research communications
Hirshfeld surface analysis and spectroscopic characterization of the di-enol tautomeric form of the compound 3,3′-[(2-sulfanylidene-1,3-dithiole-4,5-diyl)bis(sulfanediyl)]bis(pentane-2,4-dione)
aDepartment of Chemistry, University of Puerto Rico, Rio Piedras Campus, San Juan, 00927, Puerto Rico
*Correspondence e-mail: dalice.pinero@upr.edu
The reaction between [TBA]2[Zn(dmit)2] and 3-chloro-2,4-pentanedione yielded single crystals of the title compound, (3E,3′E)-3,3′-[(2-sulfanylidene-1,3-dithiole-4,5-diyl)bis(sulfanediyl)]bis(4-hydroxypent-3-en-2-one), C13H14O4S5, after solvent evaporation. The title compound crystallizes in the triclinic P with two molecules related by an inversion center present in the The central thione ring moiety contains a carbon–carbon double bond covalently linked to two sulfoxide substituents located outside of the plane of the ring. The S—C—C—S torsion angles are −176.18 (8) and −0.54 (18)°. Intramolecular hydrogen bonds occur within the two dione substituents (1.67–1.69 Å). Adjacent asymmetric units are linked by C—H⋯S (2.89–2.90 Å), S⋯S [3.569 (1) Å] and O⋯H [2.56–2.66 Å between non-stacked thione rings] short contacts.
Keywords: dithioles; redox state; non-innocent; tautomerism; crystal structure.
CCDC reference: 1984599
1. Chemical context
Dithiolene systems (McCleverty et al., 1968) are a versatile family of compounds in coordination chemistry because of their redox non-innocent behavior (Eisenberg et al., 2011). These compounds are electronically flexible and contribute to the stability of several redox processes observed in metal complexes, which are not necessarily `metal-based' (Stiefel, 2004; Periyasamy et al., 2007). Their electronic spin states can easily be clarified with the combined insights afforded by spectroscopic data, X-ray crystallography and computational analysis (Eisenberg et al., 2011; Yan et al., 2013; Lyaskovskyy et al., 2012). Dithiolene derivatives such as tetrathiafulvenyl-acetylacetonate (TTFSacacH), synthesized by Lorcy et al. (2001), have been reported as electroactive ligands with interesting redox properties. Most of these compounds employ the zinc–thiolate complex bis(tetrabutylammonium) bis(1,3-dithiole-2-thione-4,5-dithiolato)zinc(II), [TBA]2[Zn(dmit)2]2− (Comerlato et al. 2002), as a key starting material to achieve the synthesis of interesting metal complexes.
Herein, the reduction of the [Zn(dmit)2]2− dithiolene complex is utilized to aid the formation of a novel thiocarbonyl compound by its reaction with 3-chloro-2,4-pentanedione (Cl-acac) to yield the title compound (3E,3′E)-3,3′-[(2-sulfanylidene-1,3-dithiole-4,5-diyl)bis(sulfanediyl)]bis(4-hydroxypent-3-en-2-one), the di-enol tautomer of 3,3′-[(2-sulfanylidene-1,3-dithiole-4,5-diyl)bis(sulfanediyl)]bis(pentane-2,4-dione). The electrophilic nature of the acetylacetone (acac) motif and the high electron density on the sulfur atoms drive the nucleophilic substitution to completion. The title compound is a double β-dicarbonyl compound that contains two acetylacetone moieties, which are found in their enolic form in the solid state. Concerning the reactivity of the title compound, it is able to undergo acid or base-catalyzed α-hydrogen substitution reactions, in which the rate-determining step is the formation of the enol or enolate anion (Shapet'ko et al., 1975). Compared to the acid-catalyzed process, the self-enolization of most is negligible. The double β-dicarbonyl compound described herein also undergoes however, in the solid phase, the enol tautomer predominates in this equilibrium as it is stabilized relative to the keto form via resonance through the conjugated π-system and by intramolecular hydrogen bonding in the solid-state (Drexler et al. 1976; Seco et al. 1989). This aspect is confirmed by its FT–IR and NMR spectra.
