Bis(1,3-dimesitylimidazol­yl)gold(I) 2,4,8,10-tetra­phenyl-1,3,5,7,9,11-hexa­oxa-2,4,8,10-tetra­bora-6-borataspiro­[5.5]undeca­ne

Möhlmann, L.; Wendt, O.F.; Johnson, M.T.

doi:10.1107/S1600536811016357

metal-organic compounds

CRYSTALLOGRAPHIC
COMMUNICATIONS

ISSN: 2056-9890

Volume 67| Part 6| June 2011| Pages m719-m720

doi:10.1107/S1600536811016357

Open

access

Bis(1,3-dimesitylimidazolyl)gold(I) 2,4,8,10-tetraphenyl-1,3,5,7,9,11-hexaoxa-2,4,8,10-tetrabora-6-borataspiro[5.5]undecane

Lennart Möhlmann,^a Ola F. Wendt ^a and Magnus T. Johnson ^a ^*

^aCentre for Analysis and Synthesis, Department of Chemistry, Lund University, PO Box 124, S-221 00 Lund, Sweden
^*Correspondence e-mail: magnus.johnson@organic.lu.se

(Received 15 April 2011; accepted 29 April 2011; online 7 May 2011)

The Au^I atom in the title compound, [Au(C₂₁H₂₄N₂)₂](C₂₄H₂₀B₅O₆), adopts a slightly distorted linear AuC₂ coordination geometry arising from its coordination by two mesitylenic N-heterocyclic carbene ligands, forming an overall cationic complex. The dihedral angle between the imidazole rings is 57.3 (6)°. In the crystal, the components are linked by weak C—H⋯O hydrogen bonds.

Related literature

For homoleptic bis-N-heterocyclic carbene complexes of gold(I), see, for example: Raubenheimer et al. (1996 ); Wang et al. (2005 ). For carbene complexes, see: Raubenheimer et al. (1996); Gaillard et al. (2010 ). For an overview of studies on a variety of bis-N-heterocyclic carbene complexes of gold(I) and their toxicity towards cancer cells, see: Teyssot et al. (2009 ) and for implications on mitochondrial directed chemoterapeutics, see: Baker et al. (2006 ); Barnard & Berners-Price (2007 ); Hickey et al. (2008 ). For a similar spiro tetraarylpentaborate anion, see Nishihara et al. (2004 ). The title compound was obtained as a side product in the synthesis of the (1,3-dimesitylimidazolium)gold phenyl complex in an attempt to transmetallate the NHC gold(I) tert-butoxide (Johnson et al., 2011) using phenyl boronic acid. A different approach leading to the NHC gold(I) phenyl complex was reported by Pazicky et al. (2010 ). For π–π interactions, see: Haddon (1982 ).

Experimental

Crystal data

[Au(C₂₁H₂₄N₂)₂](C₂₄H₂₀B₅O₆)
M_r = 1264.26
Triclinic, $[P \overline 1]$
a = 15.388 (2) Å
b = 15.768 (2) Å
c = 16.453 (2) Å
α = 94.81 (1)°
β = 112.86 (1)°
γ = 117.65 (1)°
V = 3083.2 Å³
Z = 2
Mo Kα radiation
μ = 2.44 mm⁻¹
T = 293 K
0.20 × 0.20 × 0.10 mm

Data collection

Oxford Diffraction Xcalibur-3 CCD diffractometer
Absorption correction: multi-scan (CrysAlis RED; Oxford Diffraction, 2006 $[Oxford Diffraction (2006). CrysAlis CCD and CrysAlis RED. Oxford Diffraction, Abingdon, England.]$ ) T_min = 0.838, T_max = 1.000
19866 measured reflections
10639 independent reflections
7217 reflections with I > 2σ(I)
R_int = 0.051

Refinement

R[F² > 2σ(F²)] = 0.046
wR(F²) = 0.152
S = 1.08
10639 reflections
751 parameters
H-atom parameters constrained
Δρ_max = 1.02 e Å⁻³
Δρ_min = −0.91 e Å⁻³

Table 1
Selected geometric parameters (Å, °)

Au1—C1	1.982 (7)
Au1—C22	1.990 (8)

C1—Au1—C22	176.8 (3)

Table 2
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
C3—H3⋯O1ⁱ	0.93	2.56	3.460 (10)	164
C18—H18C⋯O5ⁱⁱ	0.96	2.55	3.421 (14)	151
C24—H24⋯O3	0.93	2.57	3.421 (13)	153
C42—H42C⋯O6ⁱⁱⁱ	0.96	2.58	3.336 (16)	136
Symmetry codes: (i) x, y, z+1; (ii) -x, -y, -z+1; (iii) -x+1, -y, -z+1.

Data collection: CrysAlis CCD (Oxford Diffraction, 2006 $[Oxford Diffraction (2006). CrysAlis CCD and CrysAlis RED. Oxford Diffraction, Abingdon, England.]$ ); cell refinement: CrysAlis RED (Oxford Diffraction, 2006 $[Oxford Diffraction (2006). CrysAlis CCD and CrysAlis RED. Oxford Diffraction, Abingdon, England.]$ ); data reduction: CrysAlis RED; program(s) used to solve structure: SIR97 (Altomare et al., 1999 ); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ); molecular graphics: DIAMOND (Brandenburg, 2006 ); software used to prepare material for publication: SHELXL97.

Supporting information

Crystal structure: contains datablock global. DOI: 10.1107/S1600536811016357/hb5850sup1.cif

checkCIF report

Comment top

The title compound was obtained as a side product in the synthesis of the (1,3-dimesitylimidazolium)gold phenyl complex in an attempt to transmetallate the NHC gold(I) tert-butoxide (Johnson et al., 2011) using phenyl boronic acid. A different approach leading to the NHC gold(I) phenyl complex was reported by Pazicky et al. (2010).

The gold atom in compound (I) adopts a slightly distorted linear coordination geometry with a C1—Au—C22 angle of 176.8 (3)°. The coordination of two neutral ligands results in a delocalized positive charge which is balanced by the spiro tetraphenylpentaborate anion. The Au—C1 and Au—C22 coordination bonds of 1.982 (9) Å and 1.989 (9) Å, respectively, do not differ significantly with each other, but are slightly shorter than for example its 1,3-dimethylbenzimidazolium analogue at 2.054 (9) Å (Wang et al. 2005). This is as expected for a less electron deficient ligand. In the tetraphenylpentaborate anion, the boroxine rings are both flat due to a partial delocalization of electrons which is a result of π–π interactions between the filled p-orbitals of oxygen and vacant p-orbitals of boron (Haddon et al. 1982). Regarding the tetracoordinate boron, the four B—O bonds are in the range 1.43 (1)–1.47 (1) Å, in excellent agreement with the m-xylyl analogue 1.45 (2)–1.49 (1) Å (Nishihara et al. 2004). There is a weak C–H···O intermolecular interaction [H···O = 2.47–2.60 Å; C–H···O = 132–155°].

Related literature top

For homoleptic bis-N-heterocyclic carbene complexes of gold(I), see, for example: Raubenheimer et al. (1996); Wang et al. (2005). For carbene complexes, see: Raubenheimer et al. (1996); Gaillard et al. (2010). For an overview of studies on a variety of bis-N-heterocyclic carbene complexes of gold(I) of their toxicity towards cancer cells, see: Teyssot et al. (2009) and for implications on mitochondrial directed chemoterapeutics, see: Baker et al. (2006); Barnard & Berners-Price (2007); Hickey et al. (2008). For a similar spiro tetraarylpentaborate anion, see Nishihara et al. (2004). The title compound was obtained as a side product in the synthesis of the (1,3-dimesitylimidazolium)gold phenyl complex in an attempt to transmetallate the NHC gold(I) tert-butoxide (Johnson et al., 2011) using phenyl boronic acid. A different approach leading to the NHC gold(I) phenyl complex was reported by Pazicky et al. (2010). For π–π interactions, see: Haddon (1982).

Experimental top

Under inert conditions, IMesAuOtBu (100 mg, 0.18 mmol) was dissolved in 5 ml toluene. PhB(OH)₂ (42 mg, 0.35 mmol) was added together with Cs₂CO₃ (114 mg, 0.35 mmol). The suspension was stirred in the dark at 50 °C for 24 h. After cooling to room temperature, the mixture was filtered through Celite and the volatiles were removed in vacuo. Recrystallization of the resulting powder left colourless plates of the title compound.

