Crystal structure of 4-({(1E,2E)-3-[3-(4-fluoro­phen­yl)-1-isopropyl-1H-indol-2-yl]allyl­idene}amino)-1H-1,2,4-triazole-5(4H)-thione

Ajaykumar D Kulkarni; Md Lutfor Rahman; Mashitah Mohd Yusoff; Huey Chong Kwong; Ching Kheng Quah

doi:10.1107/S205698901502201X

. 2015 Nov 25;71(Pt 12):1525–1527. doi: 10.1107/S205698901502201X

Crystal structure of 4-({(1E,2E)-3-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]allylidene}amino)-1H-1,2,4-triazole-5(4H)-thione

Ajaykumar D Kulkarni ^a, Md Lutfor Rahman ^b,^*, Mashitah Mohd Yusoff ^b, Huey Chong Kwong ^c, Ching Kheng Quah ^d

PMCID: PMC4719829 PMID: 26870420

The asymmetric unit of the title compound comprises two independent molecules which exist in the trans conformation with respect to the methene C= C and the acyclic N=C bonds. In the crystal, molecules are linked via N—H⋯N hydrogen bonds, forming chains along the b-axis direction.

Keywords: crystal structure; 1,2,4-triazole-3-thione; indole; Schiff base; N—H⋯N hydrogen bonds; C—H⋯π interactions; π–π interactions

Abstract

The asymmetric unit of the titled compound, C₂₂H₂₀FN₅S, comprises two independent molecules (A and B), both of which have a trans conformation with respect to the methene C=C [1.342 (2) and 1.335 (2) Å] and the acyclic N=C [1.283 (2) and 1.281 (2) Å] bonds. In molecule A, the triazole ring makes dihedral angles of 55.01 (12) and 18.17 (9)° with the benzene and indole rings, respectively. The corresponding dihedral angles for molecule B are 54.54 (11) and 14.60 (10)°, respectively. In the crystal, molecules are consolidated into –A–B–A–B– chains along [010] via N—H⋯N hydrogen bonds. The chains are further linked into layers parallel to the ac plane via π–π interactions involving inversion-related triazole rings [centroid–centroid distances = 3.3436 (11)–3.4792 (13) Å].

Chemical context

The chemistry of 1,2,4-triazole derivatives has attracted widespread attention due to their diverse biological activities and because they are a new class of antimicrobial agents (Sun et al., 2004 ▸; Verreck et al., 2003 ▸); for example fluconazole and itraconazole are used as antimicrobial drugs. Hence, metal complexes of Schiff bases derived from 1,2,4-triazole derivatives have been the subject of considerable study (Ozarowski et al., 1991 ▸; Cornelissen et al., 1992 ▸; Varma et al., 1992 ▸; Mishra & Said, 1996 ▸). A number of metal complexes with 1,2,4-triazole Schiff bases have been reported from our laboratory (Yadawe & Patil, 1997 ▸; Avaji et al., 2006 ▸; Kulkarni et al., 2009 ▸, 2011 ▸). In addition to this isatin, which is an endogenous indole, and its derivatives have been shown to exhibit a wide range of biological activities (Daisley & Shah, 1984 ▸; Pandeya et al., 1999a ▸,b ▸; Cerchiaro & Ferreira, 2006 ▸; Sridhar et al., 2002 ▸).Since triazoles are heterocyclic compounds and Schiff bases derived from isatin often act as versatile chelating agents and exhibit promising bioactivities, it is likely that a Schiff base derived from fluvastatin–triazole might also exhibit useful biological activities. In this way, it was planned to prepare a Schiff base which possesses both nitrogen and sulfur coordination cites so that it might coordinate effectively to metal ions.

Structural commentary

The asymmetric unit of the title compound (Fig. 1 ▸) is comprised of two independent molecules (A and B). Both molecules have a trans conformation with respect to the methene C=C [1.342 (2) and 1.335 (2) Å in molecules A and B, respectively] and the acyclic N=C bonds [1.283 (2) and 1.281 (2) Å in molecules A and B, respectively]. The indole rings are almost planar [maximum deviations of 0.017 (2) Å for atom C8A in molecule A and 0.027 (2) Å for atom N1B in molecule B]. In molecule A, the triazole ring makes dihedral angles of 55.01 (12) and 18.17 (9)°, respectively, with the fluorophenyl and indole rings [54.54 (11) and 14.60 (10)°, respectively, in molecule B]. The indole and fluorophenyl rings are inclined to one another by a dihedral angle of 64.78 (9)° [55.21 (8)° in molecule B]. The bond lengths and angles in the triazole-thione moiety of the title compound are comparable to those reported for related compounds (Fun et al., 2008 ▸; Kulkarni et al., 2015 ▸). graphic file with name e-71-01525-scheme1.jpg

The molecular structure of the two independent molecules (A and B) of the title compound, showing the atom labelling. Displacement ellipsoids are drawn at the 30% probability level.

Supramolecular features

In the crystal, molecules A and B are consolidated into –A–B–A–B– chains along [010] via N—H⋯N hydrogen bonds (Table 1 ▸ and Fig. 2 ▸). The chains are linked via C—H⋯π interactions (Table 1 ▸) and slipped parallel π–π interactions, involving inversion-related triazole rings, forming layers parallel to the ac plane [Cg4⋯Cg4ⁱ = 3.3436 (11) Å; Cg4 is the centroid of ring N3A–N5A/C12A/C13A; interplanar distance = 3.2317 (8) Å; slippage = 0.858 Å; symmetry code: (i) −x, −y + 1, −z, and Cg5⋯Cg5ⁱⁱ = 3.4792 (13) Å; Cg5 is the centroid of ring N3B–N5B/C12B/C13B; interplanar distance = 3.4194 (9) Å; slippage = 0.642 Å; symmetry code: (ii) −x + 2, −y + 2, −z].

Table 1. Hydrogen-bond geometry (Å, °).

Cg1 is the centroid of ring N3A–N5A/C12A/C13A, Cg2 is the centroid of ring C17B–C22B, and Cg3 is the centroid of ring C1A–C6A.

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
N4A—H4AB⋯N2B ⁱ	0.90 (2)	2.05 (2)	2.944 (2)	170 (2)
N4B—H4BB⋯N2A ⁱⁱ	0.89 (2)	2.02 (2)	2.906 (2)	170 (3)
C15B—H15E⋯Cg1ⁱⁱⁱ	0.96	2.91	3.521 (3)	123
C16A—H16B⋯Cg2^iv	0.96	2.87	3.716 (2)	148
C21A—H21A⋯Cg3^v	0.93	2.90	3.668 (2)	140

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Symmetry codes: (i) Inline graphic ; (ii) ; (iii) ; (iv) ; (v) .

The crystal packing of the title compound viewed along the a axis. The N—H⋯N hydrogen bonds are shown as dashed lines (see Table 1 ▸). H atoms not involved in hydrogen bonding have been omitted for clarity.

Database survey

A search of the Cambridge Structural Database (Version35.6, last update May 2015; Groom and Allen, 2014 ▸) using 4-(λ¹-azanyl)-5-methyl-2,4-dihydro-3H-1,2,4-triazole-3-thione as the main skeleton, revealed the presence of 57 structures containing the triazole-thione moiety but only four structures containing the fluvastatin nucleus. These include 5-(3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl)-1-(X)penta-2,4-diene-1-one (Kalalbandi et al., 2015 ▸), where X = 4-nitrophenyl (NUHNAH), 2-hydroxyphenyl (NUHNEL), 4-methoxyphenyl (NUHNIP) and 4-chlorophenyl (NUHNOV). In the four compounds the 4-fluorophenyl ring of the fluvastatin nucleus is inclined to the indole ring by dihedral angles ranging from ca 46.66 to 68.59°, compared to 55.01 (12) and 55.21 (8)° for the title compound.

