# Electronic Supplementary Material (ESI) for Organic & Biomolecular Chemistry.
# This journal is © The Royal Society of Chemistry 2017

####################################################################### 
# 
# This file contains crystal structure data downloaded from the 
# Cambridge Structural Database (CSD) hosted by the Cambridge 
# Crystallographic Data Centre (CCDC).
# 
# Full information about CCDC data access policies and citation 
# guidelines are available at http://www.ccdc.cam.ac.uk/access/V1 
# 
# Audit and citation data items may have been added by the CCDC. 
# Please retain this information to preserve the provenance of 
# this file and to allow appropriate attribution of the data. 
# 
#######################################################################

data_chensk_0118
_database_code_depnum_ccdc_archive 'CCDC 1528229'
_audit_update_record             
;
2017-01-18 deposited with the CCDC.
2017-03-17 downloaded from the CCDC.
;
_audit_creation_date             2017-01-18
_audit_creation_method           
;
Olex2 1.2
(compiled 2016.11.30 svn.r3356 for OlexSys, GUI svn.r5269)
;
_chemical_name_common            ?
_chemical_name_systematic        3i
_chemical_formula_moiety         'C24 H26 O5'
_chemical_formula_sum            'C24 H26 O5'
_chemical_formula_weight         394.45
_chemical_melting_point          381-383
loop_
_atom_type_symbol
_atom_type_description
_atom_type_scat_dispersion_real
_atom_type_scat_dispersion_imag
_atom_type_scat_source
C C 0.0033 0.0016 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
H H 0.0000 0.0000 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
O O 0.0106 0.0060 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'

_space_group_crystal_system      monoclinic
_space_group_IT_number           14
_space_group_name_H-M_alt        'P 1 21/c 1'
_space_group_name_Hall           '-P 2ybc'
loop_
_space_group_symop_id
_space_group_symop_operation_xyz
1 'x, y, z'
2 '-x, y+1/2, -z+1/2'
3 '-x, -y, -z'
4 'x, -y-1/2, z-1/2'

_cell_length_a                   12.4334(5)
_cell_length_b                   10.2160(4)
_cell_length_c                   16.6743(7)
_cell_angle_alpha                90.00
_cell_angle_beta                 99.832(4)
_cell_angle_gamma                90.00
_cell_volume                     2086.84(14)
_cell_formula_units_Z            4
_cell_measurement_reflns_used    1993
_cell_measurement_temperature    293(2)
_cell_measurement_theta_max      28.2000
_cell_measurement_theta_min      3.7980
_exptl_absorpt_coefficient_mu    0.087
_exptl_absorpt_correction_T_max  1.00000
_exptl_absorpt_correction_T_min  0.92211
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   
;
CrysAlisPro, Agilent Technologies,
Version 1.171.36.28 (release 01-02-2013 CrysAlis171 .NET)
(compiled Feb  1 2013,16:14:44)
Empirical absorption correction using spherical harmonics,
 implemented in SCALE3 ABSPACK scaling algorithm.
;
_exptl_crystal_colour            'clear light colourless'
_exptl_crystal_colour_lustre     clear
_exptl_crystal_colour_modifier   light
_exptl_crystal_colour_primary    colourless
_exptl_crystal_density_diffrn    1.255
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    'not measured'
_exptl_crystal_description       block
_exptl_crystal_F_000             840
_exptl_crystal_size_max          0.25
_exptl_crystal_size_mid          0.24
_exptl_crystal_size_min          0.21
_exptl_special_details           
;
 ? 