Computing details top

Data collection: CrysAlis CCD (Oxford Diffraction, 2006); cell refinement: CrysAlis RED (Oxford Diffraction, 2006); data reduction: CrysAlis RED (Oxford Diffraction, 2006); program(s) used to solve structure: SIR97 (Altomare et al., 1999); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: DIAMOND (Brandenburg, 2006); software used to prepare material for publication: SHELXL97 (Sheldrick, 2008).

Figures top

Fig. 1. A molecular structure of the title compound with the atom-numbering scheme. Displacement ellipsoids are drawn at the 30 % probability level.

Bis(1,3-dimesitylimidazolyl)gold(I) 2,4,8,10-tetraphenyl-1,3,5,7,9,11-hexaoxa-2,4,8,10-tetrabora- 6-borataspiro[5.5]undecane top

Crystal data top

[Au(C₂₁H₂₄N₂)₂](C₂₄H₂₀B₅O₆)	Z = 2
M_r = 1264.26	F(000) = 1288
Triclinic, P1	D_x = 1.362 Mg m⁻³
Hall symbol: -P 1	Mo Kα radiation, λ = 0.71073 Å
a = 15.388 (2) Å	Cell parameters from 7585 reflections
b = 15.768 (2) Å	θ = 2.3–33.2°
c = 16.453 (2) Å	µ = 2.44 mm⁻¹
α = 94.81 (1)°	T = 293 K
β = 112.86 (1)°	Plate, colorless
γ = 117.65 (1)°	0.20 × 0.20 × 0.10 mm
V = 3083.2 Å³

Data collection top

Oxford Diffraction Xcalibur-3 CCD diffractometer	10639 independent reflections
Radiation source: Enhance (Mo) X-ray Source	7217 reflections with I > 2σ(I)
Graphite monochromator	R_int = 0.051
Detector resolution: 16.1829 pixels mm^-1	θ_max = 25.0°, θ_min = 2.3°
ω scans	h = −18→17
Absorption correction: multi-scan (CrysAlis RED; Oxford Diffraction, 2006)	k = −13→18
T_min = 0.838, T_max = 1.000	l = −19→19
19866 measured reflections

Refinement top

Refinement on F²	Primary atom site location: structure-invariant direct methods
Least-squares matrix: full	Secondary atom site location: difference Fourier map
R[F² > 2σ(F²)] = 0.046	Hydrogen site location: inferred from neighbouring sites
wR(F²) = 0.152	H-atom parameters constrained
S = 1.08	w = 1/[σ²(F_o²) + (0.0797P)²] where P = (F_o² + 2F_c²)/3
10639 reflections	(Δ/σ)_max = 0.002
751 parameters	Δρ_max = 1.02 e Å⁻³
0 restraints	Δρ_min = −0.91 e Å⁻³

Crystal data top

[Au(C₂₁H₂₄N₂)₂](C₂₄H₂₀B₅O₆)	γ = 117.65 (1)°
M_r = 1264.26	V = 3083.2 Å³
Triclinic, P1	Z = 2
a = 15.388 (2) Å	Mo Kα radiation
b = 15.768 (2) Å	µ = 2.44 mm⁻¹
c = 16.453 (2) Å	T = 293 K
α = 94.81 (1)°	0.20 × 0.20 × 0.10 mm
β = 112.86 (1)°

Data collection top

Oxford Diffraction Xcalibur-3 CCD diffractometer	10639 independent reflections
Absorption correction: multi-scan (CrysAlis RED; Oxford Diffraction, 2006)	7217 reflections with I > 2σ(I)
T_min = 0.838, T_max = 1.000	R_int = 0.051
19866 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.046	0 restraints
wR(F²) = 0.152	H-atom parameters constrained
S = 1.08	Δρ_max = 1.02 e Å⁻³
10639 reflections	Δρ_min = −0.91 e Å⁻³
751 parameters

Special details top

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

Refinement. Refinement of F² against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F², conventional R-factors R are based on F, with F set to zero for negative F². The threshold expression of F² > 2σ(F²) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F² are statistically about twice as large as those based on F, and R- factors based on ALL data will be even larger.

