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Acta Crystallographica Section E: Structure Reports Online logoLink to Acta Crystallographica Section E: Structure Reports Online
. 2012 Jul 18;68(Pt 8):o2487. doi: 10.1107/S160053681203173X

(S)-4-tert-Butyl-2-(1,2,3,4-tetra­hydro­isoquinolin-3-yl)-1,3-thia­zole

Sunayna Pawar a, Thavendran Govender a, Hendrik G Kruger b, Glenn E M Maguire b,*
PMCID: PMC3414942  PMID: 22904929

Abstract

In the title compound, C16H20N2S, a potential tetra­hydro­isoquinoline (TIQ) thia­zole ligand, the N-containing six-membered ring of the TIQ unit adopts a half-chair conformation. There are four mol­ecules in the asymmetric unit. No classical hydrogen bonds or π–π inter­actions were found in the crystal structure.

Related literature  

For reactions associated with tetra­hydro­isoquinoline ligands, see: Chakka et al. (2010); Naicker et al. (2010); Kawthekar et al. (2010); Peters et al. (2010); Pawar et al. (2012). For related structures, see: Aubry et al. (2006); Naicker et al. (2011a ,b ); Pawar et al. (2011).graphic file with name e-68-o2487-scheme1.jpg

Experimental  

Crystal data  

  • C16H20N2S

  • M r = 272.40

  • Monoclinic, Inline graphic

  • a = 10.0534 (9) Å

  • b = 13.0076 (12) Å

  • c = 23.808 (2) Å

  • β = 102.076 (1)°

  • V = 3044.5 (5) Å3

  • Z = 8

  • Mo Kα radiation

  • μ = 0.20 mm−1

  • T = 173 K

  • 0.18 × 0.16 × 0.08 mm

Data collection  

  • Bruker Kappa DUO APEXII diffractometer

  • Absorption correction: multi-scan (SADABS; Bruker, 2006) T min = 0.965, T max = 0.984

  • 39811 measured reflections

  • 15130 independent reflections

  • 12021 reflections with I > 2σ(I)

  • R int = 0.035

  • Standard reflections: ?

Refinement  

  • R[F 2 > 2σ(F 2)] = 0.092

  • wR(F 2) = 0.299

  • S = 1.04

  • 15130 reflections

  • 710 parameters

  • 5 restraints

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

  • Δρmax = 0.99 e Å−3

  • Δρmin = −0.76 e Å−3

  • Absolute structure: Flack (1983), 7172 Friedel pairs

  • Flack parameter: 0.04 (13)

Data collection: SAINT (Bruker, 2006); cell refinement: SAINT; data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: OLEX2 (Dolomanov et al., 2009); software used to prepare material for publication: SHELXL97.

Supplementary Material

Crystal structure: contains datablock(s) I, global. DOI: 10.1107/S160053681203173X/gw2121sup1.cif

e-68-o2487-sup1.cif (43.5KB, cif)

Structure factors: contains datablock(s) I. DOI: 10.1107/S160053681203173X/gw2121Isup2.hkl

e-68-o2487-Isup2.hkl (739.5KB, hkl)

Supplementary material file. DOI: 10.1107/S160053681203173X/gw2121Isup3.cml

Additional supplementary materials: crystallographic information; 3D view; checkCIF report

Acknowledgments

The authors thank Dr Hong Su of the University of Capetown for the data collection and structure refinement.

supplementary crystallographic information

Comment

We have recently reported a range of tetrahydroisoquinoline (TIQ) structures that have been employed as ligands for catalysis of a number of reactions, Chakka et al. 2010, Naicker et al., 2010, Kawthekar et al., 2010 and Peters et al., 2010. The title compound is from a new family of TIQ thiazole derivatives that we have tested for catalytic activity in the Henry reaction, (Pawar et al., 2012).

The absolute stereochemistry was confirmed to be S at the C9 position from two-dimensional NMR spectroscopy experiments (Aubry et al., 2006), (Fig. 1). From the crystal structure it is evident that the N-containing six membered ring assumes a half chair conformation [Q = 0.493 (6) Å, θ = 49.5 (7)° and φ = 322.8 (9)°]. This is similar to our previously reported structures which also assume this conformation (Naicker et al., 2011a,b and Pawar et al. 2011). The torsion angle for C1A—N1A—C9A—C10A is -170.1 (5)°; C1B—N1B—C9B—C10B is -173.4 (5)°; C1C—N1C—C9C—C10C is -170.5 (5)° and C1D—N1D—C9D—C10D is -169.1 (5)°. For the plain formed by the atoms C1—C2—C7—C8—C9—N1 the maximum displacement from planarity for N1A is 0.446 Å and for C9A 0.299 Å; N1B is 0.384 Å and for C9B 0.296 Å; N1C is 0.427 Å and for C9C 0.258 Å and N1D is 0.286 Å and for C9D 0.473 Å. There are no hydrogen bonding or π–π interactions in the crystal lattice.

Experimental

The N-protected thiazole (3 mmol) was dissolved in THF (15 ml), to this 12 M HCl (15 ml) was added slowly and the reaction mixture was stirred at room temperature for 2 h. The reaction was monitored by TLC using EtOAc/Hexane (20:80, Rf = 0.5). After this time the THF was evaporated under vacuum. Aqueous saturated NaHCO3 solution, was then slowly poured into the mixture which was then extracted with CH2Cl2 (3 x 30 ml). The combined organic layers waere dried over MgSO4. The solvent was then evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (deactivated with 5% Et3N) with Et3N/EtOAc/Hexane (5/8/100) as the eluent to afford the TIQ thiazole as a yellow solid (0.27 g, yield 95%).

Recrystallization from mixture of hexane and dichloromethane at room temperature afforded colourless crystals suitable for X-ray analysis.

Refinement

The crystal was twinned. When the structure was attempted to be refined with a P21/c space group the R factor rose to 20%. All hydrogen atoms, except H1A, H1B, H1C and H1D, were positioned geometrically with C—H distances ranging from 0.95 Å to 0.99 Å and refined as riding on their parent atoms with Uiso (H) = 1.2 - 1.5 Ueq (C). The positions of H1A, H1B, H1C and H1D were located in difference electron density maps and refined with bond length constraints [d(N—H) = 0.97 (2) Å] and Uiso = 1.5 Ueq (N).

Figures

Fig. 1.

Fig. 1.

The crystal structure of the title compound with atomic numbering. Displacement ellipsoids are drawn at 50% probability.

