# Electronic Supplementary Material (ESI) for Organic & Biomolecular Chemistry.
# This journal is © The Royal Society of Chemistry 2016

####################################################################### 
# 
# 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_3ba
_database_code_depnum_ccdc_archive 'CCDC 1407861'
_audit_update_record             
;
2015-06-20 deposited with the CCDC.
2015-11-30 downloaded from the CCDC.
;
_audit_creation_date             2014-11-10
_audit_creation_method           
;
Olex2 1.2
(compiled 2014.09.19 svn.r3010 for OlexSys, GUI svn.r4874)
;
_chemical_name_common            ?
_chemical_name_systematic        aks_i_282_01
_chemical_formula_moiety         'C15 H16 N4 O4 S'
_chemical_formula_sum            'C15 H16 N4 O4 S'
_chemical_formula_weight         348.38
_chemical_absolute_configuration ad
_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'
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'
S S 0.1246 0.1234 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'

_space_group_crystal_system      orthorhombic
_space_group_IT_number           19
_space_group_name_H-M_alt        'P 21 21 21'
_space_group_name_Hall           'P 2ac 2ab'
loop_
_space_group_symop_id
_space_group_symop_operation_xyz
1 'x, y, z'
2 '-x+1/2, -y, z+1/2'
3 '-x, y+1/2, -z+1/2'
4 'x+1/2, -y+1/2, -z'

_cell_length_a                   5.8334(5)
_cell_length_b                   10.9763(9)
_cell_length_c                   24.922(2)
_cell_angle_alpha                90.00
_cell_angle_beta                 90.00
_cell_angle_gamma                90.00
_cell_volume                     1595.7(2)
_cell_formula_units_Z            4
_cell_measurement_reflns_used    9950
_cell_measurement_temperature    100
_cell_measurement_theta_max      ?
_cell_measurement_theta_min      ?
_exptl_absorpt_coefficient_mu    0.231
_exptl_absorpt_correction_T_max  0.7456
_exptl_absorpt_correction_T_min  0.4834
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   
;
SADABS-2012/1 (Bruker,2012) was used for absorption correction.
wR2(int) was 0.1045 before and 0.0793 after correction.
The Ratio of minimum to maximum transmission is 0.6483.
The λ/2 correction factor is 0.0015.
;
_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    1.450
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    'not measured'
_exptl_crystal_description       block
_exptl_crystal_F_000             728
_exptl_crystal_size_max          0.26
_exptl_crystal_size_mid          0.25
_exptl_crystal_size_min          0.24
_exptl_special_details           
;
 ? 
;
_diffrn_reflns_av_R_equivalents  0.0688
_diffrn_reflns_av_unetI/netI     0.0481
_diffrn_reflns_limit_h_max       6
_diffrn_reflns_limit_h_min       -6
_diffrn_reflns_limit_k_max       13
_diffrn_reflns_limit_k_min       -13
_diffrn_reflns_limit_l_max       29
_diffrn_reflns_limit_l_min       -29
_diffrn_reflns_number            25586
_diffrn_reflns_theta_full        24.99
_diffrn_reflns_theta_max         24.99
_diffrn_reflns_theta_min         3.08
_diffrn_ambient_temperature      100
_diffrn_detector_area_resol_mean ?
_diffrn_measured_fraction_theta_full 0.996
_diffrn_measured_fraction_theta_max 0.996
_diffrn_measurement_device_type  'Bruker APEX-II CCD'
_diffrn_measurement_method       'φ and ω scans'
_diffrn_radiation_monochromator  graphite
_diffrn_radiation_type           MoK\a
_diffrn_radiation_wavelength     0.71073
_diffrn_source                   'fine-focus sealed tube'
_diffrn_standards_number         0
_reflns_number_gt                2355
_reflns_number_total             2756
_reflns_threshold_expression     >2sigma(I)
_computing_cell_refinement       'SAINT v8.34A (Bruker, 2013)'
_computing_data_collection       ?
