#------------------------------------------------------------------------------
#$Date: 2016-03-26 02:12:40 +0200 (Sat, 26 Mar 2016) $
#$Revision: 180128 $
#$URL: svn://www.crystallography.net/cod/cif/7/10/26/7102619.cif $
#------------------------------------------------------------------------------
#
# This file is available in the Crystallography Open Database (COD),
# http://www.crystallography.net/
#
# All data on this site have been placed in the public domain by the
# contributors.
#
data_7102619
loop_
_publ_author_name
'Fawcett, John'
'Moralee, Andrew C'
'Percy, Jonathan M'
'Salafia, Vittoria'
'Vincent, Mark A'
'Hillier, Ian H'
_publ_section_title
;
 A surprising steric effect on a tandem cycloaddition/ring-opening
 reaction: rapid syntheses of difluorinated analogues of
 (hydroxymethyl)conduritols.
;
_journal_issue                   9
_journal_name_full
'Chemical communications (Cambridge, England)'
_journal_page_first              1062
_journal_page_last               1063
_journal_paper_doi               10.1039/b401245c
_journal_year                    2004
_chemical_formula_sum            'C14 H19 Cl4 F2 N O5 Sn'
_chemical_formula_weight         579.79
_chemical_name_systematic
;
?
;
_space_group_IT_number           14
_symmetry_cell_setting           monoclinic
_symmetry_space_group_name_Hall  '-P 2yn'
_symmetry_space_group_name_H-M   'P 1 21/n 1'
_atom_sites_solution_hydrogens   geom
_atom_sites_solution_primary     direct
_atom_sites_solution_secondary   difmap
_audit_creation_method           SHELXL-97
_cell_angle_alpha                90.00
_cell_angle_beta                 102.993(2)
_cell_angle_gamma                90.00
_cell_formula_units_Z            4
_cell_length_a                   10.4879(11)
_cell_length_b                   18.8071(19)
_cell_length_c                   10.7203(11)
_cell_measurement_reflns_used    7168
_cell_measurement_temperature    150(2)
_cell_measurement_theta_max      28.39
_cell_measurement_theta_min      2.23
_cell_volume                     2060.4(4)
_computing_cell_refinement       'Bruker SMART'
_computing_data_collection       'Bruker SMART'
_computing_data_reduction        'Bruker SAINT'
_computing_molecular_graphics    'Bruker SHELXTL'
_computing_publication_material  'Bruker SHELXTL'
_computing_structure_refinement  'SHELXL-97 (Sheldrick, 1997)'
_computing_structure_solution    'SHELXS-97 (Sheldrick, 1990)'
_diffrn_ambient_temperature      150(2)
_diffrn_measured_fraction_theta_full 0.994
_diffrn_measured_fraction_theta_max 0.994
_diffrn_measurement_device_type  'CCD area detector'
_diffrn_measurement_method       'phi and omega scans'
_diffrn_radiation_monochromator  graphite
_diffrn_radiation_source         'fine-focus sealed tube'
_diffrn_radiation_type           MoK\a
_diffrn_radiation_wavelength     0.71073
_diffrn_reflns_av_R_equivalents  0.0261
_diffrn_reflns_av_sigmaI/netI    0.0253
_diffrn_reflns_limit_h_max       11
_diffrn_reflns_limit_h_min       -12
_diffrn_reflns_limit_k_max       21
_diffrn_reflns_limit_k_min       -23
_diffrn_reflns_limit_l_max       13
_diffrn_reflns_limit_l_min       -13
_diffrn_reflns_number            10971
_diffrn_reflns_theta_full        26.00
_diffrn_reflns_theta_max         26.00
_diffrn_reflns_theta_min         2.17
_exptl_absorpt_coefficient_mu    1.802
_exptl_absorpt_correction_T_max  0.89
_exptl_absorpt_correction_T_min  0.80
_exptl_absorpt_correction_type   empirical
_exptl_absorpt_process_details
;
absorption correction based on 5879 reflections (SADABS); Rint 0.034 before
correction and 0.014 after.
;
_exptl_crystal_colour            colourless
_exptl_crystal_density_diffrn    1.869
_exptl_crystal_density_method    'not measured'
_exptl_crystal_description       block
_exptl_crystal_F_000             1144
_exptl_crystal_size_max          0.30
_exptl_crystal_size_mid          0.29
_exptl_crystal_size_min          0.19
_refine_diff_density_max         0.710
_refine_diff_density_min         -0.336
_refine_diff_density_rms         0.077
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.058
_refine_ls_hydrogen_treatment    mixed
_refine_ls_matrix_type           full
_refine_ls_number_parameters     247
_refine_ls_number_reflns         4033
_refine_ls_number_restraints     0
_refine_ls_restrained_S_all      1.058
_refine_ls_R_factor_all          0.0278
_refine_ls_R_factor_gt           0.0254
_refine_ls_shift/su_max          0.001
_refine_ls_shift/su_mean         0.000
_refine_ls_structure_factor_coef Fsqd
_refine_ls_weighting_details
'calc w=1/[σ²(Fo²)+(0.0328P)²+1.0826P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.0639
_refine_ls_wR_factor_ref         0.0651
_reflns_number_gt                3761
_reflns_number_total             4033
_reflns_threshold_expression     >2sigma(I)
_cod_data_source_file            b401245c_cif.txt
_cod_data_source_block           6a
_cod_depositor_comments
;
The following automatic conversions were performed:
'_symmetry_cell_setting' value 'Monoclinic' changed to 'monoclinic'
according to '/home/saulius/struct/CIF-dictionaries/cif_core.dic'
dictionary named 'cif_core.dic' version 2.4.1 from 2010-06-29.