2. Structural commentary
The title compound crystallizes in the triclinic P with one molecule in the (Fig. 1, Table 3). Its chemical structure consists of two 4-hydroxy-3-penten-2-one units connected to a 1,3-dithiol-1-thione ring moiety through a C—S single bond. In the two molecules are related by an inversion center. The central thione ring is conformed by a C2=C3 carbon–carbon double bond, which is in the same plane as the C1=S1 bond characteristic of the thione substituent. The angles C2—S3—C6 and C3—S4—C11 are 101.45 (7) and 103.72 (7)°, respectively. The torsion angles S4—C3—C2—S3 and S2—C2—C3—S5 are −176.18 (8) and −0.54 (18)°, respectively; the difference in the torsion angles is due to the effects of from the 4-hydroxy-3-penten-2-one moiety. The S4—C3 and S3—C2 bond lengths are 1.7608 (16) and 1.7679 (16) Å, respectively.
3. Supramolecular features
The title compound exhibits numerous intermolecular interactions, namely four C—H⋯O, three C—H⋯S, three C⋯O, one S⋯C, and one S⋯S interaction (Fig. 2, Tables 1 and 2). The five-membered thiocarbonyl-containing rings lie almost parallel to the c axis and extend in a sheet-like fashion, forming a network that propagates along the axis with all rings following the same orientation. The sheets are linked by out-of-plane C13—H13B⋯S1 short contacts, generating stacks along the a axis with S⋯S short contacts between adjacent molecules [S5⋯S5iv = 3.5688 (6) Å]. In addition, the nucleophilic atom S3 is oriented towards the electrophilic C5, leading to an S3⋯C5iii [3.471 (2) Å] contact, further contributing to the extension of the network along the c-axis direction. Molecules of the title compound also associate with neighboring molecules above and below the thiocarbonyl ring planes through the acac backbone by C4—H4⋯S1 and C9—H9⋯S1 contacts. The acac backbone lies nearly perpendicular to the rings, and there are several key interactions between the carbonyl oxygen atoms (O1, O2, and O3) and neighboring methyl hydrogen atoms (H8A and H8C) with lengths in the range 2.56-2.66 Å. However, atom O4 is not involved in any interactions with hydrogen atoms, and instead makes short contacts with both C12 and C13.
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4. Hirshfeld Surface Analysis
The Hirshfeld surface (Spackman & Jayatilaka, 2009) for the title compound mapped over dnorm is shown in Fig. 3 while Fig. 4 shows the associated two-dimensional fingerprint plots (McKinnon et al., 2007), both generated with CrystalExplorer17 (Turner et al., 2017). Red spots on the Hirshfeld surface mapped over dnorm in the color range −0.0820 to 1.5568 arbitrary units confirm the above-mentioned primary intermolecular contacts. The fingerprint plots are given for all contacts and those delineated into S⋯H/H⋯S (27.9%; Fig. 4b), H⋯H (25.8%; Fig. 4c), O⋯H/H⋯O (19.5%; Fig. 4d), C⋯H/H⋯C (9.3%; Fig. 4e), S⋯C/C⋯S (4.9%; Fig. 4f), S⋯O/O⋯S (4.8%; Fig. 4g), S⋯S (4.0%; Fig. 4h), O⋯C/C⋯O (2.0%; Fig. 4i), O⋯O (1.1%; Fig. 4j), and C⋯C (0.7%; Fig. 4k) interactions. Thus, the Hirshfeld surface analysis indicates that the most significant contributions arise from S⋯H and H⋯H contacts.
5. Database survey
A search of the Cambridge Structural Database (CSD Version 5.40, September 2019 update; Groom et al., 2016) for the title compound revealed 46 hits comprising structures including metal complexes and organic compounds. Of the latter, 31 hits are for C–S bicyclic compounds and four hits are for monocyclic C–S crystal structures. Monocyclic structures related to the title compound are bis(5-(mesitylthio)-1,3-dithiole-2-thione)-4,4′-disulfide dihydrate (LOBXEF; Cerrada et al., 1999), 4,4′-disulfanediylbis{5-[(2,4,6-triisopropylphenyl)sulfanyl]-1,3-dithiole-2-thione} (NUMXOJ; Cerrada et al., 2009) and 4,5-bis(2,4-dinitrophenylthio)-1,3-dithiole-2-thione (YISBOR; Qi et al., 1994 and YISBOR10; Qu et al., 1995). The dihedral angles in YISBOR/YISBOR10 and LOBXEF are similar to those exhibited by the title compound, unlike in NUMXOJ, which is completely different. For the mentioned compounds, the lack of C—H⋯O and C—H⋯S short contacts means they are not comparable to the title compound. The four comparative compounds show similar S⋯C short contacts, which involve the sulfur atoms of the thione ring and the carbon atoms from the substituents. In contrast to YISBOR/YISBOR10, the structures of LOBXEF and NUMXOJ exhibit an S⋯S short contact analogous to that in the title compound. The structure of NUMXOJ exhibits π–π stacking of the thione rings of neighboring molecules, similar to the title compound, and unlike LOBXEF (in which π-π stacking occurs between the benzene and thione rings) and YISBOR/YISBOR10 (where there π–π stacking between the thione ring and one benzene ring).
6. Synthesis and crystallization
The synthesis of the title compound was carried out by refluxing 1 eq. of [TBA]2[Zn(dmit)2] and 4 eq. of 3-chloro-2,4-pentanedione in 100 mL of acetonitrile under argon for 1 h, after which it was cooled and left under stirring overnight. was added and stirring continued for 1 h. The resulting mixture was filtered and washed with cold acetonitrile. The solvent was evaporated under reduced pressure, and ethyl acetate was added to precipitate ZnCl2. The remaining solution was filtered, followed by evaporation of the solvent, giving a yellow crystalline solid (67.3% yield). NMR analyses were performed on a Bruker AV-700 spectrometer using chloroform-d (CDCl3) as solvent. The solvent signals at 7.26 and 77.00 ppm were used as internal standards for proton and carbon, respectively. 1H NMR (700 MHz, CDCl3) δ 15.40 (s, 1H, interchangeable) 5.11(s, 1H, interchangeable), 2.48 (s, 12H). 13C NMR (176 MHz, CDCl3) δ 24.92, 102.30, 131.40, 197.78, 209.18.
7. Spectroscopic Characterization
Without basic catalysis, the self-enolization of most et al., 1976). However, β-dicarbonyl compounds, which can also undergo are stabilized in the enol tautomer via resonance of the conjugated π-system and intramolecular hydrogen bonding. Furthermore, the enol is the less polar of the two tautomers because the intramolecular hydrogen bond reduces the dipole–dipole repulsion of the two carbonyls in the keto form. The equilibrium of β-dicarbonyl compounds has been studied extensively and it has been shown that tautomeric interconversion between the diketo and enol forms is relatively slow and can be observed by NMR. Under normal conditions, the enolic form predominates in equilibrium (Egan et al., 1977). This effect was demonstrated to be solvent and concentration dependent. An NMR study of keto–enol in β-dicarbonyl compounds revealed that for the unsubstituted and symmetrical β-dicarbonyl compound pentane-2,4-dione, the at 310 K has a value of 2.95 with 93.3 enol % (acetone exists as 0.00025% enol) (Schubert, 1960). In addition, as these compounds are progressively diluted with non-polar solvents, the enol content of the system increases. The progressive dilution with more polar solvents than the solute was observed to increase the stability of the keto form.
