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ISSN: 2056-9890

Crystal structure and Hirshfeld surface analysis of (benzo[4,5]imidazo[2,1-b]thia­zol-2-yl)(4-chlorophen­yl)methanone

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aChemical Biology Lab, School of Chemical and Biotechnology, SASTRA Deemed University, Tirumalaisumudiram, Thanjavur, Tamil Nadu-613401, India, and bOrganic Synthesis & Catalysis Lab, Department of Chemistry, School of Chemical, and Biotechnology, SASTRA Deemed University, Thanjavur – 613 401, Tamil Nadu, India
*Correspondence e-mail: [email protected]

Edited by Y. Ozawa, University of Hyogo, Japan (Received 30 July 2026; accepted 28 September 2026; online 2 October 2026)

Thia­zolo[3,2-a]benzimidazole derivatives are biologically important heterocycles with diverse pharmacological activities such as anti­cancer and anti-inflammatory. The compound, C16H9ClN2OS, crystallizes in the monoclinic space group P21/c with two conformationally similar mol­ecules (Z′ = 2) in the asymmetric unit. The fused thia­zolo[3,2-a]benzimidazole framework is essentially planar, while the 4-chloro­benzoyl ring is inclined by ∼53° to the thia­zole ring in both mol­ecules. The crystal packing is consolidated by C—H⋯N hydrogen bonds, C—H⋯π contacts, and π–π stacking inter­actions, forming a three-dimensional supra­molecular framework. Hirshfeld surface analysis indicates that H⋯H, H⋯C/C⋯H, H⋯Cl/Cl⋯H, H⋯N/N⋯H, and H⋯O/O⋯H contacts dominate the inter­molecular inter­actions.

1. Chemical context

Benzimidazole is an important nitro­gen-containing heterocyclic scaffold with a broad spectrum of biological activities, including anti­cancer, anti­microbial, and anti-inflammatory properties (Anichina et al., 2017View full citation; Ramos Rodríguez et al., 2019View full citation). Fusion with a thia­zole ring affords thia­zolo[3,2-a]benzimidazole derivatives, which often exhibit enhanced pharmacological profiles and have shown promise against cancer, HIV, and microbial infections (Al-Rashood & Abdel-Aziz, 2010View full citation; Khaldi et al., 2020View full citation). Given that substitution patterns on the fused ring system significantly influence bioactivity, structural characterization by single-crystal X-ray diffraction is essential for establishing the mol­ecular geometry and crystal packing, which are crucial for understanding structure–activity relationships (Ramos Rodríguez et al., 2020View full citation). As part of our ongoing research on bioactive heterocycles (Al-Ansary et al., 2017View full citation), we report the crystal structure of the title compound, C16H9ClN2OS, (3).

[Scheme 1]

2. Structural commentary

The title compound crystallizes in the monoclinic space group P21/c with two crystallographically independent mol­ecules, A and B, in the asymmetric unit (Fig. 1[link]). Both mol­ecules share the same fused thia­zolobenzimidazole core, comprising a thia­zole ring (B), an imidazole ring (C), and a benzene ring (D), which adopts an essentially planar conformation in both independent mol­ecules as observed in similar reported structures (Fun et al., 2012aView full citation,bView full citation; Wang et al., 2011View full citation). However, a comparative analysis reveals subtle differences in the degree of planarity between the two mol­ecules: the inter­planar angles between rings B/C, C/D, and B/D are 1.2 (2), 1.7 (1), and 2.7 (2)° for mol­ecule A, compared to 1.0 (1), 0.8 (2), and 1.3 (2)° for mol­ecule B, indicating that mol­ecule B exhibits marginally greater coplanarity of the fused ring system, as further supported by the corresponding torsion angles (see the torsion angle table in the supporting information). In contrast, the 4-chloro­benzoyl substituents attached at the C9 position of the thia­zole ring show a significant and remarkably similar deviation from the fused ring plane in both mol­ecules, with dihedral angles between the 4-chloro­phenyl ring (A) and the thia­zole ring (B) of 53.0 (1)° for mol­ecule A and 53.1 (3)° for mol­ecule B, suggesting that this conformational preference is primarily governed by intrinsic electronic factors and steric avoidance rather than crystal packing influences. All bond lengths and bond angles (Table 1[link]) in both mol­ecules are within the expected ranges for analogous heterocyclic systems and show no statistically significant differences between the two independent mol­ecules, confirming that mol­ecules A and B are chemically equivalent but exhibit minor conformational variations, particularly in the planarity of the fused thia­zolobenzimidazole core.

Table 1
Selected geometric parameters (Å, °)

S1B—C7B 1.725 (3) N2A—C8A 1.375 (3)
S1B—C9B 1.760 (3) N2A—C6A 1.390 (3)
S1A—C7A 1.726 (3) O1A—C10A 1.220 (3)
S1A—C9A 1.762 (3) N1B—C7B 1.305 (3)
N2B—C7B 1.382 (3) N1B—C1B 1.404 (4)
N2B—C8B 1.370 (3) O1B—C10B 1.219 (3)
N2B—C6B 1.393 (3) N1A—C7A 1.305 (3)
N2A—C7A 1.383 (3) N1A—C1A 1.407 (4)
       
