# Electronic Supplementary Material (ESI) for Organic & Biomolecular Chemistry.
# This journal is © The Royal Society of Chemistry 2016

####################################################################### 
# 
# 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_rjkt1408
_database_code_depnum_ccdc_archive 'CCDC 1465173'
_audit_update_record             
;
2016-03-13 deposited with the CCDC.
2016-08-10 downloaded from the CCDC.
;
_audit_creation_date             2014-05-13
_audit_creation_method           
;
Olex2 1.2
(compiled 2014.03.20 svn.r2914 for OlexSys, GUI svn.r4816)
;
_shelxl_version_number           2013-4
_chemical_name_common            ?
_chemical_name_systematic        
'(+-)-diethyl ((1R,5S,6S)-2-oxo-6-phenyl-3-oxabicyclo[3.1.0]hexan-1-yl)phosphonate'
_chemical_formula_moiety         'C15 H19 O5 P'
_chemical_formula_sum            'C15 H19 O5 P'
_chemical_formula_weight         310.27
_chemical_melting_point          352-354
_chemical_oxdiff_formula         'C15 H19 O5 P1'
_chemical_oxdiff_usercomment     'Matthew MGL/04/67-P'
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'
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'

_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                   12.11290(15)
_cell_length_b                   10.43581(14)
_cell_length_c                   11.94338(15)
_cell_angle_alpha                90
_cell_angle_beta                 90.0578(13)
_cell_angle_gamma                90
_cell_volume                     1509.74(3)
_cell_formula_units_Z            4
_cell_measurement_reflns_used    6651
_cell_measurement_temperature    110.05(10)
_cell_measurement_theta_max      32.0880
_cell_measurement_theta_min      3.4130
_shelx_estimated_absorpt_T_max   ?
_shelx_estimated_absorpt_T_min   ?
_exptl_absorpt_coefficient_mu    0.201
_exptl_absorpt_correction_T_max  0.976
_exptl_absorpt_correction_T_min  0.963
_exptl_absorpt_correction_type   gaussian
_exptl_absorpt_process_details   
;
CrysAlisPro, Agilent Technologies,
Version 1.171.37.33 (release 27-03-2014 CrysAlis171 .NET)
(compiled Mar 27 2014,17:12:48)
Numerical absorption correction based on gaussian integration over
			a multifaceted crystal model
Empirical absorption correction using spherical harmonics,
 implemented in SCALE3 ABSPACK scaling algorithm.
;
_exptl_crystal_colour            'clear colourless'
_exptl_crystal_colour_lustre     clear
_exptl_crystal_colour_modifier   .
_exptl_crystal_colour_primary    colourless
_exptl_crystal_density_diffrn    1.365
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    ?
_exptl_crystal_description       irregular
_exptl_crystal_F_000             656
_exptl_crystal_size_max          0.2985
_exptl_crystal_size_mid          0.1689
_exptl_crystal_size_min          0.1447
_exptl_special_details           
;
 ?
;
_exptl_transmission_factor_max   ?
_exptl_transmission_factor_min   ?
_diffrn_reflns_av_R_equivalents  0.0209
_diffrn_reflns_av_unetI/netI     0.0210
_diffrn_reflns_Laue_measured_fraction_full 0.977
_diffrn_reflns_Laue_measured_fraction_max 0.954
_diffrn_reflns_limit_h_max       17
_diffrn_reflns_limit_h_min       -17
_diffrn_reflns_limit_k_max       13
_diffrn_reflns_limit_k_min       -14
_diffrn_reflns_limit_l_max       16
_diffrn_reflns_limit_l_min       -16
_diffrn_reflns_number            13086
_diffrn_reflns_point_group_measured_fraction_full 0.977
_diffrn_reflns_point_group_measured_fraction_max 0.954
_diffrn_reflns_theta_full        25.242
_diffrn_reflns_theta_max         30.032
_diffrn_reflns_theta_min         3.089
_diffrn_ambient_environment      N~2~
_diffrn_ambient_temperature      110.05(10)
_diffrn_detector                 'CCD plate'
_diffrn_detector_area_resol_mean 16.1450
_diffrn_detector_type            Eos
_diffrn_measured_fraction_theta_full 0.977
_diffrn_measured_fraction_theta_max 0.954
_diffrn_measurement_device       'four-circle diffractometer'
_diffrn_measurement_device_type  'SuperNova, Single source at offset, Eos'
_diffrn_measurement_method       'ω scans'
_diffrn_orient_matrix_UB_11      -0.0074880000
_diffrn_orient_matrix_UB_12      0.0513004000
_diffrn_orient_matrix_UB_13      -0.0382073000
_diffrn_orient_matrix_UB_21      -0.0572668000
_diffrn_orient_matrix_UB_22      0.0009036000
_diffrn_orient_matrix_UB_23      0.0124242000
_diffrn_orient_matrix_UB_31      0.0097598000
_diffrn_orient_matrix_UB_32      0.0445752000
_diffrn_orient_matrix_UB_33      0.0437157000
_diffrn_radiation_monochromator  mirror
_diffrn_radiation_probe          x-ray
_diffrn_radiation_type           MoK\a
_diffrn_radiation_wavelength     0.71073
_diffrn_source                   'SuperNova (Mo) X-ray Source'
_diffrn_special_details          ?
