# Electronic Supplementary Material (ESI) for ChemComm.
# This journal is © The Royal Society of Chemistry 2019

####################################################################### 
# 
# 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_a
_database_code_depnum_ccdc_archive 'CCDC 1940902'
_audit_update_record             
;
2019-07-16 deposited with the CCDC.	2019-09-16 downloaded from the CCDC.
;
_audit_creation_date             2019-07-16
_audit_creation_method           
;
Olex2 1.2
(compiled 2018.05.29 svn.r3508 for OlexSys, GUI svn.r5506)
;
_shelx_SHELXL_version_number     2014/7
_chemical_name_common            ?
_chemical_name_systematic        ?
_chemical_formula_moiety         'C15 H10 I N O'
_chemical_formula_sum            'C15 H10 I N O'
_chemical_formula_weight         347.14
_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'
I I -0.4742 1.8119 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
N N 0.0061 0.0033 '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'

_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      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_operation_xyz
'x, y, z'
'-x, y+1/2, -z+1/2'
'-x, -y, -z'
'x, -y-1/2, z-1/2'

_cell_length_a                   9.1325(13)
_cell_length_b                   16.190(2)
_cell_length_c                   8.6506(13)
_cell_angle_alpha                90
_cell_angle_beta                 95.062(2)
_cell_angle_gamma                90
_cell_volume                     1274.0(3)
_cell_formula_units_Z            4
_cell_measurement_reflns_used    4636
_cell_measurement_temperature    273(2)
_cell_measurement_theta_max      28.111
_cell_measurement_theta_min      2.24
_shelx_estimated_absorpt_T_max   0.662
_shelx_estimated_absorpt_T_min   0.435
_exptl_absorpt_coefficient_mu    2.499
_exptl_absorpt_correction_T_max  0.7457
_exptl_absorpt_correction_T_min  0.5206
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   
'SADABS-2016/2 (Bruker,2016/2) was used for absorption correction. wR2(int) was 0.0844 before and 0.0342 after correction. The Ratio of minimum to maximum transmission is 0.6981. The λ/2 correction factor is Not present.'
_exptl_absorpt_special_details   ?
_exptl_crystal_colour            orange
_exptl_crystal_colour_primary    orange
_exptl_crystal_density_diffrn    1.810
_exptl_crystal_density_meas      .
_exptl_crystal_density_method    ?
_exptl_crystal_description       block
_exptl_crystal_F_000             672
_exptl_crystal_size_max          0.4
_exptl_crystal_size_mid          0.36
_exptl_crystal_size_min          0.18
_exptl_transmission_factor_max   ?
_exptl_transmission_factor_min   ?
_diffrn_reflns_av_R_equivalents  0.0168
_diffrn_reflns_av_unetI/netI     0.0185
_diffrn_reflns_Laue_measured_fraction_full 0.999
_diffrn_reflns_Laue_measured_fraction_max 0.998
_diffrn_reflns_limit_h_max       11
_diffrn_reflns_limit_h_min       -10
_diffrn_reflns_limit_k_max       20
_diffrn_reflns_limit_k_min       -19
_diffrn_reflns_limit_l_max       10
_diffrn_reflns_limit_l_min       -10
_diffrn_reflns_number            7178
_diffrn_reflns_point_group_measured_fraction_full 0.999
_diffrn_reflns_point_group_measured_fraction_max 0.998
_diffrn_reflns_theta_full        25.242
_diffrn_reflns_theta_max         26.368
_diffrn_reflns_theta_min         2.239
_diffrn_ambient_temperature      273.15
_diffrn_detector_area_resol_mean ?
_diffrn_measured_fraction_theta_full 0.999
_diffrn_measured_fraction_theta_max 0.998
_diffrn_measurement_device_type  'CCD area detector'
_diffrn_measurement_method       'phi and omega scans'
_diffrn_radiation_monochromator  graphite
_diffrn_radiation_type           MoK\a
_diffrn_radiation_wavelength     0.71073
_diffrn_source                   ?
_reflns_Friedel_coverage         0.000
_reflns_Friedel_fraction_full    .
_reflns_Friedel_fraction_max     .
_reflns_number_gt                2319
_reflns_number_total             2600
_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       'SAINT V8.38A (?, 2016)'
_computing_data_collection       ?