;
_diffrn_reflns_av_R_equivalents  0.0297
_diffrn_reflns_av_unetI/netI     0.0473
_diffrn_reflns_limit_h_max       12
_diffrn_reflns_limit_h_min       -15
_diffrn_reflns_limit_k_max       11
_diffrn_reflns_limit_k_min       -12
_diffrn_reflns_limit_l_max       16
_diffrn_reflns_limit_l_min       -20
_diffrn_reflns_number            7359
_diffrn_reflns_theta_full        25.50
_diffrn_reflns_theta_max         26.02
_diffrn_reflns_theta_min         3.33
_diffrn_ambient_temperature      298
_diffrn_detector_area_resol_mean 16.0733
_diffrn_measured_fraction_theta_full 0.9969
_diffrn_measured_fraction_theta_max 0.8791
_diffrn_measurement_details      
;
#__ type_ start__ end____ width___ exp.time_
  1 omega  -91.00  -55.00   1.0000    8.0000
omega____ theta____ kappa____ phi______ frames
    -      -19.5055  -19.0000  -30.0000 36

#__ type_ start__ end____ width___ exp.time_
  2 omega  -47.00   41.00   1.0000    8.0000
omega____ theta____ kappa____ phi______ frames
    -       22.7867  -77.0000  120.0000 88

#__ type_ start__ end____ width___ exp.time_
  3 omega   -1.00   93.00   1.0000    8.0000
omega____ theta____ kappa____ phi______ frames
    -       22.7867   57.0000 -120.0000 94
;
_diffrn_measurement_device_type  'SuperNova, Dual, Cu at zero, Eos'
_diffrn_measurement_method       'ω scans'
_diffrn_orient_matrix_UB_11      -0.0051427000
_diffrn_orient_matrix_UB_12      0.0645250000
_diffrn_orient_matrix_UB_13      -0.0159145000
_diffrn_orient_matrix_UB_21      -0.0454305000
_diffrn_orient_matrix_UB_22      -0.0199419000
_diffrn_orient_matrix_UB_23      -0.0291562000
_diffrn_orient_matrix_UB_31      -0.0355408000
_diffrn_orient_matrix_UB_32      0.0161660000
_diffrn_orient_matrix_UB_33      0.0275532000
_diffrn_radiation_monochromator  mirror
_diffrn_radiation_type           'Mo K\a'
_diffrn_radiation_wavelength     0.7107
_diffrn_source                   'SuperNova (Mo) X-ray Source'
_diffrn_standards_decay_%        ?
_diffrn_standards_interval_count ?
_diffrn_standards_interval_time  ?
_diffrn_standards_number         ?
_reflns_number_gt                2925
_reflns_number_total             4111
_reflns_odcompleteness_completeness 99.69
_reflns_odcompleteness_iscentric 1
_reflns_odcompleteness_theta     26.32
_reflns_threshold_expression     >2sigma(I)
_computing_cell_refinement       
;
CrysAlisPro, Agilent Technologies,
Version 1.171.36.28 (release 01-02-2013 CrysAlis171 .NET)
(compiled Feb  1 2013,16:14:44)
;
_computing_data_collection       
;
CrysAlisPro, Agilent Technologies,
Version 1.171.36.28 (release 01-02-2013 CrysAlis171 .NET)
(compiled Feb  1 2013,16:14:44)
;
_computing_data_reduction        
;
CrysAlisPro, Agilent Technologies,
Version 1.171.36.28 (release 01-02-2013 CrysAlis171 .NET)
(compiled Feb  1 2013,16:14:44)
;
_computing_molecular_graphics    'Olex2 (Dolomanov et al., 2009)'
_computing_publication_material  'Olex2 (Dolomanov et al., 2009)'
_computing_structure_refinement  'ShelXL (Sheldrick, 2015)'
_computing_structure_solution    'ShelXS (Sheldrick, 2008)'
_refine_diff_density_max         0.227
_refine_diff_density_min         -0.211
_refine_diff_density_rms         0.042
_refine_ls_extinction_coef       ?
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.029
_refine_ls_hydrogen_treatment    constr
_refine_ls_matrix_type           full
_refine_ls_number_parameters     266
_refine_ls_number_reflns         4111
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.0796
_refine_ls_R_factor_gt           0.0546
_refine_ls_restrained_S_all      1.029
_refine_ls_shift/su_max          0.000
_refine_ls_shift/su_mean         0.000
_refine_ls_structure_factor_coef Fsqd
_refine_ls_weighting_details     
'calc w=1/[σ²(Fo²)+(0.0532P)²+0.9006P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.1282
_refine_ls_wR_factor_ref         0.1468
_refine_special_details          
;
 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 > 2sigma(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. 
