# Electronic Supplementary Material (ESI) for Chemical Science.
# This journal is © The Royal Society of Chemistry 2018

####################################################################### 
# 
# This file contains crystal structure data downloaded from the 
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# Crystallographic Data Centre (CCDC).
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# guidelines are available at http://www.ccdc.cam.ac.uk/access/V1 
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data_a86a_0m_75
_database_code_depnum_ccdc_archive 'CCDC 1849476'
_audit_update_record             
;
2018-06-14 deposited with the CCDC.
2018-11-23 downloaded from the CCDC.
;
_audit_creation_date             2018-06-14
_audit_creation_method           
; 
Olex2 1.2 
(compiled 2018.04.26 svn.r3504 for OlexSys, GUI svn.r5492) 
;
_shelxl_version_number           2014-3

_chemical_name_common            ?
_chemical_name_systematic        
; 
 ? 
;
_chemical_formula_moiety         'C14 H28 Fe N O3 P2, C F3 O3 S'
_chemical_formula_sum            'C15 H28 F3 Fe N O6 P2 S'
_chemical_formula_weight         525.23
_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 0.0033 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'
F F 0.0171 0.0103 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
Fe Fe 0.3463 0.8444 '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'
O O 0.0106 0.0060 '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'

_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      triclinic
_space_group_IT_number           2
_space_group_name_H-M_alt        'P -1'
_space_group_name_Hall           '-P 1'
loop_
_space_group_symop_operation_xyz
'x, y, z'
'-x, -y, -z'

_cell_length_a                   9.893(3)
_cell_length_b                   10.456(4)
_cell_length_c                   12.269(4)
_cell_angle_alpha                98.650(11)
_cell_angle_beta                 111.652(9)
_cell_angle_gamma                95.223(11)
_cell_volume                     1151.2(7)
_cell_formula_units_Z            2
_cell_measurement_reflns_used    566
_cell_measurement_temperature    296(2)
_cell_measurement_theta_max      26.629
_cell_measurement_theta_min      2.958
_shelx_estimated_absorpt_T_max   0.960
_shelx_estimated_absorpt_T_min   0.535
_exptl_absorpt_coefficient_mu    0.938
_exptl_absorpt_correction_T_max  0.9889
_exptl_absorpt_correction_T_min  0.7362
_exptl_absorpt_correction_type   integration
_exptl_absorpt_process_details   
'SADABS-2016/2 (Bruker,2016/2) was used for absorption correction. wR2(int) was'
_exptl_crystal_colour            colourless
_exptl_crystal_density_diffrn    1.515
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    ?
_exptl_crystal_description       prism
_exptl_crystal_F_000             544
_exptl_crystal_size_max          0.763
_exptl_crystal_size_mid          0.074
_exptl_crystal_size_min          0.044
_exptl_crystal_id                a86a


_exptl_crystal_preparation       
; 
The data crystal was mounted using oil (Parantone-N, Exxon) to a 
0.3 mm cryo-loop (Hampton Research). 
;
_exptl_special_details           
; 
One distinct cell was identified using APEX2 (Bruker, 2013).  19 
frame series were integrated and filtered for statistical outliers 
using SAINT (Bruker, 2013) then corrected for absorption by 
integration using SADABS v2012/1 (Bruker, 2012). 
No decay correction was applied. 
 
;

_exptl_transmission_factor_max   ?
_exptl_transmission_factor_min   ?
_diffrn_reflns_av_R_equivalents  0.0568
_diffrn_reflns_av_unetI/netI     0.0304
_diffrn_reflns_Laue_measured_fraction_full 1.000
_diffrn_reflns_Laue_measured_fraction_max 0.986
_diffrn_reflns_limit_h_max       13
_diffrn_reflns_limit_h_min       -13
_diffrn_reflns_limit_k_max       14
_diffrn_reflns_limit_k_min       -13
_diffrn_reflns_limit_l_max       16
_diffrn_reflns_limit_l_min       -16
_diffrn_reflns_number            55976
_diffrn_reflns_point_group_measured_fraction_full 1.000
_diffrn_reflns_point_group_measured_fraction_max 0.986
_diffrn_reflns_theta_full        25.242
_diffrn_reflns_theta_max         28.473
_diffrn_reflns_theta_min         1.822
_diffrn_ambient_temperature      296.15
_diffrn_detector_area_resol_mean ?
_diffrn_measured_fraction_theta_full 1.000
_diffrn_measured_fraction_theta_max 0.986
_diffrn_measurement_device_type  'Bruker APEX-II CCD'
_diffrn_measurement_method       'φ and ω scans'
_diffrn_radiation_type           MoK\a
_diffrn_radiation_wavelength     0.71073
_diffrn_radiation_wavelength_id  a86a
_diffrn_source                   ?
_diffrn_standards_number         0
_reflns_Friedel_coverage         0.000
_reflns_Friedel_fraction_full    .
_reflns_Friedel_fraction_max     .
_reflns_number_gt                4769
_reflns_number_total             5751
_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       'SAINT V8.34A (Bruker, 2005)'
_computing_data_collection       'APEX2 V2013.10-0 (Bruker, 2013)'