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

	x	y	z	U_iso*/U_eq
Au1	0.38230 (3)	0.16116 (2)	0.80812 (2)	0.05262 (14)
O5	0.2525 (4)	0.1693 (4)	0.2299 (3)	0.0546 (13)
O6	0.3904 (4)	0.1308 (4)	0.2674 (4)	0.0603 (14)
N2	0.4720 (5)	0.2319 (4)	1.0153 (4)	0.0499 (15)
O2	0.7074 (4)	0.3338 (4)	0.4622 (4)	0.0607 (14)
O3	0.5298 (4)	0.2002 (4)	0.4263 (4)	0.0581 (13)
O4	0.4233 (4)	0.2732 (4)	0.3694 (4)	0.0710 (17)
C1	0.3848 (6)	0.1842 (5)	0.9295 (5)	0.0443 (17)
C49	0.7431 (7)	0.4448 (6)	0.3638 (6)	0.057 (2)
O1	0.5531 (4)	0.2929 (4)	0.3195 (3)	0.0579 (13)
N1	0.2940 (6)	0.1477 (5)	0.9393 (4)	0.0557 (16)
C2	0.3269 (8)	0.1689 (6)	1.0337 (5)	0.060 (2)
H2	0.2795	0.1488	1.0598	0.072*
N3	0.3280 (6)	0.0399 (6)	0.6263 (5)	0.066 (2)
C22	0.3783 (6)	0.1303 (6)	0.6865 (5)	0.0530 (19)
C13	0.1819 (6)	0.0923 (6)	0.8632 (5)	0.0495 (18)
C4	0.5847 (7)	0.2853 (6)	1.0355 (5)	0.0508 (19)
N4	0.4279 (6)	0.1985 (6)	0.6507 (5)	0.070 (2)
C24	0.4102 (7)	0.1509 (8)	0.5677 (6)	0.065 (2)
H24	0.4375	0.1820	0.5300	0.079*
C61	0.1974 (6)	−0.0002 (5)	0.1391 (5)	0.0483 (17)
C14	0.1272 (7)	−0.0091 (6)	0.8245 (6)	0.060 (2)
C7	0.7416 (8)	0.4358 (7)	1.0543 (7)	0.076 (3)
H7	0.7770	0.5040	1.0593	0.091*
B1	0.4750 (8)	0.2237 (7)	0.3479 (7)	0.062 (3)
C34	0.2674 (7)	−0.0509 (7)	0.6360 (5)	0.057 (2)
C3	0.4360 (8)	0.2220 (6)	1.0793 (6)	0.061 (2)
H3	0.4809	0.2484	1.1437	0.073*
B4	0.3235 (7)	0.2549 (7)	0.3065 (6)	0.053 (2)
C55	0.2825 (7)	0.3239 (6)	0.3249 (6)	0.058 (2)
C5	0.6320 (7)	0.3859 (6)	1.0311 (6)	0.055 (2)
C43	0.6982 (6)	0.2235 (6)	0.5615 (6)	0.060 (2)
C66	0.2276 (7)	−0.0671 (6)	0.1204 (5)	0.057 (2)
H66	0.3027	−0.0461	0.1522	0.069*
C16	0.0202 (8)	−0.0594 (7)	0.7499 (6)	0.072 (3)
H16	−0.0189	−0.1293	0.7239	0.086*
C47	0.6888 (9)	0.1052 (7)	0.6477 (6)	0.067 (2)
H47	0.6463	0.0450	0.6561	0.081*
B5	0.2866 (8)	0.1053 (6)	0.2154 (6)	0.046 (2)
B2	0.6618 (8)	0.3522 (7)	0.3812 (7)	0.056 (2)
C35	0.1545 (8)	−0.0956 (8)	0.6019 (6)	0.068 (2)
C48	0.6397 (8)	0.1359 (7)	0.5772 (6)	0.071 (3)
H48	0.5626	0.0949	0.5383	0.085*
B3	0.6399 (8)	0.2525 (6)	0.4792 (6)	0.049 (2)
C25	0.4923 (9)	0.3063 (6)	0.6965 (6)	0.066 (2)
C20	0.1354 (8)	0.1461 (7)	0.8298 (6)	0.067 (2)
C62	0.0859 (7)	−0.0347 (7)	0.0891 (6)	0.072 (2)
H62	0.0621	0.0077	0.0993	0.086*
C19	0.0285 (8)	0.0937 (9)	0.7512 (7)	0.081 (3)
H19	−0.0029	0.1291	0.7245	0.097*
C10	0.7521 (9)	0.2952 (8)	1.0674 (7)	0.087 (3)
H10	0.7925	0.2644	1.0788	0.104*
C60	0.1821 (8)	0.3076 (7)	0.2628 (7)	0.077 (3)
H60	0.1347	0.2516	0.2090	0.092*
C38	0.1547 (9)	−0.2332 (8)	0.6637 (7)	0.083 (3)
C64	0.0418 (10)	−0.1930 (7)	0.0096 (7)	0.088 (3)
H64	−0.0105	−0.2577	−0.0335	0.106*
C17	−0.0299 (8)	−0.0094 (8)	0.7135 (6)	0.076 (3)
C11	0.6429 (8)	0.2401 (7)	1.0479 (6)	0.073 (3)
C26	0.6032 (10)	0.3520 (8)	0.7661 (8)	0.100 (4)
C56	0.3499 (8)	0.4098 (7)	0.3988 (7)	0.087 (3)
H56	0.4212	0.4255	0.4399	0.104*
C40	0.2671 (9)	−0.1834 (8)	0.6961 (7)	0.080 (3)
H40	0.3049	−0.2128	0.7261	0.096*
C46	0.7995 (11)	0.1648 (10)	0.7031 (8)	0.094 (3)
H46	0.8330	0.1424	0.7487	0.113*
C50	0.7072 (9)	0.4704 (8)	0.2884 (7)	0.087 (3)
H50	0.6320	0.4294	0.2435	0.104*
C8	0.8040 (8)	0.3937 (8)	1.0708 (7)	0.077 (3)
C53	0.9260 (9)	0.5923 (8)	0.4124 (8)	0.091 (3)
H53	1.0022	0.6327	0.4551	0.110*
C54	0.8563 (8)	0.5067 (7)	0.4283 (8)	0.087 (3)
H54	0.8858	0.4916	0.4819	0.105*
C41	0.3257 (7)	−0.0942 (7)	0.6868 (6)	0.074 (3)
C15	0.1828 (9)	−0.0663 (7)	0.8671 (7)	0.087 (3)
H15A	0.2378	−0.0563	0.8484	0.130*
H15B	0.1266	−0.1372	0.8455	0.130*
H15C	0.2185	−0.0410	0.9339	0.130*
C45	0.8633 (10)	0.2509 (12)	0.6984 (8)	0.111 (4)
H45	0.9394	0.2912	0.7411	0.134*
C37	0.1021 (8)	−0.1886 (9)	0.6225 (7)	0.095 (4)
H37	0.0267	−0.2191	0.6059	0.114*
C65	0.1522 (10)	−0.1616 (7)	0.0577 (7)	0.083 (3)
H65	0.1753	−0.2046	0.0476	0.099*
C44	0.8110 (8)	0.2829 (8)	0.6232 (7)	0.080 (3)
H44	0.8549	0.3443	0.6171	0.096*
C63	0.0079 (8)	−0.1300 (7)	0.0244 (7)	0.088 (3)
H63	−0.0671	−0.1511	−0.0089	0.105*
C42	0.4486 (8)	−0.0419 (8)	0.7250 (8)	0.103 (4)
H42A	0.4857	0.0169	0.7774	0.155*
H42B	0.4677	−0.0218	0.6778	0.155*
H42C	0.4720	−0.0868	0.7445	0.155*
C32	0.4382 (11)	0.3563 (8)	0.6753 (7)	0.088 (3)
C18	−0.1442 (8)	−0.0652 (10)	0.6316 (7)	0.113 (4)
H18A	−0.1455	−0.1023	0.5814	0.170*
H18B	−0.1640	−0.0181	0.6124	0.170*
H18C	−0.1970	−0.1115	0.6482	0.170*
C6	0.5682 (8)	0.4327 (7)	1.0191 (7)	0.079 (3)
H6A	0.6088	0.4923	1.0718	0.119*
H6B	0.4971	0.3860	1.0143	0.119*
H6C	0.5565	0.4510	0.9634	0.119*
C28	0.6574 (10)	0.4549 (9)	0.8149 (9)	0.122 (5)
H28	0.7316	0.4901	0.8620	0.146*
C57	0.3193 (11)	0.4744 (9)	0.4165 (9)	0.108 (4)
H57	0.3658	0.5290	0.4714	0.129*
C39	0.0928 (10)	−0.3329 (8)	0.6825 (9)	0.110 (4)
H39A	0.0663	−0.3221	0.7239	0.165*
H39B	0.1435	−0.3542	0.7105	0.165*
H39C	0.0304	−0.3843	0.6247	0.165*
C9	0.9243 (9)	0.4502 (11)	1.0940 (10)	0.127 (5)
H9A	0.9701	0.4943	1.1574	0.190*
H9B	0.9344	0.4894	1.0531	0.190*
H9C	0.9457	0.4030	1.0863	0.190*
C33	0.3176 (12)	0.3032 (11)	0.6007 (9)	0.138 (5)
H33A	0.3132	0.3318	0.5511	0.207*
H33B	0.2748	0.3114	0.6266	0.207*
H33C	0.2880	0.2325	0.5767	0.207*
C58	0.2200 (11)	0.4581 (10)	0.3530 (11)	0.121 (5)
H58	0.2004	0.5047	0.3606	0.145*
C21	0.1984 (10)	0.2590 (8)	0.8708 (9)	0.111 (4)
H21A	0.2570	0.2806	0.9333	0.167*
H21B	0.1480	0.2782	0.8716	0.167*
H21C	0.2306	0.2904	0.8336	0.167*
C59	0.1498 (10)	0.3724 (9)	0.2782 (9)	0.102 (4)
H59	0.0789	0.3575	0.2369	0.122*
C12	0.5882 (9)	0.1295 (7)	1.0455 (8)	0.108 (4)
H12A	0.5485	0.1187	1.0803	0.162*
H12B	0.6451	0.1148	1.0726	0.162*
H12C	0.5367	0.0858	0.9821	0.162*
C51	0.7768 (11)	0.5559 (9)	0.2732 (9)	0.120 (4)
H51	0.7487	0.5710	0.2192	0.144*
C27	0.6588 (10)	0.2926 (10)	0.7902 (9)	0.119 (4)
H27A	0.7196	0.3178	0.7763	0.179*
H27B	0.6049	0.2223	0.7542	0.179*
H27C	0.6871	0.3001	0.8554	0.179*
C31	0.4970 (14)	0.4580 (11)	0.7261 (10)	0.116 (4)
H31	0.4623	0.4940	0.7123	0.140*
C52	0.8854 (11)	0.6160 (8)	0.3386 (9)	0.109 (4)
H52	0.9321	0.6750	0.3311	0.131*