_computing_data_reduction        'SAINT v8.34A (Bruker, 2013)'
_computing_molecular_graphics    'Olex2 (Dolomanov et al., 2009)'
_computing_publication_material  'Olex2 (Dolomanov et al., 2009)'
_computing_structure_refinement  'XL (Sheldrick, 2008)'
_computing_structure_solution    'SHELXS-97 (Sheldrick, 2008)'
_refine_diff_density_max         0.270
_refine_diff_density_min         -0.407
_refine_diff_density_rms         0.057
_refine_ls_abs_structure_details 'Flack H D (1983), Acta Cryst. A39, 876-881'
_refine_ls_abs_structure_Flack   0.00(12)
_refine_ls_extinction_coef       ?
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.081
_refine_ls_hydrogen_treatment    refall
_refine_ls_matrix_type           full
_refine_ls_number_parameters     282
_refine_ls_number_reflns         2756
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.0600
_refine_ls_R_factor_gt           0.0448
_refine_ls_restrained_S_all      1.081
_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)+(0.0000P)²+1.5909P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.0726
_refine_ls_wR_factor_ref         0.0754
_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    
;
;
_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
C15 C 0.5956(7) -0.7086(3) -0.28725(15) 0.0318(10) Uani 1 d . . .
H8A H 0.017(5) -0.802(2) -0.1338(10) 0.010(7) Uiso 1 d . . .
H6 H 0.434(5) -1.038(2) 0.1041(11) 0.014(8) Uiso 1 d . . .
H4 H -0.005(6) -1.307(3) 0.0800(11) 0.028(8) Uiso 1 d . . .
H12 H 0.378(5) -0.498(3) -0.1553(11) 0.024(8) Uiso 1 d . . .
H3 H -0.236(5) -1.181(3) 0.0288(11) 0.019(8) Uiso 1 d . . .
H8B H 0.226(5) -0.820(2) -0.0952(12) 0.022(8) Uiso 1 d . . .
H15A H 0.678(6) -0.740(3) -0.3170(14) 0.041(11) Uiso 1 d . . .
H5 H 0.325(5) -1.233(3) 0.1200(12) 0.025(8) Uiso 1 d . . .
H1 H 0.221(5) -0.910(3) 0.0483(11) 0.022(8) Uiso 1 d . . .
H9A H 0.398(5) -0.932(3) -0.1613(11) 0.021(9) Uiso 1 d . . .
H11 H 0.603(5) -0.701(3) -0.1525(11) 0.016(8) Uiso 1 d . . .
H15B H 0.465(5) -0.664(2) -0.2999(10) 0.012(8) Uiso 1 d . . .
H14A H 0.417(5) -0.867(3) -0.2749(12) 0.022(9) Uiso 1 d . . .
H15C H 0.712(7) -0.649(3) -0.2657(14) 0.048(11) Uiso 1 d . . .
H14B H 0.629(6) -0.858(3) -0.2369(12) 0.029(9) Uiso 1 d . . .
H9B H 0.178(6) -0.935(3) -0.1989(12) 0.034(9) Uiso 1 d . . .
S1 S -0.01335(16) -0.98263(6) -0.10158(3) 0.0232(2) Uani 1 d . . .
O4 O 0.0055(5) -0.51901(19) -0.21588(8) 0.0352(5) Uani 1 d . . .
O1 O -0.1759(4) -1.02439(18) -0.14046(8) 0.0332(6) Uani 1 d . . .
O3 O 0.1540(4) -0.70660(17) -0.22509(8) 0.0256(5) Uani 1 d . . .
N1 N -0.1622(5) -0.94940(18) 0.00446(9) 0.0190(6) Uani 1 d . . .
N2 N -0.3136(5) -0.8779(2) 0.03092(10) 0.0233(6) Uani 1 d . . .
C1 C 0.1811(6) -0.9887(3) 0.05670(12) 0.0238(7) Uani 1 d . . .
O2 O 0.1482(4) -1.06527(19) -0.07901(8) 0.0350(6) Uani 1 d . . .
C2 C -0.0164(6) -1.0331(2) 0.03466(10) 0.0182(7) Uani 1 d . . .
C5 C 0.2452(6) -1.1832(3) 0.09668(13) 0.0251(8) Uani 1 d . . .
C8 C 0.1276(7) -0.8517(3) -0.12608(13) 0.0236(8) Uani 1 d . . .
C12 C 0.3571(6) -0.5761(3) -0.17122(12) 0.0243(8) Uani 1 d . . .
C11 C 0.4706(7) -0.6798(3) -0.17073(12) 0.0233(8) Uani 1 d . . .
