Related Experiment Video
Updated: Nov 20, 2025

Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides
Published on: May 26, 2019
One-step synthesis of hierarchical [B]-ZSM-5 using cetyltrimethylammonium bromide as mesoporogen
Büşra Karakaya YalÇin1, Bahar İpek1
1Department of Chemical Engineering, Faculty of Engineering, Middle East Technical University, Ankara Turkey.
Abstract:
One-step facile synthesis of boron containing ZSM-5 microspheres is developed using 1,6-diaminohexane as the structure-directing agent and cetyltrimethylammonium bromide as the mesoporogen. High boron incorporation up to Si/B ratio of 38 is achieved and evidenced by the stretching vibrations of B-O-Si at 667 cm-1 and 917 cm-1 using Fourier-transform infrared spectra. The morphology of the crystals resembles berry-like spheres with sizes approximately 15 μm, which is composed of aggregated nanocrystals having sizes around 450 nm, is observed using scanning electron microscopy. The textural properties, i.e. the surface areas and pore volumes are investigated using N2 adsorption at -196 °C. t-plot micropore volume of 0.11 cm3/g and mesopore volume of 0.14 cm3/g are obtained applying this synthesis method for mesopores having pore diameters within the range of 2-10 nm.
More Related Videos
07:36Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy
Published on: November 9, 2019
10:17Efficient Construction of Drug-like Bispirocyclic Scaffolds Via Organocatalytic Cycloadditions of α-Imino γ-Lactones and Alkylidene Pyrazolones
Published on: February 7, 2019
Related Concept Videos
Formation of Halohydrin from Alkenes
Radical Substitution: Allylic Bromination
α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...
Halogenation of Alkenes
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
Hydroboration-Oxidation of Alkenes