_computing_data_reduction        
; 
SAINT V8.34A, XPREP v2013/3, SADABS V2012/1, TWINABS V2012/1 
(Bruker, 2012 & 2013) 
;
_computing_molecular_graphics    'Olex2 (Dolomanov et al., 2009)'
_computing_publication_material  'Olex2 (Dolomanov et al., 2009)'
_computing_structure_refinement  'SHELX-2013-4 (Sheldrick, 2013)'

_computing_structure_solution    'SHELX-2013-4 (Sheldrick, 2013)'
_refine_diff_density_max         0.896
_refine_diff_density_min         -0.552
_refine_diff_density_rms         0.067
_refine_ls_extinction_coef       .
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.042
_refine_ls_hydrogen_treatment    constr
_refine_ls_matrix_type           full
_refine_ls_number_parameters     267
_refine_ls_number_reflns         5751
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.0407
_refine_ls_R_factor_gt           0.0298
_refine_ls_restrained_S_all      1.042
_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)+(0.0294P)²+0.7688P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.0679
_refine_ls_wR_factor_ref         0.0723
_refine_special_details          
; 
Structure was phased by direct??dual space??Paterson methods?intrinsic phasing? 
2008).  Systematic conditions suggested the un??ambiguous space group. 
The space group choice was confirmed by successful convergence of the 
full-matrix least-squares refinement on F².  The highest peaks in 
the final difference Fourier map were in the vicinity of atoms F1; the 
final map had no other significant features. 
 
;

