The invention relates to a process for preparing liquid, storage-stable isocyanate mixtures having carbodiimide (CD) and/or uretonimine (UI) groups or prepolymers derived therefrom, wherein (i) in a first step, a starting isocyanate which is an organic isocyanate or a mixture of two or more organic isocyanates is partly carbodiimidized with a catalyst K of the formula cyclo-C.sub.4H.sub.6P(O)R, where the substituent R is a saturated or unsaturated, optionally substituted, especially halogen-substituted, organic radical, and then (ii) in a second step, the carbodiimidization reaction is stopped at a temperature of 80 C. by adding a stopper, the stopper used being an organic silane S of the general formula H.sub.nSiX.sub.4-n, where n is a natural number in the range from 1 to 3, where X is a saturated or unsaturated, optionally substituted, especially halogen-substituted, organic radical.

The invention relates to a process for preparing liquid, storage-stable isocyanate mixtures having carbodiimide (CD) and/or uretonimine (UI) groups or prepolymers derived therefrom, wherein (i) in a first step, a starting isocyanate which is an organic isocyanate or a mixture of two or more organic isocyanates is partly carbodiimidized with a catalyst K of the formula cyclo-C.sub.4H.sub.6P(O)R, where the substituent R is a saturated or unsaturated, optionally substituted, especially halogen-substituted, organic radical, and then (ii) in a second step, the carbodiimidization reaction is stopped at a temperature of 80 C. by adding a stopper, the stopper used being an organic silane S of the general formula H.sub.nSiX.sub.4-n, where n is a natural number in the range from 1 to 3, where X is a saturated or unsaturated, optionally substituted, especially halogen-substituted, organic radical.

The invention relates to a process for preparing liquid, storage-stable isocyanate mixtures having carbodiimide (CD) and/or uretonimine (UI) groups or prepolymers derived therefrom, wherein (i) in a first step, a starting isocyanate which is an organic isocyanate or a mixture of two or more organic isocyanates is partly carbodiimidized with a catalyst K of the formula cyclo-C.sub.4H.sub.6P(O)R, where the substituent R is a saturated or unsaturated, optionally substituted, especially halogen-substituted, organic radical, and then (ii) in a second step, the carbodiimidization reaction is stopped at a temperature of 80 C. by adding a stopper, the stopper used being an organic silane S of the general formula H.sub.nSiX.sub.4-n, where n is a natural number in the range from 1 to 3, where X is a saturated or unsaturated, optionally substituted, especially halogen-substituted, organic radical.

The invention relates to a process for producing a polyisocyanate composition comprising addition of at least one isocyanate-inert solvent to at least one polyisocyanate, characterized in that the addition of the solvent is carried out in one or more stages and at least one of these stages is performed as a continuous dilution. The invention further relates to the polyisocyanate compositions obtainable by the process, to the use of the polyisocyanate compositions, to a two-component system containing the polyisocyanate composition and to composite systems produced with the two-component system.

The invention relates to a process for producing a polyisocyanate composition comprising addition of at least one isocyanate-inert solvent to at least one polyisocyanate, characterized in that the addition of the solvent is carried out in one or more stages and at least one of these stages is performed as a continuous dilution. The invention further relates to the polyisocyanate compositions obtainable by the process, to the use of the polyisocyanate compositions, to a two-component system containing the polyisocyanate composition and to composite systems produced with the two-component system.

The invention relates to a process for preparing liquid, storage-stable isocyanate mixtures having carbodiimide (CD) and/or uretonimine (UI) groups or prepolymers derived therefrom, wherein (i) in a first step, a starting isocyanate which is an organic isocyanate or a mixture of two or more organic isocyanates is partly carbodiimidized with a catalyst K of the formula cyclo-C.sub.4H.sub.6P(O)R, where the substituent R is a saturated or unsaturated, optionally substituted, especially halogen-substituted, organic radical, and then (ii) in a second step, the carbodiimidization reaction is stopped at a temperature of 80 C. by adding a stopper, the stopper used being an organic silane S of the general formula H.sub.nSiX.sub.4-n, where n is a natural number in the range from 1 to 3, where X is a saturated or unsaturated, optionally substituted, especially halogen-substituted, organic radical.

The invention relates to a process for preparing liquid, storage-stable isocyanate mixtures having carbodiimide (CD) and/or uretonimine (UI) groups or prepolymers derived therefrom, wherein (i) in a first step, a starting isocyanate which is an organic isocyanate or a mixture of two or more organic isocyanates is partly carbodiimidized with a catalyst K of the formula cyclo-C.sub.4H.sub.6P(O)R, where the substituent R is a saturated or unsaturated, optionally substituted, especially halogen-substituted, organic radical, and then (ii) in a second step, the carbodiimidization reaction is stopped at a temperature of 80 C. by adding a stopper, the stopper used being an organic silane S of the general formula H.sub.nSiX.sub.4-n, where n is a natural number in the range from 1 to 3, where X is a saturated or unsaturated, optionally substituted, especially halogen-substituted, organic radical.

The invention relates to a process for preparing liquid, storage-stable isocyanate mixtures having carbodiimide (CD) and/or uretonimine (UI) groups or prepolymers derived therefrom, wherein (i) in a first step, a starting isocyanate which is an organic isocyanate or a mixture of two or more organic isocyanates is partly carbodiimidized with a catalyst K of the formula cyclo-C.sub.4H.sub.6P(O)R, where the substituent R is a saturated or unsaturated, optionally substituted, especially halogen-substituted, organic radical, and then (ii) in a second step, the carbodiimidization reaction is stopped at a temperature of 80 C. by adding a stopper, the stopper used being an organic silane S of the general formula H.sub.nSiX.sub.4-n, where n is a natural number in the range from 1 to 3, where X is a saturated or unsaturated, optionally substituted, especially halogen-substituted, organic radical.

The present invention relates to a polyisocyanate composition comprising, on the basis of the total mass of the polyisocyanate composition, 97 mass % or more of a polyisocyanate; and 2.0 mass ppm to 1.010.sup.4 mass ppm of a compound represented by the formula (1): ##STR00001## wherein R.sup.1 is an aliphatic group having 6 to 70 carbon atoms, R.sup.2 is an aromatic ring, a is an integer of 1 to 5, b is an integer of 0 to 4, and the sum of a and b is 2 to 5.

Disclosed herein are compounds of the general Formula (I), and methods of synthesizing a substituted bicyclo[1.1.1]pentane using a Group VII or Group IX transition metal compound.