N3 N -0.4146(4) -0.8111(2) -0.00514(10) 0.0243(7) Uani 1 d . . .
C3 C -0.0909(6) -1.1509(3) 0.04259(13) 0.0232(8) Uani 1 d . . .
C9 C 0.2712(6) -0.8849(3) -0.17468(13) 0.0228(8) Uani 1 d . . .
N4 N -0.3321(5) -0.8373(2) -0.05496(10) 0.0220(6) Uani 1 d . . .
C13 C 0.1553(6) -0.5907(3) -0.20544(12) 0.0258(8) Uani 1 d . . .
C4 C 0.0449(6) -1.2270(3) 0.07427(12) 0.0244(8) Uani 1 d . . .
C14 C 0.5011(8) -0.8119(3) -0.25330(13) 0.0297(8) Uani 1 d . . .
C6 C 0.3140(6) -1.0649(3) 0.08769(13) 0.0249(8) Uani 1 d . . .
C10 C 0.3557(6) -0.7719(3) -0.20547(12) 0.0214(7) Uani 1 d . . .
C7 C -0.1763(6) -0.9217(2) -0.04763(11) 0.0181(7) Uani 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
C15 C14 1.518(5) . ?
S1 O1 1.431(2) . ?
S1 O2 1.424(2) . ?
S1 C8 1.765(3) . ?
S1 C7 1.777(3) . ?
O4 C13 1.204(4) . ?
O3 C13 1.363(4) . ?
O3 C10 1.462(4) . ?
N1 N2 1.353(3) . ?
N1 C2 1.460(4) . ?
N1 C7 1.336(3) . ?
N2 N3 1.301(3) . ?
C1 C2 1.366(5) . ?
C1 C6 1.378(4) . ?
C2 C3 1.379(4) . ?
C5 C4 1.381(5) . ?
C5 C6 1.377(4) . ?
C8 C9 1.517(4) . ?
C12 C11 1.317(5) . ?
C12 C13 1.463(5) . ?
C11 C10 1.491(4) . ?
N3 N4 1.362(3) . ?
C3 C4 1.396(4) . ?
C9 C10 1.539(4) . ?
N4 C7 1.311(4) . ?
C14 C10 1.527(5) . ?

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
O1 S1 C8 109.60(15) . . ?
O1 S1 C7 106.17(14) . . ?
O2 S1 O1 120.13(13) . . ?
O2 S1 C8 110.30(17) . . ?
O2 S1 C7 107.14(13) . . ?
C8 S1 C7 101.81(14) . . ?
C13 O3 C10 109.5(2) . . ?
N2 N1 C2 119.6(2) . . ?
C7 N1 N2 107.6(2) . . ?
C7 N1 C2 132.8(2) . . ?
N3 N2 N1 106.6(2) . . ?
C2 C1 C6 118.9(3) . . ?
C1 C2 N1 118.3(2) . . ?
C1 C2 C3 122.9(3) . . ?
C3 C2 N1 118.7(3) . . ?
C6 C5 C4 120.6(3) . . ?
C9 C8 S1 109.8(2) . . ?
C11 C12 C13 108.4(3) . . ?
C12 C11 C10 110.8(3) . . ?
N2 N3 N4 110.5(2) . . ?
C2 C3 C4 117.6(3) . . ?
C8 C9 C10 112.4(2) . . ?
C7 N4 N3 105.5(2) . . ?
O4 C13 O3 121.9(3) . . ?
O4 C13 C12 129.7(3) . . ?
O3 C13 C12 108.4(3) . . ?
C5 C4 C3 120.0(3) . . ?
C15 C14 C10 115.0(3) . . ?
C5 C6 C1 120.0(3) . . ?
O3 C10 C11 102.9(2) . . ?
O3 C10 C9 107.7(3) . . ?
O3 C10 C14 109.0(3) . . ?
C11 C10 C9 113.6(3) . . ?
C11 C10 C14 113.5(3) . . ?
C14 C10 C9 109.6(2) . . ?
N1 C7 S1 128.1(2) . . ?
N4 C7 S1 122.1(2) . . ?
N4 C7 N1 109.8(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_3af
_database_code_depnum_ccdc_archive 'CCDC 1407862'
_audit_update_record             
;
2015-06-20 deposited with the CCDC.