C7B—S1B—C9B 89.83 (13) N1B—C7B—N2B 114.3 (2)
C7A—S1A—C9A 89.93 (14) C9B—C8B—N2B 112.2 (2)
C7B—N2B—C6B 106.8 (2) C9A—C8A—N2A 112.7 (3)
C8B—N2B—C7B 114.8 (2) C8B—C9B—S1B 112.4 (2)
C8B—N2B—C6B 138.4 (2) C10B—C9B—S1B 120.1 (2)
C7A—N2A—C6A 106.7 (2) N1B—C1B—C6B 111.8 (2)
C8A—N2A—C7A 114.4 (2) C2B—C1B—N1B 129.5 (3)
C8A—N2A—C6A 138.9 (2) C8A—C9A—S1A 112.2 (2)
C7B—N1B—C1B 103.4 (2) C10A—C9A—S1A 119.9 (2)
C7A—N1A—C1A 103.4 (2) N2B—C6B—C1B 103.8 (2)
N2A—C7A—S1A 110.8 (2) C5B—C6B—N2B 132.5 (3)
N1A—C7A—S1A 135.0 (2) N2A—C6A—C1A 104.1 (2)
N1A—C7A—N2A 114.2 (3) C5A—C6A—N2A 132.0 (3)
N2B—C7B—S1B 110.7 (2) C6A—C1A—N1A 111.6 (3)
N1B—C7B—S1B 135.0 (2) C2A—C1A—N1A 129.8 (3)
[Figure 1]
Figure 1
The mol­ecular structures (mol­ecules A and B) of compound 3 showing 50% displacement ellipsoids.

3. Supra­molecular features and Hirshfeld surface analysis

Fig. 2[link] illustrates the packing of structure 3 along the crystallographic a-axis direction, wherein the overall cohesion of the unit cell is sustained by two inter­molecular hydrogen bonds (Table 2[link]; Fig. 3[link]), C8A—H8A⋯N1A and C8B—H8B⋯N1B, that propagate into supra­molecular chains parallel to the c axis. The crystal packing is characterized by weak C—H⋯π and aromatic π–π contacts (Fig. 4[link]). The C13B—H13B⋯Cg1 and C16A—H16A⋯Cg7 contacts provide additional inter­molecular links between neighbouring mol­ecules. Several pairs of aromatic rings exhibit centroid-to-centroid separations in the range 3.731 (2)–4.011 (2) Å, namely Cg1⋯Cg3 = 3.731 (2) Å, Cg2⋯Cg3 = 4.011 (2) Å, Cg3⋯Cg4 = 3.748 (2) Å, Cg5⋯Cg7 = 3.893 (2) Å, Cg6⋯Cg7 = 3.924 (2) Å and Cg7⋯Cg8 = 3.787 (2) Å where Cg1, Cg2, Cg3 and Cg4 denote the centroids of the S1A/C7A/N2A/C8A/C9A, N1A/C1A/C6A/N2A/C7A, C11A–C16A and S1A/C7A/N1A/C1A/C6A/N2A/C8A/C9A ring systems, respectively, while Cg5, Cg6, Cg7 and Cg8 denote the corresponding centroids of the S1B/C7B/N2B/C8B/C9B, N1B/C1B/C6B/N2B/C7B, C1B–C6B and S1B/C7B/N1B/C1B/C6B/N2B/C8B/C9B ring systems. The Cg1⋯Cg3i, Cg3⋯Cg4i and Cg7⋯Cg8ii contacts are consistent with weak aromatic π–π associations (Fig. 4[link]), while the Cg5⋯Cg7ii and Cg6⋯Cg7ii contacts, with slightly larger centroid-to-centroid separations, are indicative of weaker slipped or offset aromatic contacts [symmetry codes: (i) x, Mathematical equation − y, Mathematical equation + z; (ii) x, Mathematical equation − y, −Mathematical equation + z]. The Cg2⋯Cg3i separation of 4.011 (2) Å is comparatively long and is therefore regarded as a weak or borderline aromatic contact rather than a conventional π–π stacking inter­action. Thus, the observed contacts are not inter­preted as idealized face-to-face π–π stacks, but rather as a range of weak, slipped or offset aromatic associations arising from the relative disposition of the ring systems in the crystal. Together with the C—H⋯π contacts, these inter­actions contribute to the overall supra­molecular organization of the crystal. Overall, these weak aromatic contacts, together with the other inter­molecular inter­actions present in the crystal, contribute to the cohesion and packing of the mol­ecular structure.

Table 2
Hydrogen-bond geometry (Å, °)

Cg1, and Cg7 are the centroids of of atoms S1A/C7A/N2A/C8A/C9A and C1B–C6B, respectively.

D—H⋯A D—H H⋯A D⋯A D—H⋯A
C8A—H8A⋯N1Ai 0.93 2.30 3.206 (3) 165
C8B—H8B⋯N1Bii 0.93 2.31 3.212 (3) 163
C13B—H13B⋯Cg1ii 0.93 2.88 3.551 (4) 130
C16A—H16A⋯Cg7iii 0.93 3.00 3.832 (4) 150
Symmetry codes: (i) Mathematical equation; (ii) Mathematical equation; (iii) Mathematical equation.
[Figure 2]
Figure 2
Packing diagram for compound 3 viewed down the a axis in the crystal unit cell. The dotted lines indicate the hydrogen bonds between symmetry-related mol­ecules, which extend as C—H⋯N inter­molecular inter­actions towards the c-axis direction in the unit-cell packing.
[Figure 3]
Figure 3
Hydrogen-bonding inter­actions in the crystal structure of compound 3, showing the corresponding inter­molecular contacts (C—H⋯N) involving the two crystallographically independent mol­ecules A and B. Dashed lines indicate the hydrogen-bond inter­actions.
[Figure 4]
Figure 4
Visualization of inter­molecular C—H⋯π (blue boxes) and π–π (red and black boxes) inter­actions in the crystal of compound 3. Green dashed lines indicate inter­action distances (Å).

