Chiral Thianthrenes

The absolute configuration and stability of two thianthrene chiral sulfoxides has been determined by means of X-ray single-crystal structure determinations. The analyses and configurations allow verification that the diastereomeric sulfoxides are stable in solution and are not interconverting, which has been suggested in some studies of sulfoxides. The two thianthrene sulfoxides have slightly different Rf values, which allowed their separation using flash chromatography on silica. The spots run back-to-back, which posed a challenge for their separation. The pure, separated compounds in solution remain as separate, single spots on a Thin Layer Chromatography (TLC) plate.


Results and Discussion
In this work, enantiopure sulfoxides of the thianthrene framework 3 are prepared for the first time.This has a folded butterfly shape that is expected to invert rapidly, but we anticipated that making a sulfoxide from one of the sulfur atoms would fix the conformation.Attaching a chiral centre would give two diastereoisomers with different physical and chemical properties, allowing them to be separated and characterised, provided that the sulfoxide is stable enough to hold its configuration.The configuration of a chiral sulfur atom can be assigned using a sub-rule of the Cahn-Ingold-Prelog (CIP) sequence rules [44,45].The CIP rules are based on quadri-covalent asymmetric atoms, and a lone pair of electrons, on nitrogen or sulfur, has negligible mass.An imaginary or phantom atom, of low priority, is added on here.A configuration of either R or S can then be assigned (Figure 1).and chemical properties, allowing them to be separated and characterised, provided that the sulfoxide is stable enough to hold its configuration.The configuration of a chiral sulfur atom can be assigned using a sub-rule of the Cahn-Ingold-Prelog (CIP) sequence rules [44,45].The CIP rules are based on quadri-covalent asymmetric atoms, and a lone pair of electrons, on nitrogen or sulfur, has negligible mass.An imaginary or phantom atom, of low priority, is added on here.A configuration of either R or S can then be assigned (Figure 1).These are the first thianthrenes prepared using 1,2-difluoro-4,5-dinitrobenzene, 5.The reaction of benzenedithiol 4 with compound 5 and Na2CO3 gave 2,3-dinitrothianthrene 6 (Figure 2).Oxidation with meta-chloroperbenzoic (mcpba) acid gave an enantiomeric mixture of sulfoxides 7. The oxidation of the second sulfur atom was not observed, suggesting that one sulfoxide deactivates the other sulfur atom.Treatment with (S)-phenylethylamine 8 displaced the 3-nitro group, which is conjugated to the electronwithdrawing sulfoxide group.The two nitro groups activate each other, but the sulfoxide provides additional activation to the 3-nitro group.Only products 9 and 10 were formed in equal amounts, which is reasonable given their similar framework.They eluted as two back-to-back spots on a TLC plate with an eluent of dichloromethane/ether (90:10).Using chromatography on flash silica, they were resolved and separated, and then characterised using NMR and X-Ray single-crystal structure determinations.The proton and 13 C NMR data are virtually identical, making it impossible to distinguish the two diastereoisomers.Figure 3 shows the molecular structures of both diastereoisomers 9 and 10 side by side.The yields for each step are shown in Figure 2 by the side of the compound number.The yields are calculated as the ratio of the moles of dry product divided by the moles of starting material x 100 to convert this into a percentage.The maximum possible yield is 100%.A yield of 70-80 % is very good and over 90% is excellent and very high.Yields of 37 % and 30% are much lower and are workable over a short scheme, but a great deal of mass is lost, which makes it difficult to carry on with further steps.For example, 500 mg of compound 6 gave 191 mg of sulfoxide 7, a 37 % yield.This work was challenging because of two low yields, the back-to-back TLC spots and split material.The remaining material in each reaction had no products which were easily isolated.It was mainly baseline and intractable.Compounds 6-7 and 9-10 are crystalline solids, which dried easily in air, but compound 11, an orange/red oil, had DCM in the proton and 13 carbon NMR.This evaporated after a beaker of it was left exposed to the atmosphere for two months and the spectra re-run.These are the first thianthrenes prepared using 1,2-difluoro-4,5-dinitrobenzene, 5.The reaction of benzenedithiol 4 with compound 5 and Na 2 CO 3 gave 2,3-dinitrothianthrene 6 (Figure 2).Oxidation with meta-chloroperbenzoic (mcpba) acid gave an enantiomeric mixture of sulfoxides 7. The oxidation of the second sulfur atom was not observed, suggesting that one sulfoxide deactivates the other sulfur atom.Treatment with (S)-phenylethylamine 8 displaced the 3-nitro group, which is conjugated to the electron-withdrawing sulfoxide group.The two nitro groups activate each other, but the sulfoxide provides additional activation to the 3-nitro group.Only products 9 and 10 were formed in equal amounts, which is reasonable given their similar framework.They eluted as two back-to-back spots on a TLC plate with an eluent of dichloromethane/ether (90:10).Using chromatography on flash silica, they were resolved and separated, and then characterised using NMR and X-Ray single-crystal structure determinations.The proton and 13 C NMR data are