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. Recommanded Product: Tetrafluoroterephthalonitrile.
Huang, Lingqi;Luo, Zhiyong;Han, Wenjie;Zhang, Qi;Zhu, He;Zhu, Shiping research published 《 Direct transformation of ZIF-8 into hollow porous carbons and hollow carbon composites》, the research content is summarized as follows. Hollow porous carbons (HPCs) are a class of porous materials with advantages of high surface to volume ratio, large interior cavities, low d., and short diffusion length, which are promising in various applications. Direct carbonization of carbon precursors is the simplest and the most cost-effective method to prepare porous carbons, however, it often leads to non-hollow structures. Herein, we demonstrate the preparation of HPCs through a direct carbonization method with a two-step heating process of zeolitic imidazolate framework-8 (ZIF-8) and tetrafluoroterephthalonitrile (TFTPN). During the carbonization, ZIF-8 nanoparticles first react with TFTPN at low temperature to create polymer coatings on the surface, which are then converted into HPCs at elevated temperature The obtained HPCs show hierarchically porous structure with high sp. surface areas and pore volumes Addnl., this method has been adopted to fabricate Au@HPCs yolk-shell composites, exhibiting good catalytic performance in nitrobenzene reduction The developed synthesis strategy can enrich the toolbox for the preparation of novel HPCs and their composites.
Recommanded Product: Tetrafluoroterephthalonitrile, 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. , 1835-49-0.
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts