# 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_yanrl_0429
_database_code_depnum_ccdc_archive 'CCDC 1541467'
_audit_update_record             
;
2017-03-31 deposited with the CCDC.
2017-04-03 downloaded from the CCDC.
;
_audit_creation_date             2017-03-31
_audit_creation_method           
;
Olex2 1.2
(compiled 2017.03.02 svn.r3394 for OlexSys, GUI svn.r5324)
;
_shelx_SHELXL_version_number     2014/7
_chemical_name_common            ?
_chemical_name_systematic        ?
_chemical_formula_moiety         'C22 H15 F O S'
_chemical_formula_sum            'C22 H15 F O S'
_chemical_formula_weight         346.40
_chemical_melting_point          ?
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'
F F 0.0171 0.0103 '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'
S S 0.1246 0.1234 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'

_shelx_space_group_comment       
;
The symmetry employed for this shelxl refinement is uniquely defined
by the following loop, which should always be used as a source of
symmetry information in preference to the above space-group names.
They are only intended as comments.
;
_space_group_crystal_system      triclinic
_space_group_IT_number           2
_space_group_name_H-M_alt        'P -1'
_space_group_name_Hall           '-P 1'
loop_
_space_group_symop_operation_xyz
'x, y, z'
'-x, -y, -z'

_cell_length_a                   5.7144(13)
_cell_length_b                   12.030(3)
_cell_length_c                   12.5875(12)
_cell_angle_alpha                92.050(14)
_cell_angle_beta                 92.677(13)
_cell_angle_gamma                90.37(2)
_cell_volume                     863.8(3)
_cell_formula_units_Z            2
_cell_measurement_reflns_used    970
_cell_measurement_temperature    198(15)
_cell_measurement_theta_max      23.3000
_cell_measurement_theta_min      3.5660
_shelx_estimated_absorpt_T_max   ?
_shelx_estimated_absorpt_T_min   ?
_exptl_absorpt_coefficient_mu    0.203
_exptl_absorpt_correction_T_max  1.00000
_exptl_absorpt_correction_T_min  0.64997
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   
;
CrysAlisPro, Agilent Technologies,
Version 1.171.37.35 (release 13-08-2014 CrysAlis171 .NET)
(compiled Aug 13 2014,18:06:01)
Empirical absorption correction using spherical harmonics,
 implemented in SCALE3 ABSPACK scaling algorithm.
;
_exptl_absorpt_special_details   ?
_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    1.332
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    ?
_exptl_crystal_description       block
_exptl_crystal_F_000             360
_exptl_crystal_size_max          0.21
_exptl_crystal_size_mid          0.14
_exptl_crystal_size_min          0.12
_exptl_transmission_factor_max   ?
_exptl_transmission_factor_min   ?
_diffrn_reflns_av_R_equivalents  0.0514
_diffrn_reflns_av_unetI/netI     0.0876
_diffrn_reflns_Laue_measured_fraction_full 0.997
_diffrn_reflns_Laue_measured_fraction_max 0.997
_diffrn_reflns_limit_h_max       7
_diffrn_reflns_limit_h_min       -5
_diffrn_reflns_limit_k_max       14
_diffrn_reflns_limit_k_min       -14
_diffrn_reflns_limit_l_max       15
_diffrn_reflns_limit_l_min       -15
_diffrn_reflns_number            5738
_diffrn_reflns_point_group_measured_fraction_full 0.997
_diffrn_reflns_point_group_measured_fraction_max 0.997
_diffrn_reflns_theta_full        25.242
_diffrn_reflns_theta_max         26.022
_diffrn_reflns_theta_min         3.569
_diffrn_ambient_environment      N~2~
_diffrn_ambient_temperature      198(15)
_diffrn_detector                 'CCD plate'
_diffrn_detector_area_resol_mean 16.0733
_diffrn_detector_type            Eos
_diffrn_measured_fraction_theta_full 0.997
_diffrn_measured_fraction_theta_max 0.997
_diffrn_measurement_details      
;
#__ type_ start__ end____ width___ exp.time_
  1 omega   -5.00   91.00   2.0000    3.5000
omega____ theta____ kappa____ phi______ frames
    -       20.5854   38.0000  120.0000 48

#__ type_ start__ end____ width___ exp.time_
  2 omega   37.00   93.00   2.0000    3.5000
omega____ theta____ kappa____ phi______ frames
    -       20.5854  178.0000  -30.0000 28

#__ type_ start__ end____ width___ exp.time_
  3 omega  -46.00   44.00   2.0000    3.5000
omega____ theta____ kappa____ phi______ frames
    -       20.5854  -38.0000  -60.0000 45

#__ type_ start__ end____ width___ exp.time_
  4 omega  -19.00   21.00   2.0000    3.5000
omega____ theta____ kappa____ phi______ frames
    -      -17.1479  -99.0000  -90.0000 20

#__ type_ start__ end____ width___ exp.time_
  5 omega  -15.00   17.00   2.0000    3.5000
omega____ theta____ kappa____ phi______ frames
    -      -17.1479  -99.0000   90.0000 16

#__ type_ start__ end____ width___ exp.time_
  6 omega  -17.00   41.00   2.0000    3.5000
omega____ theta____ kappa____ phi______ frames
    -       20.5854  -99.0000 -150.0000 29
;
_diffrn_measurement_device       'four-circle diffractometer'
_diffrn_measurement_device_type  'SuperNova, Dual, Cu at zero, Eos'
_diffrn_measurement_method       'ω scans'
_diffrn_orient_matrix_UB_11      0.0255597000
_diffrn_orient_matrix_UB_12      -0.0541538000
_diffrn_orient_matrix_UB_13      0.0175619000
_diffrn_orient_matrix_UB_21      -0.1215476000
_diffrn_orient_matrix_UB_22      -0.0124978000
_diffrn_orient_matrix_UB_23      -0.0006910000
_diffrn_orient_matrix_UB_31      0.0037919000
_diffrn_orient_matrix_UB_32      -0.0198107000
_diffrn_orient_matrix_UB_33      -0.0536420000
_diffrn_radiation_monochromator  mirror
_diffrn_radiation_probe          x-ray
_diffrn_radiation_type           MoK\a
_diffrn_radiation_wavelength     0.71073
_diffrn_source                   'SuperNova (Mo) X-ray Source'
_reflns_Friedel_coverage         0.000
_reflns_Friedel_fraction_full    .
_reflns_Friedel_fraction_max     .
_reflns_number_gt                1775
_reflns_number_total             3389
_reflns_odcompleteness_completeness 99.69
_reflns_odcompleteness_iscentric 1
_reflns_odcompleteness_theta     26.32
_reflns_special_details          
;
 Reflections were merged by SHELXL according to the crystal
 class for the calculation of statistics and refinement.
 
