Misplaced Pages

NCF

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.

Cyanogen fluoride (molecular formula: FCN ; IUPAC name: carbononitridic fluoride ) is an inorganic linear compound which consists of a fluorine in a single bond with carbon , and a nitrogen in a triple bond with carbon. It is a toxic and explosive gas at room temperature. It is used in organic synthesis and can be produced by pyrolysis of cyanuric fluoride or by fluorination of cyanogen .

#889110

12-693: NCF may refer to: Cyanogen fluoride , a toxic, explosive inorganic linear compound National Capital FreeNet , an ISP in Ottawa, Canada National Championship Foundation , an organization that retroactively selected NCAA college football national champions from 1869-1870 and 1872-2000 National Christian Foundation , a US Evangelical Christian donations organization National Civic Federation , 1900–1920s US labor organization National Commerce Financial Corporation , Tennessee, NYSE symbol, 2001–2005 National Cultural Foundation of Barbados National Cyber Force ,

24-409: A 24 cm separation between the two branches. A triplet band is observed at around 451 cm . Cyanogen fluoride reacts with benzene in the presence of aluminum chloride to form benzonitrile in 20% conversion. It also reacts with olefins to yield an alpha,beta-fluoronitriles. FCN also adds to olefins which have internal double bonds in the presence of strong acid catalyst. FCN can be stored in

36-432: A British defence and intelligence unit National Cybersecurity FFRDC , a US-funded research and development center operated by MITRE Corporation in support of NIST Nederlandsche Cocaïnefabriek , a Dutch pharmaceutical company New Century Foundation , a US white supremacist organization founded in 1994 Next Century Foundation, a London-based think tank on Middle Eastern conflicts Nicaraguan Cycling Federation ,

48-508: A molecular mass of 45.015 gmol . Cyanogen fluoride has a boiling point of –46.2 °C and a melting point of –82 °C. The stretching constant for the CN bond was 17.5 mdyn/A and for the CF bond it was 8.07 mdyn/A, but this can vary depending on the interaction constant. At room temperature, the condensed phase converts rapidly to polymeric materials. Liquid FCN explodes at –41 °C when initiated by

60-467: A squib. The fluorine NMR pattern for FCN showed that there was a triplet peak centered at 80 ppm (3180 cps) with a 32-34 cps splitting between adjacent peaks because of the N nucleus. This splitting is absent near freezing point and it collapses to a singlet peak. The IR spectrum of FCN shows two doublet bands at around 2290 cm (for the C ≡ N) and 1078 cm (for the C-F). The C-F doublet band has

72-426: A stainless steel cylinders for over a year when the temperature is -78.5 °C (solid carbon dioxide temperature). Cyanogen fluoride undergoes violent reaction when in the presence of boron trifluoride or hydrogen fluoride. Pure gaseous FCN at atmospheric pressure and room temperature does not ignite by a spark or hot wire. FCN air mixtures however are more susceptible to ignition and explosion than pure FCN. FCN

84-433: Is by the fluorination of cyanogen. Nitrogen trifluoride can fluoridate cyanogen to cyanogen fluoride when both the reactants are injected downstream into the nitrogen arc plasma. With carbonyl fluoride and carbon tetrafluoride, FCN was obtained by passing these fluorides through the arc flame and injecting the cyanogen downstream into the arc plasma. Cyanogen fluoride (FCN) is a toxic, colorless gas. The linear molecule has

96-409: Is pyrolyzed (becoming a pyrolysate) at a rate of 50g/hr, and appears as fluffy white solid collected in liquid nitrogen traps. These liquid nitrogen traps are filled to atmospheric pressure with nitrogen or helium. This process yields crude cyanogen fluoride, which is then distilled in a glass column at atmospheric pressure to give pure cyanogen fluoride. Another method of synthesizing cyanogen fluoride

108-437: Is synthesized by the pyrolysis of cyanuric fluoride (C 3 N 3 F 3 ) at 1300 °C and 50mm pressure; this process gives a maximum of 50% yield. Other products observed were cyanogen and CF 3 CN. For pyrolysis, an induction heated carbon tube with an internal diameter of 0.75 inches is packed with 4 to 8 mesh carbon granules and is surrounded by graphite powder insulation and a water-jacketed shell. The cyanuric fluoride

120-419: Is useful in synthesis of important compounds such as dyes, fluorescent brighteners and photographic sensitizers. It is also very useful as a fluorinating and nitrilating agent. Beta-fluoronitriles, which are produced when FCN is reacted with olefins, are useful intermediates for preparing polymers, beta-fluorocarboxylic acids and other fluorine containing products. Useful amines can be obtained. Cyanogen fluoride

132-647: The national governing body of cycle racing in Nicaragua Nigeria Cricket Federation , the national governing body of cricket in Nigeria No-Conscription Fellowship , a British pacifist organization Nomenclature Committee for Fungi , a committee of the International Botanical Congress Topics referred to by the same term [REDACTED] This disambiguation page lists articles associated with

SECTION 10

#1732844796890

144-467: The title NCF . If an internal link led you here, you may wish to change the link to point directly to the intended article. Retrieved from " https://en.wikipedia.org/w/index.php?title=NCF&oldid=1240962605 " Category : Disambiguation pages Hidden categories: Short description is different from Wikidata All article disambiguation pages All disambiguation pages Cyanogen fluoride Cyanogen fluoride (FCN),

#889110