;
_olex2_refinement_description    
;
1. Fixed Uiso
 At 1.2 times of:
  All C(H) groups, All C(H,H) groups
 At 1.5 times of:
  All C(H,H,H) groups
2.a Ternary CH refined with riding coordinates:
 C3(H3), C5(H5)
2.b Secondary CH2 refined with riding coordinates:
 C10(H10A,H10B)
2.c Aromatic/amide H refined with riding coordinates:
 C14(H14), C15(H15), C16(H16), C17(H17), C18(H18), C20(H20), C21(H21),
 C22(H22), C23(H23), C24(H24)
2.d Idealised Me refined as rotating group:
 C6(H6A,H6B,H6C), C7(H7A,H7B,H7C), C9(H9A,H9B,H9C), C12(H12A,H12B,H12C)
;
_atom_sites_solution_hydrogens   geom
_atom_sites_solution_primary     direct
_atom_sites_solution_secondary   difmap
loop_
_atom_site_label
_atom_site_type_symbol
_atom_site_fract_x
_atom_site_fract_y
_atom_site_fract_z
_atom_site_U_iso_or_equiv
_atom_site_adp_type
_atom_site_occupancy
_atom_site_calc_flag
_atom_site_disorder_assembly
_atom_site_disorder_group
_atom_site_refinement_flags_posn
O1 O 1.07243(13) 0.31321(17) 0.12505(11) 0.0600(5) Uani 1 d . . .
O2 O 1.01157(12) 0.11290(15) 0.08694(9) 0.0449(4) Uani 1 d . . .
O3 O 0.71819(10) 0.24646(13) 0.15711(8) 0.0346(3) Uani 1 d . . .
O4 O 0.88592(12) 0.32599(16) 0.31002(9) 0.0482(4) Uani 1 d . . .
O5 O 1.05076(17) 0.2362(2) 0.34195(16) 0.0942(8) Uani 1 d . . .
C1 C 0.80587(16) 0.1803(2) 0.13849(11) 0.0330(5) Uani 1 d . . .
C2 C 0.89284(16) 0.25816(19) 0.13848(12) 0.0333(5) Uani 1 d . . .
C3 C 0.86705(16) 0.39236(19) 0.16765(12) 0.0336(5) Uani 1 d . . .
H3 H 0.8913 0.4584 0.1320 0.040 Uiso 1 calc . . R
C4 C 0.74057(16) 0.38703(19) 0.15143(12) 0.0329(5) Uani 1 d . . .
C5 C 0.78603(17) 0.0369(2) 0.12619(14) 0.0401(5) Uani 1 d . . .
H5 H 0.8534 -0.0035 0.1150 0.048 Uiso 1 calc . . R
C6 C 0.6958(2) 0.0110(3) 0.05350(18) 0.0636(8) Uani 1 d . . .
H6A H 0.6274 0.0415 0.0657 0.095 Uiso 1 calc . . GR
H6B H 0.6913 -0.0812 0.0425 0.095 Uiso 1 calc . . GR
H6C H 0.7121 0.0565 0.0067 0.095 Uiso 1 calc . . GR
C7 C 0.7582(2) -0.0243(2) 0.20367(17) 0.0608(7) Uani 1 d . . .
H7A H 0.8162 -0.0072 0.2483 0.091 Uiso 1 calc . . GR
H7B H 0.7494 -0.1171 0.1963 0.091 Uiso 1 calc . . GR
H7C H 0.6916 0.0129 0.2151 0.091 Uiso 1 calc . . GR
C8 C 1.00028(17) 0.2327(2) 0.11765(12) 0.0384(5) Uani 1 d . . .
C9 C 1.11480(19) 0.0876(3) 0.06184(16) 0.0541(6) Uani 1 d . . .