C29	0.6011 (16)	0.5039 (10)	0.7935 (10)	0.108 (4)
C30	0.6642 (14)	0.6165 (8)	0.8543 (11)	0.165 (8)
H30A	0.7294	0.6569	0.8481	0.247*
H30B	0.6865	0.6206	0.9185	0.247*
H30C	0.6153	0.6409	0.8338	0.247*
C36	0.0911 (9)	−0.0539 (10)	0.5597 (9)	0.114 (4)
H36A	0.1198	0.0093	0.6029	0.172*
H36B	0.0140	−0.0999	0.5427	0.172*
H36C	0.0965	−0.0427	0.5049	0.172*
C23	0.3475 (7)	0.0527 (8)	0.5503 (6)	0.074 (3)
H23	0.3213	0.0017	0.4979	0.089*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Au1	0.0546 (2)	0.0573 (2)	0.04296 (19)	0.02929 (16)	0.02380 (14)	0.00809 (13)
O5	0.050 (3)	0.054 (3)	0.047 (3)	0.030 (3)	0.012 (2)	0.013 (2)
O6	0.040 (3)	0.059 (3)	0.066 (4)	0.026 (3)	0.015 (3)	0.001 (3)
N2	0.061 (4)	0.053 (4)	0.034 (3)	0.032 (3)	0.020 (3)	0.013 (3)
O2	0.043 (3)	0.061 (3)	0.056 (3)	0.021 (3)	0.016 (3)	0.012 (3)
O3	0.046 (3)	0.063 (3)	0.058 (3)	0.026 (3)	0.022 (3)	0.025 (3)
O4	0.045 (3)	0.066 (4)	0.073 (4)	0.026 (3)	0.014 (3)	−0.012 (3)
C1	0.059 (5)	0.044 (4)	0.035 (4)	0.028 (4)	0.026 (4)	0.018 (3)
C49	0.052 (5)	0.048 (4)	0.054 (5)	0.019 (4)	0.020 (4)	0.009 (4)
O1	0.044 (3)	0.063 (3)	0.047 (3)	0.021 (3)	0.015 (3)	0.017 (3)
N1	0.062 (4)	0.051 (4)	0.051 (4)	0.028 (3)	0.029 (4)	0.012 (3)
C2	0.081 (6)	0.067 (5)	0.043 (5)	0.035 (5)	0.041 (5)	0.034 (4)
N3	0.054 (4)	0.071 (5)	0.056 (4)	0.030 (4)	0.022 (3)	−0.009 (4)
C22	0.044 (4)	0.059 (5)	0.055 (5)	0.024 (4)	0.029 (4)	0.013 (4)
C13	0.057 (5)	0.058 (5)	0.038 (4)	0.030 (4)	0.026 (4)	0.022 (4)
C4	0.062 (5)	0.058 (5)	0.032 (4)	0.038 (4)	0.015 (4)	0.013 (3)
N4	0.052 (4)	0.080 (5)	0.063 (5)	0.033 (4)	0.025 (4)	−0.007 (4)
C24	0.071 (6)	0.092 (7)	0.048 (5)	0.044 (6)	0.041 (5)	0.026 (5)
C61	0.047 (4)	0.053 (4)	0.038 (4)	0.022 (4)	0.020 (3)	0.015 (3)
C14	0.065 (5)	0.054 (5)	0.058 (5)	0.029 (4)	0.030 (4)	0.018 (4)
C7	0.077 (7)	0.065 (6)	0.078 (7)	0.034 (6)	0.037 (5)	0.019 (5)
B1	0.042 (5)	0.056 (6)	0.075 (7)	0.021 (5)	0.025 (5)	0.008 (5)
C34	0.052 (5)	0.072 (6)	0.039 (4)	0.034 (5)	0.017 (4)	0.003 (4)
C3	0.069 (6)	0.062 (5)	0.041 (5)	0.032 (5)	0.022 (4)	0.017 (4)
B4	0.048 (5)	0.060 (6)	0.042 (5)	0.029 (5)	0.014 (4)	0.013 (4)
C55	0.066 (6)	0.053 (5)	0.058 (5)	0.032 (4)	0.032 (4)	0.022 (4)
C5	0.065 (6)	0.053 (5)	0.057 (5)	0.033 (4)	0.036 (4)	0.033 (4)
C43	0.040 (5)	0.058 (5)	0.067 (6)	0.020 (4)	0.025 (4)	0.008 (4)
C66	0.051 (5)	0.061 (5)	0.047 (5)	0.025 (4)	0.020 (4)	0.015 (4)
C16	0.073 (6)	0.055 (5)	0.048 (5)	0.002 (5)	0.036 (5)	0.022 (4)
C47	0.098 (8)	0.093 (7)	0.057 (5)	0.066 (6)	0.054 (6)	0.052 (5)
B5	0.069 (6)	0.049 (5)	0.038 (4)	0.033 (5)	0.037 (4)	0.031 (4)
B2	0.048 (6)	0.056 (6)	0.052 (6)	0.023 (5)	0.021 (5)	0.005 (4)
C35	0.068 (6)	0.087 (7)	0.052 (5)	0.041 (6)	0.031 (5)	0.030 (5)
C48	0.058 (5)	0.075 (6)	0.070 (6)	0.037 (5)	0.026 (5)	−0.004 (5)
B3	0.055 (6)	0.048 (5)	0.047 (5)	0.027 (5)	0.027 (5)	0.013 (4)
C25	0.103 (7)	0.062 (5)	0.060 (6)	0.037 (6)	0.068 (6)	0.040 (5)
C20	0.077 (6)	0.068 (6)	0.072 (6)	0.046 (5)	0.042 (5)	0.029 (5)
C62	0.051 (5)	0.063 (6)	0.071 (6)	0.025 (5)	0.015 (4)	0.004 (5)
C19	0.065 (6)	0.101 (8)	0.081 (7)	0.052 (6)	0.031 (6)	0.031 (6)
C10	0.072 (7)	0.092 (8)	0.088 (7)	0.057 (6)	0.020 (6)	0.014 (6)
C60	0.061 (6)	0.061 (5)	0.097 (7)	0.033 (5)	0.031 (5)	0.014 (5)
C38	0.076 (7)	0.078 (7)	0.069 (6)	0.036 (6)	0.025 (5)	−0.004 (5)
C64	0.085 (8)	0.056 (6)	0.073 (7)	0.013 (6)	0.029 (6)	−0.006 (5)
C17	0.067 (6)	0.103 (8)	0.055 (6)	0.040 (6)	0.029 (5)	0.046 (6)
C11	0.064 (6)	0.065 (6)	0.068 (6)	0.041 (5)	0.008 (5)	0.001 (4)
C26	0.079 (8)	0.087 (8)	0.091 (8)	0.016 (6)	0.049 (7)	−0.008 (6)
C56	0.077 (7)	0.077 (6)	0.086 (7)	0.044 (6)	0.023 (5)	0.000 (5)
C40	0.089 (8)	0.073 (7)	0.072 (6)	0.051 (6)	0.029 (6)	0.005 (5)
C46	0.091 (9)	0.127 (10)	0.094 (9)	0.068 (8)	0.054 (8)	0.059 (8)
C50	0.075 (7)	0.077 (7)	0.067 (7)	0.023 (6)	0.021 (5)	0.022 (5)
C8	0.073 (6)	0.097 (8)	0.066 (6)	0.048 (6)	0.033 (5)	0.031 (5)
C53	0.073 (7)	0.081 (7)	0.072 (7)	0.007 (6)	0.037 (6)	0.026 (6)
C54	0.065 (6)	0.076 (7)	0.081 (7)	0.014 (5)	0.034 (6)	0.007 (5)
C41	0.059 (6)	0.068 (6)	0.074 (6)	0.033 (5)	0.022 (5)	−0.012 (5)
C15	0.096 (8)	0.068 (6)	0.080 (7)	0.045 (6)	0.028 (6)	0.026 (5)
C45	0.063 (7)	0.159 (12)	0.092 (9)	0.058 (8)	0.021 (6)	0.049 (9)
C37	0.053 (6)	0.129 (10)	0.070 (7)	0.045 (7)	0.016 (5)	−0.010 (7)
C65	0.099 (8)	0.072 (6)	0.067 (6)	0.042 (6)	0.040 (6)	0.003 (5)
C44	0.060 (6)	0.093 (7)	0.078 (7)	0.034 (5)	0.031 (5)	0.048 (6)
C63	0.061 (6)	0.071 (6)	0.079 (7)	0.019 (5)	0.016 (5)	−0.003 (5)
C42	0.067 (7)	0.103 (8)	0.129 (10)	0.060 (6)	0.027 (6)	0.010 (7)
C32	0.132 (10)	0.081 (7)	0.073 (7)	0.062 (7)	0.058 (7)	0.040 (6)
C18	0.059 (6)	0.164 (12)	0.083 (8)	0.043 (7)	0.021 (6)	0.066 (8)
C6	0.090 (7)	0.068 (6)	0.088 (7)	0.047 (6)	0.043 (6)	0.038 (5)
C28	0.082 (8)	0.094 (9)	0.118 (10)	−0.001 (7)	0.061 (7)	−0.034 (8)
C57	0.119 (10)	0.101 (8)	0.101 (9)	0.071 (8)	0.041 (8)	0.005 (7)
C39	0.098 (9)	0.077 (7)	0.120 (10)	0.030 (7)	0.047 (7)	0.014 (7)
C9	0.076 (8)	0.149 (12)	0.136 (12)	0.052 (8)	0.046 (8)	0.043 (9)
C33	0.144 (13)	0.153 (12)	0.114 (11)	0.109 (11)	0.027 (9)	0.030 (9)
C58	0.103 (10)	0.102 (9)	0.161 (13)	0.071 (8)	0.053 (9)	0.009 (9)
C21	0.123 (10)	0.070 (7)	0.144 (11)	0.059 (7)	0.058 (8)	0.037 (7)
C59	0.085 (8)	0.114 (9)	0.119 (10)	0.073 (8)	0.038 (7)	0.027 (8)
C12	0.101 (8)	0.067 (6)	0.127 (10)	0.058 (6)	0.019 (7)	0.014 (6)
C51	0.105 (9)	0.091 (8)	0.098 (9)	0.015 (8)	0.034 (8)	0.053 (7)
C27	0.083 (8)	0.124 (10)	0.114 (10)	0.060 (8)	0.020 (7)	−0.001 (8)
C31	0.150 (13)	0.117 (11)	0.110 (11)	0.090 (11)	0.064 (10)	0.040 (9)
C52	0.118 (10)	0.073 (7)	0.098 (9)	0.011 (7)	0.068 (8)	0.036 (7)
C29	0.177 (14)	0.098 (9)	0.104 (10)	0.071 (10)	0.114 (11)	0.055 (8)
C30	0.26 (2)	0.066 (8)	0.164 (14)	0.043 (10)	0.158 (15)	0.020 (8)
C36	0.056 (7)	0.138 (10)	0.133 (11)	0.053 (7)	0.034 (7)	0.026 (8)
C23	0.061 (6)	0.104 (8)	0.053 (5)	0.041 (6)	0.032 (4)	−0.003 (5)

