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

Journal logoCRYSTALLOGRAPHIC
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ISSN: 2056-9890
Volume 64| Part 5| May 2008| Pages m701-m702

catena-Poly[[[bis­­[4-(1H-1,3,7,8-tetra­aza­cyclo­penta­[l]phenanthren-2-yl)phenol-κ2N7,N8]manganese(II)]-μ-naphthalene-1,4-di­carboxyl­ato-κ2O1:O4] naphthalene-1,4-di­carboxylic acid hemisolvate monohydrate]

aDepartment of Chemistry, Jilin Normal University, Siping 136000, People's Republic of China, bXi'an Modern Chemistry Research Institute, Xi'an 710065, People's Republic of China, and cDepartment of Chemistry, University of Malaya, 50603 Kuala Lumpur, Malaysia
*Correspondence e-mail: seikweng@um.edu.my

(Received 16 January 2008; accepted 18 April 2008; online 23 April 2008)

The 1,4-dicarboxyl­ate dianions in the title compound, [Mn(C12H6O4)(C19H12N4O)2]·0.5C12H8O4·H2O, bond to two 4-(1H-1,3,7,8-tetra­azacyclo­penta­[l]phenanthren-2-yl)phenol-chelated Mn atoms to form a chain that features the metal atom in an octa­hedral coordination geometry. Adjacent chains inter­act with the uncoordinated water mol­ecules to form a three-dimensional network. The naphthalene-1,4-dicarboxylic acid solvent mol­ecule, which is disordered about a centre of inversion, occupies the space within the network but is not bonded to the network. One NH group is disordered equally over two positions.

Related literature

There are several studies of (2-phenyl-1H-1,3,7,8,-tetra­azacyclo­penta­[l]phenanthrene-chelated manganese dicarb­oxyl­ates (see, for example, Li et al., 2008[Li, H.-D., Liu, Y., Xu, M.-L. & Ng, S. W. (2008). Acta Cryst. E64, m704-m705.]). The 4-hydr­oxy-substituted N-heterocycle forms an adduct with mangan­ese(II) terephthalate (see Che et al., 2006[Che, G.-B., Lin, X.-F. & Liu, C.-B. (2006). Acta Cryst. E62, m1456-m1458.]).

[Scheme 1]

Experimental

Crystal data
  • [Mn(C12H6O4)(C19H12N4O)2]·0.5C12H8O4·H2O

  • Mr = 1019.87

  • Monoclinic, C 2/c

  • a = 48.398 (15) Å

  • b = 9.089 (2) Å

  • c = 20.598 (6) Å

  • β = 103.20 (1)°

  • V = 8821 (4) Å3

  • Z = 8

  • Mo Kα radiation

  • μ = 0.38 mm−1

  • T = 295 (2) K

  • 0.31 × 0.25 × 0.18 mm

Data collection
  • Rigaku R-AXIS RAPID diffractometer

  • Absorption correction: multi-scan (ABSCOR; Higashi, 1995[Higashi, T. (1995). ABSCOR. Rigaku Corporation, Tokyo, Japan.]) Tmin = 0.820, Tmax = 1.000 (expected range = 0.767–0.935)

  • 40785 measured reflections

  • 10014 independent reflections

  • 5868 reflections with I > 2σ(I)

  • Rint = 0.084

Refinement
  • R[F2 > 2σ(F2)] = 0.060

  • wR(F2) = 0.170

  • S = 1.03

  • 10014 reflections

  • 717 parameters

  • 116 restraints

  • H-atom parameters constrained

  • Δρmax = 1.35 e Å−3

  • Δρmin = −0.42 e Å−3

Table 1
Selected geometric parameters (Å, °)

Mn1—O1 2.146 (2)
Mn1—O3i 2.108 (2)
Mn1—N1 2.282 (3)
Mn1—N4 2.245 (3)
Mn1—N5 2.265 (3)
Mn1—N8 2.307 (3)
O1—Mn1—O3i 95.0 (1)
O1—Mn1—N1 87.1 (1)
O1—Mn1—N4 97.6 (1)
O1—Mn1—N5 97.9 (1)
O1—Mn1—N8 169.9 (1)
O3i—Mn1—N1 165.2 (1)
O3i—Mn1—N4 91.8 (1)
O3i—Mn1—N5 104.8 (1)
O3i—Mn1—N8 87.1 (1)
N1—Mn1—N4 73.4 (1)
N1—Mn1—N5 89.5 (1)
N1—Mn1—N8 93.4 (1)
N4—Mn1—N5 156.2 (1)
N4—Mn1—N8 92.2 (1)
N5—Mn1—N8 72.0 (1)
Symmetry code: (i) [x, -y+1, z+{\script{1\over 2}}].

Table 2
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A DA D—H⋯A
O5—H5O⋯N2ii 0.82 1.93 2.737 (4) 168
O6—H6O⋯O1Wiii 0.82 1.85 2.656 (4) 168
N3—H3N⋯O2iv 0.86 1.97 2.813 (4) 166
N6—H6N⋯O9 0.86 2.00 2.728 (6) 142
N7—H7N⋯O10v 0.86 1.83 2.685 (6) 178
O1W—H1W2⋯O1 0.82 1.94 2.754 (4) 173
O1W—H1W1⋯O4i 0.82 2.19 3.007 (6) 173
Symmetry codes: (i) [x, -y+1, z+{\script{1\over 2}}]; (ii) [-x+{\script{3\over 2}}, y-{\script{1\over 2}}, -z+{\script{1\over 2}}]; (iii) -x+1, -y+1, -z+1; (iv) [-x+{\script{3\over 2}}, -y+{\script{1\over 2}}, -z+1]; (v) -x+1, -y, -z+1.

Data collection: RAPID-AUTO (Rigaku, 1998[Rigaku (1998). RAPID-AUTO. Rigaku Corporation, Tokyo, Japan.]); cell refinement: RAPID-AUTO; data reduction: CrystalStructure (Rigaku/MSC, 2002[Rigaku/MSC (2002). CrystalStructure. Rigaku/MSC, The Woodlands, Texas, USA.]); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); molecular graphics: X-SEED (Barbour, 2001[Barbour, L. J. (2001). J. Supramol. Chem. 1, 189-191.]) and OLEX (Dolomanov et al., 2003[Dolomanov, O. V., Blake, A. J., Champness, N. R. & Schröder, M. (2003). J. Appl. Cryst. 36, 1283-1284.]); software used to prepare material for publication: publCIF (Westrip, 2008[Westrip, S. P. (2008). publCIF. In preparation.]).

Supporting information


Comment top

There are manganese dicarboxylate adducts of complexes of 2-phenyl-1H-1,3,7,8-tetraazacyclopenta[l]phenanthrene (Li et al., 2008). The 4-hydroxy substituted ligand forms an adduct with manganese terephthalate (Che et al., 2006) that features a carboxylate-bridged chain motif. The title naphthalene-1,4-dicarboxylate adduct also adopts a layer motif. However, there is space between the chains that is large enough for a naphthalene-1,4-dicarboxylic acid molecule as well as a water molecule to fit in. Adjacent chains are linked by hydrogen bonds into a three-dimensional network.

Related literature top

There are several studies of (2-phenyl-1H-1,3,7,8,-tetraazacyclopenta[l]phenanthrene-chelated manganese dicarboxylates (see Li et al., 2008). The 4-hydroxy substituted N-heterocycle forms an adduct with manganese terephthalate (see Che et al., 2006).

