Bloco A, Cidade Universitária, Ilha do Fundão, Rio de Janeiro, RJ, Brazil. Contents Pages
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1 Electronic Supplementary Material (ESI) for Organic & Biomolecular Chemistry. This journal is The Royal Society of Chemistry 2016 Supporting Information Copper(II) Catalyzed Synthesis of Novel Helical Luminescent Benzo[4,5]imidazo[1,2-a][1,10]phenanthrolines via an Intramolecular C H Amination Reaction Ramon Borges da Silva, a Rodolfo Inêz Teixeira, a James L. Wardell, b,c Solange M. S. V. Wardell, d and Simon J. Garden a * a Instituto de Química, Universidade Federal do Rio de Janeiro, Centro Tecnológica, Bloco A, Cidade Universitária, Ilha do Fundão, Rio de Janeiro, RJ, Brazil. b Instituto de Tecnologia em Fármacos Farmanguinhos, Fiocruz. R. Sizenando Nabuco, 100, Manguinhos, , Rio de Janeiro, RJ, Brazil. c Department of Chemistry, University of Aberdeen, Old Aberdeen, AB24 3UE, Scotland d CHEMSOL, 1 Harcourt Road, Aberdeen AB15 5NY, Scotland. * garden@iq.ufrj.br; Tel: Contents Pages 1 H, 13 C spectra of compounds H, 13 C spectra of compound H, 13 C spectra of compounds HRMS of compounds 3, 5 and D NMR of compound 3a and of compound 6a Theoretical calculations of 6a and 6aTS Absorption, emission and excitation spectra of 6a in different solvents. Crystallography Experimental and details
2 SI Figure 1: 1 H NMR: N-phenyl-1,10-phenanthroline (3a), (300 MHz, DMSO-d 6 ). SI Figure 2: 13 C NMR: N-phenyl-1,10-phenanthroline (3a), (75 MHz, DMSO-d 6 ). 2
3 SI Figure 3: 1 H NMR: N-(2-methoxyphenyl)-1,10-phenanthrolin-2-amine (3b), (200 MHz, DMSO-d 6 ). SI Figure 4: 13 C NMR: N-(2-methoxyphenyl)-1,10-phenanthrolin-2-amine (3b), (50 MHz, DMSO-d 6 ). 3
4 SI Figure 5: 1 H NMR N-o-tolyl-1,10-phenanthrolin-2-amine (3c), (500 MHz, CDCl 3 ). SI Figure 6: 13 C NMR: N-o-tolyl-1,10-phenanthrolin-2-amine (3c), (125 MHz, CDCl 3 ). 4
5 SI Figure 7: 1 H NMR: N-(2-fluorophenyl)-1,10-phenanthrolin-2-amine (3d), (500 MHz, DMSO-d 6 ) SI Figure 8: 13 C NMR: N-(2-fluorophenyl)-1,10-phenanthrolin-2-amine (3d), (125 MHz, DMSO-d 6 ) 5
6 SI Figure 9: 1 H NMR: N-(2-chlorophenyl)-1,10-phenanthrolin-2-amine (3e), (500 MHz, DMSO-d 6 ). SI Figure 10: 13 C NMR: N-(2-chlorophenyl)-1,10-phenanthrolin-2-amine (3e), (125 MHz, DMSO-d 6 ). 6
7 SI Figure 11: 1 H NMR: N-(3-methoxyphenyl)-1,10-phenanthrolin-2-amine (3f), (200 MHz, DMSO-d 6 ). SI Figure 12: 13 C NMR: N-(3-methoxyphenyl)-1,10-phenanthrolin-2-amine (3f), (50 MHz, DMSO-d 6 ). 7
8 SI Figure 13: 1 H NMR: N-m-tolyl-1,10-phenanthrolin-2-amine (3g), (300 MHz, DMSO-d 6 ). SI Figure 14: 13 C NMR: N-m-tolyl-1,10-phenanthrolin-2-amine (3g), (75 MHz, DMSOd 6 ). 8
9 SI Figure 15: 1 H NMR: N-(3-fluorophenyl)-1,10-phenanthrolin-2-amine (3h), (500 MHz, DMSO-d 6 ). SI Figure 16: 13 C NMR: N-(3-fluorophenyl)-1,10-phenanthrolin-2-amine (3h), (125 MHz, DMSO-d 6 ). 9
10 SI Figure 17: 1 H NMR: N-(3-chlorophenyl)-1,10-phenanthrolin-2-amine (3i), (300 MHz, DMSO-d 6 ). SI Figure 18: 13 C NMR: N-(3-chlorophenyl)-1,10-phenanthrolin-2-amine (3i), (75 MHz, DMSO-d 6 ). 10
11 SI Figure 19: 1 H NMR: N-(3-(trifluoromethyl)phenyl)-1,10-phenanthrolin-2-amine (3j) (200 MHz, DMSO-d 6 ). SI Figure 20: 13 C NMR: N-(3-(trifluoromethyl)phenyl)-1,10-phenanthrolin-2-amine (3j), (50 MHz, DMSO-d 6 ) 11
12 SI Figure 21: 1 H NMR: 3-(1,10-phenanthrolin-2-ylamino)benzonitrile (3k), (200 MHz, DMSO-d 6 ). SI Figure 22: 13 C NMR: 3-(1,10-phenanthrolin-2-ylamino)benzonitrile (3k), (50 MHz, DMSO-d 6 ). 12
13 SI Figure 23: 1 H NMR: N-(3-nitrophenyl)-1,10-phenanthrolin-2-amine (3l), (500 MHz, DMSO-d 6 ). SI Figure 24: 13 C NMR: N-(3-nitrophenyl)-1,10-phenanthrolin-2-amine (3l), (125 MHz, DMSO-d 6 ). 13
14 SI Figure 25: 1 H NMR: N-(4-methoxyphenyl)-1,10-phenanthrolin-2-amine (3m), (300 MHz, DMSO-d 6 ). SI Figure 26: 13 C NMR: N-(4-methoxyphenyl)-1,10-phenanthrolin-2-amine (3m), (75 MHz, DMSO-d 6 ). 14
15 SI Figure 27: 1 H NMR: N-p-tolyl-1,10-phenanthrolin-2-amine (3n), (300 MHz, DMSO-d 6 ). SI Figure 28: 13 C NMR: N-p-tolyl-1,10-phenanthrolin-2-amine (3n), (75 MHz, DMSOd 6 ). 15
16 SI Figure 29: 1 H NMR: N-(4-fluorophenyl)-1,10-phenanthrolin-2-amine (3o), (200 MHz, DMSO-d 6 ). SI Figure 30: 13 C NMR: N-(4-fluorophenyl)-1,10-phenanthrolin-2-amine (3o), (50 MHz, DMSO-d 6 ). 16
17 SI Figure 31: 1 H NMR: N-(4-chlorophenyl)-1,10-phenanthrolin-2-amine (3p), (300 MHz, DMSO-d 6 ). SI Figure 32: 13 C NMR: N-(4-chlorophenyl)-1,10-phenanthrolin-2-amine (3p), (75 MHz, DMSO-d 6 ). 17
18 SI Figure 33: 1 H NMR: N-(4-bromophenyl)-1,10-phenanthrolin-2-amine (3q), (200 MHz, DMSO-d 6 ). SI Figure 34: 13 C NMR: N-(4-bromophenyl)-1,10-phenanthrolin-2-amine (3q) (50 MHz, DMSO-d 6 ). 18
19 SI Figure 35: 1 H NMR: 4-(1,10-phenanthrolin-2-ylamino)benzonitrile (3r), (300 MHz, DMSO-d 6 ). SI Figure 36: 13 C NMR: 4-(1,10-phenanthrolin-2-ylamino)benzonitrile (3r), (75 MHz, DMSO-d 6 ). 19
20 SI Figure 37: 1 H NMR: N-(naphthalen-1-yl)-1,10-phenanthrolin-2-amine (3s) (200 MHz, CDCl 3 ). SI Figure 38: 13 C NMR: N-(naphthalen-1-yl)-1,10-phenanthrolin-2-amine (3s), (50 MHz, CDCl 3 ). 20