Geometric parameters (Å, º) top

Au1—C1	1.982 (7)	C38—C39	1.547 (15)
Au1—C22	1.990 (8)	C64—C63	1.363 (13)
O5—B4	1.370 (10)	C64—C65	1.366 (14)
O5—B5	1.378 (9)	C64—H64	0.9300
O6—B5	1.315 (10)	C17—C18	1.486 (13)
O6—B1	1.470 (10)	C11—C12	1.533 (13)
N2—C1	1.331 (9)	C26—C28	1.407 (15)
N2—C3	1.356 (10)	C26—C27	1.519 (16)
N2—C4	1.407 (10)	C56—C57	1.358 (13)
O2—B3	1.360 (10)	C56—H56	0.9300
O2—B2	1.371 (11)	C40—C41	1.334 (14)
O3—B3	1.321 (10)	C40—H40	0.9300
O3—B1	1.427 (12)	C46—C45	1.285 (16)
O4—B4	1.348 (10)	C46—H46	0.9300
O4—B1	1.453 (10)	C50—C51	1.397 (14)
C1—N1	1.324 (9)	C50—H50	0.9300
C49—C50	1.329 (12)	C8—C9	1.493 (14)
C49—C54	1.387 (12)	C53—C52	1.307 (15)
C49—B2	1.560 (13)	C53—C54	1.406 (14)
O1—B2	1.331 (10)	C53—H53	0.9300
O1—B1	1.470 (12)	C54—H54	0.9300
N1—C2	1.388 (9)	C41—C42	1.480 (12)
N1—C13	1.430 (10)	C15—H15A	0.9600
C2—C3	1.302 (11)	C15—H15B	0.9600
C2—H2	0.9300	C15—H15C	0.9600
N3—C22	1.324 (9)	C45—C44	1.463 (14)
N3—C34	1.365 (11)	C45—H45	0.9300
N3—C23	1.404 (11)	C37—H37	0.9300
C22—N4	1.334 (11)	C65—H65	0.9300
C13—C20	1.368 (11)	C44—H44	0.9300
C13—C14	1.354 (10)	C63—H63	0.9300
C4—C11	1.352 (10)	C42—H42A	0.9600
C4—C5	1.428 (11)	C42—H42B	0.9600
N4—C24	1.361 (10)	C42—H42C	0.9600
N4—C25	1.443 (11)	C32—C31	1.390 (16)
C24—C23	1.317 (12)	C32—C33	1.506 (16)
C24—H24	0.9300	C18—H18A	0.9600
C61—C62	1.372 (11)	C18—H18B	0.9600
C61—C66	1.390 (10)	C18—H18C	0.9600
C61—B5	1.555 (11)	C6—H6A	0.9600
C14—C16	1.379 (12)	C6—H6B	0.9600
C14—C15	1.547 (12)	C6—H6C	0.9600
C7—C5	1.352 (12)	C28—C29	1.378 (18)
C7—C8	1.363 (13)	C28—H28	0.9300
C7—H7	0.9300	C57—C58	1.358 (16)
C34—C35	1.366 (11)	C57—H57	0.9300
C34—C41	1.432 (12)	C39—H39A	0.9600
C3—H3	0.9300	C39—H39B	0.9600
B4—C55	1.551 (11)	C39—H39C	0.9600
C55—C56	1.352 (11)	C9—H9A	0.9600
C55—C60	1.364 (12)	C9—H9B	0.9600
C5—C6	1.446 (11)	C9—H9C	0.9600
C43—C44	1.372 (11)	C33—H33A	0.9600
C43—C48	1.367 (12)	C33—H33B	0.9600
C43—B3	1.546 (12)	C33—H33C	0.9600
C66—C65	1.356 (11)	C58—C59	1.356 (15)
C66—H66	0.9300	C58—H58	0.9300
C16—C17	1.363 (13)	C21—H21A	0.9600
C16—H16	0.9300	C21—H21B	0.9600
C47—C46	1.334 (14)	C21—H21C	0.9600
C47—C48	1.380 (12)	C59—H59	0.9300
C47—H47	0.9300	C12—H12A	0.9600
C35—C36	1.420 (14)	C12—H12B	0.9600
C35—C37	1.453 (15)	C12—H12C	0.9600
C48—H48	0.9300	C51—C52	1.345 (16)
C25—C32	1.365 (13)	C51—H51	0.9300
C25—C26	1.395 (14)	C27—H27A	0.9600
C20—C19	1.403 (13)	C27—H27B	0.9600
C20—C21	1.501 (13)	C27—H27C	0.9600
C62—C63	1.378 (12)	C31—C29	1.315 (18)
C62—H62	0.9300	C31—H31	0.9300
C19—C17	1.370 (13)	C52—H52	0.9300
C19—H19	0.9300	C29—C30	1.563 (16)
C10—C11	1.363 (13)	C30—H30A	0.9600
C10—C8	1.361 (14)	C30—H30B	0.9600
C10—H10	0.9300	C30—H30C	0.9600
C60—C59	1.372 (12)	C36—H36A	0.9600
C60—H60	0.9300	C36—H36B	0.9600
C38—C37	1.338 (14)	C36—H36C	0.9600
C38—C40	1.359 (13)	C23—H23	0.9300