is negligible and the keto form is favored almost exclusively (DrexlerIn the case of the 1H NMR study of the title compound in deuterated chloroform at 298 K, the predominant form was observed to be the enol tautomer. NMR was used to confirm the underlying symmetry the title compound possesses in solution, in which the enol tautomer predominates, as can be observed in Fig. 5. The lowest frequency signal in the 1H NMR spectrum integrates to twelve and corresponds to the methyl protons of the compound, indicating that the latter are chemically equivalent. Similarly, the enol form of the compound was observed crystallographically and in solution, exhibiting intramolecular hydrogen bonding and renders both methyl groups, as well as both carbonyls, chemically equivalent. When studying the proton spectrum, the conjugation in the six-membered pseudo-aromatic ring deshields the signal of the interchangeable proton, giving rise to a low field signal at 15.4 ppm that is lost in the baseline. Looking further into the baseline at higher fields, around 5.1 ppm, it reveals a wide signal that is almost lost in the noise and that can be assigned to the interchangeable proton in the keto tautomer (Fig. 6). The formation of this hydrogen-bridge bond is promoted by the planar structure of the enol–carbonyl resonance system because this leads to an ideal spatial orientation of the hydroxy group and carbonyl group in order to construct a strong hydrogen-bridge bond. Therefore, the monoenolic form of a β-dicarbonyl compound has a planar, six-membered cyclic structure stabilized by resonance. Decreasing the concentration of the solute in non-polar solvents has been proven to increase the concentration of the enol tautomer. 13C NMR spectrum displayed a single signal at 24.8 ppm for the methyl carbons, and a single signal at 197.7 ppm for the carbonyl carbons, supporting the statement that there is chemical equivalency between the methyl groups and, most importantly, between both carbonyl moieties. This effect has been previously demonstrated by comparing the 13C NMR spectra of the enol forms of symmetrical and unsymmetrical derivatives of β-diketones, where a different was observed for the two carbonyls in the unsymmetrical case (Shapet'ko et al., 1975). It is possible to conclude that the three signals of the 2,4-pentanedione portion of the title compound, as well as the chemical shifts observed, are indicative of a symmetrical system that results from intramolecular hydrogen-bonding in the enol tautomer.
IR peaks at 2,962 and 2,876 cm−1 are assigned to the C—H stretches (Fig. 7). The peaks between 1,575 and 1,402 cm−1 correspond to the C=C bond in the enol form. Moreover, hidden under this peak there is also the C=O stretch in the enol form, which is lowered by conjugation to the C=C bond and the O atom of the –OH group, respectively. OH stretches for β-diketones are tabulated from 3,200 to 2,400 cm−1; however, in the case of symmetric acac compounds where the enol form predominates and the interchangeable hydrogen is located between the two carbonyls, the dipole change associated to the symmetric OH stretch is null, and the signal is minimal to non-existent. Thus, evidence from NMR and IR spectroscopy indicates that the compound exists almost entirely in its enol form.
8. Refinement
Crystal data, data collection and structure . H atoms were included in geometrically calculated positions for the while the hydrogen atoms from OH groups were located from the difference-Fourier map and refined as riding: O—H = 0.82 Å, C—H = 0.93–0.98 Å with Uiso(H) =1.5Ueq(O, C-methyl) and 1.2Ueq(C) for other H atoms.
details are summarized in Table 3Supporting information
CCDC reference: 1984599
https://doi.org/10.1107/S2056989020010695/dx2025sup1.cif
contains datablock I. DOI:Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S2056989020010695/dx2025Isup2.hkl
Data collection: CrysAlis PRO (Rigaku OD, 2015); cell
CrysAlis PRO (Rigaku OD, 2015); data reduction: CrysAlis PRO (Rigaku OD, 2015); program(s) used to solve structure: SHELXT2014/5 (Sheldrick, 2015a); program(s) used to refine structure: SHELXL (Sheldrick, 2015b); molecular graphics: OLEX2 (Dolomanov et al., 2009); software used to prepare material for publication: OLEX2 (Dolomanov et al., 2009).C13H14O4S5 | Z = 2 |
Mr = 394.54 | F(000) = 408 |
Triclinic, P1 | Dx = 1.584 Mg m−3 |
a = 7.1843 (1) Å | Cu Kα radiation, λ = 1.54184 Å |
b = 9.9198 (1) Å | Cell parameters from 38605 reflections |
c = 12.5230 (2) Å | θ = 3.6–68.9° |
α = 84.319 (1)° | µ = 6.59 mm−1 |
β = 83.574 (1)° | T = 100 K |
γ = 69.151 (1)° | Block, light yellow |
V = 827.11 (2) Å3 | 0.3 × 0.28 × 0.06 mm |
Rigaku SuperNova HyPix3000 diffractometer | 3034 reflections with I > 2σ(I) |
ω scans | Rint = 0.048 |
Absorption correction: multi-scan (CrysAlisPro; Rigaku OD, 2015) | θmax = 69.1°, θmin = 3.6° |
Tmin = 0.208, Tmax = 0.673 | h = −8→8 |
45972 measured reflections | k = −12→12 |
3086 independent reflections | l = −15→15 |
Refinement on F2 | Secondary atom site location: difference Fourier map |
Least-squares matrix: full | Hydrogen site location: mixed |
R[F2 > 2σ(F2)] = 0.027 | H-atom parameters constrained |
wR(F2) = 0.073 | w = 1/[σ2(Fo2) + (0.0432P)2 + 0.5496P] where P = (Fo2 + 2Fc2)/3 |
S = 1.05 | (Δ/σ)max = 0.001 |
3072 reflections | Δρmax = 0.37 e Å−3 |
206 parameters | Δρmin = −0.31 e Å−3 |
0 restraints | Extinction correction: SHELXL-2016/6 (Sheldrick 2015b), Fc*=kFc[1+0.001xFc2λ3/sin(2θ)]-1/4 |
Primary atom site location: dual | Extinction coefficient: 0.0023 (3) |
Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds involving l.s. planes. |
x | y | z | Uiso*/Ueq | ||
S1 | 0.23650 (6) | 0.66587 (4) | 0.42463 (3) | 0.01782 (12) | |
S2 | 0.27692 (6) | 0.63562 (4) | 0.65943 (3) | 0.01461 (11) | |