21 SI Figure 39: 1 H NMR: N-(naphthalen-2-yl)-1,10-phenanthrolin-2-amine (3t), (500 MHz, DMSO-d 6, CDCl 3 ). SI Figure 40: 13 C NMR: N-(naphthalen-2-yl)-1,10-phenanthrolin-2-amine (3t), (125 MHz, DMSO-d 6, CDCl 3 ). 21
22 SI Figure 41: 1 H NMR: benzo[4,5]imidazo[1,2-a]pyridine (5), (500 MHz, CDCl 3 ). SI Figure 42: 13 C NMR: benzo[4,5]imidazo[1,2-a]pyridine (5), (125 MHz, CDCl 3 ). 22
23 SI Figure 43: 1 H NMR: benzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6a), (500 MHz, CDCl 3 ). SI Figure 44: 13 C NMR: benzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6a), (125 MHz, CDCl 3 ). 23
24 SI Figure 45: 1 H NMR: 12-methylbenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6c), (300 MHz, CDCl 3 ). SI Figure 46: 13 C NMR: 12-methylbenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6c), (75 MHz, CDCl 3 ). 24
25 SI Figure 47: 1 H NMR: 12-fluorobenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6d), (500 MHz, CDCl 3 ). SI Figure 48: 13 C NMR: 12-fluorobenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6d), (125 MHz, CDCl 3 ). 25
26 SI Figure 49: 1 H NMR: 13-methoxybenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6f), (300 MHz, CDCl 3 ). SI Figure 50: 13 C NMR: 13-methoxybenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6f), (75 MHz, CDCl 3 ). 26
27 SI Figure 51: 1 H NMR: 13-methylbenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6g), (500 MHz,CDCl 3 ). SI Figure 52: 13 C NMR: 13-methylbenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6g), (75 MHz, CDCl 3 ). 27
28 SI Figure 53: 1 H NMR: 13-fluorobenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6h), (500 MHz, CDCl 3 ). SI Figure 54: 13 C NMR: 13-fluorobenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6h), (125 MHz, CDCl 3 ). 28
29 SI Figure 55: 1 H NMR: 13-clorobenzo[4,5]imidazo[1,2-a][1,10] fenantrolina (6i), (300 MHz, CDCl 3 ) SI Figure 56: 13 C NMR: 13-chlorobenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6i), (75 MHz, CDCl 3 ). 29
30 SI Figure 57: 1 H NMR: 13-(trifluoromethyl)benzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6j), (500 MHz, CDCl 3 ). SI Figure 58: phenanthroline (6j), (125 MHz, CDCl 3 ) 13 C NMR: 13-(trifluoromethyl)benzo[4,5]imidazo[1,2-a][1,10] 30
31 SI Figure 59: 1 H NMR: 14-methoxybenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6m), (300 MHz, CDCl 3, DMSO-d 6 ). SI Figure 60: 13 C NMR: 14-methoxybenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6m), (75 MHz, CDCl 3, DMSO-d 6 ). 31
32 SI Figure 61: 1 H NMR: 14-methylbenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6n), (500 MHz, CDCl 3 ). SI Figure 62: 1 H NMR: 14-methylbenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6n), (125 MHz, CDCl 3 ). 32
