# Electronic Supplementary Material (ESI) for ChemComm.
# This journal is © The Royal Society of Chemistry 2021

####################################################################### 
# 
# 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_mo_d8v20731_0m
_database_code_depnum_ccdc_archive 'CCDC 2060841'
loop_
_audit_author_name
_audit_author_address
Tang
;Shanghai Institute of Organic Chemistry, CAS
China
;
_audit_update_record             
;
2021-02-03 deposited with the CCDC.	2021-02-24 downloaded from the CCDC.
;

_audit_creation_method           SHELXL-2013
_chemical_name_systematic        
; 
 ? 
;
_chemical_name_common            ?
_chemical_melting_point          ?
_chemical_formula_moiety         ?
_chemical_formula_sum            'C10 H13 P S'
_chemical_formula_weight         196.23

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'
P P 0.1023 0.0942 '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'

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

_cell_length_a                   9.1461(3)
_cell_length_b                   9.6810(3)
_cell_length_c                   11.8702(3)
_cell_angle_alpha                90
_cell_angle_beta                 90
_cell_angle_gamma                90
_cell_volume                     1051.03(5)
_cell_formula_units_Z            4
_cell_measurement_temperature    293(2)
_cell_measurement_reflns_used    7299
_cell_measurement_theta_min      5.431
_cell_measurement_theta_max      54.919

_exptl_crystal_description       prismatic
_exptl_crystal_colour            colorless
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    ?
_exptl_crystal_density_diffrn    1.240
_exptl_crystal_F_000             416
_exptl_transmission_factor_min   ?
_exptl_transmission_factor_max   ?
_exptl_crystal_size_max          0.170
_exptl_crystal_size_mid          0.140
_exptl_crystal_size_min          0.120
_exptl_absorpt_coefficient_mu    0.405
_shelx_estimated_absorpt_T_min   0.934
_shelx_estimated_absorpt_T_max   0.953
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_correction_T_min  0.6532
_exptl_absorpt_correction_T_max  0.7456
_exptl_absorpt_process_details   sadabs

_exptl_special_details           
; 
 ? 
;

_diffrn_ambient_temperature      293(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            9523
_diffrn_reflns_av_unetI/netI     0.0225
_diffrn_reflns_av_R_equivalents  0.0318
_diffrn_reflns_limit_h_min       -11
_diffrn_reflns_limit_h_max       11
_diffrn_reflns_limit_k_min       -11
_diffrn_reflns_limit_k_max       11
_diffrn_reflns_limit_l_min       -14
_diffrn_reflns_limit_l_max       14
_diffrn_reflns_theta_min         2.715
_diffrn_reflns_theta_max         25.995
_diffrn_reflns_theta_full        25.242
_diffrn_measured_fraction_theta_max 0.992
_diffrn_measured_fraction_theta_full 0.991
_diffrn_reflns_Laue_measured_fraction_max 0.992
_diffrn_reflns_Laue_measured_fraction_full 0.991
_diffrn_reflns_point_group_measured_fraction_max 0.993
_diffrn_reflns_point_group_measured_fraction_full 0.992
_reflns_number_total             2054
_reflns_number_gt                1998
_reflns_threshold_expression     'I > 2σ(I)'
_reflns_Friedel_coverage         0.710
_reflns_Friedel_fraction_max     0.994
_reflns_Friedel_fraction_full    0.994

_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       'Bruker APEX2'
_computing_cell_refinement       'Bruker SAINT'
_computing_data_reduction        'Bruker SAINT'
_computing_structure_solution    'SHELXS-97 (Sheldrick 2008)'
_computing_structure_refinement  'SHELXL-2013 (Sheldrick, 2013)'
_computing_molecular_graphics    'Bruker SHELXTL'
_computing_publication_material  'Bruker SHELXTL'

