# Electronic Supplementary Material (ESI) for CrystEngComm.
# 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_yu71
_database_code_depnum_ccdc_archive 'CCDC 1877411'
_audit_update_record             
;
2018-11-06 deposited with the CCDC.
2018-11-30 downloaded from the CCDC.
;
_audit_creation_date             2018-04-16
_audit_creation_method           
;
Olex2 1.2-dev
(compiled 2018.04.03 svn.r3497 for OlexSys, GUI svn.r5486)
;
_shelx_SHELXL_version_number     2018/1
_chemical_name_common            ROY
_chemical_name_systematic        
5-methyl-2-[(2-nitrophenyl)-amino]-3-thiophenecarbonitrile
_chemical_formula_moiety         'C12 H9 N3 O2 S'
_chemical_formula_sum            'C12 H9 N3 O2 S'
_chemical_formula_weight         259.28
_chemical_melting_point          114.8
loop_
_atom_type_symbol
_atom_type_description
_atom_type_scat_dispersion_real
_atom_type_scat_dispersion_imag
_atom_type_scat_source
C C 0.0181 0.0091 '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 0.0311 0.0180 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
O O 0.0492 0.0322 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
S S 0.3331 0.5567 '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                   3.8517(2)
_cell_length_b                   18.458(2)
_cell_length_c                   16.3545(12)
_cell_angle_alpha                90
_cell_angle_beta                 92.481(3)
_cell_angle_gamma                90
_cell_volume                     1161.61(17)
_cell_formula_units_Z            4
_cell_measurement_reflns_used    9985
_cell_measurement_temperature    100(2)
_cell_measurement_theta_max      73.22
_cell_measurement_theta_min      3.61
_shelx_estimated_absorpt_T_max   0.886
_shelx_estimated_absorpt_T_min   0.638
_exptl_absorpt_coefficient_mu    2.473
_exptl_absorpt_correction_T_max  0.7537
_exptl_absorpt_correction_T_min  0.6743
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   
;
SADABS-2016/2 (Krause et al., 2015) was used for absorption correction.
;
_exptl_absorpt_special_details   ?
_exptl_crystal_colour            orange
_exptl_crystal_density_diffrn    1.483
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    'not measured'
_exptl_crystal_description       Needle
_exptl_crystal_F_000             536
_exptl_crystal_size_max          0.2
_exptl_crystal_size_mid          0.1
_exptl_crystal_size_min          0.05
_exptl_transmission_factor_max   ?
_exptl_transmission_factor_min   ?
_diffrn_reflns_av_R_equivalents  0.0280
_diffrn_reflns_av_unetI/netI     0.0128
_diffrn_reflns_Laue_measured_fraction_full 0.993
_diffrn_reflns_Laue_measured_fraction_max 0.981
_diffrn_reflns_limit_h_max       4
_diffrn_reflns_limit_h_min       -4
_diffrn_reflns_limit_k_max       18
_diffrn_reflns_limit_k_min       -21
_diffrn_reflns_limit_l_max       19
_diffrn_reflns_limit_l_min       -20
_diffrn_reflns_number            19811
_diffrn_reflns_point_group_measured_fraction_full 0.993
_diffrn_reflns_point_group_measured_fraction_max 0.981
_diffrn_reflns_theta_full        67.000
_diffrn_reflns_theta_max         73.208
_diffrn_reflns_theta_min         3.613
_diffrn_ambient_temperature      100.0
_diffrn_detector                 'charge-coupled device (CCD) area detector'
_diffrn_detector_area_resol_mean 7.9
_diffrn_detector_type            'Bruker APEX II'
_diffrn_measured_fraction_theta_full 0.993
_diffrn_measured_fraction_theta_max 0.981
_diffrn_measurement_device       'three-circle diffractometer'
_diffrn_measurement_device_type  'Bruker APEX II Quazar'
_diffrn_measurement_method       '0.5° ω and 0.5° φ scans'
_diffrn_radiation_collimation    'focusing mirrors'
_diffrn_radiation_detector       'Bruker APEX II'
_diffrn_radiation_monochromator  'mirror optics'
_diffrn_radiation_probe          x-ray
_diffrn_radiation_type           CuK\a
_diffrn_radiation_wavelength     1.54178
_diffrn_source                   'microfocus sealed X-ray tube'
_diffrn_source_type              'Incoatec I\ms'
_diffrn_standards_number         0
_reflns_Friedel_coverage         0.000
_reflns_Friedel_fraction_full    .
_reflns_Friedel_fraction_max     .
_reflns_number_gt                2146
_reflns_number_total             2288
_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       'APEX3 Ver. 2017.3-0 (Bruker-AXS, 2017)'
_computing_data_collection       'APEX3 Ver. 2017.3-0 (Bruker-AXS, 2017)'
_computing_data_reduction        'APEX3 Ver. 2017.3-0 (Bruker-AXS, 2017)'
_computing_molecular_graphics    'OLEX2 (Dolomanov et al., 2009)'
_computing_publication_material  'OLEX2 (Dolomanov et al., 2009)'
_computing_structure_refinement  'XL (Sheldrick, 2015b)'
_computing_structure_solution    'XT (Sheldrick, 2015a)'
_refine_diff_density_max         0.335
_refine_diff_density_min         -0.239
_refine_diff_density_rms         0.046
_refine_ls_extinction_coef       .