Experimental top

Manganese dichloride dihydrate (0.02 g, 0.1 mmol), naphthalene-1,4-dicarboxylic acid (0.02 g, 0.1 mmol), 4-(1H-1,3,7,8-tetraazacyclopenta[l]phenanthren-2-yl)phenol4-(1H-imidazo[4,5-f][1,10]phenanthrolin-2-yl)phenol (0.03 g, 0.1 mmol) and water (15 ml) were heated in a 23 ml, Teflon-lined, stainless-steel Parr bomb at 408 K for 2 days. Crystals were obtained in 40% yield.

Refinement top

The naphthalene-1,4-dicarboxylic acid is disordered over a center-of-inversion. The fused-ring portion was refined as a rigid naphthalene group of 1.39 Å sides; the occupancy is 0.5. The C–O distances were restrained to 1.25±0.01 Å and the Ccarboxyl–Caryl distances to 1.50±0.01 Å. Other restrained were applied to the carboxyl parts. The anisotropic displacement factors of the carbon and oxygen atoms were restrained to be nearly isotropic. The acid H atoms were arbitrarily placed on the carboxyl parts.

The carbon- and nitrogen-bound H atoms were placed in calculated positions [C–H 0.93, N–H 0.86, O–H 0.82 Å and Uiso(H) 1.2Ueq(C,N,O)], and were included in the refinement in the riding-model approximation. For one of the N-heterocycles, the amino –NH group is ordered whereas for the other, it is disordered. For the second N-heterocycle, hydrogen atoms of 0.5 occupancy were placed on the two nitrogen atoms. The water H-atoms were placed in chemically sensible positions on the basis of hydrogen bonds.

The final difference Fourier map had a large peak near H14, but this could not be modeled as a water molecule.

Computing details top

Data collection: RAPID-AUTO (Rigaku, 1998); cell refinement: RAPID-AUTO (Rigaku, 1998); data reduction: CrystalStructure (Rigaku/MSC, 2002); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: X-SEED (Barbour, 2001) and OLEX (Dolomanov et al., 2003); software used to prepare material for publication: publCIF (Westrip, 2008).