Automatic conversion script
Id: cif_fix_enum 1527 2010-12-29 10:47:43Z saulius 
;
_cod_original_sg_symbol_H-M      P2(1)/n
_cod_database_code               7102619
loop_
_symmetry_equiv_pos_as_xyz
'x, y, z'
'-x+1/2, y+1/2, -z+1/2'
'-x, -y, -z'
'x-1/2, -y-1/2, z-1/2'
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_symmetry_multiplicity
_atom_site_calc_flag
_atom_site_refinement_flags
Sn1 Sn 0.732849(17) 0.482949(9) 0.775439(15) 0.02270(7) Uani 1 1 d .
Cl1 Cl 0.50709(7) 0.50333(4) 0.70984(8) 0.04142(18) Uani 1 1 d .
Cl2 Cl 0.74585(7) 0.52387(3) 0.98742(6) 0.02899(15) Uani 1 1 d .
Cl3 Cl 0.74903(7) 0.42475(4) 0.58570(6) 0.03208(16) Uani 1 1 d .
Cl4 Cl 0.82018(9) 0.58959(4) 0.71858(7) 0.0439(2) Uani 1 1 d .
F1 F 0.78495(15) 0.23688(8) 0.87737(14) 0.0310(3) Uani 1 1 d .
F2 F 0.88786(17) 0.25825(9) 0.72809(14) 0.0376(4) Uani 1 1 d .
N1 N 0.6762(2) 0.34931(11) 1.04422(19) 0.0230(4) Uani 1 1 d .
O1 O 1.12119(18) 0.24508(10) 0.92390(18) 0.0307(4) Uani 1 1 d .
O2 O 0.93782(17) 0.44521(9) 0.84473(16) 0.0230(4) Uani 1 1 d .
O3 O 1.06855(18) 0.36946(9) 0.77628(17) 0.0286(4) Uani 1 1 d .
O4 O 0.87694(16) 0.34858(9) 1.00860(15) 0.0189(3) Uani 1 1 d .
O5 O 0.70338(16) 0.37991(9) 0.84833(15) 0.0212(4) Uani 1 1 d .
C1 C 1.0874(2) 0.29510(14) 1.0102(2) 0.0244(5) Uani 1 1 d .
H1 H 1.1558 0.3319 1.0421 0.029 Uiso 1 1 calc R
C2 C 0.9553(2) 0.32511(13) 0.9250(2) 0.0187(5) Uani 1 1 d .
C3 C 0.9025(3) 0.25417(14) 0.8545(2) 0.0259(5) Uani 1 1 d .
C4 C 1.0109(3) 0.20043(14) 0.9156(3) 0.0288(6) Uani 1 1 d .
H4 H 1.0124 0.1555 0.8661 0.035 Uiso 1 1 calc R
C5 C 1.0033(3) 0.19049(15) 1.0527(3) 0.0327(6) Uani 1 1 d .
H5 H 0.9709 0.1503 1.0895 0.039 Uiso 1 1 calc R
C6 C 1.0520(2) 0.25047(15) 1.1120(2) 0.0274(6) Uani 1 1 d .
H6 H 1.0618 0.2621 1.1999 0.033 Uiso 1 1 calc R
C7 C 0.9840(2) 0.38575(13) 0.8422(2) 0.0211(5) Uani 1 1 d .
C8 C 1.1058(3) 0.42550(16) 0.6945(3) 0.0352(7) Uani 1 1 d .
H8A H 1.0274 0.4431 0.6326 0.042 Uiso 1 1 calc R
H8B H 1.1469 0.4660 0.7477 0.042 Uiso 1 1 calc R
C9 C 1.1970(5) 0.3944(2) 0.6277(4) 0.0737(13) Uani 1 1 d .
H9A H 1.2719 0.3749 0.6899 0.111 Uiso 1 1 calc R
H9B H 1.2275 0.4310 0.5761 0.111 Uiso 1 1 calc R
H9C H 1.1536 0.3563 0.5716 0.111 Uiso 1 1 calc R
C10 C 0.7476(2) 0.36033(12) 0.9620(2) 0.0200(5) Uani 1 1 d .
C11 C 0.5366(3) 0.36802(15) 1.0106(3) 0.0313(6) Uani 1 1 d .
