Patent classifications
C07F7/0879
Platinum catalyzed hydrosilylation reactions utilizing cyclodiene additives
A process and composition for the hydrosilylation of an unsaturated compound comprising reacting (a) a silyl hydride with (b) an unsaturated compound in the presence of (c) a platinum compound and (d) a cyclodiene, with the proviso that when the unsaturated compound is a terminal alkyne, the silyl hydride is other than a halosilane. The process and composition optionally comprise an inhibitor (e). The process and composition may be employed to form a variety of hydrosilylation products.
Process for the Preparation of Hydroxyl-Functionalized Polysiloxanes
A method for producing a hydroxyl-functionalized polysiloxane having secondary or tertiary hydroxyl groups, said method comprising the steps of: i) reacting a hydroxyalkyl allyl ether having a secondary or tertiary alcohol group with a siloxane under anhydrous conditions and under transition metal catalysis, said hydroxylalkyl allyl ether conforming to Formula (I)
##STR00001## wherein n is 0, 1, 2, 3, 4 or 5, preferably 0; m is 1, 2, 3, 4 or 5, preferably 1; spacer group A is constituted by a covalent bond or a C.sub.1-C.sub.20 alkylene group; R.sup.1 is hydrogen, a C.sub.1-C.sub.8 alkyl group, a C.sub.3-C.sub.10 cycloalkyl group, a C.sub.6-C.sub.18 aryl group or an aralkyl group; R.sup.a, R.sup.b, R.sup.c, R.sup.d, R.sup.2, R.sup.3, R.sup.4 and R.sup.5 may be the same or different and each is independently selected from hydrogen, a C.sub.1-C.sub.8 alkyl group, a C.sub.6-C.sub.18 aryl group or a C.sub.6-C.sub.18 aralkyl group, with the proviso that at least one of R.sup.3 and R.sup.4 is not hydrogen; and said siloxane conforming to Formula (II)
##STR00002## wherein m is 1, 2, 3, 4 or 5, preferably 1; R.sup.6, R.sup.7, R.sup.8 and R.sup.9 may be the same or different and each represent a C.sub.1-C.sub.8 alkyl group, a C.sub.3-C.sub.10 cycloalkyl group, a C.sub.6-C.sub.18 aryl group or a C.sub.6-C.sub.18 aralkyl group; and ii) in the presence of the reaction product of step i), performing a ring opening polymerization of at least one cyclic siloxane monomer.
Biodegradable super-spreading, organomodified trisiloxane
The invention relates to polyether-modified siloxanes which are both superspreading and readily biodegradable. In particular, the invention is directed to a composition including polyether-modified siloxanes of formula (I)
M.sub.aD.sub.bD.sub.cFormula (I) with M=R.sup.1.sub.3SiO.sub.1/2, D=R.sup.1.sub.2SiO.sub.2/2, D=R.sup.1R.sup.2SiO.sub.2/2, where a is 2, b is between 0 and 0.1, c is between 1.0 and 1.15, 0 and 1.05, R.sup.1 are independently hydrocarbyl having 1 to 8 carbon atoms, preferably methyl, ethyl, propyl or phenyl radicals, especially preferably methyl radicals, R.sup.2 are independently a polyether radical of the formula (II)
R.sup.3O[CH.sub.2CH.sub.2O].sub.m[CH.sub.2CH(CH.sub.3)O].sub.nR.sup.5Formula (II) where m=3.4 to 11.0, n=2.5 to 8.0, wherein m/n=1.9 to 2.8, and R.sup.3 are independently divalent hydrocarbyl radicals having 2 to 8 carbon atoms, and R.sup.5 is hydrogen, wherein the polyether-modified siloxanes of formula (I) having a biodegradability of greater than 60%.
