Crystal structure and Hirshfeld surface analysis of (2E,2'E)-1,1'-[seleno-bis-(4,1-phenyl-ene)]bis-[3-(4-chloro-phen-yl)prop-2-en-1-one].
Journal: 2019/November - Acta Crystallographica Section E: Crystallographic Communications
ISSN: 2056-9890
Abstract:
In the title com-pound, C30H20Cl2O2Se, the C-Se-C angle is 99.0 (2)°, with the dihedral angle between the planes of the attached benzene rings being 79.1 (3)°. The average endocyclic angles (Se-C-C) facing the Se atom are 122.1 (5) and 122.2 (5)°. The Se atom is essentially coplanar with the attached benzene rings, deviating by 0.075 (1) and 0.091 (1) Å. In the two phenyl-ene(4-chloro-phen-yl)prop-2-en-1-one units, the benzene rings are inclined to each other by 44.6 (3) and 7.8 (3)°. In the crystal, the mol-ecules stack up the a axis, forming layers parallel to the ac plane. There are no significant classical inter-molecular inter-actions present. Hirshfeld surface analysis, two-dimensional fingerprint plots and the mol-ecular electrostatic potential surface were used to analyse the crystal packing. The Hirshfeld surface analysis suggests that the most significant contributions to the crystal packing are by C⋯H/H⋯C contacts (17.7%).
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Acta Crystallogr E Crystallogr Commun 75(Pt 11): 1724-1728

Crystal structure and Hirshfeld surface analysis of (2<em>E</em>,2′<em>E</em>)-1,1′-[seleno­bis­(4,1-phenyl­ene)]bis­[3-(4-chloro­phen­yl)prop-2-en-1-one]

Chemical context

During the last few years, organoselenium chemistry (Procter, 2001) has been the subject of constant scientific inter­est and organoselenium com­pounds have been used intensively as important reagents and inter­mediates in organic synthesis (Zade et al., 2005). Recently, various organoselenium com­pounds have attracted growing attention in medicine. Seleno­proteins are very important for neuronal survival and function. It has been found that seleno­protein P may influence Alzheimer pathology (Bellinger et al., 2008). Furthermore, the potential of seleno­proteins to protect against oxidative stress led to the expectation that selenium would be protective against type 2 diabetes, and indeed in the 1990s, selenium was shown to have anti­diabetic and insulin mimetic effects (Steinbrenner et al., 2011). However, more recently, findings from observational epidemiological studies and randomized clinical trials have raised concern that high selenium exposure may lead to type 2 diabetes or insulin resistance at least in well-nourished populations (Stranges et al., 2010). In addition, mol­ecules involving selenium are still efficient and encouraged in medicinal chemistry (Zhao et al., 2012). Moreover, organoselenium com­pounds are of considerable inter­est in academia, as anti­cancer (Zhu &amp; Jiang, 2008), anti-oxidant (Anderson et al., 1996), anti-inflammatory and anti­allergic agents (Abdel-Hafez, 2008), and in industry because of their involvement as key inter­mediates in the synthesis of pharmaceuticals (Woods et al., 1993), fine chemicals and polymers (Hellberg et al., 1997). Moreover, chalcone derivatives are notable for their excellent blue-light transmittance and good crystallizability; they also show considerable promise as organic nonlinear optical materials (Uchida et al., 1998). In continuation of our work on chalcone organoselenium derivatives, we report herein on the crystal structure of (2E,2′E)-1,1′-[seleno­bis­(4,1-phenyl­ene)]bis­[3-(4-chloro­phen­yl)prop-2-en-1-one].

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Structural commentary

The mol­ecular structure of the title com­pound is shown in Fig. 1. The C1—Se1—C16 angle is 99.0 (2)°, which is close to the value observed in three very similar com­pounds, viz. 99.47 (10)° in bis­(4-nitro­phen­yl) selenide, where the Se atom lies on a twofold rotation axis (Zuo, 2013), 99.59 (14)° in bis­(4-acetyl­phen­yl) selenide (Bouraoui et al., 2011) and 100.03 (15)° in bis­(2-chloro­ethan-1-one-phen­yl) selenide (Bouraoui et al., 2015).

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The mol­ecular structure of the title com­pound, with the atom labelling and displacement ellipsoids drawn at the 50% probability level.