H9A H 1.1260 0.1496 0.0208 0.081 Uiso 1 calc . . GR
H9B H 1.1148 0.0005 0.0401 0.081 Uiso 1 calc . . GR
H9C H 1.1725 0.0957 0.1078 0.081 Uiso 1 calc . . GR
C10 C 0.92254(18) 0.4179(2) 0.25488(13) 0.0431(5) Uani 1 d . . .
H10A H 1.0010 0.4104 0.2585 0.052 Uiso 1 calc . . R
H10B H 0.9063 0.5062 0.2704 0.052 Uiso 1 calc . . R
C11 C 0.9575(2) 0.2421(2) 0.35060(15) 0.0508(6) Uani 1 d . . .
C12 C 0.9059(3) 0.1595(3) 0.40734(17) 0.0713(8) Uani 1 d . . .
H12A H 0.8541 0.2110 0.4303 0.107 Uiso 1 calc . . GR
H12B H 0.9612 0.1276 0.4502 0.107 Uiso 1 calc . . GR
H12C H 0.8692 0.0869 0.3781 0.107 Uiso 1 calc . . GR
C13 C 0.68315(16) 0.4571(2) 0.21254(12) 0.0340(5) Uani 1 d . . .
C14 C 0.68532(19) 0.5928(2) 0.21655(14) 0.0455(6) Uani 1 d . . .
H14 H 0.7229 0.6398 0.1823 0.055 Uiso 1 calc . . R
C15 C 0.6322(2) 0.6589(2) 0.27093(15) 0.0537(6) Uani 1 d . . .
H15 H 0.6345 0.7499 0.2730 0.064 Uiso 1 calc . . R
C16 C 0.5763(2) 0.5914(3) 0.32168(16) 0.0547(6) Uani 1 d . . .
H16 H 0.5396 0.6361 0.3575 0.066 Uiso 1 calc . . R
C17 C 0.5751(2) 0.4568(3) 0.31907(15) 0.0542(6) Uani 1 d . . .
H17 H 0.5383 0.4102 0.3540 0.065 Uiso 1 calc . . R
C18 C 0.62818(18) 0.3897(2) 0.26480(14) 0.0439(5) Uani 1 d . . .
H18 H 0.6267 0.2987 0.2637 0.053 Uiso 1 calc . . R
C19 C 0.69479(16) 0.4287(2) 0.06356(12) 0.0356(5) Uani 1 d . . .
C20 C 0.60927(19) 0.3593(2) 0.01850(15) 0.0484(6) Uani 1 d . . .
H20 H 0.5795 0.2884 0.0420 0.058 Uiso 1 calc . . R
C21 C 0.5678(2) 0.3938(3) -0.06052(16) 0.0602(7) Uani 1 d . . .
H21 H 0.5109 0.3456 -0.0899 0.072 Uiso 1 calc . . R
C22 C 0.6096(2) 0.4986(3) -0.09639(16) 0.0659(8) Uani 1 d . . .
H22 H 0.5818 0.5210 -0.1500 0.079 Uiso 1 calc . . R
C23 C 0.6927(2) 0.5699(3) -0.05244(16) 0.0642(8) Uani 1 d . . .
H23 H 0.7208 0.6420 -0.0760 0.077 Uiso 1 calc . . R
C24 C 0.73528(19) 0.5352(2) 0.02706(14) 0.0493(6) Uani 1 d . . .
H24 H 0.7918 0.5842 0.0562 0.059 Uiso 1 calc . . R


_geom_special_details            
;
 All esds (except the esd in the dihedral angle between two l.s. planes) 
 are estimated using the full covariance matrix.  The cell esds are taken 
 into account individually in the estimation of esds in distances, angles 
 and torsion angles; correlations between esds in cell parameters are only 
 used when they are defined by crystal symmetry.  An approximate (isotropic) 
 treatment of cell esds is used for estimating esds involving l.s. planes. 
;
loop_
_geom_bond_atom_site_label_1
_geom_bond_atom_site_label_2
_geom_bond_distance
_geom_bond_site_symmetry_2
_geom_bond_publ_flag
O1 C8 1.208(3) . ?
