# Electronic Supplementary Material (ESI) for Organic & Biomolecular Chemistry.
# This journal is © The Royal Society of Chemistry 2020

####################################################################### 
# 
# 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_lq-0903-2
_database_code_depnum_ccdc_archive 'CCDC 1973697'
loop_
_audit_author_name
_audit_author_address
'wqq upper'
;Southwest Minzu University
China
;
_audit_update_record             
;
2019-12-23 deposited with the CCDC.	2020-02-03 downloaded from the CCDC.
;
_audit_creation_date             2018-09-04
_audit_creation_method           
;
Olex2 1.2
(compiled 2018.05.29 svn.r3508 for OlexSys, GUI svn.r5506)
;
_shelx_SHELXL_version_number     2014/7
_chemical_name_common            ?
_chemical_name_systematic        ?
_chemical_formula_moiety         'C16 H16 Cl F3 O4'
_chemical_formula_sum            'C16 H16 Cl F3 O4'
_chemical_formula_weight         364.74
_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 0.0181 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'
Cl Cl 0.3639 0.7018 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
F F 0.0727 0.0534 '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'

_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      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_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                   5.6493(2)
_cell_length_b                   14.4444(7)
_cell_length_c                   21.6781(9)
_cell_angle_alpha                90
_cell_angle_beta                 90
_cell_angle_gamma                90
_cell_volume                     1768.95(14)
_cell_formula_units_Z            4
_cell_measurement_reflns_used    3675
_cell_measurement_temperature    297.60(10)
_cell_measurement_theta_max      71.8670
_cell_measurement_theta_min      6.8480
_shelx_estimated_absorpt_T_max   ?
_shelx_estimated_absorpt_T_min   ?
_exptl_absorpt_coefficient_mu    2.351
_exptl_absorpt_correction_T_max  1.00000
_exptl_absorpt_correction_T_min  0.41056
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   
;
CrysAlisPro, Agilent Technologies,
Version 1.171.37.35 (release 13-08-2014 CrysAlis171 .NET)
(compiled Aug 13 2014,18:06:01)
Empirical absorption correction using spherical harmonics,
 implemented in SCALE3 ABSPACK scaling algorithm.
;
_exptl_absorpt_special_details   ?
_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    1.370
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    ?
_exptl_crystal_description       block
_exptl_crystal_F_000             752
_exptl_crystal_size_max          0.7
_exptl_crystal_size_mid          0.5
_exptl_crystal_size_min          0.4
_exptl_transmission_factor_max   ?
_exptl_transmission_factor_min   ?
_diffrn_reflns_av_R_equivalents  0.0337
_diffrn_reflns_av_unetI/netI     0.0281
_diffrn_reflns_Laue_measured_fraction_full 0.998
_diffrn_reflns_Laue_measured_fraction_max 0.990
_diffrn_reflns_limit_h_max       6
_diffrn_reflns_limit_h_min       -4
_diffrn_reflns_limit_k_max       17
_diffrn_reflns_limit_k_min       -16
_diffrn_reflns_limit_l_max       26
_diffrn_reflns_limit_l_min       -25
_diffrn_reflns_number            9792
_diffrn_reflns_point_group_measured_fraction_full 0.998
_diffrn_reflns_point_group_measured_fraction_max 0.981
_diffrn_reflns_theta_full        67.684
_diffrn_reflns_theta_max         72.442
_diffrn_reflns_theta_min         5.102
_diffrn_ambient_environment      air
_diffrn_ambient_temperature      297.60(10)
_diffrn_detector                 'CCD plate'
_diffrn_detector_area_resol_mean 15.9595
_diffrn_detector_type            EosS2
_diffrn_measured_fraction_theta_full 0.998
_diffrn_measured_fraction_theta_max 0.990
_diffrn_measurement_details      
;
#__ type_ start__ end____ width___ exp.time_
  1 omega   19.00  103.00   1.0000    1.0000
omega____ theta____ kappa____ phi______ frames
    -       36.0421   57.0000    0.0000 84

#__ type_ start__ end____ width___ exp.time_
  2 omega    9.00  104.00   1.0000    1.0000
omega____ theta____ kappa____ phi______ frames
    -       36.0421   77.0000 -180.0000 95

#__ type_ start__ end____ width___ exp.time_
  3 omega   19.00  103.00   1.0000    1.0000
omega____ theta____ kappa____ phi______ frames
    -       36.0421   57.0000 -150.0000 84

#__ type_ start__ end____ width___ exp.time_
  4 omega  -31.00   53.00   1.0000    1.0000
omega____ theta____ kappa____ phi______ frames
    -       36.0421  -57.0000  -30.0000 84

#__ type_ start__ end____ width___ exp.time_
  5 omega  -32.00   63.00   1.0000    1.0000
omega____ theta____ kappa____ phi______ frames
    -       36.0421  -77.0000  150.0000 95

#__ type_ start__ end____ width___ exp.time_
  6 omega   40.00   98.00   1.0000    1.9500
omega____ theta____ kappa____ phi______ frames
    -      108.0000  -45.0000 -120.0000 58

#__ type_ start__ end____ width___ exp.time_
  7 omega   38.00   91.00   1.0000    1.9500
omega____ theta____ kappa____ phi______ frames
    -      108.0000  -30.0000   60.0000 53

#__ type_ start__ end____ width___ exp.time_
  8 omega   38.00   91.00   1.0000    1.9500
omega____ theta____ kappa____ phi______ frames
    -      108.0000  -30.0000  -90.0000 53

#__ type_ start__ end____ width___ exp.time_
  9 omega   37.00  146.00   1.0000    1.9500
omega____ theta____ kappa____ phi______ frames
    -      108.0000  -15.0000 -120.0000 109

#__ type_ start__ end____ width___ exp.time_
 10 omega   38.00   91.00   1.0000    1.9500
omega____ theta____ kappa____ phi______ frames
    -      108.0000  -30.0000  150.0000 53

#__ type_ start__ end____ width___ exp.time_
 11 omega   39.00  109.00   1.0000    1.9500
omega____ theta____ kappa____ phi______ frames
    -      108.0000  -94.0000 -120.0000 70

#__ type_ start__ end____ width___ exp.time_
 12 omega   39.00  109.00   1.0000    1.9500
omega____ theta____ kappa____ phi______ frames
    -      108.0000  -94.0000  150.0000 70

#__ type_ start__ end____ width___ exp.time_
 13 omega   40.00   98.00   1.0000    1.9500
omega____ theta____ kappa____ phi______ frames
    -      108.0000  -45.0000  120.0000 58

#__ type_ start__ end____ width___ exp.time_
 14 omega   38.00   91.00   1.0000    1.9500
omega____ theta____ kappa____ phi______ frames
    -      108.0000  -30.0000   30.0000 53

#__ type_ start__ end____ width___ exp.time_
 15 omega   19.00  103.00   1.0000    1.0000
omega____ theta____ kappa____ phi______ frames
    -       36.0421   57.0000  -90.0000 84

#__ type_ start__ end____ width___ exp.time_
 16 omega  -31.00   22.00   1.0000    1.0000
omega____ theta____ kappa____ phi______ frames
    -       36.0421  -57.0000 -150.0000 53

#__ type_ start__ end____ width___ exp.time_
 17 omega   17.00  105.00   1.0000    1.0000
omega____ theta____ kappa____ phi______ frames
    -       36.0421   38.0000  120.0000 88
;
_diffrn_measurement_device       'four-circle diffractometer'
_diffrn_measurement_device_type  'New Gemini, Dual, Cu at zero, EosS2'
_diffrn_measurement_method       'ω scans'
_diffrn_orient_matrix_UB_11      -0.0442818000
_diffrn_orient_matrix_UB_12      0.0660526000
_diffrn_orient_matrix_UB_13      0.0545674000
_diffrn_orient_matrix_UB_21      0.0389951000
_diffrn_orient_matrix_UB_22      -0.0805024000
_diffrn_orient_matrix_UB_23      0.0454744000
_diffrn_orient_matrix_UB_31      0.2663788000
_diffrn_orient_matrix_UB_32      0.0227551000
_diffrn_orient_matrix_UB_33      0.0024274000
_diffrn_radiation_monochromator  graphite
_diffrn_radiation_probe          x-ray
_diffrn_radiation_type           CuK\a
_diffrn_radiation_wavelength     1.54184
_diffrn_source                   'Enhance (Cu) X-ray Source'
_reflns_Friedel_coverage         0.695
_reflns_Friedel_fraction_full    0.998
_reflns_Friedel_fraction_max     0.968
_reflns_number_gt                2977
_reflns_number_total             3423
_reflns_odcompleteness_completeness 99.79
_reflns_odcompleteness_iscentric 1
_reflns_odcompleteness_theta     66.97
_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       
;
CrysAlisPro, Agilent Technologies,
Version 1.171.37.35 (release 13-08-2014 CrysAlis171 .NET)
(compiled Aug 13 2014,18:06:01)
;
_computing_data_collection       
;
CrysAlisPro, Agilent Technologies,
Version 1.171.37.35 (release 13-08-2014 CrysAlis171 .NET)
(compiled Aug 13 2014,18:06:01)
;
_computing_data_reduction        
;
CrysAlisPro, Agilent Technologies,
Version 1.171.37.35 (release 13-08-2014 CrysAlis171 .NET)
(compiled Aug 13 2014,18:06:01)
;
_computing_molecular_graphics    'Olex2 (Dolomanov et al., 2009)'
_computing_publication_material  'Olex2 (Dolomanov et al., 2009)'
_computing_structure_refinement  'ShelXL (Sheldrick, 2015)'
_computing_structure_solution    'ShelXT (Sheldrick, 2015)'
_refine_diff_density_max         0.484
_refine_diff_density_min         -0.804
_refine_diff_density_rms         0.134
_refine_ls_abs_structure_details 
;
 Flack x determined using 1075 quotients [(I+)-(I-)]/[(I+)+(I-)]
 (Parsons, Flack and Wagner, Acta Cryst. B69 (2013) 249-259).
;
_refine_ls_abs_structure_Flack   0.012(12)
_refine_ls_extinction_coef       .
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.034
_refine_ls_hydrogen_treatment    constr
_refine_ls_matrix_type           full
_refine_ls_number_parameters     240
_refine_ls_number_reflns         3423
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.0830
_refine_ls_R_factor_gt           0.0765
_refine_ls_restrained_S_all      1.034
_refine_ls_shift/su_max          0.000
_refine_ls_shift/su_mean         0.000
_refine_ls_structure_factor_coef Fsqd
_refine_ls_weighting_details     
'w=1/[σ²(Fo²)+(0.1408P)²+0.3350P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.1951
_refine_ls_wR_factor_ref         0.2084
_refine_special_details          ?
_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, All O(H) groups
2. Others
 Sof(C1A)=Sof(H1AA)=Sof(H1AB)=1-FVAR(1)
 Sof(C1)=Sof(H1A)=Sof(H1B)=FVAR(1)
 Sof(C2A)=Sof(H2AA)=Sof(H2AB)=Sof(H2AC)=1-FVAR(2)
 Sof(C2)=Sof(H2A)=Sof(H2B)=Sof(H2C)=FVAR(2)
3.a Ternary CH refined with riding coordinates:
 C5(H5), C4(H4A)
3.b Secondary CH2 refined with riding coordinates:
 C8(H8A,H8B), C6(H6A,H6B), C1(H1A,H1B), C1A(H1AA,H1AB)
3.c Aromatic/amide H refined with riding coordinates:
 C12(H12), C15(H15), C13(H13), C14(H14)
3.d Idealised Me refined as rotating group:
 C2(H2A,H2B,H2C), C2A(H2AA,H2AB,H2AC)
3.e Idealised tetrahedral OH refined as rotating group:
 O4(H4)
;
_atom_sites_solution_hydrogens   geom
_atom_sites_solution_primary     direct
_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
Cl1 Cl 0.7972(5) 0.3084(2) 0.75518(8) 0.1409(11) Uani 1 1 d . . . . .
O4 O 0.6962(5) 0.3791(2) 0.53674(14) 0.0586(8) Uani 1 1 d . . . . .
H4 H 0.6997 0.3538 0.5029 0.088 Uiso 1 1 calc GR . . . .
F3 F 0.4754(7) 0.4671(3) 0.43567(13) 0.0916(11) Uani 1 1 d . . . . .
O2 O 0.8908(6) 0.5171(3) 0.62720(19) 0.0728(9) Uani 1 1 d . . . . .
F2 F 0.6840(7) 0.5574(3) 0.49152(16) 0.0966(11) Uani 1 1 d . . . . .
F1 F 0.3037(8) 0.5623(3) 0.49684(18) 0.0992(12) Uani 1 1 d . . . . .
O3 O 0.2210(9) 0.2187(3) 0.57238(18) 0.0888(13) Uani 1 1 d . . . . .
O1 O 0.6223(8) 0.6285(2) 0.6191(2) 0.0865(12) Uani 1 1 d . . . . .
C5 C 0.4856(8) 0.4012(3) 0.65672(18) 0.0523(9) Uani 1 1 d . . . . .
H5 H 0.6315 0.3651 0.6520 0.063 Uiso 1 1 calc R . . . .
C9 C 0.4881(7) 0.4319(3) 0.54188(18) 0.0497(8) Uani 1 1 d . . . . .
C4 C 0.4842(7) 0.4769(3) 0.60676(17) 0.0481(8) Uani 1 1 d . . . . .
H4A H 0.3382 0.5130 0.6109 0.058 Uiso 1 1 calc R . . . .
C11 C 0.4829(8) 0.4414(3) 0.7210(2) 0.0594(10) Uani 1 1 d . . . . .
C8 C 0.2703(7) 0.3717(3) 0.5336(2) 0.0567(10) Uani 1 1 d . . . . .
H8A H 0.1297 0.4102 0.5344 0.068 Uiso 1 1 calc R . . . .
H8B H 0.2772 0.3412 0.4938 0.068 Uiso 1 1 calc R . . . .
C3 C 0.6946(8) 0.5409(3) 0.6186(2) 0.0583(10) Uani 1 1 d . . . . .
C7 C 0.2544(7) 0.3004(4) 0.5833(2) 0.0604(10) Uani 1 1 d . . . . .
C6 C 0.2739(9) 0.3348(3) 0.6482(2) 0.0597(10) Uani 1 1 d . . . . .
H6A H 0.2920 0.2825 0.6758 0.072 Uiso 1 1 calc R . . . .
H6B H 0.1290 0.3668 0.6593 0.072 Uiso 1 1 calc R . . . .
C10 C 0.4891(10) 0.5064(4) 0.4916(2) 0.0686(12) Uani 1 1 d . . . . .
C12 C 0.3390(16) 0.5150(5) 0.7368(3) 0.098(2) Uani 1 1 d . . . . .
H12 H 0.2352 0.5385 0.7074 0.117 Uiso 1 1 calc R . . . .
C16 C 0.6244(11) 0.4075(5) 0.7679(2) 0.0808(16) Uani 1 1 d . . . . .
C15 C 0.6326(15) 0.4471(8) 0.8261(3) 0.117(3) Uani 1 1 d . . . . .
H15 H 0.7323 0.4231 0.8563 0.141 Uiso 1 1 calc R . . . .
C13 C 0.344(2) 0.5550(6) 0.7947(3) 0.125(3) Uani 1 1 d . . . . .
H13 H 0.2450 0.6047 0.8038 0.150 Uiso 1 1 calc R . . . .
C14 C 0.4939(18) 0.5210(8) 0.8385(3) 0.121(3) Uani 1 1 d . . . . .
H14 H 0.5008 0.5488 0.8771 0.145 Uiso 1 1 calc R . . . .
C1 C 0.809(5) 0.7007(18) 0.6287(18) 0.153(10) Uani 0.79(8) 1 d . . P A 1
H1A H 0.7372 0.7517 0.6510 0.183 Uiso 0.79(8) 1 calc R . P A 1
H1B H 0.9292 0.6744 0.6554 0.183 Uiso 0.79(8) 1 calc R . P A 1
C2 C 0.913(5) 0.7342(16) 0.5821(10) 0.149(11) Uani 0.59(3) 1 d . . P A 1
H2A H 1.0680 0.7075 0.5786 0.224 Uiso 0.59(3) 1 calc GR . P A 1
H2B H 0.9265 0.8001 0.5867 0.224 Uiso 0.59(3) 1 calc GR . P A 1
H2C H 0.8232 0.7204 0.5457 0.224 Uiso 0.59(3) 1 calc GR . P A 1
C1A C 0.796(9) 0.690(3) 0.6436(19) 0.066(14) Uani 0.21(8) 1 d . . P A 2
H1AA H 0.9545 0.6723 0.6311 0.079 Uiso 0.21(8) 1 calc R . P A 2
H1AB H 0.7881 0.6930 0.6882 0.079 Uiso 0.21(8) 1 calc R . P A 2
C2A C 0.718(8) 0.7837(15) 0.613(2) 0.19(2) Uani 0.41(3) 1 d . . P A 2
H2AA H 0.8275 0.8000 0.5810 0.289 Uiso 0.41(3) 1 calc GR . P A 2
H2AB H 0.7150 0.8316 0.6436 0.289 Uiso 0.41(3) 1 calc GR . P A 2
H2AC H 0.5622 0.7768 0.5956 0.289 Uiso 0.41(3) 1 calc GR . P A 2