Figures top
[Figure 1] Fig. 1. Thermal ellipsoid plot of Mn(C19H12N4O)2(C12H6O4).(C12H8O4)0.5.H2O; displacement ellipsoids are drawn at the 50% probability level, and H atoms as spheres of arbitrary radius. The naphthalene-1,4-dicarboxylic acid is disordered about a center-of-inversion. [Symmetry code i: x, 1 - y, 1/2 + z].
[Figure 2] Fig. 2. Chain structure of the manganese-naphthalene-1,4-dicarboxylate network as illustrated by OLEX (Dolomanov et al., 2003).
catena-Poly[[[bis[4-(1H-1,3,7,8- tetraazacyclopenta[l]phenanthren-2-yl)phenol- κ2N7,N8]manganese(II)]-µ-naphthalene-1,4-dicarboxylato- κ2O1:O4] naphthalene-1,4-dicarboxylic acid hemisolvate monohydrate] top
Crystal data top
[Mn(C12H6O4)(C19H12N4O)2]·0.5C12H8O4·H2OF(000) = 4200
Mr = 1019.87Dx = 1.536 Mg m3
Monoclinic, C2/cMo Kα radiation, λ = 0.71073 Å
Hall symbol: -C 2ycCell parameters from 24704 reflections
a = 48.398 (15) Åθ = 3.0–27.5°
b = 9.089 (2) ŵ = 0.38 mm1
c = 20.598 (6) ÅT = 295 K
β = 103.20 (1)°Block, brown
V = 8821 (4) Å30.31 × 0.25 × 0.18 mm
Z = 8
Data collection top
Rigaku R-AXIS RAPID
diffractometer
10014 independent reflections
Radiation source: fine-focus sealed tube5868 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.084
Detector resolution: 10 pixels mm-1θmax = 27.5°, θmin = 3.0°
ω scansh = 6262
Absorption correction: multi-scan
(ABSCOR; Higashi, 1995)
k = 1111
Tmin = 0.820, Tmax = 1.000l = 2526
40785 measured reflections
Refinement top
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.060Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.170H-atom parameters constrained
S = 1.03 w = 1/[σ2(Fo2) + (0.0782P)2 + 7.7802P]
where P = (Fo2 + 2Fc2)/3
10014 reflections(Δ/σ)max = 0.001
717 parametersΔρmax = 1.35 e Å3
116 restraintsΔρmin = 0.42 e Å3
Crystal data top
[Mn(C12H6O4)(C19H12N4O)2]·0.5C12H8O4·H2OV = 8821 (4) Å3
Mr = 1019.87Z = 8
Monoclinic, C2/cMo Kα radiation
a = 48.398 (15) ŵ = 0.38 mm1
b = 9.089 (2) ÅT = 295 K
c = 20.598 (6) Å0.31 × 0.25 × 0.18 mm
β = 103.20 (1)°
Data collection top
Rigaku R-AXIS RAPID
diffractometer
10014 independent reflections
Absorption correction: multi-scan
(ABSCOR; Higashi, 1995)
5868 reflections with I > 2σ(I)
Tmin = 0.820, Tmax = 1.000Rint = 0.084
40785 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.060116 restraints
wR(F2) = 0.170H-atom parameters constrained
S = 1.03Δρmax = 1.35 e Å3
10014 reflectionsΔρmin = 0.42 e Å3
717 parameters
Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/UeqOcc. (<1)
Mn10.648562 (11)0.41289 (6)0.51035 (2)0.03142 (15)
O10.66266 (5)0.5844 (3)0.45399 (11)0.0379 (6)
O20.70748 (5)0.5903 (3)0.44417 (12)0.0468 (7)
O30.65765 (6)0.4702 (3)0.10116 (11)0.0487 (7)
O40.62358 (12)0.3337 (5)0.12178 (16)0.137 (2)
O50.80478 (5)0.5497 (3)0.28409 (12)0.0431 (6)
H5O0.79750.57130.24530.052*
O60.39480 (6)0.0139 (4)0.56796 (15)0.0580 (8)
H6O0.38280.05380.53880.070*
O1W0.64402 (6)0.8246 (3)0.51341 (13)0.0585 (8)
H1W10.63810.78820.54400.070*
H1W20.65000.75800.49350.070*
N10.64987 (6)0.2597 (3)0.42332 (13)0.0329 (6)
N20.71343 (6)0.0949 (3)0.35027 (13)0.0326 (6)
N30.74551 (6)0.0806 (3)0.44653 (13)0.0323 (6)
H3N0.76080.09580.47650.039*
N40.68967 (6)0.2888 (3)0.53848 (13)0.0323 (6)
N50.60125 (6)0.4417 (3)0.47014 (14)0.0349 (7)
N60.50889 (6)0.2640 (4)0.49973 (15)0.0427 (8)
H6N0.49630.31270.47180.051*0.50
N70.52850 (6)0.1071 (3)0.58045 (15)0.0393 (7)
H7N0.53050.04220.61150.047*0.50
N80.62546 (6)0.2431 (3)0.56234 (13)0.0328 (6)
C10.68180 (7)0.5800 (4)0.42007 (15)0.0318 (7)
C20.67164 (7)0.5539 (4)0.34578 (15)0.0334 (8)
C30.68747 (8)0.4623 (4)0.31553 (18)0.0442 (9)
H30.70460.42570.34040.053*
C40.67855 (10)0.4222 (5)0.24807 (19)0.0520 (11)
H40.69040.36590.22820.062*
C50.65281 (9)0.4650 (4)0.21179 (17)0.0453 (10)
C60.63544 (8)0.5580 (4)0.24055 (17)0.0418 (9)
C70.60821 (10)0.6066 (6)0.2051 (2)0.0636 (14)
H70.60060.56990.16260.076*
C80.59313 (10)0.7050 (7)0.2321 (2)0.0763 (17)
H80.57500.73120.20870.092*
C90.60437 (9)0.7686 (6)0.2949 (2)0.0610 (13)
H90.59440.84140.31150.073*
C100.63004 (8)0.7224 (4)0.33118 (18)0.0446 (9)
H100.63750.76470.37260.053*
C110.64569 (8)0.6109 (4)0.30714 (16)0.0362 (8)
C120.64374 (11)0.4187 (5)0.13943 (18)0.0573 (12)
C130.63068 (8)0.2504 (4)0.36630 (17)0.0391 (8)
H130.61430.30710.36120.047*
C140.63352 (8)0.1611 (4)0.31385 (18)0.0443 (9)
H140.61950.15940.27450.053*
C150.65707 (7)0.0760 (4)0.32064 (16)0.0383 (8)
H150.65920.01400.28620.046*
C160.67804 (7)0.0824 (4)0.38000 (15)0.0309 (7)
C170.67358 (7)0.1766 (4)0.43056 (15)0.0277 (7)
C180.70380 (7)0.0002 (4)0.39249 (15)0.0302 (7)
C190.73844 (7)0.1426 (4)0.38480 (16)0.0319 (7)
C200.75594 (7)0.2469 (4)0.35910 (15)0.0310 (7)
C210.74440 (8)0.3234 (4)0.30051 (17)0.0375 (8)
H210.72560.30660.27870.045*
C220.76036 (7)0.4235 (4)0.27433 (16)0.0363 (8)
H220.75230.47300.23500.044*
C230.78818 (7)0.4505 (4)0.30626 (16)0.0326 (8)
C240.80001 (8)0.3755 (4)0.36495 (17)0.0394 (9)
H240.81870.39320.38680.047*
C250.78397 (8)0.2747 (4)0.39081 (17)0.0388 (8)
H250.79210.22490.43000.047*
C260.72353 (7)0.0112 (4)0.45189 (15)0.0305 (7)
