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For example, Cp′Fe(PPh 3)(CO)I has four different signals in the 1 H NMR spectrum for the ring hydrogens and five different signals in the 13 C NMR spectrum for the ring carbons. There is therefore no symmetry within the ring even accounting for rotation around the ring–metal axis, but instead there is a diastereotopic relationship as a ...
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 ‡−).
NiCl 2 + 2 NaC 5 H 5 → Ni(C 5 H 5) 2 + 2 NaCl Organometallic complexes that include both the cyclopentadienyl anion and cyclopentadiene itself are known, one example of which is the rhodocene derivative produced from the rhodocene monomer in protic solvents .
2 t Bu − 3. These ligands are so large that their complexes behave differently from the pentamethylcyclopentadienyl analogues. Because they cannot closely approach the metal, these bulky ligands stabilize high spin complexes, such as (C 5 H 2 t Bu 3) 2 Fe 2 I 2. These large ligands stabilize highly unsaturated derivatives such as (C 5 H 2 t ...
Diene complexes can also be produced by dehalogenation of 1,4-dihalobutene derivatives: [15] Fe 2 (CO) 9 + C 6 H 4 (CH 2 Br) 2 → FeBr 2 + (C 6 H 4 (=CH 2) 2)Fe(CO) 3 + 6 CO. The Fe(CO) 3 unit serves as a protecting group for the diene, preventing the diene from participating in Diels-Alder reactions and hydrogenation.
The parent cyclopentadienone is rarely encountered, because it rapidly dimerizes. [1] Many substituted derivatives are known, notably tetraphenylcyclopentadienone. Such compounds are used as ligands in organometallic chemistry. [2] The Knölker complex, derived from a substituted cyclopentadienone, is a catalyst for transfer hydrogenation. [3]
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 ...
[2] As of early 1990s, it was present in American [3] and European [4] gasoline in small amounts, and by 2011 its share in US gasoline varied between 1 and 3%. [5] It has a research octane number of 103 and motor octane number of 95. [6] The C 6 core of methylcyclopentane is not perfectly planar and can pucker to alleviate stress in its ...