_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
Cl1 C16 1.754(7) . ?
O4 H4 0.8200 . ?
O4 C9 1.406(5) . ?
F3 C10 1.341(6) . ?
O2 C3 1.175(6) . ?
F2 C10 1.324(7) . ?
F1 C10 1.327(6) . ?
O3 C7 1.219(6) . ?
O1 C3 1.330(6) . ?
O1 C1 1.50(2) . ?
O1 C1A 1.42(4) . ?
C5 H5 0.9800 . ?
C5 C4 1.539(6) . ?
C5 C11 1.511(6) . ?
C5 C6 1.544(6) . ?
C9 C4 1.549(5) . ?
C9 C8 1.518(6) . ?
C9 C10 1.532(7) . ?
C4 H4A 0.9800 . ?
C4 C3 1.527(6) . ?
C11 C12 1.381(8) . ?
C11 C16 1.383(7) . ?
C8 H8A 0.9700 . ?
C8 H8B 0.9700 . ?
C8 C7 1.493(7) . ?
C7 C6 1.497(6) . ?
C6 H6A 0.9700 . ?
C6 H6B 0.9700 . ?
C12 H12 0.9300 . ?
C12 C13 1.382(9) . ?
C16 C15 1.387(9) . ?
C15 H15 0.9300 . ?
C15 C14 1.350(13) . ?
C13 H13 0.9300 . ?
C13 C14 1.365(14) . ?
C14 H14 0.9300 . ?
C1 H1A 0.9700 . ?
C1 H1B 0.9700 . ?
C1 C2 1.26(4) . ?
C2 H2A 0.9600 . ?
C2 H2B 0.9600 . ?
C2 H2C 0.9600 . ?
C1A H1AA 0.9700 . ?
C1A H1AB 0.9700 . ?
C1A C2A 1.57(6) . ?
C2A H2AA 0.9600 . ?
C2A H2AB 0.9600 . ?
C2A H2AC 0.9600 . ?

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 O4 H4 109.5 . . ?
C3 O1 C1 116.6(11) . . ?
C3 O1 C1A 112.6(19) . . ?
C4 C5 H5 108.0 . . ?
C4 C5 C6 110.7(3) . . ?
C11 C5 H5 108.0 . . ?
C11 C5 C4 112.1(3) . . ?
C11 C5 C6 110.0(3) . . ?
C6 C5 H5 108.0 . . ?
O4 C9 C4 108.1(3) . . ?
O4 C9 C8 110.9(3) . . ?
O4 C9 C10 108.8(3) . . ?
C8 C9 C4 109.6(3) . . ?
C8 C9 C10 108.8(4) . . ?
C10 C9 C4 110.6(4) . . ?
C5 C4 C9 109.9(3) . . ?
C5 C4 H4A 108.5 . . ?
C9 C4 H4A 108.5 . . ?
C3 C4 C5 107.9(3) . . ?
C3 C4 C9 113.3(3) . . ?
C3 C4 H4A 108.5 . . ?
C12 C11 C5 122.0(4) . . ?
C12 C11 C16 115.6(5) . . ?
C16 C11 C5 122.4(5) . . ?
C9 C8 H8A 109.4 . . ?
C9 C8 H8B 109.4 . . ?
H8A C8 H8B 108.0 . . ?
C7 C8 C9 111.0(3) . . ?
C7 C8 H8A 109.4 . . ?
C7 C8 H8B 109.4 . . ?
O2 C3 O1 124.5(4) . . ?
O2 C3 C4 125.7(4) . . ?
O1 C3 C4 109.8(4) . . ?
O3 C7 C8 122.5(4) . . ?
O3 C7 C6 121.1(4) . . ?
C8 C7 C6 116.4(4) . . ?
C5 C6 H6A 109.2 . . ?
C5 C6 H6B 109.2 . . ?
C7 C6 C5 112.1(4) . . ?
C7 C6 H6A 109.2 . . ?
C7 C6 H6B 109.2 . . ?
H6A C6 H6B 107.9 . . ?
F3 C10 C9 110.2(4) . . ?
F2 C10 F3 106.4(4) . . ?
F2 C10 F1 108.6(5) . . ?
F2 C10 C9 113.2(4) . . ?
F1 C10 F3 106.8(4) . . ?
F1 C10 C9 111.3(4) . . ?
C11 C12 H12 118.8 . . ?
C11 C12 C13 122.4(7) . . ?
C13 C12 H12 118.8 . . ?
C11 C16 Cl1 119.7(4) . . ?
C11 C16 C15 122.8(7) . . ?
C15 C16 Cl1 117.5(6) . . ?
C16 C15 H15 120.4 . . ?
C14 C15 C16 119.2(7) . . ?
C14 C15 H15 120.4 . . ?
C12 C13 H13 120.2 . . ?
C14 C13 C12 119.5(8) . . ?
C14 C13 H13 120.2 . . ?
C15 C14 C13 120.5(6) . . ?
C15 C14 H14 119.7 . . ?
C13 C14 H14 119.7 . . ?
O1 C1 H1A 107.6 . . ?
O1 C1 H1B 107.6 . . ?
H1A C1 H1B 107.0 . . ?
C2 C1 O1 119(2) . . ?
C2 C1 H1A 107.6 . . ?
C2 C1 H1B 107.6 . . ?
C1 C2 H2A 109.5 . . ?
C1 C2 H2B 109.5 . . ?
C1 C2 H2C 109.5 . . ?
H2A C2 H2B 109.5 . . ?
H2A C2 H2C 109.5 . . ?
H2B C2 H2C 109.5 . . ?
O1 C1A H1AA 111.6 . . ?
O1 C1A H1AB 111.6 . . ?
O1 C1A C2A 101(3) . . ?
H1AA C1A H1AB 109.4 . . ?
C2A C1A H1AA 111.6 . . ?
C2A C1A H1AB 111.6 . . ?
C1A C2A H2AA 109.5 . . ?
C1A C2A H2AB 109.5 . . ?
C1A C2A H2AC 109.5 . . ?
H2AA C2A H2AB 109.5 . . ?
H2AA C2A H2AC 109.5 . . ?
H2AB C2A H2AC 109.5 . . ?