The Hirshfeld surfaces (Fig. 5[link]) and corresponding two-dimensional fingerprint plots (Fig. 4[link]) of mol­ecules A and B provide a comparative view of their inter­molecular contacts and crystal-packing characteristics (Spackman et al., 2021View full citation). In both mol­ecules, the dnorm mapped surfaces show localized red regions associated with close inter­molecular contacts, particularly around the heteroatom-containing sites. The Hirshfeld fingerprint analysis (Fig. 6[link]) reveals closely comparable inter­molecular contact distributions for the two independent mol­ecules. For mol­ecule A, the major contributions arise from C⋯H/H⋯C (21.4%), H⋯H (19.3%), Cl⋯H/H⋯Cl (13.0%), N⋯H/H⋯N (10.9%) and O⋯H/H⋯O (10.2%) contacts, while the corresponding contributions for mol­ecule B are 22.8, 19.4, 10.7, 10.2 and 11.2%, respectively. The fingerprint plots are consistent with these values and show that C⋯H/H⋯C and H⋯H contacts constitute the principal contributions in both mol­ecules. The short C8A—H8A⋯N1A [3.206 (3) Å] and C8B—H8B⋯N1B [3.212 (3) Å] contacts are consistent with the comparable N⋯H/H⋯N contributions. The O⋯H/H⋯O contribution is slightly higher for mol­ecule B, consistent with the closer C—H⋯O contact observed for this mol­ecule, whereas mol­ecule A exhibits relatively larger Cl⋯H/H⋯Cl and S-associated contributions. Overall, the highly similar fingerprint profiles indicate comparable inter­molecular contact environments for mol­ecules A and B. The crystal packing is therefore consolidated by a cooperative combination of dispersive H⋯H, C⋯H/H⋯C and heteroatom-associated contacts, rather than by any single dominant inter­action. The small differences in individual contact contributions reflect variations in the local packing environments of the two crystallographically independent mol­ecules.

[Figure 5]
Figure 5
Hirshfeld surface mapped with dnorm for compound 3. Both mol­ecules A and B form two types of inter­molecular inter­actions, N—H⋯O and C—H⋯O, which contribute significantly to the cohesion of the crystal.
[Figure 6]
Figure 6
Hirshfeld surface fingerprint plots for compound 3 for mol­ecules A and B. Contacts contributing >5% to the total surface are given with their respective percentage contributions labeled; those contributing less than 5% are shown in supplementary Figs. S1A and S1B.

4. Database survey

A systematic analysis of the Cambridge Structural Database (CSD, Version 5.47; Groom et al., 2016View full citation), performed using the CCDC CONQUEST inter­face, was carried out to identify crystallographically characterized compounds structurally related to the title compound 3. The search identified two closely related derivatives, namely benzo[4,5]imidazo[2,1-b]thia­zol-2-yl(p-tol­yl)methanone (CSD refcode ABESUY) and benzo[4,5]imidazo[2,1-b]thia­zol-2-yl(4-fluoro­phen­yl)methan­one (ABESOS), reported by Ambethkar et al. (2017View full citation). These compounds contain para-methyl and para-fluoro substituents, respectively, on the phenyl ring of the benzoyl group. Their presence in the CSD provides useful structural precedents for assessing the influence of substitution on the conformation of the benzoyl-containing thia­zolobenzimidazole framework.

The CSD search was subsequently extended to related compounds containing the thia­zolo[3,2-a]benzimidazole core. Among the relevant structures, BACCUH (Chen et al., 2020View full citation) and AMUCIW (Yallur et al., 2016View full citation) are particularly useful for comparison. In these compounds, the benzoyl functionality is replaced by an aldehyde group; nevertheless, the principal geometrical characteristics and conformational features of the fused heteroaromatic framework are broadly comparable with those observed for compound 3. Both structures also display aromatic π–π stacking inter­actions, indicating that such contacts may contribute significantly to the supra­molecular organization of thia­zolo[3,2-a]benzimidazole derivatives in the solid state. Further structural comparisons can be made with the benzoyl-containing CSD entries CANHEI (Zhang et al., 2021View full citation) and CANHEI01 (Chen et al., 2022View full citation). These structures possess an unsubstituted benzoyl group and exhibit geometrical parameters broadly consistent with those determined for compound 3. The comparison suggests that modification of the peripheral substituents does not substanti­ally alter the geometry of the fused thia­zolo[3,2-a]benzimidazole skeleton, although differences in the orientation of the pendant phenyl ring can occur.

The methyl-ketone derivative FAQPAQ (Abdel-Aziz et al., 2010View full citation) represents another structurally relevant example. In this compound, the thia­zolo[3,2-a]benzimidazole unit adopts an essentially planar conformation and is associated with a pyrazolo­[1,5-a]pyrimidine system. Although its overall mol­ecular constitution differs from that of compound 3, its nearly planar heteroaromatic framework supports the conformational preference observed for the corresponding core in the present structure. The reported biological activity of FAQPAQ, including its in vitro anti­cancer activity against colon cancer, further illustrates the continued inter­est in this heterocyclic scaffold. Other related structures, such as EXIVOX (Wang et al., 2011View full citation) and QECZAB (Fun et al., 2012bView full citation), provide additional insight into the inter­molecular organization of this class of compounds. In EXIVOX, no significant classical inter­molecular hydrogen-bonding inter­actions were reported, whereas the crystal packing of QECZAB is substanti­ally influenced by π–π stacking inter­actions. These observations are consistent with the possibility that aromatic stacking and other weak inter­molecular contacts can play an important role in consolidating the crystal packing of thia­zolo[3,2-a]benzimidazole derivatives.