Crystal data

C16H20N2S F(000) = 1168
Mr = 272.40 Dx = 1.189 Mg m3
Monoclinic, P21 Mo Kα radiation, λ = 0.71073 Å
a = 10.0534 (9) Å Cell parameters from 39811 reflections
b = 13.0076 (12) Å θ = 1.6–28.4°
c = 23.808 (2) Å µ = 0.20 mm1
β = 102.076 (1)° T = 173 K
V = 3044.5 (5) Å3 Block, colourless
Z = 8 0.18 × 0.16 × 0.08 mm

Data collection

Bruker Kappa DUO APEXII diffractometer 15130 independent reflections
Radiation source: fine-focus sealed tube 12021 reflections with I > 2σ(I)
Graphite monochromator Rint = 0.035
0.5° φ scans and ω scans θmax = 28.4°, θmin = 1.6°
Absorption correction: multi-scan (SADABS; Bruker, 2006) h = −13→13
Tmin = 0.965, Tmax = 0.984 k = −17→17
39811 measured reflections l = −31→31

Refinement

Refinement on F2 Secondary atom site location: difference Fourier map
Least-squares matrix: full Hydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.092 H atoms treated by a mixture of independent and constrained refinement
wR(F2) = 0.299 w = 1/[σ2(Fo2) + (0.193P)2 + 3.4647P] where P = (Fo2 + 2Fc2)/3
S = 1.04 (Δ/σ)max = 0.001
15130 reflections Δρmax = 0.99 e Å3
710 parameters Δρmin = −0.76 e Å3
5 restraints Absolute structure: Flack (1983), 7172 Friedel pairs
Primary atom site location: structure-invariant direct methods Flack parameter: 0.04 (13)

Special details

Experimental. Half sphere of data collected using the Bruker SAINT software package. Crystal to detector distance = 30 mm; combination of φ and ω scans of 0.5°, 30 s per °, 2 iterations.
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)

x y z Uiso*/Ueq
S1A 0.09853 (14) 0.61309 (11) 0.11586 (7) 0.0419 (3)
N1A 0.3267 (5) 0.6150 (4) 0.2152 (2) 0.0378 (10)
H1A 0.264 (6) 0.604 (7) 0.240 (3) 0.057*
N2A 0.1638 (5) 0.4234 (3) 0.11006 (19) 0.0329 (9)
C1A 0.4608 (7) 0.6376 (5) 0.2515 (3) 0.0489 (15)
H1A1 0.4494 0.6893 0.2806 0.059*
H1A2 0.5193 0.6683 0.2273 0.059*
C2A 0.5322 (6) 0.5450 (5) 0.2818 (2) 0.0422 (13)
C3A 0.6510 (7) 0.5576 (7) 0.3254 (3) 0.0562 (18)
H3A 0.6837 0.6248 0.3361 0.067*
C4A 0.7189 (8) 0.4742 (8) 0.3521 (3) 0.068 (2)
H4A 0.7985 0.4846 0.3810 0.082*
C5A 0.6754 (7) 0.3759 (7) 0.3382 (3) 0.0571 (18)
H5A 0.7231 0.3191 0.3580 0.068*
C6A 0.5607 (6) 0.3594 (5) 0.2949 (3) 0.0449 (14)
H6A 0.5309 0.2914 0.2845 0.054*
C7A 0.4889 (6) 0.4442 (5) 0.2665 (2) 0.0367 (11)
C8A 0.3660 (5) 0.4250 (4) 0.2192 (2) 0.0333 (10)
H8A1 0.2868 0.4079 0.2360 0.040*
H8A2 0.3837 0.3661 0.1954 0.040*
C9A 0.3349 (5) 0.5207 (4) 0.1816 (2) 0.0280 (9)
H9A 0.4107 0.5299 0.1608 0.034*
C10A 0.2059 (5) 0.5086 (4) 0.1376 (2) 0.0278 (9)
C11A −0.0054 (6) 0.5346 (5) 0.0667 (3) 0.0424 (13)
H11A −0.0869 0.5561 0.0415 0.051*
C12A 0.0464 (5) 0.4374 (4) 0.0691 (2) 0.0351 (11)
C13A −0.0077 (5) 0.3479 (5) 0.0315 (3) 0.0403 (12)
C14A −0.0372 (8) 0.2563 (6) 0.0695 (3) 0.0591 (18)
H14A 0.0414 0.2457 0.1011 0.089*
H14B −0.0538 0.1938 0.0461 0.089*
H14C −0.1176 0.2721 0.0852 0.089*
C15A 0.1035 (7) 0.3142 (6) 0.0002 (3) 0.0547 (17)
H15A 0.1256 0.3713 −0.0231 0.082*
H15B 0.0710 0.2555 −0.0248 0.082*
H15C 0.1850 0.2941 0.0284 0.082*
C16A −0.1361 (8) 0.3772 (8) −0.0118 (4) 0.072 (2)
H16A −0.2015 0.4085 0.0084 0.107*
H16B −0.1762 0.3156 −0.0322 0.107*
H16C −0.1132 0.4266 −0.0394 0.107*
S1B 0.60664 (15) 0.34925 (11) 0.11989 (6) 0.0400 (3)
N1B 0.8906 (6) 0.3639 (4) 0.2019 (2) 0.0462 (12)
H1B 0.940 (7) 0.380 (7) 0.171 (3) 0.069*
N2B 0.6586 (5) 0.5416 (4) 0.1216 (2) 0.0374 (10)
C1B 0.9826 (6) 0.3481 (5) 0.2572 (3) 0.0439 (13)
H1B1 1.0552 0.3000 0.2519 0.053*
H1B2 0.9313 0.3148 0.2835 0.053*
C2B 1.0472 (6) 0.4433 (5) 0.2851 (2) 0.0364 (11)
C3B 1.1645 (7) 0.4370 (6) 0.3293 (3) 0.0519 (16)
H3B 1.2013 0.3716 0.3418 0.062*
C4B 1.2274 (7) 0.5265 (8) 0.3551 (3) 0.062 (2)
H4B 1.3074 0.5220 0.3844 0.074*
C5B 1.1729 (8) 0.6196 (7) 0.3377 (3) 0.0611 (19)
H5B 1.2160 0.6799 0.3553 0.073*
C6B 1.0559 (7) 0.6296 (5) 0.2950 (3) 0.0478 (14)
H6B 1.0185 0.6955 0.2841 0.057*
C7B 0.9939 (5) 0.5401 (4) 0.2681 (2) 0.0343 (11)
C8B 0.8711 (6) 0.5515 (4) 0.2204 (2) 0.0374 (11)
H8B1 0.8994 0.5803 0.1862 0.045*
