Isoindole
 |
|
| Ball-and-stick model | |
| Names | |
|---|---|
| IUPAC name
2H-Isoindole
|
|
| Identifiers | |
270-68-8  |
|
| ChEBI | CHEBI:33179 |
| ChemSpider | 2282425 |
| Jmol 3D model | Interactive image |
| PubChem | 3013853 |
|
|
|
|
| Properties | |
| C8H7N | |
| Molar mass | 117.15 g/mol |
| Vapor pressure | {{{value}}} |
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
|
 verify (what is  ?) |
|
| Infobox references | |
Isoindole in heterocyclic chemistry is a benzo-fused pyrrole.[1] The compound is an isomer of indole. Its reduced form is isoindoline. The parent isoindole is a rarely encountered in the technical literature, but substituted derivatives are useful commercially and occur naturally. Isoindoles units occur in phthalocyanines, an important family of dyes. Some alkaloids containing isoindole have been isolated and characterized.[2][3]
Contents
Synthesis
The parent isoindole was prepared by flash vacuum pyrolysis of an N-substituted isoindoline.[4] N-Substituted isoindoles, which are easier to handle, can be prepared by dehydration of isoindoline-N-oxides. They also arise by myriad other methods, e.g., starting from xylylene dibromide (C6H4(CH2Br)2).
Structure and tautomerism of 2-H-isoindoles
Unlike indole, isoindoles exhibit noticeable alternation in the C-C bond lengths, which is consistent with their description as pyrrole derivatives fused to a butadiene.
In solution, the 2H-isoindole tautomer predominates. It resembles a pyrrole more than a simple imine.[5] The degree to which the 2H predominates depends on the solvent, and can vary with the substituent in substituted isoindoles.[6]
-
File:Isoindoletautomerism.svg2H-Isoindole (right) is the predominant tautomer relative to 1H-isoindole (left)
N-Substituted isoindoles do not engage is tautomerism and are therefore simpler to study.
The commercially important phthalimide is an isoindole-1,3-dione with two carbonyl groups attached to the heterocyclic ring.
- Illustrative Isoindoline Derivatives
-
PY139.svg
Pigment yellow 139, a common high performance pigment.
-
PY185.svg
Pigment yellow 185, a common high performance pigment.
-
Copper phthalocyanine, one of the most pervasive synthetic pigments.
See also
- 1,3-Disubstituted Isoindolines.
- Isoindene with nitrogen replaced by a methylene group.
References
<templatestyles src="Reflist/styles.css" />
Cite error: Invalid <references> tag; parameter "group" is allowed only.
<references />, or <references group="..." />- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Heugebaert, Thomas S. A.; Roman, Bart I.; Stevens, Christian V. "Synthesis of isoindoles and related iso-condensed heteroaromatic pyrroles" Chemical Society Reviews 2012, volume 41, pp. 5626-5640. doi:10.1039/c2cs35093a
- ↑ See for example: Lua error in package.lua at line 80: module 'strict' not found.
- ↑ R. Bonnett and R. F. C. Brown "Isoindole" J. Chem. Soc., Chem. Commun., 1972, 393-395. doi:10.1039/C39720000393
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
