(Dimethyl­formamide)(2-methyl­propen­oato)[tris­(1-methyl-1H-benzimidazol-2-ylmeth­yl)amine]­manganese(II) perchlorate dimethyl­formamide solvate

Wu, H.; Jia, F.; Kong, J.; Kou, F.; Yuan, J.

doi:10.1107/S1600536810036457

metal-organic compounds

CRYSTALLOGRAPHIC
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ISSN: 2056-9890

Volume 66| Part 10| October 2010| Page m1270

doi:10.1107/S1600536810036457

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(Dimethylformamide)(2-methylpropenoato)[tris(1-methyl-1H-benzimidazol-2-ylmethyl)amine]manganese(II) perchlorate dimethylformamide solvate

Huilu Wu,^a ^* Fei Jia,^a Jin Kong,^a Fan Kou ^a and Jingkun Yuan ^a

^aSchool of Chemical and Biological Engineering, Lanzhou Jiaotong University, Lanzhou 730070, People's Republic of China
^*Correspondence e-mail: wuhuilu@163.com

(Received 24 August 2010; accepted 12 September 2010; online 18 September 2010)

In the title complex, [Mn(C₄H₅O₂)(C₂₇H₂₇N₇)(C₃H₇NO)]ClO₄·C₃H₇NO, the Mn^II ion is seven-coordinated in a distorted monocapped trigonal-prismatic geometry formed by a tetradentate tris(1-methyl-1H-benzimidazol-2-ylmethyl)amine molecule, a bidentate 2-methacrylate anion and a dimethylformamide molecule. The methyl groups of the coordinated dimethylformamide molecule and the perchlorate anions are disordered over two positions with occupancy factors of 0.640 (8) and 0.360 (8).

Related literature

For the biological activity of benzimidazole derivatives, see: Horton et al. (2003 ). For related structures, see: Wu et al. (2005 , 2009 ).

Experimental

Crystal data

[Mn(C₄H₅O₂)(C₂₇H₂₇N₇)(C₃H₇NO)]ClO₄·C₃H₇NO
M_r = 835.22
Triclinic, $[P \overline 1]$
a = 12.139 (5) Å
b = 12.354 (5) Å
c = 15.146 (6) Å
α = 89.168 (4)°
β = 71.098 (4)°
γ = 76.936 (5)°
V = 2088.9 (14) Å³
Z = 2
Mo Kα radiation
μ = 0.44 mm⁻¹
T = 296 K
0.38 × 0.34 × 0.30 mm

Data collection

Bruker APEXII area-detector diffractometer
Absorption correction: multi-scan (SADABS: Bruker, 2006 ) T_min = 0.851, T_max = 0.880
15471 measured reflections
7680 independent reflections
5422 reflections with I > 2σ(I)
R_int = 0.033

Refinement

R[F² > 2σ(F²)] = 0.059
wR(F²) = 0.187
S = 1.10
7680 reflections
525 parameters
8 restraints
H-atom parameters constrained
Δρ_max = 0.90 e Å⁻³
Δρ_min = −0.54 e Å⁻³

Data collection: APEX2 (Bruker, 2006); cell refinement: SAINT (Bruker, 2006); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXTL.

Supporting information

Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536810036457/is2590sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536810036457/is2590Isup2.hkl

checkCIF report

Comment top

The benzimidazole core is of a wide interest because of its diverse biological activities, and it is a well known structure in medicinal chemistry (Horton et al., 2003). We are interested in tris(2-benzimidazolylmethyl)amine and its derivatives and previously reported the crystal structure of some related complexes (Wu et al., 2009; Wu et al., 2005).

The asymmetric unit of the title compound consists of a discrete [Mn(Mentb)(2-methacrylato)(DMF)] cations, a perchlorate anions, and one molecule of DMF (Fig. 1). The Mentb ligand forms a tripodal pyramidal geometry with the manganese ion, and the remaining open axial site of the complex is occupied by a chelating 2-methacrylate anion and a monodentate DMF. The complex has a seven-coordinate manganese(II) geometry with a N₄O₃ donor set.

Related literature top

For the biological activity of benzimidazole derivatives, see: Horton et al. (2003). For related structures, see: Wu et al. (2005, 2009).

Experimental top

To a stirred solution of Mentb (0.5 mmol) in hot methanol (20 ml) was added Mn(ClO₄)₂.6 H₂O (0.5 mmol) followed by a solution of Na(2-methacrylate) (0.5 mmol) in methanol (5 ml), whereupon a colorless microcrystalline precipitate was produced and collected by filtration. After drying in air the colorless product was redissolved in DMF/methanol (1:1) and filtered. Light-yellow block-shaped crystals suitable for X-ray diffraction studies were obtained by vapor diffusion of diethyl ether into the filtrate for 4 weeks at room temperature (yield 0.34 g, 82%). Elemental analysis found: C 53.21, H 5.55, N 15.09%; calcd. for C₃₇H₄₆N₉O₈MnCl: C 53.04, H 5.39, N 15.13%.

Computing details top

Data collection: APEX2 (Bruker, 2006); cell refinement: SAINT (Bruker, 2006); data reduction: SAINT (Bruker, 2006); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXTL (Sheldrick, 2008).

Figures top

Fig. 1. Molecular structure and atom numbering of the title compound with displacement ellipsoides drawn at the 30% probability level. H atoms bonded to C atoms have been omitted for clarity.

(Dimethylformamide)(2-methylpropenoato)[tris(1-methyl-1H-benzimidazol- 2-ylmethyl)amine]manganese(II) perchlorate dimethylformamide solvate top

Crystal data top

[Mn(C₄H₅O₂)(C₂₇H₂₇N₇)(C₃H₇NO)]ClO₄·C₃H₇NO	Z = 2
M_r = 835.22	F(000) = 874
Triclinic, P1	D_x = 1.328 Mg m⁻³
Hall symbol: -P 1	Mo Kα radiation, λ = 0.71073 Å
a = 12.139 (5) Å	Cell parameters from 6078 reflections
b = 12.354 (5) Å	θ = 2.3–26.9°
c = 15.146 (6) Å	µ = 0.44 mm⁻¹
α = 89.168 (4)°	T = 296 K
β = 71.098 (4)°	Block, light-yellow
γ = 76.936 (5)°	0.38 × 0.34 × 0.30 mm
V = 2088.9 (14) Å³

Data collection top

Bruker APEXII area-detector diffractometer	7680 independent reflections
Radiation source: fine-focus sealed tube	5422 reflections with I > 2σ(I)
Graphite monochromator	R_int = 0.033
ω scans	θ_max = 25.5°, θ_min = 1.7°
Absorption correction: multi-scan (SADABS: Bruker, 2006)	h = −14→14
T_min = 0.851, T_max = 0.880	k = −14→13
15471 measured reflections	l = −18→18

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)] = 0.059	Hydrogen site location: inferred from neighbouring sites
wR(F²) = 0.187	H-atom parameters constrained
S = 1.10	w = 1/[σ²(F_o²) + (0.1111P)² + 0.1787P] where P = (F_o² + 2F_c²)/3
7680 reflections	(Δ/σ)_max = 0.001
525 parameters	Δρ_max = 0.90 e Å⁻³
8 restraints	Δρ_min = −0.54 e Å⁻³

Crystal data top

[Mn(C₄H₅O₂)(C₂₇H₂₇N₇)(C₃H₇NO)]ClO₄·C₃H₇NO	γ = 76.936 (5)°
M_r = 835.22	V = 2088.9 (14) Å³
Triclinic, P1	Z = 2
a = 12.139 (5) Å	Mo Kα radiation
b = 12.354 (5) Å	µ = 0.44 mm⁻¹
c = 15.146 (6) Å	T = 296 K
α = 89.168 (4)°	0.38 × 0.34 × 0.30 mm
β = 71.098 (4)°

Data collection top

Bruker APEXII area-detector diffractometer	7680 independent reflections
Absorption correction: multi-scan (SADABS: Bruker, 2006)	5422 reflections with I > 2σ(I)
T_min = 0.851, T_max = 0.880	R_int = 0.033
15471 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.059	8 restraints
wR(F²) = 0.187	H-atom parameters constrained
S = 1.10	Δρ_max = 0.90 e Å⁻³
7680 reflections	Δρ_min = −0.54 e Å⁻³
525 parameters