2015-11-30 downloaded from the CCDC.
;
_audit_creation_date             2014-12-02
_audit_creation_method           
;
Olex2 1.2
(compiled 2014.09.19 svn.r3010 for OlexSys, GUI svn.r4874)
;
_chemical_name_common            ?
_chemical_name_systematic        AKS_I_393_01
_chemical_formula_moiety         'C20 H17 Br N4 O4 S'
_chemical_formula_sum            'C20 H17 Br N4 O4 S'
_chemical_formula_weight         489.35
_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'
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'
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'

_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_id
_space_group_symop_operation_xyz
1 'x, y, z'
2 '-x, -y, -z'

_cell_length_a                   8.1772(5)
_cell_length_b                   9.7706(5)
_cell_length_c                   13.9947(8)
_cell_angle_alpha                70.184(2)
_cell_angle_beta                 73.970(2)
_cell_angle_gamma                83.379(2)
_cell_volume                     1010.72(10)
_cell_formula_units_Z            2
_cell_measurement_reflns_used    ?
_cell_measurement_temperature    100
_cell_measurement_theta_max      25.540
_cell_measurement_theta_min      3.088
_exptl_absorpt_coefficient_mu    2.173
_exptl_absorpt_correction_T_min  0.6126
_exptl_absorpt_correction_T_max  0.6349
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   
'SADABS-2012/1 (Bruker,2012) was used for absorption correction. wR2(int) was 0.0976 before and 0.0638 after correction. The Ratio of minimum to maximum transmission is 0.8654. The λ/2 correction factor is 0.0015.'
_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    1.608
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    'not measured'
_exptl_crystal_description       block
_exptl_crystal_F_000             496
_exptl_crystal_size_max          0.25
_exptl_crystal_size_mid          0.25
_exptl_crystal_size_min          0.23
_exptl_special_details           
;
 ?
;
_diffrn_reflns_av_R_equivalents  0.0677
_diffrn_reflns_av_unetI/netI     0.0367
_diffrn_reflns_limit_h_max       9
_diffrn_reflns_limit_h_min       -9
_diffrn_reflns_limit_k_max       11
_diffrn_reflns_limit_k_min       -11
_diffrn_reflns_limit_l_max       16
_diffrn_reflns_limit_l_min       -16
_diffrn_reflns_number            35218
_diffrn_reflns_theta_full        25.00
_diffrn_reflns_theta_max         25.00
_diffrn_reflns_theta_min         3.09
_diffrn_ambient_temperature      100
_diffrn_detector                 'Bruker APEX2 area detector'
_diffrn_detector_area_resol_mean ?
_diffrn_detector_type            'CCD area detector'
_diffrn_measured_fraction_theta_full 0.999
_diffrn_measured_fraction_theta_max 0.999
_diffrn_measurement_device       'three-circle diffractometer'
_diffrn_measurement_device_type  'Bruker APEX-II CCD'
_diffrn_measurement_method       'φ and ω scans'
_diffrn_radiation_monochromator  ?
_diffrn_radiation_probe          x-ray
_diffrn_radiation_type           MoK\a
_diffrn_radiation_wavelength     0.71073
_diffrn_source                   'microfocus sealed X-ray tube'
_diffrn_source_type              'Incoatec I\ms'
_diffrn_standards_decay_%        ?
_diffrn_standards_interval_count ?
_diffrn_standards_interval_time  ?
_diffrn_standards_number         .
_reflns_number_gt                3010
_reflns_number_total             3553
_reflns_threshold_expression     >2σ(I)
_computing_cell_refinement       ?
_computing_data_collection       ?
_computing_data_reduction        ?
_computing_molecular_graphics    'Olex2 (Dolomanov et al., 2009)'
_computing_publication_material  'Olex2 (Dolomanov et al., 2009)'
_computing_structure_refinement  'XL (Sheldrick, 2008)'
_computing_structure_solution    'olex2.solve (Bourhis et al., 2013)'
_refine_diff_density_max         0.421
_refine_diff_density_min         -0.343
_refine_diff_density_rms         0.069
_refine_ls_extinction_coef       ?
