# Electronic Supplementary Material (ESI) for Organic & Biomolecular Chemistry.
# 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_SUST_1788_0m
_database_code_depnum_ccdc_archive 'CCDC 1954603'
loop_
_audit_author_name
_audit_author_address
'shanshan liu'
;Shaanxi University of Science and Technology
China
;
_audit_update_record             
;
2019-09-19 deposited with the CCDC.	2019-11-11 downloaded from the CCDC.
;

_audit_creation_method           SHELXL-2014/7
_shelx_SHELXL_version_number     2014/7
_chemical_name_systematic        ?
_chemical_name_common            ?
_chemical_melting_point          ?
_chemical_formula_moiety         ?
_chemical_formula_sum            'C13 H10 N2 S'
_chemical_formula_weight         226.29

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'
N N 0.0061 0.0033 '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'
H H 0.0000 0.0000 '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 21/n'
_space_group_name_Hall           '-P 2yn'

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

_cell_length_a                   5.8840(6)
_cell_length_b                   8.0198(7)
_cell_length_c                   24.297(3)
_cell_angle_alpha                90
_cell_angle_beta                 95.847(7)
_cell_angle_gamma                90
_cell_volume                     1140.6(2)
_cell_formula_units_Z            4
_cell_measurement_temperature    276(2)
_cell_measurement_reflns_used    2605
_cell_measurement_theta_min      2.68
_cell_measurement_theta_max      24.38

_exptl_crystal_description       block
_exptl_crystal_colour            colourless
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    ?
_exptl_crystal_density_diffrn    1.318
_exptl_crystal_F_000             472
_exptl_transmission_factor_min   ?
_exptl_transmission_factor_max   ?
_exptl_crystal_size_max          0.150
_exptl_crystal_size_mid          0.140
_exptl_crystal_size_min          0.130
_exptl_absorpt_coefficient_mu    0.255
_shelx_estimated_absorpt_T_min   0.963
_shelx_estimated_absorpt_T_max   0.968
_exptl_absorpt_correction_type   none
_exptl_absorpt_correction_T_min  ?
_exptl_absorpt_correction_T_max  ?
_exptl_absorpt_process_details   ?
_exptl_absorpt_special_details   ?
_diffrn_ambient_temperature      276(2)
_diffrn_radiation_wavelength     0.71073
_diffrn_radiation_type           MoK\a
_diffrn_source                   ?
_diffrn_measurement_device_type  'Bruker APEX-II CCD'
_diffrn_measurement_method       'φ and ω scans'
_diffrn_detector_area_resol_mean ?
_diffrn_reflns_number            11367
_diffrn_reflns_av_unetI/netI     0.0828
_diffrn_reflns_av_R_equivalents  0.0666
_diffrn_reflns_limit_h_min       -7
_diffrn_reflns_limit_h_max       5
_diffrn_reflns_limit_k_min       -10
_diffrn_reflns_limit_k_max       10
_diffrn_reflns_limit_l_min       -32
_diffrn_reflns_limit_l_max       24
_diffrn_reflns_theta_min         2.676
_diffrn_reflns_theta_max         28.270
_diffrn_reflns_theta_full        25.242
_diffrn_measured_fraction_theta_max 0.964
_diffrn_measured_fraction_theta_full 0.979
_diffrn_reflns_Laue_measured_fraction_max 0.964
_diffrn_reflns_Laue_measured_fraction_full 0.979
_diffrn_reflns_point_group_measured_fraction_max 0.964
_diffrn_reflns_point_group_measured_fraction_full 0.979
_reflns_number_total             2722
_reflns_number_gt                1392
_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)+(0.0494P)²+0.7061P] 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         2722
_refine_ls_number_parameters     145
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.1487
_refine_ls_R_factor_gt           0.0660
_refine_ls_wR_factor_ref         0.1717
_refine_ls_wR_factor_gt          0.1480
_refine_ls_goodness_of_fit_ref   1.074
_refine_ls_restrained_S_all      1.074
_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
C1 C 0.4173(6) 0.8448(4) 0.31282(14) 0.0601(9) Uani 1 1 d . . . . .
H1 H 0.3151 0.7851 0.3320 0.072 Uiso 1 1 calc R U . . .
C2 C 0.3566(6) 0.8935(4) 0.25884(14) 0.0675(10) Uani 1 1 d . . . . .
H2 H 0.2137 0.8642 0.2416 0.081 Uiso 1 1 calc R U . . .
C3 C 0.5018(7) 0.9835(5) 0.23028(16) 0.0761(11) Uani 1 1 d . . . . .
H3 H 0.4585 1.0154 0.1939 0.091 Uiso 1 1 calc R U . . .
C4 C 0.7114(8) 1.0265(5) 0.25551(19) 0.0863(12) Uani 1 1 d . . . . .
H4 H 0.8108 1.0894 0.2365 0.104 Uiso 1 1 calc R U . . .
C5 C 0.7762(7) 0.9766(5) 0.30922(17) 0.0753(11) Uani 1 1 d . . . . .
H5 H 0.9200 1.0052 0.3260 0.090 Uiso 1 1 calc R U . . .
C6 C 0.6298(6) 0.8850(4) 0.33811(14) 0.0578(9) Uani 1 1 d . . . . .
C7 C 0.3631(7) 0.7685(4) 0.46679(14) 0.0703(11) Uani 1 1 d . . . . .
H7 H 0.3672 0.8748 0.4822 0.084 Uiso 1 1 calc R U . . .
C8 C 0.5052(6) 0.7152(4) 0.42970(14) 0.0663(10) Uani 1 1 d . . . . .
C9 C 0.4415(7) 0.5457(4) 0.41690(12) 0.0621(10) Uani 1 1 d . . . . .
C10 C 0.2579(7) 0.5105(4) 0.44806(12) 0.0593(9) Uani 1 1 d . . . . .
C11 C 0.2164(9) 0.2489(4) 0.41562(15) 0.0829(13) Uani 1 1 d . . . . .
H11 H 0.1431 0.1460 0.4143 0.100 Uiso 1 1 calc R U . . .
C12 C 0.3947(9) 0.2700(5) 0.38370(17) 0.0929(15) Uani 1 1 d . . . . .
H12 H 0.4361 0.1829 0.3615 0.111 Uiso 1 1 calc R U . . .
C13 C 0.5131(8) 0.4195(5) 0.38427(15) 0.0812(12) Uani 1 1 d . . . . .
H13 H 0.6359 0.4340 0.3635 0.097 Uiso 1 1 calc R U . . .
N1 N 0.2151(5) 0.6479(3) 0.47845(10) 0.0624(8) Uani 1 1 d . . . . .
H1A H 0.1122 0.6562 0.5010 0.075 Uiso 1 1 calc R U . . .
N2 N 0.1416(6) 0.3667(3) 0.44838(10) 0.0685(9) Uani 1 1 d . . . . .
S1 S 0.73088(18) 0.82678(14) 0.40677(4) 0.0882(4) 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 C6 1.374(4) . ?
C1 C2 1.380(4) . ?
C1 H1 0.9300 . ?
C2 C3 1.362(5) . ?
C2 H2 0.9300 . ?
C3 C4 1.364(6) . ?
C3 H3 0.9300 . ?
C4 C5 1.381(5) . ?
C4 H4 0.9300 . ?
C5 C6 1.377(5) . ?
C5 H5 0.9300 . ?
C6 S1 1.776(3) . ?
C7 N1 1.351(4) . ?
C7 C8 1.360(5) . ?
C7 H7 0.9300 . ?
C8 C9 1.436(5) . ?
C8 S1 1.739(4) . ?
C9 C13 1.378(5) . ?
C9 C10 1.409(5) . ?
C10 N2 1.341(4) . ?
C10 N1 1.364(4) . ?
C11 N2 1.338(4) . ?
C11 C12 1.377(6) . ?
C11 H11 0.9300 . ?
C12 C13 1.386(6) . ?
C12 H12 0.9300 . ?
C13 H13 0.9300 . ?
N1 H1A 0.8600 . ?