O2 C8 1.343(3) . ?
O2 C9 1.440(3) . ?
O3 C1 1.363(2) . ?
O3 C4 1.469(2) . ?
O4 C10 1.441(3) . ?
O4 C11 1.333(3) . ?
O5 C11 1.195(3) . ?
C1 C2 1.342(3) . ?
C1 C5 1.494(3) . ?
C2 C3 1.507(3) . ?
C2 C8 1.460(3) . ?
C3 H3 0.9800 . ?
C3 C4 1.550(3) . ?
C3 C10 1.522(3) . ?
C4 C13 1.519(3) . ?
C4 C19 1.538(3) . ?
C5 H5 0.9800 . ?
C5 C6 1.527(3) . ?
C5 C7 1.527(3) . ?
C6 H6A 0.9600 . ?
C6 H6B 0.9600 . ?
C6 H6C 0.9600 . ?
C7 H7A 0.9600 . ?
C7 H7B 0.9600 . ?
C7 H7C 0.9600 . ?
C9 H9A 0.9600 . ?
C9 H9B 0.9600 . ?
C9 H9C 0.9600 . ?
C10 H10A 0.9700 . ?
C10 H10B 0.9700 . ?
C11 C12 1.492(4) . ?
C12 H12A 0.9600 . ?
C12 H12B 0.9600 . ?
C12 H12C 0.9600 . ?
C13 C14 1.388(3) . ?
C13 C18 1.380(3) . ?
C14 H14 0.9300 . ?
C14 C15 1.386(3) . ?
C15 H15 0.9300 . ?
C15 C16 1.369(3) . ?
C16 H16 0.9300 . ?
C16 C17 1.377(4) . ?
C17 H17 0.9300 . ?
C17 C18 1.389(3) . ?
C18 H18 0.9300 . ?
C19 C20 1.387(3) . ?
C19 C24 1.383(3) . ?
C20 H20 0.9300 . ?
C20 C21 1.376(3) . ?
C21 H21 0.9300 . ?
C21 C22 1.371(4) . ?
C22 H22 0.9300 . ?
C22 C23 1.370(4) . ?
C23 H23 0.9300 . ?
C23 C24 1.387(3) . ?
C24 H24 0.9300 . ?

loop_
_geom_angle_atom_site_label_1
_geom_angle_atom_site_label_2
_geom_angle_atom_site_label_3
_geom_angle
_geom_angle_site_symmetry_1
_geom_angle_site_symmetry_3
_geom_angle_publ_flag
C8 O2 C9 115.54(17) . . ?
C1 O3 C4 107.60(14) . . ?
C11 O4 C10 119.10(18) . . ?
O3 C1 C5 113.45(17) . . ?
C2 C1 O3 112.45(18) . . ?
C2 C1 C5 134.04(19) . . ?
C1 C2 C3 108.85(17) . . ?
C1 C2 C8 131.61(19) . . ?
C8 C2 C3 119.53(17) . . ?
C2 C3 H3 109.0 . . ?
C2 C3 C4 100.20(15) . . ?
C2 C3 C10 112.17(17) . . ?
C4 C3 H3 109.0 . . ?
C10 C3 H3 109.0 . . ?
C10 C3 C4 116.97(17) . . ?
O3 C4 C3 102.75(15) . . ?
O3 C4 C13 107.53(15) . . ?
O3 C4 C19 106.76(16) . . ?
C13 C4 C3 116.43(16) . . ?
C13 C4 C19 111.64(16) . . ?
C19 C4 C3 110.84(16) . . ?
C1 C5 H5 108.2 . . ?
C1 C5 C6 111.12(19) . . ?
C1 C5 C7 109.95(18) . . ?
C6 C5 H5 108.2 . . ?
C7 C5 H5 108.2 . . ?
C7 C5 C6 111.0(2) . . ?
C5 C6 H6A 109.5 . . ?
C5 C6 H6B 109.5 . . ?