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.040
_refine_ls_hydrogen_treatment    mixed
_refine_ls_matrix_type           full
_refine_ls_number_parameters     168
_refine_ls_number_reflns         2288
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.0308
_refine_ls_R_factor_gt           0.0287
_refine_ls_restrained_S_all      1.040
_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)+(0.0422P)²+0.6264P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.0752
_refine_ls_wR_factor_ref         0.0765
_refine_special_details          ?
_olex2_refinement_description    
;
1. Fixed Uiso
 At 1.2 times of:
  All C(H) groups
 At 1.5 times of:
  All C(H,H,H) groups
2.a Aromatic/amide H refined with riding coordinates:
 C5(H5), C6(H6), C7(H7), C8(H8), C11(H11)
2.b Idealised Me refined as rotating group:
 C2(H2A,H2B,H2C)
;
_atom_sites_solution_hydrogens   mixed
_atom_sites_solution_primary     ?
_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 0.30513(8) 0.59827(2) 0.93012(2) 0.01556(11) Uani 1 1 d . . . . .
O1 O 0.0581(3) 0.68962(6) 0.63246(6) 0.0263(3) Uani 1 1 d . . . . .
O2 O -0.0092(3) 0.61864(6) 0.52821(6) 0.0259(2) Uani 1 1 d . . . . .
N1 N 0.3540(3) 0.64357(6) 0.76957(7) 0.0148(2) Uani 1 1 d . . . . .
H1 H 0.269(5) 0.6772(10) 0.7445(11) 0.022(4) Uiso 1 1 d . . . . .
N2 N 0.1046(3) 0.63056(6) 0.59839(7) 0.0168(2) Uani 1 1 d . . . . .
N3 N 0.8808(3) 0.80514(7) 0.78682(8) 0.0232(3) Uani 1 1 d . . . . .
C1 C 0.7514(3) 0.76674(7) 0.83158(8) 0.0167(3) Uani 1 1 d . . . . .
C2 C 0.4368(4) 0.63896(9) 1.09393(9) 0.0254(3) Uani 1 1 d . . . . .
H2A H 0.191095 0.637755 1.107134 0.038 Uiso 1 1 calc GR . . . .
H2B H 0.558256 0.675634 1.127739 0.038 Uiso 1 1 calc GR . . . .
H2C H 0.541570 0.591369 1.104861 0.038 Uiso 1 1 calc GR . . . .
C3 C 0.4117(3) 0.58184(7) 0.72501(8) 0.0128(3) Uani 1 1 d . . . . .
C4 C 0.2935(3) 0.57377(7) 0.64232(8) 0.0139(3) Uani 1 1 d . . . . .
C5 C 0.3495(3) 0.50983(7) 0.59902(8) 0.0165(3) Uani 1 1 d . . . . .
H5 H 0.263427 0.505539 0.543917 0.020 Uiso 1 1 calc R . . . .
C6 C 0.5276(4) 0.45325(8) 0.63539(8) 0.0184(3) Uani 1 1 d . . . . .
H6 H 0.566086 0.409889 0.605821 0.022 Uiso 1 1 calc R . . . .
C7 C 0.6518(3) 0.46025(7) 0.71663(8) 0.0172(3) Uani 1 1 d . . . . .
H7 H 0.776080 0.421342 0.742188 0.021 Uiso 1 1 calc R . . . .
C8 C 0.5962(3) 0.52285(7) 0.76010(8) 0.0149(3) Uani 1 1 d . . . . .
H8 H 0.684484 0.526302 0.815106 0.018 Uiso 1 1 calc R . . . .
C9 C 0.4387(3) 0.65414(7) 0.85213(8) 0.0135(3) Uani 1 1 d . . . . .
C10 C 0.5990(3) 0.71479(7) 0.88437(8) 0.0145(3) Uani 1 1 d . . . . .
C11 C 0.6110(3) 0.71670(8) 0.97182(8) 0.0174(3) Uani 1 1 d . . . . .
H11 H 0.709930 0.755466 1.003122 0.021 Uiso 1 1 calc R . . . .
C12 C 0.4665(3) 0.65752(8) 1.00531(8) 0.0175(3) 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
S1 C9 1.7355(13) . ?
S1 C12 1.7402(14) . ?
O1 N2 1.2407(15) . ?
O2 N2 1.2306(15) . ?
N1 H1 0.805(19) . ?
N1 C3 1.3757(17) . ?
N1 C9 1.3892(17) . ?
N2 C4 1.4488(17) . ?
N3 C1 1.1481(19) . ?
C1 C10 1.4328(19) . ?
C2 H2A 0.9800 . ?
