A compound represented by Chemical Formula 1 according to the present invention can coordinate with metal ions to form a bidirectional or multidirectional metal-organic hybrid structure. Thus, the present invention can synthesize various ligands using amine-aldehyde condensation, and synthesize metal-organic materials using the same.

The present invention relates to the field of polymerisation catalysts, and systems comprising said catalysts for polymerising carbon dioxide and an epoxide, a lactide and/or lactone, and/or an epoxide and an anhydride. The catalyst is of formula (I): ##STR00001## Wherein M.sub.1 and M.sub.2 are independently selected from Zn(II), Cr(II), Co(II), Cu(II), Mn(II), Ni(II), Mg(II), Fe(II), Ti(II), V(II), Cr(III)-X, Co(III)-X, Ni(III)-X, Mn(III)-X, Fe(III)-X, Ca(II), Ge(II), Al(III)-X, Ti(III)-X, V(III)-X, Ge(IV)-(X).sub.2 or Ti(IV)-(X).sub.2. R.sub.3A is different from R.sub.3B; and/or at least one occurrence of E.sub.3, E.sub.4, E.sub.5 and E.sub.6 is different to a remaining occurrence of E.sub.3, E.sub.4, E.sub.5 and E.sub.6. A ligand, a process of asymmetric N-substitution of a symmetrical ligand and a process for the reaction of: (i) carbon dioxide with an epoxide; (ii) an epoxide and an anhydride; and/or (iii) a lactide and/or a lactone, in the presence of a catalyst is also described.

A process for reducing the loss of catalyst activity of a Ziegler-Natta catalyst is provided. The process includes preparing a Ziegler-Natta (ZN) catalyst by contacting the ZN catalyst with at least one aluminum alkyl compound to produce a reduced ZN catalyst and storing and/or transporting the reduced ZN catalyst for at least 20 days at a temperature of 25 C. or less. The reduced ZN catalyst may be used for polymerizing polyolefin polymers.

Embodiments of the present disclosure directed towards polymerization catalysts having improved ethylene enchainment. As an example, the present disclosure provides a polymerization catalyst having improved ethylene enchainment, the polymerization catalyst comprising a zirconocene catalyst of Formula (I) where R.sub.1 is a C.sub.1 to C.sub.20 alkyl, aryl or aralkyl group, wherein R.sub.2 is an C.sub.1 to C.sub.20 alkyl, aryl or aralkyl group, and where R.sub.3 is a C.sub.1 to C.sub.20 alkyl or a hydrogen, and where each X is independently a halide, C.sub.1 to C.sub.20 alkyl, aralkyl group or hydrogen.

##STR00001##

The invention describes a method for dimerization of ethylene implementing a step for treatment of raw effluent by neutralization, at the outlet of the reactor, of the catalyst for dimerization of ethylene into but-1-ene by a particular alcohol.

[Problem] Provided is a method for producing an industrially advantageous hydrogenated polymer, whereby a high hydrogenation rate can be achieved by a small use amount therein at a level of not requiring a decalcification process of the catalyst. [Solution] A method for producing a hydrogenated polymer including hydrogenating, with a hydrogen molecule, a carbon-carbon double bond based on a conjugated diene structural unit of a polymer in which at least a part of a living polymer obtained by polymerizing a monomer containing one or more conjugated dienes using an organic alkali metal compound as a polymerization initiator is terminated by a hydrogen molecule, in the presence of a silane compound having at least one silyl hydride bond and an organic metal compound represented by the following general formula (I): ##STR00001##
wherein R.sup.1 to R.sup.10 are those as defined in the specification.

A process can be used for producing a distillate product with a methanol concentration greater than the concentration of methanol in the minimum boiling azeotrope of methanol and methyl(meth)acrylate, from a mixture with a methanol concentration less than the concentration of methanol in the minimum boiling azeotrope of methanol and methyl (meth)acrylate, in a distillation column. A transesterification process for preparing C.sub.6- to C.sub.2- alkyl, aryl or alkenyl (meth)acrylates from methyl(meth)actylate is also provided.

The various embodiments provide, a magnesium titanium polymerization procatalyst, and methods for making and using the same.

A novel metal organic framework, EMM-39, is described having the structure of UiO-66 and comprising bisphosphonate linking ligands. EMM-39 has acid activity and is useful as a catalyst in olefin isomerization. Also disclosed is a process of making metal organic frameworks, such as EMM-39, by heterogeneous ligand exchange, in which linking ligands having a first bonding functionality in a host metal organic framework are exchanged with linking ligands having a second different bonding functionality in the framework.

A 3D structure of the graphite-titanium-nanocomposite complex and a method of preparing the graphite-titanium-nanocomposite complex are disclosed. The Graphite-titanium-nanocomposite complex includes a metal core associated with the two phases, amine functionalized graphite, and amine functionalized titanium. The method of preparation includes amine functionalizing of graphite and titanium with coupling agents to produce amine functionalized titanium and graphite, further mixing with a metal ion solution for synthesizing an ion complex. Trisodium citrate solution and sodium borohydride solution is added to the ion complex to prepare a 3D structure of the graphite-titanium-nanocomposite complex, employed as a catalyst.