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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. The [Li(OEt 2) 4] + complex is tetrahedral.

  4. 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]

  5. Isomerization - Wikipedia

    en.wikipedia.org/wiki/Isomerization

    The compound with the formula (C 5 H 5) 2 Fe 2 (CO) 4 exists as three isomers in solution. In one isomer the CO ligands are terminal. When a pair of CO are bridging, cis and trans isomers are possible depending on the location of the C 5 H 5 groups. [7] Another example in organometallic chemistry is the linkage isomerization of ...

  6. Valence isomer - Wikipedia

    en.wikipedia.org/wiki/Valence_isomer

    Tricyclo[4,2,0,0 2,5]octa-3,7-diene. The dimer of cyclobutadiene occurs as a cis isomer and a trans isomer. Both isomers convert to COT (symmetry forbidden hence stable) with a half-life of 20 minutes at 140 °C [ 10 ]

  7. Cycloisomerization - Wikipedia

    en.wikipedia.org/wiki/Cycloisomerization

    [10] [11] Dienyl esters such as 11 were transformed into substituted bicyclo[2.2.2]octanes via an isomerization step stabilized by a hemiacetal azolium intermediate (13). [11] 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 ...

  8. Penex - Wikipedia

    en.wikipedia.org/wiki/Penex

    It was first used commercially in 1958. [2] Ideally, the isomerization catalyst converts normal pentane (nC5) to isopentane (iC5) and normal hexane (nC6) to 2,2- and 2,3-dimethylbutane. The thermodynamic equilibrium is more favorable at low temperature. [3]

  9. Photoisomerization - Wikipedia

    en.wikipedia.org/wiki/Photoisomerization

    In addition, interest in photoisomerizable molecules has been aimed at molecular devices, such as molecular switches, [3] [4] molecular motors, [5] and molecular electronics. Another class of device that uses the photoisomerization process is as an additive in liquid crystals to change their linear and nonlinear properties. [ 6 ]