virtually identical, making it impossible to distinguish the two diastereoisomers.Figure 3 shows the molecular structures of both diastereoisomers 9 and 10 side by side.The yields for each step are shown in Figure 2 by the side of the compound number.The yields are calculated as the ratio of the moles of dry product divided by the moles of starting material x 100 to convert this into a percentage.The maximum possible yield is 100%.A yield of 70-80% is very good and over 90% is excellent and very high.Yields of 37% and 30% are much lower and are workable over a short scheme, but a great deal of mass is lost, which makes it difficult to carry on with further steps.For example, 500 mg of compound 6 gave 191 mg of sulfoxide 7, a 37% yield.This work was challenging because of two low yields, the back-to-back TLC spots and split material.The remaining material in each reaction had no products which were easily isolated.It was mainly baseline and intractable.Compounds 6-7 and 9-10 are crystalline solids, which dried easily in air, but compound 11, an orange/red oil, had DCM in the proton and 13 carbon NMR.This evaporated after a beaker of it was left exposed to the atmosphere for two months and the spectra re-run.The products were characterised using X-Ray single-crystal structure determinations.A guide to crystallography is available [46].Compound 9 (Figure 3) crystallises in the trigonal space group R3 (No. 146).The dihedral angle between the C1-C6 and C7-C12 rings is 43.56 (5)°, resulting in a 'butterfly' conformation for the fused ring system; atoms S1, O1 and S2 deviate from the mean plane of C4/C5/C7/C8 by −0.746 (2), −0.142 (4) and −0.560 (2) Å, respectively.As expected, S1 is pyramidal [deviation from C5, C8 and O1 = −0.6872(9) Å], the S1-O1 bond length is 1.4890 ( 14) Å, indicating a significant degree of double-bond character, and the C5-S1-C8 bond angle is 97.10 (7)°.These data compare with the corresponding S atom displacement, S-O separation and C-S-C angle of 0.684 (2) Å, 1.489 (6) Å and 96.9 (3)°, respectively, in the centrosymmetric co-crystal of thianthrene 5-oxide with 1,4-di-iodotetrafluorobenzene [47].The dihedral angle between the C1-C6 ring and the pendant C15-C20 ring in 9 is 85.96 (6)°, and the C2-N1-C13-C14 torsion angle is 154.86 ( 16  The products were characterised using X-Ray single-crystal structure determinations.A guide to crystallography is available [46].Compound 9 (Figure 3) crystallises in the trigonal space group R3 (No. 146).The dihedral angle between the C1-C6 and C7-C12 rings is 43.56 (5) • , resulting in a 'butterfly' conformation for the fused ring system; atoms S1, O1 and S2 deviate from the mean plane of C4/C5/C7/C8 by −0.746 (2), −0.142 (4) and −0.560 (2) Å, respectively.As expected, S1 is pyramidal [deviation from C5, C8 and O1 = −0.6872(9) Å], the S1-O1 bond length is 1.4890 ( 14) Å, indicating a significant degree of double-bond character, and the C5-S1-C8 bond angle is 97.10 (7) • .These data compare with the corresponding S atom displacement, S-O separation and C-S-C angle of 0.684 (2) Å, 1.489 (6) Å and 96.9 (3) • , respectively, in the centrosymmetric co-crystal of thianthrene 5-oxide with 1,4-di-iodotetrafluorobenzene [47].The dihedral angle between the C1-C6 ring and the pendant C15-C20 ring in 9 is 85.96 (6) • , and the C2-N1-C13-C14 torsion angle is 154.86 ( 16 Compound 10 (Figure 3) crystallises in the orthorhombic space group P2 1 2 1 2 1 (No.19).The C1-C6 and C7-C12 rings of the thianthrene fused ring system subtend a dihedral angle of 52.55 (5) • , and the equivalent angle between the C1-C6 and C15-C20 rings is 81.47Although the dihedral angles between the aryl rings of the thianthrene ring systems are similar in compounds 9 and 10, the overall molecular conformations are quite different, as illustrated in an overlay plot [49] (Figure 5), which shows that the C7-C12 ring is 'flipped' up or down in the two structures due to the rigid, chiral, sulfoxide moiety.Both structures are well ordered with no suggestion of disorder.Although the dihedral angles between the aryl rings of the thianthrene ring systems are similar in compounds 9 and 10, the overall molecular conformations are quite different, as illustrated in an overlay plot [49] (Figure 5), which shows that the C7-C12 ring is 'flipped' up or down in the two structures due to the rigid, chiral, sulfoxide moiety.Both structures are well ordered with no suggestion of disorder.Thianthrenes 9 and 10 were also prepared in similar yields from the mcpba oxidation of thianthrene 11 (Figure 6).This was prepared from 2,3-dinitrothianthrene 6 through the displacement of one of the nitro groups.One of the sulfur atoms in compound 11, conjugated to the amine group, is more electron-rich, so it might have oxidised more readily, but the oxidation was still a low-yielding reaction.Sulfoxides 9 and 10 formed in equal amounts, so the energy pathways to their formation, as two different diastereoisomers, must be similar.
of thianthrene 11 (Figure 6).This was prepared from 2,3-dinitrothianthrene 6 through the displacement of one of the nitro groups.One of the sulfur atoms in compound 11, conjugated to the amine group, is more electron-rich, so it might have oxidised more readily, but the oxidation was still a low-yielding reaction.Sulfoxides 9 and 10 formed in equal amounts, so the energy pathways to their formation, as two different diastereoisomers, must be similar.

