A halosilane compound: R.sup.1CH.sub.2CH.sub.2SiR.sup.5.sub.2X is prepared by hydrosilylation reaction of a vinyl compound: R.sup.1CH═CH.sub.2 with a halogenodiorganosilane compound having formula: HSiR.sup.5.sub.2X in the co-presence of an iridium catalyst, an internal olefin compound, and an allyl halide. The halosilane compound is prepared on an industrial scale with the advantages of low costs, high yields, and high selectivity, using a small amount of iridium catalyst.

A method for producing a boron-containing compound comprises a step of reacting a first raw material compound having a carbon-carbon double bond with a second raw material compound having a conjugated diene skeleton in the presence of a metal catalyst to obtain a boron-containing compound having a 1,4-diene skeleton, wherein at least one of the first raw material compound and the second raw material compound has a boron-containing group bonded to a carbon atom constituting the carbon-carbon double bond or the conjugated diene skeleton, and the boron-containing compound has the 1,4-diene skeleton and the boron-containing group.

Provided is a catalyst which comprises a compound represented by formula (1) and which exhibits activity for at least one type of reaction selected from among hydrosilylation reaction or hydrogenation reaction with respect to an aliphatic unsaturated bond and hydrosilane reduction reaction with respect to a carbon-oxygen unsaturated bond or a carbon-nitrogen unsaturated bond. Formula (1): M.sub.n(L.sub.m) {M represents Fe, Co, or Ni having an oxidation number of 0, L represents an isocyanide ligand represented by formula (2), n denotes an integer of 1-8, and m denotes an integer of 2-12. Formula (2): (CN).sub.x—R.sup.1 (R.sup.1 represents a mono- to trivalent-organic group having 1-30 carbon atoms, optionally being substituted by a halogen atom, and optionally having interposed therein one or more atoms selected from among O, N, S, and Si; and x denotes an integer of 1-3)}.

Provided herein are a method of Ru(II)-catalyzed enantioselective synthesis of a cyclic compound and cyclic compounds formed therefrom. The method includes providing a precursor compound having an unfunctionalized C—H bond and activating the unfunctionalized C—H bond by reacting the precursor compound in the presence of co-catalysts including a Ru(II) arene complex and a chiral transient directing group (CTDG).

A moldable eraser kit includes a first silicone polymer, a second silicone polymer, an abrasive agent, a catalyst configured to catalyze a reaction between the first silicone polymer and the second silicone polymer at room temperature, and at least two containers such that the first silicone polymer, the second silicone polymer, and the catalyst are not all present in the same container. Also disclosed herein is a method of making an eraser including the steps of mixing a first silicone polymer, a second silicone polymer, a catalyst, an abrasive agent, and optionally one or more additives to form a mixture, the mixture being free of polyvinyl chloride. The method also includes molding the mixture to form a shape and curing the mixture in the shape at room temperature to form a molded eraser.

A catalyst for hydrosilylation is disclosed. The catalyst comprises a complex having a certain formula. A redox-switchable catalyst system for preparing the catalyst is also disclosed. The redox-switchable catalyst system comprises a redox-switchable catalyst and a reducing compound. The reducing compound reduces a formal oxidation state of the redox-switchable catalyst to give the catalyst, where the former is generally inactive in catalyzing hydrosilylation and the latter is catalytically active. A composition comprising the catalyst and/or the redox-switchable catalyst system, and a hydrosilylation reaction product, are also disclosed.

A mixture M includes at least one compound A, selected from (a1) a compound of the general formula (I) and/or (a2) a compound of the general formula (I′), at least one compound B, selected from (b1) a compound of the general formula (II) and/or (b2) a compound of the general formula (II′) and/or (b3) a compound of the general formula (II″), and at least one compound C, selected from cationic germanium(II) compounds of the general formula (III).

[Problem] To provide a complex compound useful as a catalyst for a hydrophosphorylation reaction and a process for producing the same.

[Means to Solve the Problem] A complex compound of the present invention is a complex compound of a resin fine particle represented by the following general formula (1):

##STR00001## wherein, R.sup.1 represents a substituted or unsubstituted hydrocarbon group, R.sup.2 represents a substituted or unsubstituted alkyl group or a substituted or unsubstituted aryl group, R.sup.3 and R.sup.4 each independently represent a hydrogen atom, a substituted or unsubstituted alkyl group or a substituted or unsubstituted aryl group, and based on the total of 100% of the values of n and m, the value of n is within the range of 20 to 100%, the value of m is within the range of 0 to 80%, and * represents bonding with the surface of the resin fine particle and a transition metal.

The synthesis and structure of beta-diketiminate manganese compounds are described, as well as their use as catalysts for the hydrosilylation and hydroboration of unsaturated organic compounds and main group element-main group element bond formation via dehydrogenative coupling.

The present invention relates to the use of n-butyllithium for catalyzing the hydroboration of an imine and a borane. A catalyst, the borane and the imine are sequentially stirred and mixed uniformly, and are reacted for 1-2 h; the mixture is exposed to air to terminate the reaction; and the reaction liquid is subjected to reduced pressure to remove the solvent, so as to obtain a borate with different substituents. The n-butyllithium disclosed in the present invention can be used for catalyzing the hydroboration of the imine and the borane in high activity under room temperature conditions, the amount of the catalyst is only 4-5 mol % of the molar weight of the imine, and the yield of the reaction can reach 90% or more.