Silicon moulding material comprising a two-stage hardening mechanism

1. Impression material with

a) at least one compound with at least two alkenyl groups as component (a),

b) at least one compound with at least one chelating group as component (b),

c) at least one organohydropolysiloxane as component (c),

d) at least one hydrosilylation catalyst as component (d) and

e) at least one compound with a chelatable metal atom as component (e),

wherein the chelating group of the component (b) exhibits no reactive groups which can react with the component (c) and/or the component (d).

2. Impression material according to claim 1 , wherein the chelating group of the compound of the component (b) is a dicarbonyl group.

3. Impression material according to claim 1 , wherein the chelating group of the component (b) exhibits no reactive groups chosen from the group consisting of hydroxylalkyl group, amino group and carboxyl group.

4. Impression material according to claim 1 or claim 2 , wherein the impression material consists of at least two components B and C, the component B comprising the components (a), (b) and (c) and the component C comprising the components (d) and (e).

5. Impression material according to claim 4 , wherein the components B and C are stable on storage for more than 3 months.

6. Impression material which can be obtained by mixing the components B and C according to claim 4 .

7. Impression material according to claim 5 , wherein, during the mixing and/or after the mixing of the components B and C, the mixture changes, in a first stage, from a relatively thin starting consistency which can pass through a mixer to a more viscous plastic phase, before it cures, in a second stage, to give its final elastic form.

8. Cured impression material, which can be obtained from an impression material according to claim 1 or claim 2 .

9. Process for the preparation of an impression of an object, an impression of which is to be taken, wherein an impression material according to claim 1 or claim 2 is used, in which, in a first step, the components (a)-(e) are mixed, in a second step, the mixture is brought into contact with a surface of an object, an impression of which is to be taken, and, subsequently, the impression is removed.

10. The process of claim 9 , characterized in that R 1 is a methyl group.

11. The process of claim 9 or 10 , characterized in that R 3 is a methylene group.

12. Impression material according to claim 1 or claim 2 , wherein the chelating group of the compound of the component (b) is a 1,3-dicarbonyl group.

13. Impression material according to claim 1 or claim 2 , wherein the compound of component (b) is as a β-dicarboxylate or β-ketoester.

14. Impression material of claim 1 or claim 2 , wherein the compounds of component (b) are compounds of the formulae

R 5 a R 1 b SiO—(SiR 1 2 O) c —(SiR 1 R 5 O) d —SiR 1 b —R 6 a

and

R 5 a R 1 b SiO—[(SiR 1 2 O) c —(SiR 1 R 5 O) d —(R 7 ) g ] h —OSiR 1 b R 5 a

with

R 1 =linear or branched alkyl, fluoroalkyl, cycloalkyl or aryl;

R 2 =linear or branched alkylene, fluoroalkylene, cycloalkylene or arylene;

R 3 =linear or branched alkylene with 1 to 10 carbon atoms, cycloalkylene or arylene;

R 4 =linear or branched alkyl, cycloalkyl, aryl, NR 1 2 , NHR 1 or alkoxy;

R 5 =R 4 —CO—R 3 f —CO—X e —R 2 —;

R 6 =R 4 —COR 3 f —CO—X e —R 2 ;

R 7 =SiR 1 2 —R 2 —X e —CO—R 3 f —CO—X e —R 2 —SiR 1 2 ;

X=O or NR 1 ; and

a=0 to 3; b=3-a; c=0 to 10 000; d=0 to 500; e=0 or 1; f=0 or 1; g=1 to 100 and h=1 to 1000.

15. Impression material according to claim 14 , wherein R 1 is a methyl group.

16. Impression material according to claim 14 , wherein R 3 is a methylene group.

17. Impression material according to claim 5 , wherein the components B and C are stable on storage for more than 6 months.

18. Impression material according to claim 17 , wherein the components B and C are stable on storage for more than 12 months.

19. Impression material according to claim 18 , wherein the components B and C are stable on storage for more than 24 months.