Materials and Methods
IR spectra were recorded on a diamond-attenuated total reflection (ATR) Fourier transform infrared (FTIR) spectrometer (Thermo Fisher Scientific, Stafford House, Boundary Way, Hemel Hempstead, UK).Ultraviolet (UV) spectra were recorded using an Evolution, UV-Vis spectrometer with EtOH as the solvent (Thermo Fisher Scientific, Stafford House, Boundary Way, Hemel Hempstead, UK).The term sh means shoulder. 1H and 13 C nuclear magnetic resonance (NMR) spectra were recorded at 400 and 100.5 MHz, respectively, using a Bruker 400 spectrometer (Research Complex at Harwell, Rutherford Appleton Laboratory, Harwell, Didcot, Oxon, UK).Chemical shifts, δ, are given in ppm and measured by comparison with the residual solvent.Coupling constants, J, are given in Hz.A broad signal is abbreviated as br.High-resolution mass spectra were obtained at the University of Wales, Swansea, using an Atmospheric Solids Analysis Probe (ASAP) (positive mode) instrument: Xevo The structures were routinely solved by dual-space methods using SHELXT [50] and the structural models were completed and optimized by refinement against |F| 2 with SHELXL-2018 [51].The N-bound H atoms were located in difference maps and their positions were freely refined.The C-bound H atoms were placed geometrically (C-H = 0.95-1.00Å) and refined as riding atoms.The methyl groups were allowed to rotate, but not to tip, to best fit the electron density.The constraint Uiso(H) = 1.2Ueq(carrier) or 1.5Ueq(methyl carrier) was applied in all cases.Full details of the structures and refinements are available in the deposited cifs.

