A method for preparing a bi-component, multi-network nanofibrous aerogel-supported heterojunction photocatalyst includes the following steps. Step 1, preparing ammoniated polyacrylonitrile nanofibers. Step 2, dispersing the ammoniated polyacrylonitrile nanofibers in water to obtain a first solution; dispersing cellulose nanofibers in water to obtain a second solution; and mixing, heating and lyophilizing the first solution with the second solution to obtain a bi-component, multi-network nanofibrous aerogel. Step 3, adding graphite carbon nitride, a ferric-iron containing reagent, 2,5-diaminoterephthalic acid, and the bi-component, multi-network nanofiber aerogel obtained in the step 2 into a N, N-dimethylformamide solvent to obtain a third solution, and carrying out a hydrothermal reaction on the third solution for 8-24 hours to obtain the bi-component, multi-network nanofibrous aerogel-supported heterojunction photocatalyst.

Catalytic hydroesterification of alkyl lactates give alkyl 2-(propionyloxy)propanoates, starting from alkyl lactate, carbon monoxide, ethylene gas, and a palladium catalyst. Pyrolysis of alkyl 2-(propionyloxy)propanoates gives acrylate esters.

D The present invention relates to ion pair catalysts (I) comprising the cationic bisguanidinium ligand (A) and diperoxomolybdate anion (B). The present invention also relates to ion pair catalysts (III) comprising the cationic bisguanidinium ligand (C) and peroxotungstate anion (D). It further relates to the use of the said catalysts in the manufacture of enantiomerically enriched sulfoxides. ##STR00001##

The invention relates to polyoxometalates represented by the formula (A.sub.n).sup.m+[MM.sub.12O.sub.y(RCOO).sub.zH.sub.q].sup.m or solvates thereof, corresponding supported polyoxometalates, and processes for their preparation, as well as corresponding metal clusters, optionally in the form of a dispersion in a liquid carrier medium or immobilized on a solid support, and processes for their preparation, as well as their use in reductive conversion of organic substrate.

The present invention relates to an organic zinc catalyst which exhibits more improved catalytic activity than conventional organic zinc catalysts during a polymerization process for the preparation of a polyalkylene carbonate resin and is capable of preventing an aggregation phenomenon during a reaction, a method for preparing the same, and a method for preparing a polyalkylene carbonate resin using the organic zinc catalyst.

The method for preparing an organic zinc catalyst includes the step of reacting a zinc precursor with a dicarboxylic acid in the presence of a polyether derivative to form a zinc dicarboxylate-based catalyst.

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

A zinc-based metal organic framework and method of making is described. The zinc-based metal organic framework is in the form of an interpenetrating diamondoid framework where each Zn.sup.2+ ion center is linked with four other Zn.sup.2+ ion centers in a distorted tetrahedral geometry. The linking occurs through diamine and dicarboxylic acid linkers. The zinc-based metal organic framework may be deposited on a transparent conducting film and used as a photoelectrode for photoelectrochemical water splitting.

The present invention refers to a process for a Rh-catalyzed Anti-Markovnikov hydrocyanation of terminal alkynes which process discloses, for the first time, the highly stereo- and regio-selective hydrocyanation of terminal alkynes to furnish E-configured alkenyl nitriles and the catalyst used in the present process.

A method for synthesizing 4-(Hydroxymethyl)benzoic acid using P-xylene (PX) as a raw material, including: dissolving PX in an organic solvent to undergo an oxidation reaction with an oxidizing agent under an action of an M-MOF catalyst; and after the oxidation reaction, performing a post-treatment to obtain the 4-(Hydroxymethyl)benzoic acid; wherein, the metal element M in the M-MOF catalyst is Fe, Cu, Cr, Mn, Cu/Fe, Cu/Cr, Cu/Mn, Fe/Mn, Cr/Fe or Cr/Mn. The by-product produced in the reaction process is little, the yield is high, and the separation is convenient. The acid-base neutralization is not required in the reaction process, reducing pollution. A one-step reaction is employed which has mild reaction conditions, short reaction time, low pollution and is convenient for industrialized mass production; and the obtained 4-(Hydroxymethyl)benzoic acid can be used for preparing medicines and liquid crystal materials having wide applications.

Compositions comprising metal organic frameworks and related methods and uses are generally provided, including use in selective carbonylation of heterocyclic compounds.