_computing_data_reduction        'SAINT V8.38A (?, 2016)'
_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    'olex2.solve (Bourhis et al., 2015)'
_refine_diff_density_max         0.345
_refine_diff_density_min         -0.968
_refine_diff_density_rms         0.093
_refine_ls_extinction_coef       .
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.085
_refine_ls_hydrogen_treatment    constr
_refine_ls_matrix_type           full
_refine_ls_number_parameters     163
_refine_ls_number_reflns         2600
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.0289
_refine_ls_R_factor_gt           0.0252
_refine_ls_restrained_S_all      1.085
_refine_ls_shift/su_max          0.001
_refine_ls_shift/su_mean         0.000
_refine_ls_structure_factor_coef Fsqd
_refine_ls_weighting_details     
'w=1/[σ²(Fo²)+(0.0403P)²+0.4801P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.0691
_refine_ls_wR_factor_ref         0.0718
_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:
 C4(H4), C6(H6), C7(H7), C8(H8), C9(H9), C11(H11), C12(H12), C13(H13),
 C14(H14), C15(H15)
;
_atom_sites_solution_hydrogens   geom
_atom_sites_solution_primary     iterative
_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
C1 C 0.6553(2) 0.33917(13) 0.7138(3) 0.0345(5) Uani 1 1 d . . . . .
C2 C 0.7106(3) 0.26508(14) 0.6739(3) 0.0385(5) Uani 1 1 d . . . . .
C3 C 0.6356(3) 0.18617(15) 0.6896(3) 0.0465(6) Uani 1 1 d . . . . .
C4 C 0.4990(3) 0.19487(15) 0.7513(3) 0.0519(7) Uani 1 1 d . . . . .
H4 H 0.4446 0.1473 0.7649 0.062 Uiso 1 1 calc R . . . .
C5 C 0.4404(3) 0.26944(15) 0.7931(3) 0.0445(6) Uani 1 1 d . . . . .
C6 C 0.3010(3) 0.27708(19) 0.8524(5) 0.0638(8) Uani 1 1 d . . . . .
H6 H 0.2461 0.2296 0.8653 0.077 Uiso 1 1 calc R . . . .
C7 C 0.2456(3) 0.3503(2) 0.8906(4) 0.0661(8) Uani 1 1 d . . . . .
H7 H 0.1531 0.3532 0.9274 0.079 Uiso 1 1 calc R . . . .
C8 C 0.3290(3) 0.42301(17) 0.8746(3) 0.0534(7) Uani 1 1 d . . . . .
H8 H 0.2928 0.4739 0.9032 0.064 Uiso 1 1 calc R . . . .
C9 C 0.4599(3) 0.41798(14) 0.8181(3) 0.0421(5) Uani 1 1 d . . . . .
H9 H 0.5137 0.4661 0.8072 0.051 Uiso 1 1 calc R . . . .
C10 C 0.7349(2) 0.41868(13) 0.6952(3) 0.0339(5) Uani 1 1 d . . . . .
C11 C 0.7235(3) 0.46038(17) 0.5540(3) 0.0506(6) Uani 1 1 d . . . . .
H11 H 0.6606 0.4409 0.4717 0.061 Uiso 1 1 calc R . . . .
C12 C 0.8056(4) 0.53044(18) 0.5366(3) 0.0589(7) Uani 1 1 d . . . . .
H12 H 0.7964 0.5586 0.4425 0.071 Uiso 1 1 calc R . . . .
C13 C 0.9006(3) 0.55944(16) 0.6554(3) 0.0506(6) Uani 1 1 d . . . . .
H13 H 0.9569 0.6063 0.6417 0.061 Uiso 1 1 calc R . . . .
C14 C 0.9119(3) 0.51879(16) 0.7943(3) 0.0504(6) Uani 1 1 d . . . . .
H14 H 0.9764 0.5383 0.8752 0.061 Uiso 1 1 calc R . . . .
C15 C 0.8288(3) 0.44893(15) 0.8164(3) 0.0451(6) Uani 1 1 d . . . . .
H15 H 0.8361 0.4225 0.9122 0.054 Uiso 1 1 calc R . . . .
I1 I 0.91695(2) 0.25757(2) 0.58940(2) 0.05290(10) Uani 1 1 d . . . . .
N1 N 0.5191(2) 0.34268(11) 0.7748(2) 0.0360(4) Uani 1 1 d . . . . .
O1 O 0.6883(3) 0.11911(12) 0.6507(3) 0.0700(6) Uani 1 1 d . . . . .


_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
C1 C2 1.358(3) . ?
C1 C10 1.494(3) . ?
C1 N1 1.395(3) . ?
C2 C3 1.462(3) . ?
C2 I1 2.084(3) . ?
C3 C4 1.407(4) . ?
C3 O1 1.246(3) . ?
C4 H4 0.9300 . ?
C4 C5 1.382(4) . ?
C5 C6 1.419(4) . ?
C5 N1 1.403(3) . ?
C6 H6 0.9300 . ?
C6 C7 1.341(4) . ?
C7 H7 0.9300 . ?
C7 C8 1.416(4) . ?
C8 H8 0.9300 . ?
C8 C9 1.333(4) . ?
C9 H9 0.9300 . ?
C9 N1 1.398(3) . ?
C10 C11 1.391(3) . ?
C10 C15 1.385(3) . ?
C11 H11 0.9300 . ?
C11 C12 1.375(4) . ?
C12 H12 0.9300 . ?
C12 C13 1.368(4) . ?
C13 H13 0.9300 . ?
C13 C14 1.366(4) . ?
C14 H14 0.9300 . ?
C14 C15 1.385(3) . ?
C15 H15 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 C1 C10 122.6(2) . . ?
C2 C1 N1 119.8(2) . . ?
N1 C1 C10 117.64(19) . . ?
C1 C2 C3 124.1(2) . . ?
C1 C2 I1 120.59(18) . . ?
C3 C2 I1 115.30(18) . . ?
C4 C3 C2 112.7(2) . . ?
O1 C3 C2 122.8(3) . . ?
O1 C3 C4 124.5(3) . . ?
C3 C4 H4 117.8 . . ?
C5 C4 C3 124.3(2) . . ?
C5 C4 H4 117.8 . . ?
C4 C5 C6 123.5(3) . . ?
C4 C5 N1 119.7(3) . . ?
N1 C5 C6 116.9(2) . . ?
C5 C6 H6 118.8 . . ?
C7 C6 C5 122.4(3) . . ?
C7 C6 H6 118.8 . . ?
C6 C7 H7 120.2 . . ?
C6 C7 C8 119.5(3) . . ?
C8 C7 H7 120.2 . . ?
C7 C8 H8 120.2 . . ?
C9 C8 C7 119.5(3) . . ?
C9 C8 H8 120.2 . . ?
C8 C9 H9 118.9 . . ?
C8 C9 N1 122.1(2) . . ?
N1 C9 H9 118.9 . . ?
C11 C10 C1 120.9(2) . . ?
C15 C10 C1 119.9(2) . . ?
C15 C10 C11 119.1(2) . . ?
C10 C11 H11 120.1 . . ?
C12 C11 C10 119.9(2) . . ?
C12 C11 H11 120.1 . . ?
C11 C12 H12 119.5 . . ?
C13 C12 C11 121.1(2) . . ?
C13 C12 H12 119.5 . . ?
C12 C13 H13 120.4 . . ?
C14 C13 C12 119.3(2) . . ?
C14 C13 H13 120.4 . . ?
C13 C14 H14 119.5 . . ?
C13 C14 C15 121.0(2) . . ?
C15 C14 H14 119.5 . . ?
C10 C15 H15 120.2 . . ?
C14 C15 C10 119.6(2) . . ?
C14 C15 H15 120.2 . . ?
C1 N1 C5 119.4(2) . . ?
C1 N1 C9 121.04(19) . . ?
C9 N1 C5 119.6(2) . . ?

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
C1 C2 C3 C4 -0.2(4) . . . . ?
C1 C2 C3 O1 179.3(3) . . . . ?
C1 C10 C11 C12 -175.5(3) . . . . ?
C1 C10 C15 C14 174.4(2) . . . . ?
C2 C1 C10 C11 84.4(3) . . . . ?
C2 C1 C10 C15 -91.4(3) . . . . ?
C2 C1 N1 C5 -0.5(3) . . . . ?
C2 C1 N1 C9 179.5(2) . . . . ?
C2 C3 C4 C5 0.1(4) . . . . ?
C3 C4 C5 C6 178.8(3) . . . . ?
C3 C4 C5 N1 -0.2(4) . . . . ?
C4 C5 C6 C7 -179.3(3) . . . . ?
C4 C5 N1 C1 0.4(4) . . . . ?
C4 C5 N1 C9 -179.6(2) . . . . ?
C5 C6 C7 C8 -1.2(6) . . . . ?
C6 C5 N1 C1 -178.6(2) . . . . ?
C6 C5 N1 C9 1.4(4) . . . . ?
C6 C7 C8 C9 1.6(5) . . . . ?
C7 C8 C9 N1 -0.5(4) . . . . ?
C8 C9 N1 C1 179.0(2) . . . . ?
C8 C9 N1 C5 -1.1(4) . . . . ?
C10 C1 C2 C3 -179.6(2) . . . . ?
C10 C1 C2 I1 2.0(3) . . . . ?
C10 C1 N1 C5 179.5(2) . . . . ?
C10 C1 N1 C9 -0.5(3) . . . . ?
C10 C11 C12 C13 1.0(5) . . . . ?
C11 C10 C15 C14 -1.4(4) . . . . ?
C11 C12 C13 C14 -1.2(5) . . . . ?
C12 C13 C14 C15 0.0(4) . . . . ?
C13 C14 C15 C10 1.3(4) . . . . ?
C15 C10 C11 C12 0.2(4) . . . . ?
I1 C2 C3 C4 178.24(18) . . . . ?
I1 C2 C3 O1 -2.3(3) . . . . ?
N1 C1 C2 C3 0.4(4) . . . . ?
N1 C1 C2 I1 -177.93(15) . . . . ?
N1 C1 C10 C11 -95.6(3) . . . . ?
N1 C1 C10 C15 88.6(3) . . . . ?
N1 C5 C6 C7 -0.3(5) . . . . ?
O1 C3 C4 C5 -179.4(3) . . . . ?

_olex2_submission_special_instructions 'No special instructions were received'
####################################################################### 
# 
# 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_a_CCDC1
_database_code_depnum_ccdc_archive 'CCDC 1940903'
_audit_update_record             
;
2019-07-16 deposited with the CCDC.	2019-09-16 downloaded from the CCDC.
;
_audit_creation_date             2019-07-16
_audit_creation_method           
;
Olex2 1.2
(compiled 2018.05.29 svn.r3508 for OlexSys, GUI svn.r5506)
;
_shelx_SHELXL_version_number     2014/7
_chemical_name_common            ?
_chemical_name_systematic        ?
_chemical_formula_moiety         'C15 H9 I2 N O'
_chemical_formula_sum            'C15 H9 I2 N O'
_chemical_formula_weight         473.03
_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'
I I -0.4742 1.8119 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
N N 0.0061 0.0033 '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'

_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      monoclinic
_space_group_IT_number           14
_space_group_name_H-M_alt        'P 1 21/n 1'
_space_group_name_Hall           '-P 2yn'
loop_
_space_group_symop_operation_xyz
'x, y, z'
'-x+1/2, y+1/2, -z+1/2'
'-x, -y, -z'
'x-1/2, -y-1/2, z-1/2'

_cell_length_a                   8.9008(15)
_cell_length_b                   17.581(3)
_cell_length_c                   9.4398(16)
_cell_angle_alpha                90
_cell_angle_beta                 101.219(2)
_cell_angle_gamma                90
_cell_volume                     1449.0(4)
_cell_formula_units_Z            4
_cell_measurement_reflns_used    4702
_cell_measurement_temperature    273(2)
_cell_measurement_theta_max      28.33
_cell_measurement_theta_min      2.32
_shelx_estimated_absorpt_T_max   0.624
_shelx_estimated_absorpt_T_min   0.263
_exptl_absorpt_coefficient_mu    4.331
_exptl_absorpt_correction_T_max  0.7457
_exptl_absorpt_correction_T_min  0.5075
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   
'SADABS-2016/2 (Bruker,2016/2) was used for absorption correction. wR2(int) was 0.1120 before and 0.0372 after correction. The Ratio of minimum to maximum transmission is 0.6806. The λ/2 correction factor is Not present.'
_exptl_absorpt_special_details   ?
_exptl_crystal_colour            violet
_exptl_crystal_colour_primary    violet
_exptl_crystal_density_diffrn    2.168
_exptl_crystal_density_meas      .
