Chang, Siqi team published research on European Polymer Journal in 2021 | 1835-49-0

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. , HPLC of Formula: 1835-49-0

Nitrile is any organic compound with a −C≡N functional group. 1835-49-0, formula is C8F4N2, Name is Tetrafluoroterephthalonitrile.The prefix cyano- is used interchangeably with the term nitrile in literature. HPLC of Formula: 1835-49-0.

Chang, Siqi;Xie, Wei;Yao, Chan;Xu, Guangjuan;Zhang, Shuran;Xu, Yanhong research published 《 Preparation of covalent triazine frameworks with multiactive sites for efficient and reversible iodine capture》, the research content is summarized as follows. Covalent triazine skeletons (CTFs) are long-chain polymers with rigid hydrophobic aromatic skeletons and polar functional groups. Here, we selected three monomers to explore a series of stable CTFs (FCTFs, NCTFs, ClCTFs) with multiple active sites at 350 and 400°C resp., which can act as a porous platform for effective and reversible iodine capture. The iodine adsorption capacities of FCTF@350, NCTF@350, ClCTF@350, FCTF@400, NCTF@400 and ClCTF@400 are 285, 232, 231, 382, 372 and 340 wt%, resp. Among them, the iodine capture capacities of FCTFs and NCTFs are higher than those of ClCTFs, which suggested that the introduction of electron-rich F and pyridine N groups can indeed improve the iodine adsorption capacity of the polymers. In addition, at 50 bar and 323 K, the CO2 capture capacity of FCTF@350, NCTF@350, ClCTF@350, FCTF@400, NCTF@400 and ClCTF@400 are 631.6, 539.2, 496.6, 876.6, 783.3, and 695.4 mg g-1, resp. This shows that polymers have good applications in CO2 capture.

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. , HPLC of Formula: 1835-49-0

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts