# Electronic Supplementary Material (ESI) for Organic & Biomolecular Chemistry.
# This journal is © The Royal Society of Chemistry 2018

####################################################################### 
# 
# 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_exp_4183
_audit_block_doi                 10.5517/ccdc.csd.cc1zlgst
_database_code_depnum_ccdc_archive 'CCDC 1835007'
_audit_update_record             
;
2018-04-05 deposited with the CCDC.
2018-12-04 downloaded from the CCDC.
;

_audit_creation_method           SHELXL-2014/7
_shelx_SHELXL_version_number     2014/7
_chemical_name_systematic        3-arylquinoline
_chemical_name_common            ?
_chemical_melting_point          ?
_chemical_formula_moiety         ?
_chemical_formula_sum            'C16 H12 Br N'
_chemical_formula_weight         298.18

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'
Br Br -0.2901 2.4595 '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'

_space_group_crystal_system      orthorhombic
_space_group_IT_number           60
_space_group_name_H-M_alt        'P b c n'
_space_group_name_Hall           '-P 2n 2ab'

_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.
;

loop_
_space_group_symop_operation_xyz
'x, y, z'
'-x+1/2, -y+1/2, z+1/2'
'-x, y, -z+1/2'
'x+1/2, -y+1/2, -z'
'-x, -y, -z'
'x-1/2, y-1/2, -z-1/2'
'x, -y, z-1/2'
'-x-1/2, y-1/2, z'

_cell_length_a                   13.856(2)
_cell_length_b                   6.4827(11)
_cell_length_c                   28.807(3)
_cell_angle_alpha                90
_cell_angle_beta                 90
_cell_angle_gamma                90
_cell_volume                     2587.5(6)
_cell_formula_units_Z            8
_cell_measurement_temperature    293(2)
_cell_measurement_reflns_used    1290
_cell_measurement_theta_min      3.7550
_cell_measurement_theta_max      25.0130

_exptl_crystal_description       block
_exptl_crystal_colour            brown
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    ?
_exptl_crystal_density_diffrn    1.531
_exptl_crystal_F_000             1200
_exptl_transmission_factor_min   ?
_exptl_transmission_factor_max   ?
_exptl_crystal_size_max          ?
_exptl_crystal_size_mid          ?
_exptl_crystal_size_min          ?
_exptl_absorpt_coefficient_mu    3.157
_shelx_estimated_absorpt_T_min   ?
_shelx_estimated_absorpt_T_max   ?
_exptl_absorpt_correction_type   ?
_exptl_absorpt_correction_T_min  ?
_exptl_absorpt_correction_T_max  ?
_exptl_absorpt_process_details   ?
_exptl_absorpt_special_details   ?
_diffrn_ambient_temperature      293(2)
_diffrn_radiation_wavelength     0.71073
_diffrn_radiation_type           MoK\a
_diffrn_source                   ?
_diffrn_measurement_device_type  'CCD area detector'
_diffrn_measurement_method       'phi and omega scans'
_diffrn_detector_area_resol_mean ?
_diffrn_reflns_number            6340
_diffrn_reflns_av_unetI/netI     0.1240
_diffrn_reflns_av_R_equivalents  0.1221
_diffrn_reflns_limit_h_min       -15
_diffrn_reflns_limit_h_max       16
_diffrn_reflns_limit_k_min       -7
_diffrn_reflns_limit_k_max       7
_diffrn_reflns_limit_l_min       -34
_diffrn_reflns_limit_l_max       32
_diffrn_reflns_theta_min         2.940
_diffrn_reflns_theta_max         25.050
_diffrn_reflns_theta_full        25.050
_diffrn_measured_fraction_theta_max 0.997
_diffrn_measured_fraction_theta_full 0.997
_diffrn_reflns_Laue_measured_fraction_max 0.997
_diffrn_reflns_Laue_measured_fraction_full 0.997
_diffrn_reflns_point_group_measured_fraction_max 0.997
_diffrn_reflns_point_group_measured_fraction_full 0.997
_reflns_number_total             2283
_reflns_number_gt                911
_reflns_threshold_expression     'I > 2σ(I)'
_reflns_Friedel_coverage         0.000
_reflns_Friedel_fraction_max     .
_reflns_Friedel_fraction_full    .

_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.
;

_computing_data_collection       ?
_computing_cell_refinement       ?
_computing_data_reduction        ?
_computing_structure_solution    ?
_computing_structure_refinement  'SHELXL-2014/7 (Sheldrick, 2014)'
_computing_molecular_graphics    ?
_computing_publication_material  ?
_refine_special_details          ?
_refine_ls_structure_factor_coef Fsqd
_refine_ls_matrix_type           full
_refine_ls_weighting_scheme      calc
_refine_ls_weighting_details     
'w=1/[σ²(Fo²)+(0.0100P)²+0.0900P] where P=(Fo²+2Fc²)/3'
_atom_sites_solution_primary     ?
_atom_sites_solution_secondary   ?
_atom_sites_solution_hydrogens   geom
_refine_ls_hydrogen_treatment    constr
_refine_ls_extinction_method     none
_refine_ls_extinction_coef       .
_refine_ls_number_reflns         2283
_refine_ls_number_parameters     164
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.1828
_refine_ls_R_factor_gt           0.0800
_refine_ls_wR_factor_ref         0.1334
_refine_ls_wR_factor_gt          0.1102
_refine_ls_goodness_of_fit_ref   1.104
_refine_ls_restrained_S_all      1.104
_refine_ls_shift/su_max          0.000
_refine_ls_shift/su_mean         0.000

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
Br17 Br 0.38139(6) 0.85640(17) 0.06250(3) 0.0937(4) Uani 1 1 d . . . . .
N3 N 0.4040(4) 0.2286(9) 0.3133(2) 0.0611(18) Uani 1 1 d . . . . .
C1 C 0.3681(4) 0.5227(11) 0.2636(2) 0.0389(18) Uani 1 1 d . . . . .
C11 C 0.3698(4) 0.5986(12) 0.2139(3) 0.0449(19) Uani 1 1 d . . . . .
C10 C 0.3522(4) 0.6463(11) 0.3006(3) 0.055(2) Uani 1 1 d . . . . .
H10 H 0.3346 0.7834 0.2964 0.066 Uiso 1 1 calc R U . . .
C9 C 0.3625(4) 0.5656(12) 0.3456(3) 0.0461(19) Uani 1 1 d . . . . .
C16 C 0.4022(5) 0.7980(11) 0.2049(3) 0.056(2) Uani 1 1 d . . . . .
H16 H 0.4214 0.8816 0.2294 0.067 Uiso 1 1 calc R U . . .
C2 C 0.3927(5) 0.3133(11) 0.2718(3) 0.057(2) Uani 1 1 d . . . . .
H2 H 0.4016 0.2290 0.2461 0.068 Uiso 1 1 calc R U . . .
C15 C 0.4064(5) 0.8729(12) 0.1606(3) 0.057(2) Uani 1 1 d . . . . .
H15 H 0.4274 1.0072 0.1554 0.069 Uiso 1 1 calc R U . . .
C12 C 0.3405(4) 0.4805(12) 0.1770(3) 0.061(2) Uani 1 1 d . . . . .
H12 H 0.3162 0.3490 0.1825 0.073 Uiso 1 1 calc R U . . .
C4 C 0.3928(5) 0.3583(12) 0.3500(3) 0.055(2) Uani 1 1 d . . . . .
C13 C 0.3462(5) 0.5540(13) 0.1312(3) 0.059(2) Uani 1 1 d . . . . .
H13 H 0.3277 0.4699 0.1067 0.071 Uiso 1 1 calc R U . . .
C8 C 0.3491(4) 0.6840(13) 0.3868(3) 0.063(2) Uani 1 1 d . . . . .
H8 H 0.3270 0.8188 0.3836 0.076 Uiso 1 1 calc R U . . .
C7 C 0.3668(5) 0.6116(15) 0.4307(3) 0.068(2) Uani 1 1 d . . . . .
C14 C 0.3790(5) 0.7484(13) 0.1229(3) 0.063(2) Uani 1 1 d . . . . .
C6 C 0.3970(6) 0.4034(15) 0.4329(3) 0.076(3) Uani 1 1 d . . . . .
H6 H 0.4090 0.3478 0.4621 0.091 Uiso 1 1 calc R U . . .
C5 C 0.4097(6) 0.2785(14) 0.3954(3) 0.076(3) Uani 1 1 d . . . . .
H5 H 0.4292 0.1424 0.3993 0.091 Uiso 1 1 calc R U . . .
C18 C 0.3515(5) 0.7375(13) 0.4736(3) 0.092(3) Uani 1 1 d . . . . .
H18A H 0.4124 0.7609 0.4885 0.139 Uiso 1 1 calc R U . . .
H18B H 0.3093 0.6649 0.4943 0.139 Uiso 1 1 calc R U . . .
H18C H 0.3231 0.8674 0.4653 0.139 Uiso 1 1 calc R U . . .


