A process can prepare an isocyanurate compound by hydrosilylation. The compound is a tris[3-(trialkoxysilyl)propyl] isocyanurate, a tris[3-(alkyldialkoxysilyl)propyl] isocyanurate, and/or a tris[3-(dialkylalkoxysilyl)propyl] isocyanurate, The process includes (A) preparing a mixture of at least one carboxylic acid, a platinum catalyst, and 1,3,5-triallyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione; (B) heating the mixture to a temperature in the range of 40 to 140 C.; (C) adding at least one H-silane among a hydrotrialkoxysilane, a hydroalkyldialkoxysilane, and a hydrodialkylalkoxysilane to the mixture; (D) adding at least one alcohol to the mixture prepared in step (C); and (E) isolating the isocyanurate compound.

Systems and methods are provided for selective oxidation of CO and/or C.sub.3 hydrocarbonaceous compounds in a reaction environment including hydrocarbons and/or hydrocarbonaceous components. The selective oxidation can be performed by exposing the CO and/or C.sub.3 hydrocarbonaceous compounds to a catalytic metal that is encapsulated in a small pore zeolite. The small pore zeolite containing the encapsulated metal can have a sufficiently small pore size to reduce or minimize the types of hydrocarbons or hydrocarbonaceous compounds that can interact with the encapsulated metal.

An organometallic complex catalyst is disclosed for use in a cross-coupling reaction. In formula (1), M is the coordination center and represents a metal atom such as Pd or an ion thereof. R.sup.1, R.sup.2, and R.sup.3 may be the same or different and are a substituent such as a hydrogen atom. R.sup.4, R.sup.5, R.sup.6, and R.sup.7 may be the same or different and are a substituent such as a hydrogen atom. X represents a halogen atom. R.sup.8 represents a substituent that has a bond and 3-20 carbon atoms. With regard to the electron-donating properties of R.sup.1-R.sup.7 with respect to the coordination center M of the ligand containing R.sup.1-R.sup.7 that is indicated in formula (2), R.sup.1-R.sup.7 are arranged in combination such that the TEP value obtained from infrared spectroscopy shifts toward the low frequency side compared to the TEP value of the ligand of formula (2-1).

##STR00001##

A compound represented by the structure of formula (I): ##STR00001## The compound is useful as a ligand for ruthenium to form an organometallic complex. The complex may be immobilized on an oxidic support to form an active, heterogeneous catalyst for the hydrogenolysis of amides to form amines and optionally alcohols.

A liquid curable silicone elastomer composition is disclosed. The composition comprises: an organopolysiloxane (A) comprising: an organopolysiloxane (A1) containing at least 2 alkenyl groups bonded to silicon atom per molecule and having a total alkenyl content of from 0.01 to 1.5 mmol/g, and an organopolysiloxane (A2) containing at least 2 alkenyl groups bonded to silicon atom per molecule and having a total alkenyl content of from 5.0 to 15.0 mmol/g; an organopolysiloxane (B) comprising an organopolysiloxane (B1) containing at least 2 silicon-bonded hydrogen atoms per molecule provided by siloxy units of the type (R.sub.2HSiO.sub.1/2)x where R is independently selected from hydrogen, an aliphatic a hydrocarbyl, an aromatic hydrocarbyl, or an organyl group and x2; a platinum based catalyst (C); an inhibitor (D) selected from the group consisting of acetylenic alcohols and their derivatives; and a silica filler (E).

A silicone-polyether copolymer has the formula X.sub.gY, where each X is an independently selected silicone moiety having a particular structure, Y is a linear or branched polyether moiety, and subscript g is on average more than 1. A method of preparing the silicone-polyether copolymer comprising reacting a polyether compound and an organosilicon compound in the presence of a hydrosilylation-reaction catalyst. A sealant is also disclosed, the sealant comprising the silicone-polyether copolymer and a condensation-reaction catalyst.

A silicone-polyether copolymer has the formula X.sub.g[Z.sub.jY.sub.o].sub.c, where each X is an independently selected silicone moiety having a particular structure, each Y is an independently selected polyether moiety, each Z is an independently selected siloxane moiety, subscript c is from 1 to 150, subscript g is >1, and each subscript j and o are independently >0 and <2, with the proviso that j+o=2 in each moiety indicated by subscript c. A method of preparing the silicone-polyether copolymer is also disclosed, and comprises reacting a polyether compound, a chain extending organosilicon compound, and an endcapping organosilicon compound in the presence of a hydrosilylation catalyst. A sealant is also disclosed, the sealant comprising the silicone-polyether copolymer and a condensation-reaction catalyst.

A silicone-polyether copolymer has the formula (X-D.sup.2).sub.g-Y, where each X is an independently selected silicone moiety having a particular structure, D.sup.2 is a divalent hydrocarbon group, subscript g is greater than 1, and Y is a linear or branched polyether moiety. A method of preparing the silicone-polyether copolymer comprising reacting a polyether compound and an organosilicon compound in the presence of a hydrosilylation-reaction catalyst. A sealant is also disclosed, the sealant comprising the silicone-polyether copolymer and a condensation-reaction catalyst.

A platinum organosiloxane complex is prepared by a process including combining A) a platinous halide; B) a ketone; C) an enone additive distinct from any other starting materials or rearrangement products thereof; and D) a polyorganosiloxane having, per molecule, 2 to 4 silicon bonded terminally unsaturated hydrocarbon groups having from 2 to 6 carbon. The platinum organosiloxane complex prepared by the process is useful as a hydrosilylation catalyst.

An isocyanate-functional silicone-polyether copolymer having a particular structure is disclosed. A method of preparing the isocyanate-functional silicone-polyether copolymer is also disclosed, the method comprising reacting a polyether compound and an organosilicon compound to give the isocyanate-functional silicone-polyether copolymer. A silicone-polyether-urethane copolymer formed therewith, as well as a method of preparing the silicone-polyether-urethane copolymer, are also disclosed. Sealants comprising the isocyanate-functional silicone-polyether copolymer and/or the silicone-polyether-urethane copolymer are further disclosed.