C270.72016 (7)0.1082 (4)0.50390 (15)0.0303 (7)
C280.69495 (7)0.1906 (4)0.49268 (15)0.0289 (7)
C290.73988 (8)0.1291 (4)0.56409 (16)0.0368 (8)
H290.75670.07510.57340.044*
C300.73462 (8)0.2288 (4)0.60954 (17)0.0417 (9)
H300.74780.24480.64940.050*
C310.70901 (8)0.3062 (4)0.59476 (16)0.0370 (8)
H310.70540.37310.62600.044*
C320.58966 (8)0.5338 (4)0.42155 (17)0.0421 (9)
H320.60170.59400.40390.051*
C330.56062 (8)0.5453 (5)0.39549 (19)0.0472 (10)
H330.55360.60910.36030.057*
C340.54270 (8)0.4625 (4)0.42190 (18)0.0448 (9)
H340.52320.47030.40590.054*
C350.55415 (7)0.3645 (4)0.47394 (17)0.0352 (8)
C360.58368 (7)0.3551 (4)0.49587 (16)0.0308 (7)
C370.53799 (7)0.2739 (4)0.50782 (17)0.0375 (8)
C380.50402 (8)0.1628 (4)0.54421 (18)0.0390 (8)
C390.47567 (8)0.1240 (4)0.55059 (18)0.0398 (9)
C400.45204 (8)0.1852 (5)0.5075 (2)0.0466 (9)
H400.45460.25070.47460.056*
C410.42516 (8)0.1502 (4)0.51280 (19)0.0441 (9)
H410.40960.19180.48350.053*
C420.42095 (8)0.0535 (4)0.56145 (19)0.0418 (9)
C430.44413 (9)0.0074 (5)0.6052 (2)0.0502 (10)
H430.44150.07190.63830.060*
C440.47111 (9)0.0282 (5)0.59918 (19)0.0482 (10)
H440.48660.01330.62850.058*
C450.54997 (7)0.1768 (4)0.55707 (16)0.0360 (8)
C460.58004 (7)0.1575 (4)0.57679 (16)0.0317 (7)
C470.59665 (7)0.2488 (4)0.54633 (15)0.0301 (7)
C480.59376 (8)0.0503 (4)0.62186 (18)0.0423 (9)
H480.58330.01480.64170.051*
C490.62277 (8)0.0435 (4)0.63611 (18)0.0422 (9)
H490.63240.02750.66530.051*
C500.63774 (8)0.1443 (4)0.60637 (17)0.0391 (9)
H500.65750.14160.61820.047*
O70.57620 (11)0.3027 (6)0.1777 (3)0.0515 (14)0.50
H7O0.58860.31120.15680.062*0.50
O80.54490 (15)0.4380 (7)0.1031 (3)0.0662 (18)0.50
O90.47578 (12)0.3147 (7)0.3757 (3)0.0619 (16)0.50
O100.46652 (12)0.0992 (7)0.3243 (3)0.0651 (17)0.50
H10O0.45750.07380.35170.078*0.50
C510.55115 (11)0.3657 (5)0.1545 (2)0.0409 (17)0.50
C520.53036 (7)0.3410 (4)0.19789 (16)0.0385 (17)0.50
C530.52596 (9)0.1961 (4)0.2146 (2)0.049 (2)0.50
H530.53520.12000.19810.059*0.50
C540.50771 (9)0.1650 (3)0.2560 (2)0.047 (2)0.50
H540.50480.06810.26720.056*0.50
C550.49387 (8)0.2788 (4)0.28073 (17)0.0461 (19)0.50
C560.49827 (9)0.4237 (4)0.2640 (2)0.042 (3)0.50
C570.51652 (9)0.4548 (3)0.22257 (19)0.041 (2)0.50
C580.52092 (14)0.5997 (4)0.2058 (3)0.044 (2)0.50
H580.53310.62050.17810.053*0.50
C590.50708 (19)0.7134 (3)0.2305 (4)0.047 (3)0.50
H590.51000.81040.21930.057*0.50
C600.48883 (19)0.6823 (4)0.2719 (4)0.068 (4)0.50
H600.47960.75840.28840.082*0.50
C610.48443 (14)0.5374 (5)0.2887 (3)0.057 (3)0.50
H610.47220.51660.31640.068*0.50
C620.47719 (9)0.2234 (7)0.3285 (3)0.050 (2)0.50
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
Mn10.0325 (3)0.0381 (3)0.0258 (2)0.0015 (2)0.0110 (2)0.0006 (2)
O10.0453 (15)0.0431 (14)0.0294 (12)0.0010 (12)0.0171 (11)0.0011 (11)
O20.0342 (15)0.0710 (19)0.0338 (13)0.0000 (14)0.0048 (11)0.0056 (13)
O30.0654 (19)0.0591 (17)0.0245 (12)0.0084 (15)0.0161 (12)0.0071 (12)
O40.217 (5)0.161 (4)0.0387 (18)0.144 (4)0.040 (2)0.035 (2)
O50.0398 (15)0.0600 (17)0.0289 (12)0.0147 (13)0.0063 (11)0.0057 (12)
O60.0341 (15)0.080 (2)0.0612 (18)0.0089 (15)0.0143 (13)0.0063 (17)
O1W0.063 (2)0.0632 (19)0.0460 (16)0.0125 (16)0.0062 (14)0.0068 (14)
N10.0311 (15)0.0399 (16)0.0290 (14)0.0017 (13)0.0099 (12)0.0012 (13)
N20.0337 (15)0.0388 (16)0.0262 (13)0.0026 (13)0.0087 (12)0.0015 (13)
N30.0321 (15)0.0394 (16)0.0254 (13)0.0046 (13)0.0063 (11)0.0030 (13)
N40.0352 (16)0.0368 (16)0.0260 (13)0.0003 (13)0.0092 (12)0.0023 (12)
N50.0364 (16)0.0382 (16)0.0323 (14)0.0028 (13)0.0124 (13)0.0040 (13)
N60.0330 (17)0.0523 (19)0.0438 (17)0.0035 (15)0.0109 (14)0.0065 (16)
N70.0322 (16)0.0495 (18)0.0385 (16)0.0004 (14)0.0128 (13)0.0016 (14)
N80.0298 (15)0.0368 (15)0.0325 (14)0.0026 (13)0.0084 (12)0.0012 (13)
C10.0367 (19)0.0358 (18)0.0249 (15)0.0006 (16)0.0112 (14)0.0000 (15)
C20.0381 (19)0.0400 (19)0.0236 (15)0.0060 (16)0.0100 (14)0.0004 (14)
C30.045 (2)0.056 (2)0.0338 (18)0.0049 (19)0.0142 (17)0.0013 (18)
C40.071 (3)0.056 (3)0.0351 (19)0.001 (2)0.025 (2)0.0081 (19)
C50.066 (3)0.047 (2)0.0250 (17)0.019 (2)0.0147 (18)0.0020 (17)
C60.046 (2)0.054 (2)0.0257 (16)0.0174 (19)0.0090 (16)0.0095 (16)
C70.053 (3)0.105 (4)0.0291 (19)0.024 (3)0.0025 (19)0.016 (2)
C80.040 (3)0.137 (5)0.052 (3)0.002 (3)0.010 (2)0.044 (3)
C90.052 (3)0.085 (3)0.052 (2)0.020 (2)0.023 (2)0.029 (2)
C100.046 (2)0.053 (2)0.0374 (19)0.0059 (19)0.0164 (17)0.0095 (18)
C110.040 (2)0.045 (2)0.0260 (16)0.0073 (17)0.0123 (15)0.0060 (15)
C120.091 (4)0.056 (3)0.0261 (18)0.027 (3)0.016 (2)0.0040 (18)
C130.0334 (19)0.048 (2)0.0349 (18)0.0104 (17)0.0046 (15)0.0018 (17)
C140.040 (2)0.057 (2)0.0319 (18)0.0058 (19)0.0005 (16)0.0063 (18)
C150.037 (2)0.050 (2)0.0259 (16)0.0047 (17)0.0036 (14)0.0065 (16)
C160.0302 (17)0.0365 (18)0.0267 (15)0.0009 (15)0.0079 (13)0.0009 (15)
C170.0292 (17)0.0319 (17)0.0240 (15)0.0016 (14)0.0101 (13)0.0026 (14)
C180.0328 (18)0.0345 (18)0.0242 (15)0.0004 (15)0.0081 (13)0.0003 (14)
C190.0349 (19)0.0378 (18)0.0245 (15)0.0003 (16)0.0100 (14)0.0001 (14)
C200.0345 (18)0.0346 (18)0.0254 (15)0.0001 (15)0.0102 (14)0.0000 (14)