CARBINOL FUNCTIONAL TRISILOXANE AND METHOD OF FORMING THE SAME
A trisiloxane having at least one carbinol functional group comprises the reaction product of (A) an initial trisiloxane and (B) an organic compound. Component (A) has a pendant silicon-bonded functional group selected from a hydrogen atom, an epoxy-containing group, an ethylenically unsaturated group, and an amine group. Typically, component (A) is free of certain terminal silicon-bonded functional groups and is free of polyoxyalkylene groups. Component (B) has a functional group reactive with the pendant silicon-bonded functional group of component (A), and has at least one hydroxyl functional group. The trisiloxane is useful for a number of applications including use as a detergent additive. The trisiloxane may be of the following general formula (I): (R13SiO1/2) (R1R3Si2/2)(R13SiO1/2) (I). In formula (I), each R1 is an independently selected hydrocarbyl group. R3 may be selected from the groups (i) to (iv) described herein. Typically, the trisiloxane has 1-6 carbinol groups.
SILICON-CONTAINING COMPOUND, URETHANE RESIN, STRETCHABLE FILM, AND METHOD FOR FORMING THE SAME
The present invention provides a silicon-containing compound shown by the following formula (1):
##STR00001##
wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, and R.sup.6 each independently represent a linear, branched, or cyclic alkyl group having 1 to 6 carbon atoms, a phenyl group, a 3,3,3-trifluoropropyl group, or a group shown by (OSiR.sup.7R.sup.8).sub.nOSiR.sup.9R.sup.10R.sup.11; R.sup.7, R.sup.8, R.sup.9, R.sup.10, and R.sup.11 have the same meanings as R.sup.1 to R.sup.6; X represents a linear or branched alkylene group having 3 to 7 carbon atoms optionally having an ether group; and n is an integer in the range of 0 to 100. This provides a stretchable film that hats excellent stretchability and strength, with the film surface having excellent repellency, and a method for forming the same; as well as a urethane resin used for the stretchable film; and a silicon-containing compound to be a material of the urethane resin.
SILICONE FORMULATIONS FOR 3D PRINTING
In one embodiment, a silicone-based ink for additive manufacturing includes a vinyl-terminated siloxane macromer, a hydrophobic reinforcing filler, and a rheology modifying additive. In another embodiment, a method of additive manufacturing with silicone-based ink includes adding a mixture that includes a vinyl-terminated siloxane macromer, a hydrophobic reinforcing filler, and a rheology modifying additive to a cartridge for additive manufacturing, extruding the mixture through the cartridge to form a structure, and curing the mixture to at least a predefined extent.
Hydrosilylation iron catalyst
A hydrosilylation iron catalyst prepared from a two-electron ligand (L) and a mononuclear, binuclear, or trinuclear complex of iron indicated by formula (1), Fe having bonds with carbon atoms included in X and the total number of Fe-carbon bonds being 2-10. As a result of using iron, the hydrosilylation iron catalyst is advantageous from a cost perspective as well as being easily synthesized. Hydrosilylation reactions can be promoted under mild conditions by using this catalyst.
Fe(X).sub.a(1)
(in the formula, each X independently indicates a C2-30 ligand that may include an unsaturated group excluding carbonyl groups (CO groups) and cyclopentadienyl groups, however at least one X includes an unsaturated group, a indicates an integer of 2-4 per Fe atom.)
SYNTHESIS OF AMINOALKYL-SUBSTITUTED DISILOXANES
Described herein is a method of preparing an aminoalkyl-substituted disiloxane. The method includes forming a mixture including a di- or polyamine containing at least one primary amine group and a silane; reacting the mixture in a first reaction; adding a hydrolysis agent to the mixture; and reacting the mixture in a second reaction to form the aminoalkyl-substituted disiloxane. Also described herein is an aminoalkyl-substituted disiloxane prepared according to the method.
NOBLE METAL-FREE HYDROSILYLATABLE MIXTURE
The invention relates to a hydrosilylatable mixture M containing: (A) a compound with at least one hydrogen atom directly bonded to Si, (B) a compound containing at least one carbon-carbon multiple bond, and (C) a compound containing at least one cationic Si(II) group. The invention also relates to a method for hydrosilylating the mixture M.
Hydroboration and borylation with cobalt catalysts
In one aspect, cobalt complexes are described herein. In some embodiments, such cobalt complexes are operable as catalysts for hydroboration and borylation applications.