C1—Au1—C22	176.8 (3)	C45—C46—C47	124.9 (11)
B4—O5—B5	119.4 (6)	C45—C46—H46	117.5
B5—O6—B1	123.6 (6)	C47—C46—H46	117.5
C1—N2—C3	110.2 (7)	C49—C50—C51	123.3 (10)
C1—N2—C4	124.3 (6)	C49—C50—H50	118.4
C3—N2—C4	125.5 (6)	C51—C50—H50	118.4
B3—O2—B2	119.1 (7)	C10—C8—C7	116.7 (9)
B3—O3—B1	122.7 (7)	C10—C8—C9	119.7 (10)
B4—O4—B1	122.3 (7)	C7—C8—C9	123.6 (11)
N2—C1—N1	106.3 (6)	C52—C53—C54	120.9 (11)
N2—C1—Au1	129.3 (6)	C52—C53—H53	119.5
N1—C1—Au1	124.3 (5)	C54—C53—H53	119.5
C50—C49—C54	116.7 (9)	C49—C54—C53	119.8 (11)
C50—C49—B2	122.0 (8)	C49—C54—H54	120.1
C54—C49—B2	121.3 (9)	C53—C54—H54	120.1
B2—O1—B1	119.5 (7)	C40—C41—C34	118.9 (9)
C1—N1—C2	108.5 (7)	C40—C41—C42	121.1 (10)
C1—N1—C13	124.2 (6)	C34—C41—C42	120.0 (10)
C2—N1—C13	127.2 (7)	C14—C15—H15A	109.5
C3—C2—N1	107.6 (7)	C14—C15—H15B	109.5
C3—C2—H2	126.2	H15A—C15—H15B	109.5
N1—C2—H2	126.2	C14—C15—H15C	109.5
C22—N3—C34	126.1 (7)	H15A—C15—H15C	109.5
C22—N3—C23	108.7 (8)	H15B—C15—H15C	109.5
C34—N3—C23	125.2 (7)	C46—C45—C44	117.2 (11)
N3—C22—N4	106.9 (7)	C46—C45—H45	121.4
N3—C22—Au1	127.4 (7)	C44—C45—H45	121.4
N4—C22—Au1	125.7 (6)	C38—C37—C35	124.5 (10)
C20—C13—C14	122.3 (8)	C38—C37—H37	117.7
C20—C13—N1	117.4 (7)	C35—C37—H37	117.7
C14—C13—N1	120.2 (7)	C64—C65—C66	119.2 (9)
C11—C4—N2	121.6 (8)	C64—C65—H65	120.4
C11—C4—C5	120.4 (8)	C66—C65—H65	120.4
N2—C4—C5	117.5 (6)	C43—C44—C45	120.8 (10)
C22—N4—C24	109.9 (7)	C43—C44—H44	119.6
C22—N4—C25	123.5 (7)	C45—C44—H44	119.6
C24—N4—C25	126.6 (8)	C64—C63—C62	119.3 (9)
C23—C24—N4	107.8 (8)	C64—C63—H63	120.3
C23—C24—H24	126.1	C62—C63—H63	120.3
N4—C24—H24	126.1	C41—C42—H42A	109.5
C62—C61—C66	116.1 (7)	C41—C42—H42B	109.5
C62—C61—B5	123.3 (7)	H42A—C42—H42B	109.5
C66—C61—B5	120.6 (7)	C41—C42—H42C	109.5
C16—C14—C13	118.4 (8)	H42A—C42—H42C	109.5
C16—C14—C15	121.6 (8)	H42B—C42—H42C	109.5
C13—C14—C15	119.9 (8)	C25—C32—C31	118.1 (12)
C5—C7—C8	124.8 (9)	C25—C32—C33	121.6 (10)
C5—C7—H7	117.6	C31—C32—C33	120.3 (12)
C8—C7—H7	117.6	C17—C18—H18A	109.5
O3—B1—O4	110.9 (8)	C17—C18—H18B	109.5
O3—B1—O6	109.8 (7)	H18A—C18—H18B	109.5
O4—B1—O6	110.4 (6)	C17—C18—H18C	109.5
O3—B1—O1	112.2 (7)	H18A—C18—H18C	109.5
O4—B1—O1	106.7 (7)	H18B—C18—H18C	109.5
O6—B1—O1	106.7 (7)	C5—C6—H6A	109.5
C35—C34—N3	119.8 (8)	C5—C6—H6B	109.5
C35—C34—C41	121.7 (9)	H6A—C6—H6B	109.5
N3—C34—C41	118.5 (8)	C5—C6—H6C	109.5
C2—C3—N2	107.3 (7)	H6A—C6—H6C	109.5
C2—C3—H3	126.4	H6B—C6—H6C	109.5
N2—C3—H3	126.4	C29—C28—C26	120.4 (13)
O4—B4—O5	120.1 (7)	C29—C28—H28	119.8
O4—B4—C55	120.5 (7)	C26—C28—H28	119.8
O5—B4—C55	119.2 (7)	C58—C57—C56	119.1 (11)
C56—C55—C60	116.2 (8)	C58—C57—H57	120.4
C56—C55—B4	121.4 (8)	C56—C57—H57	120.4
C60—C55—B4	122.0 (7)	C38—C39—H39A	109.5
C7—C5—C6	124.4 (8)	C38—C39—H39B	109.5
C7—C5—C4	115.6 (7)	H39A—C39—H39B	109.5
C6—C5—C4	119.1 (8)	C38—C39—H39C	109.5
C44—C43—C48	115.7 (9)	H39A—C39—H39C	109.5
C44—C43—B3	122.7 (8)	H39B—C39—H39C	109.5
C48—C43—B3	121.6 (8)	C8—C9—H9A	109.5
C65—C66—C61	122.8 (8)	C8—C9—H9B	109.5
C65—C66—H66	118.6	H9A—C9—H9B	109.5
C61—C66—H66	118.6	C8—C9—H9C	109.5
C14—C16—C17	121.7 (9)	H9A—C9—H9C	109.5
C14—C16—H16	119.2	H9B—C9—H9C	109.5
C17—C16—H16	119.2	C32—C33—H33A	109.5
C46—C47—C48	117.6 (10)	C32—C33—H33B	109.5
C46—C47—H47	121.2	H33A—C33—H33B	109.5
C48—C47—H47	121.2	C32—C33—H33C	109.5
O6—B5—O5	120.9 (7)	H33A—C33—H33C	109.5
O6—B5—C61	120.8 (7)	H33B—C33—H33C	109.5
O5—B5—C61	118.2 (7)	C59—C58—C57	118.6 (10)
O1—B2—O2	121.5 (8)	C59—C58—H58	120.7
O1—B2—C49	121.4 (8)	C57—C58—H58	120.7
O2—B2—C49	117.1 (7)	C20—C21—H21A	109.5
C34—C35—C36	126.0 (10)	C20—C21—H21B	109.5
C34—C35—C37	113.9 (8)	H21A—C21—H21B	109.5
C36—C35—C37	119.7 (9)	C20—C21—H21C	109.5
C43—C48—C47	123.6 (9)	H21A—C21—H21C	109.5
C43—C48—H48	118.2	H21B—C21—H21C	109.5
C47—C48—H48	118.2	C58—C59—C60	120.8 (10)
O3—B3—O2	121.0 (8)	C58—C59—H59	119.6
O3—B3—C43	122.0 (8)	C60—C59—H59	119.6
O2—B3—C43	116.9 (7)	C11—C12—H12A	109.5
C32—C25—C26	123.6 (10)	C11—C12—H12B	109.5
C32—C25—N4	118.0 (10)	H12A—C12—H12B	109.5
C26—C25—N4	118.2 (9)	C11—C12—H12C	109.5
C13—C20—C19	118.1 (8)	H12A—C12—H12C	109.5
C13—C20—C21	121.9 (9)	H12B—C12—H12C	109.5
C19—C20—C21	119.9 (9)	C52—C51—C50	118.5 (11)
C61—C62—C63	122.2 (8)	C52—C51—H51	120.8
C61—C62—H62	118.9	C50—C51—H51	120.8
C63—C62—H62	118.9	C26—C27—H27A	109.5
C17—C19—C20	120.3 (9)	C26—C27—H27B	109.5
C17—C19—H19	119.8	H27A—C27—H27B	109.5
C20—C19—H19	119.8	C26—C27—H27C	109.5
C11—C10—C8	122.5 (9)	H27A—C27—H27C	109.5
C11—C10—H10	118.8	H27B—C27—H27C	109.5
C8—C10—H10	118.8	C29—C31—C32	120.6 (13)
C55—C60—C59	121.2 (9)	C29—C31—H31	119.7
C55—C60—H60	119.4	C32—C31—H31	119.7
C59—C60—H60	119.4	C53—C52—C51	120.8 (10)
C37—C38—C40	117.6 (11)	C53—C52—H52	119.6
C37—C38—C39	121.6 (11)	C51—C52—H52	119.6
C40—C38—C39	120.5 (11)	C31—C29—C28	122.0 (13)
C63—C64—C65	120.4 (9)	C31—C29—C30	120.3 (15)
C63—C64—H64	119.8	C28—C29—C30	117.7 (16)
C65—C64—H64	119.8	C29—C30—H30A	109.5
C19—C17—C16	119.0 (9)	C29—C30—H30B	109.5
C19—C17—C18	120.4 (10)	H30A—C30—H30B	109.5
C16—C17—C18	120.5 (10)	C29—C30—H30C	109.5
C4—C11—C10	119.3 (9)	H30A—C30—H30C	109.5
C4—C11—C12	119.9 (9)	H30B—C30—H30C	109.5
C10—C11—C12	120.6 (8)	C35—C36—H36A	109.5
C25—C26—C28	115.3 (12)	C35—C36—H36B	109.5
C25—C26—C27	121.9 (10)	H36A—C36—H36B	109.5
C28—C26—C27	122.7 (12)	C35—C36—H36C	109.5
C55—C56—C57	123.7 (10)	H36A—C36—H36C	109.5
C55—C56—H56	118.2	H36B—C36—H36C	109.5
C57—C56—H56	118.2	C24—C23—N3	106.6 (7)
C41—C40—C38	123.1 (10)	C24—C23—H23	126.7
C41—C40—H40	118.5	N3—C23—H23	126.7
C38—C40—H40	118.5

