# Electronic Supplementary Material (ESI) for New Journal of Chemistry.
# This journal is © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 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_aa491
_database_code_depnum_ccdc_archive 'CCDC 1873649'
loop_
_audit_author_name
_audit_author_address
'Marcos Flores-Alamo'
;Facultad de Qu?mica, Universidad Nacional Aut?noma de M?xico
Mexico
;
_audit_update_record             
;
2018-10-16 deposited with the CCDC.	2019-03-15 downloaded from the CCDC.
;

_audit_creation_date             2018-06-22T12:12:17-00:00
_audit_creation_method           'WinGX routine CIF_UPDATE'
_audit_conform_dict_name         cif_core.dic
_audit_conform_dict_version      2.4.3
_audit_conform_dict_location     ftp://ftp.iucr.org/pub/cif_core.dic

#----------------------------------------------------------------------------#
#                   CHEMICAL INFORMATION                                     #
#----------------------------------------------------------------------------#

_chemical_formula_sum            'C12 H15 F4 P S'
_chemical_formula_moiety         'C12 H15 F4 P S'
_chemical_formula_weight         298.27
_chemical_absolute_configuration syn

#----------------------------------------------------------------------------#
#                   UNIT CELL INFORMATION                                    #
#----------------------------------------------------------------------------#

_symmetry_cell_setting           orthorhombic
_symmetry_space_group_name_H-M   'P c a 21'
_symmetry_space_group_name_Hall  'P 2c -2ac'
_symmetry_Int_Tables_number      29
loop_
_symmetry_equiv_pos_as_xyz
'x, y, z'
'-x, -y, z+1/2'
'x+1/2, -y, z'
'-x+1/2, y, z+1/2'

_cell_length_a                   12.1337(12)
_cell_length_b                   10.3273(10)
_cell_length_c                   10.8935(12)
_cell_angle_alpha                90
_cell_angle_beta                 90
_cell_angle_gamma                90
_cell_volume                     1365.0(2)
_cell_formula_units_Z            4
_cell_measurement_temperature    130(2)
_cell_measurement_reflns_used    1408
_cell_measurement_theta_min      6.553
_cell_measurement_theta_max      27.499

#----------------------------------------------------------------------------#
#                   CRYSTAL INFORMATION                                      #
#----------------------------------------------------------------------------#

_exptl_crystal_description       block
_exptl_crystal_colour            colourless
_exptl_crystal_size_max          0.18
_exptl_crystal_size_mid          0.14
_exptl_crystal_size_min          0.06
_exptl_crystal_density_diffrn    1.451
_exptl_crystal_F_000             616
loop_
_exptl_crystal_face_index_h
_exptl_crystal_face_index_k
_exptl_crystal_face_index_l
_exptl_crystal_face_perp_dist
17 2 0 0.0662
4 0 15 0.0758
-15 -7 -1 0.0601
12 10 1 0.0523
8 13 2 0.0432
0 2 -15 0.0738
3 -14 -1 0.0354
8 -13 -1 0.0477
3 -4 15 0.0724
15 -6 -1 0.0646
0 -2 15 0.0754
-17 2 -2 0.0643
-12 -10 -1 0.0508
12 10 -2 0.0567
-8 -13 0 0.0401
-2 -14 0 0.0294
3 14 1 0.0293
-3 14 1 0.0339
-15 7 -3 0.0613


#----------------------------------------------------------------------------#
#                   ABSORPTION CORRECTION                                    #
#----------------------------------------------------------------------------#

_exptl_absorpt_coefficient_mu    0.38
_exptl_absorpt_correction_type   analytical
_exptl_absorpt_process_details   
;
        CrysAlisPro, Agilent Technologies,
        Version 1.171.36.32 (release 02-08-2013 CrysAlis171 .NET)
        (compiled Aug  2 2013,16:46:58)
Analytical numeric absorption correction using a multifaceted crystal
                        model based on expressions derived by R.C. Clark & J.S.
        (Clark, R. C. & Reid, J. S. (1995). Acta Cryst. A51, 887-897)
;
_exptl_absorpt_correction_T_min  0.952
_exptl_absorpt_correction_T_max  0.98
_shelx_estimated_absorpt_T_min   0.935
_shelx_estimated_absorpt_T_max   0.978