H8B2 0.8071 0.6006 0.2323 0.045*
C9B 0.7984 (6) 0.4497 (4) 0.2043 (3) 0.0390 (12)
H9B 0.7481 0.4333 0.2352 0.047*
C10B 0.6936 (5) 0.4573 (4) 0.1491 (2) 0.0346 (11)
C11B 0.5115 (6) 0.4238 (5) 0.0688 (3) 0.0420 (12)
H11B 0.4397 0.3987 0.0395 0.050*
C12B 0.5500 (5) 0.5239 (4) 0.0745 (2) 0.0313 (10)
C13B 0.4973 (5) 0.6145 (5) 0.0360 (3) 0.0401 (12)
C14B 0.6112 (7) 0.6504 (6) 0.0065 (3) 0.0520 (17)
H14D 0.5775 0.7064 −0.0203 0.078*
H14E 0.6402 0.5929 −0.0147 0.078*
H14F 0.6886 0.6748 0.0355 0.078*
C15B 0.3705 (7) 0.5821 (7) −0.0092 (4) 0.064 (2)
H15D 0.2956 0.5670 0.0101 0.097*
H15E 0.3917 0.5207 −0.0295 0.097*
H15F 0.3439 0.6382 −0.0367 0.097*
C16B 0.4602 (7) 0.7032 (5) 0.0722 (3) 0.0516 (16)
H16D 0.4428 0.7654 0.0485 0.077*
H16E 0.5356 0.7158 0.1049 0.077*
H16F 0.3783 0.6852 0.0863 0.077*
S1C 0.49001 (18) 1.13218 (11) 0.37976 (7) 0.0457 (4)
N1C 0.6940 (6) 1.1111 (4) 0.2993 (2) 0.0506 (13)
H1C 0.746 (8) 1.109 (8) 0.3381 (15) 0.076*
N2C 0.5430 (5) 0.9411 (4) 0.3832 (2) 0.0380 (10)
C1C 0.7239 (7) 1.1284 (5) 0.2438 (3) 0.0494 (15)
H1C1 0.7998 1.1783 0.2479 0.059*
H1C2 0.6434 1.1604 0.2188 0.059*
C2C 0.7620 (6) 1.0332 (5) 0.2141 (3) 0.0415 (12)
C3C 0.8347 (7) 1.0409 (8) 0.1699 (3) 0.060 (2)
H3C 0.8608 1.1064 0.1582 0.072*
C4C 0.8679 (8) 0.9533 (8) 0.1435 (3) 0.066 (2)
H4C 0.9169 0.9583 0.1135 0.079*
C5C 0.8294 (8) 0.8560 (8) 0.1607 (3) 0.064 (2)
H5C 0.8532 0.7956 0.1427 0.077*
C6C 0.7578 (7) 0.8487 (6) 0.2034 (3) 0.0528 (15)
H6C 0.7305 0.7830 0.2144 0.063*
C7C 0.7244 (6) 0.9369 (5) 0.2312 (2) 0.0385 (12)
C8C 0.6495 (6) 0.9268 (5) 0.2803 (2) 0.0382 (12)
H8C1 0.5715 0.8795 0.2686 0.046*
H8C2 0.7116 0.8963 0.3140 0.046*
C9C 0.5986 (6) 1.0286 (5) 0.2972 (3) 0.0412 (12)
H9C 0.5175 1.0469 0.2667 0.049*
C10C 0.5504 (5) 1.0230 (4) 0.3527 (3) 0.0366 (11)
C11C 0.4493 (6) 1.0600 (5) 0.4341 (3) 0.0406 (12)
H11C 0.4064 1.0862 0.4631 0.049*
C12C 0.4867 (5) 0.9611 (4) 0.4301 (2) 0.0344 (11)
C13C 0.4733 (6) 0.8751 (5) 0.4722 (3) 0.0422 (13)
C14C 0.4029 (8) 0.7853 (6) 0.4391 (4) 0.0607 (19)
H14G 0.3969 0.7287 0.4656 0.091*
H14H 0.4548 0.7629 0.4108 0.091*
H14I 0.3112 0.8057 0.4194 0.091*
C15C 0.6172 (7) 0.8470 (6) 0.5036 (3) 0.0574 (18)
H15G 0.6126 0.7973 0.5341 0.086*
H15H 0.6646 0.9090 0.5204 0.086*
H15I 0.6666 0.8165 0.4763 0.086*
C16C 0.3907 (9) 0.9113 (7) 0.5163 (3) 0.065 (2)
H16G 0.3037 0.9399 0.4960 0.098*
H16H 0.4421 0.9642 0.5410 0.098*
H16I 0.3739 0.8528 0.5398 0.098*
S1D 0.98789 (17) 0.88108 (13) 0.38079 (7) 0.0479 (4)
N1D 1.1117 (5) 0.8850 (4) 0.2825 (2) 0.0367 (9)
H1D 1.023 (4) 0.882 (6) 0.257 (2) 0.055*
N2D 1.0684 (5) 1.0679 (4) 0.3918 (2) 0.0388 (10)
C1D 1.2058 (7) 0.8614 (5) 0.2455 (3) 0.0449 (14)
H1D1 1.1619 0.8113 0.2161 0.054*
H1D2 1.2871 0.8277 0.2690 0.054*
C2D 1.2522 (5) 0.9536 (4) 0.2152 (2) 0.0353 (11)
C3D 1.3220 (7) 0.9387 (6) 0.1714 (3) 0.0480 (14)
H3D 1.3418 0.8708 0.1609 0.058*
C4D 1.3641 (8) 1.0233 (7) 0.1421 (3) 0.0600 (19)
H4D 1.4127 1.0127 0.1124 0.072*
C5D 1.3343 (7) 1.1189 (7) 0.1569 (3) 0.0601 (19)
H5D 1.3612 1.1762 0.1371 0.072*
C6D 1.2647 (6) 1.1354 (5) 0.2008 (3) 0.0419 (12)
H6D 1.2439 1.2035 0.2105 0.050*
C7D 1.2251 (5) 1.0524 (4) 0.2309 (2) 0.0329 (10)
C8D 1.1525 (5) 1.0723 (4) 0.2792 (2) 0.0319 (10)
H8D1 1.0565 1.0908 0.2632 0.038*
H8D2 1.1961 1.1305 0.3029 0.038*
C9D 1.1581 (5) 0.9752 (4) 0.3170 (2) 0.0303 (10)
H9D 1.2551 0.9635 0.3366 0.036*
C10D 1.0758 (5) 0.9858 (4) 0.3624 (2) 0.0323 (10)
C11D 0.9375 (6) 0.9549 (6) 0.4329 (3) 0.0507 (16)
H11D 0.8815 0.9317 0.4579 0.061*
C12D 0.9900 (6) 1.0518 (5) 0.4328 (2) 0.0390 (12)
C13D 0.9748 (6) 1.1356 (6) 0.4738 (2) 0.0447 (14)
C14D 0.9180 (17) 1.2287 (8) 0.4417 (4) 0.124 (6)
H14J 0.8767 1.2729 0.4667 0.186*
H14K 0.8488 1.2085 0.4081 0.186*
H14L 0.9911 1.2663 0.4291 0.186*
C15D 1.1122 (8) 1.1564 (7) 0.5130 (4) 0.065 (2)
H15J 1.1432 1.0946 0.5354 0.098*
H15K 1.1036 1.2132 0.5390 0.098*
H15L 1.1783 1.1748 0.4897 0.098*
C16D 0.8815 (11) 1.1057 (10) 0.5137 (5) 0.094 (4)
H16J 0.7938 1.0826 0.4910 0.141*
H16K 0.8671 1.1654 0.5369 0.141*
H16L 0.9232 1.0500 0.5391 0.141*