Special details top

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

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 > σ(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	Occ. (<1)
Mn1	0.78941 (4)	0.30677 (4)	0.72233 (3)	0.04338 (18)
Cl	0.42500 (11)	0.73755 (8)	0.62722 (8)	0.0706 (3)
O1	0.9336 (2)	0.3582 (2)	0.76647 (19)	0.0655 (7)
O2	0.8252 (3)	0.2580 (2)	0.86003 (18)	0.0720 (8)
O3	0.9336 (3)	0.1338 (2)	0.6630 (2)	0.0757 (8)
O4	0.4724 (4)	0.7215 (3)	0.7008 (3)	0.1208 (14)
O5	0.3586 (10)	0.6632 (8)	0.6261 (7)	0.101 (3)	0.640 (8)
O5'	0.3062 (18)	0.740 (4)	0.669 (2)	0.262 (15)	0.360 (8)
O6	0.5290 (5)	0.7232 (11)	0.5421 (4)	0.111 (3)	0.640 (8)
O6'	0.463 (3)	0.6437 (14)	0.5688 (19)	0.190 (13)	0.360 (8)
O7	0.3568 (13)	0.8430 (9)	0.6244 (10)	0.131 (5)	0.640 (8)
O7'	0.423 (3)	0.8347 (19)	0.5935 (19)	0.172 (16)	0.360 (8)
O8	0.3489 (4)	0.2371 (5)	0.7818 (4)	0.1465 (19)
N1	0.6526 (2)	0.4681 (2)	0.79600 (18)	0.0437 (6)
N2	0.4589 (2)	0.5539 (2)	0.85885 (19)	0.0494 (7)
N3	0.6674 (3)	0.1841 (2)	0.74261 (18)	0.0477 (6)
N4	0.6038 (3)	0.0753 (2)	0.66356 (19)	0.0524 (7)
N5	0.8692 (2)	0.3485 (2)	0.57493 (18)	0.0473 (6)
N6	0.8642 (3)	0.4395 (2)	0.4480 (2)	0.0581 (8)
N7	0.6286 (2)	0.3665 (2)	0.64674 (18)	0.0451 (6)
N8	1.0068 (5)	−0.0478 (4)	0.6781 (4)	0.1245 (16)
N9	0.2678 (5)	0.0927 (5)	0.7980 (4)	0.131 (2)
C1	0.5169 (3)	0.4191 (3)	0.7206 (2)	0.0513 (8)
H1A	0.4758	0.3625	0.7501	0.062*
H1B	0.4649	0.4698	0.6935	0.062*
C2	0.5432 (3)	0.4806 (3)	0.7911 (2)	0.0448 (7)
C3	0.3310 (3)	0.5872 (4)	0.8722 (3)	0.0681 (10)
H3A	0.3158	0.6501	0.8362	0.102*
H3B	0.2871	0.6071	0.9372	0.102*
H3C	0.3059	0.5265	0.8519	0.102*
C4	0.5162 (3)	0.5930 (3)	0.9121 (2)	0.0478 (8)
C5	0.4734 (4)	0.6652 (3)	0.9913 (2)	0.0601 (10)
H5	0.3921	0.6975	1.0184	0.072*
C6	0.5565 (4)	0.6868 (3)	1.0279 (2)	0.0631 (10)
H6	0.5309	0.7347	1.0812	0.076*
C7	0.6773 (4)	0.6392 (3)	0.9874 (3)	0.0639 (10)
H7	0.7313	0.6573	1.0132	0.077*
C8	0.7203 (3)	0.5645 (3)	0.9086 (2)	0.0538 (8)
H8	0.8017	0.5323	0.8819	0.065*
C9	0.6373 (3)	0.5401 (3)	0.8718 (2)	0.0438 (7)
C10	0.6214 (3)	0.2630 (3)	0.6052 (2)	0.0517 (8)
H10A	0.6855	0.2427	0.5459	0.062*
H10B	0.5456	0.2733	0.5939	0.062*
C11	0.6318 (3)	0.1731 (3)	0.6710 (2)	0.0454 (7)
C12	0.5611 (4)	0.0362 (3)	0.5929 (3)	0.0752 (12)
H12A	0.5215	0.0991	0.5677	0.113*
H12B	0.5060	−0.0092	0.6209	0.113*
H12C	0.6279	−0.0068	0.5436	0.113*
C13	0.6210 (3)	0.0157 (3)	0.7386 (2)	0.0541 (8)
C14	0.6035 (4)	−0.0882 (3)	0.7658 (3)	0.0721 (11)
H14	0.5785	−0.1335	0.7314	0.086*
C15	0.6253 (5)	−0.1200 (4)	0.8462 (3)	0.0934 (16)
H15	0.6138	−0.1888	0.8678	0.112*
C16	0.6642 (5)	−0.0528 (4)	0.8971 (3)	0.0887 (15)
H16	0.6786	−0.0784	0.9513	0.106*
C17	0.6822 (4)	0.0506 (3)	0.8695 (3)	0.0672 (11)
H17	0.7077	0.0954	0.9040	0.081*
C18	0.6601 (3)	0.0845 (3)	0.7875 (2)	0.0523 (8)
C19	0.6679 (3)	0.4447 (3)	0.5758 (2)	0.0509 (8)
H19A	0.6445	0.5197	0.6045	0.061*
H19B	0.6306	0.4440	0.5281	0.061*
C20	0.8004 (3)	0.4101 (3)	0.5331 (2)	0.0479 (8)
C21	0.8145 (5)	0.5073 (4)	0.3826 (3)	0.0786 (13)
H21A	0.8689	0.5514	0.3497	0.118*
H21B	0.7388	0.5554	0.4169	0.118*
H21C	0.8036	0.4591	0.3385	0.118*
C22	0.9825 (4)	0.3943 (3)	0.4344 (2)	0.0570 (9)
C23	1.0863 (5)	0.3980 (4)	0.3602 (3)	0.0747 (12)
H23	1.0833	0.4373	0.3079	0.090*
C24	1.1928 (5)	0.3405 (4)	0.3687 (3)	0.0857 (14)
H24	1.2636	0.3402	0.3205	0.103*
C25	1.1982 (4)	0.2829 (4)	0.4467 (3)	0.0795 (12)
H25	1.2724	0.2454	0.4499	0.095*
C26	1.0948 (4)	0.2799 (3)	0.5206 (3)	0.0679 (10)
H26	1.0985	0.2408	0.5730	0.081*
C27	0.9862 (3)	0.3374 (3)	0.5132 (2)	0.0517 (8)
C28	0.9084 (3)	0.3102 (3)	0.8409 (3)	0.0598 (10)
C29	0.9747 (6)	0.3139 (7)	0.9058 (4)	0.1252 (15)
C31	1.0517 (5)	0.3945 (6)	0.8873 (4)	0.1252 (15)
H31A	1.0836	0.3965	0.9374	0.188*
H31B	1.0051	0.4671	0.8830	0.188*
H31C	1.1162	0.3721	0.8295	0.188*
C30	0.9638 (5)	0.2499 (6)	0.9765 (4)	0.1252 (15)
H30A	0.9134	0.2011	0.9860	0.150*
H30B	1.0065	0.2532	1.0171	0.150*
C32	0.9487 (4)	0.0529 (4)	0.7078 (4)	0.0821 (13)
H32	0.9137	0.0652	0.7723	0.099*
C33	1.0101 (11)	−0.1517 (6)	0.7264 (8)	0.1245 (16)	0.640 (8)
H33A	0.9790	−0.1347	0.7928	0.187*	0.640 (8)
H33B	1.0913	−0.1945	0.7094	0.187*	0.640 (8)
H33C	0.9623	−0.1938	0.7087	0.187*	0.640 (8)
C33'	1.0174 (19)	−0.1210 (11)	0.7540 (9)	0.1245 (16)	0.360 (8)
H33D	1.0376	−0.0826	0.7992	0.187*	0.360 (8)
H33E	1.0790	−0.1872	0.7287	0.187*	0.360 (8)
H33F	0.9425	−0.1409	0.7838	0.187*	0.360 (8)
C34	1.0828 (9)	−0.0635 (7)	0.5788 (6)	0.1245 (16)	0.640 (8)
H34A	1.0330	−0.0483	0.5400	0.187*	0.640 (8)
H34B	1.1294	−0.1389	0.5655	0.187*	0.640 (8)
H34C	1.1353	−0.0135	0.5664	0.187*	0.640 (8)
C34'	1.0205 (19)	−0.1070 (12)	0.5909 (9)	0.1245 (16)	0.360 (8)
H34D	0.9432	−0.1006	0.5845	0.187*	0.360 (8)
H34E	1.0577	−0.1841	0.5919	0.187*	0.360 (8)
H34F	1.0697	−0.0751	0.5390	0.187*	0.360 (8)