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.025
_refine_ls_hydrogen_treatment    constr
_refine_ls_matrix_type           full
_refine_ls_number_parameters     272
_refine_ls_number_reflns         3553
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.0437
_refine_ls_R_factor_gt           0.0303
_refine_ls_restrained_S_all      1.025
_refine_ls_shift/su_max          0.001
_refine_ls_shift/su_mean         0.000
_refine_ls_structure_factor_coef Fsqd
_refine_ls_weighting_details     
'calc w=1/[σ²(Fo²)+(0.0292P)²+0.5610P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.0599
_refine_ls_wR_factor_ref         0.0628
_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 > 2σ(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:
 C14(H14)
2.b Secondary CH2 refined with riding coordinates:
 C26(H26A,H26B)
2.c Aromatic/amide H refined with riding coordinates:
 C8(H8), C10(H10), C13(H13), C15(H15), C17(H17), C20(H20), C21(H21), C23(H23),
 C25(H25), C27(H27), C30(H30)
2.d Idealised Me refined as rotating group:
 C16(H16A,H16B,H16C)
;
_atom_sites_solution_hydrogens   geom
_atom_sites_solution_primary     iterative
_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
Br1 Br 0.15828(3) 0.85202(3) 0.451728(19) 0.01792(9) Uani 1 d . . .
S2 S 0.07400(8) 0.73330(7) 1.00887(5) 0.01413(15) Uani 1 d . . .
O3 O 0.5899(2) 0.56631(17) 0.84038(12) 0.0147(4) Uani 1 d . . .
O4 O -0.0335(2) 0.61515(18) 1.07646(13) 0.0206(4) Uani 1 d . . .
O5 O 0.0137(2) 0.84843(18) 0.93081(13) 0.0197(4) Uani 1 d . . .
N6 N 0.0430(2) 0.8178(2) 1.18631(15) 0.0136(4) Uani 1 d . . .
O7 O 0.7402(2) 0.4515(2) 0.72859(15) 0.0269(5) Uani 1 d . . .
C8 C 0.2782(3) 0.6664(3) 0.73737(19) 0.0148(5) Uani 1 d . . .
H8 H 0.2783 0.5714 0.7865 0.018 Uiso 1 calc . . R
N9 N 0.2783(3) 0.9222(2) 1.14625(16) 0.0189(5) Uani 1 d . . .
C10 C 0.2819(3) 0.9414(3) 0.59180(19) 0.0174(6) Uani 1 d . . .
H10 H 0.2847 1.0356 0.5412 0.021 Uiso 1 calc . . R
N11 N 0.2775(3) 0.8795(2) 1.06340(16) 0.0184(5) Uani 1 d . . .
N12 N 0.1390(3) 0.8870(2) 1.21976(16) 0.0167(5) Uani 1 d . . .
C13 C 0.2284(3) 0.6867(3) 0.64698(19) 0.0162(6) Uani 1 d . . .
H13 H 0.1937 0.6065 0.6342 0.019 Uiso 1 calc . . R
C14 C 0.3842(3) 0.7640(2) 0.85625(18) 0.0123(5) Uani 1 d . . .
H14 H 0.3726 0.8614 0.8666 0.015 Uiso 1 calc . . R
C15 C 0.3303(3) 0.9198(3) 0.68266(18) 0.0151(5) Uani 1 d . . .
H15 H 0.3661 1.0005 0.6945 0.018 Uiso 1 calc . . R
C16 C 0.6391(3) 0.7156(3) 0.9370(2) 0.0197(6) Uani 1 d . . .
H16A H 0.5746 0.6476 1.0024 0.030 Uiso 1 calc . . GR
H16B H 0.6255 0.8140 0.9422 0.030 Uiso 1 calc . . GR
H16C H 0.7599 0.6864 0.9250 0.030 Uiso 1 calc . . GR
C17 C 0.6861(3) 0.7982(3) 0.7439(2) 0.0187(6) Uani 1 d . . .
H17 H 0.7019 0.9001 0.7214 0.022 Uiso 1 calc . . R
C18 C 0.3280(3) 0.7826(3) 0.75760(18) 0.0126(5) Uani 1 d . . .
C19 C 0.5732(3) 0.7138(2) 0.84605(19) 0.0152(5) Uani 1 d . . .
C20 C -0.2583(3) 0.7840(3) 1.2098(2) 0.0223(6) Uani 1 d . . .