33 SI Figure 63: 1 H NMR: 14-fluorobenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6o), (300 MHz,CDCl 3 ). SI Figure 64: 13 C NMR: 14-fluorobenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6o), (75 MHz, CDCl 3 ). 33
34 SI Figure 65: 1 H NMR: 14-chlorobenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6p), (500 MHz, CDCl 3 ). SI Figure 66: 1 H NMR: 14-chlorobenzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6p), (125 MHz, CDCl 3 ). 34
35 SI Figure 67: HRMS of compound 3a SI Figure 68: HRMS of compound 3b. 35
36 SI Figure 69: HRMS of compound 3c SI Figure 70: HRMS of compound 3d 36
37 SI Figure 71: HRMS of compound 3e SI Figure 72: HRMS of compound 3f 37
38 SI Figure 73: HRMS of compound 3g SI Figure 74: HRMS of compound 3h 38
39 SI Figure 75: HRMS of compound 3i SI Figure 76: HRMS of compound 3j 39
40 SI Figure 77: HRMS of compound 3k SI Figure 78: HRMS of compound 3l 40
41 SI Figure 79: HRMS of compound 3m SI Figure 80: HRMS of compound 3n 41
42 SI Figure 81: HRMS of compound 3o SI Figure 82: HRMS of compound 3p 42
43 SI Figure 83: HRMS of compound 3q SI Figure 84: HRMS of compound 3r SI Figure 85: HRMS of compound 3s 43
44 SI Figure 86: HRMS of compound 3t SI Figure 87: HRMS of compound 5 44
45 SI Figure 88: HRMS of compound 6a SI Figure 89: HRMS of compound 6c 45
46 SI Figure 90: HRMS of compound 6d SI Figure 91: HRMS of compound 6f 46
47 SI Figure 92: HRMS of compound 6g SI Figure 93: HRMS of compound 6h 47
48 SI Figure 94: HRMS of compound 6i SI Figure 95: HRMS of compound 6j 48
49 SI Figure 96: HRMS of compound 6m SI Figure 97: HRMS of compound 6n 49
50 SI Figure 98: HRMS of compound 6o SI Figure 99: HRMS of compound 6p 50
51 SI Figure 100: COSY spectrum of N-phenyl-1,10-phenanthroline (3a) SI Figure 101: HMQC spectrum of N-phenyl-1,10-phenanthroline (3a) 51
52 SI Figure 102: HMBC spectrum of N-phenyl-1,10-phenanthroline (3a) SI Table 1. Heteronuclear multiple bond correlations (HMBC) 1 H NMR NH H9 H7 H12 H4 H5 H6 H8 H13 H3 H14 13 C NMR δ C C J C C J C C4a J C C J C6a J 2 J C C J W C11a J C10a/C1a J W C J C
53 SI Figure 103: COSY spectrum of benzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6a). SI Figure 104: HMQC spectrum of benzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6a). 53
54 SI Figure 105: HMBC spectrum of benzo[4,5]imidazo[1,2-a][1,10]phenanthroline (6a). SI Table 2. Heteronuclear multiple bond correlations (HMBC). 1 H H9 H15 H7 H12 H3 H5,6 H4 H8 H13 H14 13 C δ C C C C C J C4a C C C C6a C J *C1a, JU1a 1a 1a C15a a 15a C C10a C11a C J C J * Not possible to distinguish between C1a and C15a. The 13 C resonances are arbitrarily assigned. 2 J 54
