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

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ISSN: 2056-9890

1,3-Di-1-adamantylimidazolium (phthalocyaninato)lithium(I) acetone hemisolvate monohydrate

aDepartment of Chemistry, Wright State University, 3640 Colonel Glenn Hwy., Dayton Ohio 45435, USA
*Correspondence e-mail: david.grossie@wright.edu

(Received 24 November 2008; accepted 5 December 2008; online 17 December 2008)

The asymmetric unit of the title compound, (C23H33N2)[Li(C32H16N8)]·0.5C3H6O·H2O, consists of two symmetry-unrelated lithium phthalocyanine (LiPc) half-anions, centered at (1,0,0) and (0,[{\script{1\over 2}}],0), respectively, the bis­(adamant­yl)imidazolium cation (BAI+), occupying a general site, an acetone mol­ecule, disordered about the inversion centre at (0, [{\script{1\over 2}}], [{\script{1\over 2}}]) and a water mol­ecule at a general site. The LiPc anions pack in a stepped pattern enclosing the bis­(adamant­yl)imidazolium cation. Attractions between the anion and cation are mediated by a water mol­ecule which forms O—H⋯N hydrogen bonds. In addition, two C—H⋯O interactions are seen.

Related literature

Similar compounds utilizing nitro­gen-based cations have been reported by Homborg & Kalz (1978a[Homborg, H. & Kalz, W. (1978a). Z. Naturforsch. Teil B, 33, 968-975.],b[Homborg, H. & Kalz, W. (1978b). Z. Naturforsch. Teil B, 33, 1067-1071.]). For related structures see: Grossie et al. (2006[Grossie, D. A., Feld, W. A., Scanlon, L., Sandi, G. & Wawrzak, Z. (2006). Acta Cryst. E62, m827-m829.]).

[Scheme 1]

Experimental

Crystal data
  • (C23H33N2)[Li(C32H16N8)]·0.5C3H6O·H2O

  • Mr = 904.04

  • Monoclinic, P 21 /n

  • a = 15.799 (3) Å

  • b = 17.165 (4) Å

  • c = 17.831 (4) Å

  • β = 108.374 (3)°

  • V = 4588.9 (16) Å3

  • Z = 4

  • Mo Kα radiation

  • μ = 0.08 mm−1

  • T = 173 (2) K

  • 0.44 × 0.39 × 0.20 mm

Data collection
  • Bruker Smart APEXII CCD diffractometer

  • Absorption correction: multi-scan (SADABS; Bruker, 2003[Bruker (2003). SAINT-Plus and SADABS. Bruker AXS Inc., Madison (WI), USA.]) Tmin = 0.901, Tmax = 0.985

  • 54676 measured reflections

  • 14917 independent reflections

  • 11038 reflections with I > 2σ(I)

  • Rint = 0.039

Refinement
  • R[F2 > 2σ(F2)] = 0.052

  • wR(F2) = 0.129

  • S = 1.03

  • 14917 reflections

  • 649 parameters

  • 8 restraints

  • H atoms treated by a mixture of independent and constrained refinement

  • Δρmax = 0.37 e Å−3

  • Δρmin = −0.30 e Å−3

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A DA D—H⋯A
O1—H1A⋯N6 0.861 (18) 2.405 (17) 3.1618 (17) 147.1 (18)
O1—H1B⋯N3i 0.889 (18) 2.025 (19) 2.8911 (17) 164.3 (16)
C33—H33⋯O1 0.95 2.18 3.127 (2) 171
C37—H37A⋯O1 0.99 2.52 3.493 (2) 166
Symmetry code: (i) -x+1, -y+1, -z.

Data collection: SMART (Bruker, 2002[Bruker (2002). SMART. Bruker AXS Inc., Madison (WI), USA.]); cell refinement: SAINT-Plus (Bruker, 2003[Bruker (2003). SAINT-Plus and SADABS. Bruker AXS Inc., Madison (WI), USA.]); data reduction: SAINT-Plus; 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: Mercury (Macrae et al., 2006[Macrae, C. F., Edgington, P. R., McCabe, P., Pidcock, E., Shields, G. P., Taylor, R., Towler, M. & van de Streek, J. (2006). J. Appl. Cryst. 39, 453-457.]), ORTEP-3 for Windows, (Farrugia, 1997[Farrugia, L. J. (1997). J. Appl. Cryst. 30, 565.]), OSCAIL, (McArdle, 1995[McArdle, P. (1995). J. Appl. Cryst. 28, 65.]); software used to prepare material for publication: enCIFer (Allen et al., 2004[Allen, F. H., Johnson, O., Shields, G. P., Smith, B. R. & Towler, M. (2004). J. Appl. Cryst. 37, 335-338.]) and publCIF (Westrip, 2009[Westrip, S. P. (2009). publCIF. In preparation.]).

Supporting information


Comment top

The asymmetric unit of the title compound consists of two symmetry-unrelated halves of lithium phthalocyanine anions (LiPc-), centered at 1,0,0 and 0, 1/2,0, respectively; the bis(adamantyl)imidazolium cation (BAI+), occupying a general site, an acetone molecule, at 0, 1/2,0.5, and a water molecule at a general site, Fig 1. In addition, the unit cell packing provides interesting detail of the arrangement of molecules within the crystal structure, as seen in Figure 2. Similar compounds utilizing nitrogen-based cations have been reported by Homborg & Kalz (1978a, 1978b).

Although they may appear to be in Figure 2, the symmetry-related LiPc- anions are not parallel, as seen in the angle (2.39°) between their mean planes. Additionally, their intermolecular distances are quite large (10.10 Å as measured between mesonitrogens) in comparison to those seen in Li2PC (3.06–3.38 Å)(Grossie, et al., 2006) The large spacing between LiPc- molecules is easily attributed to the bulky adamantyl substituents of the BAI+ molecules, in which one cation appears to be enclosed within four LiPc- anions forming ionic pockets. This is shown in Fig. 2, which presents the organized but unique packing of molecules. Rows of symmetry-related anions along the b axis are offset from each other, stacking in a stair-step manner. These molecules appear to be nearly orthogonal to the columnar anions, in which alternating columns have slightly different orientations. It is necessary, though, to view the packing from all angles to get a true understanding of ion arrangements.

Probably the most intriguing information obtained was the role of solvent molecules within the crystal structure. It was seen in the crystal structure of Li2PC that acetone and water ligated to lithium, forming dimers that were found in between LiPc- pairs. In the current structure it can be seen that water molecules are crucial to the crystallization of the complex ions. Here, it is noticed that water forms O—H···N and C—H···O hydrogen bonds, Table 1, with the two symmetry-unrelated LiPc- anions and one BAI+ cation, acting as an intermediate to the three ions. Interatomic distances between hydrogen atoms and isoindoline and meso nitrogen of individual LiPc- ions were found to be 2.405 (17) Å and 2.025 (19) Å, respectively. The distance between the oxygen atom of water and the hydrogen on the 2- position of the BAI+ cation was calculated to be about 2.18 Å.