Atomic displacement parameters (Å2)

U11 U22 U33 U12 U13 U23
S1A 0.0386 (7) 0.0278 (6) 0.0569 (8) 0.0050 (5) 0.0043 (6) −0.0021 (6)
N1A 0.037 (2) 0.029 (2) 0.045 (2) −0.0051 (18) 0.0034 (18) −0.012 (2)
N2A 0.039 (2) 0.0227 (19) 0.034 (2) 0.0043 (16) 0.0005 (17) −0.0028 (16)
C1A 0.048 (3) 0.033 (3) 0.059 (4) −0.004 (2) −0.003 (3) −0.016 (3)
C2A 0.033 (3) 0.056 (4) 0.035 (3) −0.007 (2) 0.002 (2) −0.015 (3)
C3A 0.048 (3) 0.076 (5) 0.040 (3) −0.003 (3) −0.002 (3) −0.023 (3)
C4A 0.055 (4) 0.099 (7) 0.043 (4) 0.001 (4) −0.005 (3) −0.012 (4)
C5A 0.051 (4) 0.076 (5) 0.041 (3) 0.015 (4) 0.002 (3) 0.009 (3)
C6A 0.046 (3) 0.050 (4) 0.038 (3) 0.006 (3) 0.005 (2) 0.005 (3)
C7A 0.037 (3) 0.041 (3) 0.033 (3) 0.005 (2) 0.011 (2) 0.006 (2)
C8A 0.032 (2) 0.030 (2) 0.038 (3) −0.0001 (19) 0.006 (2) −0.001 (2)
C9A 0.027 (2) 0.024 (2) 0.034 (2) −0.0040 (16) 0.0069 (18) −0.0049 (18)
C10A 0.026 (2) 0.025 (2) 0.033 (2) 0.0010 (17) 0.0089 (18) −0.0025 (18)
C11A 0.030 (3) 0.045 (3) 0.045 (3) 0.000 (2) −0.007 (2) −0.007 (3)
C12A 0.032 (2) 0.037 (3) 0.038 (3) −0.007 (2) 0.011 (2) −0.005 (2)
C13A 0.029 (2) 0.041 (3) 0.046 (3) −0.003 (2) −0.003 (2) −0.009 (3)
C14A 0.066 (4) 0.055 (4) 0.060 (4) −0.020 (3) 0.022 (3) −0.013 (3)
C15A 0.047 (3) 0.068 (5) 0.051 (4) −0.008 (3) 0.015 (3) −0.021 (3)
C16A 0.047 (4) 0.076 (6) 0.076 (5) −0.005 (4) −0.022 (4) −0.010 (4)
S1B 0.0400 (7) 0.0309 (6) 0.0465 (8) −0.0035 (5) 0.0027 (6) 0.0004 (6)
N1B 0.046 (3) 0.039 (3) 0.048 (3) 0.009 (2) −0.004 (2) −0.005 (2)
N2B 0.029 (2) 0.033 (2) 0.044 (2) 0.0066 (18) −0.0050 (18) 0.002 (2)
C1B 0.043 (3) 0.031 (3) 0.051 (3) 0.007 (2) −0.004 (2) 0.006 (2)
C2B 0.035 (3) 0.042 (3) 0.033 (3) 0.000 (2) 0.008 (2) −0.004 (2)
C3B 0.048 (3) 0.064 (4) 0.037 (3) 0.005 (3) −0.006 (3) 0.005 (3)
C4B 0.048 (4) 0.104 (7) 0.029 (3) −0.009 (4) −0.003 (3) −0.006 (4)
C5B 0.066 (4) 0.075 (5) 0.038 (3) −0.024 (4) 0.000 (3) −0.017 (3)
C6B 0.055 (3) 0.044 (3) 0.042 (3) −0.017 (3) 0.006 (3) −0.009 (3)
C7B 0.035 (3) 0.034 (3) 0.033 (3) −0.006 (2) 0.004 (2) −0.001 (2)
C8B 0.042 (3) 0.033 (3) 0.036 (3) 0.001 (2) 0.003 (2) 0.002 (2)
C9B 0.040 (3) 0.032 (3) 0.043 (3) 0.001 (2) 0.001 (2) −0.002 (2)
C10B 0.035 (3) 0.028 (2) 0.039 (3) −0.003 (2) 0.004 (2) 0.001 (2)
C11B 0.037 (3) 0.041 (3) 0.044 (3) 0.002 (2) 0.001 (2) −0.002 (2)
C12B 0.022 (2) 0.039 (3) 0.031 (2) −0.0030 (18) 0.0011 (17) 0.002 (2)
C13B 0.031 (2) 0.044 (3) 0.045 (3) 0.002 (2) 0.010 (2) 0.009 (3)
C14B 0.048 (3) 0.061 (4) 0.050 (4) 0.002 (3) 0.015 (3) 0.026 (3)
C15B 0.044 (4) 0.064 (5) 0.074 (5) 0.002 (3) −0.015 (3) 0.017 (4)
C16B 0.045 (3) 0.042 (3) 0.066 (4) 0.017 (3) 0.008 (3) 0.016 (3)
S1C 0.0636 (9) 0.0291 (7) 0.0477 (8) 0.0017 (6) 0.0190 (7) 0.0010 (6)
N1C 0.059 (3) 0.042 (3) 0.052 (3) −0.017 (3) 0.015 (2) −0.007 (2)
N2C 0.037 (2) 0.028 (2) 0.053 (3) −0.0032 (18) 0.019 (2) −0.002 (2)
C1C 0.065 (4) 0.035 (3) 0.053 (3) −0.013 (3) 0.024 (3) 0.000 (3)
C2C 0.043 (3) 0.045 (3) 0.036 (3) −0.005 (2) 0.008 (2) 0.000 (2)
C3C 0.048 (4) 0.090 (6) 0.043 (3) −0.017 (4) 0.010 (3) 0.009 (4)
C4C 0.056 (4) 0.112 (7) 0.031 (3) −0.015 (4) 0.016 (3) −0.008 (4)
C5C 0.061 (4) 0.081 (6) 0.053 (4) 0.004 (4) 0.017 (3) −0.019 (4)
C6C 0.054 (4) 0.055 (4) 0.046 (3) 0.000 (3) 0.005 (3) −0.009 (3)
C7C 0.036 (3) 0.045 (3) 0.032 (3) −0.009 (2) 0.001 (2) 0.002 (2)
C8C 0.037 (3) 0.038 (3) 0.040 (3) −0.005 (2) 0.010 (2) −0.001 (2)
C9C 0.045 (3) 0.031 (3) 0.048 (3) 0.000 (2) 0.013 (2) 0.000 (2)
C10C 0.034 (3) 0.029 (3) 0.048 (3) −0.0045 (19) 0.013 (2) −0.008 (2)
C11C 0.048 (3) 0.038 (3) 0.041 (3) −0.004 (2) 0.019 (2) −0.003 (2)
C12C 0.029 (2) 0.038 (3) 0.035 (3) −0.003 (2) 0.0045 (19) 0.002 (2)
C13C 0.042 (3) 0.043 (3) 0.044 (3) 0.000 (2) 0.014 (2) 0.010 (3)
C14C 0.066 (4) 0.053 (4) 0.070 (5) −0.015 (3) 0.029 (4) 0.006 (4)
C15C 0.046 (3) 0.053 (4) 0.071 (5) 0.001 (3) 0.008 (3) 0.023 (4)
C16C 0.071 (5) 0.082 (6) 0.051 (4) 0.006 (4) 0.033 (4) 0.011 (4)
S1D 0.0509 (8) 0.0453 (8) 0.0521 (9) −0.0110 (7) 0.0211 (7) −0.0024 (7)
N1D 0.046 (2) 0.024 (2) 0.043 (2) 0.0009 (18) 0.016 (2) −0.0039 (18)
N2D 0.042 (2) 0.039 (3) 0.040 (2) 0.0067 (19) 0.018 (2) −0.002 (2)
C1D 0.062 (4) 0.033 (3) 0.044 (3) 0.002 (2) 0.021 (3) −0.004 (2)
C2D 0.034 (2) 0.032 (3) 0.039 (3) 0.001 (2) 0.006 (2) −0.001 (2)
C3D 0.054 (3) 0.047 (3) 0.044 (3) 0.002 (3) 0.011 (3) −0.007 (3)
C4D 0.070 (5) 0.076 (5) 0.040 (3) −0.012 (4) 0.026 (3) −0.002 (3)
C5D 0.052 (4) 0.082 (5) 0.048 (4) −0.014 (4) 0.015 (3) 0.020 (4)
C6D 0.044 (3) 0.036 (3) 0.045 (3) −0.004 (2) 0.007 (2) 0.006 (2)
C7D 0.030 (2) 0.037 (3) 0.032 (2) −0.0058 (19) 0.0069 (19) 0.001 (2)
C8D 0.038 (3) 0.027 (2) 0.030 (2) −0.0027 (19) 0.006 (2) −0.0019 (19)
C9D 0.028 (2) 0.033 (2) 0.031 (2) 0.0029 (18) 0.0077 (18) 0.0021 (19)
C10D 0.033 (2) 0.037 (3) 0.028 (2) −0.0022 (19) 0.0070 (19) 0.001 (2)
C11D 0.033 (3) 0.068 (5) 0.052 (4) −0.013 (3) 0.012 (2) −0.002 (3)
C12D 0.032 (2) 0.050 (3) 0.037 (3) 0.002 (2) 0.010 (2) −0.006 (2)
C13D 0.039 (3) 0.060 (4) 0.037 (3) 0.010 (3) 0.013 (2) −0.007 (3)
C14D 0.221 (15) 0.068 (6) 0.070 (6) 0.094 (9) 0.000 (7) −0.006 (5)
C15D 0.061 (4) 0.059 (4) 0.070 (5) 0.007 (3) 0.002 (4) −0.028 (4)
C16D 0.084 (6) 0.106 (8) 0.111 (8) −0.029 (6) 0.064 (6) −0.045 (7)

