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In chemistry, the cyclopentadienyl anion or cyclopentadienide is an aromatic species with a formula of [C 5 H 5] − and abbreviated as Cp −. [1] It is formed by the deprotonation of cyclopentadiene. The cyclopentadienyl anion is a ligand which binds to a metal in organometallic chemistry. [2]
The cyclopentadienyl cation is another textbook example of an antiaromatic compound. It is conventionally understood to be planar, cyclic, and have 4 π electrons (4n for n=1) in a conjugated system. However, it has long been questioned if the cyclopentadienyl cation is genuinely antiaromatic and recent discoveries have suggested that it may ...
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.
In chemistry, cyclopentadienyl is a radical with the formula C 5 H 5. The related cyclopentadienyl anion (which can formally be converted to the cyclopentadienyl radical by one-electron reduction) is aromatic , and forms salts and coordination compounds .
Aromaticity is found in ions as well: the cyclopropenyl cation (2e system), the cyclopentadienyl anion (6e system), the tropylium ion (6e), and the cyclooctatetraene dianion (10e). Aromatic properties have been attributed to non-benzenoid compounds such as tropone. Aromatic properties are tested to the limit in a class of compounds called ...
A cyclopentadienyl complex is a coordination complex of a metal and cyclopentadienyl groups (C 5 H − 5, abbreviated as Cp −). Cyclopentadienyl ligands almost invariably bind to metals as a pentahapto (η 5-) bonding mode. The metal–cyclopentadienyl interaction is typically drawn as a single line from the metal center to the center of the ...
Cyclopentadienyl can refer to Cyclopentadienyl anion, ... Cyclopentadienyl cation, [C 5 H 5] + See also. Pentadienyl This page was last edited on 3 July 2021 ...
The cyclopentadienyl anion (C 5 H – 5) with six π electrons is planar and readily generated from the unusually acidic cyclopentadiene (pK a 16), while the corresponding cation with four π electrons is destabilized, being harder to generate than a typical acyclic pentadienyl cations and is thought to be antiaromatic. [8] Similarly, the ...