C5 C6 H6C 109.5 . . ?
H6A C6 H6B 109.5 . . ?
H6A C6 H6C 109.5 . . ?
H6B C6 H6C 109.5 . . ?
C5 C7 H7A 109.5 . . ?
C5 C7 H7B 109.5 . . ?
C5 C7 H7C 109.5 . . ?
H7A C7 H7B 109.5 . . ?
H7A C7 H7C 109.5 . . ?
H7B C7 H7C 109.5 . . ?
O1 C8 O2 122.4(2) . . ?
O1 C8 C2 123.2(2) . . ?
O2 C8 C2 114.38(18) . . ?
O2 C9 H9A 109.5 . . ?
O2 C9 H9B 109.5 . . ?
O2 C9 H9C 109.5 . . ?
H9A C9 H9B 109.5 . . ?
H9A C9 H9C 109.5 . . ?
H9B C9 H9C 109.5 . . ?
O4 C10 C3 110.93(17) . . ?
O4 C10 H10A 109.5 . . ?
O4 C10 H10B 109.5 . . ?
C3 C10 H10A 109.5 . . ?
C3 C10 H10B 109.5 . . ?
H10A C10 H10B 108.0 . . ?
O4 C11 C12 111.3(2) . . ?
O5 C11 O4 123.3(2) . . ?
O5 C11 C12 125.4(3) . . ?
C11 C12 H12A 109.5 . . ?
C11 C12 H12B 109.5 . . ?
C11 C12 H12C 109.5 . . ?
H12A C12 H12B 109.5 . . ?
H12A C12 H12C 109.5 . . ?
H12B C12 H12C 109.5 . . ?
C14 C13 C4 119.68(19) . . ?
C18 C13 C4 121.92(18) . . ?
C18 C13 C14 118.4(2) . . ?
C13 C14 H14 119.6 . . ?
C15 C14 C13 120.7(2) . . ?
C15 C14 H14 119.6 . . ?
C14 C15 H15 119.7 . . ?
C16 C15 C14 120.5(2) . . ?
C16 C15 H15 119.7 . . ?
C15 C16 H16 120.4 . . ?
C15 C16 C17 119.2(2) . . ?
C17 C16 H16 120.4 . . ?
C16 C17 H17 119.7 . . ?
C16 C17 C18 120.7(2) . . ?
C18 C17 H17 119.7 . . ?
C13 C18 C17 120.5(2) . . ?
C13 C18 H18 119.8 . . ?
C17 C18 H18 119.8 . . ?
C20 C19 C4 119.96(19) . . ?
C24 C19 C4 122.24(19) . . ?
C24 C19 C20 117.8(2) . . ?
C19 C20 H20 119.5 . . ?
C21 C20 C19 121.0(2) . . ?
C21 C20 H20 119.5 . . ?
C20 C21 H21 119.7 . . ?
C22 C21 C20 120.7(2) . . ?
C22 C21 H21 119.7 . . ?
C21 C22 H22 120.4 . . ?
C23 C22 C21 119.3(2) . . ?
C23 C22 H22 120.4 . . ?
C22 C23 H23 119.8 . . ?
C22 C23 C24 120.3(3) . . ?
C24 C23 H23 119.8 . . ?
C19 C24 C23 120.9(2) . . ?
C19 C24 H24 119.5 . . ?
C23 C24 H24 119.5 . . ?

loop_
_geom_torsion_atom_site_label_1
_geom_torsion_atom_site_label_2
_geom_torsion_atom_site_label_3
_geom_torsion_atom_site_label_4
_geom_torsion
_geom_torsion_site_symmetry_1
_geom_torsion_site_symmetry_2
_geom_torsion_site_symmetry_3
_geom_torsion_site_symmetry_4
_geom_torsion_publ_flag
O3 C1 C2 C3 5.6(2) . . . . ?
O3 C1 C2 C8 -175.79(19) . . . . ?
O3 C1 C5 C6 63.3(2) . . . . ?