Geometric parameters (Å, º)

S1A—C11A 1.731 (6) S1C—C11C 1.715 (6)
S1A—C10A 1.745 (5) S1C—C10C 1.722 (6)
N1A—C1A 1.470 (7) N1C—C9C 1.433 (8)
N1A—C9A 1.476 (6) N1C—C1C 1.434 (8)
N1A—H1A 0.97 (2) N1C—H1C 0.96 (2)
N2A—C10A 1.312 (6) N2C—C10C 1.301 (8)
N2A—C12A 1.376 (7) N2C—C12C 1.377 (7)
C1A—C2A 1.507 (9) C1C—C2C 1.515 (9)
C1A—H1A1 0.9900 C1C—H1C1 0.9900
C1A—H1A2 0.9900 C1C—H1C2 0.9900
C2A—C7A 1.405 (9) C2C—C7C 1.394 (8)
C2A—C3A 1.418 (8) C2C—C3C 1.404 (9)
C3A—C4A 1.366 (12) C3C—C4C 1.376 (13)
C3A—H3A 0.9500 C3C—H3C 0.9500
C4A—C5A 1.369 (13) C4C—C5C 1.409 (14)
C4A—H4A 0.9500 C4C—H4C 0.9500
C5A—C6A 1.394 (9) C5C—C6C 1.366 (10)
C5A—H5A 0.9500 C5C—H5C 0.9500
C6A—C7A 1.411 (8) C6C—C7C 1.400 (9)
C6A—H6A 0.9500 C6C—H6C 0.9500
C7A—C8A 1.508 (7) C7C—C8C 1.522 (8)
C8A—C9A 1.526 (7) C8C—C9C 1.506 (8)
C8A—H8A1 0.9900 C8C—H8C1 0.9900
C8A—H8A2 0.9900 C8C—H8C2 0.9900
C9A—C10A 1.495 (7) C9C—C10C 1.500 (8)
C9A—H9A 1.0000 C9C—H9C 1.0000
C11A—C12A 1.364 (9) C11C—C12C 1.349 (8)
C11A—H11A 0.9500 C11C—H11C 0.9500
C12A—C13A 1.500 (8) C12C—C13C 1.527 (8)
C13A—C16A 1.521 (9) C13C—C14C 1.501 (10)
C13A—C15A 1.531 (9) C13C—C15C 1.527 (9)
C13A—C14A 1.562 (10) C13C—C16C 1.540 (9)
C14A—H14A 0.9800 C14C—H14G 0.9800
C14A—H14B 0.9800 C14C—H14H 0.9800
C14A—H14C 0.9800 C14C—H14I 0.9800
C15A—H15A 0.9800 C15C—H15G 0.9800
C15A—H15B 0.9800 C15C—H15H 0.9800
C15A—H15C 0.9800 C15C—H15I 0.9800
C16A—H16A 0.9800 C16C—H16G 0.9800
C16A—H16B 0.9800 C16C—H16H 0.9800
C16A—H16C 0.9800 C16C—H16I 0.9800
S1B—C11B 1.688 (6) S1D—C11D 1.726 (7)
S1B—C10B 1.723 (5) S1D—C10D 1.729 (6)
N1B—C1B 1.457 (7) N1D—C9D 1.451 (7)
N1B—C9B 1.460 (7) N1D—C1D 1.454 (7)
N1B—H1B 0.99 (2) N1D—H1D 0.97 (2)
N2B—C10B 1.288 (7) N2D—C10D 1.287 (7)
N2B—C12B 1.410 (6) N2D—C12D 1.392 (7)
C1B—C2B 1.489 (8) C1D—C2D 1.523 (8)
C1B—H1B1 0.9900 C1D—H1D1 0.9900
C1B—H1B2 0.9900 C1D—H1D2 0.9900
C2B—C7B 1.395 (8) C2D—C7D 1.382 (8)
C2B—C3B 1.408 (8) C2D—C3D 1.387 (8)
C3B—C4B 1.404 (12) C3D—C4D 1.414 (11)
C3B—H3B 0.9500 C3D—H3D 0.9500
C4B—C5B 1.358 (13) C4D—C5D 1.344 (13)
C4B—H4B 0.9500 C4D—H4D 0.9500
C5B—C6B 1.391 (10) C5D—C6D 1.392 (9)
C5B—H5B 0.9500 C5D—H5D 0.9500
C6B—C7B 1.409 (8) C6D—C7D 1.398 (8)
C6B—H6B 0.9500 C6D—H6D 0.9500
C7B—C8B 1.500 (7) C7D—C8D 1.507 (7)
C8B—C9B 1.522 (8) C8D—C9D 1.544 (7)
C8B—H8B1 0.9900 C8D—H8D1 0.9900
C8B—H8B2 0.9900 C8D—H8D2 0.9900
C9B—C10B 1.505 (7) C9D—C10D 1.501 (7)
C9B—H9B 1.0000 C9D—H9D 1.0000
C11B—C12B 1.358 (8) C11D—C12D 1.366 (10)
C11B—H11B 0.9500 C11D—H11D 0.9500
C12B—C13B 1.519 (8) C12D—C13D 1.493 (8)
C13B—C16B 1.533 (9) C13D—C14D 1.480 (11)
C13B—C14B 1.536 (8) C13D—C16D 1.520 (10)
C13B—C15B 1.544 (9) C13D—C15D 1.521 (10)
C14B—H14D 0.9800 C14D—H14J 0.9800
C14B—H14E 0.9800 C14D—H14K 0.9800
C14B—H14F 0.9800 C14D—H14L 0.9800
C15B—H15D 0.9800 C15D—H15J 0.9800
C15B—H15E 0.9800 C15D—H15K 0.9800
C15B—H15F 0.9800 C15D—H15L 0.9800
C16B—H16D 0.9800 C16D—H16J 0.9800
C16B—H16E 0.9800 C16D—H16K 0.9800
C16B—H16F 0.9800 C16D—H16L 0.9800
C11A—S1A—C10A 89.4 (3) C11C—S1C—C10C 89.4 (3)
C1A—N1A—C9A 109.7 (4) C9C—N1C—C1C 110.7 (5)
C1A—N1A—H1A 108 (4) C9C—N1C—H1C 104 (6)
C9A—N1A—H1A 109 (5) C1C—N1C—H1C 136 (5)
C10A—N2A—C12A 112.5 (4) C10C—N2C—C12C 112.3 (5)
N1A—C1A—C2A 114.1 (5) N1C—C1C—C2C 115.1 (5)
N1A—C1A—H1A1 108.7 N1C—C1C—H1C1 108.5
C2A—C1A—H1A1 108.7 C2C—C1C—H1C1 108.5
N1A—C1A—H1A2 108.7 N1C—C1C—H1C2 108.5
C2A—C1A—H1A2 108.7 C2C—C1C—H1C2 108.5
H1A1—C1A—H1A2 107.6 H1C1—C1C—H1C2 107.5
C7A—C2A—C3A 117.8 (6) C7C—C2C—C3C 119.9 (7)
C7A—C2A—C1A 122.0 (5) C7C—C2C—C1C 119.2 (5)
C3A—C2A—C1A 120.1 (6) C3C—C2C—C1C 120.9 (6)