Overall, the CSD comparison indicates that the fused thia­zolo[3,2-a]benzimidazole core generally favours an approximately planar geometry, consistent with its extended conjugated aromatic system. In compound 3, however, attachment of the benzoyl substituent introduces an additional torsional degree of freedom, allowing the pendant phenyl ring to rotate with respect to the heteroaromatic core. The magnitude of this torsional deviation is likely governed by a combination of steric and electronic effects associated with the substituent on the phenyl ring. In particular, para substitution may influence both the preferred mol­ecular conformation and the inter­molecular packing arrangement. Thus, the structural features observed for compound 3, including the planarity of the heteroaromatic core, the orientation of the benzoyl phenyl ring and the presence of π–π inter­actions, are broadly consistent with the structural trends evident from related thia­zolo[3,2-a]benzimidazole derivatives reported in the CSD.

5. Synthesis and crystallization

A mixture of 1.0 equiv of 2-mercaptobenzimidazole (1), 1.0 equiv of (E)-1-(4-chloro­phen­yl)-3-(di­methyl­amino)­prop-2-en-1-one (2), and 1.0 equiv of iodine in acetic acid (5 mL) was stirred at room temperature under open air for 2 h (Fig. 7[link]). Upon completion (monitored by TLC), the reaction mixture was poured into water, quenched with aqueous sodium thio­sulfate, and extracted with ethyl acetate. The combined organic layers were dried over Na2SO4 and concentrated under reduced pressure. The crude product, (benzo[4,5]imidazo[2,1-b]thia­zol-2-yl)(4-chloro­phen­yl)methanone (3) was purified by column chromatography and the well dried sample was crystallized using 100% ethyl­acetate as a solvent by slow evaporation method which yielded pale yellow crystal for diffraction study.

[Figure 7]
Figure 7
Synthetic route of the title compound (3).

6. Refinement

Crystal data, data collection and structure refinement details are summarized in Table 3[link]. The carbon-bound hydrogen atoms were positioned based on calculated values (C—H = 0.93 Å) and were refined as riding atoms, with Uiso(H) set to 1.2Ueq(C).

Table 3
Experimental details

Crystal data
Chemical formula C16H9ClN2OS
Mr 312.76
Crystal system, space group Monoclinic, P21/c
Temperature (K) 300
a, b, c (Å) 18.1878 (18), 12.8058 (13), 12.1917 (11)
β (°) 90.115 (4)
V (Å3) 2839.6 (5)
Z 8
Radiation type Mo Kα
μ (mm−1) 0.42
Crystal size (mm) 0.30 × 0.15 × 0.10
 
Data collection
Diffractometer Bruker APEXII CCD
Absorption correction Multi-scan (SADABS; Krause et al., 2015View full citation)
Tmin, Tmax 0.678, 0.746
No. of measured, independent and observed [I > 2σ(I)] reflections 94667, 7077, 3706
Rint 0.096
(sin θ/λ)max (Å−1) 0.668
 
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.059, 0.134, 1.11
No. of reflections 7077
No. of parameters 380
H-atom treatment H-atom parameters constrained
Δρmax, Δρmin (e Å−3) 0.38, −0.33
Computer programs: APEX3 (Bruker, 2016View full citation), SAINT (Bruker, 2017View full citation), OLEX2.solve (Bourhis et al., 2015View full citation), SHELXL2019/3 (Sheldrick, 2015View full citation) and OLEX2 (Dolomanov et al., 2009View full citation).

Supporting information


Computing details top

(Benzo[4,5]imidazo[2,1-b]thiazol-2-yl)(4-chlorophenyl)methanone top
Crystal data top
C16H9ClN2OSF(000) = 1280
Mr = 312.76Dx = 1.463 Mg m−3
Monoclinic, P21/cMo Kα radiation, λ = 0.71073 Å
a = 18.1878 (18) ÅCell parameters from 94667 reflections
b = 12.8058 (13) Åθ = 2.0–28.4°
c = 12.1917 (11) ŵ = 0.42 mm−1
β = 90.115 (4)°T = 300 K
V = 2839.6 (5) Å3Block, pale yellow
Z = 80.30 × 0.15 × 0.10 mm
Data collection top
Bruker APEXII CCD
diffractometer
7077 independent reflections
Radiation source: MoKα (0.71073)3706 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.096
φ and ω scansθmax = 28.4°, θmin = 2.0°
Absorption correction: multi-scan
(SADABS; Krause et al., 2015)
h = −24→24
Tmin = 0.678, Tmax = 0.746k = −17→17
94667 measured reflectionsl = −16→16
Refinement top
Refinement on F2Primary atom site location: iterative
Least-squares matrix: fullHydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.059H-atom parameters constrained
wR(F2) = 0.134 w = 1/[σ2(Fo2) + (0.0264P)2 + 2.3482P]
where P = (Fo2 + 2Fc2)/3
S = 1.11(Δ/σ)max < 0.001
7077 reflectionsΔρmax = 0.38 e Å−3
380 parametersΔρmin = −0.33 e Å−3
0 restraintsExtinction correction: SHELXL2019/2 (Sheldrick 2015), Fc*=kFc[1+0.001xFc2λ3/sin(2θ)]-1/4
0 constraintsExtinction coefficient: 0.0031 (3)
Special details top

