-
Cyclopentadiene is an
organic compound with the
formula C5H6. It is
often abbreviated CpH
because the
cyclopentadienyl anion is
abbreviated Cp−. This...
-
structure was
deduced in 1931. The
spontaneous dimerization of neat
cyclopentadiene at room
temperature to form
dicyclopentadiene proceeds to
around 50%...
- the
dimer "A−A".
Dicyclopentadiene is an
asymmetrical dimer of two
cyclopentadiene molecules that have
reacted in a Diels-Alder
reaction to give the product...
-
Trimethylsilyl cyclopentadiene is an
organosilicon compound with the
chemical formula C5H5Si(CH3)3. It
exists as a
colorless liquid. It is used in the...
-
dimethylformamide and
ethylene glycol, and even in water. The
reaction of
cyclopentadiene and
butenone for
example is 700
times faster in
water relative to 2...
- 5H 5]− and
abbreviated as Cp−. It is
formed by the
deprotonation of
cyclopentadiene. The
cyclopentadienyl anion is a
ligand which binds to a
metal in organometallic...
-
hafnium metal centers.
Depending on the
placement of the catalyst's
cyclopentadiene ligands, it can
produce polypropylenes with
different tacticity. 1...
-
starting point is the
cracking of dicyclopentadiene, the
dimer of
cyclopentadiene.
Cyclopentadiene is
deprotonated by
strong bases or
alkali metals. MCl2 + 2 NaC5H5...
- EPDM. It is
prepared by the Diels–Alder
reaction of
butadiene and
cyclopentadiene. LD50 is 0.10–0.05 mg/kg (intravenous,
female rabbit). It is also a...
-
produced today.
Hexachlorocyclopentadiene is
prepared by
chlorination of
cyclopentadiene to give 1,1,2,3,4,5-octachlorocyclopentane,
which in a
second step...