C210.0333 (19)0.046 (2)0.0328 (17)0.0057 (17)0.0059 (15)0.0018 (16)
C220.038 (2)0.044 (2)0.0261 (16)0.0038 (17)0.0054 (14)0.0039 (15)
C230.0329 (18)0.0381 (19)0.0286 (16)0.0056 (15)0.0105 (14)0.0018 (15)
C240.0311 (19)0.052 (2)0.0328 (18)0.0045 (17)0.0033 (15)0.0039 (17)
C250.037 (2)0.048 (2)0.0299 (17)0.0024 (17)0.0034 (15)0.0071 (16)
C260.0332 (18)0.0330 (17)0.0268 (15)0.0008 (15)0.0100 (14)0.0010 (14)
C270.0302 (17)0.0366 (18)0.0268 (15)0.0007 (15)0.0120 (13)0.0013 (14)
C280.0318 (18)0.0303 (17)0.0262 (15)0.0040 (14)0.0101 (13)0.0001 (14)
C290.0351 (19)0.046 (2)0.0290 (16)0.0058 (16)0.0063 (15)0.0019 (16)
C300.040 (2)0.054 (2)0.0295 (17)0.0006 (19)0.0056 (16)0.0060 (17)
C310.039 (2)0.043 (2)0.0289 (17)0.0010 (17)0.0090 (15)0.0066 (16)
C320.042 (2)0.049 (2)0.0361 (18)0.0013 (18)0.0110 (16)0.0100 (18)
C330.044 (2)0.054 (2)0.041 (2)0.0009 (19)0.0049 (18)0.0148 (19)
C340.037 (2)0.055 (2)0.039 (2)0.0008 (19)0.0008 (16)0.0106 (19)
C350.0342 (19)0.042 (2)0.0307 (17)0.0010 (16)0.0091 (15)0.0025 (16)
C360.0323 (18)0.0346 (18)0.0274 (16)0.0006 (15)0.0105 (14)0.0029 (14)
C370.0311 (19)0.050 (2)0.0309 (17)0.0002 (17)0.0063 (15)0.0032 (17)
C380.036 (2)0.045 (2)0.0395 (19)0.0020 (17)0.0160 (16)0.0007 (17)
C390.037 (2)0.046 (2)0.0386 (19)0.0034 (17)0.0139 (16)0.0045 (17)
C400.043 (2)0.052 (2)0.048 (2)0.0024 (19)0.0168 (18)0.0041 (19)
C410.039 (2)0.051 (2)0.043 (2)0.0001 (18)0.0112 (17)0.0025 (19)
C420.035 (2)0.050 (2)0.043 (2)0.0077 (17)0.0151 (16)0.0104 (18)
C430.046 (2)0.062 (3)0.046 (2)0.007 (2)0.0171 (19)0.006 (2)
C440.041 (2)0.060 (3)0.043 (2)0.001 (2)0.0106 (17)0.010 (2)
C450.035 (2)0.044 (2)0.0308 (17)0.0026 (17)0.0115 (15)0.0003 (16)
C460.0331 (19)0.0352 (18)0.0270 (16)0.0029 (15)0.0071 (14)0.0005 (15)
C470.0318 (18)0.0328 (17)0.0262 (15)0.0006 (15)0.0076 (14)0.0032 (14)
C480.044 (2)0.045 (2)0.0374 (19)0.0030 (18)0.0094 (17)0.0073 (17)
C490.045 (2)0.043 (2)0.0391 (19)0.0104 (18)0.0096 (17)0.0120 (17)
C500.037 (2)0.046 (2)0.0351 (18)0.0063 (17)0.0103 (16)0.0060 (17)
O70.048 (3)0.060 (3)0.053 (3)0.014 (3)0.025 (3)0.002 (3)
O80.092 (5)0.072 (4)0.044 (3)0.014 (3)0.033 (3)0.016 (3)
O90.052 (3)0.088 (4)0.050 (3)0.004 (3)0.021 (3)0.023 (3)
O100.057 (4)0.074 (4)0.068 (4)0.012 (3)0.023 (3)0.030 (3)
C510.044 (4)0.043 (4)0.039 (4)0.007 (3)0.016 (3)0.009 (3)
C520.039 (4)0.041 (4)0.036 (3)0.005 (3)0.010 (3)0.001 (3)
C530.072 (5)0.042 (4)0.033 (4)0.005 (4)0.013 (4)0.000 (4)
C540.064 (7)0.039 (3)0.033 (4)0.013 (3)0.004 (4)0.002 (4)
C550.039 (4)0.054 (4)0.044 (4)0.002 (4)0.006 (3)0.022 (4)
C560.046 (4)0.045 (4)0.029 (6)0.003 (5)0.008 (4)0.010 (3)
C570.045 (5)0.041 (5)0.031 (4)0.002 (4)0.002 (4)0.005 (4)
C580.041 (5)0.047 (5)0.045 (4)0.004 (4)0.008 (4)0.015 (4)
C590.065 (6)0.027 (4)0.050 (6)0.002 (4)0.014 (5)0.001 (4)
C600.062 (7)0.075 (6)0.072 (8)0.011 (6)0.023 (6)0.009 (6)
C610.036 (5)0.080 (7)0.057 (6)0.003 (5)0.018 (4)0.012 (5)
C620.036 (4)0.061 (5)0.055 (5)0.003 (4)0.011 (4)0.014 (4)
Geometric parameters (Å, º) top
Mn1—O12.146 (2)C21—H210.9300
Mn1—O3i2.108 (2)C22—C231.379 (5)
Mn1—N12.282 (3)C22—H220.9300
Mn1—N42.245 (3)C23—C241.392 (5)
Mn1—N52.265 (3)C24—C251.384 (5)
Mn1—N82.307 (3)C24—H240.9300
O1—C11.282 (4)C25—H250.9300
O2—C11.232 (4)C26—C271.425 (4)
O3—C121.239 (5)C27—C291.394 (4)
O3—Mn1ii2.108 (2)C27—C281.405 (5)
O4—C121.232 (5)C29—C301.368 (5)
O5—C231.354 (4)C29—H290.9300
O5—H5O0.8200C30—C311.397 (5)
O6—C421.352 (4)C30—H300.9300
O6—H6O0.8200C31—H310.9300
O1W—H1W10.8201C32—C331.389 (5)
O1W—H1W20.8200C32—H320.9300
N1—C131.323 (4)C33—C341.352 (5)
N1—C171.353 (4)C33—H330.9300
N2—C191.329 (4)C34—C351.407 (5)
N2—C181.379 (4)C34—H340.9300
N3—C191.361 (4)C35—C361.400 (5)
N3—C261.376 (4)C35—C371.423 (5)
N3—H3N0.8600C36—C471.453 (5)
N4—C311.323 (4)C37—C451.369 (5)
N4—C281.364 (4)C38—C391.452 (5)
N5—C321.327 (4)C39—C441.382 (5)
N5—C361.352 (4)C39—C401.394 (5)
N6—C381.356 (5)C40—C411.368 (5)
N6—C371.383 (4)C40—H400.9300
N6—H6N0.8600C41—C421.383 (5)
N7—C381.347 (5)C41—H410.9300
N7—C451.393 (4)C42—C431.384 (5)
N7—H7N0.8600C43—C441.378 (5)
N8—C501.318 (4)C43—H430.9300
N8—C471.359 (4)C44—H440.9300
C1—C21.515 (4)C45—C461.430 (5)
C2—C31.374 (5)C46—C471.400 (5)
C2—C111.422 (5)C46—C481.403 (5)
C3—C41.406 (5)C48—C491.369 (5)
C3—H30.9300C48—H480.9300
C4—C51.355 (6)C49—C501.394 (5)
C4—H40.9300C49—H490.9300
C5—C61.414 (6)C50—H500.9300
C5—C121.514 (5)O7—C511.327 (6)
C6—C71.423 (6)O7—H7O0.8201
C6—C111.431 (5)O8—C511.223 (6)
C7—C81.351 (7)O9—C621.291 (7)
C7—H70.9300O10—C621.236 (7)
C8—C91.409 (7)O10—H10O0.8198
C8—H80.9300C51—C521.507 (5)
C9—C101.362 (5)C52—C531.3900
C9—H90.9300C52—C571.3900
C10—C111.420 (5)C53—C541.3900
C10—H100.9300C53—H530.9300
C13—C141.383 (5)C54—C551.3900
C13—H130.9300C54—H540.9300
C14—C151.358 (5)C55—C561.3900
C14—H140.9300C55—C621.496 (5)
C15—C161.401 (4)C56—C571.3900
C15—H150.9300C56—C611.3900
C16—C171.402 (4)C57—C581.3900
C16—C181.427 (5)C58—C591.3900
C17—C281.455 (4)C58—H580.9300
C18—C261.373 (4)C59—C601.3900
C19—C201.449 (5)C59—H590.9300
C20—C251.388 (5)C60—C611.3900
C20—C211.394 (5)C60—H600.9300
C21—C221.381 (5)C61—H610.9300
O1—Mn1—O3i95.0 (1)C24—C25—H25119.5
