Category: 1835-49-0

Industrially, the main methods for producing nitriles are ammoxidation and hydrocyanation. 1835-49-0, formula is C8F4N2, Name is Tetrafluoroterephthalonitrile. Both routes are green in the sense that they do not generate stoichiometric amounts of salts. Formula: C8F4N2.

Wang, Jian-Xin;Gutierrez-Arzaluz, Luis;Wang, Xiaojia;Almalki, Maram;Yin, Jun;Czaban-Jozwiak, Justyna;Shekhah, Osama;Zhang, Yuhai;Bakr, Osman M.;Eddaoudi, Mohamed;Mohammed, Omar F. research published 《 Nearly 100% energy transfer at the interface of metal-organic frameworks for X-ray imaging scintillators》, the research content is summarized as follows. In this work, we describe a highly efficient and reabsorption-free X-ray-harvesting system using luminescent metal-organic framework (MOF)-fluorescence chromophore composite films. The ultrafast time-resolved experiments and d. functional theory calculations demonstrate that a nearly 100% energy transfer from a luminescent MOF with a high at. number to an organic chromophore with thermally activated delayed fluorescence (TADF) character can be achieved. Such an unprecedented efficiency of interfacial energy transfer and the direct harnessing of singlet and triplet excitons of the TADF chromophore led to remarkable enhancement of radioluminescence upon X-ray radiation. A low detection limit of 256 nGy/s of the fabricated X-ray imaging scintillator was achieved, about 60 times lower than the MOF and 7 times lower than the organic chromophore counterparts. More importantly, this detection limit is about 22 times lower than the standard dosage for a medical examination, making it an excellent candidate for X-ray radiog.

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. , Formula: C8F4N2

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

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

Nitriles are found in many useful compounds. Nitrile rubber is also widely used as automotive and other seals since it is resistant to fuels and oils. Organic compounds containing multiple nitrile groups are known as cyanocarbons. 1835-49-0, formula is C8F4N2, Name is Tetrafluoroterephthalonitrile. Nitriles are found in many useful compounds. One of the most common occurrences of nitriles is in Nitrile rubber. Computed Properties of 1835-49-0.

Shin, Dong Jin;Hwang, Soon Jae;Lim, Junseop;Jeon, Chae Yeon;Lee, Jun Yeob;Kwon, Jang Hyuk research published 《 Reverse intersystem crossing accelerating assistant dopant for high efficiency and long lifetime in red hyperfluorescence organic light-emitting diodes》, the research content is summarized as follows. A highly efficient deep-red hyper fluorescence device achieving long device lifetime was fabricated by adopting a newly designed 2,5-bis(12H-benzo[4,5]thieno[2,3-a]carbazole-12-yl)-3,6-di(9H-carbazol-9-yl)terephthalonitrile (12BTCzTPN) thermally activated delayed fluorescence (TADF) assistant dopant. The 12BTCzTPN was designed via donor modification of 2,3,5,6-tetra(9H-carbazol-9-yl)terephthalonitrile (4CzTPN) to increase reverse intersystem crossing (RISC) rate for fast up-conversion. The carbazole donor moiety was replaced with 12H-benzo[4,5]thieno[2,3-a]carbazole (12BTCz) donor, which induced a small singlet-triplet energy gap and large spin-orbit coupling via the heavy atom effect of sulfur, resulting in 4.5-times faster RISC rate than the 4CzTPN TADF mol. The addition of 12BTCzTPN as an assistant dopant to a deep-red hyper fluorescence device resulted in a device with a high external quantum efficiency of 19.9% and a long device lifetime of 1312 h at 3000 cd/m2, which is up to 90% of the initial luminance.

Computed Properties of 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. , 1835-49-0.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

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. Recommanded Product: Tetrafluoroterephthalonitrile.

Sizov, Victor E.;Zefirov, Vadim V.;Volkova, Yulia A.;Gusak, Danil I.;Kharitonova, Elena P.;Ponomarev, Igor I.;Gallyamov, Marat O. research published 《 Celgard/ PIM -1 proton conducting composite membrane with reduced vanadium permeability》, the research content is summarized as follows. Renewable energy systems need efficient and cheap storage devices and vanadium redox flow batteries (VRB) may become one of them. However, better performance of VRB membranes yet should be achieved. Novel composite Celgard-based films coated with PIM-1 for aqueous electrolyte VRB applications are presented. Two types of the composites with different PIM-1 loadings are obtained. Their properties are studied and compared with the original Celgard films. The deposited PIM-1 forms a smooth layer on the outer Celgard surface and penetrates inside the porous matrix, thus significantly reducing the pores diameter and affecting the transport properties of the composite film. The nanoporous structure of PIM-1 permits size-screening of H₃O⁺/hydrated vanadium ions when used in aqueous vanadium redox flow batteries applications, which allows to tailor the membrane permeability for the two types of ions and, therefore, to increase its selectivity from 4.3 x 10⁶ to 1.3 x 10⁷ mS min cm^-3, while maintaining high proton conductivity