C35	0.3276 (6)	0.1548 (7)	0.8206 (5)	0.122 (2)
H35	0.3562	0.1350	0.8701	0.146*
C36	0.2514 (11)	−0.0045 (10)	0.8492 (8)	0.230 (6)
H36A	0.3055	−0.0197	0.8846	0.345*
H36B	0.2674	−0.0670	0.8063	0.345*
H36C	0.1704	0.0083	0.8910	0.345*
C37	0.2181 (7)	0.1126 (8)	0.7233 (7)	0.190 (5)
H37A	0.1323	0.1307	0.7489	0.286*
H37B	0.2447	0.0470	0.6818	0.286*
H37C	0.2442	0.1735	0.6894	0.286*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Mn1	0.0455 (3)	0.0413 (3)	0.0407 (3)	−0.0102 (2)	−0.0107 (2)	0.0032 (2)
Cl	0.0939 (8)	0.0588 (6)	0.0796 (7)	−0.0275 (6)	−0.0500 (7)	0.0179 (5)
O1	0.0589 (16)	0.0718 (18)	0.0626 (16)	−0.0108 (14)	−0.0186 (14)	−0.0053 (14)
O2	0.0749 (19)	0.0780 (19)	0.0576 (14)	−0.0080 (16)	−0.0216 (14)	0.0110 (13)
O3	0.0718 (19)	0.0590 (18)	0.085 (2)	−0.0056 (14)	−0.0164 (16)	0.0000 (15)
O4	0.178 (4)	0.139 (3)	0.104 (3)	−0.088 (3)	−0.092 (3)	0.047 (2)
O5	0.133 (7)	0.091 (6)	0.129 (6)	−0.078 (5)	−0.076 (6)	0.039 (5)
O5'	0.100 (13)	0.31 (4)	0.31 (3)	0.021 (18)	−0.026 (16)	0.07 (3)
O6	0.066 (4)	0.176 (9)	0.081 (4)	−0.014 (4)	−0.020 (3)	0.017 (5)
O6'	0.31 (3)	0.089 (11)	0.21 (2)	0.070 (15)	−0.21 (2)	−0.072 (13)
O7	0.165 (9)	0.061 (6)	0.132 (8)	0.018 (7)	−0.033 (7)	0.007 (5)
O7'	0.36 (4)	0.11 (2)	0.15 (2)	−0.15 (3)	−0.17 (3)	0.093 (17)
O8	0.106 (3)	0.148 (5)	0.172 (5)	−0.058 (3)	−0.007 (3)	−0.030 (4)
N1	0.0414 (15)	0.0390 (14)	0.0439 (14)	−0.0062 (12)	−0.0071 (12)	0.0013 (11)
N2	0.0401 (15)	0.0471 (16)	0.0472 (15)	−0.0060 (13)	0.0012 (13)	0.0081 (13)
N3	0.0549 (17)	0.0387 (15)	0.0468 (15)	−0.0130 (13)	−0.0122 (14)	0.0066 (12)
N4	0.0658 (19)	0.0438 (16)	0.0499 (16)	−0.0199 (14)	−0.0172 (15)	0.0031 (13)
N5	0.0503 (16)	0.0414 (15)	0.0434 (14)	−0.0120 (13)	−0.0053 (13)	0.0017 (12)
N6	0.077 (2)	0.0525 (18)	0.0455 (16)	−0.0262 (16)	−0.0139 (16)	0.0113 (13)
N7	0.0509 (16)	0.0371 (14)	0.0464 (15)	−0.0133 (12)	−0.0131 (13)	0.0079 (11)
N8	0.130 (3)	0.060 (2)	0.192 (4)	0.000 (2)	−0.078 (3)	−0.022 (3)
N9	0.098 (4)	0.134 (5)	0.145 (5)	−0.048 (3)	−0.003 (3)	−0.058 (4)
C1	0.0450 (19)	0.047 (2)	0.061 (2)	−0.0115 (15)	−0.0166 (17)	0.0082 (16)
C2	0.0453 (19)	0.0389 (17)	0.0443 (17)	−0.0098 (14)	−0.0073 (15)	0.0099 (14)
C3	0.044 (2)	0.071 (3)	0.072 (3)	−0.0028 (19)	−0.0036 (19)	0.010 (2)
C4	0.055 (2)	0.0366 (17)	0.0406 (17)	−0.0086 (15)	−0.0026 (16)	0.0096 (14)
C5	0.070 (3)	0.044 (2)	0.0439 (19)	−0.0052 (18)	0.0059 (19)	0.0069 (15)
C6	0.091 (3)	0.045 (2)	0.0378 (18)	−0.007 (2)	−0.007 (2)	−0.0021 (15)
C7	0.084 (3)	0.056 (2)	0.052 (2)	−0.014 (2)	−0.024 (2)	0.0008 (17)
C8	0.056 (2)	0.050 (2)	0.0482 (19)	−0.0062 (16)	−0.0115 (17)	0.0012 (16)
C9	0.0522 (19)	0.0360 (17)	0.0358 (16)	−0.0097 (14)	−0.0048 (15)	0.0055 (13)
C10	0.067 (2)	0.0474 (19)	0.0470 (18)	−0.0198 (17)	−0.0222 (18)	0.0062 (15)
C11	0.0483 (19)	0.0400 (17)	0.0454 (17)	−0.0137 (15)	−0.0096 (15)	0.0022 (14)
C12	0.107 (4)	0.060 (2)	0.071 (3)	−0.037 (2)	−0.033 (3)	0.000 (2)
C13	0.062 (2)	0.0429 (19)	0.0512 (19)	−0.0149 (17)	−0.0080 (18)	0.0042 (15)
C14	0.093 (3)	0.047 (2)	0.073 (3)	−0.028 (2)	−0.016 (2)	0.0063 (19)
C15	0.147 (5)	0.055 (3)	0.078 (3)	−0.039 (3)	−0.027 (3)	0.026 (2)
C16	0.139 (5)	0.066 (3)	0.060 (3)	−0.030 (3)	−0.027 (3)	0.026 (2)
C17	0.091 (3)	0.055 (2)	0.055 (2)	−0.018 (2)	−0.022 (2)	0.0100 (18)
C18	0.055 (2)	0.0433 (19)	0.0521 (19)	−0.0105 (16)	−0.0105 (17)	0.0093 (15)
C19	0.066 (2)	0.0404 (18)	0.0482 (18)	−0.0148 (16)	−0.0204 (18)	0.0109 (14)
C20	0.063 (2)	0.0402 (18)	0.0401 (17)	−0.0207 (16)	−0.0112 (17)	0.0035 (14)
C21	0.108 (4)	0.079 (3)	0.059 (2)	−0.043 (3)	−0.028 (2)	0.032 (2)
C22	0.073 (3)	0.0433 (19)	0.0475 (19)	−0.0252 (18)	−0.0015 (19)	−0.0051 (15)
C23	0.093 (3)	0.065 (3)	0.055 (2)	−0.040 (3)	0.005 (2)	−0.0015 (19)
C24	0.082 (3)	0.072 (3)	0.081 (3)	−0.040 (3)	0.019 (3)	−0.010 (2)
C25	0.058 (3)	0.071 (3)	0.093 (3)	−0.019 (2)	0.001 (2)	−0.009 (3)
C26	0.061 (3)	0.059 (2)	0.073 (3)	−0.015 (2)	−0.007 (2)	−0.006 (2)
C27	0.056 (2)	0.0402 (18)	0.0497 (19)	−0.0172 (16)	−0.0013 (17)	−0.0059 (15)
C28	0.048 (2)	0.064 (2)	0.059 (2)	0.0026 (19)	−0.0163 (19)	−0.0164 (19)
C29	0.091 (2)	0.182 (4)	0.095 (2)	0.011 (2)	−0.048 (2)	−0.026 (2)
C31	0.091 (2)	0.182 (4)	0.095 (2)	0.011 (2)	−0.048 (2)	−0.026 (2)
C30	0.091 (2)	0.182 (4)	0.095 (2)	0.011 (2)	−0.048 (2)	−0.026 (2)
C32	0.067 (3)	0.054 (3)	0.113 (4)	−0.011 (2)	−0.015 (3)	0.001 (3)
C33	0.130 (3)	0.060 (2)	0.192 (4)	0.000 (2)	−0.078 (3)	−0.022 (3)
C33'	0.130 (3)	0.060 (2)	0.192 (4)	0.000 (2)	−0.078 (3)	−0.022 (3)
C34	0.130 (3)	0.060 (2)	0.192 (4)	0.000 (2)	−0.078 (3)	−0.022 (3)
C34'	0.130 (3)	0.060 (2)	0.192 (4)	0.000 (2)	−0.078 (3)	−0.022 (3)
C35	0.098 (5)	0.147 (7)	0.112 (5)	−0.042 (5)	−0.010 (4)	−0.047 (5)
C36	0.237 (13)	0.191 (11)	0.210 (11)	−0.105 (10)	0.035 (9)	−0.064 (9)
C37	0.131 (6)	0.195 (9)	0.251 (10)	0.021 (6)	−0.106 (7)	−0.111 (8)