O1—Mn1—N187.1 (1)C20—C25—H25119.5
O1—Mn1—N497.6 (1)C18—C26—N3106.0 (3)
O1—Mn1—N597.9 (1)C18—C26—C27122.7 (3)
O1—Mn1—N8169.9 (1)N3—C26—C27131.2 (3)
O3i—Mn1—N1165.2 (1)C29—C27—C28117.8 (3)
O3i—Mn1—N491.8 (1)C29—C27—C26125.4 (3)
O3i—Mn1—N5104.8 (1)C28—C27—C26116.8 (3)
O3i—Mn1—N887.1 (1)N4—C28—C27121.8 (3)
N1—Mn1—N473.4 (1)N4—C28—C17117.2 (3)
N1—Mn1—N589.5 (1)C27—C28—C17120.9 (3)
N1—Mn1—N893.4 (1)C30—C29—C27120.1 (3)
N4—Mn1—N5156.2 (1)C30—C29—H29119.9
N4—Mn1—N892.2 (1)C27—C29—H29119.9
N5—Mn1—N872.0 (1)C29—C30—C31118.6 (3)
C1—O1—Mn1129.1 (2)C29—C30—H30120.7
C12—O3—Mn1ii136.2 (3)C31—C30—H30120.7
C23—O5—H5O109.5N4—C31—C30123.1 (3)
C42—O6—H6O109.5N4—C31—H31118.5
H1W1—O1W—H1W2108.2C30—C31—H31118.5
C13—N1—C17117.9 (3)N5—C32—C33123.7 (4)
C13—N1—Mn1126.6 (2)N5—C32—H32118.1
C17—N1—Mn1115.4 (2)C33—C32—H32118.1
C19—N2—C18105.3 (3)C34—C33—C32119.2 (4)
C19—N3—C26107.0 (3)C34—C33—H33120.4
C19—N3—H3N126.5C32—C33—H33120.4
C26—N3—H3N126.5C33—C34—C35118.8 (4)
C31—N4—C28118.5 (3)C33—C34—H34120.6
C31—N4—Mn1125.0 (2)C35—C34—H34120.6
C28—N4—Mn1116.4 (2)C36—C35—C34118.7 (3)
C32—N5—C36117.9 (3)C36—C35—C37116.2 (3)
C32—N5—Mn1124.5 (2)C34—C35—C37125.1 (3)
C36—N5—Mn1117.6 (2)N5—C36—C35121.7 (3)
C38—N6—C37107.0 (3)N5—C36—C47117.4 (3)
C38—N6—H6N126.5C35—C36—C47120.9 (3)
C37—N6—H6N126.5C45—C37—N6107.1 (3)
C38—N7—C45105.6 (3)C45—C37—C35123.3 (3)
C38—N7—H7N127.2N6—C37—C35129.6 (3)
C45—N7—H7N127.2N7—C38—N6111.3 (3)
C50—N8—C47118.0 (3)N7—C38—C39126.1 (3)
C50—N8—Mn1125.8 (2)N6—C38—C39122.7 (3)
C47—N8—Mn1116.2 (2)C44—C39—C40118.0 (4)
O2—C1—O1124.5 (3)C44—C39—C38122.0 (3)
O2—C1—C2118.9 (3)C40—C39—C38120.0 (3)
O1—C1—C2116.6 (3)C41—C40—C39120.9 (4)
C3—C2—C11118.7 (3)C41—C40—H40119.6
C3—C2—C1117.8 (3)C39—C40—H40119.6
C11—C2—C1123.4 (3)C40—C41—C42120.4 (4)
C2—C3—C4121.9 (4)C40—C41—H41119.8
C2—C3—H3119.1C42—C41—H41119.8
C4—C3—H3119.1O6—C42—C41122.5 (4)
C5—C4—C3120.4 (4)O6—C42—C43117.8 (4)
C5—C4—H4119.8C41—C42—C43119.7 (4)
C3—C4—H4119.8C44—C43—C42119.4 (4)
C4—C5—C6120.0 (3)C44—C43—H43120.3
C4—C5—C12119.1 (4)C42—C43—H43120.3
C6—C5—C12120.8 (4)C43—C44—C39121.6 (4)
C5—C6—C7122.7 (4)C43—C44—H44119.2
C5—C6—C11119.5 (4)C39—C44—H44119.2
C7—C6—C11117.7 (4)C37—C45—N7109.1 (3)
C8—C7—C6121.3 (4)C37—C45—C46121.4 (3)
C8—C7—H7119.4N7—C45—C46129.6 (3)
C6—C7—H7119.4C47—C46—C48118.3 (3)
C7—C8—C9121.2 (4)C47—C46—C45116.8 (3)
C7—C8—H8119.4C48—C46—C45124.8 (3)
C9—C8—H8119.4N8—C47—C46122.1 (3)
C10—C9—C8119.3 (5)N8—C47—C36116.8 (3)
C10—C9—H9120.3C46—C47—C36121.1 (3)
C8—C9—H9120.3C49—C48—C46118.7 (4)
C9—C10—C11121.4 (4)C49—C48—H48120.6
C9—C10—H10119.3C46—C48—H48120.6
C11—C10—H10119.3C48—C49—C50119.1 (3)
C10—C11—C2122.5 (3)C48—C49—H49120.4
C10—C11—C6118.6 (3)C50—C49—H49120.4
C2—C11—C6118.9 (3)N8—C50—C49123.5 (4)
O4—C12—O3123.9 (4)N8—C50—H50118.2
O4—C12—C5119.8 (4)C49—C50—H50118.2
O3—C12—C5116.3 (4)C51—O7—H7O119.4
N1—C13—C14123.8 (3)C62—O10—H10O119.1
N1—C13—H13118.1O8—C51—O7124.6 (6)
C14—C13—H13118.1O8—C51—C52121.8 (5)
C15—C14—C13119.0 (3)O7—C51—C52113.7 (4)
C15—C14—H14120.5C53—C52—C57120.0
C13—C14—H14120.5C53—C52—C51116.7 (3)
C14—C15—C16119.3 (3)C57—C52—C51123.3 (3)
C14—C15—H15120.3C52—C53—C54120.0
C16—C15—H15120.3C52—C53—H53120.0
C17—C16—C15118.0 (3)C54—C53—H53120.0
C17—C16—C18117.6 (3)C55—C54—C53120.0
C15—C16—C18124.4 (3)C55—C54—H54120.0
N1—C17—C16122.0 (3)C53—C54—H54120.0
N1—C17—C28117.6 (3)C54—C55—C56120.0
C16—C17—C28120.5 (3)C54—C55—C62111.6 (3)
C26—C18—N2110.0 (3)C56—C55—C62128.2 (3)
C26—C18—C16121.5 (3)C55—C56—C57120.0
N2—C18—C16128.5 (3)C55—C56—C61120.0
N2—C19—N3111.6 (3)C57—C56—C61120.0
N2—C19—C20123.7 (3)C58—C57—C56120.0
N3—C19—C20124.7 (3)C58—C57—C52120.0
C25—C20—C21118.2 (3)C56—C57—C52120.0
C25—C20—C19122.5 (3)C57—C58—C59120.0
C21—C20—C19119.3 (3)C57—C58—H58120.0
C22—C21—C20121.2 (3)C59—C58—H58120.0
C22—C21—H21119.4C58—C59—C60120.0
C20—C21—H21119.4C58—C59—H59120.0
C23—C22—C21120.2 (3)C60—C59—H59120.0
C23—C22—H22119.9C61—C60—C59120.0
C21—C22—H22119.9C61—C60—H60120.0
O5—C23—C22123.2 (3)C59—C60—H60120.0
O5—C23—C24117.4 (3)C60—C61—C56120.0
C22—C23—C24119.4 (3)C60—C61—H61120.0
C25—C24—C23120.2 (3)C56—C61—H61120.0
C25—C24—H24119.9O10—C62—O9123.2 (6)
C23—C24—H24119.9O10—C62—C55122.7 (6)
C24—C25—C20120.9 (3)O9—C62—C55114.1 (5)
O3i—Mn1—O1—C1122.4 (3)C19—N3—C26—C180.4 (4)
N4—Mn1—O1—C130.0 (3)C19—N3—C26—C27176.7 (3)
N5—Mn1—O1—C1131.9 (3)C18—C26—C27—C29177.3 (3)
N1—Mn1—O1—C142.8 (3)N3—C26—C27—C290.6 (6)
N8—Mn1—O1—C1136.0 (5)C18—C26—C27—C281.8 (5)
O3i—Mn1—N1—C13177.0 (4)N3—C26—C27—C28178.4 (3)
O1—Mn1—N1—C1378.7 (3)C31—N4—C28—C270.1 (5)
N4—Mn1—N1—C13177.5 (3)Mn1—N4—C28—C27178.8 (2)
N5—Mn1—N1—C1319.3 (3)C31—N4—C28—C17178.5 (3)
N8—Mn1—N1—C1391.2 (3)Mn1—N4—C28—C170.2 (4)
O3i—Mn1—N1—C170.7 (6)C29—C27—C28—N40.3 (5)
O1—Mn1—N1—C1797.6 (2)C26—C27—C28—N4178.8 (3)
N4—Mn1—N1—C171.2 (2)C29—C27—C28—C17178.9 (3)
N5—Mn1—N1—C17164.4 (2)C26—C27—C28—C170.2 (4)
N8—Mn1—N1—C1792.5 (2)N1—C17—C28—N41.3 (4)
O3i—Mn1—N4—C310.8 (3)C16—C17—C28—N4177.4 (3)
O1—Mn1—N4—C3194.4 (3)N1—C17—C28—C27179.9 (3)
N5—Mn1—N4—C31135.3 (3)C16—C17—C28—C271.3 (5)
N1—Mn1—N4—C31179.1 (3)C28—C27—C29—C301.0 (5)