O3 C1 C5 C7 -60.0(2) . . . . ?
O3 C4 C13 C14 -176.12(18) . . . . ?
O3 C4 C13 C18 3.8(3) . . . . ?
O3 C4 C19 C20 26.2(2) . . . . ?
O3 C4 C19 C24 -154.49(19) . . . . ?
C1 O3 C4 C3 -25.86(19) . . . . ?
C1 O3 C4 C13 -149.24(15) . . . . ?
C1 O3 C4 C19 90.83(17) . . . . ?
C1 C2 C3 C4 -20.7(2) . . . . ?
C1 C2 C3 C10 104.1(2) . . . . ?
C1 C2 C8 O1 -176.0(2) . . . . ?
C1 C2 C8 O2 6.0(3) . . . . ?
C2 C1 C5 C6 -119.9(3) . . . . ?
C2 C1 C5 C7 116.8(3) . . . . ?
C2 C3 C4 O3 27.13(18) . . . . ?
C2 C3 C4 C13 144.35(17) . . . . ?
C2 C3 C4 C19 -86.61(18) . . . . ?
C2 C3 C10 O4 -61.5(2) . . . . ?
C3 C2 C8 O1 2.5(3) . . . . ?
C3 C2 C8 O2 -175.49(17) . . . . ?
C3 C4 C13 C14 69.3(2) . . . . ?
C3 C4 C13 C18 -110.7(2) . . . . ?
C3 C4 C19 C20 137.4(2) . . . . ?
C3 C4 C19 C24 -43.3(3) . . . . ?
C4 O3 C1 C2 13.6(2) . . . . ?
C4 O3 C1 C5 -168.92(16) . . . . ?
C4 C3 C10 O4 53.5(2) . . . . ?
C4 C13 C14 C15 179.0(2) . . . . ?
C4 C13 C18 C17 -179.0(2) . . . . ?
C4 C19 C20 C21 -179.2(2) . . . . ?
C4 C19 C24 C23 179.7(2) . . . . ?
C5 C1 C2 C3 -171.2(2) . . . . ?
C5 C1 C2 C8 7.4(4) . . . . ?
C8 C2 C3 C4 160.44(17) . . . . ?
C8 C2 C3 C10 -74.7(2) . . . . ?
C9 O2 C8 O1 -1.2(3) . . . . ?
C9 O2 C8 C2 176.83(18) . . . . ?
C10 O4 C11 O5 -2.3(4) . . . . ?
C10 O4 C11 C12 177.31(19) . . . . ?
C10 C3 C4 O3 -94.32(19) . . . . ?
C10 C3 C4 C13 22.9(2) . . . . ?
C10 C3 C4 C19 151.94(18) . . . . ?
C11 O4 C10 C3 115.8(2) . . . . ?
C13 C4 C19 C20 -91.1(2) . . . . ?
C13 C4 C19 C24 88.3(2) . . . . ?
C13 C14 C15 C16 -0.1(4) . . . . ?
C14 C13 C18 C17 1.0(3) . . . . ?
C14 C15 C16 C17 1.1(4) . . . . ?
C15 C16 C17 C18 -1.1(4) . . . . ?
C16 C17 C18 C13 0.0(4) . . . . ?
C18 C13 C14 C15 -0.9(3) . . . . ?
C19 C4 C13 C14 -59.3(2) . . . . ?
C19 C4 C13 C18 120.6(2) . . . . ?
C19 C20 C21 C22 -0.6(4) . . . . ?
C20 C19 C24 C23 -1.0(3) . . . . ?
C20 C21 C22 C23 -0.6(4) . . . . ?
C21 C22 C23 C24 1.0(4) . . . . ?
C22 C23 C24 C19 -0.2(4) . . . . ?
C24 C19 C20 C21 1.4(3) . . . . ?

_olex2_date_sample_data_collection 2017-01-18
_olex2_submission_special_instructions 'No special instructions were received'
_exptl_crystal_recrystallization_method 
'Re-crystallisation from solvent: petroleum ether/ethyl acetate'