_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
Br17 C14 1.877(9) . ?
N3 C2 1.324(9) . ?
N3 C4 1.359(9) . ?
C1 C10 1.353(9) . ?
C1 C2 1.420(9) . ?
C1 C11 1.512(9) . ?
C11 C12 1.371(9) . ?
C11 C16 1.393(9) . ?
C10 C9 1.405(9) . ?
C10 H10 0.9300 . ?
C9 C4 1.414(9) . ?
C9 C8 1.424(9) . ?
C16 C15 1.366(9) . ?
C16 H16 0.9300 . ?
C2 H2 0.9300 . ?
C15 C14 1.405(10) . ?
C15 H15 0.9300 . ?
C12 C13 1.405(9) . ?
C12 H12 0.9300 . ?
C4 C5 1.426(10) . ?
C13 C14 1.361(10) . ?
C13 H13 0.9300 . ?
C8 C7 1.372(10) . ?
C8 H8 0.9300 . ?
C7 C6 1.414(11) . ?
C7 C18 1.495(10) . ?
C6 C5 1.362(10) . ?
C6 H6 0.9300 . ?
C5 H5 0.9300 . ?
C18 H18A 0.9600 . ?
C18 H18B 0.9600 . ?
C18 H18C 0.9600 . ?

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 N3 C4 115.6(7) . . ?
C10 C1 C2 118.2(7) . . ?
C10 C1 C11 123.8(7) . . ?
C2 C1 C11 117.8(7) . . ?
C12 C11 C16 118.0(7) . . ?
C12 C11 C1 123.1(7) . . ?
C16 C11 C1 119.0(7) . . ?
C1 C10 C9 119.4(7) . . ?
C1 C10 H10 120.3 . . ?
C9 C10 H10 120.3 . . ?
C10 C9 C4 117.7(7) . . ?
C10 C9 C8 123.6(7) . . ?
C4 C9 C8 118.5(7) . . ?
C15 C16 C11 121.2(7) . . ?
C15 C16 H16 119.4 . . ?
C11 C16 H16 119.4 . . ?
N3 C2 C1 125.2(7) . . ?
N3 C2 H2 117.4 . . ?
C1 C2 H2 117.4 . . ?
C16 C15 C14 120.4(8) . . ?
C16 C15 H15 119.8 . . ?
C14 C15 H15 119.8 . . ?
C11 C12 C13 121.4(7) . . ?
C11 C12 H12 119.3 . . ?
C13 C12 H12 119.3 . . ?
N3 C4 C9 123.6(7) . . ?
N3 C4 C5 118.1(8) . . ?
C9 C4 C5 118.3(8) . . ?
C14 C13 C12 119.9(8) . . ?
C14 C13 H13 120.1 . . ?
C12 C13 H13 120.1 . . ?
C7 C8 C9 124.1(8) . . ?
C7 C8 H8 118.0 . . ?
C9 C8 H8 118.0 . . ?
C8 C7 C6 114.9(9) . . ?
C8 C7 C18 123.4(9) . . ?
C6 C7 C18 121.7(9) . . ?
C13 C14 C15 119.1(8) . . ?
C13 C14 Br17 121.0(7) . . ?
C15 C14 Br17 119.8(6) . . ?
C5 C6 C7 124.7(9) . . ?
C5 C6 H6 117.6 . . ?
C7 C6 H6 117.6 . . ?
C6 C5 C4 119.5(8) . . ?
C6 C5 H5 120.3 . . ?
C4 C5 H5 120.3 . . ?
C7 C18 H18A 109.5 . . ?
C7 C18 H18B 109.5 . . ?
H18A C18 H18B 109.5 . . ?
C7 C18 H18C 109.5 . . ?
H18A C18 H18C 109.5 . . ?
H18B C18 H18C 109.5 . . ?

_refine_diff_density_max         0.503
_refine_diff_density_min         -0.430
_refine_diff_density_rms         0.094


_exptl_crystal_recrystallization_method 
'Re-crystallisation from solvent: acetonitrile'