Related literature top

Similar compounds utilizing nitrogen-based cations have been reported by Homborg & Kalz (1978a,b). For related structures see: Grossie et al. (2006).

Experimental top

The 1,3-bis(1-adamantyl)imidazolium tetrafluoroborate (0.884 g) was purified by dissolving it in 70 ml of acetone and filtering the insoluble impurities. The solution was evaporated to dryness to give 0.843 g (1.98 mmol) of the pure salt, which was redissolved in 10 ml of acetone and added to a solution of 0.991 g (1.98 mmol) of dilithium phthalocyanine in 100 ml of acetone. The solution was evaporated to approximately 20–30 ml under reduced pressure to the point of crystallization, sealed and crystallized at 5°C for 72 h. The resulting solid was redissolved in 125 ml of hot acetone with stirring (some undissolved solid remained). The volume was reduced and crystallized at 5°C. The dry product isolated by filtration gave 0.893 g (55.3%) of purple crystals. m.p. 349–351°C. Anal. Calc. for C55H49LiN10 (856.99): C, 77.08; H, 5.76; N, 16.34. Found: C, 76.89; H, 5.90; N, 15.94.

Refinement top

Hydrogen atoms of the water molecule and of the methyl group of the acetone molecule were located in a difference Fourier map and refined with appropriate distance restraints. All other H-atoms were positioned geometrically and refined using a riding model with d(C-H) = 0.95Å, Uiso=1.2Ueq (C) for aromatic 1.00Å, Uiso = 1.2Ueq (C) for CH and 0.99Å, Uiso = 1.2Ueq (C) for CH2 atoms

Computing details top

Data collection: SMART (Bruker, 2002); cell refinement: SAINT-Plus (Bruker, 2003); data reduction: SAINT-Plus (Bruker, 2003); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: Mercury (Macrae et al., 2006), ORTEP-3 for Windows, (Farrugia, 1997), OSCAIL, (McArdle, 1995); software used to prepare material for publication: enCIFer (Allen et al., 2004) and publCIF (Westrip, 2009).

Figures top
[Figure 1] Fig. 1. The asymmetric unit of I. Labelled atoms are related to unlabelled atoms by the symmetry codes –x+2, -y, -z for the Li1 anion and -x, -y+1, -z for the Li2 anion. Hydrogen atoms are not shown.
[Figure 2] Fig. 2. Unit cell packing diagram, viewed along the b axis. Acetone molecules have been omitted for clarity.
1,3-Bis(1-adamantyl)imidazolium lithium phthalocyanine monohydrate acetone hemisolvate. top
Crystal data top
(C23H33N2)[Li(C32H16N8)]·0.5C3H6O·H2OF(000) = 1912
Mr = 904.04Dx = 1.309 Mg m3
Monoclinic, P21/nMelting point: 622 K
Hall symbol: -P 2ynMo Kα radiation, λ = 0.71073 Å
a = 15.799 (3) ÅCell parameters from 64888 reflections
b = 17.165 (4) Åθ = 2.4–30.1°
c = 17.831 (4) ŵ = 0.08 mm1
β = 108.374 (3)°T = 173 K
V = 4588.9 (16) Å3Block, violet
Z = 40.44 × 0.39 × 0.20 mm
Data collection top
Bruker Smart APEXII CCD
diffractometer
14917 independent reflections
Radiation source: fine-focus sealed tube11038 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.039
ω scansθmax = 31.7°, θmin = 1.7°
Absorption correction: multi-scan
(SADABS; Bruker, 2003)
h = 2223
Tmin = 0.901, Tmax = 0.985k = 2524
54676 measured reflectionsl = 2626
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)] = 0.052Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.129H atoms treated by a mixture of independent and constrained refinement
S = 1.03 w = 1/[σ2(Fo2) + (0.0482P)2 + 2.081P]
where P = (Fo2 + 2Fc2)/3
14917 reflections(Δ/σ)max = 0.001
649 parametersΔρmax = 0.37 e Å3
8 restraintsΔρmin = 0.30 e Å3
Crystal data top
(C23H33N2)[Li(C32H16N8)]·0.5C3H6O·H2OV = 4588.9 (16) Å3
Mr = 904.04Z = 4
Monoclinic, P21/nMo Kα radiation
a = 15.799 (3) ŵ = 0.08 mm1
b = 17.165 (4) ÅT = 173 K
c = 17.831 (4) Å0.44 × 0.39 × 0.20 mm
β = 108.374 (3)°
Data collection top
Bruker Smart APEXII CCD
diffractometer
14917 independent reflections
Absorption correction: multi-scan
(SADABS; Bruker, 2003)
11038 reflections with I > 2σ(I)
Tmin = 0.901, Tmax = 0.985Rint = 0.039
54676 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0528 restraints
wR(F2) = 0.129H atoms treated by a mixture of independent and constrained refinement
S = 1.03Δρmax = 0.37 e Å3
14917 reflectionsΔρmin = 0.30 e Å3
649 parameters
Special details top

Experimental. 1H NMR (300 MHz, DMSO-d6) δ = 9.35–9.25 (m, 8H, Ar—H), 9.06 (s, 1H, Ar—H), 8.12–8.02 (m, 8H, Ar—H), 8.01 (d, 2H, 3 J = 1.1 Hz, Ar—H), 2.24–2.09 (m, 18H, Al—H), 1.82–1.62 (m, 12H, Al—H); 13 C-NMR (75 MHz, DMSO-d6) δ = 154.14, 140.05, 131.23, 127.51, 119.31, 59.35, 41.46, 34.81, 28.83; IR (KBr) cm-1 = 3053 (Ar—H), 2912 (C—H), 1604 (C—C), 1583 (C—N), 1485 (C—N), 1092 (C—C), 1055 (C—N); UV/Vis (DMSO) λmax nm (log ε) = 665 (5.25), 636 (4.47), 601 (4.48), 380 (4.55), 327 (4.55), 255 (4.63);