C4A—C3A—C2A 120.7 (7) C4C—C3C—C2C 119.8 (8)
C4A—C3A—H3A 119.6 C4C—C3C—H3C 120.1
C2A—C3A—H3A 119.6 C2C—C3C—H3C 120.1
C3A—C4A—C5A 121.7 (7) C3C—C4C—C5C 120.2 (6)
C3A—C4A—H4A 119.1 C3C—C4C—H4C 119.9
C5A—C4A—H4A 119.1 C5C—C4C—H4C 119.9
C4A—C5A—C6A 119.7 (7) C6C—C5C—C4C 120.0 (8)
C4A—C5A—H5A 120.2 C6C—C5C—H5C 120.0
C6A—C5A—H5A 120.2 C4C—C5C—H5C 120.0
C5A—C6A—C7A 119.7 (7) C5C—C6C—C7C 120.7 (7)
C5A—C6A—H6A 120.1 C5C—C6C—H6C 119.7
C7A—C6A—H6A 120.1 C7C—C6C—H6C 119.7
C2A—C7A—C6A 120.3 (5) C2C—C7C—C6C 119.4 (6)
C2A—C7A—C8A 120.6 (5) C2C—C7C—C8C 120.7 (6)
C6A—C7A—C8A 119.0 (5) C6C—C7C—C8C 119.9 (6)
C7A—C8A—C9A 109.7 (4) C9C—C8C—C7C 112.3 (5)
C7A—C8A—H8A1 109.7 C9C—C8C—H8C1 109.1
C9A—C8A—H8A1 109.7 C7C—C8C—H8C1 109.1
C7A—C8A—H8A2 109.7 C9C—C8C—H8C2 109.1
C9A—C8A—H8A2 109.7 C7C—C8C—H8C2 109.1
H8A1—C8A—H8A2 108.2 H8C1—C8C—H8C2 107.9
N1A—C9A—C10A 109.2 (4) N1C—C9C—C10C 110.1 (5)
N1A—C9A—C8A 112.9 (4) N1C—C9C—C8C 113.9 (5)
C10A—C9A—C8A 111.4 (4) C10C—C9C—C8C 112.5 (5)
N1A—C9A—H9A 107.7 N1C—C9C—H9C 106.6
C10A—C9A—H9A 107.7 C10C—C9C—H9C 106.6
C8A—C9A—H9A 107.7 C8C—C9C—H9C 106.6
N2A—C10A—C9A 125.5 (4) N2C—C10C—C9C 126.8 (5)
N2A—C10A—S1A 113.2 (4) N2C—C10C—S1C 113.5 (4)
C9A—C10A—S1A 121.2 (4) C9C—C10C—S1C 119.6 (4)
C12A—C11A—S1A 110.3 (4) C12C—C11C—S1C 110.8 (4)
C12A—C11A—H11A 124.9 C12C—C11C—H11C 124.6
S1A—C11A—H11A 124.9 S1C—C11C—H11C 124.6
C11A—C12A—N2A 114.6 (5) C11C—C12C—N2C 113.9 (5)
C11A—C12A—C13A 127.3 (5) C11C—C12C—C13C 126.0 (5)
N2A—C12A—C13A 118.1 (5) N2C—C12C—C13C 120.1 (5)
C12A—C13A—C16A 111.1 (6) C14C—C13C—C12C 108.8 (5)
C12A—C13A—C15A 107.6 (5) C14C—C13C—C15C 111.3 (6)
C16A—C13A—C15A 110.2 (6) C12C—C13C—C15C 106.9 (5)
C12A—C13A—C14A 109.5 (5) C14C—C13C—C16C 109.5 (6)
C16A—C13A—C14A 110.3 (6) C12C—C13C—C16C 110.9 (6)
C15A—C13A—C14A 108.1 (6) C15C—C13C—C16C 109.3 (6)
C13A—C14A—H14A 109.5 C13C—C14C—H14G 109.5
C13A—C14A—H14B 109.5 C13C—C14C—H14H 109.5
H14A—C14A—H14B 109.5 H14G—C14C—H14H 109.5
C13A—C14A—H14C 109.5 C13C—C14C—H14I 109.5
H14A—C14A—H14C 109.5 H14G—C14C—H14I 109.5
H14B—C14A—H14C 109.5 H14H—C14C—H14I 109.5
C13A—C15A—H15A 109.5 C13C—C15C—H15G 109.5
C13A—C15A—H15B 109.5 C13C—C15C—H15H 109.5
H15A—C15A—H15B 109.5 H15G—C15C—H15H 109.5
C13A—C15A—H15C 109.5 C13C—C15C—H15I 109.5
H15A—C15A—H15C 109.5 H15G—C15C—H15I 109.5
H15B—C15A—H15C 109.5 H15H—C15C—H15I 109.5
C13A—C16A—H16A 109.5 C13C—C16C—H16G 109.5
C13A—C16A—H16B 109.5 C13C—C16C—H16H 109.5
H16A—C16A—H16B 109.5 H16G—C16C—H16H 109.5
C13A—C16A—H16C 109.5 C13C—C16C—H16I 109.5
H16A—C16A—H16C 109.5 H16G—C16C—H16I 109.5
H16B—C16A—H16C 109.5 H16H—C16C—H16I 109.5
C11B—S1B—C10B 89.2 (3) C11D—S1D—C10D 89.1 (3)
C1B—N1B—C9B 111.2 (5) C9D—N1D—C1D 109.9 (4)
C1B—N1B—H1B 112 (5) C9D—N1D—H1D 122 (5)
C9B—N1B—H1B 107 (5) C1D—N1D—H1D 104 (4)
C10B—N2B—C12B 110.4 (5) C10D—N2D—C12D 111.1 (5)
N1B—C1B—C2B 114.9 (5) N1D—C1D—C2D 115.0 (5)
N1B—C1B—H1B1 108.5 N1D—C1D—H1D1 108.5
C2B—C1B—H1B1 108.5 C2D—C1D—H1D1 108.5
N1B—C1B—H1B2 108.5 N1D—C1D—H1D2 108.5
C2B—C1B—H1B2 108.5 C2D—C1D—H1D2 108.5
H1B1—C1B—H1B2 107.5 H1D1—C1D—H1D2 107.5
C7B—C2B—C3B 118.7 (6) C7D—C2D—C3D 119.6 (5)
C7B—C2B—C1B 121.1 (5) C7D—C2D—C1D 120.5 (5)
C3B—C2B—C1B 120.2 (6) C3D—C2D—C1D 120.0 (5)
C4B—C3B—C2B 120.5 (7) C2D—C3D—C4D 120.9 (6)
C4B—C3B—H3B 119.7 C2D—C3D—H3D 119.6
C2B—C3B—H3B 119.7 C4D—C3D—H3D 119.6
C5B—C4B—C3B 119.4 (6) C5D—C4D—C3D 119.0 (6)
C5B—C4B—H4B 120.3 C5D—C4D—H4D 120.5
C3B—C4B—H4B 120.3 C3D—C4D—H4D 120.5
C4B—C5B—C6B 122.1 (7) C4D—C5D—C6D 120.9 (7)
C4B—C5B—H5B 118.9 C4D—C5D—H5D 119.5
C6B—C5B—H5B 118.9 C6D—C5D—H5D 119.5
C5B—C6B—C7B 118.7 (7) C5D—C6D—C7D 120.6 (6)
