Related Experiment Video
Updated: Jan 13, 2026

Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry
Published on: October 18, 2019
Microenvironment engineering unveils surface methoxy species origination in zeolite-catalyzed methanol chemistry
Fengqing Liu1, Xianfeng Yi2, Jiamin Yuan1
1State Key Laboratory of Magnetic Resonance Spectroscopy and Imaging, National Center for Magnetic Resonance in Wuhan, Wuhan Institute of Physics and Mathematics, Innovation Academy for Precision Measurement Science and Technology, Chinese Academy of Sciences, Wuhan, PR China.
Abstract:
Which came first, the chicken or the egg? This age-old riddle is also present for the formation sequence of the surface methoxy species and dimethyl ether in zeolite-catalyzed methanol chemistry due to their inevitable interconversion at high temperatures. The challenge is the lack of feasible reaction conditions to achieve the formation of surface methoxy species by Brønsted acids at mild temperatures. This work proposes a microenvironment design strategy to manipulate the reaction routes inside zeolite channels with the assistance of nitromethane, realizes the surface methoxy species generation catalyzed by Brønsted acids at 363 kelvin, and solves the long-standing problem of the origin and evolution of the highly active surface methoxy species during zeolite Brønsted-acid-catalyzed methanol conversion process. It is found that the surface methoxy species mainly originate from dimethyl ether decomposition under these mild conditions. These findings provide a perspective to subtly manipulate the reaction routes by tailoring the chemical microenvironment, and offer fresh insights into the zeolite-catalyzed methanol chemistry.
Related Concept Videos
Carboxylic Acids to Methylesters: Alkylation using Diazomethane
Oxidative Cleavage of Alkenes: Ozonolysis
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
Hydroboration-Oxidation of Alkenes
Oxymercuration-Reduction of Alkenes
Ethers from Alkenes: Alcohol Addition and Alkoxymercuration-Demercuration
Ethers can also be prepared from alkenes through acid-catalyzed addition of alcohols and alkoxymercuration–demercuration.
Preparation of Ethers by Acid-Catalyzed Addition of Alcohol to Alkenes
The acid-catalyzed addition of alcohol to an alkene involves treating the alkene with an excess of alcohol in the presence of an acid catalyst to form an ether under suitable conditions. The hydrogen will add to the less substituted carbon so that the nucleophile can attack the more substituted...
Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...