#----------------------------------------------------------------------------#
#                   DATA COLLECTION                                          #
#----------------------------------------------------------------------------#

_diffrn_ambient_temperature      130(2)
_diffrn_radiation_wavelength     0.71073
_diffrn_radiation_type           MoK\a
_diffrn_radiation_monochromator  graphite
_diffrn_detector_area_resol_mean 10.4685
_diffrn_orient_matrix_ub_11      -0.0465792
_diffrn_orient_matrix_ub_12      0.0410077
_diffrn_orient_matrix_ub_13      0.0055516
_diffrn_orient_matrix_ub_21      -0.0352396
_diffrn_orient_matrix_ub_22      -0.0545554
_diffrn_orient_matrix_ub_23      -0.0051834
_diffrn_orient_matrix_ub_31      0.0012281
_diffrn_orient_matrix_ub_32      -0.0078885
_diffrn_orient_matrix_ub_33      0.0646889
_diffrn_measurement_device_type  'Xcalibur, Atlas, Gemini'
_diffrn_measurement_method       'ω scans'
_diffrn_reflns_av_R_equivalents  0.0563
_diffrn_reflns_av_unetI/netI     0.0934
_diffrn_reflns_number            5780
_diffrn_reflns_limit_h_min       -16
_diffrn_reflns_limit_h_max       16
_diffrn_reflns_limit_k_min       -14
_diffrn_reflns_limit_k_max       12
_diffrn_reflns_limit_l_min       -14
_diffrn_reflns_limit_l_max       13
_diffrn_reflns_theta_min         3.741
_diffrn_reflns_theta_max         29.605
_diffrn_reflns_theta_full        25.242
_diffrn_measured_fraction_theta_full 0.997
_diffrn_measured_fraction_theta_max 0.868
_diffrn_reflns_Laue_measured_fraction_full 0.997
_diffrn_reflns_Laue_measured_fraction_max 0.868
_diffrn_reflns_point_group_measured_fraction_full 0.916
_diffrn_reflns_point_group_measured_fraction_max 0.755
_reflns_Friedel_fraction_full    0.825
_reflns_Friedel_fraction_max     0.63
_reflns_Friedel_coverage         0.654
_reflns_number_total             2905
_reflns_number_gt                2231
_reflns_threshold_expression     'I > 2σ(I)'

#----------------------------------------------------------------------------#
#                   COMPUTER PROGRAMS USED                                   #
#----------------------------------------------------------------------------#

_computing_data_collection       
;
        CrysAlisPro, Agilent Technologies,
        Version 1.171.36.32 (release 02-08-2013 CrysAlis171 .NET)
        (compiled Aug  2 2013,16:46:58)
;
_computing_cell_refinement       
;
        CrysAlisPro, Agilent Technologies,
        Version 1.171.36.32 (release 02-08-2013 CrysAlis171 .NET)
        (compiled Aug  2 2013,16:46:58)
;
_computing_data_reduction        
;
        CrysAlisPro, Agilent Technologies,
        Version 1.171.36.32 (release 02-08-2013 CrysAlis171 .NET)
        (compiled Aug  2 2013,16:46:58)
;
_computing_structure_solution    
;
      'SHELXS-2014 (Sheldrick, 2015)'
      Sheldrick, G. M. (2015). Acta Cryst. A71, 3--8.
;
_computing_structure_refinement  
;
      'SHELXS-2014 (Sheldrick, 2015)'
      Sheldrick, G. M. (2015). Acta Cryst. C71, 3--8.
;
_computing_molecular_graphics    
;
          'Ortep-3 for Windows (Farrugia, 1997)'
      L. J. Farrugia, J. Appl. Crystallogr., 1997, 30, 565.
;
_computing_publication_material  
;	
        'WinGX publication routines (Farrugia, 1999)'				 
	L. J. Farrugia, J. Appl. Crystallogr., 1999, 32, 837-838.
;


#----------------------------------------------------------------------------#
#                   STRUCTURE SOLUTION                                       #
#----------------------------------------------------------------------------#

