Part of the structure of 1,2‑dithia-3,5‑diazole highlighting the stacking motif common for these compounds.[1] Color code: yellow = S, blue = N, gray = C.

In chemistry, dithiadiazoles are a family of heterocyclic compounds with the formula RCN2S2. Two isomers have been studied: the 1,2‑dithia-3,5‑diazoles, in which the sulfur atoms are bonded to each other across the ring from the carbon atom, and the 1,3‑dithia-2,5‑diazoles, in which nitrogen and sulfur atoms alternate around the ring. In both cases, the neutral species are radicals that are of interest as examples of paramagnetic heterocycles. They have also attracted interest because of the tendency of the neutral species to form linear chain compounds, a theme in molecular electronics.

1,2-Dithia-3,5-diazoles and their oxidized derivatives

Bond distances and bond angles of 1,3-[2] and 1,2-dithiadiazolium cations.[3] Distances in picometers.

Structures

The structures of both the 1,2-dithia-3,5-diazolium cations and the neutral 1,2-dithia-3,5-diazoles are fairly similar. These are planar five-membered rings. With one electron in a π*-level, the neutral ring has longer bonds vs the cation. The elongation is a few percent. For example, the S–S distance in the neutral HCN2S2 is 207 vs 201 pm in the cation.[1] Melting cracks these dimers to produce a paramagnetic liquid.[4]: 177, 182  Dithiadiazole radicals equilibrate with their (diamagnetic) spin-paired dimers via weak S---S interactions. The neutral species' slight dipole moment places a positive charge on the sulfur atoms.[4]: 156 

For the 1,2-dithia-3,5-diazolium salts, their bright colors vary with the R side chain and the counterion.[4]: 159–160 

Synthesis

The traditional entry to dithiadiazoles is reduction the mono-cation RCN2S+
2. These cations are obtained by the addition of nitriles and thiazyl chloride:

2 RCN + 4 NSCl → 2 [RCN2S2]+Cl− + Cl2 + N2

For large-scale syntheses, a mixture of ammonium chloride and sulfur dichloride under a chlorine atmosphere substitutes cheaply for thiazyl chloride, but product yields are small. Alternatively, sulfur dichloride reacts with amidines to give dithiadiazolium chlorides, albeit with sensitivity to reaction conditions.[4]: 148–150 

The dithidiazolium cations are reduced by treatment with iodide and thiocyanate:

2 [RCN2S2]+[I]- → 2 RCN2S•
2 + I2

A variety of reducing agents can be employed.[4]: 161, 174–175 

Reactions

Molecule of 4,4′-bis(1,2,3,5-dithiadiazolyl) (BDTDA)
BDTDA honeycomb lattice on copper, STM image

Halogens typically reoxidize dithiadiazoles to dithiazolium cations:

2 RCN2S•
2 + X2 → 2[ RCN2S2X +]X-

Dithiadiazoles react with low-valent metal ion by oxidative addition of the S–S bonds.[5] The products feature bidentate dithiolate-like ligands, each sulfur functioning as a bridging ligand.[4]: 192–194 

Dithiadiazolium salts hydrolyze to amidine-hydrochloride salts, sulfur dioxide, and elemental sulfur.[4]: 171 

1,3-Dithia-2,5-diazoles

1,3-Dithia-2,5-diazolium salts, which lack the S–S bond, are less common than the 1,2,3,5 isomer. The neutral 1,3-dithia-2,5-diazoles are even rarer.

The synthesis of these salts involves addition of dithionitronium hexafluoroarsenate ([SNS]+[AsF6]-) to a nitrile. The conversion is an example of a 1,3-Dipolar cycloaddition.[4]: 195–200 

The sulfur atoms bear a slight positive charge.[4]: 201–202 

The electrophilicity of dithiadiazolium salts is indicated by their tendency to polymerize THF. They hydrolyze to an amide through a poorly-understood mechanism.[4]: 206–209 

The singly-reduced dithiazole radical is unstable, isomerizing to 1,2‑dithia-3,5‑diazole or forming uncharacterized brown polymers.[4]: 144, 204, 216–217 

References

  1. 1 2 Cordes, A. W.; Bryan, C. D.; Davis, W. M.; De Laat, R. H.; Glarum, S. H.; Goddard, J. D.; Haddon, R. C.; Hicks, R. G.; Kennepohl, D. K. (1993). "Prototypal 1,2,3,5-dithia- and -diselenadiazolyl [HCN2E2]• (E = sulfur, selenium): Molecular and electronic structures of the radicals and their dimers, by theory and experiment". Journal of the American Chemical Society. 115 (16): 7232–7239. doi:10.1021/ja00069a022.
  2. ↑ MacLean, Gregory K.; Passmore, Jack; Rao, M. N. Sudheedra; Schriver, Melbourne J.; White, Peter S.; Bethell, Donald; Pilkington, Roger S.; Sutcliffe, Leslie H. (1985). "Preparation of 1,3,2-dithiazolium hexafluoroarsenate(V), preparation and crystal structures of 5-methyl-1,3,2,4-dithiadiazolium and 4-methyl-1,3,2-dithiazolium hexafluoroarsenate(V) and the reduction of these salts to stable free radicals". Journal of the Chemical Society, Dalton Transactions (7): 1405. doi:10.1039/dt9850001405.
  3. ↑ Bryan, C. D.; Cordes, A. W.; Fleming, R. M.; George, N. A.; Glarum, S. H.; Haddon, R. C.; MacKinnon, C. D.; Oakley, R. T.; Palstra, T. T. M.; Perel, A. S. (1995). "Charge Transfer Salts of Benzene-Bridged 1,2,3,5-Dithiadiazolyl Diradicals. Preparation, Structures, and Transport Properties of 1,3- and 1,4-[(S2N2C)C6H4(CN2S2)][X] (X = I, Br)". Journal of the American Chemical Society. 117 (26): 6880–6888. doi:10.1021/ja00131a009. S2CID 96841129.
  4. 1 2 3 4 5 6 7 8 9 10 11 Rawson, Jeremy M.; Banister, Arthur J.; Lavender, Ian (1995). "The Chemistry of Dithiadiazolylium and Dithiadiazolyl Rings". Adv. Heterocyc. Chem. 62. doi:10.1016/S0065-2725(08)60422-5.
  5. ↑ Lau, Hiu Fung; Ang, Pearly Chwee Ying; Ng, Victor Wee Lin; Kuan, Seah Ling; Goh, Lai Yoong; Borisov, Alexey S.; Hazendonk, Paul; Roemmele, Tracey L.; Boeré, René T.; Webster, Richard D. (2008). "Coupling of CpCr(CO)3 and Heterocyclic Dithiadiazolyl Radicals. Synthetic, X-ray Diffraction, Dynamic NMR, EPR, CV, and DFT Studies". Inorganic Chemistry. 47 (2): 632–644. doi:10.1021/ic702128f. PMID 18161967.


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