_olex2_submission_special_instructions 'No special instructions were received'
_exptl_crystal_recrystallization_method 'Vapour deposition'
####################################################################### 
# 
# 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_lq-1d-150k
_database_code_depnum_ccdc_archive 'CCDC 1973712'
loop_
_audit_author_name
_audit_author_address
'wqq down'
;Southwest Minzu University
China
;
_audit_update_record             
;
2019-12-23 deposited with the CCDC.	2020-02-03 downloaded from the CCDC.
;
_audit_creation_date             2018-07-20
_audit_creation_method           
;
Olex2 1.2
(compiled 2018.05.29 svn.r3508 for OlexSys, GUI svn.r5506)
;
_shelx_SHELXL_version_number     2014/7
_chemical_name_common            ?
_chemical_name_systematic        ?
_chemical_formula_moiety         'C14 H15 F3 O4 S'
_chemical_formula_sum            'C14 H15 F3 O4 S'
_chemical_formula_weight         336.32
_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 0.0181 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'
F F 0.0727 0.0534 '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           5
_space_group_name_H-M_alt        'I 1 2 1'
_space_group_name_Hall           'I 2y'
loop_
_space_group_symop_operation_xyz
'x, y, z'
'-x, y, -z'
'x+1/2, y+1/2, z+1/2'
'-x+1/2, y+1/2, -z+1/2'

_cell_length_a                   17.4373(11)
_cell_length_b                   5.6433(3)
_cell_length_c                   16.0752(9)
_cell_angle_alpha                90
_cell_angle_beta                 103.086(6)
_cell_angle_gamma                90
_cell_volume                     1540.78(16)
_cell_formula_units_Z            4
_cell_measurement_reflns_used    4518
_cell_measurement_temperature    157(10)
_cell_measurement_theta_max      72.9890
_cell_measurement_theta_min      4.2520
_shelx_estimated_absorpt_T_max   ?
_shelx_estimated_absorpt_T_min   ?
_exptl_absorpt_coefficient_mu    2.323
_exptl_absorpt_correction_T_max  1.00000
_exptl_absorpt_correction_T_min  0.55043
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   
;
CrysAlisPro 1.171.38.46 (Rigaku Oxford Diffraction, 2015)
Empirical absorption correction using spherical harmonics,
 implemented in SCALE3 ABSPACK scaling algorithm.
;
_exptl_absorpt_special_details   ?
_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    ?
_exptl_crystal_description       block
_exptl_crystal_F_000             696
_exptl_crystal_size_max          0.5
_exptl_crystal_size_mid          0.4
_exptl_crystal_size_min          0.2
_exptl_transmission_factor_max   ?
_exptl_transmission_factor_min   ?
_diffrn_reflns_av_R_equivalents  0.0615
_diffrn_reflns_av_unetI/netI     0.0476
_diffrn_reflns_Laue_measured_fraction_full 0.999
_diffrn_reflns_Laue_measured_fraction_max 0.987
_diffrn_reflns_limit_h_max       21
_diffrn_reflns_limit_h_min       -21
_diffrn_reflns_limit_k_max       6
_diffrn_reflns_limit_k_min       -6
_diffrn_reflns_limit_l_max       19
_diffrn_reflns_limit_l_min       -19
_diffrn_reflns_number            8038
_diffrn_reflns_point_group_measured_fraction_full 0.919
_diffrn_reflns_point_group_measured_fraction_max 0.891
_diffrn_reflns_theta_full        67.684
_diffrn_reflns_theta_max         73.331
_diffrn_reflns_theta_min         4.252
_diffrn_ambient_environment      N~2~
_diffrn_ambient_temperature      157(10)
_diffrn_detector                 'CCD plate'
_diffrn_detector_area_resol_mean 15.9595
_diffrn_detector_type            EosS2
_diffrn_measured_fraction_theta_full 0.999
_diffrn_measured_fraction_theta_max 0.987
_diffrn_measurement_details      
;
List of Runs (angles in degrees, time in seconds):