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
xyzUiso*/UeqOcc. (<1)
Li11.00000.00000.00000.0221 (7)
N10.84511 (7)0.01780 (6)0.09200 (6)0.0183 (2)
N20.94090 (7)0.08811 (6)0.03257 (6)0.0173 (2)
N31.01005 (7)0.19613 (6)0.01323 (6)0.0182 (2)
N41.06695 (7)0.07380 (6)0.04398 (6)0.0178 (2)
C10.87993 (8)0.08236 (7)0.07194 (7)0.0167 (2)
C20.85314 (8)0.15984 (7)0.08970 (7)0.0173 (2)
C30.79734 (9)0.18458 (8)0.13159 (8)0.0213 (3)
H30.76540.14830.15260.026*
C40.78994 (10)0.26408 (8)0.14163 (8)0.0240 (3)
H40.75240.28280.17010.029*
C50.83698 (10)0.31696 (8)0.11036 (9)0.0256 (3)
H50.83100.37110.11830.031*
C60.89232 (9)0.29251 (8)0.06800 (8)0.0222 (3)
H60.92370.32900.04660.027*
C70.90028 (9)0.21275 (7)0.05796 (7)0.0179 (2)
C80.95462 (8)0.16503 (7)0.02226 (7)0.0173 (2)
C91.06334 (8)0.15280 (7)0.04204 (7)0.0172 (2)
C101.12886 (8)0.18684 (7)0.07575 (7)0.0174 (2)
C111.15259 (9)0.26268 (8)0.08836 (8)0.0201 (2)
H111.12300.30620.07500.024*
C121.22089 (9)0.27270 (8)0.12104 (8)0.0221 (3)
H121.23820.32400.13010.026*
C131.26472 (9)0.20899 (8)0.14097 (8)0.0228 (3)
H131.31150.21770.16290.027*
C141.24094 (9)0.13324 (8)0.12920 (8)0.0213 (3)
H141.27040.08980.14280.026*
C151.17233 (9)0.12325 (7)0.09671 (8)0.0181 (2)
C161.13064 (9)0.05364 (7)0.07705 (7)0.0177 (2)
Li20.00000.50000.00000.0223 (7)
N50.00519 (7)0.50482 (6)0.18826 (6)0.0193 (2)
N60.08896 (7)0.49153 (7)0.10472 (6)0.0192 (2)
N70.22215 (7)0.47223 (6)0.06714 (7)0.0195 (2)
N80.09266 (7)0.48310 (7)0.04998 (6)0.0187 (2)
C170.07282 (9)0.49409 (7)0.17554 (7)0.0183 (2)
C180.15585 (9)0.48247 (7)0.24040 (8)0.0187 (2)
C190.17516 (10)0.47967 (8)0.32180 (8)0.0229 (3)
H190.12970.48630.34570.027*
C200.26314 (10)0.46682 (9)0.36727 (8)0.0279 (3)
H200.27820.46490.42320.033*
C210.32991 (10)0.45674 (9)0.33197 (9)0.0286 (3)
H210.38950.44750.36430.034*
C220.31062 (9)0.45991 (8)0.25046 (8)0.0237 (3)
H220.35610.45340.22660.028*
C230.22251 (9)0.47299 (8)0.20492 (8)0.0196 (2)
C240.17785 (9)0.47881 (7)0.11946 (8)0.0187 (2)
C250.18188 (9)0.47596 (7)0.01094 (8)0.0183 (2)
C260.23144 (9)0.47344 (7)0.06777 (8)0.0183 (2)
C270.32210 (9)0.47045 (8)0.05927 (8)0.0213 (3)
H270.36570.46650.00860.026*
C280.34626 (10)0.47343 (8)0.12769 (9)0.0251 (3)
H280.40770.47190.12350.030*
C290.28251 (10)0.47858 (9)0.20269 (9)0.0255 (3)
H290.30130.47990.24830.031*
C300.19217 (10)0.48184 (8)0.21123 (8)0.0224 (3)
H300.14870.48570.26190.027*
C310.16757 (9)0.47920 (7)0.14276 (8)0.0185 (2)
C320.08121 (9)0.48562 (7)0.12921 (8)0.0179 (2)
N90.21347 (8)0.75837 (7)0.32337 (7)0.0206 (2)
N100.31358 (8)0.73900 (7)0.26556 (7)0.0210 (2)
C330.22743 (9)0.73102 (8)0.25812 (8)0.0212 (3)
H330.18320.70940.21370.025*
C340.29366 (9)0.78481 (9)0.37394 (8)0.0238 (3)
H340.30330.80710.42470.029*
C350.35583 (9)0.77306 (9)0.33786 (8)0.0245 (3)
H350.41730.78590.35840.029*
C360.12688 (9)0.75260 (8)0.33990 (8)0.0191 (2)
C370.05180 (9)0.78827 (8)0.27195 (8)0.0205 (3)
H37A0.04710.76070.22200.025*
H37B0.06490.84380.26540.025*
C380.03623 (9)0.78110 (8)0.29063 (8)0.0222 (3)
H380.08550.80460.24660.027*
C390.02848 (10)0.82412 (9)0.36785 (9)0.0258 (3)
H39A0.01550.87990.36240.031*
H39B0.08560.82040.37960.031*
C400.04642 (10)0.78776 (9)0.43521 (8)0.0262 (3)
H400.05120.81560.48560.031*
C410.13491 (9)0.79498 (9)0.41737 (8)0.0245 (3)
H41A0.14910.85060.41270.029*
H41B0.18370.77170.46100.029*
C420.05610 (10)0.69499 (9)0.29889 (9)0.0252 (3)
H42A0.06120.66730.24890.030*
H42B0.11350.68960.30980.030*
C430.01881 (10)0.65890 (8)0.36645 (9)0.0263 (3)
H430.00550.60260.37190.032*
C440.02643 (11)0.70154 (10)0.44379 (9)0.0300 (3)
H44A0.03010.69630.45630.036*
H44B0.07480.67810.48760.036*
C450.10709 (10)0.66639 (8)0.34806 (9)0.0242 (3)
H45A0.15600.64260.39120.029*
H45B0.10270.63860.29830.029*
C460.35926 (9)0.71388 (8)0.20826 (7)0.0188 (2)
C470.29214 (9)0.67521 (8)0.13680 (8)0.0218 (3)
H47A0.24410.71240.11050.026*
H47B0.26480.62950.15400.026*
C480.34101 (9)0.64948 (9)0.07899 (8)0.0240 (3)
H480.29770.62410.03190.029*
C490.38222 (11)0.72049 (10)0.05245 (9)0.0301 (3)
H49A0.33490.75830.02620.036*
H49B0.41250.70440.01400.036*
C500.44974 (11)0.75862 (9)0.12455 (9)0.0294 (3)
H500.47730.80480.10710.035*
C510.52255 (10)0.70054 (10)0.16613 (9)0.0302 (3)
H51A0.56550.72550.21280.036*
H51B0.55530.68420.12970.036*
C520.48106 (9)0.62939 (9)0.19228 (8)0.0243 (3)
H520.52890.59120.21890.029*
C530.43204 (9)0.65519 (8)0.24972 (8)0.0221 (3)
H53A0.47470.67950.29700.027*
H53B0.40490.60940.26710.027*
C540.41484 (9)0.59165 (9)0.11957 (9)0.0254 (3)
H54A0.44630.57520.08220.030*
H54B0.38840.54480.13570.030*
C550.40064 (10)0.78504 (8)0.18204 (9)0.0266 (3)
H55A0.44300.81070.22860.032*
H55B0.35340.82300.15570.032*