Geometric parameters (Å, º) top

Mn1—N5	2.231 (3)	C10—C11	1.493 (4)
Mn1—O1	2.278 (3)	C10—H10A	0.9700
Mn1—N3	2.301 (3)	C10—H10B	0.9700
Mn1—O2	2.310 (3)	C12—H12A	0.9600
Mn1—N1	2.311 (3)	C12—H12B	0.9600
Mn1—O3	2.405 (3)	C12—H12C	0.9600
Mn1—N7	2.538 (3)	C13—C14	1.384 (5)
Cl—O7'	1.30 (2)	C13—C18	1.388 (5)
Cl—O5	1.356 (5)	C14—C15	1.362 (6)
Cl—O6'	1.365 (12)	C14—H14	0.9300
Cl—O5'	1.37 (2)	C15—C16	1.392 (7)
Cl—O7	1.385 (11)	C15—H15	0.9300
Cl—O4	1.403 (3)	C16—C17	1.380 (6)
Cl—O6	1.462 (6)	C16—H16	0.9300
O1—C28	1.248 (5)	C17—C18	1.393 (5)
O2—C28	1.272 (5)	C17—H17	0.9300
O3—C32	1.212 (5)	C19—C20	1.487 (5)
O8—C35	1.203 (9)	C19—H19A	0.9700
N1—C2	1.328 (4)	C19—H19B	0.9700
N1—C9	1.401 (4)	C21—H21A	0.9600
N2—C2	1.359 (4)	C21—H21B	0.9600
N2—C4	1.377 (4)	C21—H21C	0.9600
N2—C3	1.460 (4)	C22—C27	1.386 (5)
N3—C11	1.310 (4)	C22—C23	1.400 (6)
N3—C18	1.403 (4)	C23—C24	1.373 (7)
N4—C11	1.343 (4)	C23—H23	0.9300
N4—C13	1.391 (4)	C24—C25	1.382 (7)
N4—C12	1.461 (4)	C24—H24	0.9300
N5—C20	1.312 (4)	C25—C26	1.393 (6)
N5—C27	1.401 (4)	C25—H25	0.9300
N6—C20	1.364 (4)	C26—C27	1.388 (5)
N6—C22	1.365 (5)	C26—H26	0.9300
N6—C21	1.477 (5)	C28—C29	1.464 (6)
N7—C10	1.465 (4)	C29—C30	1.312 (10)
N7—C1	1.466 (4)	C29—C31	1.478 (10)
N7—C19	1.471 (4)	C31—H31A	0.9600
N8—C32	1.289 (6)	C31—H31B	0.9600
N8—C34'	1.462 (7)	C31—H31C	0.9600
N8—C33	1.467 (6)	C30—H30A	0.9300
N8—C33'	1.473 (7)	C30—H30B	0.9300
N8—C34	1.476 (7)	C32—H32	0.9300
N9—C35	1.286 (7)	C33—H33A	0.9600
N9—C36	1.437 (12)	C33—H33B	0.9600
N9—C37	1.439 (10)	C33—H33C	0.9600
C1—C2	1.475 (5)	C33'—H33D	0.9600
C1—H1A	0.9700	C33'—H33E	0.9600
C1—H1B	0.9700	C33'—H33F	0.9600
C3—H3A	0.9600	C34—H34A	0.9600
C3—H3B	0.9600	C34—H34B	0.9600
C3—H3C	0.9600	C34—H34C	0.9600
C4—C5	1.387 (5)	C34'—H34D	0.9600
C4—C9	1.399 (5)	C34'—H34E	0.9600
C5—C6	1.373 (6)	C34'—H34F	0.9600
C5—H5	0.9300	C35—H35	0.9300
C6—C7	1.382 (6)	C36—H36A	0.9600
C6—H6	0.9300	C36—H36B	0.9600
C7—C8	1.400 (5)	C36—H36C	0.9600
C7—H7	0.9300	C37—H37A	0.9600
C8—C9	1.387 (5)	C37—H37B	0.9600
C8—H8	0.9300	C37—H37C	0.9600

