Anionic platinum carbonyl cluster has been ion paired with cinchonidium groups that are chemically bound to the surface of MCM-41 and fumed silica. In the hydrogenation of methyl pyruvate or acetophenone the fumed silica-based catalyst gives zero enantioselectivity, but under optimum conditions enantiomeric excesses of > 90 and ∼ 40%, respectively, are obtained with the MCM-41-based catalyst.

Covalent grafting of MCM-41 with 3-chloropropyl trimethoxysilane and subsequent reaction respectively with acacdien and complexation with MoO2(acac)2 afforded MoO2acacdien@MCM-41. X-ray diffraction and nitrogen sorption analyses revealed the preservation of the textural properties of the support as well as accessibility of the channel system despite sequential reduction in surface area, pore vo...

The goal of this research was to investigate the potential of newly synthesized gold complex trichloro(2,4,6-trimethylpyridine)Au(III) as an anticancer agent. The gold(III) complex was synthesized and grafted on nanoporous silica, MCM-41, to produce AuCl(3)@PF-MCM- 41 (AuCl(3) grafted on pyridine-functionalized MCM-41). The toxicity of trichloro(2,4,6- trimethylpyridine)Au(III) and AuCl(3)@PF-M...

A Pd-based heterogeneous catalyst (Pd(II)-MCM-41) derived from post-synthesis modification of mesoporous silica, MCM-41, has been successfully employed in catalytic Stille and Sonogashira cross-coupling reactions. The catalyst affords good yields in all cross-coupling reactions. Notably, the catalyst is capable of activating less reactive chlorobenzene with moderate yield in both the coupling r...

A series of MCM-41 supported Ni catalysts with high metal dispersion was successfully synthesized by simple co-impregnation using proper ethylene glycol (EG). The acquired Ni-based catalysts performed the outstanding hydrogenolysis activity of guaiacol. The effects of the synthesis parameters including drying temperature, calcination temperature, and metal loading on the physical properties of ...

A heterogeneous catalyst, nanosized MCM-41-Pd, was used to catalyze the Sonogashira coupling of aryl and heteroaryl halides with terminal alkynes in the presence of CuI and triphenylphosphine. The coupling products were obtained in high yields using low Pd loadings to 0.01 mol%, and the nanosized MCM-41-Pd catalyst was recovered by centrifugation of the reaction solution and re-used in further ...

The catalytic performance of incorporated V-MCM-41 catalysts for the partial direct oxidation of methane to formaldehyde with molecular oxygen has been investigated. V-MCM-41 catalysts containing 0.56–1.86 wt.% V have been prepared by incorporating the vanadium ions into the framework of mesoporous siliceous MCM-41, resulting in a highly ordered structure with large BET surface area and high su...

In this study, we demonstrate the production of long-chain hydrocarbons (C8+) from 2-methylfuran (2MF) and butanal in a single step reactive process by utilizing a bi-functional catalyst with both acid and metallic sites. Our approach utilizes a solid acid for the hydroalkylation function and as a support as well as a transition metal as hydrodeoxygenation catalyst. A series of solid acids was ...

Fe-substituted MCM-41 molecular sieves with ca. 1, 2, and 3 wt % Fe were synthesized hydrothermally using different sources of colloidal silica (HiSil and Cab-O-Sil) and characterized by ICP, XRD, N2 physisorption, UV-vis, EPR, TPR, and X-ray absorption. Catalysts synthesized from Cab-O-Sil showed higher structural order and stability than those from HiSil. The local environment of Fe in the me...

The hydroformylation of alkenes is a major commercial process used for the production of oxygenated organic compounds. When the hydroformylation reaction is performed using a homogeneous catalyst, an organic or aqueous solvent is employed, and a significant effort must be expended to recover the catalyst so it can be recycled. Development of a selective heterogeneous catalyst would allow simpli...