C3—N2—C1—N1	2.4 (8)	C44—C43—C48—C47	−2.3 (12)
C4—N2—C1—N1	−177.0 (6)	B3—C43—C48—C47	177.6 (7)
C3—N2—C1—Au1	−174.1 (5)	C46—C47—C48—C43	0.1 (13)
C4—N2—C1—Au1	6.4 (10)	B1—O3—B3—O2	1.1 (11)
C22—Au1—C1—N2	96 (5)	B1—O3—B3—C43	−177.6 (7)
C22—Au1—C1—N1	−80 (6)	B2—O2—B3—O3	−9.8 (11)
N2—C1—N1—C2	−3.5 (8)	B2—O2—B3—C43	168.9 (7)
Au1—C1—N1—C2	173.3 (5)	C44—C43—B3—O3	−172.8 (8)
N2—C1—N1—C13	179.0 (6)	C48—C43—B3—O3	7.3 (11)
Au1—C1—N1—C13	−4.2 (10)	C44—C43—B3—O2	8.5 (11)
C1—N1—C2—C3	3.4 (9)	C48—C43—B3—O2	−171.4 (7)
C13—N1—C2—C3	−179.2 (7)	C22—N4—C25—C32	−92.8 (10)
C34—N3—C22—N4	180.0 (7)	C24—N4—C25—C32	88.7 (10)
C23—N3—C22—N4	0.2 (9)	C22—N4—C25—C26	81.4 (10)
C34—N3—C22—Au1	0.6 (12)	C24—N4—C25—C26	−97.1 (11)
C23—N3—C22—Au1	−179.1 (6)	C14—C13—C20—C19	−1.6 (13)
C1—Au1—C22—N3	24 (6)	N1—C13—C20—C19	175.7 (8)
C1—Au1—C22—N4	−155 (5)	C14—C13—C20—C21	−177.5 (9)
C1—N1—C13—C20	−90.9 (9)	N1—C13—C20—C21	−0.2 (13)
C2—N1—C13—C20	92.1 (10)	C66—C61—C62—C63	0.2 (14)
C1—N1—C13—C14	86.5 (10)	B5—C61—C62—C63	−177.5 (9)
C2—N1—C13—C14	−90.5 (9)	C13—C20—C19—C17	4.3 (14)
C1—N2—C4—C11	−91.3 (9)	C21—C20—C19—C17	−179.7 (10)
C3—N2—C4—C11	89.4 (10)	C56—C55—C60—C59	−3.7 (15)
C1—N2—C4—C5	81.2 (9)	B4—C55—C60—C59	−176.7 (10)
C3—N2—C4—C5	−98.1 (9)	C20—C19—C17—C16	−4.0 (15)
N3—C22—N4—C24	−0.9 (9)	C20—C19—C17—C18	178.5 (9)
Au1—C22—N4—C24	178.4 (5)	C14—C16—C17—C19	0.9 (14)
N3—C22—N4—C25	−179.6 (8)	C14—C16—C17—C18	178.4 (9)
Au1—C22—N4—C25	−0.2 (12)	N2—C4—C11—C10	−180.0 (8)
C22—N4—C24—C23	1.3 (10)	C5—C4—C11—C10	7.8 (13)
C25—N4—C24—C23	179.9 (9)	N2—C4—C11—C12	−3.4 (12)
C20—C13—C14—C16	−1.3 (12)	C5—C4—C11—C12	−175.7 (8)
N1—C13—C14—C16	−178.6 (7)	C8—C10—C11—C4	−3.1 (15)
C20—C13—C14—C15	−178.3 (9)	C8—C10—C11—C12	−179.6 (10)
N1—C13—C14—C15	4.4 (12)	C32—C25—C26—C28	0.5 (15)
B3—O3—B1—O4	−104.5 (8)	N4—C25—C26—C28	−173.3 (9)
B3—O3—B1—O6	133.2 (7)	C32—C25—C26—C27	177.4 (10)
B3—O3—B1—O1	14.7 (10)	N4—C25—C26—C27	3.6 (15)
B4—O4—B1—O3	−142.2 (8)	C60—C55—C56—C57	4.8 (16)
B4—O4—B1—O6	−20.3 (12)	B4—C55—C56—C57	177.9 (11)
B4—O4—B1—O1	95.3 (9)	C37—C38—C40—C41	−1.4 (14)
B5—O6—B1—O3	131.3 (7)	C39—C38—C40—C41	−175.9 (9)
B5—O6—B1—O4	8.7 (12)	C48—C47—C46—C45	3.1 (17)
B5—O6—B1—O1	−106.8 (8)	C54—C49—C50—C51	−1.3 (16)
B2—O1—B1—O3	−23.1 (10)	B2—C49—C50—C51	176.6 (10)
B2—O1—B1—O4	98.6 (8)	C11—C10—C8—C7	0.5 (15)
B2—O1—B1—O6	−143.4 (7)	C11—C10—C8—C9	179.1 (10)
C22—N3—C34—C35	90.5 (10)	C5—C7—C8—C10	−3.0 (15)
C23—N3—C34—C35	−89.7 (10)	C5—C7—C8—C9	178.4 (10)
C22—N3—C34—C41	−86.1 (10)	C50—C49—C54—C53	0.9 (14)
C23—N3—C34—C41	93.7 (10)	B2—C49—C54—C53	−177.0 (9)
N1—C2—C3—N2	−1.8 (9)	C52—C53—C54—C49	1.6 (17)
C1—N2—C3—C2	−0.3 (9)	C38—C40—C41—C34	−3.5 (14)
C4—N2—C3—C2	179.1 (7)	C38—C40—C41—C42	178.7 (9)
B1—O4—B4—O5	18.6 (13)	C35—C34—C41—C40	4.0 (12)
B1—O4—B4—C55	−167.8 (8)	N3—C34—C41—C40	−179.5 (7)
B5—O5—B4—O4	−3.4 (12)	C35—C34—C41—C42	−178.2 (8)
B5—O5—B4—C55	−177.1 (7)	N3—C34—C41—C42	−1.7 (11)
O4—B4—C55—C56	7.2 (14)	C47—C46—C45—C44	−3.5 (19)
O5—B4—C55—C56	−179.1 (9)	C40—C38—C37—C35	6.3 (15)
O4—B4—C55—C60	179.9 (9)	C39—C38—C37—C35	−179.3 (9)
O5—B4—C55—C60	−6.4 (13)	C34—C35—C37—C38	−5.6 (14)
C8—C7—C5—C6	176.1 (9)	C36—C35—C37—C38	−178.7 (10)
C8—C7—C5—C4	7.4 (14)	C63—C64—C65—C66	0.0 (16)
C11—C4—C5—C7	−9.7 (11)	C61—C66—C65—C64	0.8 (14)
N2—C4—C5—C7	177.7 (7)	C48—C43—C44—C45	1.8 (14)
C11—C4—C5—C6	−179.1 (8)	B3—C43—C44—C45	−178.1 (9)
N2—C4—C5—C6	8.3 (11)	C46—C45—C44—C43	1.0 (17)
C62—C61—C66—C65	−0.9 (12)	C65—C64—C63—C62	−0.7 (17)
B5—C61—C66—C65	176.9 (8)	C61—C62—C63—C64	0.6 (16)
C13—C14—C16—C17	1.7 (13)	C26—C25—C32—C31	−0.2 (15)
C15—C14—C16—C17	178.6 (9)	N4—C25—C32—C31	173.6 (9)
B1—O6—B5—O5	4.7 (12)	C26—C25—C32—C33	−178.9 (11)
B1—O6—B5—C61	−172.2 (8)	N4—C25—C32—C33	−5.1 (15)
B4—O5—B5—O6	−8.1 (11)	C25—C26—C28—C29	0.4 (17)
B4—O5—B5—C61	168.8 (7)	C27—C26—C28—C29	−176.5 (11)
C62—C61—B5—O6	173.4 (8)	C55—C56—C57—C58	−6 (2)
C66—C61—B5—O6	−4.2 (11)	C56—C57—C58—C59	6 (2)
C62—C61—B5—O5	−3.5 (11)	C57—C58—C59—C60	−5 (2)
C66—C61—B5—O5	178.8 (7)	C55—C60—C59—C58	4.1 (19)
B1—O1—B2—O2	16.4 (11)	C49—C50—C51—C52	−1 (2)
B1—O1—B2—C49	−164.3 (7)	C25—C32—C31—C29	−1.0 (19)
B3—O2—B2—O1	0.7 (11)	C33—C32—C31—C29	177.7 (13)
B3—O2—B2—C49	−178.6 (6)	C54—C53—C52—C51	−4 (2)
C50—C49—B2—O1	2.0 (13)	C50—C51—C52—C53	3 (2)
C54—C49—B2—O1	179.7 (8)	C32—C31—C29—C28	2 (2)
C50—C49—B2—O2	−178.7 (8)	C32—C31—C29—C30	−176.2 (11)
C54—C49—B2—O2	−0.9 (12)	C26—C28—C29—C31	−2 (2)
N3—C34—C35—C36	−3.6 (14)	C26—C28—C29—C30	176.6 (10)
C41—C34—C35—C36	172.9 (9)	N4—C24—C23—N3	−1.1 (10)
N3—C34—C35—C37	−176.2 (7)	C22—N3—C23—C24	0.6 (10)
C41—C34—C35—C37	0.3 (12)	C34—N3—C23—C24	−179.2 (8)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
C3—H3···O1ⁱ	0.93	2.56	3.460 (10)	164
C18—H18C···O5ⁱⁱ	0.96	2.55	3.421 (14)	151
C24—H24···O3	0.93	2.57	3.421 (13)	153
C42—H42C···O6ⁱⁱⁱ	0.96	2.58	3.336 (16)	136