H20 H -0.2472 0.8326 1.1370 0.027 Uiso 1 calc . . R
C21 C -0.2903(4) 0.6492(3) 1.4235(2) 0.0279(7) Uani 1 d . . .
H21 H -0.3026 0.6054 1.4969 0.033 Uiso 1 calc . . R
C22 C 0.7032(3) 0.5632(3) 0.7480(2) 0.0195(6) Uani 1 d . . .
C23 C -0.1327(3) 0.6954(3) 1.3576(2) 0.0205(6) Uani 1 d . . .
H23 H -0.0352 0.6806 1.3846 0.025 Uiso 1 calc . . R
C24 C 0.1314(3) 0.8150(2) 1.09041(19) 0.0140(5) Uani 1 d . . .
C25 C 0.7606(3) 0.7119(3) 0.6892(2) 0.0222(6) Uani 1 d . . .
H25 H 0.8391 0.7414 0.6222 0.027 Uiso 1 calc . . R
C26 C 0.2707(3) 0.6591(3) 0.95411(18) 0.0145(5) Uani 1 d . . .
H26A H 0.3350 0.6216 1.0086 0.017 Uiso 1 calc . . R
H26B H 0.2474 0.5752 0.9358 0.017 Uiso 1 calc . . R
C27 C -0.4135(3) 0.7320(3) 1.2765(3) 0.0294(7) Uani 1 d . . .
H27 H -0.5099 0.7414 1.2491 0.035 Uiso 1 calc . . R
C28 C -0.1197(3) 0.7632(3) 1.25210(19) 0.0159(6) Uani 1 d . . .
C29 C 0.2295(3) 0.8244(3) 0.57543(18) 0.0144(5) Uani 1 d . . .
C30 C -0.4290(4) 0.6665(3) 1.3829(2) 0.0316(7) Uani 1 d . . .
H30 H -0.5367 0.6332 1.4284 0.038 Uiso 1 calc . . R


_geom_special_details            
;
 All s.u.'s (except the s.u. in the dihedral angle between two l.s. planes)
 are estimated using the full covariance matrix.  The cell s.u.'s are taken
 into account individually in the estimation of s.u.'s in distances, angles
 and torsion angles; correlations between s.u.'s in cell parameters are only
 used when they are defined by crystal symmetry.  An approximate (isotropic)
 treatment of cell s.u.'s is used for estimating s.u.'s 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
Br1 C29 1.901(2) . ?
S2 O4 1.4265(18) . ?
S2 O5 1.4277(17) . ?
S2 C24 1.778(2) . ?
S2 C26 1.768(2) . ?
O3 C19 1.458(3) . ?
O3 C22 1.375(3) . ?
N6 N12 1.354(3) . ?
N6 C24 1.345(3) . ?
N6 C28 1.434(3) . ?
O7 C22 1.198(3) . ?
C8 H8 0.9500 . ?
C8 C13 1.379(3) . ?
C8 C18 1.387(3) . ?
N9 N11 1.361(3) . ?
N9 N12 1.295(3) . ?
C10 H10 0.9500 . ?
C10 C15 1.376(3) . ?
C10 C29 1.374(3) . ?
N11 C24 1.315(3) . ?
C13 H13 0.9500 . ?
C13 C29 1.377(3) . ?
C14 H14 1.0000 . ?
C14 C18 1.520(3) . ?
C14 C19 1.549(3) . ?
C14 C26 1.534(3) . ?
C15 H15 0.9500 . ?
C15 C18 1.393(3) . ?
C16 H16A 0.9800 . ?
C16 H16B 0.9800 . ?
C16 H16C 0.9800 . ?
C16 C19 1.519(3) . ?
C17 H17 0.9500 . ?
C17 C19 1.491(3) . ?
C17 C25 1.315(4) . ?
C20 H20 0.9500 . ?
C20 C27 1.383(4) . ?
C20 C28 1.383(4) . ?
C21 H21 0.9500 . ?
C21 C23 1.382(4) . ?
C21 C30 1.372(4) . ?
C22 C25 1.463(4) . ?
C23 H23 0.9500 . ?
C23 C28 1.377(3) . ?
C25 H25 0.9500 . ?
C26 H26A 0.9900 . ?
