8-Hydroxyquinoline

Last updated
8-Hydroxyquinoline
8-Hydroxychinolin.svg
8-Hydroxyquinoline 3D ball.png
8-Hydroxychinolin.jpg
Names
Preferred IUPAC name
Quinolin-8-ol
Other names
1-Azanaphthalene-8-ol, Fennosan H 30, Hydroxybenzopyridine, Oxybenzopyridine, Oxychinolin, Oxyquinoline, Phenopyridine, Quinophenol, Oxine, 8-Quinolinol
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.005.193 OOjs UI icon edit-ltr-progressive.svg
KEGG
PubChem CID
UNII
  • InChI=1S/C9H7NO/c11-8-5-1-3-7-4-2-6-10-9(7)8/h1-6,11H Yes check.svgY
    Key: MCJGNVYPOGVAJF-UHFFFAOYSA-N Yes check.svgY
  • InChI=1/C9H7NO/c11-8-5-1-3-7-4-2-6-10-9(7)8/h1-6,11H
    Key: MCJGNVYPOGVAJF-UHFFFAOYAG
  • C1=CC2=C(C(=C1)O)N=CC=C2
Properties
C9H7NO
Molar mass 145.16 g/mol
AppearanceWhite crystalline powder
Density 1.034 g/cm3
Melting point 76 °C (169 °F; 349 K)
Boiling point 276 °C (529 °F; 549 K)
Pharmacology
G01AC30 ( WHO ) A01AB07 ( WHO ) D08AH03 ( WHO ) R02AA14 ( WHO )
Hazards
GHS labelling:
GHS-pictogram-skull.svg GHS-pictogram-silhouette.svg GHS-pictogram-acid.svg GHS-pictogram-pollu.svg
Danger
H301, H317, H318, H360D, H410
P202, P273, P280, P301+P310, P302+P352, P305+P351+P338
Safety data sheet (SDS) External MSDS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

8-Hydroxyquinoline (also known as oxine) is an organic compound derived from the heterocycle quinoline. A colorless solid, its conjugate base is a chelating agent, which is used for the quantitative determination of metal ions.

Contents

In aqueous solution 8-hydroxyquinoline has a pKa value of ca. 9.9 [1] It reacts with metal ions, losing the proton and forming 8-hydroxyquinolinato-chelate complexes.

Tris(8-hydroxyquinolinato)aluminium Mer-tris(8-hydroxyquinoline)aluminium(III)-from-xtal-2000-CM-3D-ellipsoids.png
Tris(8-hydroxyquinolinato)aluminium

The aluminium complex, [3] is a common component of organic light-emitting diodes (OLEDs). Substituents on the quinoline ring affect the luminescence properties. [4]

In its photo-induced excited-state, 8-hydroxyquinoline converts to zwitterionic isomers, in which the hydrogen atom is transferred from oxygen to nitrogen. [5]

History

8-hydroxyquinoline was first obtained by Hugo Weidel and his student Albert Cobenzl in 1880. They decarboxylated so-called oxycinchoninic acid (from cinchonine) and characterized the resulting compound as melting at about 70°C. They identified that the hydroxy group is on the benzene ring (but not its particular place) and called the compound oxyquinoline and α-quinophenol. [6]

In the following year more chemists found other ways to make the compound. Zdenko Hans Skraup discovered a way to synthesize substituted quinolines from substituted phenols and described three isomers of oxyquinoline, identifying the structure of 8-hydroxyquinoline. [7] Otto Fischer  [ de ] and his student Karl Bedall made the compound from a sulphonic acid independently at about the same time, but misidentified its structure. [8] [9]

By 1888 azo dyes were made from the compound. [10]

In the 1920s insoluble chelates of 8-hydroxyquinoline were discovered. [11]

Bioactivity

The complexes as well as the heterocycle itself exhibit antiseptic, disinfectant, and pesticide properties, [12] [13] functioning as a transcription inhibitor. [14] [ dubious – discuss ] Its solution in alcohol is used in liquid bandages. It once was of interest as an anti-cancer drug. [15]

A thiol analogue, 8-mercaptoquinoline is also known. [16]

The roots of the invasive plant Centaurea diffusa release 8-hydroxyquinoline, which has a negative effect on plants that have not co-evolved with it. [17]