N5—Mn1—O1	92.23 (10)	N4—C11—C10	123.6 (3)
N5—Mn1—N3	115.22 (10)	N4—C12—H12A	109.5
O1—Mn1—N3	145.55 (10)	N4—C12—H12B	109.5
N5—Mn1—O2	145.57 (11)	H12A—C12—H12B	109.5
O1—Mn1—O2	56.72 (11)	N4—C12—H12C	109.5
N3—Mn1—O2	90.47 (10)	H12A—C12—H12C	109.5
N5—Mn1—N1	105.01 (10)	H12B—C12—H12C	109.5
O1—Mn1—N1	90.47 (10)	C14—C13—C18	123.6 (3)
N3—Mn1—N1	101.20 (10)	C14—C13—N4	131.2 (3)
O2—Mn1—N1	90.95 (10)	C18—C13—N4	105.3 (3)
N5—Mn1—O3	80.88 (11)	C15—C14—C13	115.8 (4)
O1—Mn1—O3	86.30 (10)	C15—C14—H14	122.1
N3—Mn1—O3	78.50 (10)	C13—C14—H14	122.1
O2—Mn1—O3	82.48 (11)	C14—C15—C16	122.1 (4)
N1—Mn1—O3	173.41 (9)	C14—C15—H15	119.0
N5—Mn1—N7	69.34 (10)	C16—C15—H15	119.0
O1—Mn1—N7	145.78 (10)	C17—C16—C15	122.0 (4)
N3—Mn1—N7	67.56 (9)	C17—C16—H16	119.0
O2—Mn1—N7	144.83 (10)	C15—C16—H16	119.0
N1—Mn1—N7	68.32 (9)	C16—C17—C18	116.7 (4)
O3—Mn1—N7	117.15 (10)	C16—C17—H17	121.7
O7'—Cl—O6'	120.4 (15)	C18—C17—H17	121.7
O7'—Cl—O5'	102.9 (18)	C13—C18—C17	119.9 (3)
O6'—Cl—O5'	101.4 (18)	C13—C18—N3	109.6 (3)
O5—Cl—O7	107.9 (8)	C17—C18—N3	130.5 (3)
O7'—Cl—O4	114.3 (9)	N7—C19—C20	108.4 (3)
O5—Cl—O4	111.4 (3)	N7—C19—H19A	110.0
O6'—Cl—O4	110.8 (5)	C20—C19—H19A	110.0
O5'—Cl—O4	104.3 (13)	N7—C19—H19B	110.0
O7—Cl—O4	116.3 (7)	C20—C19—H19B	110.0
O5—Cl—O6	111.2 (5)	H19A—C19—H19B	108.4
O7—Cl—O6	104.7 (6)	N5—C20—N6	112.4 (3)
O4—Cl—O6	105.2 (3)	N5—C20—C19	123.0 (3)
C28—O1—Mn1	92.8 (2)	N6—C20—C19	124.6 (3)
C28—O2—Mn1	90.7 (2)	N6—C21—H21A	109.5
C32—O3—Mn1	125.4 (3)	N6—C21—H21B	109.5
C2—N1—C9	104.4 (3)	H21A—C21—H21B	109.5
C2—N1—Mn1	115.8 (2)	N6—C21—H21C	109.5
C9—N1—Mn1	135.5 (2)	H21A—C21—H21C	109.5
C2—N2—C4	107.6 (3)	H21B—C21—H21C	109.5
C2—N2—C3	126.6 (3)	N6—C22—C27	106.0 (3)
C4—N2—C3	125.8 (3)	N6—C22—C23	131.8 (4)
C11—N3—C18	104.4 (3)	C27—C22—C23	122.2 (4)
C11—N3—Mn1	113.6 (2)	C24—C23—C22	116.5 (4)
C18—N3—Mn1	135.2 (2)	C24—C23—H23	121.7
C11—N4—C13	106.8 (3)	C22—C23—H23	121.7
C11—N4—C12	128.2 (3)	C23—C24—C25	122.1 (4)
C13—N4—C12	125.0 (3)	C23—C24—H24	118.9
C20—N5—C27	105.0 (3)	C25—C24—H24	118.9
C20—N5—Mn1	119.5 (2)	C24—C25—C26	121.3 (5)
C27—N5—Mn1	134.8 (2)	C24—C25—H25	119.4
C20—N6—C22	107.3 (3)	C26—C25—H25	119.4
C20—N6—C21	126.3 (3)	C27—C26—C25	117.5 (4)
C22—N6—C21	126.4 (3)	C27—C26—H26	121.3
C10—N7—C1	112.4 (3)	C25—C26—H26	121.3
C10—N7—C19	112.2 (2)	C22—C27—C26	120.4 (4)
C1—N7—C19	111.6 (3)	C22—C27—N5	109.2 (3)
C10—N7—Mn1	104.70 (18)	C26—C27—N5	130.3 (3)
C1—N7—Mn1	107.67 (18)	O1—C28—O2	119.7 (3)
C19—N7—Mn1	107.78 (19)	O1—C28—C29	119.9 (5)
C32—N8—C34'	128.0 (7)	O2—C28—C29	120.3 (5)
C32—N8—C33	130.8 (7)	C30—C29—C28	121.0 (7)
C32—N8—C33'	113.2 (8)	C30—C29—C31	122.9 (5)
C34'—N8—C33'	114.1 (7)	C28—C29—C31	116.1 (6)
C32—N8—C34	115.8 (6)	C29—C31—H31A	109.5
C33—N8—C34	113.4 (6)	C29—C31—H31B	109.5
C35—N9—C36	118.1 (9)	H31A—C31—H31B	109.5
C35—N9—C37	124.4 (8)	C29—C31—H31C	109.5
C36—N9—C37	117.6 (7)	H31A—C31—H31C	109.5
N7—C1—C2	110.0 (3)	H31B—C31—H31C	109.5
N7—C1—H1A	109.7	C29—C30—H30A	120.0
C2—C1—H1A	109.7	C29—C30—H30B	120.0
N7—C1—H1B	109.7	H30A—C30—H30B	120.0
C2—C1—H1B	109.7	O3—C32—N8	128.8 (6)
H1A—C1—H1B	108.2	O3—C32—H32	115.6
N1—C2—N2	112.8 (3)	N8—C32—H32	115.6
N1—C2—C1	123.1 (3)	N8—C33—H33A	109.5
N2—C2—C1	124.1 (3)	N8—C33—H33B	109.5
N2—C3—H3A	109.5	N8—C33—H33C	109.5
N2—C3—H3B	109.5	N8—C33'—H33D	109.5
H3A—C3—H3B	109.5	N8—C33'—H33E	109.5
N2—C3—H3C	109.5	H33D—C33'—H33E	109.5
H3A—C3—H3C	109.5	N8—C33'—H33F	109.5
H3B—C3—H3C	109.5	H33D—C33'—H33F	109.5
N2—C4—C5	131.9 (3)	H33E—C33'—H33F	109.5
N2—C4—C9	105.3 (3)	N8—C34—H34A	109.5
C5—C4—C9	122.8 (3)	N8—C34—H34B	109.5
C6—C5—C4	116.9 (4)	N8—C34—H34C	109.5
C6—C5—H5	121.6	N8—C34'—H34D	109.5
C4—C5—H5	121.6	N8—C34'—H34E	109.5
C5—C6—C7	121.6 (3)	H34D—C34'—H34E	109.5
C5—C6—H6	119.2	N8—C34'—H34F	109.5
C7—C6—H6	119.2	H34D—C34'—H34F	109.5
C6—C7—C8	121.6 (4)	H34E—C34'—H34F	109.5
C6—C7—H7	119.2	O8—C35—N9	124.0 (8)
C8—C7—H7	119.2	O8—C35—H35	118.0
C9—C8—C7	117.6 (4)	N9—C35—H35	118.0
C9—C8—H8	121.2	N9—C36—H36A	109.5
C7—C8—H8	121.2	N9—C36—H36B	109.5
C8—C9—C4	119.5 (3)	H36A—C36—H36B	109.5
C8—C9—N1	130.6 (3)	N9—C36—H36C	109.5
C4—C9—N1	109.9 (3)	H36A—C36—H36C	109.5
N7—C10—C11	108.8 (2)	H36B—C36—H36C	109.5
N7—C10—H10A	109.9	N9—C37—H37A	109.5
C11—C10—H10A	109.9	N9—C37—H37B	109.5
N7—C10—H10B	109.9	H37A—C37—H37B	109.5
C11—C10—H10B	109.9	N9—C37—H37C	109.5
H10A—C10—H10B	108.3	H37A—C37—H37C	109.5
N3—C11—N4	114.0 (3)	H37B—C37—H37C	109.5
N3—C11—C10	122.5 (3)