 _reflns_Friedel_fraction is defined as the number of unique
 Friedel pairs measured divided by the number that would be
 possible theoretically, ignoring centric projections and
 systematic absences.
;
_reflns_threshold_expression     'I > 2σ(I)'
_computing_cell_refinement       
;
CrysAlisPro, Agilent Technologies,
Version 1.171.37.35 (release 13-08-2014 CrysAlis171 .NET)
(compiled Aug 13 2014,18:06:01)
;
_computing_data_collection       
;
CrysAlisPro, Agilent Technologies,
Version 1.171.37.35 (release 13-08-2014 CrysAlis171 .NET)
(compiled Aug 13 2014,18:06:01)
;
_computing_data_reduction        
;
CrysAlisPro, Agilent Technologies,
Version 1.171.37.35 (release 13-08-2014 CrysAlis171 .NET)
(compiled Aug 13 2014,18:06:01)
;
_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         0.265
_refine_diff_density_min         -0.255
_refine_diff_density_rms         0.048
_refine_ls_extinction_coef       .
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.061
_refine_ls_hydrogen_treatment    constr
_refine_ls_matrix_type           full
_refine_ls_number_parameters     226
_refine_ls_number_reflns         3389
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.1215
_refine_ls_R_factor_gt           0.0619
_refine_ls_restrained_S_all      1.061
_refine_ls_shift/su_max          0.000
_refine_ls_shift/su_mean         0.000
_refine_ls_structure_factor_coef Fsqd
_refine_ls_weighting_details     
'w=1/[σ²(Fo²)+(0.0470P)²+0.0221P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.1214
_refine_ls_wR_factor_ref         0.1656
_refine_special_details          ?
_olex2_refinement_description    
;
1. Fixed Uiso
 At 1.2 times of:
  All C(H) groups
2.a Aromatic/amide H refined with riding coordinates:
 C22(H22), C3(H3), C6(H6), C16(H16), C18(H18), C15(H15), C10(H10), C20(H20),
 C12(H12), C13(H13), C19(H19), C14(H14), C7(H7), C8(H8), C9(H9)
;
_atom_sites_solution_hydrogens   geom
_atom_sites_solution_primary     direct
_atom_sites_solution_secondary   ?
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_site_symmetry_order
_atom_site_calc_flag
_atom_site_refinement_flags_posn
_atom_site_refinement_flags_adp
_atom_site_refinement_flags_occupancy
_atom_site_disorder_assembly
_atom_site_disorder_group
S1 S 0.30744(17) 0.25556(10) -0.00195(7) 0.0739(4) Uani 1 1 d . . . . .
O1 O 0.0477(4) 0.35366(17) 0.26895(14) 0.0499(6) Uani 1 1 d . . . . .
C1 C 0.1982(5) 0.2896(3) 0.2101(2) 0.0464(8) Uani 1 1 d . . . . .
F1 F 0.0047(4) 0.1496(2) -0.37395(15) 0.1022(9) Uani 1 1 d . . . . .
C4 C -0.1013(6) 0.4073(3) 0.1993(2) 0.0503(8) Uani 1 1 d . . . . .
C22 C 0.1268(6) 0.1983(3) -0.1986(2) 0.0566(9) Uani 1 1 d . . . . .
H22 H 0.2515 0.2386 -0.2232 0.068 Uiso 1 1 calc R . . . .
C5 C -0.2722(6) 0.4803(3) 0.2471(2) 0.0517(8) Uani 1 1 d . . . . .
C11 C 0.3669(6) 0.2251(3) 0.2732(2) 0.0493(8) Uani 1 1 d . . . . .
C17 C 0.0930(6) 0.1921(3) -0.0901(2) 0.0509(8) Uani 1 1 d . . . . .
C3 C -0.0450(6) 0.3802(3) 0.0993(2) 0.0552(9) Uani 1 1 d . . . . .
H3 H -0.1181 0.4060 0.0375 0.066 Uiso 1 1 calc R . . . .
C6 C -0.4599(6) 0.5216(3) 0.1864(3) 0.0653(10) Uani 1 1 d . . . . .
H6 H -0.4753 0.5021 0.1142 0.078 Uiso 1 1 calc R . . . .
C16 C 0.3307(6) 0.2067(3) 0.3795(2) 0.0619(10) Uani 1 1 d . . . . .
H16 H 0.1983 0.2350 0.4107 0.074 Uiso 1 1 calc R . . . .
C21 C -0.0298(7) 0.1430(3) -0.2680(3) 0.0616(10) Uani 1 1 d . . . . .
C18 C -0.0959(7) 0.1326(3) -0.0564(3) 0.0651(10) Uani 1 1 d . . . . .
H18 H -0.1187 0.1280 0.0160 0.078 Uiso 1 1 calc R . . . .
C2 C 0.1474(6) 0.3046(3) 0.1044(2) 0.0523(8) Uani 1 1 d . . . . .
C15 C 0.4909(7) 0.1463(3) 0.4392(3) 0.0742(12) Uani 1 1 d . . . . .
H15 H 0.4650 0.1347 0.5104 0.089 Uiso 1 1 calc R . . . .