_exptl_crystal_density_method    ?
_exptl_crystal_description       prism
_exptl_crystal_F_000             880
_exptl_crystal_size_max          0.42
_exptl_crystal_size_mid          0.3
_exptl_crystal_size_min          0.12
_exptl_transmission_factor_max   ?
_exptl_transmission_factor_min   ?
_diffrn_reflns_av_R_equivalents  0.0203
_diffrn_reflns_av_unetI/netI     0.0225
_diffrn_reflns_Laue_measured_fraction_full 1.000
_diffrn_reflns_Laue_measured_fraction_max 0.998
_diffrn_reflns_limit_h_max       11
_diffrn_reflns_limit_h_min       -7
_diffrn_reflns_limit_k_max       21
_diffrn_reflns_limit_k_min       -21
_diffrn_reflns_limit_l_max       11
_diffrn_reflns_limit_l_min       -11
_diffrn_reflns_number            8190
_diffrn_reflns_point_group_measured_fraction_full 1.000
_diffrn_reflns_point_group_measured_fraction_max 0.998
_diffrn_reflns_theta_full        25.242
_diffrn_reflns_theta_max         26.372
_diffrn_reflns_theta_min         2.317
_diffrn_ambient_temperature      273.15
_diffrn_detector_area_resol_mean ?
_diffrn_measured_fraction_theta_full 1.000
_diffrn_measured_fraction_theta_max 0.998
_diffrn_measurement_device_type  'CCD area detector'
_diffrn_measurement_method       'phi and omega scans'
_diffrn_radiation_monochromator  graphite
_diffrn_radiation_type           MoK\a
_diffrn_radiation_wavelength     0.71073
_diffrn_source                   ?
_reflns_Friedel_coverage         0.000
_reflns_Friedel_fraction_full    .
_reflns_Friedel_fraction_max     .
_reflns_number_gt                2573
_reflns_number_total             2949
_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       'SAINT V8.38A (?, 2016)'
_computing_data_collection       ?
_computing_data_reduction        'SAINT V8.38A (?, 2016)'
_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    'ShelXT (Sheldrick, 2015)'
_refine_diff_density_max         0.961
_refine_diff_density_min         -0.802
_refine_diff_density_rms         0.071
_refine_ls_extinction_coef       .
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.053
_refine_ls_hydrogen_treatment    constr
_refine_ls_matrix_type           full
_refine_ls_number_parameters     172
_refine_ls_number_reflns         2949
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.0281
_refine_ls_R_factor_gt           0.0233
_refine_ls_restrained_S_all      1.053
_refine_ls_shift/su_max          0.002
_refine_ls_shift/su_mean         0.000
_refine_ls_structure_factor_coef Fsqd
_refine_ls_weighting_details     
'w=1/[σ²(Fo²)+(0.0216P)²+1.2262P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.0531
_refine_ls_wR_factor_ref         0.0554
_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:
 C6(H6), C7(H7), C8(H8), C9(H9), C11(H11), C12(H12), C13(H13), C14(H14),
 C15(H15)
;
_atom_sites_solution_hydrogens   geom
_atom_sites_solution_primary     dual
_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
C1 C 0.7320(3) 0.43066(16) 0.4423(3) 0.0319(6) Uani 1 1 d . . . . .
C2 C 0.7768(3) 0.50113(16) 0.4905(3) 0.0333(6) Uani 1 1 d . . . . .
C3 C 0.8027(3) 0.56459(16) 0.3982(3) 0.0338(6) Uani 1 1 d . . . . .
C4 C 0.7679(4) 0.54535(16) 0.2486(3) 0.0368(7) Uani 1 1 d . . . . .
C5 C 0.7237(4) 0.47354(16) 0.1974(3) 0.0378(7) Uani 1 1 d . . . . .
C6 C 0.6891(5) 0.4538(2) 0.0478(4) 0.0591(10) Uani 1 1 d . . . . .
H6 H 0.6906 0.4919 -0.0202 0.071 Uiso 1 1 calc R . . . .
C7 C 0.6545(5) 0.3825(2) 0.0011(4) 0.0642(11) Uani 1 1 d . . . . .
H7 H 0.6331 0.3717 -0.0973 0.077 Uiso 1 1 calc R . . . .