N5—Mn1—O1—C28	−164.5 (2)	C5—C6—C7—C8	−1.7 (6)
N3—Mn1—O1—C28	−20.3 (3)	C6—C7—C8—C9	0.4 (5)
O2—Mn1—O1—C28	−0.4 (2)	C7—C8—C9—C4	2.1 (5)
N1—Mn1—O1—C28	90.5 (2)	C7—C8—C9—N1	−178.5 (3)
O3—Mn1—O1—C28	−83.8 (2)	N2—C4—C9—C8	178.4 (3)
N7—Mn1—O1—C28	140.3 (2)	C5—C4—C9—C8	−3.6 (5)
N5—Mn1—O2—C28	29.2 (3)	N2—C4—C9—N1	−1.1 (3)
O1—Mn1—O2—C28	0.3 (2)	C5—C4—C9—N1	176.9 (3)
N3—Mn1—O2—C28	169.2 (2)	C2—N1—C9—C8	−178.1 (3)
N1—Mn1—O2—C28	−89.6 (2)	Mn1—N1—C9—C8	27.5 (5)
O3—Mn1—O2—C28	90.9 (2)	C2—N1—C9—C4	1.2 (3)
N7—Mn1—O2—C28	−141.4 (2)	Mn1—N1—C9—C4	−153.1 (2)
N5—Mn1—O3—C32	−179.4 (4)	C1—N7—C10—C11	−76.5 (3)
O1—Mn1—O3—C32	87.7 (4)	C19—N7—C10—C11	156.7 (3)
N3—Mn1—O3—C32	−61.2 (4)	Mn1—N7—C10—C11	40.1 (3)
O2—Mn1—O3—C32	30.8 (4)	C18—N3—C11—N4	−1.1 (4)
N1—Mn1—O3—C32	26.9 (10)	Mn1—N3—C11—N4	154.6 (2)
N7—Mn1—O3—C32	−118.4 (4)	C18—N3—C11—C10	177.7 (3)
N5—Mn1—N1—C2	87.7 (2)	Mn1—N3—C11—C10	−26.6 (4)
O1—Mn1—N1—C2	−179.9 (2)	C13—N4—C11—N3	0.9 (4)
N3—Mn1—N1—C2	−32.5 (2)	C12—N4—C11—N3	179.8 (4)
O2—Mn1—N1—C2	−123.1 (2)	C13—N4—C11—C10	−177.9 (3)
O3—Mn1—N1—C2	−119.3 (8)	C12—N4—C11—C10	1.0 (6)
N7—Mn1—N1—C2	27.7 (2)	N7—C10—C11—N3	−13.2 (5)
N5—Mn1—N1—C9	−120.1 (3)	N7—C10—C11—N4	165.5 (3)
O1—Mn1—N1—C9	−27.6 (3)	C11—N4—C13—C14	178.6 (4)
N3—Mn1—N1—C9	119.7 (3)	C12—N4—C13—C14	−0.3 (7)
O2—Mn1—N1—C9	29.1 (3)	C11—N4—C13—C18	−0.3 (4)
O3—Mn1—N1—C9	32.9 (10)	C12—N4—C13—C18	−179.2 (4)
N7—Mn1—N1—C9	179.9 (3)	C18—C13—C14—C15	1.1 (6)
N5—Mn1—N3—C11	−16.8 (3)	N4—C13—C14—C15	−177.6 (4)
O1—Mn1—N3—C11	−156.5 (2)	C13—C14—C15—C16	−0.8 (8)
O2—Mn1—N3—C11	−173.1 (2)	C14—C15—C16—C17	0.5 (9)
N1—Mn1—N3—C11	95.9 (2)	C15—C16—C17—C18	−0.4 (8)
O3—Mn1—N3—C11	−90.9 (2)	C14—C13—C18—C17	−1.0 (6)
N7—Mn1—N3—C11	35.1 (2)	N4—C13—C18—C17	178.0 (4)
N5—Mn1—N3—C18	128.7 (3)	C14—C13—C18—N3	−179.3 (4)
O1—Mn1—N3—C18	−11.0 (4)	N4—C13—C18—N3	−0.3 (4)
O2—Mn1—N3—C18	−27.6 (3)	C16—C17—C18—C13	0.6 (6)
N1—Mn1—N3—C18	−118.6 (3)	C16—C17—C18—N3	178.5 (4)
O3—Mn1—N3—C18	54.7 (3)	C11—N3—C18—C13	0.8 (4)
N7—Mn1—N3—C18	−179.3 (3)	Mn1—N3—C18—C13	−146.8 (3)
O1—Mn1—N5—C20	−130.9 (2)	C11—N3—C18—C17	−177.2 (4)
N3—Mn1—N5—C20	70.5 (3)	Mn1—N3—C18—C17	35.2 (6)
O2—Mn1—N5—C20	−154.8 (2)	C10—N7—C19—C20	−80.3 (3)
N1—Mn1—N5—C20	−39.9 (2)	C1—N7—C19—C20	152.5 (3)
O3—Mn1—N5—C20	143.2 (2)	Mn1—N7—C19—C20	34.4 (3)
N7—Mn1—N5—C20	19.5 (2)	C27—N5—C20—N6	0.4 (4)
O1—Mn1—N5—C27	38.2 (3)	Mn1—N5—C20—N6	172.5 (2)
N3—Mn1—N5—C27	−120.3 (3)	C27—N5—C20—C19	−178.6 (3)
O2—Mn1—N5—C27	14.3 (4)	Mn1—N5—C20—C19	−6.6 (4)
N1—Mn1—N5—C27	129.3 (3)	C22—N6—C20—N5	−0.5 (4)
O3—Mn1—N5—C27	−47.7 (3)	C21—N6—C20—N5	179.3 (3)
N7—Mn1—N5—C27	−171.4 (3)	C22—N6—C20—C19	178.5 (3)
N5—Mn1—N7—C10	90.4 (2)	C21—N6—C20—C19	−1.7 (5)
O1—Mn1—N7—C10	151.6 (2)	N7—C19—C20—N5	−22.2 (4)
N3—Mn1—N7—C10	−40.06 (19)	N7—C19—C20—N6	158.9 (3)
O2—Mn1—N7—C10	−95.3 (2)	C20—N6—C22—C27	0.3 (4)
N1—Mn1—N7—C10	−153.0 (2)	C21—N6—C22—C27	−179.4 (3)
O3—Mn1—N7—C10	22.9 (2)	C20—N6—C22—C23	−179.8 (4)
N5—Mn1—N7—C1	−149.8 (2)	C21—N6—C22—C23	0.4 (6)
O1—Mn1—N7—C1	−88.5 (2)	N6—C22—C23—C24	−178.8 (4)
N3—Mn1—N7—C1	79.8 (2)	C27—C22—C23—C24	1.0 (6)
O2—Mn1—N7—C1	24.6 (3)	C22—C23—C24—C25	−0.8 (6)
N1—Mn1—N7—C1	−33.21 (19)	C23—C24—C25—C26	0.5 (7)
O3—Mn1—N7—C1	142.76 (19)	C24—C25—C26—C27	−0.3 (6)
N5—Mn1—N7—C19	−29.3 (2)	N6—C22—C27—C26	179.0 (3)
O1—Mn1—N7—C19	32.0 (3)	C23—C22—C27—C26	−0.9 (5)
N3—Mn1—N7—C19	−159.7 (2)	N6—C22—C27—N5	−0.1 (4)
O2—Mn1—N7—C19	145.1 (2)	C23—C22—C27—N5	−180.0 (3)
N1—Mn1—N7—C19	87.3 (2)	C25—C26—C27—C22	0.5 (5)
O3—Mn1—N7—C19	−96.7 (2)	C25—C26—C27—N5	179.4 (3)
C10—N7—C1—C2	149.6 (3)	C20—N5—C27—C22	−0.2 (4)
C19—N7—C1—C2	−83.3 (3)	Mn1—N5—C27—C22	−170.4 (2)
Mn1—N7—C1—C2	34.8 (3)	C20—N5—C27—C26	−179.1 (4)
C9—N1—C2—N2	−0.9 (3)	Mn1—N5—C27—C26	10.7 (5)
Mn1—N1—C2—N2	159.4 (2)	Mn1—O1—C28—O2	0.6 (4)
C9—N1—C2—C1	−179.6 (3)	Mn1—O1—C28—C29	−179.5 (4)
Mn1—N1—C2—C1	−19.3 (4)	Mn1—O2—C28—O1	−0.6 (4)
C4—N2—C2—N1	0.3 (3)	Mn1—O2—C28—C29	179.5 (4)
C3—N2—C2—N1	179.1 (3)	O1—C28—C29—C30	−168.8 (5)
C4—N2—C2—C1	179.0 (3)	O2—C28—C29—C30	11.1 (8)
C3—N2—C2—C1	−2.2 (5)	O1—C28—C29—C31	12.1 (7)
N7—C1—C2—N1	−13.6 (4)	O2—C28—C29—C31	−168.0 (5)
N7—C1—C2—N2	167.9 (3)	Mn1—O3—C32—N8	165.8 (4)
C2—N2—C4—C5	−177.2 (3)	C34'—N8—C32—O3	−32.7 (14)
C3—N2—C4—C5	3.9 (5)	C33—N8—C32—O3	−167.5 (7)
C2—N2—C4—C9	0.5 (3)	C33'—N8—C32—O3	173.4 (10)
C3—N2—C4—C9	−178.4 (3)	C34—N8—C32—O3	12.1 (9)
N2—C4—C5—C6	179.8 (3)	C36—N9—C35—O8	178.6 (8)
C9—C4—C5—C6	2.4 (5)	C37—N9—C35—O8	0.0 (11)
C4—C5—C6—C7	0.3 (5)