C5B—C6B—H6B 120.6 C5D—C6D—H6D 119.7
C7B—C6B—H6B 120.6 C7D—C6D—H6D 119.7
C2B—C7B—C6B 120.5 (5) C2D—C7D—C6D 119.0 (5)
C2B—C7B—C8B 120.9 (5) C2D—C7D—C8D 121.3 (5)
C6B—C7B—C8B 118.6 (5) C6D—C7D—C8D 119.6 (5)
C7B—C8B—C9B 112.4 (5) C7D—C8D—C9D 109.8 (4)
C7B—C8B—H8B1 109.1 C7D—C8D—H8D1 109.7
C9B—C8B—H8B1 109.1 C9D—C8D—H8D1 109.7
C7B—C8B—H8B2 109.1 C7D—C8D—H8D2 109.7
C9B—C8B—H8B2 109.1 C9D—C8D—H8D2 109.7
H8B1—C8B—H8B2 107.8 H8D1—C8D—H8D2 108.2
N1B—C9B—C10B 110.5 (5) N1D—C9D—C10D 108.8 (4)
N1B—C9B—C8B 113.5 (5) N1D—C9D—C8D 111.3 (4)
C10B—C9B—C8B 112.0 (5) C10D—C9D—C8D 112.7 (4)
N1B—C9B—H9B 106.8 N1D—C9D—H9D 108.0
C10B—C9B—H9B 106.8 C10D—C9D—H9D 108.0
C8B—C9B—H9B 106.8 C8D—C9D—H9D 108.0
N2B—C10B—C9B 124.5 (5) N2D—C10D—C9D 124.9 (5)
N2B—C10B—S1B 115.3 (4) N2D—C10D—S1D 115.2 (4)
C9B—C10B—S1B 120.1 (4) C9D—C10D—S1D 119.8 (4)
C12B—C11B—S1B 111.8 (4) C12D—C11D—S1D 109.9 (5)
C12B—C11B—H11B 124.1 C12D—C11D—H11D 125.1
S1B—C11B—H11B 124.1 S1D—C11D—H11D 125.1
C11B—C12B—N2B 113.2 (5) C11D—C12D—N2D 114.6 (5)
C11B—C12B—C13B 128.8 (5) C11D—C12D—C13D 125.4 (6)
N2B—C12B—C13B 117.9 (5) N2D—C12D—C13D 119.9 (5)
C12B—C13B—C16B 109.8 (5) C14D—C13D—C12D 110.0 (6)
C12B—C13B—C14B 108.3 (5) C14D—C13D—C16D 108.1 (9)
C16B—C13B—C14B 108.7 (6) C12D—C13D—C16D 112.6 (7)
C12B—C13B—C15B 110.0 (5) C14D—C13D—C15D 111.9 (9)
C16B—C13B—C15B 109.5 (6) C12D—C13D—C15D 109.1 (5)
C14B—C13B—C15B 110.5 (6) C16D—C13D—C15D 105.2 (6)
C13B—C14B—H14D 109.5 C13D—C14D—H14J 109.5
C13B—C14B—H14E 109.5 C13D—C14D—H14K 109.5
H14D—C14B—H14E 109.5 H14J—C14D—H14K 109.5
C13B—C14B—H14F 109.5 C13D—C14D—H14L 109.5
H14D—C14B—H14F 109.5 H14J—C14D—H14L 109.5
H14E—C14B—H14F 109.5 H14K—C14D—H14L 109.5
C13B—C15B—H15D 109.5 C13D—C15D—H15J 109.5
C13B—C15B—H15E 109.5 C13D—C15D—H15K 109.5
H15D—C15B—H15E 109.5 H15J—C15D—H15K 109.5
C13B—C15B—H15F 109.5 C13D—C15D—H15L 109.5
H15D—C15B—H15F 109.5 H15J—C15D—H15L 109.5
H15E—C15B—H15F 109.5 H15K—C15D—H15L 109.5
C13B—C16B—H16D 109.5 C13D—C16D—H16J 109.5
C13B—C16B—H16E 109.5 C13D—C16D—H16K 109.5
H16D—C16B—H16E 109.5 H16J—C16D—H16K 109.5
C13B—C16B—H16F 109.5 C13D—C16D—H16L 109.5
H16D—C16B—H16F 109.5 H16J—C16D—H16L 109.5
H16E—C16B—H16F 109.5 H16K—C16D—H16L 109.5
C9A—N1A—C1A—C2A −44.2 (7) C9C—N1C—C1C—C2C −49.9 (8)
N1A—C1A—C2A—C7A 13.9 (9) N1C—C1C—C2C—C7C 20.6 (9)
N1A—C1A—C2A—C3A −169.5 (6) N1C—C1C—C2C—C3C −159.2 (6)
C7A—C2A—C3A—C4A −1.3 (10) C7C—C2C—C3C—C4C 0.3 (10)
C1A—C2A—C3A—C4A −178.1 (7) C1C—C2C—C3C—C4C −179.9 (7)
C2A—C3A—C4A—C5A −0.3 (13) C2C—C3C—C4C—C5C −0.1 (11)
C3A—C4A—C5A—C6A 1.5 (13) C3C—C4C—C5C—C6C 0.6 (12)
C4A—C5A—C6A—C7A −1.2 (11) C4C—C5C—C6C—C7C −1.3 (11)
C3A—C2A—C7A—C6A 1.5 (9) C3C—C2C—C7C—C6C −0.9 (9)
C1A—C2A—C7A—C6A 178.3 (6) C1C—C2C—C7C—C6C 179.2 (6)
C3A—C2A—C7A—C8A −178.0 (5) C3C—C2C—C7C—C8C 178.0 (6)
C1A—C2A—C7A—C8A −1.3 (8) C1C—C2C—C7C—C8C −1.8 (9)
C5A—C6A—C7A—C2A −0.3 (9) C5C—C6C—C7C—C2C 1.5 (10)
C5A—C6A—C7A—C8A 179.2 (5) C5C—C6C—C7C—C8C −177.5 (6)
C2A—C7A—C8A—C9A 19.0 (7) C2C—C7C—C8C—C9C 12.1 (8)
C6A—C7A—C8A—C9A −160.6 (5) C6C—C7C—C8C—C9C −169.0 (6)
C1A—N1A—C9A—C10A −170.1 (5) C1C—N1C—C9C—C10C −170.5 (6)
C1A—N1A—C9A—C8A 65.3 (6) C1C—N1C—C9C—C8C 62.1 (8)
C7A—C8A—C9A—N1A −51.2 (6) C7C—C8C—C9C—N1C −42.2 (7)
C7A—C8A—C9A—C10A −174.5 (4) C7C—C8C—C9C—C10C −168.4 (5)
C12A—N2A—C10A—C9A −175.5 (5) C12C—N2C—C10C—C9C −176.4 (5)
C12A—N2A—C10A—S1A 1.8 (6) C12C—N2C—C10C—S1C 0.7 (6)
N1A—C9A—C10A—N2A −162.6 (5) N1C—C9C—C10C—N2C −132.1 (6)
C8A—C9A—C10A—N2A −37.2 (7) C8C—C9C—C10C—N2C −3.8 (9)
N1A—C9A—C10A—S1A 20.4 (6) N1C—C9C—C10C—S1C 51.0 (7)
C8A—C9A—C10A—S1A 145.7 (4) C8C—C9C—C10C—S1C 179.2 (4)