In the title com­pound, inner benzene rings A (atoms C1–C6) and C (C16–C21) (see Scheme) are inclined to each other by 79.1 (3)°. This is similar to the same angle observed for the acetyl­phenyl derivative, viz. 87.08 (15)°, but considerably different to that observed for the 4-nitro­phenyl derivative, viz. 63.76 (10)°.

In each phenyl­ene-(4-chloro­phen­yl)prop-2-en-1-one unit, the C=C has an E configuration. The C=C bond lengths C8=C9 and C23=C24 are 1.317 (8) and 1.325 (8) Å, respectively, which confirms their double-bond character. Benzene rings A and B (C10–C15) of one unit are inclined to one another by 44.6 (3)°, while rings C and D (C25–C30) of the other unit are almost coplanar, with a dihedral angle of 7.8 (3)°. The outer benzene rings, B and D, are almost normal to one another, with a dihedral angle of 84.4 (3)°.

Supra­molecular features

In the crystal, mol­ecules stack up the a axis, forming layers parallel to the ac plane (Fig. 2). There are no significant classical inter­molecular inter­actions present (PLATON; Spek, 2009). The shortest atom–atom contacts in the crystal (Figs. 3 and 4) are given in Table 1 and are discussed in §4 (Hirshfeld surface analysis).

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A view along the b axis of the crystal packing of the title com­pound, showing the layer-like structure.

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A view of the Hirshfeld surface mapped over dnorm in the colour range −0.0711 to 1.3645 a.u.

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A view of the Hirshfeld surface plotted over the calculated electrostatic potential energy in the range −0.0489 to 0.0448 a.u.

Table 1

Short contacts (Å) in the crystal of the title com­pound
Atom 1Atom 2Length (Å)vdW length (Å)
H3H102.4980.098
O2H192.632−0.088
H12O22.7590.039
O1H32.7700.050
O2H202.8180.098
H2C62.9220.022
C3H42.9430.043
H3C152.9640.064
O2C293.217−0.003
O2C303.3140.094
C5C83.4610.061
Se1C173.475−0.125
C20C233.4800.080
Cl2Cl13.5490.049

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

Hirshfeld surface analysis

Insight into the inter­molecular inter­actions in the crystal were obtained from an analysis of the Hirshfeld surface (Spackman &amp; Jayatilaka, 2009) and the two-dimensional fingerprint plots (McKinnon et al., 2007). The program CrystalExplorer (Turner et al., 2017) was used to generate both the Hirshfeld surfaces, mapped over dnorm, and the electrostatic potential for the title com­pound. The function dnorm is a ratio enclosing the distances of any surface point to the nearest inter­ior (di) and exterior (de) atom and the van der Waals (vdW) radii of the atoms. The function dnorm will be equal to zero when inter­molecular distances are close to the van der Waals contacts. They are indicated by a white colour on the Hirshfeld surface, while contacts longer than the sum of the vdW radii with positive dnorm values are coloured blue.

The analysis of the Hirshfeld surface (HS) mapped over dnorm is shown in Fig. 4. The H⋯O contacts between the corresponding donor and acceptor atoms are visualized as bright-red spots on the side (zone 4) of the Hirshfeld surface (Fig. 4). Three other red spots exist, corresponding to the C⋯Se, Cl⋯Cl and C⋯O contacts, viz. zones 1, 2 and 3, respectively (Fig. 4). These contacts are considered to be the strongest when com­paring them to the sum of the vdW radii [Table 1; calculated using Mercury (Macrae et al., 2008)].

A view of the mol­ecular electrostatic potential using the 6-31G(d) basis set with the density functional theory (DFT) method for the title com­pound is shown in Fig. 5. The H⋯O donors and acceptors are shown as blue and red areas around the atoms related with positive (hydrogen-bond donors) and negative (hydrogen-bond acceptors) electrostatic potentials, respectively.

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Hirshfeld surface mapped over dnorm to visualize some of the short inter­molecular contacts in the crystal (see Table 1).

The full two-dimensional fingerprint plot for the title com­pound is given in Fig. 6(a). Those for the most significant contacts contributing to the HS are given in Fig. 6(b) for H⋯H, Fig. 6(c) for C⋯H/H⋯C, Fig. 6(d) for O⋯H/H⋯O, Fig. 6(e) for Cl⋯H/H⋯Cl and Fig. 6(f) for C⋯C. A full list of the relative percentage contributions of the close contacts to the HS of the title com­pound are given in Table 2.

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(a) The full two-dimensional fingerprint plot for the title com­pound and those delineated into (b) H⋯H, (c) C⋯H/H⋯C, (d) O⋯H/H⋯O, (e) Cl⋯H/H⋯Cl and (f) C⋯C contacts.

Table 2

Relative percentage contributions of the close contacts to the Hirshfeld surface of the title com­pound
ContactPercentage contribution
H⋯H36.0
C⋯H/H⋯C17.7
O⋯H/H⋯O11.5
Cl⋯H/H⋯Cl11.0
C⋯C10.5
C⋯Cl4.3
C⋯Se3.5
Se⋯H/H⋯Se2.8
Cl⋯Cl2.4
C⋯O0.3

A contribution of 36.0% was found for the H⋯H contacts (Fig. 6b), representing the largest contribution, and is displayed on the fingerprint plots by a pair of very short spikes at de + di = 2.3 Å; the vdW radius for this inter­action is 2.18 Å, which means it is a weak inter­action.

The C⋯H/H⋯C (17.7%, Fig. 6c) and Cl⋯H/H⋯Cl (Fig. 6e) contacts are seen as pairs of spikes at de + di = 2.9 and 2.9 Å, respectively.

The plot of O⋯H/H⋯O contacts between H atoms located inside the Hirshfeld surface and oxygen from outside and vice versa is shown in Fig. 6(d). These contacts account for 11.5% and are characterized by two symmetrical peaks with de + di = 2.5 Å; this reveals the presence of strong O⋯H contacts.

The C⋯C contacts (Fig. 6f) give a contribution of 10.5%, while the C⋯Cl, C⋯Se, Se⋯H/H⋯Se and Cl⋯Cl contacts in the structure give weak contributions of 4.3, 3.5, 2.8 and 2.4%, respectively, to the Hirshfeld surface.

Database survey

A search of the Cambridge Structural Database (CSD, Version 5.40, last update May 2019; Groom et al., 2016) for 4,4′-substituted bis­(phen­yl) selenides yielded six relevant hits. These are bis­(2-chloro­ethan-1-one-phen­yl) selenide (CSD refcode HUYRUC; Bouraoui et al., 2015), bis­(4-nitro­phen­yl) selenide (IDIOG; Zuo, 2013), bis­(4-meth­oxy­phen­yl) selenide (LAFNAK; Verma et al., 2016), bis­(4-acetyl­phen­yl) selenide (UPAGAU; Bouraoui et al., 2011), bis­(phen­yl) selenide itself (YEWYUX; Bhandary et al., 2018) and bis­(p-tol­yl) selenide (TOLYSE; Blackmore &amp; Abrahams, 1955). In IDIOG, the Se atom lies on a twofold rotation axis, and only YEWYUX and TOLYSE crystallize in chiral space groups, i.e. P21 and P212121, respectively.

In the title com­pound (Fig. 1), the C—Se—C angle is 99.0 (2)°, similar to the value observed in five of the com­pounds mentioned above, viz. 100.03 (15), 99.47 (10), 102.25 (19), 99.59 (14) and 98.31 (16)° for HUYRUQ, IDITOG, LAFNAK, UPAGAU and YEWYUX, respectively. In the sixth com­pound, TOLYSE, the dihedral angle is 105.65 (19)°. The two inner benzene rings, A and C, in the title com­pound are inclined to each other by 79.1 (3)°. This value is quite different to that observed in the five com­pounds mentioned above, i.e. 69.92 (17), 63.76 (10), 69.6 (2), 87.08 (15), 68.46 (18) and ca 56.99° for HUYRUQ, IDITOG, LAFNAK, UPAGAU, YEWYUX and TOLYSE, respectively.

Synthesis and crystallization

The title com­pound was prepared according to a method proposed by Mechehoud et al. (2010). 2-Chloro-1-(4-chloro­phen­yl)ethan-1-one (ClC8H6COCl; 36.5 mmol) and anhydrous aluminium chloride (5 g, 37.5 mmol, 3 equiv.) were taken up in dry methyl­ene chloride (100 ml). The reaction mixture was cooled to 273–278 K, protected from atmospheric moisture and stirred continuously for 15 min. A solution of diphenyl selenide (3 g, 1.87 mmol) in CH2Cl2 was added dropwise over a period of 5 min. The reaction mixture was allowed to reach room temperature gradually and then stirred at this temperature overnight. The solution was then washed with ice water–HCl (80 ml) and extracted with CH2Cl2. The organic layer was separated and dried (Na2SO4). Removal of the solvent under reduced pressure afforded the crude product, which was recrystallized from petroleum ether to yield 4.2 g of the title com­pound. Yellow single crystals suitable for X-ray diffraction analysis were obtained by recrystallization from CH2Cl2.

Refinement

Crystal data, data collection and structure refinement details are summarized in Table 3. The H atoms could all be located in a difference Fourier map. During refinement, they were included in calculated positions and refined as riding on the parent C atom, with C—H = 0.93 Å and Uiso(H) = 1.2Ueq(C).

Table 3

Experimental details
Crystal data
Chemical formulaC30H20Cl2O2Se
Mr562.32
Crystal system, space groupTriclinic, P1
Temperature (K)293
a, b, c (Å)4.9468 (3), 5.8712 (6), 21.3530 (18)
α, β, γ (°)85.019 (8), 84.094 (6), 86.465 (7)
V)613.68 (9)
Z1
Radiation typeMo Kα
μ (mm)1.77
Crystal size (mm)0.03 × 0.02 × 0.01
Data collection
DiffractometerAgilent Technologies Xcalibur Eos
No. of measured, independent and observed [I > 2σ(I)] reflections5341, 3672, 2465
Rint0.030
(sin θ/λ)max)0.661
Refinement
R[F > 2σ(F)], wR(F), S0.038, 0.074, 0.81
No. of reflections3672
No. of parameters317
No. of restraints3
H-atom treatmentH-atom parameters constrained
Δρmax, Δρmin (e Å)0.41, −0.32
Absolute structureRefined as an inversion twin
Absolute structure parameter0.002 (11)

Computer programs: CrysAlis PRO (Agilent, 2013), SHELXS97 (Sheldrick, 2008), Mercury (Macrae et al., 2008), SHELXL2018 (Sheldrick, 2015), PLATON (Spek, 2009) and publCIF (Westrip, 2010).

Laboratoire de Cristallographie, Département de Physique, Université des Frères Mentouri-Constantine, 25000 Constantine, Algeria,
Université de Ouargla, Faculté des Mathématiques et Sciences de la Matiére, Route de Ghardaia, Ouargla 30000, Algeria,
Laboratoire VAREN, Département de Chimie, Faculté des Sciences Exactes, Université Mentouri-Constantine, 25000 Constantine, Algeria,
Unité de Recherche de Chimie de l’Environnement et Moléculaire Structurale (CHEMS), Faculté des Sciences Exactes, Département de Chimie, Université des Frères Mentouri Constantine, Constantine 25000, Algeria,
Faculté de Technologie, Université Mohamed Boudiaf, M’sila, Algeria,
Laboratoire de Chimie Appliquée et Environnement, LCAE-URAC18, COSTE, Faculté des Sciences, Université Mohamed Premier, BP524, 60000, Oujda, Morocco,
Faculté Pluridisciplinaire Nador BP 300, Selouane 62702, Nador, Morocco,
Correspondence e-mail: rf.oohay@iuoitehcaliehuos, rf.oohay@rinazuot
Received 2019 Sep 9; Accepted 2019 Oct 15.
This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.

Abstract

In the title com­pound, C30H20Cl2O2Se, the C—Se—C angle is 99.0 (2)°, with the dihedral angle between the planes of the attached benzene rings being 79.1 (3)°. The average endocyclic angles (Se—C—C) facing the Se atom are 122.1 (5) and 122.2 (5)°. The Se atom is essentially coplanar with the attached benzene rings, deviating by 0.075 (1) and 0.091 (1) Å. In the two phenyl­ene(4-chloro­phen­yl)prop-2-en-1-one units, the benzene rings are inclined to each other by 44.6 (3) and 7.8 (3)°. In the crystal, the mol­ecules stack up the a axis, forming layers parallel to the ac plane. There are no significant classical inter­molecular inter­actions present. Hirshfeld surface analysis, two-dimensional fingerprint plots and the mol­ecular electrostatic potential surface were used to analyse the crystal packing. The Hirshfeld surface analysis suggests that the most significant contributions to the crystal packing are by C⋯H/H⋯C contacts (17.7%).

Keywords: crystal structure, organoselenium, selenium, Hirshfeld surface analysis
Abstract

Crystal structure: contains datablock(s) Global, I. DOI: 10.1107/S2056989019014038/su5517sup1.cif

Click here to view.(238K, cif)

CCDC references: 1959404, 1959404

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

Acknowledgments

This work was supported by the Laboratoire de Cristallographie, Departement de Physique, Universite Constantine 1, Algeria. We also thank Mr F. Saidi, Engineer at the Laboratory of Crystallography, University Constantine 1, for assistance in collecting data on the Xcalibur X-ray diffractometer.

Acknowledgments

supplementary crystallographic information

Crystal data

C30H20Cl2O2SeZ = 1
Mr = 562.32F(000) = 284
Triclinic, P1Dx = 1.522 Mg m3
a = 4.9468 (3) ÅMo Kα radiation, λ = 0.71073 Å
b = 5.8712 (6) ÅCell parameters from 1538 reflections
c = 21.3530 (18) Åθ = 3.9–28.9°
α = 85.019 (8)°µ = 1.77 mm1
β = 84.094 (6)°T = 293 K
γ = 86.465 (7)°Prism, yellow
V = 613.68 (9) Å30.03 × 0.02 × 0.01 mm

Data collection

Agilent Technologies Xcalibur Eos diffractometerRint = 0.030
Graphite monochromatorθmax = 28.0°, θmin = 2.9°
ω scansh = −6→6
5341 measured reflectionsk = −7→5
3672 independent reflectionsl = −28→28
2465 reflections with I > 2σ(I)

Refinement

Refinement on F2Secondary atom site location: difference Fourier map
Least-squares matrix: fullHydrogen site location: inferred from neighbouring sites
R[F > 2σ(F)] = 0.038H-atom parameters constrained
wR(F) = 0.074w = 1/[σ(Fo) + (0.0181P)] where P = (Fo + 2Fc)/3
S = 0.81(Δ/σ)max < 0.001
3672 reflectionsΔρmax = 0.41 e Å3
317 parametersΔρmin = −0.32 e Å3
3 restraintsAbsolute structure: Refined as an inversion twin
Primary atom site location: structure-invariant direct methodsAbsolute structure parameter: 0.002 (11)

Special details

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.
Refinement. Refined as a 2-component inversion twin.

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

xyzUiso*/Ueq
Se10.41094 (7)0.32993 (9)0.51703 (4)0.0688 (2)
Cl12.5172 (3)0.7697 (3)0.08312 (8)0.0590 (4)
Cl22.0618 (3)−0.0037 (3)0.97993 (8)0.0649 (5)
O11.4087 (9)−0.1409 (9)0.3126 (3)0.0780 (15)
O20.9496 (10)0.8409 (8)0.7498 (2)0.0823 (16)
C10.7186 (10)0.2486 (11)0.4597 (3)0.0479 (15)
C20.8352 (11)0.0295 (12)0.4605 (3)0.0615 (18)
H10.768523−0.0813840.4909390.074*
C31.0483 (12)−0.0293 (12)0.4171 (3)0.0593 (17)
H21.122475−0.1788500.4182210.071*
C41.1520 (10)0.1346 (11)0.3718 (3)0.0444 (14)
C51.0451 (11)0.3551 (11)0.3723 (3)0.0503 (16)
H31.1203880.4689320.3439790.060*
C60.8227 (12)0.4092 (12)0.4153 (3)0.0553 (18)
H40.7442400.5573700.4135260.066*
C71.3680 (11)0.0604 (11)0.3220 (3)0.0507 (15)
C81.5292 (10)0.2372 (11)0.2840 (3)0.0461 (15)
H51.5229980.3837710.2975880.055*
C91.6809 (10)0.1939 (11)0.2315 (3)0.0457 (15)
H61.6662130.0512070.2167210.055*
C101.8698 (9)0.3462 (10)0.1941 (3)0.0439 (14)
C112.0024 (10)0.2799 (11)0.1368 (3)0.0499 (15)
H71.9583060.1437560.1220560.060*
C122.1960 (11)0.4092 (11)0.1015 (3)0.0534 (16)
H82.2775200.3648130.0629000.064*
C132.2653 (10)0.6084 (11)0.1255 (3)0.0464 (15)
C142.1353 (11)0.6771 (12)0.1810 (3)0.0479 (15)
H92.1807940.8130020.1956440.057*
C151.9411 (10)0.5512 (11)0.2153 (3)0.0484 (15)
H101.8557300.6015510.2528600.058*
C160.5992 (10)0.4225 (11)0.5837 (3)0.0498 (16)
C170.7975 (12)0.2824 (11)0.6111 (3)0.0577 (18)
H110.8486150.1417570.5952850.069*
C180.9211 (12)0.3470 (11)0.6615 (3)0.0542 (16)
H121.0519620.2485470.6794060.065*
C190.8519 (11)0.5582 (11)0.6859 (3)0.0457 (14)
C200.6508 (12)0.6967 (12)0.6588 (3)0.0580 (17)
H130.5969470.8361790.6750610.070*
C210.5295 (10)0.6326 (11)0.6087 (3)0.0509 (15)
H140.3983110.7310000.5909200.061*
C220.9847 (12)0.6393 (11)0.7381 (3)0.0540 (16)
C231.1622 (12)0.4833 (11)0.7744 (3)0.0510 (16)
H151.1862380.3319340.7643540.061*
C241.2909 (10)0.5463 (11)0.8210 (3)0.0499 (15)
H161.2587450.6979690.8303600.060*
C251.4776 (10)0.4073 (10)0.8597 (3)0.0453 (14)
C261.5525 (11)0.4873 (11)0.9142 (3)0.0574 (17)
H171.4812610.6293890.9258720.069*
C271.7295 (11)0.3629 (12)0.9516 (3)0.0553 (16)
H181.7756000.4196910.9882240.066*
C281.8357 (10)0.1557 (11)0.9342 (3)0.0505 (16)
C291.7647 (11)0.0694 (11)0.8801 (3)0.0529 (17)
H191.836285−0.0732160.8688690.063*
C301.5893 (10)0.1942 (10)0.8431 (3)0.0522 (16)
H201.5441350.1363660.8066090.063*

Atomic displacement parameters (Å)

U11U22U33U12U13U23
Se10.0439 (3)0.1060 (6)0.0592 (4)−0.0158 (3)0.0067 (3)−0.0279 (4)
Cl10.0504 (8)0.0624 (11)0.0618 (11)−0.0106 (7)0.0025 (7)0.0047 (9)
Cl20.0606 (9)0.0696 (12)0.0622 (11)0.0083 (9)−0.0051 (8)−0.0008 (10)
O10.101 (4)0.052 (3)0.075 (4)−0.015 (3)0.031 (3)−0.013 (3)
O20.130 (4)0.054 (3)0.068 (3)0.025 (3)−0.035 (3)−0.024 (3)
C10.038 (3)0.067 (5)0.042 (4)−0.014 (3)−0.004 (2)−0.013 (3)
C20.061 (4)0.075 (5)0.047 (4)−0.024 (4)0.017 (3)−0.010 (4)
C30.066 (4)0.053 (4)0.057 (5)−0.020 (3)0.011 (3)−0.004 (4)
C40.040 (3)0.060 (4)0.036 (3)−0.012 (3)−0.003 (2)−0.014 (3)
C50.057 (4)0.059 (4)0.033 (4)−0.009 (3)0.004 (3)−0.002 (3)
C60.051 (4)0.061 (5)0.057 (5)−0.010 (3)−0.004 (3)−0.019 (4)
C70.056 (3)0.054 (4)0.043 (4)−0.016 (3)0.007 (3)−0.013 (3)
C80.046 (3)0.053 (4)0.039 (4)−0.007 (3)0.006 (3)−0.016 (3)
C90.041 (3)0.050 (4)0.046 (4)0.002 (3)−0.004 (3)−0.002 (3)
C100.039 (3)0.048 (4)0.045 (3)0.003 (3)0.000 (2)−0.010 (3)
C110.060 (4)0.046 (4)0.045 (4)−0.002 (3)0.002 (3)−0.017 (3)
C120.056 (4)0.063 (5)0.040 (4)−0.012 (3)0.012 (3)−0.011 (3)
C130.037 (3)0.056 (4)0.042 (3)0.007 (3)−0.003 (2)0.012 (3)
C140.053 (3)0.050 (4)0.040 (4)−0.003 (3)−0.001 (3)−0.004 (3)
C150.048 (3)0.059 (4)0.038 (3)0.002 (3)0.002 (3)−0.013 (3)
C160.036 (3)0.062 (4)0.050 (4)−0.019 (3)0.013 (3)−0.010 (3)
C170.061 (4)0.047 (4)0.065 (5)−0.003 (3)0.007 (3)−0.016 (4)
C180.064 (4)0.053 (4)0.045 (4)−0.008 (3)0.006 (3)−0.012 (3)
C190.049 (3)0.050 (4)0.036 (3)−0.003 (3)0.006 (3)−0.005 (3)
C200.064 (4)0.059 (4)0.049 (4)0.002 (3)0.009 (3)−0.014 (3)
C210.045 (3)0.060 (4)0.047 (4)0.000 (3)0.003 (3)−0.009 (3)
C220.066 (4)0.054 (4)0.037 (3)0.016 (3)0.004 (3)−0.003 (3)
C230.075 (4)0.038 (4)0.039 (4)−0.003 (3)0.004 (3)−0.002 (3)
C240.056 (3)0.049 (4)0.042 (3)0.002 (3)0.006 (3)−0.004 (3)
C250.045 (3)0.046 (4)0.044 (4)−0.005 (3)0.006 (3)−0.009 (3)
C260.059 (4)0.052 (4)0.061 (5)0.000 (3)0.006 (3)−0.015 (4)
C270.050 (3)0.069 (5)0.047 (4)0.008 (3)−0.002 (3)−0.019 (3)
C280.040 (3)0.059 (4)0.049 (4)−0.002 (3)0.006 (3)0.001 (3)
C290.060 (4)0.042 (4)0.057 (4)0.016 (3)−0.012 (3)−0.012 (3)
C300.056 (3)0.052 (4)0.050 (4)−0.004 (3)−0.002 (3)−0.020 (3)

Geometric parameters (Å, º)

Se1—C11.916 (5)C14—C151.362 (8)
Se1—C161.913 (6)C14—H90.9300
Cl1—C131.741 (6)C15—H100.9300
Cl2—C281.737 (6)C16—C171.385 (8)
O1—C71.217 (7)C16—C211.396 (8)
O2—C221.229 (7)C17—C181.383 (9)
C1—C21.376 (8)C17—H110.9300
C1—C61.364 (8)C18—C191.396 (8)
C2—C31.377 (8)C18—H120.9300
C2—H10.9300C19—C201.387 (7)
C3—C41.386 (8)C19—C221.477 (8)
C3—H20.9300C20—C211.371 (8)
C4—C51.368 (8)C20—H130.9300
C4—C71.500 (7)C21—H140.9300
C5—C61.398 (8)C22—C231.459 (7)
C5—H30.9300C23—C241.325 (8)
C6—H40.9300C23—H150.9300
C7—C81.482 (8)C24—C251.466 (7)
C8—C91.317 (8)C24—H160.9300
C8—H50.9300C25—C261.383 (8)
C9—C101.462 (8)C25—C301.395 (7)
C9—H60.9300C26—C271.380 (8)
C10—C111.401 (7)C26—H170.9300
C10—C151.400 (8)C27—C281.361 (8)
C11—C121.380 (7)C27—H180.9300
C11—H70.9300C28—C291.387 (8)
C12—C131.392 (8)C29—C301.369 (7)
C12—H80.9300C29—H190.9300
C13—C141.369 (8)C30—H200.9300
C1—Se1—C1699.0 (2)C17—C16—C21117.4 (6)
C2—C1—C6118.2 (5)C17—C16—Se1122.2 (5)
C2—C1—Se1122.1 (5)C21—C16—Se1120.3 (5)
C6—C1—Se1119.7 (5)C18—C17—C16121.4 (6)
C1—C2—C3121.5 (6)C18—C17—H11119.3
C1—C2—H1119.2C16—C17—H11119.3
C3—C2—H1119.2C17—C18—C19120.8 (6)
C2—C3—C4120.0 (6)C17—C18—H12119.6
C2—C3—H2120.0C19—C18—H12119.6
C4—C3—H2120.0C20—C19—C18117.6 (6)
C5—C4—C3119.0 (5)C20—C19—C22119.4 (6)
C5—C4—C7122.4 (5)C18—C19—C22123.0 (6)
C3—C4—C7118.5 (6)C21—C20—C19121.5 (6)
C4—C5—C6120.0 (6)C21—C20—H13119.3
C4—C5—H3120.0C19—C20—H13119.3
C6—C5—H3120.0C20—C21—C16121.3 (6)
C1—C6—C5121.2 (6)C20—C21—H14119.4
C1—C6—H4119.4C16—C21—H14119.4
C5—C6—H4119.4O2—C22—C19119.4 (6)
O1—C7—C8120.5 (6)O2—C22—C23120.2 (6)
O1—C7—C4120.7 (6)C19—C22—C23120.4 (6)
C8—C7—C4118.7 (6)C24—C23—C22123.3 (6)
C9—C8—C7122.3 (6)C24—C23—H15118.3
C9—C8—H5118.9C22—C23—H15118.3
C7—C8—H5118.9C23—C24—C25128.2 (6)
C8—C9—C10127.0 (6)C23—C24—H16115.9
C8—C9—H6116.5C25—C24—H16115.9
C10—C9—H6116.5C26—C25—C30117.6 (5)
C11—C10—C15117.6 (6)C26—C25—C24120.2 (6)
C11—C10—C9119.8 (6)C30—C25—C24122.2 (6)
C15—C10—C9122.5 (6)C27—C26—C25122.1 (6)
C12—C11—C10122.4 (6)C27—C26—H17118.9
C12—C11—H7118.8C25—C26—H17118.9
C10—C11—H7118.8C28—C27—C26119.0 (6)
C13—C12—C11117.8 (6)C28—C27—H18120.5
C13—C12—H8121.1C26—C27—H18120.5
C11—C12—H8121.1C27—C28—C29120.6 (5)
C12—C13—C14120.5 (6)C27—C28—Cl2120.1 (5)
C12—C13—Cl1118.7 (5)C29—C28—Cl2119.3 (5)
C14—C13—Cl1120.8 (6)C30—C29—C28120.0 (6)
C15—C14—C13121.6 (7)C30—C29—H19120.0
C15—C14—H9119.2C28—C29—H19120.0
C13—C14—H9119.2C29—C30—C25120.7 (6)
C14—C15—C10120.1 (6)C29—C30—H20119.7
C14—C15—H10120.0C25—C30—H20119.7
C10—C15—H10120.0
C6—C1—C2—C3−1.1 (9)C21—C16—C17—C180.4 (9)
Se1—C1—C2—C3176.9 (5)Se1—C16—C17—C18−176.5 (5)
C1—C2—C3—C40.7 (10)C16—C17—C18—C19−0.9 (10)
C2—C3—C4—C52.0 (9)C17—C18—C19—C201.6 (9)
C2—C3—C4—C7−174.9 (6)C17—C18—C19—C22−177.7 (6)
C3—C4—C5—C6−4.2 (9)C18—C19—C20—C21−2.0 (9)
C7—C4—C5—C6172.5 (6)C22—C19—C20—C21177.4 (5)
C2—C1—C6—C5−1.3 (9)C19—C20—C21—C161.5 (9)
Se1—C1—C6—C5−179.3 (5)C17—C16—C21—C20−0.7 (8)
C4—C5—C6—C14.0 (10)Se1—C16—C21—C20176.2 (4)
C5—C4—C7—O1−160.6 (6)C20—C19—C22—O2−12.2 (9)
C3—C4—C7—O116.1 (9)C18—C19—C22—O2167.1 (6)
C5—C4—C7—C818.7 (8)C20—C19—C22—C23169.6 (6)
C3—C4—C7—C8−164.5 (5)C18—C19—C22—C23−11.1 (9)
O1—C7—C8—C913.7 (10)O2—C22—C23—C240.5 (10)
C4—C7—C8—C9−165.7 (5)C19—C22—C23—C24178.8 (5)
C7—C8—C9—C10−172.9 (5)C22—C23—C24—C25−178.6 (5)
C8—C9—C10—C11−175.5 (6)C23—C24—C25—C26−167.4 (6)
C8—C9—C10—C159.4 (8)C23—C24—C25—C3013.7 (9)
C15—C10—C11—C12−0.3 (8)C30—C25—C26—C27−0.5 (9)
C9—C10—C11—C12−175.6 (5)C24—C25—C26—C27−179.4 (5)
C10—C11—C12—C132.1 (8)C25—C26—C27—C280.6 (10)
C11—C12—C13—C14−2.9 (8)C26—C27—C28—C29−0.8 (9)
C11—C12—C13—Cl1177.9 (4)C26—C27—C28—Cl2179.3 (5)
C12—C13—C14—C151.9 (9)C27—C28—C29—C300.9 (9)
Cl1—C13—C14—C15−178.9 (4)Cl2—C28—C29—C30−179.2 (5)
C13—C14—C15—C100.0 (8)C28—C29—C30—C25−0.8 (9)
C11—C10—C15—C14−0.8 (8)C26—C25—C30—C290.6 (9)
C9—C10—C15—C14174.4 (5)C24—C25—C30—C29179.5 (5)

Hydrogen-bond geometry (Å, º)

D—H···AD—HH···AD···AD—H···A
C29—H19···O2i0.932.633.218 (8)122

Symmetry code: (i) x+1, y−1, z.

supplementary crystallographic information
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