O10.06786 (8)0.67405 (6)0.11486 (7)0.0297 (2)
H1A0.0548 (13)0.6284 (10)0.0945 (12)0.045*
H1B0.0393 (13)0.7070 (11)0.0768 (10)0.045*
O20.0403 (2)0.44760 (18)0.39840 (18)0.0555 (7)0.50
C560.0162 (3)0.4789 (2)0.4612 (2)0.0451 (9)0.50
C570.0801 (2)0.47921 (16)0.50835 (16)0.0646 (7)
H57A0.1107 (14)0.4355 (14)0.4973 (17)0.097*
H57B0.0942 (15)0.4617 (18)0.5603 (12)0.097*
H57C0.1131 (14)0.5205 (14)0.4976 (16)0.097*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
Li10.0250 (17)0.0152 (14)0.0268 (17)0.0003 (12)0.0094 (14)0.0006 (12)
N10.0193 (5)0.0163 (5)0.0190 (5)0.0001 (4)0.0058 (4)0.0004 (4)
N20.0191 (5)0.0153 (5)0.0171 (5)0.0011 (4)0.0052 (4)0.0003 (4)
N30.0199 (5)0.0168 (5)0.0177 (5)0.0000 (4)0.0056 (4)0.0007 (4)
N40.0191 (5)0.0151 (5)0.0194 (5)0.0001 (4)0.0064 (4)0.0010 (4)
C10.0175 (6)0.0162 (5)0.0154 (5)0.0004 (4)0.0038 (4)0.0011 (4)
C20.0184 (6)0.0161 (5)0.0162 (6)0.0010 (4)0.0036 (5)0.0009 (4)
C30.0215 (6)0.0214 (6)0.0214 (6)0.0017 (5)0.0073 (5)0.0006 (5)
C40.0251 (7)0.0235 (6)0.0239 (7)0.0061 (5)0.0085 (5)0.0022 (5)
C50.0304 (7)0.0180 (6)0.0272 (7)0.0051 (5)0.0075 (6)0.0026 (5)
C60.0248 (7)0.0162 (6)0.0245 (7)0.0011 (5)0.0060 (5)0.0001 (5)
C70.0191 (6)0.0163 (5)0.0168 (6)0.0019 (4)0.0035 (5)0.0001 (4)
C80.0182 (6)0.0156 (5)0.0165 (6)0.0004 (4)0.0033 (5)0.0001 (4)
C90.0183 (6)0.0152 (5)0.0166 (6)0.0016 (4)0.0034 (5)0.0001 (4)
C100.0185 (6)0.0168 (5)0.0156 (5)0.0022 (4)0.0039 (4)0.0005 (4)
C110.0231 (6)0.0170 (6)0.0189 (6)0.0031 (5)0.0049 (5)0.0008 (5)
C120.0242 (7)0.0197 (6)0.0213 (6)0.0064 (5)0.0056 (5)0.0008 (5)
C130.0215 (6)0.0247 (6)0.0231 (6)0.0061 (5)0.0083 (5)0.0003 (5)
C140.0210 (6)0.0210 (6)0.0225 (6)0.0013 (5)0.0075 (5)0.0006 (5)
C150.0192 (6)0.0172 (5)0.0175 (6)0.0016 (5)0.0054 (5)0.0010 (4)
C160.0187 (6)0.0165 (5)0.0171 (6)0.0011 (4)0.0046 (5)0.0001 (4)
Li20.0212 (16)0.0281 (17)0.0162 (15)0.0012 (13)0.0040 (12)0.0005 (13)
N50.0207 (5)0.0195 (5)0.0172 (5)0.0008 (4)0.0052 (4)0.0001 (4)
N60.0185 (5)0.0233 (5)0.0155 (5)0.0016 (4)0.0047 (4)0.0006 (4)
N70.0193 (5)0.0208 (5)0.0176 (5)0.0020 (4)0.0046 (4)0.0005 (4)
N80.0179 (5)0.0215 (5)0.0160 (5)0.0010 (4)0.0043 (4)0.0004 (4)
C170.0192 (6)0.0184 (6)0.0164 (6)0.0002 (5)0.0042 (5)0.0002 (5)
C180.0202 (6)0.0168 (5)0.0175 (6)0.0008 (5)0.0036 (5)0.0003 (5)
C190.0276 (7)0.0225 (6)0.0169 (6)0.0025 (5)0.0047 (5)0.0004 (5)
C200.0320 (8)0.0305 (7)0.0163 (6)0.0040 (6)0.0004 (6)0.0013 (5)
C210.0241 (7)0.0334 (8)0.0218 (7)0.0057 (6)0.0022 (5)0.0019 (6)
C220.0205 (6)0.0263 (7)0.0217 (7)0.0042 (5)0.0028 (5)0.0007 (5)
C230.0213 (6)0.0183 (6)0.0171 (6)0.0021 (5)0.0027 (5)0.0007 (5)
C240.0184 (6)0.0190 (6)0.0174 (6)0.0009 (5)0.0038 (5)0.0001 (5)
C250.0180 (6)0.0181 (6)0.0185 (6)0.0016 (5)0.0052 (5)0.0010 (5)
C260.0204 (6)0.0155 (5)0.0194 (6)0.0007 (5)0.0068 (5)0.0015 (4)
C270.0199 (6)0.0213 (6)0.0224 (6)0.0007 (5)0.0063 (5)0.0025 (5)
C280.0218 (7)0.0266 (7)0.0296 (7)0.0014 (5)0.0122 (6)0.0024 (6)
C290.0284 (7)0.0276 (7)0.0248 (7)0.0010 (6)0.0143 (6)0.0002 (5)
C300.0262 (7)0.0221 (6)0.0201 (6)0.0012 (5)0.0089 (5)0.0007 (5)
C310.0205 (6)0.0154 (5)0.0203 (6)0.0012 (5)0.0074 (5)0.0010 (5)
C320.0198 (6)0.0169 (5)0.0175 (6)0.0002 (5)0.0065 (5)0.0010 (4)
N90.0190 (5)0.0252 (6)0.0181 (5)0.0013 (4)0.0064 (4)0.0031 (4)
N100.0189 (5)0.0261 (6)0.0180 (5)0.0018 (4)0.0059 (4)0.0028 (4)
C330.0185 (6)0.0275 (7)0.0173 (6)0.0018 (5)0.0054 (5)0.0022 (5)
C340.0203 (6)0.0303 (7)0.0196 (6)0.0003 (5)0.0048 (5)0.0059 (5)
C350.0198 (6)0.0318 (7)0.0206 (6)0.0002 (5)0.0047 (5)0.0063 (5)
C360.0190 (6)0.0223 (6)0.0175 (6)0.0013 (5)0.0078 (5)0.0012 (5)
C370.0211 (6)0.0226 (6)0.0187 (6)0.0001 (5)0.0073 (5)0.0011 (5)
C380.0200 (6)0.0246 (6)0.0223 (6)0.0011 (5)0.0071 (5)0.0009 (5)
C390.0246 (7)0.0260 (7)0.0305 (7)0.0011 (5)0.0140 (6)0.0044 (6)
C400.0267 (7)0.0349 (8)0.0202 (6)0.0023 (6)0.0120 (5)0.0080 (6)
C410.0225 (7)0.0336 (7)0.0189 (6)0.0012 (6)0.0085 (5)0.0069 (5)
C420.0247 (7)0.0276 (7)0.0256 (7)0.0065 (5)0.0113 (6)0.0046 (5)
C430.0315 (8)0.0223 (6)0.0286 (7)0.0010 (6)0.0146 (6)0.0030 (5)
C440.0327 (8)0.0385 (8)0.0226 (7)0.0008 (6)0.0142 (6)0.0050 (6)
C450.0283 (7)0.0219 (6)0.0243 (7)0.0036 (5)0.0108 (6)0.0020 (5)
C460.0176 (6)0.0239 (6)0.0161 (6)0.0005 (5)0.0072 (5)0.0011 (5)
C470.0164 (6)0.0301 (7)0.0189 (6)0.0002 (5)0.0057 (5)0.0037 (5)
C480.0199 (6)0.0342 (7)0.0177 (6)0.0007 (5)0.0057 (5)0.0044 (5)
C490.0334 (8)0.0388 (8)0.0206 (7)0.0006 (6)0.0121 (6)0.0029 (6)
C500.0348 (8)0.0307 (7)0.0284 (7)0.0084 (6)0.0180 (6)0.0012 (6)
C510.0200 (7)0.0452 (9)0.0278 (7)0.0074 (6)0.0112 (6)0.0105 (7)
C520.0182 (6)0.0320 (7)0.0226 (7)0.0049 (5)0.0061 (5)0.0035 (5)