C11A—S1A—C10A—N2A −0.6 (4) C11C—S1C—C10C—N2C −1.6 (5)
C11A—S1A—C10A—C9A 176.8 (4) C11C—S1C—C10C—C9C 175.7 (5)
C10A—S1A—C11A—C12A −0.7 (5) C10C—S1C—C11C—C12C 2.1 (5)
S1A—C11A—C12A—N2A 1.8 (7) S1C—C11C—C12C—N2C −2.2 (7)
S1A—C11A—C12A—C13A −176.1 (5) S1C—C11C—C12C—C13C 177.0 (4)
C10A—N2A—C12A—C11A −2.4 (7) C10C—N2C—C12C—C11C 1.0 (7)
C10A—N2A—C12A—C13A 175.8 (5) C10C—N2C—C12C—C13C −178.2 (5)
C11A—C12A—C13A—C16A −1.2 (9) C11C—C12C—C13C—C14C 129.0 (7)
N2A—C12A—C13A—C16A −179.1 (6) N2C—C12C—C13C—C14C −51.9 (7)
C11A—C12A—C13A—C15A 119.5 (7) C11C—C12C—C13C—C15C −110.6 (7)
N2A—C12A—C13A—C15A −58.4 (7) N2C—C12C—C13C—C15C 68.5 (7)
C11A—C12A—C13A—C14A −123.3 (7) C11C—C12C—C13C—C16C 8.5 (9)
N2A—C12A—C13A—C14A 58.8 (7) N2C—C12C—C13C—C16C −172.4 (6)
C9B—N1B—C1B—C2B −46.4 (8) C9D—N1D—C1D—C2D −44.6 (7)
N1B—C1B—C2B—C7B 17.8 (8) N1D—C1D—C2D—C7D 11.4 (8)
N1B—C1B—C2B—C3B −161.9 (6) N1D—C1D—C2D—C3D −168.6 (6)
C7B—C2B—C3B—C4B −0.9 (9) C7D—C2D—C3D—C4D −1.0 (10)
C1B—C2B—C3B—C4B 178.8 (6) C1D—C2D—C3D—C4D 179.0 (6)
C2B—C3B—C4B—C5B 1.1 (11) C2D—C3D—C4D—C5D −0.6 (12)
C3B—C4B—C5B—C6B 0.0 (12) C3D—C4D—C5D—C6D 0.8 (12)
C4B—C5B—C6B—C7B −1.4 (11) C4D—C5D—C6D—C7D 0.6 (11)
C3B—C2B—C7B—C6B −0.4 (8) C3D—C2D—C7D—C6D 2.3 (8)
C1B—C2B—C7B—C6B 179.9 (6) C1D—C2D—C7D—C6D −177.7 (5)
C3B—C2B—C7B—C8B 178.6 (5) C3D—C2D—C7D—C8D −178.5 (5)
C1B—C2B—C7B—C8B −1.2 (8) C1D—C2D—C7D—C8D 1.5 (8)
C5B—C6B—C7B—C2B 1.5 (9) C5D—C6D—C7D—C2D −2.1 (9)
C5B—C6B—C7B—C8B −177.5 (6) C5D—C6D—C7D—C8D 178.7 (6)
C2B—C7B—C8B—C9B 13.0 (8) C2D—C7D—C8D—C9D 17.9 (7)
C6B—C7B—C8B—C9B −168.0 (5) C6D—C7D—C8D—C9D −163.0 (5)
C1B—N1B—C9B—C10B −173.3 (5) C1D—N1D—C9D—C10D −169.1 (4)
C1B—N1B—C9B—C8B 59.8 (7) C1D—N1D—C9D—C8D 66.2 (6)
C7B—C8B—C9B—N1B −42.3 (7) C7D—C8D—C9D—N1D −51.7 (6)
C7B—C8B—C9B—C10B −168.3 (5) C7D—C8D—C9D—C10D −174.3 (4)
C12B—N2B—C10B—C9B −174.8 (5) C12D—N2D—C10D—C9D −176.7 (5)
C12B—N2B—C10B—S1B 2.9 (6) C12D—N2D—C10D—S1D 0.5 (6)
N1B—C9B—C10B—N2B −134.5 (6) N1D—C9D—C10D—N2D −163.7 (5)
C8B—C9B—C10B—N2B −6.8 (8) C8D—C9D—C10D—N2D −39.7 (7)
N1B—C9B—C10B—S1B 48.0 (6) N1D—C9D—C10D—S1D 19.3 (6)
C8B—C9B—C10B—S1B 175.6 (4) C8D—C9D—C10D—S1D 143.2 (4)
C11B—S1B—C10B—N2B −2.6 (5) C11D—S1D—C10D—N2D −0.2 (5)
C11B—S1B—C10B—C9B 175.1 (5) C11D—S1D—C10D—C9D 177.1 (4)
C10B—S1B—C11B—C12B 1.5 (5) C10D—S1D—C11D—C12D −0.1 (5)
S1B—C11B—C12B—N2B −0.3 (7) S1D—C11D—C12D—N2D 0.4 (7)
S1B—C11B—C12B—C13B 176.0 (4) S1D—C11D—C12D—C13D −176.5 (5)
C10B—N2B—C12B—C11B −1.6 (7) C10D—N2D—C12D—C11D −0.6 (7)
C10B—N2B—C12B—C13B −178.4 (5) C10D—N2D—C12D—C13D 176.6 (5)
C11B—C12B—C13B—C16B 129.8 (6) C11D—C12D—C13D—C14D −126.0 (10)
N2B—C12B—C13B—C16B −54.0 (6) N2D—C12D—C13D—C14D 57.2 (10)
C11B—C12B—C13B—C14B −111.6 (7) C11D—C12D—C13D—C16D −5.4 (10)
N2B—C12B—C13B—C14B 64.5 (7) N2D—C12D—C13D—C16D 177.8 (7)
C11B—C12B—C13B—C15B 9.2 (9) C11D—C12D—C13D—C15D 110.9 (8)
N2B—C12B—C13B—C15B −174.6 (6) N2D—C12D—C13D—C15D −65.9 (8)

Footnotes

Supplementary data and figures for this paper are available from the IUCr electronic archives (Reference: GW2121).

References

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Crystal structure: contains datablock(s) I, global. DOI: 10.1107/S160053681203173X/gw2121sup1.cif

e-68-o2487-sup1.cif (43.5KB, cif)

Structure factors: contains datablock(s) I. DOI: 10.1107/S160053681203173X/gw2121Isup2.hkl

e-68-o2487-Isup2.hkl (739.5KB, hkl)

Supplementary material file. DOI: 10.1107/S160053681203173X/gw2121Isup3.cml

Additional supplementary materials: crystallographic information; 3D view; checkCIF report


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