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.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/Ueq
S1B0.15689 (4)0.87765 (7)0.91119 (6)0.0579 (3)
S1A0.34650 (4)0.36471 (7)0.99192 (6)0.0572 (2)
Cl1B0.13842 (6)0.94112 (9)0.21428 (7)0.0852 (3)
Cl1A0.37444 (7)0.45888 (10)0.30319 (8)0.0999 (4)
N2B0.26281 (12)0.77668 (19)0.82212 (16)0.0444 (6)
N2A0.23686 (13)0.2692 (2)0.90499 (17)0.0474 (6)
O1A0.46914 (12)0.3712 (2)0.82364 (18)0.0708 (7)
N1B0.27979 (13)0.7804 (2)1.00557 (17)0.0505 (6)
O1B0.03999 (13)0.9172 (2)0.74099 (18)0.0804 (8)
N1A0.21787 (14)0.2853 (2)1.08714 (18)0.0532 (7)
C7A0.26191 (16)0.3049 (2)1.0054 (2)0.0480 (7)
C7B0.23775 (15)0.8083 (2)0.9238 (2)0.0466 (7)
C8B0.21990 (16)0.8074 (2)0.7354 (2)0.0496 (8)
H8B0.2303380.7917040.6625950.060*
C8A0.28273 (16)0.2910 (2)0.8184 (2)0.0492 (8)
H8A0.2725670.2722340.7462680.059*
C9B0.16081 (16)0.8629 (2)0.7678 (2)0.0483 (7)
C1B0.33663 (16)0.7245 (2)0.9545 (2)0.0482 (7)
C9A0.34387 (16)0.3422 (2)0.8494 (2)0.0496 (8)
C6B0.32728 (15)0.7205 (2)0.8401 (2)0.0455 (7)
C5A0.12219 (17)0.1675 (3)0.8555 (2)0.0548 (8)
H5A0.1309290.1608400.7807380.066*
C6A0.17003 (16)0.2200 (2)0.9242 (2)0.0474 (7)
C10B0.09936 (17)0.8982 (3)0.6993 (2)0.0540 (8)
C1A0.15944 (16)0.2308 (2)1.0375 (2)0.0499 (8)
C11B0.11086 (16)0.9082 (2)0.5789 (2)0.0498 (8)
C5B0.37464 (17)0.6696 (3)0.7704 (2)0.0554 (8)
H5B0.3669150.6678520.6949530.066*
C11A0.39723 (16)0.3855 (2)0.6625 (2)0.0482 (7)
C3B0.44454 (18)0.6231 (3)0.9315 (3)0.0605 (9)
H3B0.4850910.5889140.9611010.073*
C2A0.09724 (17)0.1867 (3)1.0844 (3)0.0578 (8)
H2A0.0884120.1921511.1593270.069*
C2B0.39681 (17)0.6737 (3)1.0008 (3)0.0574 (8)
H2B0.4045100.6740551.0762670.069*
C10A0.40817 (17)0.3665 (2)0.7820 (2)0.0524 (8)
C4B0.43413 (17)0.6213 (3)0.8186 (3)0.0590 (8)
H4B0.4680620.5867490.7746760.071*
C4A0.06062 (17)0.1256 (3)0.9047 (3)0.0612 (9)
H4A0.0261780.0906670.8618370.073*
C16A0.45472 (17)0.3662 (3)0.5907 (3)0.0582 (8)
H16A0.4985790.3389390.6175700.070*
C3A0.04902 (18)0.1345 (3)1.0165 (3)0.0620 (9)
H3A0.0072620.1041481.0468300.074*
C16B0.05378 (17)0.8820 (3)0.5086 (2)0.0589 (9)
H16B0.0095400.8579250.5371720.071*
C14B0.12725 (19)0.9288 (3)0.3553 (2)0.0562 (8)
C12B0.17583 (18)0.9459 (3)0.5350 (3)0.0584 (8)
H12B0.2142420.9642600.5816680.070*
C13B0.18442 (18)0.9566 (3)0.4230 (3)0.0597 (9)
H13B0.2281240.9821440.3940280.072*
C12A0.33295 (17)0.4283 (3)0.6207 (3)0.0567 (8)
H12A0.2940900.4425770.6677990.068*
C15B0.06211 (18)0.8912 (3)0.3964 (3)0.0635 (9)
H15B0.0241280.8721870.3492700.076*
C14A0.3837 (2)0.4293 (3)0.4417 (3)0.0624 (9)
C13A0.32574 (19)0.4500 (3)0.5107 (3)0.0613 (9)
H13A0.2823000.4782020.4833180.074*
C15A0.44796 (19)0.3868 (3)0.4805 (3)0.0684 (10)
H15A0.4864260.3720460.4327610.082*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
S1B0.0545 (5)0.0800 (6)0.0391 (4)0.0107 (4)0.0005 (3)−0.0064 (4)
S1A0.0545 (5)0.0729 (6)0.0441 (4)−0.0056 (4)−0.0096 (3)−0.0040 (4)
Cl1B0.1001 (8)0.1075 (9)0.0479 (5)0.0073 (6)−0.0047 (5)0.0176 (5)
Cl1A0.1188 (9)0.1223 (10)0.0586 (6)−0.0032 (7)0.0062 (6)0.0263 (6)
