Abstract: A process for preparing a storage-stable silane-terminated polymer of formula (I) or (II) where D is linear or branched hydrocarbon group, A is polymer backbone selected from group, R1, R1?, R2 and R2? are each linear, branched or cyclic hydrocarbon radical having 1 to 10 carbon atoms, n is 1, 2 or 3, x and y are natural numbers between 1 and 10, G is linear or branched hydrocarbon group having 1 to 20 hydrocarbon atoms, F is linear, branched or cyclic organic radical containing no isocyanate-reactive groups, m is natural number greater than 1, E is reactive group reacting with isocyanate group and selected from group consisting of NH2, NHR4 and SH, and R4 is linear, branched or cyclic hydrocarbon radical having 1 to 10 carbon atoms.

Abstract: The use of an organocarbonate-modified prepolymer having at least an average of 1.5 carbonate, thiocarbonate, carbamate or thiocarbamate groups bonded directly to the polymer backbone each via an oxygen atom, where each of these oxygen atoms has its origin in the reaction of a primary, secondary or tertiary hydroxyl group of the polymer backbone and a reactive compound selected from the group consisting of a diorganocarbonate, a diorganothiocarbonate, a cyclic carbonate, a cyclic thiocarbonate, an N,N-diheterocyclourea derivative and an N,N-diheterocyclothiourea derivative. Also, the preparation of the alkoxysilane polymers.

Abstract: A method for producing an alkoxysilane polymer via a carbamate, thiocarbonate or carbonate-terminated prepolymer (IIIa) or (IIIb) includes reaction of a polymer backbone of formula (I) terminated with at least two amino, mercapto or hydroxyl groups and with a chloroformate of formula (IIa) or a pyrocarbonate of formula (Ilb) (I) (IIa) (IIb) (IIIa) (IIIb), wherein R1 and R3 represent a linear or branched, saturated or unsaturated alkyl or alkenyl group with 1 to 10 carbon atoms or a mono- or polycyclic aliphatic or aromatic ring system with 5 to 18 carbon atoms in the ring system, which is optionally substituted by one or more groups R2, X is oxygen or sulphur, n is 0 for a linear or branched, saturated or unsaturated alkyl or alkenyl group and is 0.1 or 2 for a mono- or polycyclic aliphatic or aromatic ring system, and A represents a polymer backbone.

Abstract: The use of an organocarbonate-modified prepolymer having at least an average of 1.5 carbonate, thiocarbonate, carbamate or thiocarbamate groups bonded directly to the polymer backbone each via an oxygen atom, where each of these oxygen atoms has its origin in the reaction of a primary, secondary or tertiary hydroxyl group of the polymer backbone and a reactive compound selected from the group consisting of a diorganocarbonate, a diorganothiocarbonate, a cyclic carbonate, a cyclic thiocarbonate, an N,N-diheterocyclourea derivative and an N,N-diheterocyclothiourea derivative. Also, the preparation of the alkoxysilane polymers.