Synthesis and crystallization

The title compound was synthesized by refluxing a hot ethanolic solution (30 ml) of 3-substituted-4-amino-5-mercapto-1,2,4-triazole (0.01 mol) and a hot ethanolic solution (30 ml) of fluvastatin (0.01 mol) for 4–5 h with addition of a catalytic amount of concentrated hydrochloric acid. The product obtained after evaporation of the solvent was filtered and recrystallized from hot ethanol. Single crystals were obtained by slow evaporation of a solution in chloroform (yield 74%; m.p. 464 K). ¹H NMR (D6-DMSO): 10.4 (s, 1H, NH), 10.01 (s, 1H, CH=N), 7.1–7.7 (m, 8H, Ar–H), 7.3 (s, 1H, triazole-H), 6.47–6.55 (d, 2H, –CH=CH–), 6.47–6.56 (s, 6H, isopropyl group). IR (KBr, cm⁻¹): 3224, 3176 (N—H), 2754 (C—H), 1616 (C=N), 1600–1500 (C=C), 1105 (C=S). FAB–MS: m/z 405. Analysis: observed(calculated) C, 65.11 (65.18); H, 4.81 (4.93); N, 17.19 (17.28).

Refinement

Crystal data, data collection and structure refinement details are summarized in Table 2 ▸. C-bound H atoms were positioned geometrically [C—H = 0.95–0.97 Å] and refined using a riding model with U _iso(H) = 1.2 or 1.5U _eq(C). All N-bound H atoms were located from a difference Fourier map and freely refined [N—H = 0.90 (3)–0.91 (3) Å].

Table 2. Experimental details.

Crystal data
Chemical formula	C₂₂H₂₀FN₅S
M _r	405.49
Crystal system, space group	Triclinic, P
Temperature (K)	297
a, b, c (Å)	9.9283 (4), 11.5343 (5), 18.4694 (7)
α, β, γ (°)	99.8886 (13), 94.9582 (14), 98.4315 (14)
V (Å³)	2047.54 (14)
Z	4
Radiation type	Mo Kα
μ (mm⁻¹)	0.19
Crystal size (mm)	0.66 × 0.60 × 0.46

Data collection
Diffractometer	Bruker APEXII DUO CCD area detector
Absorption correction	Multi-scan (SADABS; Bruker, 2009 ▸)
T _min, T _max	0.730, 0.830
No. of measured, independent and observed [I > 2σ(I)] reflections	78666, 12002, 7987
R _int	0.048
(sin θ/λ)_max (Å⁻¹)	0.707

Refinement
R[F ² > 2σ(F ²)], wR(F ²), S	0.053, 0.135, 1.02
No. of reflections	12002
No. of parameters	535
H-atom treatment	H atoms treated by a mixture of independent and constrained refinement
Δρ_max, Δρ_min (e Å⁻³)	0.32, −0.35

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Computer programs: APEX2 and SAINT (Bruker, 2009 ▸), SHELXS97 (Sheldrick, 2008 ▸), SHELXL2013 (Sheldrick, 2015 ▸), Mercury (Macrae et al., 2008 ▸) and PLATON (Spek, 2009 ▸).

Supplementary Material

Crystal structure: contains datablock(s) I. DOI: 10.1107/S205698901502201X/su5237sup1.cif

e-71-01525-sup1.cif^{(2.5MB, cif)}

Structure factors: contains datablock(s) I. DOI: 10.1107/S205698901502201X/su5237Isup2.hkl

e-71-01525-Isup2.hkl^{(657KB, hkl)}

Click here for additional data file.^{(7.6KB, cml)}

Supporting information file. DOI: 10.1107/S205698901502201X/su5237Isup3.cml

CCDC reference: 1437565

Additional supporting information: crystallographic information; 3D view; checkCIF report

Acknowledgments

This research was supported by a PRGS Research Grant (No. RDU 130121).

supplementary crystallographic information

Crystal data

C₂₂H₂₀FN₅S	Z = 4
M_r = 405.49	F(000) = 848
Triclinic, P1	D_x = 1.315 Mg m⁻³
a = 9.9283 (4) Å	Mo Kα radiation, λ = 0.71073 Å
b = 11.5343 (5) Å	Cell parameters from 9367 reflections
c = 18.4694 (7) Å	θ = 2.3–27.8°
α = 99.8886 (13)°	µ = 0.19 mm⁻¹
β = 94.9582 (14)°	T = 297 K
γ = 98.4315 (14)°	Block, yellow
V = 2047.54 (14) Å³	0.66 × 0.60 × 0.46 mm

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Data collection

Bruker APEXII DUO CCD area-detector diffractometer	12002 independent reflections
Radiation source: fine-focus sealed tube	7987 reflections with I > 2σ(I)
Graphite monochromator	R_int = 0.048
φ and ω scans	θ_max = 30.2°, θ_min = 1.8°
Absorption correction: multi-scan (SADABS; Bruker, 2009)	h = −13→14
T_min = 0.730, T_max = 0.830	k = −16→16
78666 measured reflections	l = −26→26

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Refinement

Refinement on F²	0 restraints
Least-squares matrix: full	Hydrogen site location: mixed
R[F² > 2σ(F²)] = 0.053	H atoms treated by a mixture of independent and constrained refinement
wR(F²) = 0.135	w = 1/[σ²(F_o²) + (0.0463P)² + 1.0061P] where P = (F_o² + 2F_c²)/3
S = 1.02	(Δ/σ)_max = 0.001
12002 reflections	Δρ_max = 0.32 e Å⁻³
535 parameters	Δρ_min = −0.35 e Å⁻³

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Special details

Geometry. All e.s.d.'s (except the e.s.d. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell e.s.d.'s are taken into account individually in the estimation of e.s.d.'s in distances, angles and torsion angles; correlations between e.s.d.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell e.s.d.'s is used for estimating e.s.d.'s involving l.s. planes.

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Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å²)