C530.0194 (6)0.0274 (7)0.0194 (6)0.0027 (5)0.0058 (5)0.0003 (5)
C540.0227 (7)0.0293 (7)0.0254 (7)0.0001 (5)0.0092 (5)0.0068 (6)
C550.0313 (8)0.0233 (7)0.0271 (7)0.0022 (6)0.0121 (6)0.0006 (5)
O10.0350 (6)0.0229 (5)0.0269 (6)0.0015 (4)0.0035 (5)0.0014 (4)
O20.071 (2)0.0482 (17)0.0459 (17)0.0024 (15)0.0170 (15)0.0017 (13)
C560.065 (3)0.0350 (18)0.0354 (19)0.0166 (17)0.0160 (18)0.0093 (15)
C570.0824 (19)0.0574 (15)0.0572 (14)0.0113 (13)0.0265 (14)0.0118 (12)
Geometric parameters (Å, º) top
Li1—N21.9592 (11)N9—C331.3358 (17)
Li1—N2i1.9592 (11)N9—C341.3798 (18)
Li1—N41.9650 (11)N9—C361.4906 (17)
Li1—N4i1.9650 (11)N10—C331.3323 (17)
N1—C11.3352 (16)N10—C351.3808 (17)
N1—C16i1.3365 (16)N10—C461.4885 (16)
N2—C81.3597 (16)C33—H330.9500
N2—C11.3625 (16)C34—C351.3481 (19)
N3—C91.3411 (16)C34—H340.9500
N3—C81.3424 (16)C35—H350.9500
N4—C91.3581 (16)C36—C451.529 (2)
N4—C161.3617 (16)C36—C411.5307 (18)
C1—C21.4603 (17)C36—C371.5309 (19)
C2—C31.3895 (18)C37—C381.5337 (19)
C2—C71.4020 (18)C37—H37A0.9900
C3—C41.3859 (19)C37—H37B0.9900
C3—H30.9500C38—C421.528 (2)
C4—C51.396 (2)C38—C391.533 (2)
C4—H40.9500C38—H381.0000
C5—C61.388 (2)C39—C401.528 (2)
C5—H50.9500C39—H39A0.9900
C6—C71.3914 (18)C39—H39B0.9900
C6—H60.9500C40—C441.531 (2)
C7—C81.4688 (18)C40—C411.5335 (19)
C9—C101.4720 (18)C40—H401.0000
C10—C111.3923 (18)C41—H41A0.9900
C10—C151.4016 (18)C41—H41B0.9900
C11—C121.3892 (19)C42—C431.529 (2)
C11—H110.9500C42—H42A0.9900
C12—C131.399 (2)C42—H42B0.9900
C12—H120.9500C43—C441.532 (2)
C13—C141.3875 (19)C43—C451.535 (2)
C13—H130.9500C43—H431.0000
C14—C151.3913 (18)C44—H44A0.9900
C14—H140.9500C44—H44B0.9900
C15—C161.4593 (18)C45—H45A0.9900
C16—N1i1.3365 (16)C45—H45B0.9900
Li2—N61.9567 (11)C46—C551.5267 (19)
Li2—N6ii1.9567 (11)C46—C471.5287 (18)
Li2—N81.9606 (11)C46—C531.5322 (19)
Li2—N8ii1.9606 (11)C47—C481.5347 (19)
N5—C171.3343 (17)C47—H47A0.9900
N5—C32ii1.3345 (17)C47—H47B0.9900
N6—C241.3625 (17)C48—C491.526 (2)
N6—C171.3656 (17)C48—C541.529 (2)
N7—C241.3357 (17)C48—H481.0000
N7—C251.3374 (17)C49—C501.534 (2)
N8—C251.3667 (17)C49—H49A0.9900
N8—C321.3672 (17)C49—H49B0.9900
C17—C181.4634 (18)C50—C511.526 (2)
C18—C191.3867 (18)C50—C551.536 (2)
C18—C231.3984 (19)C50—H501.0000
C19—C201.388 (2)C51—C521.527 (2)
C19—H190.9500C51—H51A0.9900
C20—C211.399 (2)C51—H51B0.9900
C20—H200.9500C52—C541.530 (2)
C21—C221.389 (2)C52—C531.5315 (19)
C21—H210.9500C52—H521.0000
C22—C231.3910 (19)C53—H53A0.9900
C22—H220.9500C53—H53B0.9900
C23—C241.4671 (18)C54—H54A0.9900
C25—C261.4636 (18)C54—H54B0.9900
C26—C271.3930 (19)C55—H55A0.9900
C26—C311.4019 (19)C55—H55B0.9900
C27—C281.3894 (19)O1—H1A0.862 (15)
C27—H270.9500O1—H1B0.890 (15)
C28—C291.400 (2)O2—C561.191 (5)
C28—H280.9500C56—C57iii1.476 (5)
C29—C301.388 (2)C56—C571.487 (5)
C29—H290.9500C56—C56iii1.503 (8)
C30—C311.3939 (18)C57—C56iii1.476 (5)
C30—H300.9500C57—H57A0.948 (18)
C31—C321.4628 (18)C57—H57B0.931 (18)
C32—N5ii1.3345 (17)C57—H57C0.935 (18)
N2—Li1—N2i180.00 (8)N10—C35—H35126.3
N2—Li1—N489.28 (5)N9—C36—C45108.13 (11)
N2i—Li1—N490.72 (5)N9—C36—C41109.07 (11)
N2—Li1—N4i90.72 (5)C45—C36—C41109.59 (11)
N2i—Li1—N4i89.28 (5)N9—C36—C37110.33 (10)
N4—Li1—N4i180.00 (8)C45—C36—C37109.37 (11)
C1—N1—C16i122.68 (11)C41—C36—C37110.32 (11)
C8—N2—C1107.98 (10)C36—C37—C38109.00 (11)
C8—N2—Li1126.75 (9)C36—C37—H37A109.9
C1—N2—Li1125.25 (8)C38—C37—H37A109.9
C9—N3—C8122.79 (11)C36—C37—H37B109.9
C9—N4—C16107.90 (11)C38—C37—H37B109.9
C9—N4—Li1126.97 (9)H37A—C37—H37B108.3
C16—N4—Li1124.98 (9)C42—C38—C39109.88 (12)
N1—C1—N2128.03 (11)C42—C38—C37109.06 (11)
N1—C1—C2121.71 (11)C39—C38—C37109.59 (11)
N2—C1—C2110.25 (11)C42—C38—H38109.4
C3—C2—C7121.79 (12)C39—C38—H38109.4
C3—C2—C1132.17 (12)C37—C38—H38109.4
C7—C2—C1105.98 (11)C40—C39—C38109.39 (11)
C4—C3—C2117.65 (13)C40—C39—H39A109.8
C4—C3—H3121.2C38—C39—H39A109.8
C2—C3—H3121.2C40—C39—H39B109.8
C3—C4—C5120.76 (13)C38—C39—H39B109.8
C3—C4—H4119.6H39A—C39—H39B108.2
C5—C4—H4119.6C39—C40—C44109.89 (12)
C6—C5—C4121.77 (13)C39—C40—C41109.54 (12)
C6—C5—H5119.1C44—C40—C41109.21 (12)
C4—C5—H5119.1C39—C40—H40109.4
C5—C6—C7117.74 (13)C44—C40—H40109.4
C5—C6—H6121.1C41—C40—H40109.4
C7—C6—H6121.1C36—C41—C40109.10 (11)
C6—C7—C2120.29 (12)C36—C41—H41A109.9
C6—C7—C8133.90 (12)C40—C41—H41A109.9
C2—C7—C8105.72 (11)C36—C41—H41B109.9
N3—C8—N2127.26 (12)C40—C41—H41B109.9
N3—C8—C7122.66 (11)H41A—C41—H41B108.3
N2—C8—C7110.07 (11)C38—C42—C43109.65 (12)
N3—C9—N4126.87 (12)C38—C42—H42A109.7
N3—C9—C10122.93 (11)C43—C42—H42A109.7
N4—C9—C10110.20 (11)C38—C42—H42B109.7
C11—C10—C15120.37 (12)C43—C42—H42B109.7
C11—C10—C9134.17 (12)H42A—C42—H42B108.2
C15—C10—C9105.46 (11)C42—C43—C44109.72 (12)
C12—C11—C10117.89 (12)C42—C43—C45109.12 (11)