C10 C -0.2550(7) 0.5112(3) 0.3546(3) 0.0706(11) Uani 1 1 d . . . . .
H10 H -0.1327 0.4846 0.3977 0.085 Uiso 1 1 calc R . . . .
C20 C -0.2175(7) 0.0861(3) -0.2369(3) 0.0725(11) Uani 1 1 d . . . . .
H20 H -0.3220 0.0517 -0.2868 0.087 Uiso 1 1 calc R . . . .
C12 C 0.5681(6) 0.1802(3) 0.2294(3) 0.0592(9) Uani 1 1 d . . . . .
H12 H 0.5965 0.1914 0.1584 0.071 Uiso 1 1 calc R . . . .
C13 C 0.7243(6) 0.1196(3) 0.2902(3) 0.0704(11) Uani 1 1 d . . . . .
H13 H 0.8560 0.0897 0.2595 0.085 Uiso 1 1 calc R . . . .
C19 C -0.2509(7) 0.0801(3) -0.1294(3) 0.0780(12) Uani 1 1 d . . . . .
H19 H -0.3780 0.0406 -0.1061 0.094 Uiso 1 1 calc R . . . .
C14 C 0.6878(7) 0.1030(3) 0.3950(3) 0.0755(12) Uani 1 1 d . . . . .
H14 H 0.7949 0.0629 0.4360 0.091 Uiso 1 1 calc R . . . .
C7 C -0.6241(7) 0.5908(3) 0.2307(4) 0.0792(12) Uani 1 1 d . . . . .
H7 H -0.7485 0.6170 0.1887 0.095 Uiso 1 1 calc R . . . .
C8 C -0.6027(8) 0.6205(3) 0.3366(4) 0.0835(13) Uani 1 1 d . . . . .
H8 H -0.7127 0.6671 0.3667 0.100 Uiso 1 1 calc R . . . .
C9 C -0.4204(8) 0.5819(3) 0.3980(3) 0.0839(13) Uani 1 1 d . . . . .
H9 H -0.4061 0.6031 0.4698 0.101 Uiso 1 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
S1 C17 1.765(3) . ?
S1 C2 1.744(3) . ?
O1 C1 1.382(3) . ?
O1 C4 1.374(3) . ?
C1 C11 1.464(4) . ?
C1 C2 1.367(4) . ?
F1 C21 1.362(4) . ?
C4 C5 1.454(4) . ?
C4 C3 1.344(4) . ?
C22 H22 0.9300 . ?
C22 C17 1.393(4) . ?
C22 C21 1.372(5) . ?
C5 C6 1.392(4) . ?
C5 C10 1.390(4) . ?
C11 C16 1.389(4) . ?
C11 C12 1.401(4) . ?
C17 C18 1.383(5) . ?
C3 H3 0.9300 . ?
C3 C2 1.432(4) . ?
C6 H6 0.9300 . ?
C6 C7 1.382(5) . ?
C16 H16 0.9300 . ?
C16 C15 1.383(4) . ?
C21 C20 1.350(5) . ?
C18 H18 0.9300 . ?
C18 C19 1.379(5) . ?
C15 H15 0.9300 . ?
C15 C14 1.376(5) . ?
C10 H10 0.9300 . ?
C10 C9 1.393(5) . ?
C20 H20 0.9300 . ?
C20 C19 1.380(5) . ?
C12 H12 0.9300 . ?
C12 C13 1.377(4) . ?
C13 H13 0.9300 . ?
C13 C14 1.367(5) . ?
C19 H19 0.9300 . ?
C14 H14 0.9300 . ?
C7 H7 0.9300 . ?
C7 C8 1.367(5) . ?
C8 H8 0.9300 . ?
C8 C9 1.362(5) . ?
C9 H9 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
C2 S1 C17 103.65(15) . . ?
C4 O1 C1 108.1(2) . . ?
O1 C1 C11 114.9(2) . . ?
C2 C1 O1 108.7(3) . . ?
C2 C1 C11 136.4(3) . . ?
O1 C4 C5 116.1(2) . . ?
C3 C4 O1 108.9(3) . . ?
C3 C4 C5 135.0(3) . . ?
C17 C22 H22 121.1 . . ?
C21 C22 H22 121.1 . . ?
C21 C22 C17 117.8(3) . . ?
C6 C5 C4 121.0(3) . . ?
C10 C5 C4 121.5(3) . . ?
C10 C5 C6 117.6(3) . . ?
C16 C11 C1 120.3(3) . . ?
C16 C11 C12 117.9(3) . . ?
C12 C11 C1 121.8(3) . . ?
C22 C17 S1 117.1(3) . . ?
C18 C17 S1 123.3(3) . . ?
C18 C17 C22 119.5(3) . . ?
C4 C3 H3 126.0 . . ?
C4 C3 C2 108.0(3) . . ?
C2 C3 H3 126.0 . . ?
C5 C6 H6 119.2 . . ?
C7 C6 C5 121.6(3) . . ?
C7 C6 H6 119.2 . . ?
C11 C16 H16 119.9 . . ?
C15 C16 C11 120.3(3) . . ?
C15 C16 H16 119.9 . . ?
F1 C21 C22 117.4(4) . . ?
C20 C21 F1 119.0(4) . . ?
C20 C21 C22 123.6(3) . . ?
C17 C18 H18 119.8 . . ?
C19 C18 C17 120.5(3) . . ?
C19 C18 H18 119.8 . . ?
C1 C2 S1 126.8(3) . . ?
C1 C2 C3 106.3(3) . . ?
C3 C2 S1 126.6(2) . . ?
C16 C15 H15 119.5 . . ?
C14 C15 C16 121.1(3) . . ?
C14 C15 H15 119.5 . . ?
C5 C10 H10 119.9 . . ?
C5 C10 C9 120.2(4) . . ?
C9 C10 H10 119.9 . . ?
C21 C20 H20 120.8 . . ?
C21 C20 C19 118.5(4) . . ?
C19 C20 H20 120.8 . . ?
C11 C12 H12 119.6 . . ?
C13 C12 C11 120.9(3) . . ?
C13 C12 H12 119.6 . . ?
C12 C13 H13 119.7 . . ?
C14 C13 C12 120.7(3) . . ?
C14 C13 H13 119.7 . . ?
C18 C19 C20 120.1(4) . . ?
C18 C19 H19 120.0 . . ?
C20 C19 H19 120.0 . . ?
C15 C14 H14 120.4 . . ?
C13 C14 C15 119.2(3) . . ?
C13 C14 H14 120.4 . . ?
C6 C7 H7 120.1 . . ?
C8 C7 C6 119.7(4) . . ?
C8 C7 H7 120.1 . . ?
C7 C8 H8 120.0 . . ?
C9 C8 C7 120.0(4) . . ?
C9 C8 H8 120.0 . . ?
C10 C9 H9 119.6 . . ?
C8 C9 C10 120.9(4) . . ?
C8 C9 H9 119.6 . . ?

