Nitriles used to be known as cyanides; the smallest organic nitrile is ethanenitrile, CH3CN, (old name: methyl cyanide or acetonitrile – and sometimes now called ethanonitrile). 1835-49-0, formula is C8F4N2, Name is Tetrafluoroterephthalonitrile. Nitriles are found in many useful compounds, including methyl cyanoacrylate, used in super glue, and nitrile rubber, a nitrile-containing polymer used in latex-free laboratory and medical gloves. Product Details of C8F4N2.
Sun, Yunhao;Niu, Qiang;Yang, Shize;Zhang, Pengfei research published 《 Observation of Cobalt Species Evolution in Mesoporous Carbon by In-Situ STEM-HAADF Imaging and Related Hydrogenation Process》, the research content is summarized as follows. Metal decorated-mesoporous carbons (MMCs) has attractive features from both mesoporous materials (large pore size, high pore volume) and metal species (reactive surface). Cobalt@mesoporous carbon (Co@MC) catalyst was successfully manufactured by mechanochem. synthesis method for hydrogenation of phenol to prepare cyclohexanone. Unlike traditional hard-templating and soft-templating methods, the essence of this strategy lies in the combination of carbonization and ligand-protected metal reduction By using Fourier transform-IR spectroscopy, X-ray diffraction and N2 adsorption-desorption, Co@MC catalyst was well studied. In particular, the effect of calcination temperature in terms of growth and aggregation of cobalt species was detailly explored by in-situ scanning transmission electron microscopy-high angle angular dark field. A series of mesoporous carbons with cobalt species readily tuned from clusters to nanoparticles were measured in phenol hydrogenation (Conv. Phenol: >99 %, Sel. Cyclohexanone: >99 %).
1835-49-0, Tetrafluoroterephthalonitrile can react with alkyl grignard reagents to form 4-alkyltetraflurorobenzonitriles. It acts as a four electron donor ligand. Tetrafluoroterephthalonitrile can be used to synthesize polymers of intrinsic microporosity. It has been used to study UV rearranged polymers of teh PIM-1 type membrane for the efficient separation of H2 and CO2.
Tetrafluoroterephthalonitrile reacts with alkyl Grignard reagents to form corresponding 4-alkyltetrafluorobenzonitriles. Tetrafluoroterephthalonitrile acts as a four-electron donor ligand and forms tungsten(II)η 2-nitrile complexes.
Tetrafluoroterephthalonitrile is a hydroxyl group-containing organic chemical compound . It has been used in analytical chemistry as a reagent for the determination of peptide binding constants and disulfide bonds. Tetrafluoroterephthalonitrile binds to nucleophilic sites on proteins, such as the pim-1 protein, and can be used to transport other molecules across cell membranes. In addition, it has been used to produce polymers for use in analytical chemistry. This chemical is also able to bind with magnetic particles under constant pressure conditions, which makes it useful for optical sensor applications. , Product Details of C8F4N2
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts