Crystal structure of [5-bromo-2-(pyridin-2-yl-κN)phenyl-κC1](pentane-2,4-dionato-κ2O,O′)platinum(II)

Fukuda, K.; Sugaya, T.; Ishihara, K.

doi:10.1107/S2056989015017478

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Volume 71| Part 10| October 2015| Pages 1259-1261

doi:10.1107/S2056989015017478

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Crystal structure of [5-bromo-2-(pyridin-2-yl-κN)phenyl-κC¹](pentane-2,4-dionato-κ²O,O′)platinum(II)

Keito Fukuda,^a Tomoaki Sugaya ^a ^* and Koji Ishihara ^a

^aDepartment of Chemistry and Biochemistry, School of Advanced Science and Engineering, Waseda University, Okubo, Shinjuku-ku, Tokyo 169-8555, Japan
^*Correspondence e-mail: tom-s@aoni.waseda.jp

Edited by M. Weil, Vienna University of Technology, Austria (Received 7 September 2015; accepted 18 September 2015; online 30 September 2015)

The title cyclometalated platinum(II) complex with 2-(4-bromophenyl)pyridinato and acetylacetonato ligands, [Pt(C₁₁H₇BrN)(C₅H₇O₂)], consists of two crystallographically non-equivalent dimers, each stacked by π–π interactions with distances of ≃ 3.4 Å. In both dimers, the platinum(II) complexes are arranged antiparallel to each other. Each complex exhibits a slightly distorted square-planar coordination environment around the central Pt(II) atom. The dihedral angles between two chelate rings including the Pt^II atom in these complexes are 0.08 (12) and 1.54 (9)°.

Keywords: crystal structure; platinum(II); cyclometalated complex; acetylacetonato ligand; π–π interactions.

CCDC reference: 1425736

1. Chemical context

Square-planar cyclometalated platinum(II) complexes with luminescent properties have recently attracted attention because of their potential applications (Chi & Chou, 2010 ; Ma et al., 2013 ), such as DNA probing, as chemical sensors or as organic light-emitting diodes (OLEDs). In particular, platinum(II) complexes including β-diketonate anions (e.g. acetylacetonate) as an ancillary ligand have been widely studied because of their excellent stabilities and high quantum yields. Although these complexes afford luminescence in the solid state, their crystal structures have not been sufficiently explored. We report herein the crystal structure of the cyclometalated platinum(II) complex with 2-(4-bromophenyl)pyridinato (Brppy, C₁₁H₇BrN) and acetylacetonato (acac, C₅H₇O₂) ligands, [Pt(Brppy)(acac)].

2. Structural commentary

The asymmetric unit of the title compound contains two complex molecules with very similar configurations (r.m.s. deviation of fit of two molecules = 0.07 Å). The structure of one of the complex molecules of the title compound is shown in Fig. 1. In both complexes, the Pt^II atom is coordinated by C and N atoms of the bidentate Brppy ligand and two O atoms of the acac ligand. The coordination environments around the central Pt^II atoms (Pt1 and Pt2) are slightly distorted from an ideal square-planar configuration, with angles around Pt1 in the range 81.89 (18)–93.04 (17)° and around Pt2 in the range 81.73 (18)–93.57 (16)°. The Pt—C bond lengths [Pt1—C11 = 1.970 (5) and Pt2—C27 = 1.969 (5) Å] are slightly shorter than the Pt—N bond lengths [Pt1—N1 = 1.995 (4) and Pt2—N2 = 1.999 (4) Å] due to the stronger electron-donating ability of a C atom compared to that of an N atom. Pt—O bond lengths are compiled in Table 1. The phenyl and pyridyl rings are approximately coplanar [the dihedral angle between the N1,C1–C5 and C6–C11 rings is 1.31 (17)° while that between the N2,C17–C21 and C22–C27 rings is 3.12 (13)°]. In addition, the dihedral angles between two planes composed of the two chelate rings in the cyclometalated complex are 0.08 (12)° (involving Pt1) and 1.54 (9)° (involving Pt2).

Table 1
Selected bond lengths (Å)

O1—Pt1	2.077 (3)	O3—Pt2	2.081 (3)
O2—Pt1	2.007 (3)	O4—Pt2	2.005 (3)

Figure 1
Molecular structure of one of the two independent Pt^II complexes of the title compound, with displacement ellipsoids drawn at the 50% probability level.

3. Supramolecular features

As shown in Figs. 2 and 3, in the unit cell two non-equivalent dimers are formed by π–π interactions between individual complexes. Each non-equivalent dimer is in a head-to-tail form. In each unit cell both types of head-to-tail dimers stacked with an intermolecular π–π interaction are perpendicular to each other. The π-plane of one Pt^II complex (Pt1) is directed to the b axis, on the other hand, that of the other complex (Pt2) is directed to the a axis. The shortest intermolecular contacts are C4⋯C15ⁱ = 3.406 (7) and C22⋯O3ⁱⁱ = 3.402 (6) Å [symmetry codes: (i) –x + $[{3\over 2}]$ , –y + $[{1\over 2}]$ , −z + 1; (ii) –x + $[{1\over 2}]$ , –y + $[{1\over 2}]$ , –z + 1]. Weak C—H⋯O and C—H⋯Br interactions might also help to consolidate the crystal packing (Table 2). There is almost no interaction between the two Pt^II atoms in each dimers because the z-axes of Pt1 and Pt2 are not coaxial. In fact, the Pt—Pt contacts [Pt1⋯Pt1ⁱ = 3.688 (1) and Pt2⋯Pt2ⁱⁱ = 3.723 (1) Å] are longer than the van der Waals diameter of the Pt atom (3.5 Å; Bondi, 1964 )

Table 2
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
C1—H1⋯O1	0.95	2.40	2.999 (7)	121
C4—H4⋯O4ⁱ	0.95	2.58	3.281 (6)	131
C17—H17⋯O3	0.95	2.45	3.034 (6)	120
C17—H17⋯Br1ⁱⁱ	0.95	2.87	3.693 (6)	145
Symmetry codes: (i) $[-x+{\script{1\over 2}}, -y+{\script{1\over 2}}, -z+1]$ ; (ii) $[x-{\script{1\over 2}}, -y+{\script{1\over 2}}, z+{\script{1\over 2}}]$ .

Figure 2
Crystal packing of the title complex, viewed perpendicular to the ab plane. Dashed lines represent the shortest intermolecular contacts. Red wires represent the Pt1 molecule, and blue wires the Pt2 molecule. H atoms are omitted for clarity. [Symmetry codes: (i) –x + $[{3\over 2}]$ , –y + $[{1\over 2}]$ , –z + 1; (ii) –x + $[{1\over 2}]$ , –y + $[{1\over 2}]$ , –z + 1.]

Figure 3
Crystal packing of the title complex, viewed perpendicular to the ac plane. Red wires represent the Pt1 molecule, and blue wires the Pt2 molecule. H atoms are omitted for clarity.

4. Synthesis and crystallization

The title complex was synthesized according to a traditional two-step preparation method via the dichlorido-bridged dimer complex [Pt(C₁₁H₇BrN)(μ-Cl)]₂ (Cockburn et al., 1973 ; Liu et al., 2009 ), though one-pot synthesis has been reported recently (Hudson et al., 2012 ).

[Pt(C₁₁H₇BrN)(μ-Cl)]₂: A mixture of 2-(4-bromophenyl)pyridine (0.585 g, 2.5 mmol) and K₂PtCl₄ (1.00 g, 2.4 mmol) in a 2-ethoxyethanol–water mixture (45 ml/15 ml) was stirred for 6 h at 333 K under an Ar atmosphere. After cooling to room temperature, the yellow–green precipitate was filtered off, washed with dichloromethane, and dried in vacuo. Yield: 0.535 g, (48.2%).

[Pt(C₁₁H₇BrN)(C₅H₇O₂)]: A mixture of the dichlorido-bridged dimer complex (0.185 g, 0.20 mmol), acetylacetone (0.020 g, 0.20 mmol) and Na₂CO₃ (0.211 g, 2.0 mmol) in 2-ethoxyethanol was stirred for 7 h at 323 K under an Ar atmosphere. After cooling to room temperature, the yellow precipitate was filtered off and dried in vacuo. Yield: 0.200 g (47.6%)

Yellow single crystals suitable for X-ray structural analysis were grown by vapor diffusion of hexane into the dichloromethane solution of the title complex.

Analysis found (calculated for C₁₆H₁₄BrNO₂Pt): C, 36.15 (36.45); H, 2.25 (2.68); N, 2.59 (2.66). UV–vis [CHCl₃, λ_max nm⁻¹ (∊ / L mol⁻¹ cm⁻¹)]: 262 (29800), 280 (27500), 317 (sh, 11700), 330 (sh, 9400), 363 (6400), 389 (4200). ¹H NMR (CDCl₃, 298 K); 8.97 (d, J_Pt-H = 40.0 Hz, J = 6.0 Hz, 1H), 7.81 (t, J = 6.0 Hz, 1H), 7.71 (s, J_Pt-H = 40.0 Hz, 1H), 7.57 (d, J = 6.0 Hz, 1H), 7.31-7.45 (m, 2H), 7.14 (t, J = 6.0 Hz, 1H), 5.48 (s, 1H), 2.03 (s, 3H), 2.01 (s, 3H).

5. Refinement

Crystal data, data collection and structure refinement details are summarized in Table 3. All H atoms were placed in geometrically idealized positions and refined using a riding model, with C—H = 0.95 Å, U_iso(H) = 1.2U_eq(C) for Csp²–H, and U_iso(H) = 1.5U_eq(C) for methyl H atoms.

Table 3
Experimental details

Crystal data
Chemical formula	[Pt(C₁₁H₇BrN)(C₅H₇O₂)]
M_r	527.28
Crystal system, space group	Monoclinic, C2/c
Temperature (K)	200
a, b, c (Å)	17.557 (2), 17.876 (2), 19.832 (2)
β (°)	91.397 (1)
V (Å³)	6222.4 (13)
Z	16
Radiation type	Mo Kα
μ (mm⁻¹)	11.59
Crystal size (mm)	0.18 × 0.06 × 0.02

Data collection
Diffractometer	Bruker APEXII CCD area detector
Absorption correction	Multi-scan (SADABS; Bruker, 2014 )
T_min, T_max	0.48, 0.80
No. of measured, independent and observed [I > 2σ(I)] reflections	35025, 7103, 6001
R_int	0.038
(sin θ/λ)_max (Å⁻¹)	0.649

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.027, 0.070, 1.01
No. of reflections	7103
No. of parameters	383
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	3.66, −1.20
Computer programs: APEX2 and SAINT (Bruker, 2014), SHELXS97 (Sheldrick, 2008 ), SHELXL2014 (Sheldrick, 2015 ), ORTEP-3 for Windows (Farrugia, 2012 ) and Mercury (Macrae et al., 2008 ).

Supporting information

CCDC reference: 1425736

Crystal structure: contains datablock I. DOI: 10.1107/S2056989015017478/wm5214sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S2056989015017478/wm5214Isup2.hkl

Supporting information file. DOI: 10.1107/S2056989015017478/wm5214Isup3.tif

checkCIF report

Chemical context top

Square-planar cyclometalated platinum(II) complexes with luminescent properties have recently attracted attention because of their potential applications (Chi & Chou, 2010; Ma et al., 2013), such as DNA probing, as chemical sensors or as organic light-emitting diodes (OLEDs). In particular, platinum(II) complexes including β-diketonate anions (e.g. acetylacetonate) as an ancillary ligand have been widely studied because of their excellent stabilities and high quantum yields. Although these complexes afford luminescence in the solid state, their crystal structures have not been sufficiently explored. We report herein the crystal structure of the cyclometalated platinum(II) complex with 2-(4-bromophenyl)pyridinato (Brppy, C₁₁H₇BrN) and acetylacetonato (acac, C₅H₇O₂) ligands, [Pt(Brppy)(acac)].

Structural commentary top

The asymmetric unit of the title compound contains two complex molecules with very similar configurations. The structure of one of the complex molecules of the title compound is shown in Fig. 1. In both complexes, the Pt^II atom is coordinated by C and N atoms of the bidentate Brppy ligand and two O atoms of the acac ligand. The coordination environments around the central Pt^II atoms (Pt1 and Pt2) are slightly distorted from an ideal square-planar configuration, with angles around Pt1 in the range 81.89 (18)–93.04 (17)° and around Pt2 in the range 81.73 (18)–93.57 (16)°. The Pt—C bond lengths [Pt1—C11 = 1.970 (5) and Pt2—C27 = 1.969 (5) Å] are slightly shorter than the Pt—N bond lengths [Pt1—N1 = 1.995 (4) and Pt2—N2 = 1.999 (4) Å] due to the stronger electron-donating ability of a C atom compared to that of an N atom. Pt—O bond lengths are compiled in Table 1. The phenyl and pyridyl rings are approximately coplanar [(N1,C1,N2,C3,C4,C5)^(C6,C7,C8,C9,C10,C11) = 1.31 (17)°; (N2,C17,C18,C19,C20,C21)^(C22,C23,C24,C25,C26,C27) = 3.12 (13)°]. In addition, the dihedral angles between two planes composed of the two chelate rings in the cyclometalated complex are 0.08 (12)° (involving Pt1) and 1.54 (9)° (involving Pt2).

As shown in Figs. 2 and 3, in the unit cell two non-equivalent dimers are formed by π–π interactions between individual complexes [give numerical details]. Each nonequivalent dimer is in a head-to-tail form.

Supramolecular features top

As mentioned above, in each unit cell both types of head-to-tail dimers stacked with an intermolecular π–π interaction are perpendicular to each other. The π-plane of one Pt^II complex (Pt1) is directed to the b axis, on the other hand, that of the other complex (Pt2) is directed to the a axis. The shortest intermolecular contacts are C4···C15ⁱ = 3.406 (7) and C22···O3ⁱⁱ = 3.402 (6) Å [symmetry codes: (i) –x + 3/2, –y + 1/2, –z + 1; (ii) –x + 1/2, –y + 1/2, –z + 1]. Weak C—H···O and C—H···Br interactions might also help to consolidate the crystal packing (Table 2). There is almost no interaction between the two Pt^II atoms of adjacent dimers because the z-axes of Pt1 and Pt2 are not coaxial. In fact, the Pt—Pt contacts [Pt1···Pt1ⁱ = 3.688 (1) and Pt2···Pt2ⁱⁱ = 3.723 (1) Å] are longer than the van der Waals diameter of the Pt atom (3.5 Å; Bondi, 1964)

Synthesis and crystallization top

The title complex was synthesized according to a traditional two-step preparation method via the dichlorido-bridged dimer complex [Pt(C₁₁H₇BrN)(µ-Cl)]₂ (Cockburn et al., 1973; Liu et al., 2009), though one-pot synthesis has been reported recently (Hudson et al., 2012).

[Pt(C₁₁H₇BrN)(µ-Cl)]₂: A mixture of 2-(4-bromophenyl)pyridine (0.585 g, 2.5 mmol) and K₂PtCl₄ (1.00 g, 2.4 mmol) in a 2-ethoxyethanol–water mixture (45 ml/15 ml) was stirred for 6 h at 333 K under an Ar atmosphere. After cooling to room temperature, the yellow–green precipitate was filtered off, washed with dichloromethane, and dried in vacuo. Yield: 0.535 g, (48.2 %).

Yellow single crystals suitable for X-ray structural analysis were grown by vapor diffusion of hexane into the dichloromethane solution of the title complex.

Analysis found (calculated for C₁₆H₁₄BrNO₂Pt): C, 36.15 (36.45); H, 2.25 (2.68); N, 2.59 (2.66). UV–vis [CHCl₃, λ_max / nm (ε / L mol^–1 cm^–1)]: 262 (29800), 280 (27500), 317 (sh, 11700), 330 (sh, 9400), 363 (6400), 389 (4200). ¹H NMR (CDCl₃, 298 K); 8.97 (d, J_Pt—H = 40.0 Hz, J = 6.0 Hz, 1H), 7.81 (t, J = 6.0 Hz, 1H), 7.71 (s, J_Pt—H = 40.0 Hz, 1H), 7.57 (d, J = 6.0 Hz, 1H), 7.31-7.45 (m, 2H), 7.14 (t, J = 6.0 Hz, 1H), 5.48 (s, 1H), 2.03 (s, 3H), 2.01 (s, 3H).

Refinement top

Related literature top

For related literature, see: Bondi (1964); Cockburn et al. (1973); Hudson et al. (2012); Liu et al. (2009); Chi & Chou (2010); Ma et al. (2013).

Computing details top

Data collection: APEX2 (Bruker, 2014); cell refinement: SAINT (Bruker, 2014); data reduction: SAINT (Bruker, 2014); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL2014 (Sheldrick, 2015); molecular graphics: ORTEP-3 for Windows (Farrugia, 2012) and Mercury (Macrae et al., 2008); software used to prepare material for publication: SHELXL2014 (Sheldrick, 2015).

Figures top

	Fig. 1. Molecular structure of one of the two independent Pt^II complexes of the title compound, with displacement ellipsoids drawn at the 50% probability level.
	Fig. 2. Crystal packing of the title complex, viewed perpendicular to the ab plane. Dashed lines represent the shortest intermolecular contacts. Red wires represent the Pt1 molecule, and blue wires the Pt2 molecule. H atoms are omitted for clarity. [Symmetry codes: (i) –x + 3/2, –y + 1/2, –z + 1; (ii) –x + 1/2, –y + 1/2, –z + 1.]
	Fig. 3. Crystal packing of the title complex, viewed perpendicular to the ac plane. Red wires represent the Pt1 molecule, and blue wires the Pt2 molecule. H atoms are omitted for clarity.

[5-Bromo-2-(pyridin-2-yl-κN)phenyl-κC¹](pentane-2,4-dionato-κ²O,O')platinum(II) top

Crystal data top

[Pt(C₁₁H₇BrN)(C₅H₇O₂)]	F(000) = 3936
M_r = 527.28	D_x = 2.251 Mg m⁻³
Monoclinic, C2/c	Mo Kα radiation, λ = 0.71073 Å
a = 17.557 (2) Å	Cell parameters from 9927 reflections
b = 17.876 (2) Å	θ = 2.3–27.3°
c = 19.832 (2) Å	µ = 11.59 mm⁻¹
β = 91.397 (1)°	T = 200 K
V = 6222.4 (13) Å³	Lath, yellow
Z = 16	0.18 × 0.06 × 0.02 mm

Data collection top

Bruker APEXII CCD area detector diffractometer	7103 independent reflections
Radiation source: Bruker TXS fine-focus rotating anode	6001 reflections with I > 2σ(I)
Bruker Helios multilayer confocal mirror monochromator	R_int = 0.038
Detector resolution: 8.333 pixels mm^-1	θ_max = 27.5°, θ_min = 1.6°
phi and ω scans	h = −22→22
Absorption correction: multi-scan (SADABS; Bruker, 2014)	k = −23→23
T_min = 0.48, T_max = 0.80	l = −25→25
35025 measured reflections

Refinement top

Refinement on F²	0 restraints
Least-squares matrix: full	Hydrogen site location: inferred from neighbouring sites
R[F² > 2σ(F²)] = 0.027	H-atom parameters constrained
wR(F²) = 0.070	w = 1/[σ²(F_o²) + (0.0368P)² + 16.0306P] where P = (F_o² + 2F_c²)/3
S = 1.01	(Δ/σ)_max = 0.001
7103 reflections	Δρ_max = 3.66 e Å⁻³
383 parameters	Δρ_min = −1.19 e Å⁻³

Crystal data top

[Pt(C₁₁H₇BrN)(C₅H₇O₂)]	V = 6222.4 (13) Å³
M_r = 527.28	Z = 16
Monoclinic, C2/c	Mo Kα radiation
a = 17.557 (2) Å	µ = 11.59 mm⁻¹
b = 17.876 (2) Å	T = 200 K
c = 19.832 (2) Å	0.18 × 0.06 × 0.02 mm
β = 91.397 (1)°

Data collection top

Bruker APEXII CCD area detector diffractometer	7103 independent reflections
Absorption correction: multi-scan (SADABS; Bruker, 2014)	6001 reflections with I > 2σ(I)
T_min = 0.48, T_max = 0.80	R_int = 0.038
35025 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.027	0 restraints
wR(F²) = 0.070	H-atom parameters constrained
S = 1.01	w = 1/[σ²(F_o²) + (0.0368P)² + 16.0306P] where P = (F_o² + 2F_c²)/3
7103 reflections	Δρ_max = 3.66 e Å⁻³
383 parameters	Δρ_min = −1.19 e Å⁻³

Special details top

Geometry. Distance SDEV

3.4016 (0.0055) C22 - O3_$6 3.4056 (0.0070) C4 - C15_$5 3.6879 (0.0005) Pt1 - Pt1_$5 3.7230 (0.0005) Pt2 - Pt2_$6

$5 1.5 - x, 0.5 - y, 1 - z $6 0.5 - x, 0.5 - y, 1 - z

Least-squares planes (x,y,z in crystal coordinates) and deviations from them (* indicates atom used to define plane)

17.0464 (0.0086) x + 3.5524 (0.0343) y - 3.1157 (0.0389) z = 1.9362 (0.0174)

* -0.0159 (0.0032) C22 * 0.0106 (0.0035) C23 * 0.0050 (0.0037) C24 * -0.0152 (0.0036) C25 * 0.0096 (0.0034) C26 * 0.0059 (0.0032) C27

Rms deviation of fitted atoms = 0.0112

17.1816 (0.0082) x + 3.3837 (0.0389) y - 2.0681 (0.0436) z = 2.4419 (0.0278)

Angle to previous plane (with approximate e.s.d.) = 3.118 (0.129)

* -0.0040 (0.0032) N2 * 0.0023 (0.0037) C17 * 0.0000 (0.0041) C18 * -0.0004 (0.0041) C19 * -0.0014 (0.0038) C20 * 0.0036 (0.0033) C21

Rms deviation of fitted atoms = 0.0025

3.5018 (0.0341) x + 17.1159 (0.0108) y - 4.2313 (0.0388) z = 3.1261 (0.0262)

Angle to previous plane (with approximate e.s.d.) = 66.846 (0.177)

* 0.0047 (0.0032) C6 * -0.0001 (0.0036) C7 * -0.0055 (0.0037) C8 * 0.0064 (0.0036) C9 * -0.0015 (0.0033) C10 * -0.0040 (0.0031) C11

Rms deviation of fitted atoms = 0.0043

3.8621 (0.0359) x + 17.0726 (0.0113) y - 4.0479 (0.0426) z = 3.4669 (0.0355)

Angle to previous plane (with approximate e.s.d.) = 1.309 (0.166)

* -0.0056 (0.0031) N1 * 0.0048 (0.0038) C1 * -0.0003 (0.0042) C2 * -0.0032 (0.0042) C3 * 0.0024 (0.0037) C4 * 0.0019 (0.0032) C5

Rms deviation of fitted atoms = 0.0035

17.0575 (0.0059) x + 3.8901 (0.0226) y - 2.3217 (0.0295) z = 2.4371 (0.0163)

Angle to previous plane (with approximate e.s.d.) = 63.889 (0.149)

* 0.0136 (0.0026) O3 * 0.0004 (0.0034) C29 * -0.0121 (0.0038) C30 * -0.0006 (0.0035) C31 * 0.0149 (0.0026) O4 * -0.0162 (0.0018) Pt2

Rms deviation of fitted atoms = 0.0117

17.1494 (0.0057) x + 3.4219 (0.0232) y - 2.3782 (0.0383) z = 2.2709 (0.0209)

Angle to previous plane (with approximate e.s.d.) = 1.538 (0.086)

* -0.0073 (0.0024) N2 * 0.0020 (0.0029) C21 * 0.0076 (0.0030) C22 * -0.0104 (0.0026) C27 * 0.0081 (0.0018) Pt2

Rms deviation of fitted atoms = 0.0076

3.7521 (0.0218) x + 17.0640 (0.0077) y - 4.2225 (0.0285) z = 3.2745 (0.0235)

Angle to previous plane (with approximate e.s.d.) = 65.705 (0.111)

* -0.0132 (0.0026) O1 * -0.0080 (0.0035) C13 * 0.0257 (0.0037) C14 * -0.0103 (0.0034) C15 * -0.0121 (0.0026) O2 * 0.0179 (0.0017) Pt1

Rms deviation of fitted atoms = 0.0157

3.7578 (0.0215) x + 17.0576 (0.0090) y - 4.2485 (0.0367) z = 3.2795 (0.0249)

Angle to previous plane (with approximate e.s.d.) = 0.080 (0.123)

* -0.0089 (0.0023) N1 * 0.0120 (0.0028) C5 * -0.0086 (0.0028) C6 * 0.0027 (0.0024) C11 * 0.0028 (0.0017) Pt1

Rms deviation of fitted atoms = 0.0079

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

	x	y	z	U_iso*/U_eq
Br1	0.63794 (4)	0.11449 (4)	0.24876 (3)	0.06869 (19)
Br2	0.13287 (5)	0.08166 (4)	0.25166 (3)	0.06997 (19)
C1	0.6968 (3)	0.1984 (3)	0.6440 (3)	0.0478 (12)
H1	0.7459	0.1928	0.6646	0.057*
C2	0.6367 (4)	0.2211 (3)	0.6835 (3)	0.0614 (16)
H2	0.6441	0.2304	0.7304	0.074*
C3	0.5655 (4)	0.2296 (3)	0.6522 (3)	0.0626 (17)
H3	0.5231	0.2449	0.6777	0.075*
C4	0.5565 (3)	0.2159 (3)	0.5846 (3)	0.0484 (13)
H4	0.5080	0.2221	0.5632	0.058*
C5	0.6187 (3)	0.1929 (2)	0.5470 (3)	0.0368 (10)
C6	0.6190 (3)	0.1739 (2)	0.4758 (3)	0.0355 (10)
C7	0.5543 (3)	0.1762 (3)	0.4328 (3)	0.0467 (12)
H7	0.5065	0.1904	0.4502	0.056*
C8	0.5596 (3)	0.1583 (3)	0.3660 (3)	0.0493 (14)
H8	0.5160	0.1593	0.3367	0.059*
C9	0.6299 (3)	0.1388 (3)	0.3424 (3)	0.0455 (12)
C10	0.6949 (3)	0.1351 (3)	0.3833 (2)	0.0392 (11)
H10	0.7421	0.1207	0.3649	0.047*
C11	0.6905 (3)	0.1526 (2)	0.4509 (2)	0.0342 (10)
C12	0.9693 (4)	0.1381 (4)	0.6572 (3)	0.0652 (17)
H12A	0.9552	0.1822	0.6835	0.098*
H12B	1.0234	0.1410	0.6463	0.098*
H12C	0.9602	0.0928	0.6837	0.098*
C13	0.9223 (3)	0.1355 (3)	0.5936 (3)	0.0445 (12)
C14	0.9569 (3)	0.1148 (3)	0.5327 (3)	0.0475 (13)
H14	1.0104	0.1067	0.5349	0.057*
C15	0.9213 (3)	0.1051 (3)	0.4705 (3)	0.0395 (11)
C16	0.9671 (3)	0.0762 (3)	0.4126 (3)	0.0514 (14)
H16A	0.9435	0.0305	0.3947	0.077*
H16B	1.0192	0.0653	0.4286	0.077*
H16C	0.9684	0.1142	0.3770	0.077*
C17	0.1737 (3)	0.2277 (3)	0.6336 (3)	0.0477 (13)
H17	0.1651	0.2790	0.6435	0.057*
C18	0.1893 (3)	0.1793 (4)	0.6855 (3)	0.0591 (15)
H18	0.1913	0.1967	0.7308	0.071*
C19	0.2023 (3)	0.1049 (4)	0.6714 (3)	0.0629 (17)
H19	0.2133	0.0706	0.7069	0.075*
C20	0.1990 (3)	0.0805 (3)	0.6053 (3)	0.0511 (13)
H20	0.2077	0.0293	0.5951	0.061*
C21	0.1831 (3)	0.1312 (3)	0.5538 (3)	0.0411 (11)
C22	0.1765 (2)	0.1157 (3)	0.4814 (3)	0.0377 (11)
C23	0.1874 (3)	0.0452 (3)	0.4521 (3)	0.0452 (12)
H23	0.2023	0.0040	0.4796	0.054*
C24	0.1767 (3)	0.0357 (3)	0.3844 (3)	0.0482 (13)
H24	0.1836	−0.0121	0.3645	0.058*
C25	0.1556 (3)	0.0967 (3)	0.3451 (3)	0.0444 (12)
C26	0.1472 (3)	0.1677 (3)	0.3722 (3)	0.0410 (11)
H26	0.1346	0.2089	0.3438	0.049*
C27	0.1574 (3)	0.1782 (3)	0.4412 (3)	0.0360 (10)
C28	0.1093 (4)	0.4917 (3)	0.5815 (3)	0.0568 (15)
H28A	0.0791	0.4731	0.6189	0.085*
H28B	0.0838	0.5352	0.5611	0.085*
H28C	0.1600	0.5062	0.5985	0.085*
C29	0.1167 (3)	0.4308 (3)	0.5292 (3)	0.0435 (12)
C30	0.1027 (3)	0.4486 (3)	0.4614 (3)	0.0490 (13)
H30	0.0888	0.4990	0.4520	0.059*
C31	0.1067 (3)	0.4011 (3)	0.4063 (3)	0.0433 (12)
C32	0.0874 (4)	0.4303 (3)	0.3369 (3)	0.0617 (16)
H32A	0.1263	0.4141	0.3055	0.093*
H32B	0.0855	0.4851	0.3379	0.093*
H32C	0.0376	0.4108	0.3219	0.093*
N1	0.6882 (2)	0.1843 (2)	0.5787 (2)	0.0349 (8)
N2	0.1701 (2)	0.2051 (2)	0.5697 (2)	0.0368 (9)
O1	0.85200 (19)	0.15218 (18)	0.59970 (18)	0.0418 (8)
O2	0.85083 (18)	0.11665 (19)	0.45482 (17)	0.0402 (8)
O3	0.13515 (19)	0.36673 (18)	0.55181 (18)	0.0410 (8)
O4	0.1237 (2)	0.33092 (18)	0.40711 (17)	0.0400 (8)
Pt1	0.77288 (2)	0.15171 (2)	0.52011 (2)	0.03211 (6)
Pt2	0.14668 (2)	0.27243 (2)	0.49142 (2)	0.03308 (6)

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Br1	0.0827 (5)	0.0827 (5)	0.0401 (3)	−0.0135 (4)	−0.0115 (3)	0.0119 (3)
Br2	0.0957 (5)	0.0599 (4)	0.0547 (4)	−0.0007 (3)	0.0093 (3)	−0.0143 (3)
C1	0.052 (3)	0.043 (3)	0.047 (3)	0.001 (2)	0.000 (2)	−0.003 (2)
C2	0.071 (4)	0.056 (4)	0.057 (4)	0.003 (3)	0.008 (3)	−0.005 (3)
C3	0.064 (4)	0.052 (4)	0.073 (4)	0.006 (3)	0.027 (3)	−0.001 (3)
C4	0.036 (3)	0.039 (3)	0.070 (4)	0.006 (2)	0.009 (3)	0.006 (3)
C5	0.032 (2)	0.023 (2)	0.056 (3)	−0.0007 (18)	0.001 (2)	0.009 (2)
C6	0.027 (2)	0.026 (2)	0.053 (3)	−0.0041 (18)	−0.004 (2)	0.009 (2)
C7	0.031 (3)	0.049 (3)	0.060 (3)	0.000 (2)	−0.004 (2)	0.008 (3)
C8	0.038 (3)	0.045 (3)	0.063 (4)	−0.007 (2)	−0.019 (3)	0.017 (3)
C9	0.050 (3)	0.046 (3)	0.040 (3)	−0.008 (2)	−0.007 (2)	0.009 (2)
C10	0.037 (3)	0.035 (2)	0.046 (3)	−0.004 (2)	−0.001 (2)	0.009 (2)
C11	0.033 (2)	0.024 (2)	0.045 (3)	−0.0028 (18)	−0.002 (2)	0.0079 (19)
C12	0.048 (4)	0.079 (5)	0.068 (4)	−0.001 (3)	−0.020 (3)	0.008 (3)
C13	0.036 (3)	0.043 (3)	0.054 (3)	−0.008 (2)	−0.011 (2)	0.014 (2)
C14	0.028 (2)	0.046 (3)	0.068 (4)	0.003 (2)	−0.006 (2)	0.013 (3)
C15	0.027 (2)	0.040 (3)	0.051 (3)	0.001 (2)	0.001 (2)	0.013 (2)
C16	0.035 (3)	0.052 (3)	0.067 (4)	0.004 (2)	0.006 (2)	0.014 (3)
C17	0.041 (3)	0.051 (3)	0.051 (3)	−0.001 (2)	0.000 (2)	0.002 (2)
C18	0.057 (4)	0.071 (4)	0.049 (3)	−0.007 (3)	−0.009 (3)	0.013 (3)
C19	0.053 (4)	0.074 (4)	0.061 (4)	−0.006 (3)	−0.011 (3)	0.025 (3)
C20	0.043 (3)	0.045 (3)	0.065 (4)	−0.001 (2)	−0.006 (3)	0.016 (3)
C21	0.027 (2)	0.036 (3)	0.060 (3)	−0.0026 (19)	0.000 (2)	0.010 (2)
C22	0.022 (2)	0.028 (2)	0.064 (3)	−0.0004 (17)	0.005 (2)	0.009 (2)
C23	0.035 (3)	0.031 (3)	0.070 (4)	0.002 (2)	0.007 (2)	0.005 (2)
C24	0.046 (3)	0.029 (3)	0.069 (4)	0.000 (2)	0.010 (3)	−0.005 (2)
C25	0.042 (3)	0.039 (3)	0.053 (3)	−0.003 (2)	0.014 (2)	−0.006 (2)
C26	0.037 (3)	0.032 (2)	0.054 (3)	−0.001 (2)	0.008 (2)	0.003 (2)
C27	0.028 (2)	0.028 (2)	0.052 (3)	−0.0004 (18)	0.005 (2)	0.005 (2)
C28	0.062 (4)	0.042 (3)	0.067 (4)	0.003 (3)	0.004 (3)	−0.010 (3)
C29	0.033 (3)	0.031 (2)	0.067 (3)	−0.004 (2)	0.008 (2)	0.001 (2)
C30	0.049 (3)	0.032 (3)	0.066 (4)	0.003 (2)	0.007 (3)	0.006 (2)
C31	0.045 (3)	0.027 (2)	0.058 (3)	−0.002 (2)	0.008 (2)	0.009 (2)
C32	0.085 (5)	0.037 (3)	0.063 (4)	0.007 (3)	0.004 (3)	0.011 (3)
N1	0.033 (2)	0.0284 (19)	0.043 (2)	0.0001 (16)	0.0005 (17)	0.0037 (16)
N2	0.0235 (19)	0.037 (2)	0.050 (2)	−0.0018 (16)	0.0014 (16)	0.0063 (18)
O1	0.0344 (19)	0.043 (2)	0.048 (2)	−0.0013 (14)	−0.0061 (15)	0.0071 (15)
O2	0.0295 (17)	0.0403 (19)	0.051 (2)	0.0019 (14)	0.0007 (14)	0.0059 (15)
O3	0.0366 (18)	0.0320 (17)	0.055 (2)	−0.0009 (14)	0.0031 (15)	−0.0027 (15)
O4	0.045 (2)	0.0295 (17)	0.0461 (19)	0.0016 (14)	0.0055 (15)	0.0068 (14)
Pt1	0.02610 (9)	0.02845 (10)	0.04157 (11)	−0.00042 (6)	−0.00348 (7)	0.00636 (7)
Pt2	0.02732 (10)	0.02679 (9)	0.04527 (11)	−0.00091 (6)	0.00418 (7)	0.00340 (7)

Geometric parameters (Å, º) top

C9—C10	1.385 (7)	C16—H16A	0.9800
C6—C11	1.414 (7)	C16—H16B	0.9800
C10—C11	1.380 (7)	C16—H16C	0.9800
C12—C13	1.492 (8)	C17—H17	0.9500
C13—C14	1.413 (8)	C18—H18	0.9500
C14—C15	1.382 (7)	C19—H19	0.9500
C15—C16	1.508 (7)	C2—H2	0.9500
C17—C18	1.368 (8)	C20—H20	0.9500
C18—C19	1.378 (9)	C23—H23	0.9500
C1—C2	1.390 (8)	C24—H24	0.9500
C19—C20	1.381 (9)	C26—H26	0.9500
C20—C21	1.389 (7)	C28—H28A	0.9800
C21—C22	1.463 (7)	C28—H28B	0.9800
C22—C23	1.402 (7)	C28—H28C	0.9800
C23—C24	1.362 (8)	C3—H3	0.9500
Br2—C25	1.905 (5)	C30—H30	0.9500
C24—C25	1.386 (8)	C32—H32A	0.9800
C25—C26	1.388 (7)	C32—H32B	0.9800
C22—C27	1.407 (6)	C32—H32C	0.9800
C26—C27	1.388 (7)	C4—H4	0.9500
C28—C29	1.511 (7)	C7—H7	0.9500
C2—C3	1.392 (9)	C8—H8	0.9500
C29—C30	1.397 (8)	C1—N1	1.325 (6)
C30—C31	1.387 (8)	C5—N1	1.367 (6)
C31—C32	1.504 (8)	C17—N2	1.331 (7)
C3—C4	1.367 (9)	C21—N2	1.378 (6)
C4—C5	1.400 (7)	C13—O1	1.279 (6)
C5—C6	1.452 (7)	C15—O2	1.284 (5)
C6—C7	1.404 (7)	C29—O3	1.270 (6)
C7—C8	1.369 (8)	C31—O4	1.290 (6)
Br1—C9	1.915 (5)	C11—Pt1	1.970 (5)
C8—C9	1.376 (8)	N1—Pt1	1.995 (4)
C1—H1	0.9500	O1—Pt1	2.077 (3)
C10—H10	0.9500	O2—Pt1	2.007 (3)
C12—H12A	0.9800	C27—Pt2	1.969 (5)
C12—H12B	0.9800	N2—Pt2	1.999 (4)
C12—H12C	0.9800	O3—Pt2	2.081 (3)
C14—H14	0.9500	O4—Pt2	2.005 (3)

N1—C1—C2	122.5 (5)	C21—C20—H20	120.1
N1—C1—H1	118.8	N2—C21—C20	119.2 (5)
C2—C1—H1	118.8	N2—C21—C22	113.4 (4)
C1—C2—C3	117.8 (6)	C20—C21—C22	127.4 (5)
C1—C2—H2	121.1	C23—C22—C27	120.8 (5)
C3—C2—H2	121.1	C23—C22—C21	124.6 (4)
C4—C3—C2	119.9 (6)	C27—C22—C21	114.6 (4)
C4—C3—H3	120.0	C24—C23—C22	120.3 (5)
C2—C3—H3	120.0	C24—C23—H23	119.9
C3—C4—C5	120.2 (5)	C22—C23—H23	119.9
C3—C4—H4	119.9	C23—C24—C25	119.0 (5)
C5—C4—H4	119.9	C23—C24—H24	120.5
N1—C5—C4	119.1 (5)	C25—C24—H24	120.5
N1—C5—C6	113.4 (4)	C24—C25—C26	122.0 (5)
C4—C5—C6	127.5 (5)	C24—C25—Br2	118.9 (4)
C7—C6—C11	120.6 (5)	C26—C25—Br2	119.0 (4)
C7—C6—C5	124.2 (5)	C27—C26—C25	119.5 (5)
C11—C6—C5	115.2 (4)	C27—C26—H26	120.2
C8—C7—C6	120.5 (5)	C25—C26—H26	120.2
C8—C7—H7	119.8	C26—C27—C22	118.3 (5)
C6—C7—H7	119.8	C26—C27—Pt2	127.0 (4)
C7—C8—C9	118.2 (5)	C22—C27—Pt2	114.7 (4)
C7—C8—H8	120.9	C29—C28—H28A	109.5
C9—C8—H8	120.9	C29—C28—H28B	109.5
C8—C9—C10	123.1 (5)	H28A—C28—H28B	109.5
C8—C9—Br1	118.4 (4)	C29—C28—H28C	109.5
C10—C9—Br1	118.5 (4)	H28A—C28—H28C	109.5
C11—C10—C9	119.6 (5)	H28B—C28—H28C	109.5
C11—C10—H10	120.2	O3—C29—C30	125.6 (5)
C9—C10—H10	120.2	O3—C29—C28	115.7 (5)
C10—C11—C6	118.1 (4)	C30—C29—C28	118.7 (5)
C10—C11—Pt1	128.2 (4)	C31—C30—C29	127.4 (5)
C6—C11—Pt1	113.7 (4)	C31—C30—H30	116.3
C13—C12—H12A	109.5	C29—C30—H30	116.3
C13—C12—H12B	109.5	O4—C31—C30	127.0 (5)
H12A—C12—H12B	109.5	O4—C31—C32	113.3 (5)
C13—C12—H12C	109.5	C30—C31—C32	119.7 (5)
H12A—C12—H12C	109.5	C31—C32—H32A	109.5
H12B—C12—H12C	109.5	C31—C32—H32B	109.5
O1—C13—C14	125.3 (5)	H32A—C32—H32B	109.5
O1—C13—C12	115.3 (5)	C31—C32—H32C	109.5
C14—C13—C12	119.4 (5)	H32A—C32—H32C	109.5
C15—C14—C13	126.9 (5)	H32B—C32—H32C	109.5
C15—C14—H14	116.5	C1—N1—C5	120.5 (4)
C13—C14—H14	116.5	C1—N1—Pt1	123.8 (3)
O2—C15—C14	127.5 (5)	C5—N1—Pt1	115.7 (3)
O2—C15—C16	113.6 (5)	C17—N2—C21	120.4 (4)
C14—C15—C16	119.0 (4)	C17—N2—Pt2	124.1 (4)
C15—C16—H16A	109.5	C21—N2—Pt2	115.6 (3)
C15—C16—H16B	109.5	C13—O1—Pt1	123.8 (3)
H16A—C16—H16B	109.5	C15—O2—Pt1	124.2 (3)
C15—C16—H16C	109.5	C29—O3—Pt2	123.8 (4)
H16A—C16—H16C	109.5	C31—O4—Pt2	124.0 (3)
H16B—C16—H16C	109.5	C11—Pt1—N1	81.89 (18)
N2—C17—C18	121.9 (6)	C11—Pt1—O2	93.04 (17)
N2—C17—H17	119.1	N1—Pt1—O2	174.80 (15)
C18—C17—H17	119.1	C11—Pt1—O1	174.72 (17)
C17—C18—C19	119.3 (6)	N1—Pt1—O1	92.90 (15)
C17—C18—H18	120.3	O2—Pt1—O1	92.15 (14)
C19—C18—H18	120.3	C27—Pt2—N2	81.73 (18)
C18—C19—C20	119.6 (5)	C27—Pt2—O4	92.57 (17)
C18—C19—H19	120.2	N2—Pt2—O4	174.29 (15)
C20—C19—H19	120.2	C27—Pt2—O3	175.20 (17)
C19—C20—C21	119.7 (6)	N2—Pt2—O3	93.57 (16)
C19—C20—H20	120.1	O4—Pt2—O3	92.12 (13)

N1—C1—C2—C3	−0.6 (9)	C21—C22—C23—C24	177.1 (5)
C1—C2—C3—C4	−0.2 (9)	C22—C23—C24—C25	0.6 (8)
C2—C3—C4—C5	0.4 (9)	C23—C24—C25—C26	1.9 (8)
C3—C4—C5—N1	0.1 (7)	C23—C24—C25—Br2	−175.1 (4)
C3—C4—C5—C6	178.0 (5)	C24—C25—C26—C27	−2.4 (8)
N1—C5—C6—C7	178.2 (4)	Br2—C25—C26—C27	174.6 (4)
C4—C5—C6—C7	0.2 (8)	C25—C26—C27—C22	0.3 (7)
N1—C5—C6—C11	−2.2 (6)	C25—C26—C27—Pt2	−178.7 (4)
C4—C5—C6—C11	179.8 (4)	C23—C22—C27—C26	2.1 (7)
C11—C6—C7—C8	−0.4 (7)	C21—C22—C27—C26	−177.6 (4)
C5—C6—C7—C8	179.2 (5)	C23—C22—C27—Pt2	−178.8 (3)
C6—C7—C8—C9	−0.6 (8)	C21—C22—C27—Pt2	1.5 (5)
C7—C8—C9—C10	1.2 (8)	O3—C29—C30—C31	−0.6 (9)
C7—C8—C9—Br1	−179.5 (4)	C28—C29—C30—C31	179.8 (5)
C8—C9—C10—C11	−0.9 (8)	C29—C30—C31—O4	0.5 (9)
Br1—C9—C10—C11	179.8 (3)	C29—C30—C31—C32	178.3 (5)
C9—C10—C11—C6	−0.1 (7)	C2—C1—N1—C5	1.2 (8)
C9—C10—C11—Pt1	179.7 (4)	C2—C1—N1—Pt1	179.9 (4)
C7—C6—C11—C10	0.7 (7)	C4—C5—N1—C1	−0.9 (7)
C5—C6—C11—C10	−178.9 (4)	C6—C5—N1—C1	−179.1 (4)
C7—C6—C11—Pt1	−179.1 (4)	C4—C5—N1—Pt1	−179.7 (3)
C5—C6—C11—Pt1	1.3 (5)	C6—C5—N1—Pt1	2.1 (5)
O1—C13—C14—C15	−3.6 (9)	C18—C17—N2—C21	−0.8 (8)
C12—C13—C14—C15	175.8 (5)	C18—C17—N2—Pt2	179.5 (4)
C13—C14—C15—O2	3.9 (9)	C20—C21—N2—C17	0.9 (7)
C13—C14—C15—C16	−174.6 (5)	C22—C21—N2—C17	179.7 (4)
N2—C17—C18—C19	0.4 (9)	C20—C21—N2—Pt2	−179.4 (4)
C17—C18—C19—C20	−0.1 (9)	C22—C21—N2—Pt2	−0.6 (5)
C18—C19—C20—C21	0.3 (8)	C14—C13—O1—Pt1	0.3 (7)
C19—C20—C21—N2	−0.6 (8)	C12—C13—O1—Pt1	−179.0 (4)
C19—C20—C21—C22	−179.2 (5)	C14—C15—O2—Pt1	−0.7 (7)
N2—C21—C22—C23	179.7 (4)	C16—C15—O2—Pt1	177.9 (3)
C20—C21—C22—C23	−1.7 (8)	C30—C29—O3—Pt2	−1.2 (7)
N2—C21—C22—C27	−0.6 (6)	C28—C29—O3—Pt2	178.4 (3)
C20—C21—C22—C27	178.0 (5)	C30—C31—O4—Pt2	1.5 (7)
C27—C22—C23—C24	−2.6 (7)	C32—C31—O4—Pt2	−176.5 (4)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
C1—H1···O1	0.95	2.40	2.999 (7)	121
C4—H4···O4ⁱ	0.95	2.58	3.281 (6)	131
C17—H17···O3	0.95	2.45	3.034 (6)	120
C17—H17···Br1ⁱⁱ	0.95	2.87	3.693 (6)	145

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

Selected bond lengths (Å) top

O1—Pt1	2.077 (3)	O3—Pt2	2.081 (3)
O2—Pt1	2.007 (3)	O4—Pt2	2.005 (3)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
C1—H1···O1	0.95	2.40	2.999 (7)	120.6
C4—H4···O4ⁱ	0.95	2.58	3.281 (6)	130.9
C17—H17···O3	0.95	2.45	3.034 (6)	119.8
C17—H17···Br1ⁱⁱ	0.95	2.87	3.693 (6)	145.0

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

Experimental details

Crystal data
Chemical formula	[Pt(C₁₁H₇BrN)(C₅H₇O₂)]
M_r	527.28
Crystal system, space group	Monoclinic, C2/c
Temperature (K)	200
a, b, c (Å)	17.557 (2), 17.876 (2), 19.832 (2)
β (°)	91.397 (1)
V (Å³)	6222.4 (13)
Z	16
Radiation type	Mo Kα
µ (mm⁻¹)	11.59
Crystal size (mm)	0.18 × 0.06 × 0.02

Data collection
Diffractometer	Bruker APEXII CCD area detector diffractometer
Absorption correction	Multi-scan (SADABS; Bruker, 2014)
T_min, T_max	0.48, 0.80
No. of measured, independent and observed [I > 2σ(I)] reflections	35025, 7103, 6001
R_int	0.038
(sin θ/λ)_max (Å⁻¹)	0.649

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.027, 0.070, 1.01
No. of reflections	7103
No. of parameters	383
H-atom treatment	H-atom parameters constrained
	w = 1/[σ²(F_o²) + (0.0368P)² + 16.0306P] where P = (F_o² + 2F_c²)/3
Δρ_max, Δρ_min (e Å⁻³)	3.66, −1.19

Computer programs: APEX2 (Bruker, 2014), SAINT (Bruker, 2014), SHELXS97 (Sheldrick, 2008), SHELXL2014 (Sheldrick, 2015), ORTEP-3 for Windows (Farrugia, 2012) and Mercury (Macrae et al., 2008).

Acknowledgements

The authors thank Professor Takashi Fujihara (Saitama University) for providing an opportunity for X-ray crystallographic analysis. This work was supported by JSPS KAKENHI Grant-in-Aid for Young Scientists (B) (25810052 to TS), and partially by JSPS KAKENHI Grant No. 2540150.

References

Bondi, A. (1964). J. Phys. Chem. 68, 441–451. CrossRef CAS Web of Science Google Scholar
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Volume 71| Part 10| October 2015| Pages 1259-1261

doi:10.1107/S2056989015017478

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