_olex2_refinement_description    
; 
1. Fixed Uiso 
 At 1.2 times of: 
  All C(H,H) groups, All N(H) groups 
 At 1.5 times of: 
  All C(H,H,H) groups 
2.a Ternary CH refined with riding coordinates: 
 N1(H1) 
2.b Secondary CH2 refined with riding coordinates: 
 C4(H4A,H4B), C6(H6A,H6B), C8(H8A,H8B), C10(H10A,H10B), C12(H12A,H12B), 
 C13(H13A,H13B) 
2.c Idealised Me refined as rotating group: 
 C5(H5A,H5B,H5C), C7(H7A,H7B,H7C), C9(H9A,H9B,H9C), C11(H11A,H11B,H11C), 
 C14(H14A,H14B,H14C) 
;
_atom_sites_solution_hydrogens   geom
_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
Fe1 Fe 0.33547(3) 0.65453(2) 0.82739(2) 0.01071(7) Uani 1 1 d . . . . .
P1 P 0.48300(5) 0.73001(4) 0.74632(4) 0.01115(9) Uani 1 1 d . . . . .
P2 P 0.17632(5) 0.78318(4) 0.74889(4) 0.01127(9) Uani 1 1 d . . . . .
O1 O 0.32748(17) 0.38880(13) 0.70458(13) 0.0273(3) Uani 1 1 d . . . . .
O2 O 0.13594(16) 0.55013(14) 0.93140(13) 0.0256(3) Uani 1 1 d . . . . .
O3 O 0.56225(17) 0.77660(17) 1.06164(13) 0.0355(4) Uani 1 1 d . . . . .
N1 N 0.35744(16) 0.95141(13) 0.67365(13) 0.0125(3) Uani 1 1 d . . . . .
H1 H 0.3170 0.8942 0.5943 0.015 Uiso 1 1 calc R . . . .
C1 C 0.3288(2) 0.49395(17) 0.75117(16) 0.0170(4) Uani 1 1 d . . . . .
C2 C 0.2140(2) 0.59044(17) 0.89021(16) 0.0170(4) Uani 1 1 d . . . . .
C3 C 0.4715(2) 0.72899(19) 0.96887(16) 0.0194(4) Uani 1 1 d . . . . .
C4 C 0.67967(19) 0.72451(18) 0.82211(17) 0.0187(4) Uani 1 1 d . . . . .
H4A H 0.7335 0.7659 0.7813 0.022 Uiso 1 1 calc R . . . .
H4B H 0.7147 0.7740 0.9035 0.022 Uiso 1 1 calc R . . . .
C5 C 0.7114(2) 0.5837(2) 0.8248(2) 0.0262(4) Uani 1 1 d . . . . .
H5A H 0.6830 0.5360 0.7445 0.039 Uiso 1 1 calc GR . . . .
H5B H 0.6564 0.5415 0.8633 0.039 Uiso 1 1 calc GR . . . .
H5C H 0.8148 0.5855 0.8684 0.039 Uiso 1 1 calc GR . . . .
C6 C 0.4413(2) 0.65666(17) 0.58964(15) 0.0150(3) Uani 1 1 d . . . . .
H6A H 0.4346 0.5624 0.5826 0.018 Uiso 1 1 calc R . . . .
H6B H 0.3449 0.6741 0.5413 0.018 Uiso 1 1 calc R . . . .
C7 C 0.5498(2) 0.70229(19) 0.53627(17) 0.0198(4) Uani 1 1 d . . . . .
H7A H 0.5086 0.6697 0.4514 0.030 Uiso 1 1 calc GR . . . .
H7B H 0.6403 0.6695 0.5716 0.030 Uiso 1 1 calc GR . . . .
H7C H 0.5687 0.7963 0.5522 0.030 Uiso 1 1 calc GR . . . .
C8 C 0.0253(2) 0.72032(18) 0.60293(16) 0.0178(4) Uani 1 1 d . . . . .
H8A H -0.0409 0.7842 0.5854 0.021 Uiso 1 1 calc R . . . .
H8B H 0.0653 0.7087 0.5415 0.021 Uiso 1 1 calc R . . . .
C9 C -0.0616(2) 0.58985(19) 0.59904(17) 0.0217(4) Uani 1 1 d . . . . .
H9A H -0.1380 0.5598 0.5208 0.033 Uiso 1 1 calc GR . . . .
H9B H -0.1048 0.6017 0.6575 0.033 Uiso 1 1 calc GR . . . .
H9C H 0.0034 0.5262 0.6163 0.033 Uiso 1 1 calc GR . . . .
C10 C 0.0756(2) 0.84471(18) 0.84023(17) 0.0184(4) Uani 1 1 d . . . . .