_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)+(0.0437P)²+0.0703P] 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     SHELXL
_refine_ls_extinction_coef       0.188(15)
_refine_ls_extinction_expression Fc^*^=kFc[1+0.001xFc²λ³/sin(2θ)]^-1/4^
_refine_ls_abs_structure_details 
; 
 Flack x determined using 809 quotients [(I+)-(I-)]/[(I+)+(I-)] 
 (Parsons and Flack (2004), Acta Cryst. A60, s61). 
;
_refine_ls_abs_structure_Flack   0.00(3)
_chemical_absolute_configuration ad
_refine_ls_number_reflns         2054
_refine_ls_number_parameters     111
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.0247
_refine_ls_R_factor_gt           0.0238
_refine_ls_wR_factor_ref         0.0668
_refine_ls_wR_factor_gt          0.0656
_refine_ls_goodness_of_fit_ref   1.054
_refine_ls_restrained_S_all      1.054
_refine_ls_shift/su_max          0.001
_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
S1 S 0.60278(7) 0.37474(6) 0.57619(5) 0.0461(2) Uani 1 1 d . . . . .
P1 P 0.64867(5) 0.48833(5) 0.44472(4) 0.03441(18) Uani 1 1 d . . . . .
C1 C 0.6779(3) 0.6668(2) 0.4773(2) 0.0501(6) Uani 1 1 d . . . . .
H1 H 0.6925 0.7273 0.4121 0.060 Uiso 1 1 calc R U . . .
C2 C 0.7611(3) 0.7064(3) 0.5809(2) 0.0606(7) Uani 1 1 d . . . . .
H2A H 0.7949 0.6326 0.6297 0.073 Uiso 1 1 calc R U . . .
H2B H 0.8261 0.7853 0.5761 0.073 Uiso 1 1 calc R U . . .
C3 C 0.6033(3) 0.7323(3) 0.5758(3) 0.0714(8) Uani 1 1 d . . . . .
H3A H 0.5712 0.8273 0.5679 0.086 Uiso 1 1 calc R U . . .
H3B H 0.5401 0.6746 0.6215 0.086 Uiso 1 1 calc R U . . .
C4 C 0.8134(3) 0.4350(3) 0.3736(2) 0.0533(6) Uani 1 1 d . . . . .
H4A H 0.8941 0.4386 0.4252 0.080 Uiso 1 1 calc R U . . .
H4B H 0.8320 0.4958 0.3113 0.080 Uiso 1 1 calc R U . . .
H4C H 0.8018 0.3423 0.3464 0.080 Uiso 1 1 calc R U . . .
C5 C 0.5049(2) 0.4904(2) 0.33965(16) 0.0336(4) Uani 1 1 d . . . . .
C6 C 0.3746(2) 0.4212(2) 0.35776(19) 0.0404(5) Uani 1 1 d . . . . .
H6 H 0.3624 0.3681 0.4223 0.048 Uiso 1 1 calc R U . . .
C7 C 0.2618(3) 0.4311(3) 0.2796(2) 0.0515(6) Uani 1 1 d . . . . .
H7 H 0.1742 0.3849 0.2923 0.062 Uiso 1 1 calc R U . . .
C8 C 0.2797(3) 0.5093(3) 0.1831(2) 0.0538(6) Uani 1 1 d . . . . .
H8 H 0.2039 0.5163 0.1311 0.065 Uiso 1 1 calc R U . . .
C9 C 0.4104(3) 0.5770(3) 0.1641(2) 0.0516(6) Uani 1 1 d . . . . .
H9 H 0.4231 0.6285 0.0987 0.062 Uiso 1 1 calc R U . . .
C10 C 0.5222(3) 0.5686(2) 0.2416(2) 0.0445(5) Uani 1 1 d . . . . .
H10 H 0.6095 0.6151 0.2287 0.053 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
S1 P1 1.9547(7) . ?
P1 C1 1.791(2) . ?
P1 C4 1.802(2) . ?
P1 C5 1.812(2) . ?
C1 C2 1.496(3) . ?
C1 C3 1.495(4) . ?
C1 H1 0.9800 . ?
C2 C3 1.466(4) . ?
C2 H2A 0.9700 . ?
C2 H2B 0.9700 . ?
C3 H3A 0.9700 . ?
C3 H3B 0.9700 . ?
C4 H4A 0.9600 . ?
C4 H4B 0.9600 . ?
C4 H4C 0.9600 . ?
C5 C6 1.384(3) . ?
C5 C10 1.397(3) . ?
C6 C7 1.391(3) . ?
C6 H6 0.9300 . ?
C7 C8 1.383(4) . ?
C7 H7 0.9300 . ?
C8 C9 1.382(4) . ?
C8 H8 0.9300 . ?
C9 C10 1.378(4) . ?
C9 H9 0.9300 . ?
C10 H10 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
C1 P1 C4 104.65(13) . . ?
C1 P1 C5 104.25(10) . . ?
C4 P1 C5 106.69(10) . . ?
C1 P1 S1 113.73(8) . . ?
C4 P1 S1 113.10(9) . . ?
C5 P1 S1 113.56(7) . . ?
C2 C1 C3 58.71(18) . . ?
C2 C1 P1 120.02(19) . . ?
C3 C1 P1 120.7(2) . . ?
C2 C1 H1 115.3 . . ?
C3 C1 H1 115.3 . . ?
P1 C1 H1 115.3 . . ?
C3 C2 C1 60.60(19) . . ?
C3 C2 H2A 117.7 . . ?
C1 C2 H2A 117.7 . . ?
C3 C2 H2B 117.7 . . ?
C1 C2 H2B 117.7 . . ?
H2A C2 H2B 114.8 . . ?
C2 C3 C1 60.70(18) . . ?
C2 C3 H3A 117.7 . . ?
C1 C3 H3A 117.7 . . ?
C2 C3 H3B 117.7 . . ?
C1 C3 H3B 117.7 . . ?
H3A C3 H3B 114.8 . . ?
P1 C4 H4A 109.5 . . ?
P1 C4 H4B 109.5 . . ?
H4A C4 H4B 109.5 . . ?
P1 C4 H4C 109.5 . . ?
H4A C4 H4C 109.5 . . ?
H4B C4 H4C 109.5 . . ?
C6 C5 C10 119.28(19) . . ?
C6 C5 P1 120.85(15) . . ?
C10 C5 P1 119.79(16) . . ?
C5 C6 C7 120.1(2) . . ?
C5 C6 H6 119.9 . . ?
C7 C6 H6 119.9 . . ?
C8 C7 C6 120.2(2) . . ?
C8 C7 H7 119.9 . . ?
C6 C7 H7 119.9 . . ?
C7 C8 C9 119.8(2) . . ?
C7 C8 H8 120.1 . . ?
C9 C8 H8 120.1 . . ?
C10 C9 C8 120.3(2) . . ?
C10 C9 H9 119.8 . . ?
C8 C9 H9 119.8 . . ?
C9 C10 C5 120.3(2) . . ?
C9 C10 H10 119.9 . . ?
C5 C10 H10 119.9 . . ?