_reflns_Friedel_coverage         0.000
_reflns_Friedel_fraction_full    .
_reflns_Friedel_fraction_max     .
_reflns_number_gt                3798
_reflns_number_total             4207
_reflns_odcompleteness_completeness 95.19
_reflns_odcompleteness_iscentric 1
_reflns_odcompleteness_theta     29.97
_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 1.171.37.33 (release 27-03-2014 CrysAlis171 .NET)
(compiled Mar 27 2014,17:12:48)
;
_computing_data_collection       
;
CrysAlisPro, Agilent Technologies,
Version 1.171.37.33 (release 27-03-2014 CrysAlis171 .NET)
(compiled Mar 27 2014,17:12:48)
;
_computing_data_reduction        
;
CrysAlisPro, Agilent Technologies,
Version 1.171.37.33 (release 27-03-2014 CrysAlis171 .NET)
(compiled Mar 27 2014,17:12:48)
;
_computing_molecular_graphics    'Olex2 (Dolomanov et al., 2009)'
_computing_publication_material  'Olex2 (Dolomanov et al., 2009)'
_computing_structure_refinement  'ShelXL (Sheldrick, 2008)'
_computing_structure_solution    'ShelXS (Sheldrick, 2008)'
_refine_diff_density_max         0.388
_refine_diff_density_min         -0.339
_refine_diff_density_rms         0.047
_refine_ls_extinction_coef       .
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.080
_refine_ls_hydrogen_treatment    constr
_refine_ls_matrix_type           full
_refine_ls_number_parameters     197
_refine_ls_number_reflns         4207
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.0368
_refine_ls_R_factor_gt           0.0328
_refine_ls_restrained_S_all      1.080
_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)+(0.0373P)²+0.6632P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.0859
_refine_ls_wR_factor_ref         0.0886
_refine_special_details          
;
One of the ethyl groups was disordered with the terminal methyl modelled in two positions with
refined occupancies of 0.878:0.122(6).  The ADP of these methyls were constrained to be equal.
;
_olex2_refinement_description    
;
1. Fixed Uiso
 At 1.2 times of:
  All C(H) groups, All C(H,H) groups, All C(H,H,H,H) groups
 At 1.5 times of:
  All C(H,H,H) groups
2. Uiso/Uaniso restraints and constraints
Uanis(C15A) = Uanis(C15B)
3. Others
 Sof(H14C)=Sof(H14D)=Sof(C15B)=Sof(H15D)=Sof(H15E)=Sof(H15F)=1-FVAR(1)
 Sof(H14A)=Sof(H14B)=Sof(C15A)=Sof(H15A)=Sof(H15B)=Sof(H15C)=FVAR(1)
4.a Ternary CH refined with riding coordinates:
 C3(H3), C4(H4)
4.b Secondary CH2 refined with riding coordinates:
 C5(H5A,H5B), C12(H12A,H12B), C14(H14A,H14B), C14(H14C,H14D)
4.c Aromatic/amide H refined with riding coordinates:
 C7(H7), C8(H8), C9(H9), C10(H10), C11(H11)
4.d Idealised Me refined as rotating group:
 C13(H13A,H13B,H13C), C15A(H15A,H15B,H15C), C15B(H15D,H15E,H15F)
;
_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
C1 C 0.45418(9) 0.06531(11) 0.85109(9) 0.0165(2) Uani 1 1 d . . . . .
C2 C 0.37325(9) -0.00018(10) 0.77579(9) 0.01413(19) Uani 1 1 d . . . . .
C3 C 0.42672(9) -0.03563(11) 0.66178(9) 0.0158(2) Uani 1 1 d . . . . .
H3 H 0.4998 0.0021 0.6492 0.019 Uiso 1 1 calc R . . . .