N8—Mn1—N4—C3188.0 (3)C26—C27—C29—C30178.0 (3)
O3i—Mn1—N4—C28179.4 (2)C27—C29—C30—C311.2 (6)
O1—Mn1—N4—C2884.1 (2)C28—N4—C31—C300.1 (5)
N5—Mn1—N4—C2846.1 (4)Mn1—N4—C31—C30178.5 (3)
N1—Mn1—N4—C280.5 (2)C29—C30—C31—N40.7 (6)
N8—Mn1—N4—C2893.4 (2)C36—N5—C32—C330.5 (6)
O3i—Mn1—N5—C32102.6 (3)Mn1—N5—C32—C33177.0 (3)
O1—Mn1—N5—C325.3 (3)N5—C32—C33—C342.3 (6)
N4—Mn1—N5—C32124.9 (3)C32—C33—C34—C351.6 (6)
N1—Mn1—N5—C3281.7 (3)C33—C34—C35—C360.8 (6)
N8—Mn1—N5—C32175.4 (3)C33—C34—C35—C37178.1 (4)
O3i—Mn1—N5—C3679.9 (3)C32—N5—C36—C352.0 (5)
O1—Mn1—N5—C36177.2 (2)Mn1—N5—C36—C35179.7 (3)
N4—Mn1—N5—C3652.6 (4)C32—N5—C36—C47176.5 (3)
N1—Mn1—N5—C3695.8 (2)Mn1—N5—C36—C471.1 (4)
N8—Mn1—N5—C362.0 (2)C34—C35—C36—N52.7 (5)
O3i—Mn1—N8—C5075.1 (3)C37—C35—C36—N5176.3 (3)
O1—Mn1—N8—C50177.4 (5)C34—C35—C36—C47175.9 (3)
N4—Mn1—N8—C5016.5 (3)C37—C35—C36—C475.2 (5)
N5—Mn1—N8—C50178.3 (3)C38—N6—C37—C450.4 (4)
N1—Mn1—N8—C5090.0 (3)C38—N6—C37—C35179.4 (4)
O3i—Mn1—N8—C47103.7 (2)C36—C35—C37—C453.0 (5)
O1—Mn1—N8—C471.5 (7)C34—C35—C37—C45178.1 (4)
N4—Mn1—N8—C47164.6 (2)C36—C35—C37—N6176.8 (4)
N5—Mn1—N8—C472.8 (2)C34—C35—C37—N62.1 (7)
N1—Mn1—N8—C4791.1 (2)C45—N7—C38—N60.3 (4)
Mn1—O1—C1—O280.7 (4)C45—N7—C38—C39179.8 (4)
Mn1—O1—C1—C296.7 (3)C37—N6—C38—N70.1 (4)
O2—C1—C2—C337.7 (5)C37—N6—C38—C39179.4 (3)
O1—C1—C2—C3139.9 (4)N7—C38—C39—C443.9 (6)
O2—C1—C2—C11146.9 (4)N6—C38—C39—C44175.5 (4)
O1—C1—C2—C1135.6 (5)N7—C38—C39—C40176.9 (4)
C11—C2—C3—C40.8 (6)N6—C38—C39—C403.7 (6)
C1—C2—C3—C4174.8 (3)C44—C39—C40—C410.6 (6)
C2—C3—C4—C54.7 (6)C38—C39—C40—C41179.8 (4)
C3—C4—C5—C63.8 (6)C39—C40—C41—C420.2 (6)
C3—C4—C5—C12179.4 (4)C40—C41—C42—O6178.9 (4)
C4—C5—C6—C7179.9 (4)C40—C41—C42—C430.4 (6)
C12—C5—C6—C73.4 (6)O6—C42—C43—C44178.7 (4)
C4—C5—C6—C112.4 (6)C41—C42—C43—C440.6 (6)
C12—C5—C6—C11174.3 (3)C42—C43—C44—C390.2 (7)
C5—C6—C7—C8174.5 (4)C40—C39—C44—C430.3 (6)
C11—C6—C7—C83.3 (6)C38—C39—C44—C43179.6 (4)
C6—C7—C8—C93.1 (7)N6—C37—C45—N70.7 (4)
C7—C8—C9—C104.7 (7)C35—C37—C45—N7179.2 (3)
C8—C9—C10—C110.3 (6)N6—C37—C45—C46178.6 (3)
C9—C10—C11—C2175.8 (4)C35—C37—C45—C461.6 (6)
C9—C10—C11—C66.6 (5)C38—N7—C45—C370.6 (4)
C3—C2—C11—C10170.6 (3)C38—N7—C45—C46178.5 (4)
C1—C2—C11—C1014.0 (5)C37—C45—C46—C473.9 (5)
C3—C2—C11—C66.9 (5)N7—C45—C46—C47177.1 (3)
C1—C2—C11—C6168.4 (3)C37—C45—C46—C48173.3 (3)
C5—C6—C11—C10169.9 (3)N7—C45—C46—C485.8 (6)
C7—C6—C11—C108.0 (5)C50—N8—C47—C462.4 (5)
C5—C6—C11—C27.8 (5)Mn1—N8—C47—C46176.6 (2)
C7—C6—C11—C2174.4 (3)C50—N8—C47—C36177.8 (3)
Mn1ii—O3—C12—O453.9 (8)Mn1—N8—C47—C363.3 (4)
Mn1ii—O3—C12—C5126.4 (4)C48—C46—C47—N84.4 (5)
C4—C5—C12—O4113.9 (6)C45—C46—C47—N8178.2 (3)
C6—C5—C12—O469.4 (7)C48—C46—C47—C36175.8 (3)
C4—C5—C12—O365.9 (6)C45—C46—C47—C361.6 (5)
C6—C5—C12—O3110.9 (5)N5—C36—C47—N81.5 (4)
C17—N1—C13—C140.2 (6)C35—C36—C47—N8177.1 (3)
Mn1—N1—C13—C14176.1 (3)N5—C36—C47—C46178.4 (3)
N1—C13—C14—C150.8 (6)C35—C36—C47—C463.0 (5)
C13—C14—C15—C161.0 (6)C47—C46—C48—C492.6 (5)
C14—C15—C16—C170.6 (5)C45—C46—C48—C49179.7 (4)
C14—C15—C16—C18179.1 (3)C46—C48—C49—C501.0 (6)
C13—N1—C17—C160.3 (5)C47—N8—C50—C491.5 (5)
Mn1—N1—C17—C16176.9 (2)Mn1—N8—C50—C49179.7 (3)
C13—N1—C17—C28178.3 (3)C48—C49—C50—N83.2 (6)
Mn1—N1—C17—C281.7 (4)O8—C51—C52—C53127.7 (3)
C15—C16—C17—N10.1 (5)O7—C51—C52—C5352.4 (3)
C18—C16—C17—N1179.8 (3)O8—C51—C52—C5754.2 (3)
C15—C16—C17—C28178.5 (3)O7—C51—C52—C57125.7 (3)
C18—C16—C17—C281.2 (5)C57—C52—C53—C540.0
C19—N2—C18—C261.5 (4)C51—C52—C53—C54178.2 (2)
C19—N2—C18—C16179.4 (3)C52—C53—C54—C550.0
C17—C16—C18—C260.3 (5)C53—C54—C55—C560.0
C15—C16—C18—C26180.0 (3)C53—C54—C55—C62175.3 (2)
C17—C16—C18—N2177.4 (3)C54—C55—C56—C570.0
C15—C16—C18—N22.3 (6)C62—C55—C56—C57174.4 (2)
C18—N2—C19—N31.2 (4)C54—C55—C56—C61180.0
C18—N2—C19—C20179.2 (3)C62—C55—C56—C615.6 (2)
C26—N3—C19—N20.6 (4)C55—C56—C57—C58180.0
C26—N3—C19—C20179.9 (3)C61—C56—C57—C580.0
N2—C19—C20—C25168.0 (3)C55—C56—C57—C520.0
N3—C19—C20—C2511.5 (5)C61—C56—C57—C52180.0
N2—C19—C20—C2112.3 (5)C53—C52—C57—C58180.0
N3—C19—C20—C21168.2 (3)C51—C52—C57—C582.0 (2)
C25—C20—C21—C220.4 (5)C53—C52—C57—C560.0
C19—C20—C21—C22179.9 (3)C51—C52—C57—C56178.0 (2)
C20—C21—C22—C230.4 (6)C56—C57—C58—C590.0
C21—C22—C23—O5178.4 (3)C52—C57—C58—C59180.0
C21—C22—C23—C240.2 (5)C57—C58—C59—C600.0
O5—C23—C24—C25178.8 (3)C58—C59—C60—C610.0
C22—C23—C24—C250.2 (6)C59—C60—C61—C560.0
C23—C24—C25—C200.2 (6)C55—C56—C61—C60180.0
C21—C20—C25—C240.0 (5)C57—C56—C61—C600.0
C19—C20—C25—C24179.8 (3)C54—C55—C62—O1030.3 (3)
N2—C18—C26—N31.1 (4)C56—C55—C62—O10154.9 (3)
C16—C18—C26—N3179.2 (3)C54—C55—C62—O9147.5 (3)
N2—C18—C26—C27176.2 (3)C56—C55—C62—O927.3 (3)
C16—C18—C26—C271.8 (5)
Symmetry codes: (i) x, y+1, z+1/2; (ii) x, y+1, z1/2.
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
O5—H5O···N2iii0.821.932.737 (4)168
O6—H6O···O1Wiv0.821.852.656 (4)168
N3—H3N···O2v0.861.972.813 (4)166
N6—H6N···O90.862.002.728 (6)142
N7—H7N···O10vi0.861.832.685 (6)178
O1W—H1W2···O10.821.942.754 (4)173
O1W—H1W1···O4i0.822.193.007 (6)173
Symmetry codes: (i) x, y+1, z+1/2; (iii) x+3/2, y1/2, z+1/2; (iv) x+1, y+1, z+1; (v) x+3/2, y+1/2, z+1; (vi) x+1, y, z+1.