C26 H26B 0.9900 . ?
C27 H27 0.9500 . ?
C27 C30 1.383(4) . ?
C30 H30 0.9500 . ?

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
O4 S2 O5 120.12(11) . . ?
O4 S2 C24 107.06(11) . . ?
O4 S2 C26 107.77(11) . . ?
O5 S2 C24 106.53(11) . . ?
O5 S2 C26 111.52(11) . . ?
C26 S2 C24 102.29(12) . . ?
C22 O3 C19 109.88(18) . . ?
N12 N6 C28 120.0(2) . . ?
C24 N6 N12 107.04(19) . . ?
C24 N6 C28 132.9(2) . . ?
C13 C8 H8 119.5 . . ?
C13 C8 C18 121.0(2) . . ?
C18 C8 H8 119.5 . . ?
N12 N9 N11 111.10(19) . . ?
C15 C10 H10 120.6 . . ?
C29 C10 H10 120.6 . . ?
C29 C10 C15 118.9(2) . . ?
C24 N11 N9 105.1(2) . . ?
N9 N12 N6 106.86(19) . . ?
C8 C13 H13 120.3 . . ?
C29 C13 C8 119.4(2) . . ?
C29 C13 H13 120.3 . . ?
C18 C14 H14 107.4 . . ?
C18 C14 C19 112.29(19) . . ?
C18 C14 C26 111.94(19) . . ?
C19 C14 H14 107.4 . . ?
C26 C14 H14 107.4 . . ?
C26 C14 C19 110.03(19) . . ?
C10 C15 H15 119.2 . . ?
C10 C15 C18 121.5(2) . . ?
C18 C15 H15 119.2 . . ?
H16A C16 H16B 109.5 . . ?
H16A C16 H16C 109.5 . . ?
H16B C16 H16C 109.5 . . ?
C19 C16 H16A 109.5 . . ?
C19 C16 H16B 109.5 . . ?
C19 C16 H16C 109.5 . . ?
C19 C17 H17 124.7 . . ?
C25 C17 H17 124.7 . . ?
C25 C17 C19 110.6(2) . . ?
C8 C18 C14 122.4(2) . . ?
C8 C18 C15 118.0(2) . . ?
C15 C18 C14 119.6(2) . . ?
O3 C19 C14 108.29(18) . . ?
O3 C19 C16 109.20(19) . . ?
O3 C19 C17 102.9(2) . . ?
C16 C19 C14 113.1(2) . . ?
C17 C19 C14 112.17(19) . . ?
C17 C19 C16 110.5(2) . . ?
C27 C20 H20 121.0 . . ?
C28 C20 H20 121.0 . . ?
C28 C20 C27 118.1(3) . . ?
C23 C21 H21 120.0 . . ?
C30 C21 H21 120.0 . . ?
C30 C21 C23 120.0(3) . . ?
O3 C22 C25 107.4(2) . . ?
O7 C22 O3 121.1(2) . . ?
O7 C22 C25 131.5(3) . . ?
C21 C23 H23 120.6 . . ?
C28 C23 C21 118.8(3) . . ?
C28 C23 H23 120.6 . . ?
N6 C24 S2 127.86(19) . . ?
N11 C24 S2 122.20(19) . . ?
N11 C24 N6 109.9(2) . . ?
C17 C25 C22 109.2(2) . . ?
C17 C25 H25 125.4 . . ?
C22 C25 H25 125.4 . . ?
S2 C26 H26A 108.3 . . ?
S2 C26 H26B 108.3 . . ?
C14 C26 S2 115.74(17) . . ?
C14 C26 H26A 108.3 . . ?
C14 C26 H26B 108.3 . . ?
H26A C26 H26B 107.4 . . ?
C20 C27 H27 119.9 . . ?
C30 C27 C20 120.2(3) . . ?
C30 C27 H27 119.9 . . ?
C20 C28 N6 120.0(2) . . ?
C23 C28 N6 117.7(2) . . ?
C23 C28 C20 122.2(2) . . ?
C10 C29 Br1 119.66(18) . . ?
C10 C29 C13 121.1(2) . . ?
C13 C29 Br1 119.21(18) . . ?
C21 C30 C27 120.6(3) . . ?
C21 C30 H30 119.7 . . ?