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
C6 C1 C2 119.6(4) . . ?
C6 C1 H1 120.2 . . ?
C2 C1 H1 120.2 . . ?
C3 C2 C1 121.3(3) . . ?
C3 C2 H2 119.4 . . ?
C1 C2 H2 119.4 . . ?
C2 C3 C4 119.4(4) . . ?
C2 C3 H3 120.3 . . ?
C4 C3 H3 120.3 . . ?
C3 C4 C5 120.1(4) . . ?
C3 C4 H4 120.0 . . ?
C5 C4 H4 120.0 . . ?
C6 C5 C4 120.6(4) . . ?
C6 C5 H5 119.7 . . ?
C4 C5 H5 119.7 . . ?
C1 C6 C5 119.0(3) . . ?
C1 C6 S1 124.1(3) . . ?
C5 C6 S1 116.9(3) . . ?
N1 C7 C8 111.5(3) . . ?
N1 C7 H7 124.2 . . ?
C8 C7 H7 124.2 . . ?
C7 C8 C9 106.1(3) . . ?
C7 C8 S1 126.3(3) . . ?
C9 C8 S1 127.5(3) . . ?
C13 C9 C10 117.3(3) . . ?
C13 C9 C8 137.0(4) . . ?
C10 C9 C8 105.7(3) . . ?
N2 C10 N1 124.7(4) . . ?
N2 C10 C9 126.5(3) . . ?
N1 C10 C9 108.8(3) . . ?
N2 C11 C12 124.3(4) . . ?
N2 C11 H11 117.8 . . ?
C12 C11 H11 117.8 . . ?
C11 C12 C13 120.8(4) . . ?
C11 C12 H12 119.6 . . ?
C13 C12 H12 119.6 . . ?
C9 C13 C12 117.3(4) . . ?
C9 C13 H13 121.4 . . ?
C12 C13 H13 121.4 . . ?
C7 N1 C10 107.9(3) . . ?
C7 N1 H1A 126.1 . . ?
C10 N1 H1A 126.1 . . ?
C11 N2 C10 113.9(4) . . ?
C8 S1 C6 104.04(16) . . ?

_refine_diff_density_max         0.228
_refine_diff_density_min         -0.261
_refine_diff_density_rms         0.048