	x	y	z	U_iso*/U_eq
S1A	0.08455 (7)	0.69136 (4)	0.16534 (3)	0.05868 (16)
F1A	−0.31446 (17)	0.78739 (11)	0.47019 (10)	0.0905 (5)
N1A	−0.10366 (15)	0.16736 (12)	0.33308 (8)	0.0362 (3)
N2A	0.09099 (16)	0.39301 (12)	0.11449 (8)	0.0380 (3)
N3A	0.12047 (15)	0.48279 (12)	0.07369 (8)	0.0365 (3)
N4A	0.18107 (18)	0.64187 (14)	0.03380 (9)	0.0465 (4)
H4AB	0.204 (2)	0.719 (2)	0.0296 (13)	0.073 (7)*
N5A	0.20935 (18)	0.55200 (14)	−0.01880 (9)	0.0480 (4)
C1A	−0.13898 (18)	0.14893 (14)	0.40148 (9)	0.0362 (4)
C2A	−0.1351 (2)	0.05110 (16)	0.43631 (10)	0.0456 (4)
H2AA	−0.1068	−0.0177	0.4130	0.055*
C3A	−0.1746 (2)	0.05986 (18)	0.50619 (11)	0.0523 (5)
H3AA	−0.1719	−0.0042	0.5304	0.063*
C4A	−0.2188 (2)	0.16190 (18)	0.54209 (11)	0.0514 (5)
H4AA	−0.2443	0.1647	0.5895	0.062*
C5A	−0.22476 (19)	0.25805 (16)	0.50808 (10)	0.0437 (4)
H5AA	−0.2552	0.3256	0.5317	0.052*
C6A	−0.18407 (17)	0.25233 (14)	0.43690 (9)	0.0347 (3)
C7A	−0.17501 (16)	0.33564 (14)	0.38866 (9)	0.0332 (3)
C8A	−0.12480 (17)	0.28220 (14)	0.32566 (9)	0.0327 (3)
C9A	−0.09289 (17)	0.34389 (14)	0.26649 (9)	0.0353 (3)
H9AA	−0.1367	0.4096	0.2654	0.042*
C10A	−0.01208 (18)	0.32505 (14)	0.21247 (9)	0.0370 (4)
H10A	0.0286	0.2569	0.2059	0.044*
C11A	0.01137 (18)	0.40985 (14)	0.16505 (9)	0.0362 (4)
H11A	−0.0310	0.4771	0.1708	0.043*
C12A	0.12757 (19)	0.60532 (15)	0.09206 (10)	0.0389 (4)
C13A	0.17236 (19)	0.45754 (16)	0.00762 (10)	0.0423 (4)
H13A	0.1800	0.3809	−0.0155	0.051*
C14A	−0.07844 (19)	0.07247 (14)	0.27346 (10)	0.0394 (4)
H14A	−0.0741	0.1071	0.2287	0.047*
C15A	0.0590 (2)	0.0347 (2)	0.28984 (13)	0.0601 (6)
H15A	0.0701	−0.0299	0.2517	0.090*
H15B	0.0631	0.0092	0.3367	0.090*
H15C	0.1309	0.1009	0.2916	0.090*
C16A	−0.1958 (2)	−0.03206 (18)	0.25663 (12)	0.0545 (5)
H16A	−0.1871	−0.0821	0.2106	0.082*
H16B	−0.2813	−0.0028	0.2531	0.082*
H16C	−0.1931	−0.0774	0.2956	0.082*
C17A	−0.21013 (17)	0.45672 (14)	0.40646 (9)	0.0349 (3)
C18A	−0.34346 (19)	0.47005 (16)	0.41822 (11)	0.0434 (4)
H18A	−0.4101	0.4025	0.4124	0.052*
C19A	−0.3798 (2)	0.58122 (18)	0.43839 (12)	0.0517 (5)
H19A	−0.4699	0.5893	0.4453	0.062*
C20A	−0.2803 (2)	0.67830 (17)	0.44782 (12)	0.0550 (5)
C21A	−0.1487 (2)	0.67053 (18)	0.43688 (15)	0.0667 (6)
H21A	−0.0829	0.7389	0.4434	0.080*
C22A	−0.1138 (2)	0.55868 (17)	0.41574 (13)	0.0550 (5)
H22A	−0.0238	0.5523	0.4077	0.066*
S1B	0.68905 (7)	0.83235 (5)	0.03129 (3)	0.06422 (17)
F1B	0.46558 (19)	0.78643 (12)	0.34049 (10)	0.0933 (5)
N1B	0.49537 (16)	1.38803 (13)	0.20432 (8)	0.0401 (3)
N2B	0.75225 (17)	1.11714 (12)	−0.00035 (8)	0.0452 (4)
N3B	0.81061 (17)	1.01944 (12)	−0.03051 (8)	0.0432 (4)
N4B	0.8607 (2)	0.85069 (15)	−0.07253 (10)	0.0563 (5)
H4BB	0.866 (3)	0.773 (2)	−0.0831 (14)	0.080 (8)*
N5B	0.9290 (2)	0.92793 (15)	−0.11091 (10)	0.0652 (5)
C1B	0.40567 (18)	1.41730 (15)	0.25539 (9)	0.0383 (4)
C2B	0.3447 (2)	1.51889 (16)	0.27086 (10)	0.0454 (4)
H2BA	0.3608	1.5806	0.2447	0.054*
C3B	0.2599 (2)	1.52490 (18)	0.32609 (11)	0.0500 (5)
H3BA	0.2178	1.5917	0.3370	0.060*
C4B	0.23559 (19)	1.43340 (18)	0.36616 (11)	0.0480 (5)
H4BA	0.1802	1.4413	0.4042	0.058*
C5B	0.29213 (18)	1.33217 (17)	0.35015 (10)	0.0424 (4)
H5BA	0.2738	1.2706	0.3763	0.051*
C6B	0.37813 (17)	1.32248 (15)	0.29381 (9)	0.0368 (4)
C7B	0.45102 (17)	1.23172 (15)	0.26345 (9)	0.0365 (4)
C8B	0.52169 (18)	1.27408 (15)	0.20931 (9)	0.0373 (4)
C9B	0.60246 (18)	1.20425 (15)	0.16399 (10)	0.0391 (4)
H9BA	0.6333	1.1443	0.1855	0.047*
C10B	0.6420 (2)	1.20839 (15)	0.09709 (10)	0.0420 (4)
H10B	0.6236	1.2692	0.0725	0.050*
C11B	0.71322 (19)	1.11722 (15)	0.06399 (10)	0.0408 (4)
H11B	0.7314	1.0574	0.0895	0.049*
C12B	0.7857 (2)	0.90104 (15)	−0.02282 (10)	0.0437 (4)
C13B	0.8952 (3)	1.02883 (18)	−0.08422 (12)	0.0575 (6)
H13B	0.9251	1.0998	−0.0998	0.069*
C14B	0.5777 (2)	1.47295 (16)	0.16779 (10)	0.0432 (4)
H14B	0.6475	1.4314	0.1454	0.052*
C15B	0.4908 (3)	1.5060 (2)	0.10514 (12)	0.0648 (6)
H15D	0.5475	1.5581	0.0805	0.097*
H15E	0.4198	1.5459	0.1248	0.097*
H15F	0.4503	1.4350	0.0705	0.097*
C16B	0.6536 (2)	1.58146 (18)	0.22234 (13)	0.0576 (5)
H16D	0.7206	1.6251	0.1983	0.086*
H16E	0.6987	1.5561	0.2636	0.086*
H16F	0.5896	1.6318	0.2396	0.086*
C17B	0.45015 (17)	1.11375 (15)	0.28393 (10)	0.0381 (4)
C18B	0.4860 (2)	1.10356 (16)	0.35652 (11)	0.0457 (4)
H18B	0.5065	1.1721	0.3929	0.055*
C19B	0.4921 (2)	0.99369 (19)	0.37605 (13)	0.0559 (5)
H19B	0.5177	0.9876	0.4247	0.067*
C20B	0.4592 (2)	0.89457 (17)	0.32175 (15)	0.0586 (6)
C21B	0.4200 (2)	0.89917 (18)	0.25037 (14)	0.0615 (6)
H21B	0.3967	0.8296	0.2149	0.074*
C22B	0.4154 (2)	1.00955 (17)	0.23120 (12)	0.0504 (5)
H22B	0.3887	1.0140	0.1824	0.060*

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Atomic displacement parameters (Å²)