C4 C 0.42238(9) -0.13155(11) 0.75355(9) 0.0168(2) Uani 1 1 d . . . . .
H4 H 0.3735 -0.2059 0.7466 0.020 Uiso 1 1 calc R . . . .
C5 C 0.52382(10) -0.14009(12) 0.82731(10) 0.0213(2) Uani 1 1 d . . . . .
H5A H 0.5109 -0.1979 0.8895 0.026 Uiso 1 1 calc R . . . .
H5B H 0.5866 -0.1710 0.7848 0.026 Uiso 1 1 calc R . . . .
C6 C 0.35739(9) -0.04927(10) 0.55844(9) 0.0151(2) Uani 1 1 d . . . . .
C7 C 0.33226(9) 0.05939(11) 0.49525(9) 0.0172(2) Uani 1 1 d . . . . .
H7 H 0.3572 0.1393 0.5187 0.021 Uiso 1 1 calc R . . . .
C8 C 0.27005(10) 0.04932(12) 0.39732(10) 0.0200(2) Uani 1 1 d . . . . .
H8 H 0.2541 0.1221 0.3554 0.024 Uiso 1 1 calc R . . . .
C9 C 0.23209(10) -0.06958(12) 0.36278(10) 0.0226(2) Uani 1 1 d . . . . .
H9 H 0.1901 -0.0765 0.2979 0.027 Uiso 1 1 calc R . . . .
C10 C 0.25669(10) -0.17846(12) 0.42488(10) 0.0228(2) Uani 1 1 d . . . . .
H10 H 0.2307 -0.2581 0.4017 0.027 Uiso 1 1 calc R . . . .
C11 C 0.32021(10) -0.16854(11) 0.52179(10) 0.0194(2) Uani 1 1 d . . . . .
H11 H 0.3379 -0.2419 0.5623 0.023 Uiso 1 1 calc R . . . .
C12 C 0.07959(10) -0.05112(13) 0.65388(12) 0.0265(3) Uani 1 1 d . . . . .
H12A H 0.1056 -0.0092 0.5864 0.032 Uiso 1 1 calc R . . . .
H12B H 0.0249 0.0036 0.6890 0.032 Uiso 1 1 calc R . . . .
C13 C 0.02957(11) -0.17845(15) 0.62554(13) 0.0344(3) Uani 1 1 d . . . . .
H13A H -0.0297 -0.1664 0.5732 0.052 Uiso 1 1 calc GR . . . .
H13B H 0.0016 -0.2177 0.6924 0.052 Uiso 1 1 calc GR . . . .
H13C H 0.0848 -0.2328 0.5929 0.052 Uiso 1 1 calc GR . . . .
C14 C 0.20450(10) 0.10973(12) 1.00446(10) 0.0221(2) Uani 1 1 d . . . . .
H14A H 0.1977 0.1944 0.9717 0.027 Uiso 0.878(6) 1 calc R . P A 1
H14B H 0.2744 0.1053 1.0439 0.027 Uiso 0.878(6) 1 calc R . P A 1
H14C H 0.2801 0.1349 1.0197 0.027 Uiso 0.122(6) 1 calc R . P A 2
H14D H 0.1633 0.1851 0.9817 0.027 Uiso 0.122(6) 1 calc R . P A 2
C15A C 0.11117(19) 0.08675(18) 1.08476(13) 0.0276(4) Uani 0.878(6) 1 d . . P A
1
H15A H 0.0421 0.1012 1.0473 0.041 Uiso 0.878(6) 1 calc GR . P A 1
H15B H 0.1177 0.1444 1.1471 0.041 Uiso 0.878(6) 1 calc GR . P A 1
H15C H 0.1141 -0.0001 1.1112 0.041 Uiso 0.878(6) 1 calc GR . P A 1
C15B C 0.1571(15) 0.0553(14) 1.0997(10) 0.0276(4) Uani 0.122(6) 1 d . . P A 2
H15D H 0.0819 0.0323 1.0839 0.041 Uiso 0.122(6) 1 calc GR . P A 2
H15E H 0.1589 0.1161 1.1600 0.041 Uiso 0.122(6) 1 calc GR . P A 2
H15F H 0.1978 -0.0199 1.1206 0.041 Uiso 0.122(6) 1 calc GR . P A 2
O1 O 0.54378(7) -0.01031(9) 0.86760(7) 0.02146(18) Uani 1 1 d . . . . .
O2 O 0.44713(7) 0.17012(8) 0.89253(7) 0.02092(18) Uani 1 1 d . . . . .