N2B0.0497 (14)0.0530 (16)0.0304 (11)0.0036 (12)−0.0023 (10)−0.0024 (11)
N2A0.0508 (15)0.0585 (17)0.0329 (12)−0.0029 (12)−0.0046 (10)0.0018 (11)
O1A0.0494 (13)0.0950 (19)0.0679 (15)−0.0010 (13)−0.0091 (11)0.0039 (13)
N1B0.0559 (15)0.0625 (18)0.0333 (12)0.0021 (13)−0.0019 (11)0.0010 (12)
O1B0.0607 (15)0.125 (2)0.0555 (14)0.0245 (15)−0.0010 (12)−0.0075 (14)
N1A0.0583 (16)0.0636 (18)0.0375 (13)0.0015 (14)−0.0052 (12)0.0008 (12)
C7A0.0531 (18)0.055 (2)0.0359 (15)0.0030 (15)−0.0086 (13)0.0006 (14)
C7B0.0499 (17)0.057 (2)0.0328 (14)−0.0007 (15)−0.0001 (12)−0.0027 (14)
C8B0.0564 (18)0.061 (2)0.0316 (14)−0.0004 (16)−0.0038 (13)0.0019 (14)
C8A0.0535 (18)0.056 (2)0.0380 (15)−0.0022 (16)0.0008 (13)0.0014 (14)
C9B0.0508 (17)0.059 (2)0.0351 (14)0.0021 (16)−0.0033 (13)−0.0024 (14)
C1B0.0518 (18)0.051 (2)0.0413 (16)−0.0027 (15)−0.0057 (13)0.0030 (14)
C9A0.0480 (18)0.060 (2)0.0402 (15)0.0002 (15)−0.0033 (13)0.0003 (14)
C6B0.0435 (16)0.0521 (19)0.0408 (15)−0.0006 (15)−0.0011 (12)0.0050 (14)
C5A0.059 (2)0.062 (2)0.0436 (16)−0.0039 (17)−0.0080 (14)0.0015 (15)
C6A0.0480 (17)0.052 (2)0.0418 (16)−0.0041 (15)−0.0020 (13)0.0052 (14)
C10B0.0536 (19)0.063 (2)0.0456 (17)0.0052 (17)−0.0051 (14)−0.0062 (15)
C1A0.0543 (19)0.054 (2)0.0416 (16)0.0054 (16)−0.0016 (14)0.0051 (14)
C11B0.0508 (18)0.053 (2)0.0458 (16)0.0089 (15)−0.0082 (14)0.0001 (14)
C5B0.060 (2)0.062 (2)0.0443 (16)0.0053 (17)0.0046 (15)0.0020 (16)
C11A0.0459 (17)0.0456 (19)0.0532 (17)−0.0021 (14)0.0010 (14)−0.0008 (15)
C3B0.0536 (19)0.056 (2)0.072 (2)0.0004 (17)−0.0110 (17)0.0080 (18)
C2A0.061 (2)0.066 (2)0.0459 (17)0.0057 (18)0.0063 (15)0.0067 (16)
C2B0.060 (2)0.063 (2)0.0490 (17)−0.0053 (17)−0.0116 (15)0.0064 (16)
C10A0.0501 (19)0.052 (2)0.0550 (18)0.0032 (16)−0.0030 (15)−0.0015 (16)
C4B0.0532 (19)0.057 (2)0.067 (2)0.0048 (17)0.0034 (16)−0.0012 (17)
C4A0.055 (2)0.065 (2)0.064 (2)−0.0047 (18)−0.0072 (16)0.0036 (18)
C16A0.0518 (19)0.062 (2)0.060 (2)0.0036 (17)0.0056 (15)0.0036 (17)
C3A0.0540 (19)0.064 (2)0.068 (2)0.0002 (18)0.0056 (17)0.0080 (19)
C16B0.0507 (18)0.074 (2)0.0519 (18)0.0000 (17)−0.0050 (15)0.0032 (17)
C14B0.066 (2)0.056 (2)0.0466 (17)0.0067 (17)−0.0092 (15)0.0073 (16)
C12B0.062 (2)0.061 (2)0.0527 (19)−0.0036 (17)−0.0145 (15)0.0049 (16)
C13B0.061 (2)0.060 (2)0.058 (2)−0.0060 (17)−0.0053 (16)0.0117 (17)
C12A0.0518 (19)0.062 (2)0.0559 (19)0.0025 (16)0.0046 (15)0.0040 (17)
C15B0.059 (2)0.079 (3)0.0525 (19)−0.0017 (19)−0.0197 (16)0.0015 (18)
C14A0.074 (2)0.064 (2)0.0491 (18)−0.0061 (19)0.0062 (17)0.0084 (17)
C13A0.063 (2)0.057 (2)0.064 (2)0.0017 (17)−0.0048 (17)0.0090 (17)
C15A0.065 (2)0.079 (3)0.061 (2)0.000 (2)0.0168 (17)0.0056 (19)
Geometric parameters (Å, º) top
S1B—C7B1.725 (3)C11B—C16B1.386 (4)
S1B—C9B1.760 (3)C11B—C12B1.385 (4)
S1A—C7A1.726 (3)C5B—H5B0.9300
S1A—C9A1.762 (3)C5B—C4B1.377 (4)
Cl1B—C14B1.739 (3)C11A—C10A1.491 (4)
Cl1A—C14A1.739 (3)C11A—C16A1.387 (4)
N2B—C7B1.382 (3)C11A—C12A1.387 (4)
N2B—C8B1.370 (3)C3B—H3B0.9300
N2B—C6B1.393 (3)C3B—C2B1.376 (4)
N2A—C7A1.383 (3)C3B—C4B1.389 (4)