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

Experimental details

Crystal data
Chemical formula	[Au(C₂₁H₂₄N₂)₂](C₂₄H₂₀B₅O₆)
M_r	1264.26
Crystal system, space group	Triclinic, P1
Temperature (K)	293
a, b, c (Å)	15.388 (2), 15.768 (2), 16.453 (2)
α, β, γ (°)	94.81 (1), 112.86 (1), 117.65 (1)
V (Å³)	3083.2
Z	2
Radiation type	Mo Kα
µ (mm⁻¹)	2.44
Crystal size (mm)	0.20 × 0.20 × 0.10

Data collection
Diffractometer	Oxford Diffraction Xcalibur-3 CCD diffractometer
Absorption correction	Multi-scan (CrysAlis RED; Oxford Diffraction, 2006)
T_min, T_max	0.838, 1.000
No. of measured, independent and observed [I > 2σ(I)] reflections	19866, 10639, 7217
R_int	0.051
(sin θ/λ)_max (Å⁻¹)	0.595

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.046, 0.152, 1.08
No. of reflections	10639
No. of parameters	751
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	1.02, −0.91

Computer programs: CrysAlis CCD (Oxford Diffraction, 2006), CrysAlis RED (Oxford Diffraction, 2006), SIR97 (Altomare et al., 1999), SHELXL97 (Sheldrick, 2008), DIAMOND (Brandenburg, 2006).

Selected geometric parameters (Å, º) top

Au1—C1	1.982 (7)	Au1—C22	1.990 (8)

C1—Au1—C22	176.8 (3)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
C3—H3···O1ⁱ	0.93	2.56	3.460 (10)	164
C18—H18C···O5ⁱⁱ	0.96	2.55	3.421 (14)	151
C24—H24···O3	0.93	2.57	3.421 (13)	153
C42—H42C···O6ⁱⁱⁱ	0.96	2.58	3.336 (16)	136

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

Acknowledgements

Financial support from the Swedish Research Council and the Knut and Alice Wallenberg Foundation is gratefully acknowledged.

References

Altomare, A., Burla, M. C., Camalli, M., Cascarano, G. L., Giacovazzo, C., Guagliardi, A., Moliterni, A. G. G., Polidori, G. & Spagna, R. (1999). J. Appl. Cryst. 32, 115–119. Web of Science CrossRef CAS IUCr Journals Google Scholar
Baker, M. V., Barnard, P. J., Berners-Price, S. J., Brayshaw, S. K., Hickey, J. L., Skelton, B. W. & White, A. H. (2006). Dalton Trans. pp. 3708–3715. Web of Science CSD CrossRef Google Scholar
Barnard, P. J. & Berners-Price, S. J. (2007). Coord. Chem. Rev. 251, 1889–1902. Web of Science CrossRef CAS Google Scholar
Brandenburg, K. (2006). DIAMOND. Crystal Impact GbR, Bonn, Germany. Google Scholar
Gaillard, S., Nun, P., Slawin, A. M. Z. & Nolan, S. P. (2010). Organometallics, 29, 5402–5408. CrossRef CAS Google Scholar
Haddon, R. C. (1982). Pure Appl. Chem. 54, 1129–1142. CrossRef CAS Google Scholar
Hickey, J. L., Ruhayel, R. A., Barnard, P. J., Baker, M. V., Berners-Price, S. J. & Filipovska, A. (2008). J. Am. Chem. Soc. 130, 12570–12571. Web of Science CrossRef PubMed CAS Google Scholar
Johnson, M. T., van Rensburg, J. M. J., Axelsson, M., Ahlquist, M. S. G. & Wendt, O. F. (2011). In preparation. Google Scholar
Nishihara, Y., Nara, K., Nishide, Y. & Osakada, K. (2004). Dalton Trans. pp. 1366–1375. CrossRef Google Scholar
Oxford Diffraction (2006). CrysAlis CCD and CrysAlis RED. Oxford Diffraction, Abingdon, England. Google Scholar
Pazicky, M., Loos, A., Ferreira, M. J., Serra, D., Vinokurov, N., Rominger, F., Jakel, C., Hashmi, A. S. K. & Limbach, M. (2010). Organometallics, 29, 4448–4458. CAS Google Scholar
Raubenheimer, H. G., Lindeque, L. & Cronje, S. (1996). J. Organomet. Chem. 511, 177–184. CrossRef CAS Google Scholar
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. Web of Science CrossRef CAS IUCr Journals Google Scholar
Teyssot, M., Jarrousse, A., Manin, M., Chevry, A., Roche, S., Norre, F., Beaudoin, C., Morel, L., Boyer, D., Mahioue, R. & Gautier, A. (2009). Dalton Trans. pp. 6894–6902. Web of Science CrossRef PubMed Google Scholar
Wang, H. M. J., Vasam, C. S., Tsai, T. Y. R., Chen, S., Chang, A. H. H. & Lin, I. J. B. (2005). Organometallics, 24, 486–493. CrossRef Google Scholar

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.

CRYSTALLOGRAPHIC
COMMUNICATIONS

ISSN: 2056-9890

Volume 67| Part 6| June 2011| Pages m719-m720

doi:10.1107/S1600536811016357

Open

access

Format		BIBTeX
		EndNote
		RefMan
		Refer
		Medline
		CIF
		SGML
		Plain Text

Format		BIBTeX
		EndNote
		RefMan
		Refer
		Medline
		CIF
		SGML
		Plain Text

Search IUCr Journals		doi		Advanced search
Author		volume	page

metal-organic compounds\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

Bis(1,3-dimesitylimidazol­yl)gold(I) 2,4,8,10-tetra­phenyl-1,3,5,7,9,11-hexa­oxa-2,4,8,10-tetra­bora-6-borata­spiro­[5.5]undeca­ne

Related literature

Experimental

Crystal data

Data collection

Refinement

Supporting information

Acknowledgements

References

metal-organic compounds

Bis(1,3-dimesitylimidazolyl)gold(I) 2,4,8,10-tetraphenyl-1,3,5,7,9,11-hexaoxa-2,4,8,10-tetrabora-6-borataspiro[5.5]undecane