C12—C11—H11121.1C44—C43—C45109.47 (12)
C10—C11—H11121.1C42—C43—H43109.5
C11—C12—C13121.46 (12)C44—C43—H43109.5
C11—C12—H12119.3C45—C43—H43109.5
C13—C12—H12119.3C40—C44—C43109.39 (12)
C14—C13—C12120.97 (13)C40—C44—H44A109.8
C14—C13—H13119.5C43—C44—H44A109.8
C12—C13—H13119.5C40—C44—H44B109.8
C13—C14—C15117.54 (13)C43—C44—H44B109.8
C13—C14—H14121.2H44A—C44—H44B108.2
C15—C14—H14121.2C36—C45—C43109.16 (11)
C14—C15—C10121.77 (12)C36—C45—H45A109.8
C14—C15—C16132.13 (12)C43—C45—H45A109.8
C10—C15—C16106.10 (11)C36—C45—H45B109.8
N1i—C16—N4128.09 (12)C43—C45—H45B109.8
N1i—C16—C15121.59 (12)H45A—C45—H45B108.3
N4—C16—C15110.31 (11)N10—C46—C55109.00 (11)
N6—Li2—N6ii180.00 (7)N10—C46—C47109.81 (10)
N6—Li2—N890.47 (5)C55—C46—C47110.10 (11)
N6ii—Li2—N889.53 (5)N10—C46—C53108.16 (10)
N6—Li2—N8ii89.53 (5)C55—C46—C53110.19 (11)
N6ii—Li2—N8ii90.47 (5)C47—C46—C53109.55 (11)
N8—Li2—N8ii180.00 (3)C46—C47—C48108.73 (11)
C17—N5—C32ii122.18 (11)C46—C47—H47A109.9
C24—N6—C17107.97 (11)C48—C47—H47A109.9
C24—N6—Li2125.63 (9)C46—C47—H47B109.9
C17—N6—Li2126.35 (9)C48—C47—H47B109.9
C24—N7—C25122.74 (12)H47A—C47—H47B108.3
C25—N8—C32107.97 (11)C49—C48—C54109.21 (12)
C25—N8—Li2125.43 (9)C49—C48—C47109.43 (12)
C32—N8—Li2126.19 (9)C54—C48—C47109.83 (11)
N5—C17—N6127.84 (12)C49—C48—H48109.5
N5—C17—C18122.04 (12)C54—C48—H48109.5
N6—C17—C18110.13 (11)C47—C48—H48109.5
C19—C18—C23121.39 (12)C48—C49—C50109.44 (12)
C19—C18—C17132.72 (13)C48—C49—H49A109.8
C23—C18—C17105.89 (11)C50—C49—H49A109.8
C18—C19—C20117.78 (13)C48—C49—H49B109.8
C18—C19—H19121.1C50—C49—H49B109.8
C20—C19—H19121.1H49A—C49—H49B108.2
C19—C20—C21120.99 (13)C51—C50—C49110.30 (13)
C19—C20—H20119.5C51—C50—C55109.30 (12)
C21—C20—H20119.5C49—C50—C55108.73 (13)
C22—C21—C20121.20 (13)C51—C50—H50109.5
C22—C21—H21119.4C49—C50—H50109.5
C20—C21—H21119.4C55—C50—H50109.5
C21—C22—C23117.79 (13)C50—C51—C52109.91 (12)
C21—C22—H22121.1C50—C51—H51A109.7
C23—C22—H22121.1C52—C51—H51A109.7
C22—C23—C18120.83 (12)C50—C51—H51B109.7
C22—C23—C24133.03 (13)C52—C51—H51B109.7
C18—C23—C24106.13 (11)H51A—C51—H51B108.2
N7—C24—N6127.88 (12)C51—C52—C54108.96 (12)
N7—C24—C23122.24 (12)C51—C52—C53109.23 (12)
N6—C24—C23109.88 (11)C54—C52—C53109.53 (11)
N7—C25—N8127.62 (12)C51—C52—H52109.7
N7—C25—C26122.45 (12)C54—C52—H52109.7
N8—C25—C26109.93 (11)C53—C52—H52109.7
C27—C26—C31120.84 (12)C52—C53—C46109.16 (11)
C27—C26—C25132.99 (12)C52—C53—H53A109.8
C31—C26—C25106.09 (11)C46—C53—H53A109.8
C28—C27—C26117.44 (13)C52—C53—H53B109.8
C28—C27—H27121.3C46—C53—H53B109.8
C26—C27—H27121.3H53A—C53—H53B108.3
C27—C28—C29121.79 (13)C48—C54—C52110.00 (12)
C27—C28—H28119.1C48—C54—H54A109.7
C29—C28—H28119.1C52—C54—H54A109.7
C30—C29—C28120.83 (13)C48—C54—H54B109.7
C30—C29—H29119.6C52—C54—H54B109.7
C28—C29—H29119.6H54A—C54—H54B108.2
C29—C30—C31117.62 (13)C46—C55—C50108.86 (12)
C29—C30—H30121.2C46—C55—H55A109.9
C31—C30—H30121.2C50—C55—H55A109.9
C30—C31—C26121.48 (12)C46—C55—H55B109.9
C30—C31—C32132.41 (13)C50—C55—H55B109.9
C26—C31—C32106.03 (11)H55A—C55—H55B108.3
N5ii—C32—N8127.75 (12)H1A—O1—H1B105.0 (18)
N5ii—C32—C31122.23 (12)O2—C56—C57iii120.8 (4)
N8—C32—C31109.99 (11)O2—C56—C57120.0 (4)
C33—N9—C34108.36 (11)C57iii—C56—C57119.1 (3)
C33—N9—C36124.24 (11)O2—C56—C56iii177.4 (5)
C34—N9—C36127.12 (11)C57iii—C56—C56iii59.9 (3)
C33—N10—C35108.33 (11)C57—C56—C56iii59.2 (3)
C33—N10—C46127.08 (11)C56iii—C57—C5660.9 (3)
C35—N10—C46124.55 (11)C56iii—C57—H57A156.5 (19)
N10—C33—N9108.73 (12)C56—C57—H57A112.2 (15)
N10—C33—H33125.6C56iii—C57—H57B76.6 (18)
N9—C33—H33125.6C56—C57—H57B116.3 (15)
C35—C34—N9107.22 (12)H57A—C57—H57B88 (2)
C35—C34—H34126.4C56iii—C57—H57C101.4 (18)
N9—C34—H34126.4C56—C57—H57C115.1 (15)
C34—C35—N10107.36 (12)H57A—C57—H57C102 (3)
C34—C35—H35126.3H57B—C57—H57C118 (3)
N4—Li1—N2—C80.79 (11)C24—N7—C25—N83.2 (2)
N4i—Li1—N2—C8179.21 (11)C24—N7—C25—C26176.20 (12)
N4—Li1—N2—C1178.85 (10)C32—N8—C25—N7179.25 (13)
N4i—Li1—N2—C11.15 (10)Li2—N8—C25—N76.3 (2)
N2—Li1—N4—C91.91 (11)C32—N8—C25—C260.18 (14)
N2i—Li1—N4—C9178.09 (11)Li2—N8—C25—C26173.14 (8)
N2—Li1—N4—C16176.80 (11)N7—C25—C26—C273.0 (2)
N2i—Li1—N4—C163.20 (11)N8—C25—C26—C27176.45 (14)
C16i—N1—C1—N22.2 (2)N7—C25—C26—C31179.63 (12)
C16i—N1—C1—C2179.29 (12)N8—C25—C26—C310.17 (14)
C8—N2—C1—N1177.65 (12)C31—C26—C27—C280.03 (19)
Li1—N2—C1—N13.99 (19)C25—C26—C27—C28176.19 (13)
C8—N2—C1—C21.00 (14)C26—C27—C28—C290.5 (2)
Li1—N2—C1—C2177.36 (8)C27—C28—C29—C300.8 (2)
N1—C1—C2—C35.0 (2)C28—C29—C30—C310.5 (2)
N2—C1—C2—C3176.21 (13)C29—C30—C31—C260.0 (2)
N1—C1—C2—C7177.94 (12)C29—C30—C31—C32176.01 (14)
N2—C1—C2—C70.80 (14)C27—C26—C31—C300.24 (19)
C7—C2—C3—C40.38 (19)C25—C26—C31—C30177.36 (12)