H11A H 0.5235 0.4087 0.9506 0.038 Uiso 1 1 calc R
H11B H 0.5085 0.3829 1.0889 0.038 Uiso 1 1 calc R
C12 C 0.4536(3) 0.30654(18) 0.9499(3) 0.0426(7) Uani 1 1 d .
H12A H 0.4763 0.2943 0.8687 0.064 Uiso 1 1 calc R
H12B H 0.3610 0.3199 0.9338 0.064 Uiso 1 1 calc R
H12C H 0.4695 0.2655 1.0075 0.064 Uiso 1 1 calc R
C13 C 0.7291(3) 0.31724(14) 1.1705(2) 0.0275(6) Uani 1 1 d .
H13A H 0.7965 0.2817 1.1627 0.033 Uiso 1 1 calc R
H13B H 0.6580 0.2922 1.1994 0.033 Uiso 1 1 calc R
C14 C 0.7889(3) 0.37190(16) 1.2694(3) 0.0362(7) Uani 1 1 d .
H14A H 0.8641 0.3941 1.2447 0.054 Uiso 1 1 calc R
H14B H 0.8178 0.3488 1.3528 0.054 Uiso 1 1 calc R
H14C H 0.7236 0.4084 1.2748 0.054 Uiso 1 1 calc R
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'
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'
F F 0.0171 0.0103 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
Sn Sn -0.6537 1.4246 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
Cl Cl 0.1484 0.1585 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
loop_
_geom_angle_atom_site_label_1
_geom_angle_atom_site_label_2
_geom_angle_atom_site_label_3
_geom_angle
O5 Sn1 O2 78.30(6)
O5 Sn1 Cl4 165.61(5)
O2 Sn1 Cl4 87.43(5)
O5 Sn1 Cl1 92.21(5)
O2 Sn1 Cl1 170.42(5)
Cl4 Sn1 Cl1 102.10(3)
O5 Sn1 Cl3 86.48(5)
O2 Sn1 Cl3 83.57(5)
Cl4 Sn1 Cl3 93.73(3)
Cl1 Sn1 Cl3 94.65(3)
O5 Sn1 Cl2 85.75(5)
O2 Sn1 Cl2 86.60(5)
Cl4 Sn1 Cl2 91.71(3)
Cl1 Sn1 Cl2 94.07(3)
Cl3 Sn1 Cl2 168.53(2)
C10 N1 C11 119.4(2)
C10 N1 C13 122.4(2)
C11 N1 C13 118.2(2)
C4 O1 C1 96.54(19)
C7 O2 Sn1 129.98(16)
C7 O3 C8 117.5(2)
C10 O4 C2 119.57(18)
C10 O5 Sn1 124.58(15)
O1 C1 C6 104.1(2)
O1 C1 C2 100.06(19)
C6 C1 C2 107.1(2)
O4 C2 C7 110.85(19)
O4 C2 C3 112.16(19)
C7 C2 C3 116.86(19)
O4 C2 C1 107.68(17)
C7 C2 C1 110.0(2)
C3 C2 C1 98.21(19)
F2 C3 F1 107.3(2)
F2 C3 C4 111.9(2)
F1 C3 C4 112.3(2)
F2 C3 C2 112.8(2)
F1 C3 C2 110.78(19)
C4 C3 C2 101.8(2)
O1 C4 C5 103.6(2)
O1 C4 C3 98.7(2)
C5 C4 C3 107.4(2)
C6 C5 C4 105.1(2)
C5 C6 C1 105.0(2)
O2 C7 O3 123.7(2)
O2 C7 C2 122.9(2)
O3 C7 C2 113.2(2)
C9 C8 O3 107.4(3)
O5 C10 N1 124.3(2)
O5 C10 O4 121.7(2)
N1 C10 O4 114.0(2)
N1 C11 C12 111.7(2)
N1 C13 C14 112.2(2)
loop_
_geom_bond_atom_site_label_1
_geom_bond_atom_site_label_2
_geom_bond_distance
Sn1 O5 2.1378(16)
Sn1 O2 2.2268(17)
Sn1 Cl4 2.3418(7)
Sn1 Cl1 2.3450(8)
Sn1 Cl3 2.3494(7)
Sn1 Cl2 2.3740(7)
F1 C3 1.350(3)
F2 C3 1.332(3)
N1 C10 1.295(3)
N1 C11 1.469(3)
N1 C13 1.472(3)
O1 C4 1.416(3)
O1 C1 1.419(3)
O2 C7 1.221(3)
O3 C7 1.289(3)
O3 C8 1.478(3)
O4 C10 1.354(3)
O4 C2 1.416(3)
O5 C10 1.258(3)
C1 C6 1.488(4)
C1 C2 1.582(3)
C2 C7 1.517(3)
C2 C3 1.571(3)
C3 C4 1.551(4)
C4 C5 1.502(4)
C5 C6 1.338(4)
C8 C9 1.442(5)
C11 C12 1.505(4)
C13 C14 1.508(4)