See also

References

  1. ↑ Albert, A.; Phillips, J. N. (1956). "264. Ionization Constants of Heterocyclic Substances. Part II. Hydroxy-Derivatives of Nitrogenous Six-Membered Ring-Compounds". Journal of the Chemical Society (Resumed). 1956: 1294–1304. doi:10.1039/JR9560001294.
  2. ↑ Cölle, M.; Dinnebier, R. E.; Brütting, W. (2002). "The structure of the blue luminescent δ-phase of tris(8-hydroxyquinoline)aluminium(III) (Alq3)". Chemical Communications. 2002 (23): 2908–9. doi:10.1039/b209164j. PMID   12478807. S2CID   96135270.
  3. ↑ Katakura, R.; Koide, Y. (2006). "Configuration-Specific Synthesis of the Facial and Meridional Isomers of Tris(8-hydroxyquinolinate)aluminum (Alq3)". Inorganic Chemistry. 45 (15): 5730–5732. doi:10.1021/ic060594s. PMID   16841973.
  4. ↑ Montes, V. A.; Pohl, R.; Shinar, J.; Anzenbacher, P. Jr. (2006). "Effective Manipulation of the Electronic Effects and Its Influence on the Emission of 5-Substituted Tris(8-quinolinolate) Aluminum(III) Complexes". Chemistry: A European Journal. 12 (17): 4523–4535. doi:10.1002/chem.200501403. PMID   16619313.
  5. ↑ Bardez, E.; Devol, I.; Larrey, B.; Valeur, B. (1997). "Excited-State Processes in 8-Hydroxyquinoline: Photoinduced Tautomerization and Solvation Effects". The Journal of Physical Chemistry B. 101 (39): 7786–7793. doi:10.1021/jp971293u.
  6. ↑ Weidel, H.; Cobenzl, A. (1880). "Über Derivate der Cinchoninsäure und des Chinolins". Monatshefte für Chemie und verwandte Teile anderer Wissenschaften (in German). 1 (1): 844–868. doi:10.1007/BF01517113. ISSN   1434-4475.
  7. ↑ DE 14976,Skraup, Zdenko Hanus,"Verfahren zur Darstellung der Oxychinoline durch Behandlung von Mononitro- und Monamido-Phenolen mit Glycerin und Schwefelsäure",published 1881-09-10,issued 1881-02-16
  8. ↑ Bedall, Karl; Fischer, Otto (1881). "Ueber Oxychinolin aus Chinolinsulfosäure" . Berichte der Deutschen Chemischen Gesellschaft (in German). 14 (1): 442–443. doi:10.1002/cber.188101401101. ISSN   1099-0682.
  9. ↑ Fischer, Otto (1882). "Zur Geschichte der Oxychinoline". Berichte der Deutschen Chemischen Gesellschaft (in German). 15 (2): 1979–1981. doi:10.1002/cber.188201502123. ISSN   1099-0682.
  10. ↑ Journal of the Society of Dyers and Colourists. Society of Dyers and Colourists. 1888.
  11. ↑ Berg, R. (1927). "Neue Wege zur Bestimmung und Trennung der Metalle mit Hilfe von o-Oxychinolin" . Zeitschrift für analytische Chemie (in German). 71 (5): 171–185. doi:10.1007/BF01390921. ISSN   1618-2650.
  12. ↑ Phillips, J. P. (1956). "The Reactions of 8-Quinolinol". Chemical Reviews. 56 (2): 271–297. doi:10.1021/cr50008a003.
  13. ↑ "8-Hydroxyquinoline". Medical Dictionary Online. Archived from the original on 2016-10-09. Retrieved 2016-03-09.
  14. ↑ "8-Hydroxyquinoline". Sigma-Aldrich. Retrieved 2022-02-15.
  15. ↑ Shen, A. Y.; Wu, S. N.; Chiu, C. T. (1999). "Synthesis and Cytotoxicity Evaluation of some 8-Hydroxyquinoline Derivatives". Journal of Pharmacy and Pharmacology. 51 (5): 543–548. doi: 10.1211/0022357991772826 . PMID   10411213. S2CID   33085238.
  16. ↑ Fleischer, H. (2005). "Structural Chemistry of Complexes of (n-1)d10ns Metal Ions with β-N-Donor Substituted Thiolate Ligands (m=0, 2)". Coordination Chemistry Reviews. 249 (7–8): 799–827. doi:10.1016/j.ccr.2004.08.024.
  17. ↑ Vivanco, J.M.; Bais, H.P.; Stermitz, F.R.; Thelen, G.C.; Callaway, R.M. (2004). "Biogeographical variation in community response to root allelochemistry: novel weapons and exotic invasion". Ecology Letters. 7 (4): 285–292. Bibcode:2004EcolL...7..285V. doi:10.1111/j.1461-0248.2004.00576.x.
This page is based on this Wikipedia article
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.