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  2. Cyclopentadiene - Wikipedia

    en.wikipedia.org/wiki/Cyclopentadiene

    Melting point: −90 °C; −130 °F; 183 K Boiling point: 39 to 43 °C; 102 to 109 °F; 312 to 316 K ... Cyclopentadiene is an organic compound with the formula C 5 ...

  3. Melting points of the elements (data page) - Wikipedia

    en.wikipedia.org/wiki/Melting_points_of_the...

    The Gmelin rare earths handbook lists 1522 °C and 1550 °C as two melting points given in the literature, the most recent reference [Handbook on the chemistry and physics of rare earths, vol.12 (1989)] is given with 1529 °C.

  4. Dicyclopentadiene - Wikipedia

    en.wikipedia.org/wiki/Dicyclopentadiene

    At temperatures above about 125 °C in the vapor phase, dissociation to cyclopentadiene monomer starts to become thermodynamically favored (the dissociation constant K d = [cyclopentadiene] 2 / [dicyclopentadiene] > 1). For instance, the values of K d at 149 °C and 195 °C were found to be 277 and 2200, respectively. [10]

  5. Cyclopentene - Wikipedia

    en.wikipedia.org/wiki/Cyclopentene

    Melting point: −135 °C (−211 °F; 138 K) Boiling point: ... It can also be produced by the catalytic hydrogenation of cyclopentadiene. [6] Reactions

  6. Cyclopentadienyliron dicarbonyl dimer - Wikipedia

    en.wikipedia.org/wiki/Cyclopentadienyliron_di...

    2 Fe(CO) 5 + C 10 H 12 → (η 5-C 5 H 5) 2 Fe 2 (CO) 4 + 6 CO + H 2. In this preparation, dicyclopentadiene cracks to give cyclopentadiene, which reacts with Fe(CO) 5 with loss of CO. Thereafter, the pathways for the photochemical and thermal routes differ subtly but both entail formation of a hydride intermediate. [5] The method is used in ...

  7. Sodium cyclopentadienide - Wikipedia

    en.wikipedia.org/wiki/Sodium_cyclopentadienide

    2 Na + 2 C 5 H 6 → 2 NaC 5 H 5 + H 2. The conversion can be conducted by heating a suspension of molten sodium in dicyclopentadiene. [2] In former times, the sodium was provided in the form of "sodium wire" or "sodium sand", a fine dispersion of sodium prepared by melting sodium in refluxing xylene and rapidly stirring.

  8. Arsole - Wikipedia

    en.wikipedia.org/wiki/Arsole

    Substitution of all hydrogen atoms in arsole with phenyl groups yields yellow needles of crystalline pentaphenylarsole, which has a melting point of 215 °C. This complex can be prepared, at a yield of 50–93%, by reacting 1,4-diiodo-1,2,3,4-tetraphenylbutadiene [ 12 ] or 1,4-dilithio-1,2,3,4-tetraphenylbutadiene with phenylarsenous dichloride ...

  9. Tetraphenylcyclopentadienone - Wikipedia

    en.wikipedia.org/wiki/Tetraphenylcyclopentadienone

    Tetraphenylcyclopentadienone is an organic compound with the formula (C 6 H 5 C) 4 C 4 C=O. It is classified as a cyclic dienone. It is a dark purple to black crystalline solid that is soluble in organic solvents. It is an easily made building block for many organic and organometallic compounds.