkyl or acyl group comprising 1 to 8 carbon atoms.

17. The process according to claim 16 , wherein the at least one crosslinker of formula (IV) is selected from the group consisting of methyltriacetoxysilane, ethyltriacetoxysilane, dimethyldiacetoxysilane, methyltrimethoxysilane, methyltriethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, tetramethoxysilane, tetraethoxysilane, phenyltriethoxysilane, phenyltrimethoxysilane, propyltrimethoxysilane, propyltriethoxysilane, dimethyldimethoxysilane, dimethyldiethoxysilane, dimethoxyphenylmethylsilane, and diethoxyphenylmethylsilane.

18. The process according to claim 9 , wherein an acetic ester, formed from the R 2 radical and the acetoxy group, is removed during the reaction.

19. The process according to claim 18 , wherein the acetic ester formed is removed from the reaction by distillation and/or optionally, with application of an auxiliary vacuum.

20. The process according to claim 9 , wherein acetoxysiloxanes are reacted to completion.

21. A method of producing a coating, comprising:

mixing the condensation compound according to claim 1 into a coating, to obtain a coating having an anti-adhesive property, an anti-graffiti property, and/or an anti-fouling property.

22. A coated product, having a coating comprising the condensation compound according to claim 1 .

23. The condensation compound according to claim 1 , wherein

said end-equilibrated acetoxy group-bearing siloxane of formula (I) and/or formula (II) is an α,ω-Diacetoxysiloxane having an average siloxane chain length of 15;

said at least one alkoxy-functional polysiloxane of formula (III) is a poly(methyltrimethoxysilane); and

said catalyst is tetraisopropyl titanate.

24. The condensation compound according to claim 1 , wherein

said end-equilibrated acetoxy group-bearing siloxane of formula (I) and/or formula (II) is an α,ω-Diacetoxysiloxane having an average siloxane chain length of 10;

said at least one alkoxy-functional polysiloxane of formula (III) is a methoxy-functional phenyl(methyl)silicone resin; and

said catalyst is tetraisopropyl titanate.

25. The curable condensation compound according to claim 1 , wherein said the end-equilibrated acetoxy group-bearing siloxanes of formula (I) and/or formula (II) which has been neutralized, is the result of neutralization of a trifluoromethanesulfonic acid.

26. A coating method comprising applying the curable condensation compound according to claim 1 in the absence of a solvent, to a surface.