C2 H2B 0.9800 . ?
C2 H2C 0.9800 . ?
C2 C12 1.4984(19) . ?
C3 C4 1.4160(18) . ?
C3 C8 1.4088(19) . ?
C4 C5 1.3980(19) . ?
C5 H5 0.9500 . ?
C5 C6 1.371(2) . ?
C6 H6 0.9500 . ?
C6 C7 1.398(2) . ?
C7 H7 0.9500 . ?
C7 C8 1.3782(19) . ?
C8 H8 0.9500 . ?
C9 C10 1.3726(19) . ?
C10 C11 1.4294(18) . ?
C11 H11 0.9500 . ?
C11 C12 1.352(2) . ?

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
C9 S1 C12 92.16(7) . . ?
C3 N1 H1 116.1(13) . . ?
C3 N1 C9 126.49(12) . . ?
C9 N1 H1 117.4(13) . . ?
O1 N2 C4 119.47(11) . . ?
O2 N2 O1 121.57(12) . . ?
O2 N2 C4 118.96(11) . . ?
N3 C1 C10 176.11(15) . . ?
H2A C2 H2B 109.5 . . ?
H2A C2 H2C 109.5 . . ?
H2B C2 H2C 109.5 . . ?
C12 C2 H2A 109.5 . . ?
C12 C2 H2B 109.5 . . ?
C12 C2 H2C 109.5 . . ?
N1 C3 C4 122.71(12) . . ?
N1 C3 C8 120.97(12) . . ?
C8 C3 C4 116.33(12) . . ?
C3 C4 N2 122.10(12) . . ?
C5 C4 N2 116.41(12) . . ?
C5 C4 C3 121.48(12) . . ?
C4 C5 H5 119.7 . . ?
C6 C5 C4 120.58(12) . . ?
C6 C5 H5 119.7 . . ?
C5 C6 H6 120.5 . . ?
C5 C6 C7 119.07(13) . . ?
C7 C6 H6 120.5 . . ?
C6 C7 H7 119.6 . . ?
C8 C7 C6 120.88(13) . . ?
C8 C7 H7 119.6 . . ?
C3 C8 H8 119.2 . . ?
C7 C8 C3 121.65(12) . . ?
C7 C8 H8 119.2 . . ?
N1 C9 S1 124.48(10) . . ?
C10 C9 S1 110.19(10) . . ?
C10 C9 N1 124.81(12) . . ?
C9 C10 C1 120.24(12) . . ?
C9 C10 C11 113.50(12) . . ?
C11 C10 C1 126.16(12) . . ?
C10 C11 H11 123.5 . . ?
C12 C11 C10 112.91(12) . . ?
C12 C11 H11 123.5 . . ?
C2 C12 S1 119.99(11) . . ?
C11 C12 S1 111.22(10) . . ?
C11 C12 C2 128.78(13) . . ?

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 C9 C10 C1 175.99(10) . . . . ?
S1 C9 C10 C11 -0.66(14) . . . . ?
O1 N2 C4 C3 3.58(19) . . . . ?
O1 N2 C4 C5 -177.25(12) . . . . ?
O2 N2 C4 C3 -175.69(12) . . . . ?
O2 N2 C4 C5 3.47(18) . . . . ?
N1 C3 C4 N2 0.48(19) . . . . ?
N1 C3 C4 C5 -178.64(12) . . . . ?
N1 C3 C8 C7 179.05(12) . . . . ?
N1 C9 C10 C1 -12.0(2) . . . . ?
N1 C9 C10 C11 171.34(12) . . . . ?
N2 C4 C5 C6 179.61(12) . . . . ?
C1 C10 C11 C12 -175.35(13) . . . . ?
C3 N1 C9 S1 -55.05(17) . . . . ?
C3 N1 C9 C10 134.07(14) . . . . ?
C3 C4 C5 C6 -1.2(2) . . . . ?
C4 C3 C8 C7 -1.29(19) . . . . ?
C4 C5 C6 C7 0.2(2) . . . . ?
C5 C6 C7 C8 0.2(2) . . . . ?
C6 C7 C8 C3 0.4(2) . . . . ?
C8 C3 C4 N2 -179.16(11) . . . . ?
C8 C3 C4 C5 1.71(18) . . . . ?
C9 S1 C12 C2 -178.97(12) . . . . ?
C9 S1 C12 C11 0.49(11) . . . . ?
C9 N1 C3 C4 175.18(12) . . . . ?
C9 N1 C3 C8 -5.2(2) . . . . ?
C9 C10 C11 C12 1.06(17) . . . . ?
C10 C11 C12 S1 -0.95(15) . . . . ?
C10 C11 C12 C2 178.46(13) . . . . ?
C12 S1 C9 N1 -171.93(11) . . . . ?
C12 S1 C9 C10 0.11(10) . . . . ?

_olex2_submission_special_instructions 'No special instructions were received'
_exptl_crystal_recrystallization_method 
'Re-crystallisation from solvent: methanol, acetonitrile'