55 Theoretical calculations SI Table 3. Calculated energies of 6a (energy minimum) and 6aTS, the transition state leading to chirality inversion. [B3LYP/6-31+G(d)] 6a 6aTS (-45 cm -1 )* Total Electronic Energy= Zero-point correction= Thermal correction to Energy= Thermal correction to Enthalpy= Thermal correction to Gibbs Free Energy= Sum of electronic and zero-point Energies= Sum of electronic and thermal Energies= Sum of electronic and thermal Enthalpies= Sum of electronic and thermal Free Energies= * imaginary vibration (an in and out of molecular plane wagging motion of the arms of the structure giving rise to either of the enantiomers). Coordinates for the structures 6a and 6aTS Compound 6a Compound 6aTS C C C C C C C C C C H C C H H H H H H C C C C H C
56 H H H N N N C Absorption, emission and excitation spectra of 6a in different solvents. SI Figure 106: Normalized absorption spectra ( ), excitation (---) and emission ( ) of 6a in acetonitrile. 56
57 SI Figure 107: Normalized Absorption ( ), excitation (---) and emission spectra ( ) of 6a in methanol. 57
58 SI Figure 108: Normalized absorption ( ), excitation (---) and emission spectra ( ) of 6a in dichloromethane. 58
59 Crystallography experimental and details Data for compound 6j were obtained with Mo-Kα radiation at 100(2) K by means of a XtaLAB AFC12 (RCD3): Kappa single diffractometer by the NCS crystallographic service, based at the University of Southampton. Data collection, data reduction and unit cell refinement were achieved with CrysAlisPro g. (1) Correction for absorption was achieved by CrysAlisPro g (1) Empirical absorption correction using spherical harmonics, implemented in SCALE3 ABSPACK scaling algorithm. The program MERCURY (2) were used in the preparation of the Figures. SHELXL97 (3) and PLATON (4) were used in the calculation of molecular geometry. The structures were solved by direct methods using SHELXS-97 (3) and fully refined by means of the program SHELXL-97. (3) All hydrogen atoms were placed in calculated positions. References 1. CrysAlisPro g Rigaku Oxford Diffraction, MERCURY 3.9 Cambridge Crystallographic Data Centre: Cambridge, UK. 3. Sheldrick, G.M. A short history of SHELX. Acta Crystallogr. Sect. A Found. Crystallogr. 2008, 64, Spek, A.L. Single-crystal structure validation with the program PLATON. J. Appl. Crystallogr. 2003, 36,
