Dithiolium salt

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1,2- and 1,3-dithiolium cations.

Dithiolium salts are compounds of the formula [(RC)3S2]+X (R = H, alkyl, aryl, etc.). These salts consist of a planar organic cation with a variety of anions such as halides. The five-membered ring cations are observed in either of two isomers, 1,2- and 1,3-dithiolium cations. These cations differ with respect to the relative positions of the pair of sulfur atoms. Both isomers feature a planar ring, which is aromatic owing to the presence of 6π electrons.[1] For example, the 1,2-ditholium ring can be represented as an allyl cation of the three carbons,[2] with each sulfur atom donating one of its lone pairs of electrons to give a total of three pairs.

Structure of diphenyl-1,2-dithiolium cation (as its bisulfate salt). Selected distances: S-S = 2.019(5); S-C=173(1); Cring-Cring = 1.38(1) Å.[3]

Preparation, occurrence, reactions[]

1,2-Dithiolium cations are typically prepared from 1,3-diketones by treatment with H2S and oxidants such as bromine.[2]

(RCO)2CH2 + 2 H2S + Br2 → [(RC)3S2]+Br + 2 H2O + HBr

1,3-Dithiolium cations are often prepared by alkylation of the corresponding unsaturated dithio- or trithiocarbonates:

[(RC)2S2C=E] + R+ → [(RC)2S2CER]+

The analogous reaction of electrophiles with 1,2-dithiole-2-ones affords 1,2-dithiolium cations.

The oxidation of tetrathiafulvalenes gives cations that exhibit the character of 1,3-dithiolium cations.

References[]

  1. ^ Noël Lozac'h, Madeleine Stavaux (1981). "The 1,2- and 1,3-Dithiolium Ions". Advances in Heterocyclic Chemistry. 27: 151–239. doi:10.1016/S0065-2725(08)60997-6.CS1 maint: uses authors parameter (link)
  2. ^ a b Hendrickson, A. R.; Martin, R. L. (1973). "Improved synthesis of alkyl substituted 1,2-dithiolium salts". Journal of Organic Chemistry. 38: 2548–9. doi:10.1021/jo00954a028.CS1 maint: uses authors parameter (link)
  3. ^ E. Uhlemann, F. Weller (1992). "3,5-Diphenyl-1,2-dithiolium-hydrogensulfat—Bildung und Struktur" [3.5-Diphenyl-l,2-dithiolium Hydrogensulphate—Synthesis and Structure]. Z. Naturforsch. B (in German). 47 (11): 1501–1504. doi:10.1515/znb-1992-1102.CS1 maint: uses authors parameter (link)
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