Provided herein are metal organic frameworks comprising metal nodes and N-donor organic ligands. Methods for capturing chemical species from fluid compositions comprise contacting a metal organic framework characterized by the formula [M.sub.aM.sub.bF.sub.6-n(O/H.sub.2O).sub.w(Ligand).sub.x(solvent).sub.y].sub.z with a fluid composition and capturing one or more chemical species from the fluid composition.

Polydentate macrocyclic NHCs (NHC ligands) and related methods are disclosed. Such ligands advantageously facilitate a variety of ligand coordination modes and stabilize oxidation states of metal complexes with a number of coordination environments and shapes. The NHC ligands described herein comprise pendant groups configured to facilitate a variety of reactions including: cis-trans isomerization, proton shuttling and facilitating changes in coordination environments as a result of redox reactions.

The present invention provides a curing catalyst for an organic polymer or an organopolysiloxane, which has a high safety and a practical curing speed, and improves the adhesion of a cured product to a substrate, and can be produced at low cost.

An aspect of the present invention provides a curing catalyst [B] for an organic polymer or an organopolysiloxane, which is used for curing an organic polymer [A1] or an organopolysiloxane [A2] having a reactive hydrolyzable silicon-containing group, wherein the catalyst [B] contains a titanium compound [B1] represented by the following formula and a secondary amine compound or a tertiary amine compound [B2].

(R.sup.1O).sub.nTi-A.sub.4-n

(In the formula, R.sup.1 is a hydrocarbon group having 1 to 10 carbon atoms, and A is a carboxylic acid residue, and n is 1 or 2.)

Disclosed herein is a catalyst system comprising (i) a heterocyclic 2-[(phosphinyl)aminyl]imine transition metal compound complex having Structure I wherein T is oxygen or sulfur, R.sup.1 and R.sup.2 are each independently a C.sub.1 to C.sub.20 organyl group consisting essentially of inert functional groups, R.sup.3 is hydrogen or a C.sub.1 to C.sub.20 organyl group, L is a C.sub.1 to C.sub.20 organylene group consisting essentially of inert functional groups, MX.sub.p represents a transition metal compound where M is a transition metal, X is a monoanion, and p is an integer from 1 to 6, Q is a neutral ligand, and q ranges from 0 to 6, and (ii) an organoaluminum compound. Also disclosed herein is a process comprising contacting (i) ethylene, (ii) a catalyst system comprising (a) a heterocyclic transition metal compound complex having Structure I as described herein and (b) an organoaluminum compound, and (iii) optionally hydrogen to form an oligomer product. ##STR00001##

Tin-containing catalysts are provided comprising a compound of formula I. I: ##STR00001##
L1, L2, L3, and L4 are each independently selected from O, S, OC(O), OC(S), SC(O), SC(S), OS(O).sub.2O, OS(O).sub.2 N(R6)-, and OP(O)(R6)-, wherein R6 represents hydrogen or a monovalent aliphatic, araliphatic, cycloaliphatic or aromatic group having up to 20 carbon atoms. R1, R2, R3, R1, R2, and R3 each independently represent a divalent aliphatic, araliphatic, cycloaliphatic or aromatic group having up to 20 carbon atoms; and R4, R5, R4, and R5 each independently represent hydrogen or a monovalent residue derived from reaction of a respective NH group with an isocyanate, an ethylenically unsaturated compound, a lactone, a dilactone, a thiolactone, a lactam, a thiolactam, a carboxylic acid or derivative thereof, or an epoxide. Also provided are curable compositions containing these catalysts and methods of controlling the rate of cure of curable compositions.

This application pertains to group 5 metal complexes having the structure of Formula I:

##STR00001##

and their potential utility in catalyzing -alkylation of secondary amine-containing moieties.

Metal ion-directed carboxylic acid functionalized polyoxometalate hybrid compounds, and their preparation method and applications in catalyzing the degradation of chemical warfare agent simulants. In the synthesis, Na.sub.2MoO.sub.4, p-hydroxybenzonic acid (PHBA), alanine (Ala), KCl, transition metal cations and As.sub.2O.sub.3 as raw materials and water are used as solvent. At room temperature, 2-chloroethyl ethyl sulfide (CEES) and the prepared polyoxometalate hybrid compounds were mixed together in anhydrous ethanol and stirred, and H.sub.2O.sub.2 was subsequently added into the reaction system. The catalytic reaction for the degradation of CEES was finished within 5 min under stirring. In the catalytic hydrolysis of diethyl cyanophosphonate (DECP), the catalyst, DECP, DMF and H.sub.2O were put together and mixed fully. The prepared polyoxometalate hybrid compounds have the advantages of high conversion, high selectivity and easy recyclability in catalyzing the degradation of two types of chemical warfare agent simulant.

The present invention discloses a cobalt compound of formula (I), a process for the preparation and use thereof. The present invention further relates to a pharmaceutical composition and a method inhibition of Tau Aggregation in a subject in need thereof using compound of formula (I).

##STR00001##

The present invention is directed to catalytic compositions and to curable compositions containing them. Catalytic compositions of the present invention consist essentially of: (i) a metal compound; and (ii) a compound different from (i) that catalyzes an addition reaction between an ethylenically unsaturated compound and a thiol, wherein said catalytic composition is essentially free of vanadium compounds. Curable compositions according to the present invention comprise: (a) a polyene, (b) a polythiol, and (c) a catalytic component, which consists of the afore-mentioned catalytic composition.

Disclosed herein are metal-organic frameworks and methods of making and use thereof.