C8 C 0.6511(4) 0.32402(19) 0.1032(4) 0.0524(9) Uani 1 1 d . . . . .
H8 H 0.6313 0.2740 0.0731 0.063 Uiso 1 1 calc R . . . .
C9 C 0.6765(4) 0.34146(17) 0.2432(4) 0.0430(7) Uani 1 1 d . . . . .
H9 H 0.6724 0.3029 0.3097 0.052 Uiso 1 1 calc R . . . .
C10 C 0.6963(3) 0.36737(16) 0.5371(3) 0.0339(6) Uani 1 1 d . . . . .
C11 C 0.8117(4) 0.32250(18) 0.6150(3) 0.0426(7) Uani 1 1 d . . . . .
H11 H 0.9135 0.3313 0.6099 0.051 Uiso 1 1 calc R . . . .
C12 C 0.7735(4) 0.26438(19) 0.7005(4) 0.0514(9) Uani 1 1 d . . . . .
H12 H 0.8506 0.2344 0.7534 0.062 Uiso 1 1 calc R . . . .
C13 C 0.6233(5) 0.25027(18) 0.7084(4) 0.0500(9) Uani 1 1 d . . . . .
H13 H 0.5990 0.2110 0.7661 0.060 Uiso 1 1 calc R . . . .
C14 C 0.5103(4) 0.2944(2) 0.6308(4) 0.0512(9) Uani 1 1 d . . . . .
H14 H 0.4087 0.2851 0.6360 0.061 Uiso 1 1 calc R . . . .
C15 C 0.5453(4) 0.35274(19) 0.5447(4) 0.0437(7) Uani 1 1 d . . . . .
H15 H 0.4673 0.3822 0.4918 0.052 Uiso 1 1 calc R . . . .
I1 I 0.81118(3) 0.52731(2) 0.71045(2) 0.05047(9) Uani 1 1 d . . . . .
I2 I 0.79848(3) 0.63197(2) 0.10471(2) 0.05786(9) Uani 1 1 d . . . . .
N1 N 0.7092(3) 0.41551(13) 0.2938(3) 0.0340(5) Uani 1 1 d . . . . .
O1 O 0.8466(3) 0.62817(11) 0.4477(2) 0.0447(5) Uani 1 1 d . . . . .


_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
C1 C2 1.353(4) . ?
C1 C10 1.501(4) . ?
C1 N1 1.402(4) . ?
C2 C3 1.462(4) . ?
C2 I1 2.090(3) . ?
C3 C4 1.426(4) . ?
C3 O1 1.245(3) . ?
C4 C5 1.381(4) . ?
C4 I2 2.093(3) . ?
C5 C6 1.429(5) . ?
C5 N1 1.390(4) . ?
C6 H6 0.9300 . ?
C6 C7 1.344(5) . ?
C7 H7 0.9300 . ?
C7 C8 1.413(5) . ?
C8 H8 0.9300 . ?
C8 C9 1.332(5) . ?
C9 H9 0.9300 . ?
C9 N1 1.398(4) . ?
C10 C11 1.387(4) . ?
C10 C15 1.384(4) . ?
C11 H11 0.9300 . ?
C11 C12 1.385(4) . ?
C12 H12 0.9300 . ?
C12 C13 1.376(5) . ?
C13 H13 0.9300 . ?
C13 C14 1.365(5) . ?
C14 H14 0.9300 . ?
C14 C15 1.381(4) . ?
C15 H15 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 C1 C10 124.1(3) . . ?
C2 C1 N1 119.1(2) . . ?
N1 C1 C10 116.7(2) . . ?
C1 C2 C3 124.7(3) . . ?
C1 C2 I1 120.8(2) . . ?
C3 C2 I1 114.5(2) . . ?
C4 C3 C2 112.4(2) . . ?
O1 C3 C2 122.4(3) . . ?
O1 C3 C4 125.2(3) . . ?
C3 C4 I2 116.1(2) . . ?
C5 C4 C3 123.7(3) . . ?
C5 C4 I2 120.1(2) . . ?
C4 C5 C6 124.1(3) . . ?
C4 C5 N1 119.9(3) . . ?
N1 C5 C6 116.0(3) . . ?
C5 C6 H6 118.6 . . ?
C7 C6 C5 122.9(3) . . ?
