This invention relates to a Cu-BTC MOF which is water stable. The Cu-BTC MOF has been modified by substituting some of the BTC ligand (1,3,5, benzene tricarboxylic acid) with 5-aminoisophthalic acid (AIA). The resultant MOF retains at least 40% of its as synthesized surface area after exposure to liquid water at 60 C. for 6 hours. This is an unexpected result versus the MOF containing only the BTC ligand. This MOF can be used to abate contaminants such as ammonia in gas streams and especially air streams.

This invention relates to a Cu-BTC MOF which is water stable. The Cu-BTC MOF has open coordination sites and has been post synthesis modified by partially occupying the open sites with a ligand such as acetonitrile (CH.sub.3CN). The resultant MOF retains at least 40% of its as synthesized surface area after exposure to liquid water at 60 C. for 6 hours. This is an unexpected result versus the MOF which has not been post treated with ligands such as acetonitrile. This MOF can be used to abate contaminants such as ammonia in gas streams and especially air streams.

Provided is a method for preparing a solution B comprising at least one catalyst in at least one second solvent, comprising at least the following steps of (A) providing a solution A comprising the at least one catalyst in at least one first solvent, (B) treating the solution A from step (A) with activated carbon, (C) removing the activated carbon from the solution A, and (D) exchanging the at least one first solvent in solution A for at least one second solvent in order to obtain the solution B comprising the at least one catalyst in at least one second solvent, to a solution of at least one catalyst in at least one second solvent, obtainable by the method according to the invention, to the use of this solution for preparing a composition comprising the at least one catalyst, the at least one second solvent, at least one polyisocyanate and at least one NCO-reactive compound, to the use of this composition for producing a single-layered or multi-layered coating system and a corresponding process.

Disclosed are complexes and methods of using the complexes as catalysts for addition of amines to unsaturated electrophiles, as well as novel compounds produced by the disclosed complexes and methods. The disclosed methods may utilize the disclosed complexes as catalysts for adding unprotected primary amines and secondary amines to unsaturated electrophiles in an enantioselective manner to produce novel compounds which may include amino substituted succinimide compounds.

A procatalyst for the polymerization of ethylene and optionally one or more alpha-olefins having the structure shown in formula (I) below. Formula (I) is provided. Also provided is a polymerization process using the inventive procatalyst. ##STR00001##

Processes to prepare lightly branched surfactant products comprise combining at least one olefin and a coordination-insertion catalyst under conditions such that at least one oligomer product is formed. The surfactant products comprise a main carbon chain containing an average of between 0.5 and 2.5 branches, wherein more than 50% of the branches are ethyl branches, wherein the branches are located more than one carbon away from each end of the main carbon chain in more than 20% of surfactant product molecules.

A catalyst system has been designed that disrupts the sedimentation process. The catalyst system achieves this by saturating key feed components before the feed components are stripped into their incompatible aromatic cores. The efficacy of this disruptive catalyst system is particularly evident in a hydrocracker configuration that runs in two-stage-recycle operation. The catalyst is a self-supported multi-metallic catalyst prepared from a precursor in the hydroxide form, and the catalyst must be toward the top level of the second stage of the two-stage system.

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.

The present invention is directed at stabilization of aqueous urea solutions containing organometallic catalyst precursors. Stabilization can be achieved by monitoring and controlling the solution pH.

A tetraanionic OCO pincer ligand metal-oxo-alkylidene complex is prepared from a trianionic pincer ligand supported metal-alkylidyne. The metal can be tungsten or other group 5-7 transition metal. The tetraanionic pincer ligand metal-oxo-alkylidene complex, a trianionic OCO pincer ligand metal complex, or a trianionic ONO pincer ligand metal complex can be used to polymerize cycloalkenes. The poly(cycloalkene)s are predominantly cis-alkene macrocyclics.