enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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. Lithium tetrafluoroborate - Wikipedia

    en.wikipedia.org/wiki/Lithium_tetrafluoroborate

    8 bf 3 + 6 lih → b 2 h 6 + 6 libf 4 LiBF 4 can also be synthesized from LiF and BF 3 in an appropriate solvent that is resistant to fluorination by BF 3 (e.g. HF , BrF 3 , or liquified SO 2 ): [ 5 ]

  6. 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]

  7. Cycloisomerization - Wikipedia

    en.wikipedia.org/wiki/Cycloisomerization

    The activation barrier of isomerization of 1,3–hexadiene through a [1,5]–shift is 41 Kcal mol–1 and is expected to increase with conjugation to the ester, thus uncatalyzed isomerization is unlikely. [11] This provides the advantage of bypassing a high barrier of activation, providing access to previously unobtainable IMDA derivatives.

  8. Penex - Wikipedia

    en.wikipedia.org/wiki/Penex

    Penex unit (simplified) The Penex process is a continuous catalytic process used in the refining of crude oil.It isomerizes light naphtha (C 5 /C 6) into higher-octane, branched C 5 /C 6 molecules.

  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 ...