Tailoring of the Properties of Amorphous Mesoporous Titanosilicates Active in Acetone Condensation.

Amorphous mesoporous materials are promising as catalysts for processes involving or forming bulk molecules. In a reaction such as acetone condensation to form mesitylene, an effective catalyst should not only have a developed porous structure but also have active centers of acidic and basic types. The sol-gel approach allows one to obtain titanosilicates with such characteristics.

The Dimerization and Oligomerization of Alkenes Catalyzed with Transition Metal Complexes: Catalytic Systems and Reaction Mechanisms.

Dimers and oligomers of alkenes represent a category of compounds that are in great demand in diverse industrial sectors. Among the developing synthetic methods, the catalysis of alkene dimerization and oligomerization using transition metal salts and complexes is of undoubted interest for practical applications. This approach demonstrates substantial potential, offering not only elevated reaction rates but also precise control over the chemo-, regio-, and stereoselectivity of the reactions.

The mechanism of the replacement of aluminum atoms in 1-ethyl-3-alkylalumolanes by boron atoms with boron halides.

In this study, the mechanism of the replacement reaction of an aluminum atom by a boron atom in the 1-ethyl-3-substituted alumolanes with boron halides is proposed. Theoretical and experimental justifications based on the DFT quantum chemical calculations of the energy parameters of possible reaction routes coupled with monitoring of the reaction between 1-ethyl-3-butylalumolane and BF·EtO, BCl and BBr using H, C, B and Al NMR spectroscopy are provided.

Catalytic Properties of Zirconocene-Based Systems in 1-Hexene Oligomerization and Structure of Metal Hydride Reaction Centers.

Despite large-scale investigations of homogeneous single-site metallocene catalysts and systems based on them, there are still unsolved problems related to the control of their activity and chemo- and stereoselectivity. A solution to these problems is required to develop efficient methods for the synthesis of practically useful products of alkene transformations, such as dimers, oligomers, and polymers. Here we studied the catalytic activity of structurally diverse zirconocenes (LZrCl, L = Cp, CMe, Ind, L = MeCCp, MeSiCp, MeCCp, -MeCInd, -HCInd, BIPh(Ind), HC[THInd]), and co-catalysts activating the system, namely HAlBu, MMAO-12, and (PhC)[B(CF)], at low activator/Zr ratios in a 1-hexene oligomerization reaction.