S3 | 0.31242 (6) | 0.48313 (4) | 0.88104 (3) | 0.01525 (12) | |
S4 | 0.24878 (6) | 0.21427 (4) | 0.76744 (3) | 0.01430 (11) | |
S5 | 0.22936 (6) | 0.40181 (4) | 0.55835 (3) | 0.01485 (11) | |
O1 | 0.58163 (18) | 0.77059 (13) | 0.86405 (10) | 0.0219 (3) | |
O2 | 0.22982 (18) | 0.89341 (12) | 0.91407 (10) | 0.0208 (3) | |
H2 | 0.348293 | 0.879765 | 0.896703 | 0.031* | |
O3 | 0.79489 (17) | −0.06088 (12) | 0.69638 (10) | 0.0204 (3) | |
O4 | 0.56236 (18) | −0.12438 (12) | 0.60106 (10) | 0.0212 (3) | |
H4 | 0.667516 | −0.126626 | 0.622140 | 0.032* | |
C1 | 0.2480 (2) | 0.57110 (16) | 0.54050 (13) | 0.0137 (3) | |
C2 | 0.2827 (2) | 0.48345 (16) | 0.74276 (13) | 0.0129 (3) | |
C3 | 0.2616 (2) | 0.37325 (16) | 0.69608 (13) | 0.0129 (3) | |
C4 | 0.7301 (3) | 0.5227 (2) | 0.83018 (15) | 0.0232 (4) | |
H4A | 0.728193 | 0.505999 | 0.756173 | 0.035* | |
H4B | 0.725804 | 0.439335 | 0.874947 | 0.035* | |
H4C | 0.850316 | 0.540141 | 0.839425 | 0.035* | |
C5 | 0.5532 (3) | 0.65102 (18) | 0.86127 (13) | 0.0175 (3) | |
C6 | 0.3570 (2) | 0.64631 (17) | 0.88533 (13) | 0.0146 (3) | |
C7 | 0.1978 (2) | 0.77374 (18) | 0.91381 (13) | 0.0163 (3) | |
C8 | −0.0110 (3) | 0.78032 (18) | 0.94305 (15) | 0.0206 (4) | |
H8A | −0.080210 | 0.861593 | 0.985597 | 0.031* | |
H8B | −0.010564 | 0.692988 | 0.983764 | 0.031* | |
H8C | −0.077272 | 0.790640 | 0.878697 | 0.031* | |
C9 | 0.6980 (3) | 0.13033 (18) | 0.81362 (15) | 0.0213 (4) | |
H9A | 0.632959 | 0.118292 | 0.883274 | 0.032* | |
H9B | 0.650861 | 0.230598 | 0.789056 | 0.032* | |
H9C | 0.839859 | 0.097756 | 0.818419 | 0.032* | |
C10 | 0.6520 (2) | 0.04366 (17) | 0.73592 (14) | 0.0170 (3) | |
C11 | 0.4523 (2) | 0.07528 (16) | 0.70716 (13) | 0.0148 (3) | |
C12 | 0.4160 (2) | −0.01363 (17) | 0.63824 (14) | 0.0168 (3) | |
C13 | 0.2157 (3) | 0.00525 (18) | 0.60412 (15) | 0.0203 (4) | |
H13A | 0.231343 | −0.053312 | 0.544829 | 0.030* | |
H13B | 0.148642 | 0.104954 | 0.582310 | 0.030* | |
H13C | 0.137979 | −0.023707 | 0.663218 | 0.030* |
U11 | U22 | U33 | U12 | U13 | U23 | |
S1 | 0.0235 (2) | 0.0160 (2) | 0.0145 (2) | −0.00766 (16) | −0.00267 (16) | 0.00069 (15) |
S2 | 0.0234 (2) | 0.00936 (19) | 0.0133 (2) | −0.00776 (15) | −0.00300 (15) | −0.00126 (14) |
S3 | 0.0252 (2) | 0.0117 (2) | 0.0117 (2) | −0.00935 (15) | −0.00231 (15) | −0.00187 (14) |
S4 | 0.0192 (2) | 0.00921 (19) | 0.0154 (2) | −0.00658 (15) | 0.00134 (15) | −0.00193 (15) |
S5 | 0.0223 (2) | 0.01119 (19) | 0.0137 (2) | −0.00800 (15) | −0.00379 (15) | −0.00224 (14) |
O1 | 0.0268 (6) | 0.0210 (6) | 0.0239 (7) | −0.0153 (5) | −0.0035 (5) | −0.0008 (5) |
O2 | 0.0266 (6) | 0.0135 (6) | 0.0254 (7) | −0.0100 (5) | −0.0020 (5) | −0.0051 (5) |
O3 | 0.0195 (6) | 0.0155 (6) | 0.0250 (7) | −0.0051 (5) | −0.0005 (5) | −0.0012 (5) |
O4 | 0.0227 (6) | 0.0145 (6) | 0.0259 (7) | −0.0046 (5) | −0.0007 (5) | −0.0076 (5) |
C1 | 0.0137 (7) | 0.0102 (7) | 0.0173 (8) | −0.0036 (6) | −0.0020 (6) | −0.0029 (6) |