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
S1A	0.0947 (4)	0.0325 (2)	0.0520 (3)	0.0121 (2)	0.0265 (3)	0.0061 (2)
F1A	0.0981 (11)	0.0402 (7)	0.1313 (14)	0.0313 (7)	0.0106 (10)	−0.0051 (8)
N1A	0.0483 (8)	0.0295 (7)	0.0346 (7)	0.0111 (6)	0.0152 (6)	0.0072 (5)
N2A	0.0550 (9)	0.0260 (6)	0.0376 (7)	0.0088 (6)	0.0146 (7)	0.0121 (6)
N3A	0.0479 (8)	0.0286 (7)	0.0376 (7)	0.0096 (6)	0.0131 (6)	0.0114 (6)
N4A	0.0640 (10)	0.0333 (8)	0.0484 (9)	0.0096 (7)	0.0189 (8)	0.0175 (7)
N5A	0.0635 (10)	0.0417 (8)	0.0469 (9)	0.0156 (7)	0.0223 (8)	0.0166 (7)
C1A	0.0429 (9)	0.0326 (8)	0.0347 (8)	0.0064 (7)	0.0105 (7)	0.0074 (6)
C2A	0.0606 (12)	0.0351 (9)	0.0444 (10)	0.0101 (8)	0.0125 (9)	0.0112 (7)
C3A	0.0697 (13)	0.0430 (10)	0.0476 (11)	0.0036 (9)	0.0131 (10)	0.0193 (9)
C4A	0.0645 (13)	0.0532 (11)	0.0378 (10)	0.0021 (10)	0.0180 (9)	0.0124 (8)
C5A	0.0506 (11)	0.0411 (9)	0.0385 (9)	0.0034 (8)	0.0164 (8)	0.0028 (7)
C6A	0.0374 (8)	0.0314 (8)	0.0348 (8)	0.0031 (6)	0.0095 (7)	0.0042 (6)
C7A	0.0347 (8)	0.0297 (7)	0.0358 (8)	0.0052 (6)	0.0096 (7)	0.0048 (6)
C8A	0.0368 (8)	0.0282 (7)	0.0348 (8)	0.0066 (6)	0.0088 (7)	0.0071 (6)
C9A	0.0427 (9)	0.0286 (7)	0.0371 (9)	0.0088 (7)	0.0087 (7)	0.0082 (6)
C10A	0.0492 (10)	0.0281 (8)	0.0371 (9)	0.0092 (7)	0.0111 (7)	0.0094 (6)
C11A	0.0440 (9)	0.0293 (8)	0.0379 (9)	0.0084 (7)	0.0091 (7)	0.0092 (6)
C12A	0.0477 (10)	0.0298 (8)	0.0430 (9)	0.0088 (7)	0.0094 (8)	0.0127 (7)
C13A	0.0536 (11)	0.0370 (9)	0.0423 (10)	0.0131 (8)	0.0180 (8)	0.0126 (7)
C14A	0.0531 (10)	0.0301 (8)	0.0365 (9)	0.0092 (7)	0.0146 (8)	0.0038 (7)
C15A	0.0558 (12)	0.0563 (12)	0.0698 (14)	0.0210 (10)	0.0184 (11)	0.0006 (10)
C16A	0.0670 (13)	0.0414 (10)	0.0508 (11)	0.0011 (9)	0.0041 (10)	0.0046 (9)
C17A	0.0406 (9)	0.0300 (8)	0.0343 (8)	0.0070 (7)	0.0084 (7)	0.0041 (6)
C18A	0.0397 (9)	0.0354 (9)	0.0527 (11)	0.0045 (7)	0.0058 (8)	0.0024 (8)
C19A	0.0455 (11)	0.0490 (11)	0.0618 (13)	0.0183 (9)	0.0090 (9)	0.0032 (9)
C20A	0.0655 (13)	0.0330 (9)	0.0664 (13)	0.0190 (9)	0.0055 (11)	0.0010 (9)
C21A	0.0585 (13)	0.0295 (9)	0.107 (2)	0.0000 (9)	0.0110 (13)	0.0033 (11)
C22A	0.0391 (10)	0.0373 (10)	0.0883 (16)	0.0051 (8)	0.0153 (10)	0.0083 (10)
S1B	0.0919 (4)	0.0371 (3)	0.0697 (4)	0.0092 (3)	0.0418 (3)	0.0115 (2)
F1B	0.1249 (13)	0.0413 (7)	0.1258 (14)	0.0180 (8)	0.0379 (11)	0.0337 (8)
N1B	0.0509 (9)	0.0360 (7)	0.0381 (8)	0.0176 (6)	0.0147 (7)	0.0067 (6)
N2B	0.0683 (10)	0.0299 (7)	0.0451 (8)	0.0209 (7)	0.0244 (8)	0.0081 (6)
N3B	0.0665 (10)	0.0301 (7)	0.0410 (8)	0.0192 (7)	0.0242 (7)	0.0100 (6)
N4B	0.0911 (14)	0.0338 (8)	0.0544 (10)	0.0246 (9)	0.0361 (9)	0.0113 (7)
N5B	0.1056 (15)	0.0434 (9)	0.0627 (11)	0.0304 (10)	0.0506 (11)	0.0185 (8)
C1B	0.0421 (9)	0.0383 (9)	0.0343 (8)	0.0118 (7)	0.0076 (7)	0.0003 (7)
C2B	0.0550 (11)	0.0393 (9)	0.0434 (10)	0.0172 (8)	0.0089 (8)	0.0027 (8)
C3B	0.0521 (11)	0.0485 (11)	0.0484 (11)	0.0216 (9)	0.0076 (9)	−0.0057 (9)
C4B	0.0422 (10)	0.0556 (11)	0.0439 (10)	0.0119 (8)	0.0127 (8)	−0.0043 (9)
C5B	0.0403 (9)	0.0449 (10)	0.0403 (9)	0.0066 (8)	0.0089 (7)	0.0012 (8)
C6B	0.0365 (9)	0.0371 (8)	0.0348 (8)	0.0073 (7)	0.0051 (7)	−0.0004 (7)
C7B	0.0396 (9)	0.0344 (8)	0.0350 (8)	0.0086 (7)	0.0070 (7)	0.0017 (7)
C8B	0.0432 (9)	0.0342 (8)	0.0370 (9)	0.0133 (7)	0.0101 (7)	0.0049 (7)
C9B	0.0471 (10)	0.0335 (8)	0.0397 (9)	0.0144 (7)	0.0114 (8)	0.0050 (7)
C10B	0.0567 (11)	0.0332 (8)	0.0405 (9)	0.0178 (8)	0.0150 (8)	0.0059 (7)
C11B	0.0548 (11)	0.0313 (8)	0.0401 (9)	0.0142 (7)	0.0143 (8)	0.0073 (7)
C12B	0.0632 (12)	0.0309 (8)	0.0409 (9)	0.0150 (8)	0.0161 (8)	0.0062 (7)
C13B	0.0915 (16)	0.0388 (10)	0.0548 (12)	0.0238 (10)	0.0413 (11)	0.0166 (9)
C14B	0.0551 (11)	0.0391 (9)	0.0408 (9)	0.0166 (8)	0.0158 (8)	0.0096 (7)
C15B	0.0834 (16)	0.0719 (15)	0.0486 (12)	0.0267 (13)	0.0121 (11)	0.0237 (11)
C16B	0.0616 (13)	0.0447 (11)	0.0674 (14)	0.0100 (9)	0.0150 (11)	0.0081 (10)
C17B	0.0349 (8)	0.0329 (8)	0.0461 (10)	0.0047 (7)	0.0108 (7)	0.0037 (7)
C18B	0.0521 (11)	0.0359 (9)	0.0477 (10)	0.0006 (8)	0.0119 (8)	0.0062 (8)
C19B	0.0648 (13)	0.0498 (11)	0.0580 (12)	0.0071 (10)	0.0150 (10)	0.0215 (10)
C20B	0.0613 (13)	0.0345 (10)	0.0853 (17)	0.0063 (9)	0.0265 (12)	0.0185 (10)
C21B	0.0618 (13)	0.0336 (10)	0.0814 (17)	−0.0006 (9)	0.0130 (12)	−0.0057 (10)
C22B	0.0521 (11)	0.0423 (10)	0.0519 (11)	0.0050 (8)	0.0039 (9)	−0.0015 (8)