H10A H 0.0149 0.9053 0.8009 0.022 Uiso 1 1 calc R . . . .
H10B H 0.0101 0.7716 0.8431 0.022 Uiso 1 1 calc R . . . .
C11 C 0.1730(2) 0.9139(2) 0.96846(18) 0.0249(4) Uani 1 1 d . . . . .
H11A H 0.2345 0.9896 0.9670 0.037 Uiso 1 1 calc GR . . . .
H11B H 0.2336 0.8550 1.0085 0.037 Uiso 1 1 calc GR . . . .
H11C H 0.1120 0.9406 1.0103 0.037 Uiso 1 1 calc GR . . . .
C12 C 0.24176(19) 0.94504(16) 0.72534(16) 0.0139(3) Uani 1 1 d . . . . .
H12A H 0.1570 0.9767 0.6731 0.017 Uiso 1 1 calc R . . . .
H12B H 0.2799 1.0056 0.8019 0.017 Uiso 1 1 calc R . . . .
C13 C 0.49649(19) 0.90756(16) 0.74701(16) 0.0139(3) Uani 1 1 d . . . . .
H13A H 0.5287 0.9543 0.8291 0.017 Uiso 1 1 calc R . . . .
H13B H 0.5720 0.9325 0.7180 0.017 Uiso 1 1 calc R . . . .
C14 C 0.3917(2) 1.08965(17) 0.65836(17) 0.0186(4) Uani 1 1 d . . . . .
H14A H 0.3032 1.1157 0.6074 0.028 Uiso 1 1 calc GR . . . .
H14B H 0.4633 1.0934 0.6229 0.028 Uiso 1 1 calc GR . . . .
H14C H 0.4302 1.1478 0.7351 0.028 Uiso 1 1 calc GR . . . .
S1 S 0.16993(5) 0.90722(4) 0.35192(4) 0.01411(9) Uani 1 1 d . . . . .
F1 F 0.1366(2) 0.70895(16) 0.18309(14) 0.0624(5) Uani 1 1 d . . . . .
F2 F 0.0103(2) 0.67665(15) 0.28832(15) 0.0752(6) Uani 1 1 d . . . . .
F3 F -0.05573(17) 0.79815(16) 0.15690(13) 0.0526(4) Uani 1 1 d . . . . .
O4 O 0.29148(16) 0.85597(15) 0.43183(12) 0.0281(3) Uani 1 1 d . . . . .
O5 O 0.07290(16) 0.95277(16) 0.40643(14) 0.0310(3) Uani 1 1 d . . . . .
O6 O 0.21115(16) 0.99337(14) 0.28452(13) 0.0280(3) Uani 1 1 d . . . . .
C15 C 0.0595(3) 0.7644(2) 0.23858(19) 0.0342(5) 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
Fe1 P1 2.2000(7) . ?
Fe1 P2 2.2073(7) . ?
Fe1 C1 1.7778(19) . ?
Fe1 C2 1.7833(19) . ?
Fe1 C3 1.763(2) . ?
P1 C4 1.8317(19) . ?
P1 C6 1.8351(18) . ?
P1 C13 1.8477(19) . ?
P2 C8 1.8342(19) . ?
P2 C10 1.8405(18) . ?
P2 C12 1.8582(18) . ?
O1 C1 1.157(2) . ?
O2 C2 1.150(2) . ?
O3 C3 1.159(2) . ?
N1 H1 0.9800 . ?
N1 C12 1.500(2) . ?
N1 C13 1.496(2) . ?
N1 C14 1.509(2) . ?
C4 H4A 0.9700 . ?
C4 H4B 0.9700 . ?
C4 C5 1.536(3) . ?
C5 H5A 0.9600 . ?
C5 H5B 0.9600 . ?
C5 H5C 0.9600 . ?
C6 H6A 0.9700 . ?
C6 H6B 0.9700 . ?
C6 C7 1.525(2) . ?
C7 H7A 0.9600 . ?
C7 H7B 0.9600 . ?
C7 H7C 0.9600 . ?
C8 H8A 0.9700 . ?
C8 H8B 0.9700 . ?
C8 C9 1.529(3) . ?
C9 H9A 0.9600 . ?
C9 H9B 0.9600 . ?
C9 H9C 0.9600 . ?
C10 H10A 0.9700 . ?
C10 H10B 0.9700 . ?
C10 C11 1.529(3) . ?
C11 H11A 0.9600 . ?
C11 H11B 0.9600 . ?
C11 H11C 0.9600 . ?
C12 H12A 0.9700 . ?
C12 H12B 0.9700 . ?
C13 H13A 0.9700 . ?
C13 H13B 0.9700 . ?
C14 H14A 0.9600 . ?
C14 H14B 0.9600 . ?
C14 H14C 0.9600 . ?
S1 O4 1.4491(14) . ?
S1 O5 1.4341(15) . ?
S1 O6 1.4379(14) . ?
S1 C15 1.821(2) . ?
F1 C15 1.314(3) . ?
F2 C15 1.326(3) . ?
F3 C15 1.329(3) . ?