  # Type    Start    End  Width  tₑₓₚ   ω     θ     κ     φ   Frames
#--------------------------------------------------------------------------
  1  ω    -55.00  33.00   1.00    1.00    --  -36.29  38.00   0.00   88
  2  ω   -104.00 -20.00   1.00    1.00    --  -36.29 -57.00-150.00   84
  3  ω   -104.00 -20.00   1.00    1.00    --  -36.29 -57.00 150.00   84
  4  ω     20.00 104.00   1.00    1.00    --   36.29  57.00  60.00   84
  5  ω      1.00  75.00   1.00    1.00    --   36.29 -99.00  90.00   74
  6  ω     23.00  90.00   1.00    1.00    --   36.29-125.00 -30.00   67
  7  ω     20.00 104.00   1.00    1.00    --   36.29  57.00  90.00   84
  8  ω     20.00 104.00   1.00    1.00    --   36.29  57.00  30.00   84
  9  ω     57.00 151.00   1.00    3.20    --  108.71 178.00 150.00   94
 10  ω     91.00 177.00   1.00    3.20    --  108.71  45.00 -30.00   86
 11  ω     87.00 178.00   1.00    3.20    --  108.71  30.00-120.00   91
 12  ω     42.00 127.00   1.00    3.20    --  108.71 -61.00 150.00   85
 13  ω    100.00 178.00   1.00    3.20    --  108.71 111.00 150.00   78
 14  ω     91.00 176.00   1.00    3.20    --  108.71  61.00 -60.00   85
 15  ω     39.00 109.00   1.00    3.20    --  108.71 -94.00   0.00   70
 16  ω     91.00 177.00   1.00    3.20    --  108.71  45.00 -90.00   86
 17  ω     39.00 109.00   1.00    3.20    --  108.71 -94.00 -90.00   70
 18  ω     42.00 127.00   1.00    3.20    --  108.71 -61.00   0.00   85
 19  ω     39.00 115.00   1.00    3.20    --  108.71-111.00-180.00   76
 20  ω     40.00 126.00   1.00    3.20    --  108.71 -45.00-120.00   86
 21  ω    -53.00  31.00   1.00    1.00    --  -36.29  57.00-150.00   84
 22  ω     10.00 104.00   1.00    1.00    --   36.29  77.00-180.00   94
 23  ω    -31.00  53.00   1.00    1.00    --   36.29 -57.00  60.00   84
 24  ω     10.00 104.00   1.00    1.00    --   36.29  77.00 -30.00   94
 25  ω     17.00 105.00   1.00    1.00    --   36.29  38.00 -30.00   88
 26  ω     87.00 178.00   1.00    3.20    --  108.71  30.00 150.00   91
 27  ω     70.00 178.00   1.00    3.20    --  108.71  15.00  90.00  108
 28  ω     91.00 170.00   1.00    3.20    --  108.71  61.00   0.00   79
;
_diffrn_measurement_device       'four-circle diffractometer'
_diffrn_measurement_device_type  'New Gemini, Dual, Cu at zero, EosS2'
_diffrn_measurement_method       'ω scans'
_diffrn_orient_matrix_type       
'CrysAlisPro convention (1999,Acta A55,543-557)'
_diffrn_orient_matrix_UB_11      -0.0415865000
_diffrn_orient_matrix_UB_12      -0.0167105000
_diffrn_orient_matrix_UB_13      -0.0952059000
_diffrn_orient_matrix_UB_21      -0.0687117000
_diffrn_orient_matrix_UB_22      0.1496248000
_diffrn_orient_matrix_UB_23      0.0170648000
_diffrn_orient_matrix_UB_31      0.0420756000
_diffrn_orient_matrix_UB_32      0.2277619000
_diffrn_orient_matrix_UB_33      -0.0181673000
_diffrn_radiation_monochromator  graphite
_diffrn_radiation_probe          x-ray
_diffrn_radiation_type           CuK\a
_diffrn_radiation_wavelength     1.54184
_diffrn_source                   'fine-focus sealed X-ray tube'
_diffrn_source_type              'Enhance (Cu) X-ray Source'
_reflns_Friedel_coverage         0.633
_reflns_Friedel_fraction_full    0.818
_reflns_Friedel_fraction_max     0.773
_reflns_number_gt                2633
_reflns_number_total             2763
_reflns_odcompleteness_completeness 99.93
_reflns_odcompleteness_iscentric 1
_reflns_odcompleteness_theta     66.97
_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       'CrysAlisPro 1.171.38.46 (Rigaku OD, 2015)'
_computing_data_collection       'CrysAlisPro 1.171.38.46 (Rigaku OD, 2015)'
_computing_data_reduction        'CrysAlisPro 1.171.38.46 (Rigaku OD, 2015)'
_computing_molecular_graphics    'Olex2 (Dolomanov et al., 2009)'
_computing_publication_material  'Olex2 (Dolomanov et al., 2009)'
_computing_structure_refinement  'ShelXL (Sheldrick, 2015)'
_computing_structure_solution    'ShelXT (Sheldrick, 2015)'
_refine_diff_density_max         0.590
_refine_diff_density_min         -0.513
_refine_diff_density_rms         0.111
_refine_ls_abs_structure_details 
;
 Flack x determined using 893 quotients [(I+)-(I-)]/[(I+)+(I-)]
 (Parsons, Flack and Wagner, Acta Cryst. B69 (2013) 249-259).
;
_refine_ls_abs_structure_Flack   0.02(3)
_refine_ls_extinction_coef       .
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.052
_refine_ls_hydrogen_treatment    constr
_refine_ls_matrix_type           full
_refine_ls_number_parameters     201
_refine_ls_number_reflns         2763
_refine_ls_number_restraints     1
_refine_ls_R_factor_all          0.0851
_refine_ls_R_factor_gt           0.0831
_refine_ls_restrained_S_all      1.052
_refine_ls_shift/su_max          0.000
_refine_ls_shift/su_mean         0.000
_refine_ls_structure_factor_coef Fsqd
_refine_ls_weighting_details     
'w=1/[σ²(Fo²)+(0.1890P)²+0.2667P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.2220
_refine_ls_wR_factor_ref         0.2261
_refine_special_details          ?
_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, All O(H) groups
2.a Ternary CH refined with riding coordinates:
 C5(H5), C10(H10)
2.b Secondary CH2 refined with riding coordinates:
 C8(H8A,H8B), C6(H6A,H6B), C13(H13A,H13B)
2.c Aromatic/amide H refined with riding coordinates:
 C3(H3), C2(H2A), C1(H1)
2.d Idealised Me refined as rotating group:
 C14(H14A,H14B,H14C)
2.e Idealised tetrahedral OH refined as rotating group:
 O2(H2)
;
_atom_sites_solution_hydrogens   geom
_atom_sites_solution_primary     direct
_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 0.55510(8) 0.3940(3) 0.34271(8) 0.0438(5) Uani 1 1 d . . . . .
F1 F 0.91629(19) 0.6223(8) 0.6536(2) 0.0471(9) Uani 1 1 d . . . . .
F3 F 0.89453(19) 0.4285(8) 0.5363(2) 0.0497(9) Uani 1 1 d . . . . .
F2 F 0.8790(2) 0.8053(8) 0.5343(3) 0.0519(10) Uani 1 1 d . . . . .
O2 O 0.7628(2) 0.7729(7) 0.6272(2) 0.0338(8) Uani 1 1 d . . . . .
H2 H 0.7920 0.7771 0.6750 0.051 Uiso 1 1 calc GR . . . .
O3 O 0.7321(3) 0.1956(9) 0.4349(3) 0.0448(10) Uani 1 1 d . . . . .
O1 O 0.6742(2) 0.2323(8) 0.6984(2) 0.0390(9) Uani 1 1 d . . . . .
O4 O 0.7789(3) 0.5044(10) 0.3742(3) 0.0474(11) Uani 1 1 d . . . . .
C3 C 0.5299(3) 0.7966(10) 0.4048(3) 0.0309(10) Uani 1 1 d . . . . .
H3 H 0.5332 0.9294 0.4397 0.037 Uiso 1 1 calc R . . . .
C7 C 0.6908(3) 0.2972(10) 0.6337(3) 0.0331(10) Uani 1 1 d . . . . .
C9 C 0.7826(3) 0.5751(10) 0.5818(3) 0.0320(10) Uani 1 1 d . . . . .
C12 C 0.7450(3) 0.4044(12) 0.4309(3) 0.0359(11) Uani 1 1 d . . . . .
C8 C 0.7752(3) 0.3448(10) 0.6281(3) 0.0343(11) Uani 1 1 d . . . . .
H8A H 0.8084 0.3521 0.6853 0.041 Uiso 1 1 calc R . . . .
H8B H 0.7936 0.2150 0.5982 0.041 Uiso 1 1 calc R . . . .
C5 C 0.6410(3) 0.5625(10) 0.5051(3) 0.0309(10) Uani 1 1 d . . . . .
H5 H 0.6344 0.6924 0.5434 0.037 Uiso 1 1 calc R . . . .
C10 C 0.7256(3) 0.5871(10) 0.4921(3) 0.0325(10) Uani 1 1 d . . . . .
H10 H 0.7306 0.7445 0.4682 0.039 Uiso 1 1 calc R . . . .
C4 C 0.5780(3) 0.6003(10) 0.4243(3) 0.0329(10) Uani 1 1 d . . . . .
C6 C 0.6290(3) 0.3332(11) 0.5526(3) 0.0362(12) Uani 1 1 d . . . . .
H6A H 0.5776 0.3377 0.5662 0.043 Uiso 1 1 calc R . . . .
H6B H 0.6298 0.1990 0.5151 0.043 Uiso 1 1 calc R . . . .
C11 C 0.8688(3) 0.6080(12) 0.5753(4) 0.0413(13) Uani 1 1 d . . . . .
C2 C 0.4753(3) 0.7722(12) 0.3258(4) 0.0417(12) Uani 1 1 d . . . . .
H2A H 0.4384 0.8883 0.3038 0.050 Uiso 1 1 calc R . . . .
C1 C 0.4808(4) 0.5694(13) 0.2855(4) 0.0455(14) Uani 1 1 d . . . . .
H1 H 0.4487 0.5276 0.2331 0.055 Uiso 1 1 calc R . . . .
C13 C 0.8084(6) 0.3432(18) 0.3175(5) 0.071(2) Uani 1 1 d . . . . .
H13A H 0.7689 0.3189 0.2650 0.085 Uiso 1 1 calc R . . . .
H13B H 0.8218 0.1909 0.3449 0.085 Uiso 1 1 calc R . . . .
C14 C 0.8795(9) 0.458(3) 0.2994(11) 0.137(7) Uani 1 1 d . . . . .
H14A H 0.8930 0.3831 0.2512 0.206 Uiso 1 1 calc GR . . . .
H14B H 0.9225 0.4434 0.3484 0.206 Uiso 1 1 calc GR . . . .
H14C H 0.8688 0.6231 0.2871 0.206 Uiso 1 1 calc GR . . . .


