Related Experiment Video
Updated: Aug 17, 2026
Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes
Published on: June 24, 2022
Nanoporous reactor with tunable selectivity on alkylation of ethylbenzene
Ajayan Vinu1, Kandaiyan Shanmugapriya, Govindasamy Chandrasekar
1International Center for Young Scientists, National Institute for Materials Science, 1-1 Namiki, Tsukuba 305-0044, Japan.
Abstract:
As nanoporous reactor, mesoporous silicates containing aluminum acidic site with n(Si)/n(Al) ratio up to 7 (AISBA-15) were prepared through a simple one-pot synthesis, which was recently developed by parts of us. The obtained materials were satisfactorily characterized by XRD and nitrogen adsorption/desorption and have regularly arranged hexagonal structures with pore diameters in the 9.6-11.8-nm range. The density and strength of the acid sites were determined using temperature-programmed desorption (TPD) of pyridine and controlled distribution between weak, moderate, and strong acid sites was demonstrated. The alkylation of ethylbenzene in a fixed-bed flow-type reactor using the AISBA-15 nanoporous reactor was carried out under various conditions such as temperature, feed ratio, flow rate, and time on stream. Interestingly, perfect regioselectivity between the m-isomer and the o-/p-isomers of diethylbenzene was achieved, where 100% selectivity of the m-isomer or the o-/p-isomers can be obtained by simply tuning the reaction temperature by using AISBA-15 catalyst with appropriate aluminum content.
Related Concept Videos
02:17Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
02:24Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
02:17Regioselectivity of Electrophilic Additions to Alkenes: Markovnikov's Rule
The hydrohalogenation of an unsymmetrical alkene can yield two haloalkane products, depending on which vinylic carbon takes up the halogen. However, one product usually predominates, where hydrogen adds to the vinylic carbon bearing the...
02:27Preparation of Alkynes: Alkylation Reaction
Alkylation of terminal alkynes with primary alkyl halides in the presence of a strong base like sodium amide is one of the common methods for the synthesis of longer carbon-chain alkynes. For example, treatment of 1-propyne with sodium amide followed by reaction with ethyl bromide yields 2-pentyne.
00:53Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
02:13Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the surface of...