C27 C30 H30 119.7 . . ?

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 C22 C25 C17 0.3(3) . . . . ?
O4 S2 C24 N6 -27.7(2) . . . . ?
O4 S2 C24 N11 149.8(2) . . . . ?
O4 S2 C26 C14 162.73(17) . . . . ?
O5 S2 C24 N6 102.0(2) . . . . ?
O5 S2 C24 N11 -80.5(2) . . . . ?
O5 S2 C26 C14 28.9(2) . . . . ?
O7 C22 C25 C17 -178.6(3) . . . . ?
C8 C13 C29 Br1 -179.28(18) . . . . ?
C8 C13 C29 C10 1.1(4) . . . . ?
N9 N11 C24 S2 -177.48(17) . . . . ?
N9 N11 C24 N6 0.4(3) . . . . ?
C10 C15 C18 C8 1.1(4) . . . . ?
C10 C15 C18 C14 179.4(2) . . . . ?
N11 N9 N12 N6 0.6(3) . . . . ?
N12 N6 C24 S2 177.67(17) . . . . ?
N12 N6 C24 N11 0.0(3) . . . . ?
N12 N6 C28 C20 136.0(2) . . . . ?
N12 N6 C28 C23 -41.8(3) . . . . ?
N12 N9 N11 C24 -0.6(3) . . . . ?
C13 C8 C18 C14 -179.8(2) . . . . ?
C13 C8 C18 C15 -1.5(4) . . . . ?
C15 C10 C29 Br1 178.89(18) . . . . ?
C15 C10 C29 C13 -1.4(4) . . . . ?
C18 C8 C13 C29 0.5(4) . . . . ?
C18 C14 C19 O3 -67.1(2) . . . . ?
C18 C14 C19 C16 171.66(19) . . . . ?
C18 C14 C19 C17 45.8(3) . . . . ?
C18 C14 C26 S2 -79.7(2) . . . . ?
C19 O3 C22 O7 177.6(2) . . . . ?
C19 O3 C22 C25 -1.4(3) . . . . ?
C19 C14 C18 C8 82.4(3) . . . . ?
C19 C14 C18 C15 -95.8(3) . . . . ?
C19 C14 C26 S2 154.67(17) . . . . ?
C19 C17 C25 C22 1.0(3) . . . . ?
C20 C27 C30 C21 -1.5(4) . . . . ?
C21 C23 C28 N6 176.4(2) . . . . ?
C21 C23 C28 C20 -1.3(4) . . . . ?
C22 O3 C19 C14 120.8(2) . . . . ?
C22 O3 C19 C16 -115.6(2) . . . . ?
C22 O3 C19 C17 1.9(2) . . . . ?
C23 C21 C30 C27 -1.0(4) . . . . ?
C24 S2 C26 C14 -84.62(19) . . . . ?
C24 N6 N12 N9 -0.3(2) . . . . ?
C24 N6 C28 C20 -44.7(4) . . . . ?
C24 N6 C28 C23 137.6(3) . . . . ?
C25 C17 C19 O3 -1.8(3) . . . . ?
C25 C17 C19 C14 -117.9(2) . . . . ?
C25 C17 C19 C16 114.8(2) . . . . ?
C26 S2 C24 N6 -140.9(2) . . . . ?
C26 S2 C24 N11 36.6(2) . . . . ?
C26 C14 C18 C8 -42.0(3) . . . . ?
C26 C14 C18 C15 139.8(2) . . . . ?
C26 C14 C19 O3 58.3(2) . . . . ?
C26 C14 C19 C16 -62.9(3) . . . . ?
C26 C14 C19 C17 171.2(2) . . . . ?
C27 C20 C28 N6 -178.8(2) . . . . ?
C27 C20 C28 C23 -1.1(4) . . . . ?
C28 N6 N12 N9 179.2(2) . . . . ?
C28 N6 C24 S2 -1.7(4) . . . . ?
C28 N6 C24 N11 -179.4(2) . . . . ?
C28 C20 C27 C30 2.5(4) . . . . ?
C29 C10 C15 C18 0.3(4) . . . . ?
C30 C21 C23 C28 2.3(4) . . . . ?

_olex2_submission_original_sample_id AKS_I_393_01
_olex2_submission_special_instructions 'No special instructions were received'
