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  2. Methylcyclopentadiene - Wikipedia

    en.wikipedia.org/wiki/Methylcyclopentadiene

    These isomers are the organic precursor to the methylcyclopentadienyl ligand (C 5 H 4 Me, often denoted as Cp′), commonly found in organometallic chemistry. As with cyclopentadiene , methylcyclopentadiene is prepared by thermal cracking of its Diels–Alder dimer, followed by distillation for removal of cyclopentadiene, a common impurity.

  3. Cyclopentadiene - Wikipedia

    en.wikipedia.org/wiki/Cyclopentadiene

    Cyclopentadiene is an organic compound with the formula C 5 H 6. [6] It is often abbreviated CpH because the cyclopentadienyl anion is abbreviated Cp − . This colorless liquid has a strong and unpleasant odor .

  4. Pentamethylcyclopentadiene - Wikipedia

    en.wikipedia.org/wiki/Pentamethylcyclopentadiene

    1,2,3,4,5-Pentamethylcyclopentadiene is a cyclic diene with the formula C 5 (CH 3) 5 H, often written C 5 Me 5 H, where Me is CH 3. [3] It is a colorless liquid. [1]1,2,3,4,5-Pentamethylcyclopentadiene is the precursor to the ligand 1,2,3,4,5-pentamethylcyclopentadienyl, which is often denoted Cp* (C 5 Me 5) and read as "C P star", the "star" signifying the five methyl groups radiating from ...

  5. Cyclopentene - Wikipedia

    en.wikipedia.org/wiki/Cyclopentene

    Cyclopentene is a chemical compound with the formula (CH 2) 3 (CH) 2. It is a colorless liquid with a petrol-like odor. It has few applications, and thus is mainly used as a minor component of gasoline, present in concentrations of less than 1%. [1] [2] It is one of the principal cycloalkenes.

  6. Pentadiene - Wikipedia

    en.wikipedia.org/wiki/Pentadiene

    2,3-pentadiene, H 3 C−CH=C=CH−CH 3, with two enantiomers (R and S). [5] It and 1,2-pentadiene are the least common isomers of pentadiene. Well known derivatives containing pentadiene groups include hexadienes , cyclopentadiene , and especially three fatty acids linoleic acid , α- linolenic acid , and arachidonic acid as well as their ...

  7. Cyclopentadienyl complex - Wikipedia

    en.wikipedia.org/wiki/Cyclopentadienyl_complex

    These ligands are more basic and more lipophilic. Replacing methyl groups with larger substituents results in cyclopentadienes that are so encumbered that pentaalkyl derivatives are no longer possible. Well-studied ligands of this type include C 5 R 4 H − (R = iso-Pr) and 1,2,4-C 5 R 3 H 2 − (R = tert-Bu).

  8. Di-tert-butylcyclopentadiene - Wikipedia

    en.wikipedia.org/wiki/Di-tert-butylcyclopentadiene

    Di-tert-butylcyclopentadiene is an organic compound with the formula (Me 3 C) 2 C 5 H 4, where Me = methyl.It is a colorless liquid that is soluble in organic solvents. The compound is the conjugate acid of the di-tert-butylcyclopentadienyl ligand, (Me 3 C) 2 C 5 H 3 − [1] (sometimes abbreviated Cp ‡−).

  9. Trimethylsilyl cyclopentadiene - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilyl_cyclopentadiene

    Trimethylsilyl cyclopentadiene is an organosilicon compound with the chemical formula C 5 H 5 Si(CH 3) 3. It exists as a colorless liquid. It exists as a colorless liquid. It is used in the synthesis of some metal cyclopentadienyl complexes and has attracted interest for its fluxional structure .