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Geometric parameters (Å, º)

S1A—C12A	1.6621 (18)	S1B—C12B	1.6618 (19)
F1A—C20A	1.356 (2)	F1B—C20B	1.359 (2)
N1A—C1A	1.382 (2)	N1B—C1B	1.386 (2)
N1A—C8A	1.399 (2)	N1B—C8B	1.394 (2)
N1A—C14A	1.479 (2)	N1B—C14B	1.473 (2)
N2A—C11A	1.283 (2)	N2B—C11B	1.281 (2)
N2A—N3A	1.3940 (18)	N2B—N3B	1.3955 (18)
N3A—C13A	1.368 (2)	N3B—C13B	1.362 (2)
N3A—C12A	1.385 (2)	N3B—C12B	1.386 (2)
N4A—C12A	1.344 (2)	N4B—C12B	1.341 (2)
N4A—N5A	1.372 (2)	N4B—N5B	1.371 (2)
N4A—H4AB	0.91 (3)	N4B—H4BB	0.90 (3)
N5A—C13A	1.287 (2)	N5B—C13B	1.287 (2)
C1A—C2A	1.395 (2)	C1B—C2B	1.394 (2)
C1A—C6A	1.411 (2)	C1B—C6B	1.409 (2)
C2A—C3A	1.373 (3)	C2B—C3B	1.377 (3)
C2A—H2AA	0.9300	C2B—H2BA	0.9300
C3A—C4A	1.396 (3)	C3B—C4B	1.394 (3)
C3A—H3AA	0.9300	C3B—H3BA	0.9300
C4A—C5A	1.371 (3)	C4B—C5B	1.367 (3)
C4A—H4AA	0.9300	C4B—H4BA	0.9300
C5A—C6A	1.402 (2)	C5B—C6B	1.402 (2)
C5A—H5AA	0.9300	C5B—H5BA	0.9300
C6A—C7A	1.417 (2)	C6B—C7B	1.423 (2)
C7A—C8A	1.388 (2)	C7B—C8B	1.385 (2)
C7A—C17A	1.478 (2)	C7B—C17B	1.473 (2)
C8A—C9A	1.436 (2)	C8B—C9B	1.437 (2)
C9A—C10A	1.342 (2)	C9B—C10B	1.335 (2)
C9A—H9AA	0.9300	C9B—H9BA	0.9300
C10A—C11A	1.429 (2)	C10B—C11B	1.432 (2)
C10A—H10A	0.9300	C10B—H10B	0.9300
C11A—H11A	0.9300	C11B—H11B	0.9300
C13A—H13A	0.9300	C13B—H13B	0.9300
C14A—C15A	1.514 (3)	C14B—C15B	1.518 (3)
C14A—C16A	1.518 (3)	C14B—C16B	1.520 (3)
C14A—H14A	0.9800	C14B—H14B	0.9800
C15A—H15A	0.9600	C15B—H15D	0.9600
C15A—H15B	0.9600	C15B—H15E	0.9600
C15A—H15C	0.9600	C15B—H15F	0.9600
C16A—H16A	0.9600	C16B—H16D	0.9600
C16A—H16B	0.9600	C16B—H16E	0.9600
C16A—H16C	0.9600	C16B—H16F	0.9600
C17A—C22A	1.379 (2)	C17B—C18B	1.386 (3)
C17A—C18A	1.386 (2)	C17B—C22B	1.389 (2)
C18A—C19A	1.381 (2)	C18B—C19B	1.384 (3)
C18A—H18A	0.9300	C18B—H18B	0.9300
C19A—C20A	1.356 (3)	C19B—C20B	1.364 (3)
C19A—H19A	0.9300	C19B—H19B	0.9300
C20A—C21A	1.353 (3)	C20B—C21B	1.354 (3)
C21A—C22A	1.385 (3)	C21B—C22B	1.385 (3)
C21A—H21A	0.9300	C21B—H21B	0.9300
C22A—H22A	0.9300	C22B—H22B	0.9300