_atom_sites_solution_hydrogens   geom

#----------------------------------------------------------------------------#
#                   REFINEMENT INFORMATION                                   #
#----------------------------------------------------------------------------#

_refine_ls_structure_factor_coef Fsqd
_refine_ls_matrix_type           full
_refine_ls_weighting_scheme      calc
_refine_ls_weighting_details     
'w=1/[σ²(Fo²)+(0.0394P)²] where P=(Fo²+2Fc²)/3'
_refine_ls_hydrogen_treatment    constr
_refine_ls_extinction_method     none
_refine_ls_number_reflns         2905
_refine_ls_number_parameters     166
_refine_ls_number_restraints     1
_refine_ls_R_factor_all          0.0729
_refine_ls_R_factor_gt           0.0483
_refine_ls_wR_factor_ref         0.1046
_refine_ls_wR_factor_gt          0.0921
_refine_ls_goodness_of_fit_ref   1.005
_refine_ls_restrained_S_all      1.005
_refine_ls_shift/su_max          0
_refine_ls_shift/su_mean         0
_refine_ls_abs_structure_details 
;
 Flack x determined using 722 quotients [(I+)-(I-)]/[(I+)+(I-)]
 (Parsons, Flack and Wagner, Acta Cryst. B69 (2013) 249-259).
;
_refine_ls_abs_structure_Flack   -0.03(11)
_refine_diff_density_max         0.486
_refine_diff_density_min         -0.407
_refine_diff_density_rms         0.084

#----------------------------------------------------------------------------#
#                   CONSTRAINTS AND RESTRAINTS                               #
#----------------------------------------------------------------------------#


#----------------------------------------------------------------------------#
#                   ATOMIC TYPES, COORDINATES AND THERMAL PARAMETERS         #
#----------------------------------------------------------------------------#

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 0 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
F F 0.0171 0.0103 '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'

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 0.4804(4) 0.5969(4) 0.5026(5) 0.0211(10) Uani 1 1 d . . . . .
C2 C 0.5499(4) 0.4982(4) 0.4606(4) 0.0204(10) Uani 1 1 d . . . . .
C3 C 0.5268(3) 0.3700(4) 0.4781(5) 0.0194(10) Uani 1 1 d . . . . .
C4 C 0.4323(4) 0.3242(4) 0.5391(4) 0.0198(11) Uani 1 1 d . . . . .
C5 C 0.3633(4) 0.4240(5) 0.5799(5) 0.0219(10) Uani 1 1 d . . . . .
C6 C 0.3859(4) 0.5516(4) 0.5637(5) 0.0223(10) Uani 1 1 d . . . . .
C7 C 0.5020(4) 0.8430(5) 0.6362(4) 0.0200(10) Uani 1 1 d . . . . .
H7A H 0.506544 0.938085 0.625724 0.024 Uiso 1 1 calc R U . . .
H7B H 0.431944 0.82364 0.679071 0.024 Uiso 1 1 calc R U . . .
C8 C 0.5974(4) 0.7988(5) 0.7166(5) 0.0267(12) Uani 1 1 d . . . . .
H8A H 0.594571 0.704537 0.726389 0.04 Uiso 1 1 calc R U . . .
H8B H 0.591909 0.840196 0.797332 0.04 Uiso 1 1 calc R U . . .
H8C H 0.667315 0.823239 0.67788 0.04 Uiso 1 1 calc R U . . .
C9 C 0.3807(4) 0.8344(5) 0.4074(5) 0.0238(11) Uani 1 1 d . . . . .
H9A H 0.314866 0.823486 0.460043 0.029 Uiso 1 1 calc R U . . .
H9B H 0.392328 0.928515 0.39567 0.029 Uiso 1 1 calc R U . . .
C10 C 0.3575(4) 0.7735(6) 0.2834(5) 0.0363(13) Uani 1 1 d . . . . .
H10A H 0.419444 0.790277 0.227915 0.054 Uiso 1 1 calc R U . . .
H10B H 0.290096 0.811052 0.248805 0.054 Uiso 1 1 calc R U . . .
H10C H 0.347867 0.679888 0.293287 0.054 Uiso 1 1 calc R U . . .
C11 C 0.6230(4) 0.8061(5) 0.4036(5) 0.0213(11) Uani 1 1 d . . . . .
H11A H 0.686827 0.766839 0.446179 0.026 Uiso 1 1 calc R U . . .
H11B H 0.618631 0.768016 0.320304 0.026 Uiso 1 1 calc R U . . .
C12 C 0.6404(4) 0.9522(5) 0.3931(5) 0.0291(11) Uani 1 1 d . . . . .
H12A H 0.576359 0.99159 0.352876 0.044 Uiso 1 1 calc R U . . .
H12B H 0.706681 0.969487 0.34441 0.044 Uiso 1 1 calc R U . . .
H12C H 0.649237 0.989369 0.475301 0.044 Uiso 1 1 calc R U . . .
F1 F 0.6434(2) 0.5300(3) 0.3997(3) 0.0309(7) Uani 1 1 d . . . . .
F2 F 0.6003(2) 0.2831(3) 0.4327(3) 0.0321(7) Uani 1 1 d . . . . .
F3 F 0.2690(2) 0.3938(3) 0.6393(3) 0.0332(7) Uani 1 1 d . . . . .
F4 F 0.3127(2) 0.6399(3) 0.6069(3) 0.0358(8) Uani 1 1 d . . . . .
P1 P 0.49869(10) 0.76848(10) 0.48679(12) 0.0175(2) Uani 1 1 d . . . . .
S1 S 0.40176(10) 0.16351(11) 0.56027(12) 0.0242(3) Uani 1 1 d . . . . .