Experimental details

Crystal data
Chemical formula[Mn(C12H6O4)(C19H12N4O)2]·0.5C12H8O4·H2O
Mr1019.87
Crystal system, space groupMonoclinic, C2/c
Temperature (K)295
a, b, c (Å)48.398 (15), 9.089 (2), 20.598 (6)
β (°) 103.20 (1)
V3)8821 (4)
Z8
Radiation typeMo Kα
µ (mm1)0.38
Crystal size (mm)0.31 × 0.25 × 0.18
Data collection
DiffractometerRigaku R-AXIS RAPID
diffractometer
Absorption correctionMulti-scan
(ABSCOR; Higashi, 1995)
Tmin, Tmax0.820, 1.000
No. of measured, independent and
observed [I > 2σ(I)] reflections
40785, 10014, 5868
Rint0.084
(sin θ/λ)max1)0.649
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.060, 0.170, 1.03
No. of reflections10014
No. of parameters717
No. of restraints116
H-atom treatmentH-atom parameters constrained
Δρmax, Δρmin (e Å3)1.35, 0.42

Computer programs: RAPID-AUTO (Rigaku, 1998), CrystalStructure (Rigaku/MSC, 2002), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), X-SEED (Barbour, 2001) and OLEX (Dolomanov et al., 2003), publCIF (Westrip, 2008).

Selected geometric parameters (Å, º) top
Mn1—O12.146 (2)Mn1—N42.245 (3)
Mn1—O3i2.108 (2)Mn1—N52.265 (3)
Mn1—N12.282 (3)Mn1—N82.307 (3)
O1—Mn1—O3i95.0 (1)O3i—Mn1—N887.1 (1)
O1—Mn1—N187.1 (1)N1—Mn1—N473.4 (1)
O1—Mn1—N497.6 (1)N1—Mn1—N589.5 (1)
O1—Mn1—N597.9 (1)N1—Mn1—N893.4 (1)
O1—Mn1—N8169.9 (1)N4—Mn1—N5156.2 (1)
O3i—Mn1—N1165.2 (1)N4—Mn1—N892.2 (1)
O3i—Mn1—N491.8 (1)N5—Mn1—N872.0 (1)
O3i—Mn1—N5104.8 (1)
Symmetry code: (i) x, y+1, z+1/2.
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
O5—H5O···N2ii0.821.932.737 (4)168
O6—H6O···O1Wiii0.821.852.656 (4)168
N3—H3N···O2iv0.861.972.813 (4)166
N6—H6N···O90.862.002.728 (6)142
N7—H7N···O10v0.861.832.685 (6)178
O1W—H1W2···O10.821.942.754 (4)173
O1W—H1W1···O4i0.822.193.007 (6)173
Symmetry codes: (i) x, y+1, z+1/2; (ii) x+3/2, y1/2, z+1/2; (iii) x+1, y+1, z+1; (iv) x+3/2, y+1/2, z+1; (v) x+1, y, z+1.
 

Acknowledgements

The authors thank the Natural Science Foundation of Jilin Province (grant No. 20060516), the Doctoral Foundation of Jilin Normal University (grant No. 2006006), the Science and Technology Institute Foundation of Siping City (grant No. 2005016), the Subject and Base Construction Foundation of Jilin Normal University (grant No. 2006041) and the University of Malaya for supporting this work.

References

First citationBarbour, L. J. (2001). J. Supramol. Chem. 1, 189–191.  CrossRef CAS Google Scholar
First citationChe, G.-B., Lin, X.-F. & Liu, C.-B. (2006). Acta Cryst. E62, m1456–m1458.  Web of Science CSD CrossRef IUCr Journals Google Scholar
First citationDolomanov, O. V., Blake, A. J., Champness, N. R. & Schröder, M. (2003). J. Appl. Cryst. 36, 1283–1284.  Web of Science CrossRef CAS IUCr Journals Google Scholar
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First citationLi, H.-D., Liu, Y., Xu, M.-L. & Ng, S. W. (2008). Acta Cryst. E64, m704–m705.  Web of Science CSD CrossRef IUCr Journals Google Scholar
First citationRigaku (1998). RAPID-AUTO. Rigaku Corporation, Tokyo, Japan.  Google Scholar
First citationRigaku/MSC (2002). CrystalStructure. Rigaku/MSC, The Woodlands, Texas, USA.  Google Scholar
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First citationWestrip, S. P. (2008). publCIF. In preparation.  Google Scholar

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Volume 64| Part 5| May 2008| Pages m701-m702
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