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
C4 P1 C1 C2 -83.6(2) . . . . ?
C5 P1 C1 C2 164.5(2) . . . . ?
S1 P1 C1 C2 40.3(2) . . . . ?
C4 P1 C1 C3 -152.8(2) . . . . ?
C5 P1 C1 C3 95.3(2) . . . . ?
S1 P1 C1 C3 -28.9(2) . . . . ?
P1 C1 C2 C3 -109.8(3) . . . . ?
P1 C1 C3 C2 108.7(2) . . . . ?
C1 P1 C5 C6 -121.56(18) . . . . ?
C4 P1 C5 C6 128.05(18) . . . . ?
S1 P1 C5 C6 2.76(19) . . . . ?
C1 P1 C5 C10 55.03(19) . . . . ?
C4 P1 C5 C10 -55.4(2) . . . . ?
S1 P1 C5 C10 179.34(15) . . . . ?
C10 C5 C6 C7 -0.7(3) . . . . ?
P1 C5 C6 C7 175.87(18) . . . . ?
C5 C6 C7 C8 0.4(4) . . . . ?
C6 C7 C8 C9 0.4(4) . . . . ?
C7 C8 C9 C10 -1.0(4) . . . . ?
C8 C9 C10 C5 0.6(4) . . . . ?
C6 C5 C10 C9 0.2(3) . . . . ?
P1 C5 C10 C9 -176.42(18) . . . . ?

_refine_diff_density_max         0.253
_refine_diff_density_min         -0.170
_refine_diff_density_rms         0.036

_shelxl_version_number           2013-4