#----------------------------------------------------------------------------#
#                   MOLECULAR GEOMETRY                                       #
#----------------------------------------------------------------------------#

_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 C2 1.400(6) . ?
C1 C6 1.405(6) . ?
C1 P1 1.795(5) . ?
C2 F1 1.355(5) . ?
C2 C3 1.366(6) . ?
C3 F2 1.359(5) . ?
C3 C4 1.408(6) . ?
C4 C5 1.401(7) . ?
C4 S1 1.716(5) . ?
C5 F3 1.351(5) . ?
C5 C6 1.358(6) . ?
C6 F4 1.357(5) . ?
C7 C8 1.522(7) . ?
C7 P1 1.801(5) . ?
C7 H7A 0.99 . ?
C7 H7B 0.99 . ?
C8 H8A 0.98 . ?
C8 H8B 0.98 . ?
C8 H8C 0.98 . ?
C9 C10 1.516(7) . ?
C9 P1 1.806(4) . ?
C9 H9A 0.99 . ?
C9 H9B 0.99 . ?
C10 H10A 0.98 . ?
C10 H10B 0.98 . ?
C10 H10C 0.98 . ?
C11 C12 1.528(7) . ?
C11 P1 1.802(5) . ?
C11 H11A 0.99 . ?
C11 H11B 0.99 . ?
C12 H12A 0.98 . ?
C12 H12B 0.98 . ?
C12 H12C 0.98 . ?