O3 O 0.20414(7) 0.17082(8) 0.75111(7) 0.02042(17) Uani 1 1 d . . . . .
O4 O 0.17142(7) -0.07327(8) 0.73031(7) 0.01950(17) Uani 1 1 d . . . . .
O5 O 0.20129(7) 0.01278(8) 0.91657(7) 0.02064(17) Uani 1 1 d . . . . .
P1 P 0.23081(2) 0.04143(3) 0.79066(2) 0.01451(8) 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
C1 C2 1.4950(14) . ?
C1 O1 1.3562(13) . ?
C1 O2 1.2036(14) . ?
C2 C3 1.5532(15) . ?
C2 C4 1.5181(15) . ?
C2 P1 1.7882(11) . ?
C3 C4 1.4853(15) . ?
C3 C6 1.4988(14) . ?
C4 C5 1.5138(15) . ?
C5 O1 1.4575(15) . ?
C6 C7 1.3955(15) . ?
C6 C11 1.3940(15) . ?
C7 C8 1.3946(15) . ?
C8 C9 1.3859(17) . ?
C9 C10 1.3892(17) . ?
C10 C11 1.3930(15) . ?
C12 C13 1.4989(18) . ?
C12 O4 1.4568(13) . ?
C14 C15A 1.502(2) . ?
C14 C15B 1.395(13) . ?
C14 O5 1.4585(14) . ?
O3 P1 1.4664(8) . ?
O4 P1 1.5712(8) . ?
O5 P1 1.5747(9) . ?

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
O1 C1 C2 110.22(9) . . ?
O2 C1 C2 128.03(10) . . ?
O2 C1 O1 121.74(10) . . ?
C1 C2 C3 111.26(9) . . ?
C1 C2 C4 105.14(8) . . ?
C1 C2 P1 117.47(8) . . ?
C3 C2 P1 123.24(7) . . ?
C4 C2 C3 57.83(7) . . ?
C4 C2 P1 127.97(8) . . ?
C4 C3 C2 59.90(7) . . ?
C4 C3 C6 121.56(10) . . ?
C6 C3 C2 120.71(9) . . ?
C3 C4 C2 62.27(7) . . ?
C3 C4 C5 116.10(10) . . ?
C5 C4 C2 105.63(9) . . ?
O1 C5 C4 105.77(9) . . ?
C7 C6 C3 119.33(10) . . ?
C11 C6 C3 121.59(10) . . ?
C11 C6 C7 119.04(9) . . ?
C8 C7 C6 120.65(10) . . ?
C9 C8 C7 119.73(10) . . ?
C8 C9 C10 120.17(10) . . ?
C9 C10 C11 120.05(11) . . ?
C10 C11 C6 120.35(11) . . ?
O4 C12 C13 108.00(11) . . ?
C15B C14 O5 107.1(5) . . ?
O5 C14 C15A 109.22(10) . . ?
C1 O1 C5 111.12(8) . . ?
C12 O4 P1 121.04(8) . . ?
C14 O5 P1 123.35(8) . . ?
O3 P1 C2 113.82(5) . . ?
O3 P1 O4 116.94(5) . . ?
O3 P1 O5 115.62(5) . . ?
O4 P1 C2 102.17(5) . . ?
O4 P1 O5 100.90(5) . . ?
O5 P1 C2 105.59(5) . . ?

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
C1 C2 C3 C4 94.96(10) . . . . ?
C1 C2 C3 C6 -153.98(10) . . . . ?
C1 C2 C4 C3 -105.87(9) . . . . ?
C1 C2 C4 C5 5.78(12) . . . . ?
C1 C2 P1 O3 70.62(9) . . . . ?
C1 C2 P1 O4 -162.38(8) . . . . ?
C1 C2 P1 O5 -57.26(9) . . . . ?
C2 C1 O1 C5 -11.94(13) . . . . ?
C2 C3 C4 C5 -94.67(10) . . . . ?
C2 C3 C6 C7 85.37(13) . . . . ?
C2 C3 C6 C11 -96.70(13) . . . . ?
C2 C4 C5 O1 -12.37(12) . . . . ?
C3 C2 C4 C5 111.65(10) . . . . ?
C3 C2 P1 O3 -75.42(10) . . . . ?
C3 C2 P1 O4 51.58(10) . . . . ?
C3 C2 P1 O5 156.71(8) . . . . ?
C3 C4 C5 O1 53.99(13) . . . . ?
C3 C6 C7 C8 178.54(11) . . . . ?
C3 C6 C11 C10 -179.43(11) . . . . ?
