Patent classifications
C07F7/1872
Guanidine-Functionalized Particles and Methods of Making and Using
Guanidine-functionalized particles and methods of making and using such particles.
LITHIUM ALKYLSILICONATE COMPOSITION, COATING, AND METHOD OF MAKING SAME
A method of making a lithium alkylsiliconate composition comprising adding an alkylalkoxysilane to a first mixture comprising lithium hydroxide and water to form a second mixture comprising a lithium alkylsiliconate and an alcohol, wherein i) the mole ratio of lithium hydroxide to alkylalkoxysilane is from 0.9 to less than 1.1 and the water is from 89 to 93 mol %, or ii) the mole ratio of lithium hydroxide to alkylalkoxysilane is from 1.1 to 1.4 and the water is from greater than 93 to 99 mole %.
Guanidine-functionalized particles and methods of making and using
Guanidine-functionalized particles and methods of making and using such particles.
Polyglyoxylates, manufacture and use thereof
Self-immolative polymers degrade by an end-to-end depolymerization mechanism in response to the cleavage of a stabilizing end-cap from the polymer terminus. Examples include homopolymers, mixed polymers including block copolymers, suitable for a variety of applications. A polyglyoxylate can be end-capped or capped with a linker as in a block copolymer.
SILANE COUPLING AGENT AND METHOD OF MANUFACTURING WIRE GRID PATTERN USING THE SAME
A method of manufacturing a wire grid pattern includes providing a laminate having a base member, a metal layer disposed on the base member, a mask layer disposed on the metal layer and containing a metal oxide, an adhesive layer disposed on the mask layer, and a patterned resin layer disposed on the adhesive layer and formed by irradiation of first light; and irradiating the laminate with second light. The adhesive layer may comprise a silane coupling agent.
Alkoxysilane-functionalized allophanates
The present invention relates to alkoxysilane-functionalized allophanates, to methods for production thereof, and to the use thereof. In particular, the alkoxysilane-functionalized allophanate includes the reaction product of A) at least one alkoxysilane group-containing monourethane A) of the formula 1
R.sub.n(OR.sup.1).sub.3-nSiR.sup.2NH(CO)OR.sup.3formula 1,
where R, R.sup.1, R.sup.2 and R.sup.3 are each independently hydrocarbyl radicals having 1-8 carbon atoms, which may be linear, branched or cyclic, or else may be integrated together to form a cyclic system, and n is 0-2, and B) at least one diisocyanate B), in a molar ratio of A) to B) of 3:1 to 1.5:1.
Silane coupling agent and method of manufacturing wire grid pattern using the same
A method of manufacturing a wire grid pattern includes providing a laminate having a base member, a metal layer disposed on the base member, a mask layer disposed on the metal layer and containing a metal oxide, an adhesive layer disposed on the mask layer, and a patterned resin layer disposed on the adhesive layer and formed by irradiation of first light; and irradiating the laminate with second light. The adhesive layer may comprise a silane coupling agent.
DIRECT SYNTHESIS OF ALKOXYSILANES USING COPPER-ALUMINUM ALLOY CATALYSTS
An improved catalyzed reaction of silicon metal with alcohol is provided for the formation of alkoxysilanes, particularly trialkoxysilanes. The Direct Synthesis reaction of silicon metal and alcohol employs a catalytically effective amount of a copper-aluminum alloy as a catalyst precursor and further benefits from an effective catalyst-promoting amount of a catalyst promoter.
Versatile and functionalised intermediates for the synthesis of vitamin D and novel vitamin D derivatives
Novel intermediates for the complete synthesis of vitamin D are provided that allow a great versatility of functional groups in the final vitamin derivatives. Vitamin derivatives that are epimeric in position 3 and vitamin derivatives with a wide range of functionalities in position 18, including compounds with isotopic labelling are provided.
Fluoroalkylsilanes and coatings therefrom
Novel fluoroalkysilanes of the following formula are described; R.sub.fOCHFCF.sub.2O(CH.sub.2).sub.nSi(R).sub.xX.sub.3x, wherein R.sub.f is a perfluoroalkyl group, optionally substituted by one or more in-chain -Q-, S or NR.sup.f1-heteroatoms, where R.sub.f.sup.1 is a -perfluoroalkyl; X is a hydrolysable group; R is a C.sub.1C.sub.4 alkyl group; n is at least 3; and x is 1 to 3.