C1—C2—C3—C4176.23 (13)C27—C26—C31—C32176.71 (12)
C2—C3—C4—C50.2 (2)C25—C26—C31—C320.41 (13)
C3—C4—C5—C60.3 (2)C25—N8—C32—N5ii177.29 (13)
C4—C5—C6—C70.5 (2)Li2—N8—C32—N5ii4.40 (19)
C5—C6—C7—C20.3 (2)C25—N8—C32—C310.45 (14)
C5—C6—C7—C8175.63 (14)Li2—N8—C32—C31173.34 (8)
C3—C2—C7—C60.2 (2)C30—C31—C32—N5ii0.9 (2)
C1—C2—C7—C6177.23 (12)C26—C31—C32—N5ii177.34 (12)
C3—C2—C7—C8177.10 (12)C30—C31—C32—N8177.02 (14)
C1—C2—C7—C80.29 (13)C26—C31—C32—N80.55 (14)
C9—N3—C8—N22.3 (2)C35—N10—C33—N90.38 (16)
C9—N3—C8—C7176.25 (12)C46—N10—C33—N9177.78 (12)
C1—N2—C8—N3179.48 (12)C34—N9—C33—N100.13 (16)
Li1—N2—C8—N31.15 (19)C36—N9—C33—N10174.13 (12)
C1—N2—C8—C70.81 (14)C33—N9—C34—C350.17 (17)
Li1—N2—C8—C7177.52 (8)C36—N9—C34—C35174.22 (13)
C6—C7—C8—N32.7 (2)N9—C34—C35—N100.40 (17)
C2—C7—C8—N3179.05 (12)C33—N10—C35—C340.48 (17)
C6—C7—C8—N2176.03 (14)C46—N10—C35—C34177.73 (13)
C2—C7—C8—N20.30 (14)C33—N9—C36—C4564.57 (16)
C8—N3—C9—N43.6 (2)C34—N9—C36—C45108.59 (15)
C8—N3—C9—C10175.40 (12)C33—N9—C36—C41176.32 (13)
C16—N4—C9—N3179.22 (12)C34—N9—C36—C4110.52 (19)
Li1—N4—C9—N33.61 (19)C33—N9—C36—C3755.00 (17)
C16—N4—C9—C100.14 (14)C34—N9—C36—C37131.84 (14)
Li1—N4—C9—C10175.46 (8)N9—C36—C37—C38179.77 (11)
N3—C9—C10—C111.2 (2)C45—C36—C37—C3860.96 (14)
N4—C9—C10—C11179.65 (14)C41—C36—C37—C3859.65 (14)
N3—C9—C10—C15178.30 (12)C36—C37—C38—C4260.66 (14)
N4—C9—C10—C150.82 (14)C36—C37—C38—C3959.67 (14)
C15—C10—C11—C120.87 (19)C42—C38—C39—C4059.37 (15)
C9—C10—C11—C12178.61 (13)C37—C38—C39—C4060.45 (15)
C10—C11—C12—C130.1 (2)C38—C39—C40—C4459.55 (15)
C11—C12—C13—C140.4 (2)C38—C39—C40—C4160.44 (15)
C12—C13—C14—C150.2 (2)N9—C36—C41—C40178.95 (11)
C13—C14—C15—C100.6 (2)C45—C36—C41—C4060.75 (15)
C13—C14—C15—C16179.63 (13)C37—C36—C41—C4059.72 (15)
C11—C10—C15—C141.1 (2)C39—C40—C41—C3659.79 (15)
C9—C10—C15—C14178.49 (12)C44—C40—C41—C3660.61 (15)
C11—C10—C15—C16179.02 (12)C39—C38—C42—C4359.47 (15)
C9—C10—C15—C161.36 (13)C37—C38—C42—C4360.67 (14)
C9—N4—C16—N1i178.37 (13)C38—C42—C43—C4459.57 (15)
Li1—N4—C16—N1i5.92 (19)C38—C42—C43—C4560.37 (15)
C9—N4—C16—C151.03 (14)C39—C40—C44—C4359.74 (15)
Li1—N4—C16—C15174.68 (8)C41—C40—C44—C4360.45 (16)
C14—C15—C16—N1i2.3 (2)C42—C43—C44—C4059.58 (16)
C10—C15—C16—N1i177.90 (12)C45—C43—C44—C4060.15 (16)
C14—C15—C16—N4178.29 (14)N9—C36—C45—C43179.11 (11)
C10—C15—C16—N41.54 (14)C41—C36—C45—C4360.33 (15)
N8—Li2—N6—C240.27 (11)C37—C36—C45—C4360.72 (14)
N8ii—Li2—N6—C24179.73 (11)C42—C43—C45—C3660.18 (15)
N8—Li2—N6—C17176.88 (11)C44—C43—C45—C3659.92 (15)
N8ii—Li2—N6—C173.12 (11)C33—N10—C46—C55120.09 (15)
N6—Li2—N8—C254.10 (11)C35—N10—C46—C5562.03 (17)
N6ii—Li2—N8—C25175.90 (11)C33—N10—C46—C470.60 (19)
N6—Li2—N8—C32175.80 (11)C35—N10—C46—C47177.28 (13)
N6ii—Li2—N8—C324.20 (11)C33—N10—C46—C53120.10 (14)
C32ii—N5—C17—N60.5 (2)C35—N10—C46—C5357.77 (17)
C32ii—N5—C17—C18179.08 (12)N10—C46—C47—C48179.67 (11)
C24—N6—C17—N5179.52 (13)C55—C46—C47—C4860.31 (15)
Li2—N6—C17—N52.0 (2)C53—C46—C47—C4861.02 (14)
C24—N6—C17—C180.07 (15)C46—C47—C48—C4959.97 (15)
Li2—N6—C17—C18177.63 (9)C46—C47—C48—C5459.90 (15)
N5—C17—C18—C190.0 (2)C54—C48—C49—C5059.32 (16)
N6—C17—C18—C19179.67 (14)C47—C48—C49—C5060.93 (16)
N5—C17—C18—C23179.73 (12)C48—C49—C50—C5158.81 (16)
N6—C17—C18—C230.11 (15)C48—C49—C50—C5561.02 (16)
C23—C18—C19—C200.2 (2)C49—C50—C51—C5258.90 (15)
C17—C18—C19—C20179.54 (14)C55—C50—C51—C5260.58 (15)
C18—C19—C20—C210.3 (2)C50—C51—C52—C5459.22 (15)
C19—C20—C21—C220.6 (2)C50—C51—C52—C5360.39 (15)
C20—C21—C22—C230.4 (2)C51—C52—C53—C4659.54 (15)
C21—C22—C23—C180.1 (2)C54—C52—C53—C4659.72 (15)
C21—C22—C23—C24179.03 (14)N10—C46—C53—C52179.12 (11)
C19—C18—C23—C220.4 (2)C55—C46—C53—C5260.06 (14)
C17—C18—C23—C22179.42 (12)C47—C46—C53—C5261.21 (14)
C19—C18—C23—C24179.58 (12)C49—C48—C54—C5260.81 (15)
C17—C18—C23—C240.23 (14)C47—C48—C54—C5259.20 (15)
C25—N7—C24—N61.5 (2)C51—C52—C54—C4860.47 (15)
C25—N7—C24—C23178.69 (12)C53—C52—C54—C4858.95 (16)
C17—N6—C24—N7179.97 (13)N10—C46—C55—C50178.57 (11)
Li2—N6—C24—N72.4 (2)C47—C46—C55—C5060.91 (15)
C17—N6—C24—C230.22 (15)C53—C46—C55—C5060.03 (15)
Li2—N6—C24—C23177.80 (9)C51—C50—C55—C4659.87 (16)
C22—C23—C24—N70.8 (2)C49—C50—C55—C4660.58 (16)
C18—C23—C24—N7179.89 (12)O2—C56—C57—C56iii177.2 (5)
C22—C23—C24—N6179.34 (14)C57iii—C56—C57—C56iii0.000 (1)
C18—C23—C24—N60.28 (15)
Symmetry codes: (i) x+2, y, z; (ii) x, y+1, z; (iii) x, y+1, z+1.
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
O1—H1A···N60.86 (2)2.41 (2)3.1618 (17)147 (2)
O1—H1B···N3iv0.89 (2)2.03 (2)2.8911 (17)164 (2)
C33—H33···O10.952.183.127 (2)171
C37—H37A···O10.992.523.493 (2)166
Symmetry code: (iv) x+1, y+1, z.