_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 C4 1.731(5) . ?
S1 C1 1.721(7) . ?
F1 C11 1.343(6) . ?
F3 C11 1.323(7) . ?
F2 C11 1.326(7) . ?
O2 H2 0.8200 . ?
O2 C9 1.418(6) . ?
O3 C12 1.204(9) . ?
O1 C7 1.199(6) . ?
O4 C12 1.320(7) . ?
O4 C13 1.461(8) . ?
C3 H3 0.9300 . ?
C3 C4 1.383(8) . ?
C3 C2 1.411(7) . ?
C7 C8 1.519(7) . ?
C7 C6 1.506(6) . ?
C9 C8 1.517(8) . ?
C9 C10 1.556(7) . ?
C9 C11 1.541(7) . ?
C12 C10 1.516(7) . ?
C8 H8A 0.9700 . ?
C8 H8B 0.9700 . ?
C5 H5 0.9800 . ?
C5 C10 1.542(7) . ?
C5 C4 1.514(7) . ?
C5 C6 1.541(7) . ?
C10 H10 0.9800 . ?
C6 H6A 0.9700 . ?
C6 H6B 0.9700 . ?
C2 H2A 0.9300 . ?
C2 C1 1.329(10) . ?
C1 H1 0.9300 . ?
C13 H13A 0.9700 . ?
C13 H13B 0.9700 . ?
C13 C14 1.485(17) . ?
C14 H14A 0.9600 . ?
C14 H14B 0.9600 . ?
C14 H14C 0.9600 . ?