C1A—N1A—C8A	107.86 (13)	C1B—N1B—C8B	107.49 (14)
C1A—N1A—C14A	124.51 (13)	C1B—N1B—C14B	125.46 (14)
C8A—N1A—C14A	126.36 (13)	C8B—N1B—C14B	124.92 (14)
C11A—N2A—N3A	117.96 (13)	C11B—N2B—N3B	116.57 (14)
C13A—N3A—C12A	108.07 (14)	C13B—N3B—C12B	108.25 (14)
C13A—N3A—N2A	119.78 (13)	C13B—N3B—N2B	120.17 (14)
C12A—N3A—N2A	131.35 (14)	C12B—N3B—N2B	131.03 (15)
C12A—N4A—N5A	114.68 (15)	C12B—N4B—N5B	114.71 (15)
C12A—N4A—H4AB	124.6 (16)	C12B—N4B—H4BB	125.5 (17)
N5A—N4A—H4AB	120.5 (16)	N5B—N4B—H4BB	119.8 (17)
C13A—N5A—N4A	103.21 (14)	C13B—N5B—N4B	103.27 (15)
N1A—C1A—C2A	131.02 (15)	N1B—C1B—C2B	130.38 (17)
N1A—C1A—C6A	108.27 (14)	N1B—C1B—C6B	108.73 (14)
C2A—C1A—C6A	120.71 (15)	C2B—C1B—C6B	120.88 (16)
C3A—C2A—C1A	117.77 (17)	C3B—C2B—C1B	117.91 (18)
C3A—C2A—H2AA	121.1	C3B—C2B—H2BA	121.0
C1A—C2A—H2AA	121.1	C1B—C2B—H2BA	121.0
C2A—C3A—C4A	122.14 (18)	C2B—C3B—C4B	121.70 (17)
C2A—C3A—H3AA	118.9	C2B—C3B—H3BA	119.1
C4A—C3A—H3AA	118.9	C4B—C3B—H3BA	119.1
C5A—C4A—C3A	120.66 (17)	C5B—C4B—C3B	120.80 (17)
C5A—C4A—H4AA	119.7	C5B—C4B—H4BA	119.6
C3A—C4A—H4AA	119.7	C3B—C4B—H4BA	119.6
C4A—C5A—C6A	118.62 (17)	C4B—C5B—C6B	119.06 (18)
C4A—C5A—H5AA	120.7	C4B—C5B—H5BA	120.5
C6A—C5A—H5AA	120.7	C6B—C5B—H5BA	120.5
C5A—C6A—C1A	120.09 (15)	C5B—C6B—C1B	119.59 (15)
C5A—C6A—C7A	132.27 (15)	C5B—C6B—C7B	133.36 (17)
C1A—C6A—C7A	107.63 (14)	C1B—C6B—C7B	107.05 (14)
C8A—C7A—C6A	106.91 (14)	C8B—C7B—C6B	107.00 (15)
C8A—C7A—C17A	128.82 (14)	C8B—C7B—C17B	125.95 (15)
C6A—C7A—C17A	124.25 (14)	C6B—C7B—C17B	127.04 (15)
C7A—C8A—N1A	109.33 (13)	C7B—C8B—N1B	109.70 (14)
C7A—C8A—C9A	122.57 (14)	C7B—C8B—C9B	122.96 (15)
N1A—C8A—C9A	127.96 (14)	N1B—C8B—C9B	127.25 (15)
C10A—C9A—C8A	132.44 (15)	C10B—C9B—C8B	132.70 (16)
C10A—C9A—H9AA	113.8	C10B—C9B—H9BA	113.7
C8A—C9A—H9AA	113.8	C8B—C9B—H9BA	113.7
C9A—C10A—C11A	119.92 (15)	C9B—C10B—C11B	118.64 (16)
C9A—C10A—H10A	120.0	C9B—C10B—H10B	120.7
C11A—C10A—H10A	120.0	C11B—C10B—H10B	120.7
N2A—C11A—C10A	119.84 (15)	N2B—C11B—C10B	120.80 (16)
N2A—C11A—H11A	120.1	N2B—C11B—H11B	119.6
C10A—C11A—H11A	120.1	C10B—C11B—H11B	119.6
N4A—C12A—N3A	101.82 (14)	N4B—C12B—N3B	101.69 (15)
N4A—C12A—S1A	126.62 (13)	N4B—C12B—S1B	126.76 (14)
N3A—C12A—S1A	131.56 (13)	N3B—C12B—S1B	131.55 (13)
N5A—C13A—N3A	112.20 (16)	N5B—C13B—N3B	112.06 (17)
N5A—C13A—H13A	123.9	N5B—C13B—H13B	124.0
N3A—C13A—H13A	123.9	N3B—C13B—H13B	124.0
N1A—C14A—C15A	111.43 (16)	N1B—C14B—C15B	110.91 (17)
N1A—C14A—C16A	111.89 (15)	N1B—C14B—C16B	112.39 (15)
C15A—C14A—C16A	112.67 (16)	C15B—C14B—C16B	112.68 (17)
N1A—C14A—H14A	106.8	N1B—C14B—H14B	106.8
C15A—C14A—H14A	106.8	C15B—C14B—H14B	106.8
C16A—C14A—H14A	106.8	C16B—C14B—H14B	106.8
C14A—C15A—H15A	109.5	C14B—C15B—H15D	109.5
C14A—C15A—H15B	109.5	C14B—C15B—H15E	109.5
H15A—C15A—H15B	109.5	H15D—C15B—H15E	109.5
C14A—C15A—H15C	109.5	C14B—C15B—H15F	109.5
H15A—C15A—H15C	109.5	H15D—C15B—H15F	109.5
H15B—C15A—H15C	109.5	H15E—C15B—H15F	109.5
C14A—C16A—H16A	109.5	C14B—C16B—H16D	109.5
C14A—C16A—H16B	109.5	C14B—C16B—H16E	109.5
H16A—C16A—H16B	109.5	H16D—C16B—H16E	109.5
C14A—C16A—H16C	109.5	C14B—C16B—H16F	109.5
H16A—C16A—H16C	109.5	H16D—C16B—H16F	109.5
H16B—C16A—H16C	109.5	H16E—C16B—H16F	109.5
C22A—C17A—C18A	117.71 (16)	C18B—C17B—C22B	117.97 (17)
C22A—C17A—C7A	122.67 (15)	C18B—C17B—C7B	120.80 (15)
C18A—C17A—C7A	119.54 (15)	C22B—C17B—C7B	121.23 (17)
C19A—C18A—C17A	121.63 (17)	C19B—C18B—C17B	121.48 (18)
C19A—C18A—H18A	119.2	C19B—C18B—H18B	119.3
C17A—C18A—H18A	119.2	C17B—C18B—H18B	119.3
C20A—C19A—C18A	118.09 (18)	C20B—C19B—C18B	118.0 (2)
C20A—C19A—H19A	121.0	C20B—C19B—H19B	121.0
C18A—C19A—H19A	121.0	C18B—C19B—H19B	121.0
C21A—C20A—C19A	122.76 (18)	C21B—C20B—F1B	118.8 (2)
C21A—C20A—F1A	118.94 (19)	C21B—C20B—C19B	122.98 (19)
C19A—C20A—F1A	118.30 (19)	F1B—C20B—C19B	118.3 (2)
C20A—C21A—C22A	118.65 (19)	C20B—C21B—C22B	118.66 (19)
C20A—C21A—H21A	120.7	C20B—C21B—H21B	120.7
C22A—C21A—H21A	120.7	C22B—C21B—H21B	120.7
C17A—C22A—C21A	121.14 (18)	C21B—C22B—C17B	120.9 (2)
C17A—C22A—H22A	119.4	C21B—C22B—H22B	119.6
C21A—C22A—H22A	119.4	C17B—C22B—H22B	119.6