60 SI Table 4. Crystal data and structure refinement for 6j. Identification code Compound 6j, CCDC Empirical formula C38H20F6N6 (pair of enantiomers) Formula weight Temperature 100(2) K Wavelength Agst Crystal system Monoclinic Space group P2(1)/c Unit cell dimensions a = (4)Agst alpha = 90deg b = (2)Agst beta = (3)deg c = (7)Agst gamma = 90deg Volume (14) Agst@3 Z 4 Density (calculated) Mg/m@3 Absorption coefficient mm@-1 F(000) 1376 Crystal size x x mm Theta range for data collection to deg. Index ranges -18<=h<=20; -9<=k<=9; -33<=l<=23 Reflections collected Independent reflections 6501 [R(int) = ] Reflections observed (>2sigma) 5111 Data Completeness Absorption correction Semi-empirical from equivalents Max. and min. transmission and Refinement method Full-matrix least-squares on F@2 Data / restraints / parameters 6501 / 0 / 451 Goodness-of-fit on F@ Final R indices [I>2sigma(I)] R~1 = wr~2 = R indices (all data) R~1 = wr~2 = Largest diff. peak and hole and e.agst@-3 Atom labelling of molecule A Atom labelling of molecule B 60
61 Molecule A Molecule B View of Molecule A View of molecule B A figure showing the stacking of the molecules. Intermolecular interactions linking molecules are π- - - π and C- H- - - π interactions and C- H- - - N hydrogen bonds. 61
62 A view of the packing of the molecules within the crystal. 62
63 SI Table 5. Atomic coordinates ( x 10@4) and equivalent isotropic displacement parameters (Å@2 x 10@3) for 6j. U(eq) is defined as one third of the trace of the orthogonalized Uij tensor. Atom x y z U(eq) F(1) 8000(1) 10266(2) 9195(1) 32(1) F(23) 7865(1) 4454(2) 9432(1) 31(1) F(21) 9163(1) 3450(2) 9509(1) 36(1) F(2) 7108(1) 8079(2) 9274(1) 37(1) F(22) 8922(1) 6375(2) 9524(1) 35(1) F(3) 6725(1) 10899(2) 9368(1) 39(1) N(21) 8966(1) 5057(2) 7105(1) 18(1) N(1) 5859(1) 9939(2) 6938(1) 18(1) N(31) 10064(1) 6129(2) 7693(1) 21(1) N(10) 7518(1) 9649(2) 6588(1) 20(1) N(30) 7158(1) 4881(2) 6792(1) 21(1) N(11) 5072(1) 11257(2) 7539(1) 22(1) C(10A) 6819(1) 9121(3) 6258(1) 18(1) C(15A) 6350(1) 9805(3) 7431(1) 18(1) C(35) 7987(1) 4112(3) 7815(1) 19(1) C(35A) 8695(1) 4903(3) 7613(1) 17(1) C(15) 7110(1) 8897(3) 7614(1) 18(1) C(21A) 8610(1) 4568(3) 6592(1) 17(1) C(22) 9812(1) 5733(3) 7194(1) 19(1) C(1A) 5987(1) 9401(3) 6423(1) 18(1) C(33) 8653(1) 4869(3) 8698(1) 20(1) C(34) 7976(1) 4129(3) 8358(1) 20(1) C(30A) 7706(1) 4342(3) 6445(1) 18(1) C(14) 7369(1) 8958(3) 8149(1) 19(1) C(13) 6884(1) 9877(3) 8502(1) 19(1) C(32) 9364(1) 5609(3) 8504(1) 20(1) C(26A) 7420(1) 3701(3) 5929(1) 21(1) C(24A) 9163(1) 4438(3) 6200(1) 20(1) C(31A) 9385(1) 5609(3) 7958(1) 18(1) C(23) 10333(1) 