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
P1 Fe1 P2 91.03(3) . . ?
C1 Fe1 P1 88.88(6) . . ?
C1 Fe1 P2 122.49(6) . . ?
C1 Fe1 C2 90.00(8) . . ?
C2 Fe1 P1 178.70(6) . . ?
C2 Fe1 P2 89.02(6) . . ?
C3 Fe1 P1 88.20(7) . . ?
C3 Fe1 P2 113.45(7) . . ?
C3 Fe1 C1 124.02(9) . . ?
C3 Fe1 C2 92.97(9) . . ?
C4 P1 Fe1 117.03(7) . . ?
C4 P1 C6 103.77(9) . . ?
C4 P1 C13 98.13(8) . . ?
C6 P1 Fe1 117.01(6) . . ?
C6 P1 C13 103.34(8) . . ?
C13 P1 Fe1 114.98(6) . . ?
C8 P2 Fe1 119.24(6) . . ?
C8 P2 C10 101.43(9) . . ?
C8 P2 C12 100.10(8) . . ?
C10 P2 Fe1 115.25(6) . . ?
C10 P2 C12 96.64(8) . . ?
C12 P2 Fe1 120.23(6) . . ?
C12 N1 H1 108.0 . . ?
C12 N1 C14 109.29(13) . . ?
C13 N1 H1 108.0 . . ?
C13 N1 C12 113.68(13) . . ?
C13 N1 C14 109.63(13) . . ?
C14 N1 H1 108.0 . . ?
O1 C1 Fe1 178.03(17) . . ?
O2 C2 Fe1 179.41(17) . . ?
O3 C3 Fe1 179.00(19) . . ?
P1 C4 H4A 109.2 . . ?
P1 C4 H4B 109.2 . . ?
H4A C4 H4B 107.9 . . ?
C5 C4 P1 112.22(13) . . ?
C5 C4 H4A 109.2 . . ?
C5 C4 H4B 109.2 . . ?
C4 C5 H5A 109.5 . . ?
C4 C5 H5B 109.5 . . ?
C4 C5 H5C 109.5 . . ?
H5A C5 H5B 109.5 . . ?
H5A C5 H5C 109.5 . . ?
H5B C5 H5C 109.5 . . ?
P1 C6 H6A 108.1 . . ?
P1 C6 H6B 108.1 . . ?
H6A C6 H6B 107.3 . . ?
C7 C6 P1 116.90(13) . . ?
C7 C6 H6A 108.1 . . ?
C7 C6 H6B 108.1 . . ?
C6 C7 H7A 109.5 . . ?
C6 C7 H7B 109.5 . . ?
C6 C7 H7C 109.5 . . ?
H7A C7 H7B 109.5 . . ?
H7A C7 H7C 109.5 . . ?
H7B C7 H7C 109.5 . . ?
P2 C8 H8A 109.2 . . ?
P2 C8 H8B 109.2 . . ?
H8A C8 H8B 107.9 . . ?
C9 C8 P2 112.27(13) . . ?
C9 C8 H8A 109.2 . . ?
C9 C8 H8B 109.2 . . ?
C8 C9 H9A 109.5 . . ?
C8 C9 H9B 109.5 . . ?
C8 C9 H9C 109.5 . . ?
H9A C9 H9B 109.5 . . ?
H9A C9 H9C 109.5 . . ?
H9B C9 H9C 109.5 . . ?
P2 C10 H10A 108.6 . . ?
P2 C10 H10B 108.6 . . ?
H10A C10 H10B 107.5 . . ?
C11 C10 P2 114.85(13) . . ?
C11 C10 H10A 108.6 . . ?
C11 C10 H10B 108.6 . . ?
C10 C11 H11A 109.5 . . ?
C10 C11 H11B 109.5 . . ?
C10 C11 H11C 109.5 . . ?
H11A C11 H11B 109.5 . . ?
H11A C11 H11C 109.5 . . ?
H11B C11 H11C 109.5 . . ?
P2 C12 H12A 107.9 . . ?
P2 C12 H12B 107.9 . . ?
N1 C12 P2 117.67(11) . . ?
N1 C12 H12A 107.9 . . ?
N1 C12 H12B 107.9 . . ?
H12A C12 H12B 107.2 . . ?
P1 C13 H13A 108.4 . . ?
P1 C13 H13B 108.4 . . ?
N1 C13 P1 115.42(11) . . ?
N1 C13 H13A 108.4 . . ?
N1 C13 H13B 108.4 . . ?
H13A C13 H13B 107.5 . . ?
N1 C14 H14A 109.5 . . ?
N1 C14 H14B 109.5 . . ?
N1 C14 H14C 109.5 . . ?
H14A C14 H14B 109.5 . . ?
H14A C14 H14C 109.5 . . ?
H14B C14 H14C 109.5 . . ?
O4 S1 C15 104.17(10) . . ?
O5 S1 O4 113.20(9) . . ?
O5 S1 O6 115.24(10) . . ?
O5 S1 C15 104.40(11) . . ?
O6 S1 O4 114.44(9) . . ?
O6 S1 C15 103.64(10) . . ?
F1 C15 S1 111.29(18) . . ?
F1 C15 F2 108.5(2) . . ?
F1 C15 F3 107.75(19) . . ?
F2 C15 S1 110.30(16) . . ?
F2 C15 F3 108.3(2) . . ?
F3 C15 S1 110.61(16) . . ?

_olex2_submission_special_instructions 'No special instructions were received'
loop_
_exptl_crystal_face_index_h
_exptl_crystal_face_index_k
_exptl_crystal_face_index_l
_exptl_crystal_face_perp_dist
0.00 0.00 1.00 0.0320
0.00 0.00 -1.00 0.0250
-1.00 0.00 0.00 0.2530
1.00 0.00 0.00 0.3390
0.00 1.00 0.00 0.0220
0.00 -1.00 0.00 0.0220