C11A—N2A—N3A—C13A	−162.30 (17)	C11B—N2B—N3B—C13B	−157.5 (2)
C11A—N2A—N3A—C12A	29.3 (3)	C11B—N2B—N3B—C12B	32.0 (3)
C12A—N4A—N5A—C13A	0.0 (2)	C12B—N4B—N5B—C13B	0.0 (3)
C8A—N1A—C1A—C2A	−178.94 (19)	C8B—N1B—C1B—C2B	−177.88 (19)
C14A—N1A—C1A—C2A	13.3 (3)	C14B—N1B—C1B—C2B	18.1 (3)
C8A—N1A—C1A—C6A	0.66 (19)	C8B—N1B—C1B—C6B	1.4 (2)
C14A—N1A—C1A—C6A	−167.09 (15)	C14B—N1B—C1B—C6B	−162.60 (16)
N1A—C1A—C2A—C3A	178.64 (19)	N1B—C1B—C2B—C3B	−179.10 (19)
C6A—C1A—C2A—C3A	−0.9 (3)	C6B—C1B—C2B—C3B	1.7 (3)
C1A—C2A—C3A—C4A	0.6 (3)	C1B—C2B—C3B—C4B	0.5 (3)
C2A—C3A—C4A—C5A	0.3 (3)	C2B—C3B—C4B—C5B	−2.1 (3)
C3A—C4A—C5A—C6A	−0.8 (3)	C3B—C4B—C5B—C6B	1.5 (3)
C4A—C5A—C6A—C1A	0.4 (3)	C4B—C5B—C6B—C1B	0.6 (3)
C4A—C5A—C6A—C7A	−178.17 (19)	C4B—C5B—C6B—C7B	−179.50 (19)
N1A—C1A—C6A—C5A	−179.20 (16)	N1B—C1B—C6B—C5B	178.37 (16)
C2A—C1A—C6A—C5A	0.4 (3)	C2B—C1B—C6B—C5B	−2.3 (3)
N1A—C1A—C6A—C7A	−0.31 (19)	N1B—C1B—C6B—C7B	−1.53 (19)
C2A—C1A—C6A—C7A	179.35 (17)	C2B—C1B—C6B—C7B	177.81 (17)
C5A—C6A—C7A—C8A	178.54 (19)	C5B—C6B—C7B—C8B	−178.80 (19)
C1A—C6A—C7A—C8A	−0.17 (19)	C1B—C6B—C7B—C8B	1.08 (19)
C5A—C6A—C7A—C17A	0.2 (3)	C5B—C6B—C7B—C17B	2.4 (3)
C1A—C6A—C7A—C17A	−178.53 (15)	C1B—C6B—C7B—C17B	−177.68 (17)
C6A—C7A—C8A—N1A	0.59 (19)	C6B—C7B—C8B—N1B	−0.3 (2)
C17A—C7A—C8A—N1A	178.84 (16)	C17B—C7B—C8B—N1B	178.53 (16)
C6A—C7A—C8A—C9A	−175.47 (16)	C6B—C7B—C8B—C9B	−177.13 (16)
C17A—C7A—C8A—C9A	2.8 (3)	C17B—C7B—C8B—C9B	1.7 (3)
C1A—N1A—C8A—C7A	−0.78 (19)	C1B—N1B—C8B—C7B	−0.7 (2)
C14A—N1A—C8A—C7A	166.68 (16)	C14B—N1B—C8B—C7B	163.39 (16)
C1A—N1A—C8A—C9A	175.00 (17)	C1B—N1B—C8B—C9B	176.01 (17)
C14A—N1A—C8A—C9A	−17.5 (3)	C14B—N1B—C8B—C9B	−19.9 (3)
C7A—C8A—C9A—C10A	158.93 (19)	C7B—C8B—C9B—C10B	155.7 (2)
N1A—C8A—C9A—C10A	−16.4 (3)	N1B—C8B—C9B—C10B	−20.6 (3)
C8A—C9A—C10A—C11A	−173.41 (18)	C8B—C9B—C10B—C11B	−174.33 (19)
N3A—N2A—C11A—C10A	−174.54 (15)	N3B—N2B—C11B—C10B	−174.83 (17)
C9A—C10A—C11A—N2A	178.49 (17)	C9B—C10B—C11B—N2B	179.52 (19)
N5A—N4A—C12A—N3A	−0.8 (2)	N5B—N4B—C12B—N3B	−0.6 (2)
N5A—N4A—C12A—S1A	178.96 (15)	N5B—N4B—C12B—S1B	178.81 (17)
C13A—N3A—C12A—N4A	1.21 (19)	C13B—N3B—C12B—N4B	1.0 (2)
N2A—N3A—C12A—N4A	170.61 (17)	N2B—N3B—C12B—N4B	172.32 (19)
C13A—N3A—C12A—S1A	−178.51 (16)	C13B—N3B—C12B—S1B	−178.40 (19)
N2A—N3A—C12A—S1A	−9.1 (3)	N2B—N3B—C12B—S1B	−7.1 (3)
N4A—N5A—C13A—N3A	0.8 (2)	N4B—N5B—C13B—N3B	0.7 (3)
C12A—N3A—C13A—N5A	−1.4 (2)	C12B—N3B—C13B—N5B	−1.1 (3)
N2A—N3A—C13A—N5A	−172.20 (16)	N2B—N3B—C13B—N5B	−173.56 (19)
C1A—N1A—C14A—C15A	−75.0 (2)	C1B—N1B—C14B—C15B	−78.5 (2)
C8A—N1A—C14A—C15A	119.51 (19)	C8B—N1B—C14B—C15B	120.25 (19)
C1A—N1A—C14A—C16A	52.1 (2)	C1B—N1B—C14B—C16B	48.7 (2)
C8A—N1A—C14A—C16A	−113.34 (19)	C8B—N1B—C14B—C16B	−112.61 (19)
C8A—C7A—C17A—C22A	−64.4 (3)	C8B—C7B—C17B—C18B	125.1 (2)
C6A—C7A—C17A—C22A	113.6 (2)	C6B—C7B—C17B—C18B	−56.4 (3)
C8A—C7A—C17A—C18A	119.0 (2)	C8B—C7B—C17B—C22B	−54.0 (3)
C6A—C7A—C17A—C18A	−63.0 (2)	C6B—C7B—C17B—C22B	124.5 (2)
C22A—C17A—C18A—C19A	0.2 (3)	C22B—C17B—C18B—C19B	2.2 (3)
C7A—C17A—C18A—C19A	176.91 (17)	C7B—C17B—C18B—C19B	−176.87 (18)
C17A—C18A—C19A—C20A	−1.1 (3)	C17B—C18B—C19B—C20B	−1.1 (3)
C18A—C19A—C20A—C21A	1.4 (4)	C18B—C19B—C20B—C21B	−0.7 (3)
C18A—C19A—C20A—F1A	−177.68 (19)	C18B—C19B—C20B—F1B	179.67 (19)
C19A—C20A—C21A—C22A	−0.5 (4)	F1B—C20B—C21B—C22B	−179.12 (19)
F1A—C20A—C21A—C22A	178.5 (2)	C19B—C20B—C21B—C22B	1.2 (3)
C18A—C17A—C22A—C21A	0.7 (3)	C20B—C21B—C22B—C17B	0.0 (3)
C7A—C17A—C22A—C21A	−176.0 (2)	C18B—C17B—C22B—C21B	−1.6 (3)
C20A—C21A—C22A—C17A	−0.5 (4)	C7B—C17B—C22B—C21B	177.44 (18)

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Hydrogen-bond geometry (Å, º)

Cg1 is the centroid of ring N3A–N5A/C12A/C13A, Cg2 is the centroid of ring C17B–C22B, and Cg3 is the centroid of ring C1A–C6A.

D—H···A	D—H	H···A	D···A	D—H···A
N4A—H4AB···N2Bⁱ	0.90 (2)	2.05 (2)	2.944 (2)	170 (2)
N4B—H4BB···N2Aⁱⁱ	0.89 (2)	2.02 (2)	2.906 (2)	170 (3)
C15B—H15E···Cg1ⁱⁱⁱ	0.96	2.91	3.521 (3)	123
C16A—H16B···Cg2^iv	0.96	2.87	3.716 (2)	148
C21A—H21A···Cg3^v	0.93	2.90	3.668 (2)	140

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Symmetry codes: (i) −x+1, −y+2, −z; (ii) −x+1, −y+1, −z; (iii) x, y+1, z; (iv) x−1, y−1, z; (v) −x, −y+1, −z+1.

