Diterminally silanol-modified perfluoropolyether compounds of the general formula (1)

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(wherein each R.sup.1 is independently an unsubstituted divalent hydrocarbon group of 1 to 10 carbon atoms, each R.sup.2 is independently a substituted or unsubstituted monovalent hydrocarbon group of 1 to 10 carbon atoms, Rf is a perfluoropolyether group, and ‘n’ is independently at each occurrence an integer from 0 to 8) are provided. Such compounds, when reacted as an intermediate with a reactive silicon compound, afford compounds of excellent durability.

The present invention aims to provide a (meth)acrylic-modified silicone macromonomer, which may be used as a raw material for a (meth)acrylic copolymer capable of forming a coating having excellent antifouling properties and surface smoothness. A (meth)acrylic-modified silicone macromonomer of formula (b1) is provided, which has 1 to 80 branches attached to a linear polysiloxane backbone and the branch has a (poly)oxyalkylene structure of the formula —(C.sub.aH.sub.2aO).sub.b— and a (meth)acryloyl group at a terminal. The (meth)acrylic-modified silicone macromonomer is a raw material for a polymer used in an antifouling paint.

Provided herein are stationary phase compositions comprising a chromatographic surface of porous or non-porous core material comprising a surface modifier for use in chromatographic separations.

A fluorochemical surface treating agent comprising a hydrolyzable group-containing silane modified with a fluorooxyalkylene-containing polymer and/or a partial hydrolytic condensate thereof forms a water/oil repellent layer having chemical resistance and mar resistance.

Coating compositions comprising a compound having at least two cyclic carbonate groups and a siloxane group (called “carbonate compound”).

One-pot synthetic methods are disclosed for synthesizing curable, antimicrobial silsesquioxane-silica hybrids by hydrolytically co-condensing a tetraalkoxysilane with two different trialkoxysilanes. Particles are also disclosed that are substantially spherical and have an ordered lamellar internal structure. In addition, polymers prepared front the curable, antimicrobial silsesquioxane-silica hybrids and co-monomers are disclosed.

Electrolytes and electrolyte additives for energy storage devices comprising a silicon compound are disclosed. The energy storage device comprises a first electrode and a second electrode, wherein at least one of the first electrode and the second electrode is a Si-based electrode, a separator between the first electrode and the second electrode, an electrolyte, and at least one electrolyte additive selected from a silicon compound.

Embodiments in accordance with the present invention encompass compositions comprising a soluble photoacid generator, a organopalladium compound, a photosensitizer and one or more olefinic monomers which undergo vinyl addition polymerization when said composition is exposed to a suitable actinic radiation to form a substantially transparent film. The monomers employed therein have a range of optical and mechanical properties, and thus these compositions can be tailored to form films having various opto-electronic properties. Accordingly, compositions of this invention are useful in various applications, including as coatings, encapsulants, fillers, leveling agents, among others.

Silicone compounds, delivery compositions, compositions, packaged products and displays comprising such silicone compounds, and processes for making and using such benefit agent delivery compositions, compositions, packaged products and displays. Such compositions have improved deposition and retention properties that may impart improved benefit characteristics to a composition and/or situs.

Novel compositions and systems for closure of wounds are disclosed. The compositions provide devices of improved flexibility and elasticity and are readily applied to wound sites or over wound closure devices. The present invention is also directed to a novel platinum catalyst for use in such compositions. The catalyst provides for rapid curing on topical surfaces such as skin and bonds to such surfaces in about 2-5 minutes.