5768(3) 6773(1) 22(1) C(6A) 6884(1) 8454(3) 5738(1) 20(1) C(11A) 5850(1) 10674(3) 7786(1) 20(1) C(12) 6117(1) 10719(3) 8326(1) 21(1) C(5) 5355(1) 8590(3) 5535(1) 24(1) C(4A) 5264(1) 9285(3) 6048(1) 21(1) C(16) 7176(1) 9796(3) 9077(1) 24(1) C(6) 6130(1) 8138(3) 5388(1) 23(1) C(2) 5082(1) 10754(3) 7043(1) 20(1) C(9) 8277(1) 9446(3) 6422(1) 22(1) C(3) 4377(1) 10781(3) 6640(1) 22(1) C(28) 5983(1) 3994(3) 6152(1) 25(1) C(27) 6528(1) 3498(3) 5796(1) 24(1) C(29) 6327(1) 4713(3) 6643(1) 23(1) C(7) 7712(1) 8223(3) 5586(1) 22(1) C(8) 8408(1) 8713(3) 5925(1) 23(1) C(25) 8852(1) 3784(3) 5689(1) 23(1) C(26) 8012(1) 3368(3) 5559(1) 24(1) C(4) 4454(1) 9992(3) 6171(1) 23(1) C(36) 8646(1) 4787(3) 9284(1) 25(1) C(24) 10034(1) 5057(3) 6303(1) 22(1) 63
64 SI Table 6. Bond lengths [Å] and angles [ o ] for 6j. Bond Length [Å] Angle [ o ] F(1)-C(16) 1.341(2) C(21A)-N(21)-C(35A) (17) F(23)-C(36) 1.346(3) C(21A)-N(21)-C(22) (16) F(21)-C(36) 1.349(3) C(35A)-N(21)-C(22) (16) F(2)-C(16) 1.349(3) C(15A)-N(1)-C(1A) (17) F(22)-C(36) 1.350(3) C(15A)-N(1)-C(2) (16) F(3)-C(16) 1.344(2) C(1A)-N(1)-C(2) (16) N(21)-C(21A) 1.408(2) C(22)-N(31)-C(31A) (16) N(21)-C(35A) 1.409(3) C(9)-N(10)-C(10A) (18) N(21)-C(22) 1.411(2) C(29)-N(30)-C(30A) (18) N(1)-C(15A) 1.402(2) C(2)-N(11)-C(11A) (17) N(1)-C(1A) 1.403(3) N(10)-C(10A)-C(6A) (18) N(1)-C(2) 1.410(3) N(10)-C(10A)-C(1A) (18) N(31)-C(22) 1.318(3) C(6A)-C(10A)-C(1A) (18) N(31)-C(31A) 1.378(3) C(15)-C(15A)-N(1) (18) N(10)-C(9) 1.319(3) C(15)-C(15A)-C(11A) (18) N(10)-C(10A) 1.361(3) N(1)-C(15A)-C(11A) (17) N(30)-C(29) 1.325(3) C(34)-C(35)-C(35A) (19) N(30)-C(30A) 1.357(3) C(34)-C(35)-H(35) N(11)-C(2) 1.315(3) C(35A)-C(35)-H(35) N(11)-C(11A) 1.378(3) C(35)-C(35A)-N(21) (19) C(10A)-C(6A) 1.422(3) C(35)-C(35A)-C(31A) (18) C(10A)-C(1A) 1.434(3) N(21)-C(35A)-C(31A) (16) C(15A)-C(15) 1.398(3) C(14)-C(15)-C(15A) (18) C(15A)-C(11A) 1.410(3) C(14)-C(15)-H(15) C(35)-C(34) 1.384(3) C(15A)-C(15)-H(15) C(35)-C(35A) 1.400(3) C(24A)-C(21A)-N(21) (17) C(35)-H(35) C(24A)-C(21A)-C(30A) (18) C(35A)-C(31A) 1.414(3) N(21)-C(21A)-C(30A) (17) C(15)-C(14) 1.378(3) N(31)-C(22)-N(21) (17) C(15)-H(15) N(31)-C(22)-C(23) (18) C(21A)-C(24A) 1.399(3) N(21)-C(22)-C(23) (18) C(21A)-C(30A) 1.439(3) C(4A)-C(1A)-N(1) (18) C(22)-C(23) 1.422(3) C(4A)-C(1A)-C(10A) (18) C(1A)-C(4A) 1.403(3) N(1)-C(1A)-C(10A) (17) C(33)-C(32) 1.381(3) C(32)-C(33)-C(34) (19) C(33)-C(34) 1.402(3) C(32)-C(33)-C(36) (19) C(33)-C(36) 1.495(3) C(34)-C(33)-C(36) (18) C(34)-H(34) C(35)-C(34)-C(33) (19) C(30A)-C(26A) 1.419(3) C(35)-C(34)-H(34) C(14)-C(13) 