Materials and Methods
IR spectra were recorded on a diamond-attenuated total reflection (ATR) Fourier transform infrared (FTIR) spectrometer (Thermo Fisher Scientific, Stafford House, Boundary Way, Hemel Hempstead, UK).Ultraviolet (UV) spectra were recorded using an Evolution, UV-Vis spectrometer with EtOH as the solvent (Thermo Fisher Scientific, Stafford House, Boundary Way, Hemel Hempstead, UK).The term sh means shoulder. 1H and 13  The structures were routinely solved by dual-space methods using SHELXT [50] and the structural models were completed and optimized by refinement against |F| 2 with SHELXL-2018 [51].The N-bound H atoms were located in difference maps and their positions were freely refined.The C-bound H atoms were placed geometrically (C-H = 0.95-1.00Å) and refined as riding atoms.The methyl groups were allowed to rotate, but not to tip, to best fit the electron density.The constraint U iso (H) = 1.2U eq (carrier) or 1.5U eq (methyl carrier) was applied in all cases.Full details of the structures and refinements are available in the deposited cifs.

Conclusions
2,3-Dinitrothianthrene 6 was prepared by means of a novel one-pot condensation of benzenedithiol 4 with 4,5-difluoro-1,2-dinitrobenzene 5.The activated fluorine atoms are displaced preferentially to a nitro group by the thiol groups.After oxidation of just one diarylthio ether to a sulfoxide, a nitro group conjugated to the sulfoxide and another nitro group was displaced by the chiral amine (S)-phenylethylamine 8, chosen because of its availability and spatial difference.Two diastereomeric products 9 and 10 were produced, which ran back-to-back on a TLC plate eluting with dichloromethane/ether (98:2).These were separated using chromatography on flash silica and fully characterised.The absolute configuration of each diastereoisomer was established using X-ray crystal structure determinations.The more polar compound has a configuration 9 (SR) and the less polar spot has a configuration 10 (SS).These different configurations are apparent in the crystal structures as they flip the unsubstituted aryl ring in different orientations.The separation of the two diastereoisomers proves their stability as they are not interconverting and helps overcome concerns from others that sulfur-based chiral centres are not sufficiently stable for synthetic studies [23][24][25][26][27][28][29].An alternative but similar pathway was developed to access thianthrenes 9 and 10 through the reaction of 2,3-dinitrothianthrene 6 with (S)phenylethylamine 8 followed by the mcpba selective oxidation of the more electron-rich sulfur atom.Compound 11 was an oil, presumably because of its asymmetry, but with the conjugation of the amine to the sulfoxide, it became crystalline.The yield of sulfoxide formation was similar to that obtained by the mcpba oxidation of 2,3-dinitrothianthrene 6.The sulfur oxidation yield is not influenced by an amine donor or a nitro group acceptor, but we did not observe the over-oxidation of the thianthrene ring to a sulfone or even a bis-sulfoxide, using two equivalents of mcpba.In summary, the crystal structures of these sulfoxides establish the absolute configuration of the chiral sulfur atom and prove the stability of the two diastereoisomers.

Figure 3 .
Figure 3.The molecular structures of 9 (left) and 10 (right) showing 50% displacement ellipsoids.The hydrogen bonds are shown as double-dashed lines.The sulfoxides orientate in the direction of the thianthrene puckering.Oxygen is red, blue is nitrogen and yellow is sulfur.

Figure 3 .
Figure 3.The molecular structures of 9 (left) and 10 (right) showing 50% displacement ellipsoids.The hydrogen bonds are shown as double-dashed lines.The sulfoxides orientate in the direction of the thianthrene puckering.Oxygen is red, blue is nitrogen and yellow is sulfur.