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

Nitriles are found in many useful compounds. Nitrile rubber is also widely used as automotive and other seals since it is resistant to fuels and oils. Organic compounds containing multiple nitrile groups are known as cyanocarbons. 1835-49-0, formula is C8F4N2, Name is Tetrafluoroterephthalonitrile. Nitriles are found in many useful compounds. One of the most common occurrences of nitriles is in Nitrile rubber. Recommanded Product: Tetrafluoroterephthalonitrile.

Ricci, Eleonora;Benedetti, Francesco M.;Noto, Antonella;Merkel, Timothy C.;Jin, Jianyong;De Angelis, Maria Grazia research published 《 Enabling experimental characterization and prediction of ternary mixed-gas sorption in polymers: C₂H₆/CO₂/CH₄ in PIM-1》, the research content is summarized as follows. In this work, a new exptl. protocol was designed to measure sorption of ternary gas mixtures in polymer membranes for the first time. We measured the sorption isotherms of binary and ternary mixtures of C₂H₆, CO₂, and CH₄ in PIM-1, using a pressure decay apparatus, working at constant composition and variable pressure of the gas phase. The results show competitive sorption effects in all gas mixtures analyzed, affecting each species in proportion to the total sorbed concentration of the other components. It was found that the presence of C₂H₆ in the mixture reduces the sorption of both CH₄ and CO₂ to a similar extent, so that the CO₂/CH₄ solubility-selectivity is not markedly affected. The exptl. data were used to validate predictions of the Non-Equilibrium Lattice Fluid (NELF) model of binary and ternary sorption isotherms. The NELF model is generally in close agreement, both in the prediction of pressure and mixture composition effects, proving to be a reliable tool to assess mixed-gas sorption, even in complex scenarios.

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. , Recommanded Product: Tetrafluoroterephthalonitrile

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Inorganic compounds containing the −C≡N group are not called nitriles, but cyanides instead.1835-49-0, formula is C8F4N2, Name is Tetrafluoroterephthalonitrile. Though both nitriles and cyanides can be derived from cyanide salts, most nitriles are not nearly as toxic. Related Products of 1835-49-0.

Rochat, Sebastien;Tian, Mi;Atri, Ria;Mays, Timothy J.;Burrows, Andrew D. research published 《 Enhancement of gas storage and separation properties of microporous polymers by simple chemical modifications》, the research content is summarized as follows. Owing to their large surface area and good solvent processability, polymers of intrinsic microporosity (PIMs) have been widely investigated for gas storage and separation processes. In this article, we show how chem. modifying the polymers can fine-tune their properties for specific, targeted applications. We find that converting the archetypal microporous polymer PIM-1 into a polycarboxylate salt enhances its separation capabilities for H₂/CO₂ mixtures (relevant to hydrogen production), whereas appending multiple amine groups significantly improves gas separation properties for N₂/CO₂ mixtures (relevant to flue gas treatment). Adsorption-based separation processes have received less attention than size-sieving processes in porous polymeric materials, however they could provide a suitable alternative technol. to energy-intensive separation processes such as cryogenic distillation We also report the hydrogen storage properties of the modified polymers, which we find to depend on the chem. modification carried out. By coupling the simplicity of the proposed chem. modifications with the scalability and porous properties of PIMs, we provide a blueprint to create new multifunctional materials with adapted properties for targeted applications.

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. , Related Products of 1835-49-0

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Nitriles are found in many useful compounds. Nitrile rubber is also widely used as automotive and other seals since it is resistant to fuels and oils. Organic compounds containing multiple nitrile groups are known as cyanocarbons. 1835-49-0, formula is C8F4N2, Name is Tetrafluoroterephthalonitrile. Nitriles are found in many useful compounds. One of the most common occurrences of nitriles is in Nitrile rubber. Recommanded Product: Tetrafluoroterephthalonitrile.

Rong, Siyi;Su, Pengcheng;Chen, Shizheng;Jia, Miaomiao;Li, Wanbin research published 《 Sub-5 nm porous polymer decoration toward superhydrophobic MOFs with enhanced stability and processability》, the research content is summarized as follows. Metal-organic frameworks (MOFs) show great potential for various applications, but many of them suffer from the drawbacks of hydrolysis propensity and poor processability. Herein, we employ polymers of intrinsic microporosity (PIMs) with hydrophobic pores to decorate MOFs toward substantially improved water stability and shapeability. Through simple PIM-1 decoration, the sub-5 nm polymer layers can be uniformly deposited on MOF surfaces with almost no deterioration in porosity. Owing to the existence of superhydrophobic coating and the obstruction of water entrance into MOFs, the PIM-1 coated CuBTC exhibits impressive water resistance and excellent pore preservation ability after exposure in water, even in acidic and alk. solutions Moreover, polymer decoration improves the processability of MOFs, while various MOF/PIM-1 bulk wafers and oil-water separators can be obtained straightforwardly.