C2 | 0.0153 (7) | 0.0113 (7) | 0.0120 (8) | −0.0046 (6) | −0.0007 (6) | −0.0013 (6) |
C3 | 0.0161 (7) | 0.0101 (7) | 0.0127 (8) | −0.0047 (6) | −0.0016 (6) | −0.0011 (6) |
C4 | 0.0216 (8) | 0.0263 (9) | 0.0233 (9) | −0.0089 (7) | −0.0015 (7) | −0.0072 (7) |
C5 | 0.0247 (8) | 0.0186 (8) | 0.0114 (8) | −0.0096 (7) | −0.0048 (6) | −0.0006 (6) |
C6 | 0.0223 (8) | 0.0128 (7) | 0.0119 (8) | −0.0093 (6) | −0.0030 (6) | −0.0022 (6) |
C7 | 0.0256 (8) | 0.0161 (8) | 0.0097 (8) | −0.0093 (7) | −0.0047 (6) | −0.0011 (6) |
C8 | 0.0224 (8) | 0.0163 (8) | 0.0227 (9) | −0.0061 (7) | −0.0001 (7) | −0.0041 (7) |
C9 | 0.0256 (9) | 0.0185 (8) | 0.0221 (9) | −0.0089 (7) | −0.0070 (7) | −0.0017 (7) |
C10 | 0.0237 (8) | 0.0110 (7) | 0.0166 (8) | −0.0076 (6) | −0.0004 (6) | 0.0027 (6) |
C11 | 0.0194 (8) | 0.0083 (7) | 0.0166 (8) | −0.0055 (6) | 0.0004 (6) | −0.0008 (6) |
C12 | 0.0236 (8) | 0.0105 (7) | 0.0170 (8) | −0.0079 (6) | 0.0013 (6) | 0.0004 (6) |
C13 | 0.0246 (8) | 0.0137 (8) | 0.0252 (9) | −0.0091 (7) | −0.0021 (7) | −0.0047 (7) |
S1—C1 | 1.6424 (17) | C4—H4C | 0.9600 |
S2—C1 | 1.7389 (16) | C4—C5 | 1.491 (2) |
S2—C2 | 1.7385 (16) | C5—C6 | 1.424 (2) |
S3—C2 | 1.7679 (16) | C6—C7 | 1.415 (2) |
S3—C6 | 1.7653 (16) | C7—C8 | 1.483 (2) |
S4—C3 | 1.7608 (16) | C8—H8A | 0.9600 |
S4—C11 | 1.7700 (16) | C8—H8B | 0.9600 |
S5—C1 | 1.7225 (16) | C8—H8C | 0.9600 |
S5—C3 | 1.7479 (16) | C9—H9A | 0.9600 |
O1—C5 | 1.278 (2) | C9—H9B | 0.9600 |
O2—H2 | 0.8200 | C9—H9C | 0.9600 |
O2—C7 | 1.287 (2) | C9—C10 | 1.495 (2) |
O3—C10 | 1.267 (2) | C10—C11 | 1.435 (2) |
O4—H4 | 0.8200 | C11—C12 | 1.399 (2) |
O4—C12 | 1.303 (2) | C12—C13 | 1.489 (2) |
C2—C3 | 1.351 (2) | C13—H13A | 0.9600 |
C4—H4A | 0.9600 | C13—H13B | 0.9600 |
C4—H4B | 0.9600 | C13—H13C | 0.9600 |
C10···O1i | 3.178 (2) | S3···C5iii | 3.471 (2) |
C12···O4ii | 3.180 (2) | S5···S5iv | 3.5688 (6) |
C13···O4ii | 3.219 (2) | ||
C2—S2—C1 | 97.02 (7) | C6—C7—C8 | 123.84 (15) |
C6—S3—C2 | 101.45 (7) | C7—C8—H8A | 109.5 |
C3—S4—C11 | 103.72 (7) | C7—C8—H8B | 109.5 |
C1—S5—C3 | 97.48 (7) | C7—C8—H8C | 109.5 |
C7—O2—H2 | 109.5 | H8A—C8—H8B | 109.5 |
C12—O4—H4 | 109.5 | H8A—C8—H8C | 109.5 |
S1—C1—S2 | 122.31 (9) | H8B—C8—H8C | 109.5 |
S1—C1—S5 | 124.58 (10) | H9A—C9—H9B | 109.5 |
S5—C1—S2 | 113.10 (9) | H9A—C9—H9C | 109.5 |
S2—C2—S3 | 118.79 (9) | H9B—C9—H9C | 109.5 |
C3—C2—S2 | 116.65 (13) | C10—C9—H9A | 109.5 |
C3—C2—S3 | 124.56 (13) | C10—C9—H9B | 109.5 |
S5—C3—S4 | 120.39 (9) | C10—C9—H9C | 109.5 |
C2—C3—S4 | 123.78 (13) | O3—C10—C9 | 118.05 (15) |
C2—C3—S5 | 115.69 (12) | O3—C10—C11 | 120.25 (15) |
H4A—C4—H4B | 109.5 | C11—C10—C9 | 121.69 (14) |
H4A—C4—H4C | 109.5 | C10—C11—S4 | 120.87 (12) |
H4B—C4—H4C | 109.5 | C12—C11—S4 | 119.52 (12) |
C5—C4—H4A | 109.5 | C12—C11—C10 | 119.34 (14) |
C5—C4—H4B | 109.5 | O4—C12—C11 | 120.13 (15) |
C5—C4—H4C | 109.5 | O4—C12—C13 | 115.14 (14) |
O1—C5—C4 | 117.29 (15) | C11—C12—C13 | 124.71 (15) |