N2A—C8A1.375 (3)C2A—H2A0.9300
N2A—C6A1.390 (3)C2A—C3A1.378 (4)
O1A—C10A1.220 (3)C2B—H2B0.9300
N1B—C7B1.305 (3)C4B—H4B0.9300
N1B—C1B1.404 (4)C4A—H4A0.9300
O1B—C10B1.219 (3)C4A—C3A1.384 (4)
N1A—C7A1.305 (3)C16A—H16A0.9300
N1A—C1A1.407 (4)C16A—C15A1.375 (4)
C8B—H8B0.9300C3A—H3A0.9300
C8B—C9B1.349 (4)C16B—H16B0.9300
C8A—H8A0.9300C16B—C15B1.381 (4)
C8A—C9A1.345 (4)C14B—C13B1.373 (4)
C9B—C10B1.466 (4)C14B—C15B1.374 (4)
C1B—C6B1.405 (4)C12B—H12B0.9300
C1B—C2B1.392 (4)C12B—C13B1.382 (4)
C9A—C10A1.464 (4)C13B—H13B0.9300
C6B—C5B1.376 (4)C12A—H12A0.9300
C5A—H5A0.9300C12A—C13A1.375 (4)
C5A—C6A1.381 (4)C15B—H15B0.9300
C5A—C4A1.380 (4)C14A—C13A1.375 (4)
C6A—C1A1.402 (4)C14A—C15A1.372 (5)
C10B—C11B1.488 (4)C13A—H13A0.9300
C1A—C2A1.389 (4)C15A—H15A0.9300
C7B—S1B—C9B89.83 (13)C16A—C11A—C12A118.3 (3)
C7A—S1A—C9A89.93 (14)C12A—C11A—C10A122.3 (3)
C7B—N2B—C6B106.8 (2)C2B—C3B—H3B118.9
C8B—N2B—C7B114.8 (2)C2B—C3B—C4B122.1 (3)
C8B—N2B—C6B138.4 (2)C4B—C3B—H3B118.9
C7A—N2A—C6A106.7 (2)C1A—C2A—H2A121.0
C8A—N2A—C7A114.4 (2)C3A—C2A—C1A117.9 (3)
C8A—N2A—C6A138.9 (2)C3A—C2A—H2A121.0
C7B—N1B—C1B103.4 (2)C1B—C2B—H2B121.1
C7A—N1A—C1A103.4 (2)C3B—C2B—C1B117.8 (3)
N2A—C7A—S1A110.8 (2)C3B—C2B—H2B121.1
N1A—C7A—S1A135.0 (2)O1A—C10A—C9A120.2 (3)
N1A—C7A—N2A114.2 (3)O1A—C10A—C11A121.2 (3)
N2B—C7B—S1B110.7 (2)C9A—C10A—C11A118.6 (3)
N1B—C7B—S1B135.0 (2)C5B—C4B—C3B121.4 (3)
N1B—C7B—N2B114.3 (2)C5B—C4B—H4B119.3
N2B—C8B—H8B123.9C3B—C4B—H4B119.3
C9B—C8B—N2B112.2 (2)C5A—C4A—H4A119.3
C9B—C8B—H8B123.9C5A—C4A—C3A121.4 (3)
N2A—C8A—H8A123.7C3A—C4A—H4A119.3
C9A—C8A—N2A112.7 (3)C11A—C16A—H16A119.4
C9A—C8A—H8A123.7C15A—C16A—C11A121.1 (3)
C8B—C9B—S1B112.4 (2)C15A—C16A—H16A119.4
C8B—C9B—C10B127.1 (3)C2A—C3A—C4A122.2 (3)
C10B—C9B—S1B120.1 (2)C2A—C3A—H3A118.9
N1B—C1B—C6B111.8 (2)C4A—C3A—H3A118.9
C2B—C1B—N1B129.5 (3)C11B—C16B—H16B119.7
C2B—C1B—C6B118.7 (3)C15B—C16B—C11B120.5 (3)
C8A—C9A—S1A112.2 (2)C15B—C16B—H16B119.7
C8A—C9A—C10A127.4 (3)C13B—C14B—Cl1B118.8 (3)
C10A—C9A—S1A119.9 (2)C13B—C14B—C15B121.6 (3)
N2B—C6B—C1B103.8 (2)C15B—C14B—Cl1B119.6 (2)
C5B—C6B—N2B132.5 (3)C11B—C12B—H12B119.5
C5B—C6B—C1B123.8 (3)C13B—C12B—C11B121.0 (3)
C6A—C5A—H5A122.1C13B—C12B—H12B119.5
C4A—C5A—H5A122.1C14B—C13B—C12B118.8 (3)
C4A—C5A—C6A115.9 (3)C14B—C13B—H13B120.6
N2A—C6A—C1A104.1 (2)C12B—C13B—H13B120.6
C5A—C6A—N2A132.0 (3)C11A—C12A—H12A119.4
C5A—C6A—C1A123.9 (3)C13A—C12A—C11A121.1 (3)
O1B—C10B—C9B119.9 (3)C13A—C12A—H12A119.4
O1B—C10B—C11B121.4 (3)C16B—C15B—H15B120.4
C9B—C10B—C11B118.7 (3)C14B—C15B—C16B119.1 (3)
C6A—C1A—N1A111.6 (3)C14B—C15B—H15B120.4
C2A—C1A—N1A129.8 (3)C13A—C14A—Cl1A118.6 (3)
C2A—C1A—C6A118.6 (3)C15A—C14A—Cl1A120.1 (3)
C16B—C11B—C10B118.8 (3)C15A—C14A—C13A121.3 (3)
C12B—C11B—C10B122.2 (3)C12A—C13A—H13A120.5
C12B—C11B—C16B119.0 (3)C14A—C13A—C12A119.0 (3)
C6B—C5B—H5B121.9C14A—C13A—H13A120.5
C6B—C5B—C4B116.2 (3)C16A—C15A—H15A120.4
C4B—C5B—H5B121.9C14A—C15A—C16A119.1 (3)
C16A—C11A—C10A119.3 (3)C14A—C15A—H15A120.4
S1B—C9B—C10B—O1B−15.4 (5)C9B—C10B—C11B—C16B143.2 (3)
S1B—C9B—C10B—C11B165.7 (2)C9B—C10B—C11B—C12B−38.8 (5)