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 C1 C6 113.9(4) . . ?
C2 C1 P1 127.8(4) . . ?
C6 C1 P1 118.3(3) . . ?
F1 C2 C3 118.3(4) . . ?
F1 C2 C1 119.2(4) . . ?
C3 C2 C1 122.4(4) . . ?
F2 C3 C2 117.1(4) . . ?
F2 C3 C4 119.0(4) . . ?
C2 C3 C4 123.9(4) . . ?
C5 C4 C3 112.9(4) . . ?
C5 C4 S1 122.7(4) . . ?
C3 C4 S1 124.3(3) . . ?
F3 C5 C6 117.3(4) . . ?
F3 C5 C4 119.2(4) . . ?
C6 C5 C4 123.5(4) . . ?
F4 C6 C5 118.3(4) . . ?
F4 C6 C1 118.4(4) . . ?
C5 C6 C1 123.3(4) . . ?
C8 C7 P1 114.1(3) . . ?
C8 C7 H7A 108.7 . . ?
P1 C7 H7A 108.7 . . ?
C8 C7 H7B 108.7 . . ?
P1 C7 H7B 108.7 . . ?
H7A C7 H7B 107.6 . . ?
C7 C8 H8A 109.5 . . ?
C7 C8 H8B 109.5 . . ?
H8A C8 H8B 109.5 . . ?
C7 C8 H8C 109.5 . . ?
H8A C8 H8C 109.5 . . ?
H8B C8 H8C 109.5 . . ?
C10 C9 P1 114.7(3) . . ?
C10 C9 H9A 108.6 . . ?
P1 C9 H9A 108.6 . . ?
C10 C9 H9B 108.6 . . ?
P1 C9 H9B 108.6 . . ?
H9A C9 H9B 107.6 . . ?
C9 C10 H10A 109.5 . . ?
C9 C10 H10B 109.5 . . ?
H10A C10 H10B 109.5 . . ?
C9 C10 H10C 109.5 . . ?
H10A C10 H10C 109.5 . . ?
H10B C10 H10C 109.5 . . ?
C12 C11 P1 111.5(4) . . ?
C12 C11 H11A 109.3 . . ?
P1 C11 H11A 109.3 . . ?
C12 C11 H11B 109.3 . . ?
P1 C11 H11B 109.3 . . ?
H11A C11 H11B 108 . . ?
C11 C12 H12A 109.5 . . ?
C11 C12 H12B 109.5 . . ?
H12A C12 H12B 109.5 . . ?
C11 C12 H12C 109.5 . . ?
H12A C12 H12C 109.5 . . ?
H12B C12 H12C 109.5 . . ?
C1 P1 C11 111.4(2) . . ?
C1 P1 C7 109.8(2) . . ?
C11 P1 C7 110.1(2) . . ?
C1 P1 C9 108.7(2) . . ?
C11 P1 C9 109.9(2) . . ?
C7 P1 C9 106.8(2) . . ?

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
C6 C1 C2 F1 179.6(4) . . . . ?
P1 C1 C2 F1 -0.2(7) . . . . ?
C6 C1 C2 C3 0.0(7) . . . . ?
P1 C1 C2 C3 -179.8(4) . . . . ?
F1 C2 C3 F2 0.1(7) . . . . ?
C1 C2 C3 F2 179.7(4) . . . . ?
F1 C2 C3 C4 -179.6(4) . . . . ?
C1 C2 C3 C4 0.0(8) . . . . ?
F2 C3 C4 C5 -179.4(4) . . . . ?
C2 C3 C4 C5 0.3(7) . . . . ?
F2 C3 C4 S1 -0.3(7) . . . . ?
C2 C3 C4 S1 179.3(4) . . . . ?
C3 C4 C5 F3 179.5(4) . . . . ?
S1 C4 C5 F3 0.5(6) . . . . ?
C3 C4 C5 C6 -0.7(7) . . . . ?
S1 C4 C5 C6 -179.8(4) . . . . ?
F3 C5 C6 F4 -0.4(7) . . . . ?
C4 C5 C6 F4 179.8(5) . . . . ?
F3 C5 C6 C1 -179.4(5) . . . . ?
C4 C5 C6 C1 0.8(9) . . . . ?
C2 C1 C6 F4 -179.4(4) . . . . ?
P1 C1 C6 F4 0.4(7) . . . . ?
C2 C1 C6 C5 -0.4(8) . . . . ?
P1 C1 C6 C5 179.4(4) . . . . ?
C2 C1 P1 C11 1.0(5) . . . . ?
C6 C1 P1 C11 -178.9(4) . . . . ?
C2 C1 P1 C7 -121.3(5) . . . . ?
C6 C1 P1 C7 58.9(5) . . . . ?
C2 C1 P1 C9 122.2(5) . . . . ?
C6 C1 P1 C9 -57.6(5) . . . . ?
C12 C11 P1 C1 -178.4(3) . . . . ?
C12 C11 P1 C7 -56.4(4) . . . . ?
C12 C11 P1 C9 61.0(4) . . . . ?
C8 C7 P1 C1 62.6(4) . . . . ?
C8 C7 P1 C11 -60.4(4) . . . . ?
C8 C7 P1 C9 -179.8(4) . . . . ?
C10 C9 P1 C1 -56.0(4) . . . . ?
C10 C9 P1 C11 66.1(4) . . . . ?
C10 C9 P1 C7 -174.4(4) . . . . ?