Experimental details

Crystal data
Chemical formula	[Mn(C₄H₅O₂)(C₂₇H₂₇N₇)(C₃H₇NO)]ClO₄·C₃H₇NO
M_r	835.22
Crystal system, space group	Triclinic, P1
Temperature (K)	296
a, b, c (Å)	12.139 (5), 12.354 (5), 15.146 (6)
α, β, γ (°)	89.168 (4), 71.098 (4), 76.936 (5)
V (Å³)	2088.9 (14)
Z	2
Radiation type	Mo Kα
µ (mm⁻¹)	0.44
Crystal size (mm)	0.38 × 0.34 × 0.30

Data collection
Diffractometer	Bruker APEXII area-detector diffractometer
Absorption correction	Multi-scan (SADABS: Bruker, 2006)
T_min, T_max	0.851, 0.880
No. of measured, independent and observed [I > 2σ(I)] reflections	15471, 7680, 5422
R_int	0.033
(sin θ/λ)_max (Å⁻¹)	0.606

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.059, 0.187, 1.10
No. of reflections	7680
No. of parameters	525
No. of restraints	8
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.90, −0.54

Computer programs: APEX2 (Bruker, 2006), SAINT (Bruker, 2006), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), SHELXTL (Sheldrick, 2008).

Acknowledgements

We are grateful for financial support and a grant from the `Qing Lan' Talent Engineering Funds of Lanzhou Jiaotong University. A grant from the Middle-Young Age Science Foundation (grant No. 3YS061-A25–023) and the `Long Yuan Qing Nian' of Gansu Province is also acknowledged.

References

Bruker (2006). APEX2, SAINT and SADABS. Bruker AXS Inc., Madison, Wisconsin, USA Google Scholar
Horton, D. A., Bourne, G. T. & Smythe, M. L. (2003). Chem. Rev. 103, 893–930. Web of Science CrossRef PubMed CAS Google Scholar
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. Web of Science CrossRef CAS IUCr Journals Google Scholar
Wu, H. L., Huang, X. C., Yuan, J. K., Li, K., Ding, J., Yun, R. R., Dong, W. K. & Fan, X. Y. (2009). J. Coord. Chem. 62, 3446–3453. Web of Science CrossRef CAS Google Scholar
Wu, H. L., Ying, W., Pen, L., Gao, Y. C. & Yu, K. B. (2005). Synth. React. Inorg. Met. Org. Chem. 34, 553–558. Google Scholar

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