S1A—C9A—C10A—O1A22.5 (4)C1B—N1B—C7B—S1B179.7 (3)
S1A—C9A—C10A—C11A−157.4 (2)C1B—N1B—C7B—N2B−0.9 (3)
Cl1B—C14B—C13B—C12B−179.4 (3)C1B—C6B—C5B—C4B−0.4 (5)
Cl1B—C14B—C15B—C16B−179.9 (3)C9A—S1A—C7A—N2A1.5 (2)
Cl1A—C14A—C13A—C12A−179.1 (3)C9A—S1A—C7A—N1A−179.6 (3)
Cl1A—C14A—C15A—C16A178.5 (3)C6B—N2B—C7B—S1B−179.2 (2)
N2B—C8B—C9B—S1B−0.5 (3)C6B—N2B—C7B—N1B1.2 (4)
N2B—C8B—C9B—C10B−172.8 (3)C6B—N2B—C8B—C9B179.8 (3)
N2B—C6B—C5B—C4B−180.0 (3)C6B—C1B—C2B—C3B0.7 (5)
N2A—C8A—C9A—S1A0.5 (3)C6B—C5B—C4B—C3B0.9 (5)
N2A—C8A—C9A—C10A172.1 (3)C5A—C6A—C1A—N1A178.3 (3)
N2A—C6A—C1A—N1A0.0 (3)C5A—C6A—C1A—C2A−0.1 (5)
N2A—C6A—C1A—C2A−178.3 (3)C5A—C4A—C3A—C2A1.1 (5)
N1B—C1B—C6B—N2B0.4 (3)C6A—N2A—C7A—S1A178.3 (2)
N1B—C1B—C6B—C5B−179.2 (3)C6A—N2A—C7A—N1A−0.9 (4)
N1B—C1B—C2B—C3B179.2 (3)C6A—N2A—C8A—C9A−179.1 (3)
O1B—C10B—C11B—C16B−35.7 (5)C6A—C5A—C4A—C3A−1.2 (5)
O1B—C10B—C11B—C12B142.3 (4)C6A—C1A—C2A—C3A−0.1 (5)
N1A—C1A—C2A—C3A−178.2 (3)C10B—C11B—C16B—C15B179.4 (3)
C7A—S1A—C9A—C8A−1.1 (3)C10B—C11B—C12B—C13B−178.5 (3)
C7A—S1A—C9A—C10A−173.4 (3)C1A—N1A—C7A—S1A−178.0 (3)
C7A—N2A—C8A—C9A0.7 (4)C1A—N1A—C7A—N2A0.9 (3)
C7A—N2A—C6A—C5A−177.5 (3)C1A—C2A—C3A—C4A−0.4 (5)
C7A—N2A—C6A—C1A0.5 (3)C11B—C16B—C15B—C14B−1.3 (5)
C7A—N1A—C1A—C6A−0.6 (3)C11B—C12B—C13B—C14B−0.2 (5)
C7A—N1A—C1A—C2A177.6 (3)C11A—C16A—C15A—C14A1.5 (5)
C7B—S1B—C9B—C8B0.8 (3)C11A—C12A—C13A—C14A−0.5 (5)
C7B—S1B—C9B—C10B173.7 (3)C2B—C1B—C6B—N2B179.2 (3)
C7B—N2B—C8B—C9B−0.2 (4)C2B—C1B—C6B—C5B−0.4 (5)
C7B—N2B—C6B—C1B−0.9 (3)C2B—C3B—C4B—C5B−0.7 (5)
C7B—N2B—C6B—C5B178.7 (3)C10A—C11A—C16A—C15A−177.3 (3)
C7B—N1B—C1B—C6B0.3 (3)C10A—C11A—C12A—C13A176.6 (3)
C7B—N1B—C1B—C2B−178.4 (3)C4B—C3B—C2B—C1B−0.1 (5)
C8B—N2B—C7B—S1B0.8 (3)C4A—C5A—C6A—N2A178.5 (3)
C8B—N2B—C7B—N1B−178.8 (3)C4A—C5A—C6A—C1A0.8 (5)
C8B—N2B—C6B—C1B179.0 (3)C16A—C11A—C10A—O1A26.5 (5)
C8B—N2B—C6B—C5B−1.3 (6)C16A—C11A—C10A—C9A−153.6 (3)
C8B—C9B—C10B—O1B156.5 (3)C16A—C11A—C12A—C13A0.8 (5)
C8B—C9B—C10B—C11B−22.5 (5)C16B—C11B—C12B—C13B−0.5 (5)
C8A—N2A—C7A—S1A−1.5 (3)C12B—C11B—C16B—C15B1.3 (5)
C8A—N2A—C7A—N1A179.3 (3)C13B—C14B—C15B—C16B0.6 (5)
C8A—N2A—C6A—C5A2.2 (6)C12A—C11A—C10A—O1A−149.3 (3)
C8A—N2A—C6A—C1A−179.8 (3)C12A—C11A—C10A—C9A30.6 (5)
C8A—C9A—C10A—O1A−148.5 (3)C12A—C11A—C16A—C15A−1.4 (5)
C8A—C9A—C10A—C11A31.6 (5)C15B—C14B—C13B—C12B0.2 (5)
C9B—S1B—C7B—N2B−0.9 (2)C13A—C14A—C15A—C16A−1.1 (6)
C9B—S1B—C7B—N1B178.6 (3)C15A—C14A—C13A—C12A0.6 (5)
Hydrogen-bond geometry (Å, º) top
Cg1, and Cg7 are the centroids of of atoms S1A/C7A/N2A/C8A/C9A and C1B–C6B, respectively.
D—H···AD—HH···AD···AD—H···A
C8A—H8A···N1Ai0.932.303.206 (3)165
C8B—H8B···N1Bii0.932.313.212 (3)163
C13B—H13B···Cg1ii0.932.883.551 (4)130
C16A—H16A···Cg7iii0.933.003.832 (4)150
Symmetry codes: (i) x, −y+1/2, z−1/2; (ii) x, −y+3/2, z−1/2; (iii) −x+1, y−1/2, −z+3/2.
 

Acknowledgements

The authors gratefully acknowledge the Vellore Institute of Technology (VIT) for providing the single crystal X-ray diffraction data.

References

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