C7 C6 H6 118.6 . . ?
C6 C7 H7 120.4 . . ?
C6 C7 C8 119.2(3) . . ?
C8 C7 H7 120.4 . . ?
C7 C8 H8 120.4 . . ?
C9 C8 C7 119.1(3) . . ?
C9 C8 H8 120.4 . . ?
C8 C9 H9 118.7 . . ?
C8 C9 N1 122.5(3) . . ?
N1 C9 H9 118.7 . . ?
C11 C10 C1 121.1(3) . . ?
C15 C10 C1 119.3(3) . . ?
C15 C10 C11 119.6(3) . . ?
C10 C11 H11 120.4 . . ?
C12 C11 C10 119.2(3) . . ?
C12 C11 H11 120.4 . . ?
C11 C12 H12 119.5 . . ?
C13 C12 C11 121.1(3) . . ?
C13 C12 H12 119.5 . . ?
C12 C13 H13 120.3 . . ?
C14 C13 C12 119.3(3) . . ?
C14 C13 H13 120.3 . . ?
C13 C14 H14 119.6 . . ?
C13 C14 C15 120.8(3) . . ?
C15 C14 H14 119.6 . . ?
C10 C15 H15 120.0 . . ?
C14 C15 C10 120.0(3) . . ?
C14 C15 H15 120.0 . . ?
C5 N1 C1 120.1(2) . . ?
C5 N1 C9 120.0(2) . . ?
C9 N1 C1 119.9(2) . . ?

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
C1 C2 C3 C4 3.0(4) . . . . ?
C1 C2 C3 O1 -178.7(3) . . . . ?
C1 C10 C11 C12 -179.6(3) . . . . ?
C1 C10 C15 C14 179.6(3) . . . . ?
C2 C1 C10 C11 -83.0(4) . . . . ?
C2 C1 C10 C15 98.2(4) . . . . ?
C2 C1 N1 C5 -3.8(4) . . . . ?
C2 C1 N1 C9 174.2(3) . . . . ?
C2 C3 C4 C5 -3.7(4) . . . . ?
C2 C3 C4 I2 179.4(2) . . . . ?
C3 C4 C5 C6 -179.8(3) . . . . ?
C3 C4 C5 N1 0.9(5) . . . . ?
C4 C5 C6 C7 176.2(4) . . . . ?
C4 C5 N1 C1 3.1(4) . . . . ?
C4 C5 N1 C9 -174.9(3) . . . . ?
C5 C6 C7 C8 0.3(7) . . . . ?
C6 C5 N1 C1 -176.3(3) . . . . ?
C6 C5 N1 C9 5.8(4) . . . . ?
C6 C7 C8 C9 2.5(6) . . . . ?
C7 C8 C9 N1 -1.1(6) . . . . ?
C8 C9 N1 C1 178.8(3) . . . . ?
C8 C9 N1 C5 -3.3(5) . . . . ?
C10 C1 C2 C3 -176.0(3) . . . . ?
C10 C1 C2 I1 3.0(4) . . . . ?
C10 C1 N1 C5 173.1(3) . . . . ?
C10 C1 N1 C9 -9.0(4) . . . . ?
C10 C11 C12 C13 0.4(5) . . . . ?
C11 C10 C15 C14 0.8(5) . . . . ?
C11 C12 C13 C14 -0.1(5) . . . . ?
C12 C13 C14 C15 0.1(5) . . . . ?
C13 C14 C15 C10 -0.5(5) . . . . ?
C15 C10 C11 C12 -0.8(5) . . . . ?
I1 C2 C3 C4 -176.1(2) . . . . ?
I1 C2 C3 O1 2.2(4) . . . . ?
I2 C4 C5 C6 -3.1(5) . . . . ?
I2 C4 C5 N1 177.6(2) . . . . ?
N1 C1 C2 C3 0.5(4) . . . . ?
N1 C1 C2 I1 179.58(19) . . . . ?
N1 C1 C10 C11 100.4(3) . . . . ?
N1 C1 C10 C15 -78.4(4) . . . . ?
N1 C5 C6 C7 -4.4(6) . . . . ?
O1 C3 C4 C5 178.0(3) . . . . ?
O1 C3 C4 I2 1.2(4) . . . . ?

_olex2_submission_special_instructions 'No special instructions were received'