Figure 4 .
Figure 4. Fragment of a hydrogen-bonded [001] chain of molecules in the extended structure of compound 10.Note that the NH group participates in both intramolecular and intermolecular links.Oxygen is red, blue is nitrogen and yellow is sulfur..

Figure 5 .
Figure 5.An overlay view of 9 (red) and 10 (blue) showing the different orientations of the terminal aryl ring owing to the rigid sulfoxide chiral centre.Atoms C1-C6 in the two structures are superimposed (the blue ring comes forward and the red ring goes back).

Figure 4 .
Figure 4. Fragment of a hydrogen-bonded [001] chain of molecules in the extended structure of compound 10.Note that the NH group participates in both intramolecular and intermolecular links.Oxygen is red, blue is nitrogen and yellow is sulfur..Although the dihedral angles between the aryl rings of the thianthrene ring systems are similar in compounds 9 and 10, the overall molecular conformations are quite different, as illustrated in an overlay plot[49] (Figure5), which shows that the C7-C12 ring is 'flipped' up or down in the two structures due to the rigid, chiral, sulfoxide moiety.Both structures are well ordered with no suggestion of disorder.

Figure 4 .
Figure 4. Fragment of a hydrogen-bonded [001] chain of molecules in the extended structure of compound 10.Note that the NH group participates in both intramolecular and intermolecular links.Oxygen is red, blue is nitrogen and yellow is sulfur..

Figure 5 .
Figure 5.An overlay view of 9 (red) and 10 (blue) showing the different orientations of the terminal aryl ring owing to the rigid sulfoxide chiral centre.Atoms C1-C6 in the two structures are superimposed (the blue ring comes forward and the red ring goes back).

Figure 5 .
Figure 5.An overlay view of 9 (red) and 10 (blue) showing the different orientations of the terminal aryl ring owing to the rigid sulfoxide chiral centre.Atoms C1-C6 in the two structures are superimposed (the blue ring comes forward and the red ring goes back).

Figure 6 .
Figure 6.An alternative pathway to thianthrenes 9 and 10.Supplementary materials are available from the electronic site below.

Figure 6 .
Figure 6.An alternative pathway to thianthrenes 9 and 10.Supplementary Materials are available from the electronic site below.
C nuclear magnetic resonance (NMR) spectra were recorded at 400 and 100.5 MHz, respectively, using a Bruker 400 spectrometer (Research Complex at Harwell, Rutherford Appleton Laboratory, Harwell, Didcot, Oxon, UK).Chemical shifts, δ, are given in ppm and measured by comparison with the residual solvent.Coupling constants, J, are given in Hz.A broad signal is abbreviated as br.High-resolution mass spectra were obtained at the University of Wales, Swansea, using an Atmospheric Solids Analysis Probe (ASAP) (positive mode) instrument: Xevo G2-S ASAP (Waters Corporation, 34 Maple Street, Milford, MA, USA).Melting points were determined on a Cole-Palmer MP-200D Stuart digital melting point apparatus (9 Orion Court, Ambuscade Road, Colmworth Business Park, St Neots, Cambridgeshire, UK).All chemicals were purchased from Sigma-Aldrich, Gillingham, UK.The crystal structures of 9 (yellow plate 0.10 × 0.05 × 0.03 mm) and 10 (yellow slab, 0.12 × 0.10 × 0.03 mm) were established using intensity data collected on a Rigaku CCD diffractometer (Mo Kα radiation, λ = 0.71073 Å for 9 and Cu Kα radiation, λ = 1.54178Å for 10) at 100 K. (Malvern Panalytical Ltd., Barn B, 2 Cygnus Business Park, Middle Watch, Swavesey, Cambridge, UK).

Author Contributions:
Methodology, M.J.P.; Software, W.T.A.H.; Formal analysis, W.T.A.H.; Investigation, M.J.P.; Writing-original draft, M.J.P.; Writing-review & editing, W.T.A.H.; Project administration, M.J.P.All authors have read and agreed to the published version of the manuscript.Funding:The authors received no financial support for the research, authorship and/or publication of this article.