References

Avaji, P. G., Reddy, B. N., Patil, S. A. & Badami, P. S. (2006). Transition Met. Chem. 31, 842–848.
Bruker (2009). APEX2, SAINT and SADABS. Bruker AXS Inc., Madison, Wisconsin, USA.
Cerchiaro, G. & Ferreira, A. M. da C. (2006). J. Braz. Chem. Soc. 17, 1473–1485.
Cornelissen, J. P., Van Diemen, J. H., Groeneveld, L. R., Haasnoot, J. G., Spek, A. L. & Reedijk, J. (1992). Inorg. Chem. 31, 198–202.
Daisley, R. W. & Shah, V. K. (1984). J. Pharm. Sci. 73, 407–408. [DOI] [PubMed]
Fun, H.-K., Jebas, S. R., Sujith, K. V., Patil, P. S., Kalluraya, B. & Dharmaprakash, S. M. (2008). Acta Cryst. E64, o1528–o1529. [DOI] [PMC free article] [PubMed]
Groom, C. R. & Allen, F. H. (2014). Angew. Chem. Int. Ed. 53, 662–671. [DOI] [PubMed]
Kalalbandi, V. K. A., Seetharamappa, J. & Katrahalli, U. (2015). RSC Adv. 5, 38748–38759.
Kulkarni, A. D., Patil, S. A. & Badami, P. S. (2009). J. Sulfur Chem. 30, 145–159.
Kulkarni, A. D., Patil, S. A., Naik, V. H. & Badami, P. S. (2011). Med. Chem. Res. 20, 346–354.
Kulkarni, A. D., Rahman, M. L., Mohd. Yusoff, M., Kwong, H. C. & Quah, C. K. (2015). Acta Cryst. E71, 1411–1413. [DOI] [PMC free article] [PubMed]
Macrae, C. F., Bruno, I. J., Chisholm, J. A., Edgington, P. R., McCabe, P., Pidcock, E., Rodriguez-Monge, L., Taylor, R., van de Streek, J. & Wood, P. A. (2008). J. Appl. Cryst. 41, 466–470.
Mishra, L. & Said, M. K. (1996). Indian J. Chem. Sect. A, 35, 304–307.
Ozarowski, A., Shunzhong, Y., McGarvey, B. R., Mislankar, A. & Drake, J. E. (1991). Inorg. Chem. 30, 3167–3174.
Pandeya, S. N., Sriram, D., Declecq, E., Pannecouque, C. & Mitvrouw, M. (1999a). Indian J. Pharm. Sci. 60, 207–212.
Pandeya, S. N., Sriram, D., Nath, G. & DeClercq, E. (1999b). Eur. J. Pharm. Sci. 9, 25–31. [DOI] [PubMed]
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. [DOI] [PubMed]
Sheldrick, G. M. (2015). Acta Cryst. C71, 3–8.
Spek, A. L. (2009). Acta Cryst. D65, 148–155. [DOI] [PMC free article] [PubMed]
Sridhar, S. K., Pandeya, S. N., Stables, J. P. & Ramesh, A. (2002). Eur. J. Pharm. Sci. 16, 129–132. [DOI] [PubMed]
Sun, S., Lou, H., Gao, Y., Fan, P., Ma, B., Ge, W. & Wang, X. J. (2004). J. Pharm. Biomed. Anal. 34, 1117–1124. [DOI] [PubMed]
Varma, R. C., Varma, K., Verma, R. K. & Bhattacharjee, N. C. J. (1992). Indian Chem. Soc. 69, 577–578.
Verreck, G., Six, K., Van den Mooter, G., Baert, L., Peeters, J. & Brewster, M. E. (2003). Int. J. Pharm. 251, 165–174. [DOI] [PubMed]
Yadawe, M. S. & Patil, S. A. (1997). Transition Met. Chem. 22, 220–224.

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Crystal structure: contains datablock(s) I. DOI: 10.1107/S205698901502201X/su5237sup1.cif

e-71-01525-sup1.cif^{(2.5MB, cif)}

Structure factors: contains datablock(s) I. DOI: 10.1107/S205698901502201X/su5237Isup2.hkl

e-71-01525-Isup2.hkl^{(657KB, hkl)}

Click here for additional data file.^{(7.6KB, cml)}

Supporting information file. DOI: 10.1107/S205698901502201X/su5237Isup3.cml

CCDC reference: 1437565

Additional supporting information: crystallographic information; 3D view; checkCIF report

[bb1] Avaji, P. G., Reddy, B. N., Patil, S. A. & Badami, P. S. (2006). Transition Met. Chem. 31, 842–848.

[bb2] Bruker (2009). APEX2, SAINT and SADABS. Bruker AXS Inc., Madison, Wisconsin, USA.

[bb3] Cerchiaro, G. & Ferreira, A. M. da C. (2006). J. Braz. Chem. Soc. 17, 1473–1485.

[bb4] Cornelissen, J. P., Van Diemen, J. H., Groeneveld, L. R., Haasnoot, J. G., Spek, A. L. & Reedijk, J. (1992). Inorg. Chem. 31, 198–202.

[bb5] Daisley, R. W. & Shah, V. K. (1984). J. Pharm. Sci. 73, 407–408. [DOI] [PubMed]

[bb6] Fun, H.-K., Jebas, S. R., Sujith, K. V., Patil, P. S., Kalluraya, B. & Dharmaprakash, S. M. (2008). Acta Cryst. E64, o1528–o1529. [DOI] [PMC free article] [PubMed]

[bb7] Groom, C. R. & Allen, F. H. (2014). Angew. Chem. Int. Ed. 53, 662–671. [DOI] [PubMed]

[bb8] Kalalbandi, V. K. A., Seetharamappa, J. & Katrahalli, U. (2015). RSC Adv. 5, 38748–38759.

[bb9] Kulkarni, A. D., Patil, S. A. & Badami, P. S. (2009). J. Sulfur Chem. 30, 145–159.

[bb10] Kulkarni, A. D., Patil, S. A., Naik, V. H. & Badami, P. S. (2011). Med. Chem. Res. 20, 346–354.

[bb11] Kulkarni, A. D., Rahman, M. L., Mohd. Yusoff, M., Kwong, H. C. & Quah, C. K. (2015). Acta Cryst. E71, 1411–1413. [DOI] [PMC free article] [PubMed]

[bb12] Macrae, C. F., Bruno, I. J., Chisholm, J. A., Edgington, P. R., McCabe, P., Pidcock, E., Rodriguez-Monge, L., Taylor, R., van de Streek, J. & Wood, P. A. (2008). J. Appl. Cryst. 41, 466–470.

[bb13] Mishra, L. & Said, M. K. (1996). Indian J. Chem. Sect. A, 35, 304–307.

[bb14] Ozarowski, A., Shunzhong, Y., McGarvey, B. R., Mislankar, A. & Drake, J. E. (1991). Inorg. Chem. 30, 3167–3174.

[bb15] Pandeya, S. N., Sriram, D., Declecq, E., Pannecouque, C. & Mitvrouw, M. (1999a). Indian J. Pharm. Sci. 60, 207–212.

[bb16] Pandeya, S. N., Sriram, D., Nath, G. & DeClercq, E. (1999b). Eur. J. Pharm. Sci. 9, 25–31. [DOI] [PubMed]

[bb17] Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. [DOI] [PubMed]

[bb18] Sheldrick, G. M. (2015). Acta Cryst. C71, 3–8.

[bb19] Spek, A. L. (2009). Acta Cryst. D65, 148–155. [DOI] [PMC free article] [PubMed]

[bb20] Sridhar, S. K., Pandeya, S. N., Stables, J. P. & Ramesh, A. (2002). Eur. J. Pharm. Sci. 16, 129–132. [DOI] [PubMed]

[bb21] Sun, S., Lou, H., Gao, Y., Fan, P., Ma, B., Ge, W. & Wang, X. J. (2004). J. Pharm. Biomed. Anal. 34, 1117–1124. [DOI] [PubMed]

[bb22] Varma, R. C., Varma, K., Verma, R. K. & Bhattacharjee, N. C. J. (1992). Indian Chem. Soc. 69, 577–578.

[bb23] Verreck, G., Six, K., Van den Mooter, G., Baert, L., Peeters, J. & Brewster, M. E. (2003). Int. J. Pharm. 251, 165–174. [DOI] [PubMed]

[bb24] Yadawe, M. S. & Patil, S. A. (1997). Transition Met. Chem. 22, 220–224.

PERMALINK

Crystal structure of 4-({(1E,2E)-3-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]allylidene}amino)-1H-1,2,4-triazole-5(4H)-thione

Ajaykumar D Kulkarni

Md Lutfor Rahman

Mashitah Mohd Yusoff

Huey Chong Kwong

Ching Kheng Quah

Abstract

Chemical context

Structural commentary

Figure 1.