Search results
Results from the WOW.Com Content Network
1,2,3,4,5-Pentakis(4-butylphenyl)-1,3-cyclopentadiene is an organochemical compound from the diene group and a cyclopentadiene derivative. The anion of this compound is used as a sterically demanding ligand, often abbreviated as Cp [BIG] , in the organometallic chemistry of sandwich compounds .
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 .
In the case of hexa-1,5-diene, the rearrangement is degenerate (the product is identical to the starting material), so K = 1 by necessity. In asymmetric dienes one often needs to consider the stereochemistry, which in the case of pericyclic reactions, such as the Cope rearrangement, can be predicted with the Woodward–Hoffmann rules and ...
[2] [1] Illustrative of the unusual complexes made possible with these bulky ligands is molecular iron nitrido complex (t Bu 3 C 5 H 2) 2 Fe 2 N 2. [3] In contrast to (C 5 Me 5) 2 Ir 2 Cl 4, (t Bu 3 C 5 H 2)IrCl 2 is monomeric. [4]
In organometallic chemistry, (diene)iron tricarbonyl describes a diverse family of related coordination complexes consisting of a diene ligand coordinated to a Fe(CO) 3 center. Often the diene is conjugated, e.g., butadiene , but the family includes nonconjugated dienes as well.
1,4-Pentadiene can be prepared from 1,5-pentadiol via the diacetate. [6] 1,3-Pentadiene, like 1,3-butadiene, undergoes a variety of cycloaddition reactions. For example, it forms a sulfolene upon treatment with sulfur dioxide. [7]
Typical examples of this type of complex are group 14 metal complexes such as CpSiMe 3. An example of both is (Cp 2 Fe(CO) 2). It is probable that η 1-Cp complexes are intermediates in the formation of η 5-Cp complexes. Still rarer, the Cp unit can bond to the metal via three carbons. In these η 3-Cp complexes, the bonding resembles that in ...
The central ring can serve as a diene in Diels–Alder reactions with various dienophiles. For example, reaction with benzyne leads to 1,2,3,4-tetraphenylnaphthalene and reaction with diphenylacetylene leads to hexaphenylbenzene. [5] In this way, it is a precursor to graphene-like molecules, [6] such as coronene.