C4 C2 C3 C6 111.06(11) . . . . ?
C4 C2 P1 O3 -148.20(9) . . . . ?
C4 C2 P1 O4 -21.20(10) . . . . ?
C4 C2 P1 O5 83.93(10) . . . . ?
C4 C3 C6 C7 156.73(11) . . . . ?
C4 C3 C6 C11 -25.35(16) . . . . ?
C4 C5 O1 C1 15.34(12) . . . . ?
C6 C3 C4 C2 -109.68(11) . . . . ?
C6 C3 C4 C5 155.65(10) . . . . ?
C6 C7 C8 C9 0.47(18) . . . . ?
C7 C6 C11 C10 -1.50(17) . . . . ?
C7 C8 C9 C10 -0.55(18) . . . . ?
C8 C9 C10 C11 -0.39(19) . . . . ?
C9 C10 C11 C6 1.43(19) . . . . ?
C11 C6 C7 C8 0.56(17) . . . . ?
C12 O4 P1 C2 -136.13(9) . . . . ?
C12 O4 P1 O3 -11.17(11) . . . . ?
C12 O4 P1 O5 115.11(10) . . . . ?
C13 C12 O4 P1 -170.76(9) . . . . ?
C14 O5 P1 C2 94.79(9) . . . . ?
C14 O5 P1 O3 -31.99(10) . . . . ?
C14 O5 P1 O4 -159.15(9) . . . . ?
C15A C14 O5 P1 143.08(12) . . . . ?
C15B C14 O5 P1 170.8(8) . . . . ?
O1 C1 C2 C3 -57.43(12) . . . . ?
O1 C1 C2 C4 3.45(12) . . . . ?
O1 C1 C2 P1 152.66(8) . . . . ?
O2 C1 C2 C3 121.49(13) . . . . ?
O2 C1 C2 C4 -177.63(11) . . . . ?
O2 C1 C2 P1 -28.42(16) . . . . ?
O2 C1 O1 C5 169.06(11) . . . . ?
P1 C2 C3 C4 -117.18(10) . . . . ?
P1 C2 C3 C6 -6.12(14) . . . . ?
P1 C2 C4 C3 109.30(10) . . . . ?
P1 C2 C4 C5 -139.05(9) . . . . ?

loop_
_exptl_crystal_face_index_h
_exptl_crystal_face_index_k
_exptl_crystal_face_index_l
_exptl_crystal_face_perp_dist
_exptl_oxdiff_crystal_face_indexfrac_h
_exptl_oxdiff_crystal_face_indexfrac_k
_exptl_oxdiff_crystal_face_indexfrac_l
_exptl_oxdiff_crystal_face_x
_exptl_oxdiff_crystal_face_y
_exptl_oxdiff_crystal_face_z
-1 0 0 0.1074 -0.9993 -0.0009 -0.0013 0.0075 0.0572 -0.0098
-2 -4 -3 0.1693 -1.9913 -4.0010 -2.9990 -0.0758 0.0732 -0.3289
-2 -1 -2 0.1391 -1.9958 -1.0023 -2.0014 0.0400 0.0885 -0.1517
0 3 -5 0.0724 0.0003 2.9952 -5.0014 0.3447 -0.0594 -0.0851
0 -3 5 0.0724 -0.0003 -2.9952 5.0014 -0.3447 0.0594 0.0851
0 -4 5 0.0765 0.0010 -3.9945 5.0022 -0.3960 0.0585 0.0406
1 2 -2 0.0939 0.9984 1.9984 -1.9999 0.1715 -0.0802 0.0114
-2 0 5 0.0825 -2.0027 0.0011 4.9966 -0.1759 0.1768 0.1989
-5 -4 2 0.1026 -4.9933 -4.0007 1.9963 -0.2441 0.3071 -0.1398
-1 2 1 0.0673 -1.0026 1.9984 0.9970 0.0719 0.0716 0.1229
1 0 -4 0.1136 1.0025 -0.0014 -3.9980 0.1452 -0.1071 -0.1651
1 0 0 0.0614 0.9993 0.0009 0.0013 -0.0075 -0.0572 0.0098
-2 1 -2 0.1169 -1.9983 0.9964 -2.0030 0.1426 0.0905 -0.0626
5 -4 1 0.1026 5.0009 -3.9924 1.0093 -0.2808 -0.2775 -0.0850

_exptl_crystal_recrystallization_method 'Re-crystallisation from solvent'
_solvent_exptl_crystal_recrystallization_method 'diethyl ether/chloroform'