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 S1 C4 92.0(3) . . ?
C9 O2 H2 109.5 . . ?
C12 O4 C13 116.1(6) . . ?
C4 C3 H3 123.9 . . ?
C4 C3 C2 112.2(5) . . ?
C2 C3 H3 123.9 . . ?
O1 C7 C8 122.3(4) . . ?
O1 C7 C6 121.7(5) . . ?
C6 C7 C8 116.0(4) . . ?
O2 C9 C8 111.4(4) . . ?
O2 C9 C10 105.3(4) . . ?
O2 C9 C11 107.1(4) . . ?
C8 C9 C10 112.6(4) . . ?
C8 C9 C11 109.2(4) . . ?
C11 C9 C10 111.1(4) . . ?
O3 C12 O4 125.0(5) . . ?
O3 C12 C10 124.0(5) . . ?
O4 C12 C10 111.0(6) . . ?
C7 C8 H8A 109.3 . . ?
C7 C8 H8B 109.3 . . ?
C9 C8 C7 111.8(4) . . ?
C9 C8 H8A 109.3 . . ?
C9 C8 H8B 109.3 . . ?
H8A C8 H8B 107.9 . . ?
C10 C5 H5 105.6 . . ?
C4 C5 H5 105.6 . . ?
C4 C5 C10 113.7(4) . . ?
C4 C5 C6 113.0(4) . . ?
C6 C5 H5 105.6 . . ?
C6 C5 C10 112.5(4) . . ?
C9 C10 H10 107.9 . . ?
C12 C10 C9 112.5(4) . . ?
C12 C10 C5 112.8(4) . . ?
C12 C10 H10 107.9 . . ?
C5 C10 C9 107.5(4) . . ?
C5 C10 H10 107.9 . . ?
C3 C4 S1 110.0(4) . . ?
C3 C4 C5 126.3(5) . . ?
C5 C4 S1 123.6(4) . . ?
C7 C6 C5 113.1(4) . . ?
C7 C6 H6A 109.0 . . ?
C7 C6 H6B 109.0 . . ?
C5 C6 H6A 109.0 . . ?
C5 C6 H6B 109.0 . . ?
H6A C6 H6B 107.8 . . ?
F1 C11 C9 110.4(4) . . ?
F3 C11 F1 106.6(5) . . ?
F3 C11 F2 108.0(4) . . ?
F3 C11 C9 112.4(5) . . ?
F2 C11 F1 106.9(5) . . ?
F2 C11 C9 112.2(5) . . ?
C3 C2 H2A 122.8 . . ?
C1 C2 C3 114.4(6) . . ?
C1 C2 H2A 122.8 . . ?
S1 C1 H1 124.3 . . ?
C2 C1 S1 111.4(4) . . ?
C2 C1 H1 124.3 . . ?
O4 C13 H13A 110.5 . . ?
O4 C13 H13B 110.5 . . ?
O4 C13 C14 106.0(9) . . ?
H13A C13 H13B 108.7 . . ?
C14 C13 H13A 110.5 . . ?
C14 C13 H13B 110.5 . . ?
C13 C14 H14A 109.5 . . ?
C13 C14 H14B 109.5 . . ?
C13 C14 H14C 109.5 . . ?
H14A C14 H14B 109.5 . . ?
H14A C14 H14C 109.5 . . ?
H14B C14 H14C 109.5 . . ?

_olex2_submission_special_instructions 'No special instructions were received'
_oxdiff_exptl_absorpt_empirical_details 
;
Empirical correction (ABSPACK) includes:
- Absorption correction using spherical harmonics
- Frame scaling
- Detector area scaling
;
_oxdiff_exptl_absorpt_empirical_full_max 2.874
_oxdiff_exptl_absorpt_empirical_full_min 0.313
_exptl_crystal_recrystallization_method 'Vapour deposition'
