Thioxanthen-9-one Chemical Properties

Melting point:

210-213 °C(lit.)

Boiling point:

371-373 °C715 mm Hg(lit.)

Density 

1.2247 (rough estimate)

refractive index 

1.5700 (estimate)

Flash point:

371-373°C/715mm

storage temp. 

2-8°C

solubility 

Chloroform (Slightly), Methanol (Slightly)

color 

Pale Yellow to Light Yellow

Water Solubility 

practically insoluble

Merck 

14,9369

BRN 

140978

Stability:

Stable. Incompatible with strong oxidizing agents.

InChIKey

YRHRIQCWCFGUEQ-UHFFFAOYSA-N

CAS DataBase Reference

492-22-8(CAS DataBase Reference)

NIST Chemistry Reference

Thioxanthone(492-22-8)

EPA Substance Registry System

Thioxanthone (492-22-8)

Safety Information

Hazard Codes 

Xi

Risk Statements 

36/37/38

Safety Statements 

22-24/25-37/39-26

WGK Germany 

3

Hazard Note 

Irritant

TSCA 

Yes

HS Code 

29349990

MSDS

• Language:English Provider:9-Oxothioxanthene
• Language:English Provider:SigmaAldrich
• Language:English Provider:ACROS
• Language:English Provider:ALFA

Thioxanthen-9-one Usage And Synthesis

Description

Thioxanthone is a heterocyclic compound that is a sulfur analog of xanthone.
Thioxanthone can be prepared by the reaction of diphenyl sulfide with phosgene in the presence of catalytic aluminium chloride. This synthesis can be seen as a special case of the Friedel-Crafts acylation. The reduction product is thioxanthene.
Thioxanthone dissolves in concentrated sulfuric acid to give a yellow colored liquid with intense green fluorescence. A mixture of the thioxanthone derivatives of 2- and 4-isopropylthioxanthone (ITX) is used in the printing industry. Pharmaceutical drugs that are derivatives of thioxanthone include hycanthone and lucanthone.

Chemical Properties

slightly yellow crystalline powder

Uses

Thioxanthen-9-one is a reagent and a starting material for the synthesis of Metixene Hydrochloride. It is also used for highly functional group tolerant and chemoselective oxidation of aromatic or aliphatic sulfides to sulfoxides with hydrogen peroxide.

Synthesis Reference(s)

Tetrahedron Letters, 35, p. 2195, 1994 DOI: 10.1016/S0040-4039(00)76794-3

Reactivity Profile

Thioxanthen-9-one can mediate reactions via triplet energy transfer (EnT), hydrogen atom transfer (HAT) or single electron transfer (SET). Apart from the use in polymerisation chemistry, thioxanthone and its derivatives have been employed in a wide variety of chemical transformations, such as photoisomerisation reactions, photoinduced rearrangements, [2 + 2] photocycloadditions, Paterno–Buchi cycloadditions, photoredox catalysis and cross-coupling reactions leading to C–O, C–N, C–P and other bond formation[1].

Purification Methods

It forms yellow needles from CHCl3 or EtOH and sublimes in vacuo. It is soluble in CS2, hot AcOH, and dissolves in conc H2SO4 to give a yellow colour with green fluorescence in VIS light. The sulfone has m 187o (from EtOH), and the hydrazone has m 115o (yellow leaflets from EtOH/*C6H6). The oxime has m 194-196o (from pet ether). [Szmant et al. J Org Chem 18 745 1953, Ullmann et al. Chem Ber 49 2509 1916, NMR: Sharpless et al. Org Magn Res 6 115 1974, Beilstein 17 H 357, 17 I 191, 17 III/IV 5302, 17/10 V 437.]

Structure and conformation

Thioxanthen-9-one (TX) is a aromatic ketone. In comparison with other aromatic ketones, TX has a high triplet energy and a relatively long triplet lifetime, while it has the ability to participate successfully in merger reactions with metal complexes. The conformation of TX is not fixed, but it interconverts from a planar (C2v) to a non-planar conformation. In the case of TX, the intersystem crossing of an electron normally occurs from a non-bonding orbital (n) to an anti-bonding pi orbital (π*) (nπ* configuration) and occurs 103 times faster than in the case of migration from the same type of molecular orbital (ππ* migration).Theoretical studies support that TX's low lying triplet state is close enough to the singlet state, favoring in this way internal conversion (IC) and ISC upon photoexcitation. Due to its high triplet energy, TX is an efficient sensitizer for oxygen, leading to singlet oxygen, since the excitation of oxygen requires around 23 kcal mol^-1[1].

References

[1] Nikitas N, et al. Thioxanthone: a powerful photocatalyst for organic reactions. Organic & Biomolecular Chemistry, 2021; 19: 5237-5253.

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