O1—C5—C6 | 119.46 (15) | C12—C13—H13A | 109.5 |
C6—C5—C4 | 123.24 (15) | C12—C13—H13B | 109.5 |
C5—C6—S3 | 120.55 (12) | C12—C13—H13C | 109.5 |
C7—C6—S3 | 120.13 (12) | H13A—C13—H13B | 109.5 |
C7—C6—C5 | 119.32 (14) | H13A—C13—H13C | 109.5 |
O2—C7—C6 | 119.97 (15) | H13B—C13—H13C | 109.5 |
O2—C7—C8 | 116.18 (15) | ||
S2—C2—C3—S4 | −176.18 (8) | C2—S3—C6—C5 | −84.62 (14) |
S2—C2—C3—S5 | −0.54 (18) | C2—S3—C6—C7 | 95.98 (14) |
S3—C2—C3—S4 | 3.1 (2) | C3—S4—C11—C10 | 80.09 (14) |
S3—C2—C3—S5 | 178.72 (8) | C3—S4—C11—C12 | −105.92 (14) |
S3—C6—C7—O2 | −178.14 (12) | C3—S5—C1—S1 | 178.43 (11) |
S3—C6—C7—C8 | 1.0 (2) | C3—S5—C1—S2 | −2.54 (10) |
S4—C11—C12—O4 | −173.78 (12) | C4—C5—C6—S3 | 0.8 (2) |
S4—C11—C12—C13 | 4.5 (2) | C4—C5—C6—C7 | −179.82 (15) |
O1—C5—C6—S3 | 179.45 (12) | C5—C6—C7—O2 | 2.4 (2) |
O1—C5—C6—C7 | −1.1 (2) | C5—C6—C7—C8 | −178.41 (15) |
O3—C10—C11—S4 | 176.35 (12) | C6—S3—C2—S2 | −6.57 (11) |
O3—C10—C11—C12 | 2.3 (2) | C6—S3—C2—C3 | 174.19 (14) |
C1—S2—C2—S3 | 179.61 (9) | C9—C10—C11—S4 | −2.8 (2) |
C1—S2—C2—C3 | −1.09 (14) | C9—C10—C11—C12 | −176.84 (15) |
C1—S5—C3—S4 | 177.69 (10) | C10—C11—C12—O4 | 0.3 (2) |
C1—S5—C3—C2 | 1.89 (14) | C10—C11—C12—C13 | 178.60 (15) |
C2—S2—C1—S1 | −178.63 (10) | C11—S4—C3—S5 | 63.50 (11) |
C2—S2—C1—S5 | 2.31 (10) | C11—S4—C3—C2 | −121.05 (15) |
Symmetry codes: (i) x, y−1, z; (ii) −x+1, −y, −z+1; (iii) −x+1, −y+1, −z+2; (iv) −x, −y+1, −z+1. |
D—H···A | D—H | H···A | D···A | D—H···A |
O2—H2···O1 | 0.82 | 1.67 | 2.4228 (17) | 151 |
O4—H4···O3 | 0.82 | 1.69 | 2.4406 (17) | 151 |
C13—H13C···O3v | 0.96 | 2.60 | 3.374 (3) | 138 |
C8—H8C···O3vi | 0.96 | 2.66 | 3.522 (2) | 150 |
C8—H8A···O2vii | 0.96 | 2.66 | 3.612 (2) | 170 |
C8—H8C···O1v | 0.96 | 2.56 | 3.228 (3) | 127 |
C9—H9B···S1viii | 0.96 | 2.90 | 3.5184 (19) | 123 |
C13—H13B···S1iv | 0.96 | 2.89 | 3.7165 (19) | 144 |
C4—H4A···S1viii | 0.96 | 2.90 | 3.7987 (19) | 156 |
Symmetry codes: (iv) −x, −y+1, −z+1; (v) x−1, y, z; (vi) x−1, y+1, z; (vii) −x, −y+2, −z+2; (viii) −x+1, −y+1, −z+1. |
C1=S1 | 1.6424 (17) |
C2=C3 | 1.351 (2) |
S2-C2 | 1.7385 (16) |
S3-C2 | 1.7679 (16) |
S5-C3 | 1.7479 (16) |
S4-C3 | 1.7608 (16) |
O1=C5 | 1.278 (2) |
O2-C7 | 1.287 (2) |
O3=C10 | 1.267 (2) |
O4-C12 | 1.303 (2) |
O2-H2 | 0.8200 |
O4-H4 | 0.8200 |
S2-C2-S3 | 118.79 (9) |
S5-C3-S4 | 120.39 (9) |
C6-S3-C2 | 101.45 (7) |
C3-S4-C11 | 103.72 (7) |
C7-C6-C5 | 119.32 (14) |
C12-C11-C10 | 119.34 (14) |
Funding information
The authors acknowledge the facility of the Molecular Science Research Center (MSRC) and Materials Characterization Center (MCC) at the University of Puerto Rico for their assistance and instrumentation facilities. The National Science Foundation grant No. 1626103 is also acknowledged. KC is thankful to the Research Initiative for Scientific Enhancement (RISE) Program under grant No. 5R25GM061151–18.
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