Experimental details

Crystal data
Chemical formula(C23H33N2)[Li(C32H16N8)]·0.5C3H6O·H2O
Mr904.04
Crystal system, space groupMonoclinic, P21/n
Temperature (K)173
a, b, c (Å)15.799 (3), 17.165 (4), 17.831 (4)
β (°) 108.374 (3)
V3)4588.9 (16)
Z4
Radiation typeMo Kα
µ (mm1)0.08
Crystal size (mm)0.44 × 0.39 × 0.20
Data collection
DiffractometerBruker Smart APEXII CCD
diffractometer
Absorption correctionMulti-scan
(SADABS; Bruker, 2003)
Tmin, Tmax0.901, 0.985
No. of measured, independent and
observed [I > 2σ(I)] reflections
54676, 14917, 11038
Rint0.039
(sin θ/λ)max1)0.740
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.052, 0.129, 1.03
No. of reflections14917
No. of parameters649
No. of restraints8
H-atom treatmentH atoms treated by a mixture of independent and constrained refinement
Δρmax, Δρmin (e Å3)0.37, 0.30

Computer programs: SMART (Bruker, 2002), SAINT-Plus (Bruker, 2003), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), Mercury (Macrae et al., 2006), ORTEP-3 for Windows, (Farrugia, 1997), OSCAIL, (McArdle, 1995), enCIFer (Allen et al., 2004) and publCIF (Westrip, 2009).

Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
O1—H1A···N60.861 (18)2.405 (17)3.1618 (17)147.1 (18)
O1—H1B···N3i0.889 (18)2.025 (19)2.8911 (17)164.3 (16)
C33—H33···O10.952.183.127 (2)171
C37—H37A···O10.992.523.493 (2)166
Symmetry code: (i) x+1, y+1, z.
 

Acknowledgements

The authors acknowledge the diffractometer time granted by A. Hunter, Youngstown State University.

References

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