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
S1 C17 C18 C19 -176.6(3) . . . . ?
O1 C1 C11 C16 17.4(5) . . . . ?
O1 C1 C11 C12 -162.7(3) . . . . ?
O1 C1 C2 S1 172.0(2) . . . . ?
O1 C1 C2 C3 -0.8(4) . . . . ?
O1 C4 C5 C6 -167.3(3) . . . . ?
O1 C4 C5 C10 12.5(5) . . . . ?
O1 C4 C3 C2 0.7(4) . . . . ?
C1 O1 C4 C5 -179.3(3) . . . . ?
C1 O1 C4 C3 -1.2(4) . . . . ?
C1 C11 C16 C15 -179.7(3) . . . . ?
C1 C11 C12 C13 -179.8(3) . . . . ?
F1 C21 C20 C19 -180.0(3) . . . . ?
C4 O1 C1 C11 -179.0(3) . . . . ?
C4 O1 C1 C2 1.3(3) . . . . ?
C4 C5 C6 C7 179.8(3) . . . . ?
C4 C5 C10 C9 179.6(3) . . . . ?
C4 C3 C2 S1 -172.7(3) . . . . ?
C4 C3 C2 C1 0.1(4) . . . . ?
C22 C17 C18 C19 -0.3(5) . . . . ?
C22 C21 C20 C19 -1.9(6) . . . . ?
C5 C4 C3 C2 178.2(4) . . . . ?
C5 C6 C7 C8 0.4(6) . . . . ?
C5 C10 C9 C8 1.0(6) . . . . ?
C11 C1 C2 S1 -7.6(6) . . . . ?
C11 C1 C2 C3 179.5(4) . . . . ?
C11 C16 C15 C14 -0.3(6) . . . . ?
C11 C12 C13 C14 -0.7(6) . . . . ?
C17 S1 C2 C1 131.0(3) . . . . ?
C17 S1 C2 C3 -57.6(3) . . . . ?
C17 C22 C21 F1 -180.0(3) . . . . ?
C17 C22 C21 C20 2.0(5) . . . . ?
C17 C18 C19 C20 0.3(6) . . . . ?
C3 C4 C5 C6 15.3(6) . . . . ?
C3 C4 C5 C10 -164.9(4) . . . . ?
C6 C5 C10 C9 -0.7(5) . . . . ?
C6 C7 C8 C9 0.0(6) . . . . ?
C16 C11 C12 C13 0.0(5) . . . . ?
C16 C15 C14 C13 -0.4(6) . . . . ?
C21 C22 C17 S1 175.7(2) . . . . ?
C21 C22 C17 C18 -0.8(5) . . . . ?
C21 C20 C19 C18 0.7(6) . . . . ?
C2 S1 C17 C22 146.2(3) . . . . ?
C2 S1 C17 C18 -37.4(3) . . . . ?
C2 C1 C11 C16 -163.0(4) . . . . ?
C2 C1 C11 C12 16.9(6) . . . . ?
C10 C5 C6 C7 0.0(6) . . . . ?
C12 C11 C16 C15 0.4(5) . . . . ?
C12 C13 C14 C15 0.9(6) . . . . ?
C7 C8 C9 C10 -0.6(7) . . . . ?

_olex2_date_sample_data_collection 2016-04-29
_olex2_submission_special_instructions 'No special instructions were received'
