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  2. Tris(pentafluorophenyl)borane - Wikipedia

    en.wikipedia.org/wiki/Tris(pentafluorophenyl)borane

    Tris(pentafluorophenyl)borane, sometimes referred to as "BCF", is the chemical compound (C 6 F 5) 3 B.It is a white, volatile solid. The molecule consists of three pentafluorophenyl groups attached in a "paddle-wheel" manner to a central boron atom; the BC 3 core is planar.

  3. Lithium tetrakis(pentafluorophenyl)borate - Wikipedia

    en.wikipedia.org/wiki/Lithium_tetrakis(pentafluo...

    The anion is tetrahedral with B-C bond lengths of approximately 1.65 Angstroms. The salt has only been obtained as the etherate, and the crystallography confirms that four ether (OEt 2) molecules are bound to the lithium cation, with Li-O bond lengths of approximately 1.95 Å.

  4. Isomerization - Wikipedia

    en.wikipedia.org/wiki/Isomerization

    In chemistry, isomerization or isomerisation is the process in which a molecule, polyatomic ion or molecular fragment is transformed into an isomer with a different chemical structure. [1] Enolization is an example of isomerization, as is tautomerization .

  5. Organoxenon chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoxenon_chemistry

    Organoxenon compounds are frequently prepared from organocadmium species including Cd(Ar F) 2 (where Ar F is a fluorine-containing arene), C 6 F 5 SiF 3, and C 6 F 5 SiMe 3 (used along with fluoride). With the use of stronger Lewis acids, such as C 6 F 5 BF 2, ionic compounds like [RXe][Ar F BF 3] can be produced.

  6. Penex - Wikipedia

    en.wikipedia.org/wiki/Penex

    Ideally, the isomerization catalyst converts normal pentane (nC5) to isopentane (iC5) and normal hexane (nC6) to 2,2- and 2,3-dimethylbutane. ... This page was last ...

  7. Bromopentafluorobenzene - Wikipedia

    en.wikipedia.org/wiki/Bromopentafluorobenzene

    Bromopentafluorobenzene is an organofluorine compound with the formula C 6 F 5 Br. It is a colorless liquid that is used to prepare pentafluophenyl compounds. These syntheses typically proceed via the intermediacy of C 6 F 5 Li or the Grignard reagent. [1]

  8. Beckmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Beckmann_rearrangement

    In the third step, an isomerization step protonates the nitrogen atom leading to the amide. The Beckmann rearrangement mechanism The same computation with a hydroxonium ion and 6 molecules of water has the same result, but when the migrating substituent is a phenyl group, the mechanism favors the formation of an intermediate three-membered π ...

  9. Brookhart's acid - Wikipedia

    en.wikipedia.org/wiki/Brookhart's_Acid

    In solution, the compound slowly degrades to m-C 6 H 3 (CF 3) 2 and BAr′ 3. [1] [H(OEt 2) 2][B(C 6 F 5) 4] is a related compound with a slightly different weakly coordinating anion; it was first reported in 2000. An X-ray crystal structure of that compound was obtained, showing the acidic proton coordinated by both ethereal oxygen centers ...