1.408(3) C(33)-C(34)-H(34) C(14)-H(14) N(30)-C(30A)-C(26A) (18) C(13)-C(12) 1.380(3) N(30)-C(30A)-C(21A) (18) C(13)-C(16) 1.486(3) C(26A)-C(30A)-C(21A) (18) C(32)-C(31A) 1.393(3) C(15)-C(14)-C(13) (19) C(32)-H(32) C(15)-C(14)-H(14) C(26A)-C(27) 1.413(3) C(13)-C(14)-H(14) C(26A)-C(26) 1.415(3) C(12)-C(13)-C(14) (19) C(24A)-C(25) 1.419(3) C(12)-C(13)-C(16) (18) C(24A)-C(24) 1.436(3) C(14)-C(13)-C(16) (18) 64
65 C(23)-C(24) 1.338(3) C(33)-C(32)-C(31A) (18) C(23)-H(23) C(33)-C(32)-H(32) C(6A)-C(7) 1.410(3) C(31A)-C(32)-H(32) C(6A)-C(6) 1.422(3) C(27)-C(26A)-C(26) (19) C(11A)-C(12) 1.393(3) C(27)-C(26A)-C(30A) (19) C(12)-H(12) C(26)-C(26A)-C(30A) (19) C(5)-C(6) 1.354(3) C(21A)-C(24A)-C(25) (19) C(5)-C(4A) 1.422(3) C(21A)-C(24A)-C(24) (19) C(5)-H(5) C(25)-C(24A)-C(24) (18) C(4A)-C(4) 1.439(3) N(31)-C(31A)-C(32) (18) C(6)-H(6) N(31)-C(31A)-C(35A) (17) C(2)-C(3) 1.425(3) C(32)-C(31A)-C(35A) (18) C(9)-C(8) 1.407(3) C(24)-C(23)-C(22) (19) C(9)-H(9) C(24)-C(23)-H(23) C(3)-C(4) 1.341(3) C(22)-C(23)-H(23) C(3)-H(3) C(7)-C(6A)-C(6) (19) C(28)-C(27) 1.363(3) C(7)-C(6A)-C(10A) (18) C(28)-C(29) 1.407(3) C(6)-C(6A)-C(10A) (18) C(28)-H(28) N(11)-C(11A)-C(12) (19) C(27)-H(27) N(11)-C(11A)-C(15A) (18) C(29)-H(29) C(12)-C(11A)-C(15A) (18) C(7)-C(8) 1.363(3) C(13)-C(12)-C(11A) (19) C(7)-H(7) C(13)-C(12)-H(12) C(8)-H(8) C(11A)-C(12)-H(12) C(25)-C(26) 1.359(3) C(6)-C(5)-C(4A) (19) C(25)-H(25) C(6)-C(5)-H(5) C(26)-H(26) C(4A)-C(5)-H(5) C(4)-H(4) C(1A)-C(4A)-C(5) (19) C(24)-H(24) C(1A)-C(4A)-C(4) (19) C(5)-C(4A)-C(4) (19) F(1)-C(16)-F(3) (17) F(1)-C(16)-F(2) (17) F(3)-C(16)-F(2) (17) F(1)-C(16)-C(13) (17) F(3)-C(16)-C(13) (18) F(2)-C(16)-C(13) (17) C(5)-C(6)-C(6A) 120.0(2) C(5)-C(6)-H(6) C(6A)-C(6)-H(6) N(11)-C(2)-N(1) (17) N(11)-C(2)-C(3) (19) N(1)-C(2)-C(3) (18) N(10)-C(9)-C(8) (19) N(10)-C(9)-H(9) C(8)-C(9)-H(9) C(4)-C(3)-C(2) (19) C(4)-C(3)-H(3) C(2)-C(3)-H(3) C(27)-C(28)-C(29) (19) C(27)-C(28)-H(28) C(29)-C(28)-H(28) C(28)-C(27)-C(26A) 119.6(2) 65
66 C(28)-C(27)-H(27) C(26A)-C(27)-H(27) N(30)-C(29)-C(28) 123.8(2) N(30)-C(29)-H(29) C(28)-C(29)-H(29) C(8)-C(7)-C(6A) (19) C(8)-C(7)-H(7) C(6A)-C(7)-H(7) C(7)-C(8)-C(9) (19) C(7)-C(8)-H(8) C(9)-C(8)-H(8) C(26)-C(25)-C(24A) (19) C(26)-C(25)-H(25) C(24A)-C(25)-H(25) C(25)-C(26)-C(26A) (19) C(25)-C(26)-H(26) C(26A)-C(26)-H(26) C(3)-C(4)-C(4A) (19) C(3)-C(4)-H(4) C(4A)-C(4)-H(4) F(23)-C(36)-F(21) (17) F(23)-C(36)-F(22) (17) F(21)-C(36)-F(22) (17) F(23)-C(36)-C(33) (18) F(21)-C(36)-C(33) (18) F(22)-C(36)-C(33) (18) C(23)-C(24)-C(24A) (19) C(23)-C(24)-H(24) C(24A)-C(24)-H(24)
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