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. , Recommanded Product: Tetrafluoroterephthalonitrile

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Inorganic compounds containing the −C≡N group are not called nitriles, but cyanides instead.1835-49-0, formula is C8F4N2, Name is Tetrafluoroterephthalonitrile. Though both nitriles and cyanides can be derived from cyanide salts, most nitriles are not nearly as toxic. Related Products of 1835-49-0.

Saadatkish, Niloufar;Karimi-Sabet, Javad;Sharif, Alireza research published 《 A molecular dynamics simulation study on the solubilities of monomers of a PIM-1 polymer in supercritical carbon dioxide》, the research content is summarized as follows. The absolute solubilities of tetrahydroxy-3,3,3′,3′-tetramethyl-1,1′-spirobisindane (TTSBI) and tetrafluoroterephthalonitrile (TFTPN), the monomers of a polymer of intrinsic microporosity-1 (PIM-1), in supercritical carbon dioxide (SCCO₂), are studied by mol. dynamics (MD) simulation method. Solvation free energies of the monomers in SCCO₂ are simulated at different temperatures and pressures by the thermodn. integration method. Furthermore, a new procedure is proposed to calculate the external pressure dependency of the monomers vapor pressures by MD simulation. These two quantities are used to estimate the absolute solubility of each monomer in SCCO₂ medium. TFTPN showed higher solubility (than TTSBI) which was ascribed to its CO₂-philic structure and low vapor pressure. Exptl. measured solubilities are in good agreement with the simulated ones confirming the accuracy of the proposed method for the calculation of vapor pressures. Finally, SCCO₂ medium is suggested as a suitable medium for synthesis of PIM-1 polymer provided that small amounts of a cosolvent are used or high external pressures (greater than 30 MPa) are applied.

Related Products of 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. , 1835-49-0.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

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. Safety of Tetrafluoroterephthalonitrile.

Senosy, Ibrahim A.;Lu, Zhi-Heng;Zhou, Dong-Dong;Abdelrahman, Talat M.;Chen, Min;Zhuang, Lv-Yun;Liu, Xiao;Cao, Yi-Wen;Li, Jian-Hong;Hua Yang, Zhong- research published 《 Construction of a magnetic solid-phase extraction method for the analysis of azole pesticides residue in medicinal plants》, the research content is summarized as follows. In this work, a sensitive and cost-effective method for the quant. anal. of azole pesticides residues in six medicinal plants was established based on magnetic cyclodextrin crosslinked with tetrafluoroterephthalonitrile (Fe3O4@TFN-CDPs) coupled with high-performance liquid chromatog. (HPLC). Through characterization anal., the outer shell of Fe3O4@TFN-CDPs has observed coating with a network of the polymer and forming a core-shell structure. Under the optimum conditions, the limits of detection (LODs) and limits of qualification (LOQs) of target pesticides were ranged from 0.011 to 0.106μg Kg-1 and from 0.036 to 0.354μg Kg-1, resp. Finally, the achieved recoveries of pesticides in six medicinal samples fluctuated from 60.1% to 102.3%. Altogether, this method based on Fe3O4@TFN-CDPs composites provided a new idea for the anal. of trace pesticides in complicated matrixes.

Safety of 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

Industrially, the main methods for producing nitriles are ammoxidation and hydrocyanation. 1835-49-0, formula is C8F4N2, Name is Tetrafluoroterephthalonitrile. Both routes are green in the sense that they do not generate stoichiometric amounts of salts. Category: nitriles-buliding-blocks.

Poulard, Laurelie;Kasemthaveechok, Sitthichok;Coehlo, Max;Kumar, Ramar Arun;Frederic, Lucas;Sumsalee, Patthira;d′Anfray, Timothee;Wu, Sen;Wang, Jingxiang;Matulaitis, Tomas;Crassous, Jeanne;Zysman-Colman, Eli;Favereau, Ludovic;Pieters, Gregory research published 《 Circularly polarized-thermally activated delayed fluorescent materials based on chiral bicarbazole donors》, the research content is summarized as follows. We describe herein a mol. design to generate circularly polarized thermally activated delayed fluorescence emitters in which chiral bicarbazole donors are connected to acceptor units via a rigid 8-membered cycle and how the nature of the donor and acceptor units affect the photophys. and chiroptical properties.

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. , Category: nitriles-buliding-blocks

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts