####################################################################### 
# 
# 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_1
_database_code_depnum_ccdc_archive 'CCDC 892694'
_audit_update_record             
;
2012-07-18 deposited with the CCDC.
2015-06-01 downloaded from the CCDC.
;

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

_chemical_name_systematic        
;
?
;
_chemical_formula_moiety         'C19 H16 Br N2 O7 Re'
_chemical_formula_sum            'C19 H16 Br N2 O7 Re'
_chemical_formula_weight         650.45
_chemical_compound_source        'synthesis as described'

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

_symmetry_cell_setting           triclinic
_symmetry_space_group_name_H-M   'P -1'
_symmetry_space_group_name_Hall  '-P 1'
_symmetry_Int_Tables_number      2
loop_
_symmetry_equiv_pos_as_xyz
'x, y, z'
'-x, -y, -z'

_cell_length_a                   6.4256(2)
_cell_length_b                   12.2609(4)
_cell_length_c                   13.0947(5)
_cell_angle_alpha                94.561(2)
_cell_angle_beta                 101.729(2)
_cell_angle_gamma                94.970(2)
_cell_volume                     1001.31(6)
_cell_formula_units_Z            2
_cell_measurement_temperature    193(2)
_cell_measurement_reflns_used    9836
_cell_measurement_theta_min      3.19
_cell_measurement_theta_max      30.66
_cell_measurement_wavelength     0.71073

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

_exptl_crystal_description       plate
_exptl_crystal_colour            orange
_exptl_crystal_size_max          0.2
_exptl_crystal_size_mid          0.16
_exptl_crystal_size_min          0.08
_exptl_crystal_density_diffrn    2.157
_exptl_crystal_density_method    'not measured'
_exptl_crystal_F_000             620
_exptl_special_details           
;
?
;

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

_exptl_absorpt_coefficient_mu    8.108
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   'SADABS (Bruker-AXS)'
_exptl_absorpt_correction_T_min  0.2939
_exptl_absorpt_correction_T_max  0.5632

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

_diffrn_ambient_temperature      193(2)
_diffrn_radiation_wavelength     0.71073
_diffrn_radiation_type           MoK\a
_diffrn_radiation_source         'microfocus sealed tube'
_diffrn_radiation_monochromator  'multilayer optics'
_diffrn_measurement_device_type  'Bruker Kappa APEX II Quazar'
_diffrn_measurement_method       'phi and omega scans'
_diffrn_standards_number         0
_diffrn_standards_interval_count 0
_diffrn_standards_interval_time  0
_diffrn_standards_decay_%        0
_diffrn_radiation_probe          x-ray
_diffrn_reflns_av_R_equivalents  0.0331
_diffrn_reflns_av_unetI/netI     0.0306
_diffrn_reflns_number            23473
_diffrn_reflns_limit_h_min       -8
_diffrn_reflns_limit_h_max       9
_diffrn_reflns_limit_k_min       -17
_diffrn_reflns_limit_k_max       17
_diffrn_reflns_limit_l_min       -17
_diffrn_reflns_limit_l_max       18
_diffrn_reflns_theta_min         1.6
_diffrn_reflns_theta_max         30.68
_diffrn_reflns_theta_full        30.68
_diffrn_measured_fraction_theta_full 0.986
_diffrn_measured_fraction_theta_max 0.986
_reflns_number_total             6129
_reflns_number_gt                5850
_reflns_threshold_expression     >2sigma(I)

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

_computing_data_collection       'Bruker APEX2'
_computing_cell_refinement       'Bruker SAINT'
_computing_data_reduction        'Bruker SAINT'
_computing_structure_solution    'SHELXS-97 (Sheldrick, 1990)'
_computing_structure_refinement  'SHELXL-97 (Sheldrick, 2008)'
_computing_molecular_graphics    'Ortep-3 for Windows (Farrugia, 1997)'
_computing_publication_material  'WinGX publication routines (Farrugia, 1999)'

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

_atom_sites_solution_primary     direct
_atom_sites_solution_secondary   difmap
_atom_sites_solution_hydrogens   geom

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

_refine_special_details          
;
Refinement of F² against ALL reflections. The weighted R-factor wR and
goodness of fit S are based on F², conventional R-factors R are based
on F, with F set to zero for negative F². The threshold expression of
F² > 2sigma(F²) is used only for calculating R-factors(gt) etc. and is
not relevant to the choice of reflections for refinement. R-factors based
on F² are statistically about twice as large as those based on F, and R-
factors based on ALL data will be even larger.
;
_refine_ls_structure_factor_coef Fsqd
_refine_ls_matrix_type           full
_refine_ls_weighting_scheme      calc
_refine_ls_weighting_details     
'calc w=1/[σ²(Fo²)+(0.0000P)²+5.2563P] where P=(Fo²+2Fc²)/3'
_refine_ls_hydrogen_treatment    constr
_refine_ls_extinction_method     none
_refine_ls_number_reflns         6129
_refine_ls_number_parameters     302
_refine_ls_number_restraints     43
_refine_ls_R_factor_all          0.0347
_refine_ls_R_factor_gt           0.0326
_refine_ls_wR_factor_ref         0.0795
_refine_ls_wR_factor_gt          0.0786
_refine_ls_goodness_of_fit_ref   1.196
_refine_ls_restrained_S_all      1.197
_refine_ls_shift/su_max          0.002
_refine_ls_shift/su_mean         0
_refine_diff_density_max         1.092
_refine_diff_density_min         -2.099
_refine_diff_density_rms         0.142

#----------------------------------------------------------------------------#
# 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'
N N 0.0061 0.0033 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
O O 0.0106 0.006 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
Br Br -0.2901 2.4595 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
Re Re -1.0185 7.231 '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_symmetry_multiplicity
_atom_site_calc_flag
_atom_site_refinement_flags
_atom_site_disorder_assembly
_atom_site_disorder_group
C1 C 0.8279(8) 0.7235(4) 0.2078(4) 0.0326(10) Uani 1 1 d . A .
C2 C 1.2449(9) 0.7252(4) 0.3117(4) 0.0343(10) Uani 1 1 d . A .
C4 C 0.5871(7) 0.4733(4) 0.1355(3) 0.0258(8) Uani 1 1 d . . .
H4 H 0.5418 0.5429 0.1196 0.031 Uiso 1 1 calc R . .
C5 C 0.4444(7) 0.3798(4) 0.1005(3) 0.0279(9) Uani 1 1 d . . .
H5 H 0.3042 0.3852 0.062 0.034 Uiso 1 1 calc R . .
C7 C 0.7189(7) 0.2732(4) 0.1783(3) 0.0258(8) Uani 1 1 d . . .
H7 H 0.7684 0.2041 0.1928 0.031 Uiso 1 1 calc R . .
C8 C 0.8529(6) 0.3700(3) 0.2119(3) 0.0220(7) Uani 1 1 d . . .
C9 C 1.0721(6) 0.3716(3) 0.2727(3) 0.0221(7) Uani 1 1 d . . .
C10 C 1.1603(7) 0.2782(4) 0.3057(3) 0.0253(8) Uani 1 1 d . . .
H10 H 1.077 0.2087 0.2907 0.03 Uiso 1 1 calc R . .
C11 C 1.3701(7) 0.2859(4) 0.3608(3) 0.0251(8) Uani 1 1 d . . .
C12 C 1.4872(7) 0.3887(4) 0.3827(3) 0.0259(8) Uani 1 1 d . . .
H12 H 1.6324 0.3967 0.419 0.031 Uiso 1 1 calc R . .
C13 C 1.3877(7) 0.4791(4) 0.3504(3) 0.0244(8) Uani 1 1 d . . .
H13 H 1.4663 0.5497 0.3673 0.029 Uiso 1 1 calc R . .
C17 C 1.4594(8) 0.1830(4) 0.3949(4) 0.0293(9) Uani 1 1 d . . .
C18 C 1.7795(9) 0.0981(4) 0.4473(5) 0.0414(12) Uani 1 1 d . . .
H18A H 1.7084 0.066 0.5 0.05 Uiso 1 1 calc R . .
H18B H 1.9299 0.1229 0.4818 0.05 Uiso 1 1 calc R . .
C19 C 1.7748(10) 0.0113(5) 0.3590(5) 0.0459(13) Uani 1 1 d . . .
H19A H 1.6266 -0.0189 0.3294 0.069 Uiso 1 1 calc R . .
H19B H 1.8578 -0.0477 0.3855 0.069 Uiso 1 1 calc R . .
H19C H 1.8368 0.0439 0.3046 0.069 Uiso 1 1 calc R . .
N1 N 0.7863(6) 0.4697(3) 0.1907(3) 0.0223(7) Uani 1 1 d . A .
N2 N 1.1842(6) 0.4720(3) 0.2959(3) 0.0232(7) Uani 1 1 d . A .
O1 O 0.7128(8) 0.7867(4) 0.1822(4) 0.0555(11) Uani 1 1 d . . .
O2 O 1.3865(7) 0.7893(4) 0.3476(4) 0.0534(11) Uani 1 1 d . . .
O6 O 1.6721(5) 0.1933(3) 0.4106(3) 0.0343(7) Uani 1 1 d . . .
O7 O 1.3484(6) 0.1019(3) 0.4054(3) 0.0411(9) Uani 1 1 d . . .
Re1 Re 1.01549(3) 0.612858(14) 0.251239(13) 0.02339(5) Uani 1 1 d D . .
Br1 Br 1.12296(18) 0.59986(10) 0.07444(10) 0.0295(3) Uani 0.439(2) 1 d PDU A 1
C3 C 0.922(2) 0.6293(12) 0.3851(9) 0.0363(10) Uani 0.439(2) 1 d PDU A 1
O3 O 0.8620(14) 0.6438(9) 0.4620(7) 0.0383(9) Uani 0.439(2) 1 d PDU A 1
Br1' Br 0.91122(15) 0.60769(9) 0.42978(8) 0.0366(3) Uani 0.561(2) 1 d PDU A 2
C3' C 1.1157(15) 0.6234(9) 0.1222(8) 0.0318(9) Uani 0.561(2) 1 d PDU A 2
O3' O 1.1884(11) 0.6368(6) 0.0465(5) 0.0355(8) Uani 0.561(2) 1 d PDU A 2
O5 O 0.1734(7) 0.1805(4) 0.0458(4) 0.0534(12) Uani 1 1 d . . .
C14 C 0.3540(8) 0.1773(4) 0.0910(4) 0.0369(11) Uani 1 1 d . . .
C6 C 0.5110(7) 0.2786(4) 0.1231(3) 0.0271(8) Uani 1 1 d . . .
O4 O 0.4415(7) 0.0874(3) 0.1197(4) 0.0582(13) Uani 1 1 d . . .
C15 C 0.3088(12) -0.0209(6) 0.0883(7) 0.067(2) Uani 1 1 d . . .
H15A H 0.2264 -0.0229 0.0154 0.08 Uiso 1 1 calc R . .
H15B H 0.4024 -0.0811 0.0915 0.08 Uiso 1 1 calc R . .
C16 C 0.1649(15) -0.0359(8) 0.1582(6) 0.079(3) Uani 1 1 d . . .
H16A H 0.247 -0.0317 0.2304 0.118 Uiso 1 1 calc R . .
H16B H 0.0814 -0.108 0.1395 0.118 Uiso 1 1 calc R . .
H16C H 0.0681 0.0219 0.1522 0.118 Uiso 1 1 calc R . .



#----------------------------------------------------------------------------#
# 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 O1 1.141(6) . ?
C1 Re1 1.935(5) . ?
C2 O2 1.145(6) . ?
C2 Re1 1.923(5) . ?
C4 N1 1.342(5) . ?
C4 C5 1.389(6) . ?
C4 H4 0.95 . ?
C5 C6 1.381(7) . ?
C5 H5 0.95 . ?
C7 C8 1.390(6) . ?
C7 C6 1.393(6) . ?
C7 H7 0.95 . ?
C8 N1 1.359(5) . ?
C8 C9 1.468(6) . ?
C9 N2 1.350(5) . ?
C9 C10 1.383(6) . ?
C10 C11 1.385(6) . ?
C10 H10 0.95 . ?
C11 C12 1.389(6) . ?
C11 C17 1.493(6) . ?
C12 C13 1.379(6) . ?
C12 H12 0.95 . ?
C13 N2 1.348(5) . ?
C13 H13 0.95 . ?
C17 O7 1.206(6) . ?
C17 O6 1.333(6) . ?
C18 O6 1.471(6) . ?
C18 C19 1.501(8) . ?
C18 H18A 0.99 . ?
C18 H18B 0.99 . ?
C19 H19A 0.98 . ?
C19 H19B 0.98 . ?
C19 H19C 0.98 . ?
N1 Re1 2.176(3) . ?
N2 Re1 2.175(4) . ?
Re1 C3' 1.937(9) . ?
Re1 C3 1.966(11) . ?
Re1 Br1 2.5441(13) . ?
Re1 Br1' 2.5636(11) . ?
C3 O3 1.157(12) . ?
C3' O3' 1.195(11) . ?
O5 C14 1.196(6) . ?
C14 O4 1.327(7) . ?
C14 C6 1.505(6) . ?
O4 C15 1.495(7) . ?
C15 C16 1.438(12) . ?
C15 H15A 0.99 . ?
C15 H15B 0.99 . ?
C16 H16A 0.98 . ?
C16 H16B 0.98 . ?
C16 H16C 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
O1 C1 Re1 178.2(5) . . ?
O2 C2 Re1 177.6(5) . . ?
N1 C4 C5 122.8(4) . . ?
N1 C4 H4 118.6 . . ?
C5 C4 H4 118.6 . . ?
C6 C5 C4 118.5(4) . . ?
C6 C5 H5 120.7 . . ?
C4 C5 H5 120.7 . . ?
C8 C7 C6 119.2(4) . . ?
C8 C7 H7 120.4 . . ?
C6 C7 H7 120.4 . . ?
N1 C8 C7 121.4(4) . . ?
N1 C8 C9 116.1(4) . . ?
C7 C8 C9 122.6(4) . . ?
N2 C9 C10 121.4(4) . . ?
N2 C9 C8 115.3(4) . . ?
C10 C9 C8 123.4(4) . . ?
C9 C10 C11 120.0(4) . . ?
C9 C10 H10 120 . . ?
C11 C10 H10 120 . . ?
C10 C11 C12 118.7(4) . . ?
C10 C11 C17 118.4(4) . . ?
C12 C11 C17 123.0(4) . . ?
C13 C12 C11 118.4(4) . . ?
C13 C12 H12 120.8 . . ?
C11 C12 H12 120.8 . . ?
N2 C13 C12 123.1(4) . . ?
N2 C13 H13 118.4 . . ?
C12 C13 H13 118.4 . . ?
O7 C17 O6 125.8(4) . . ?
O7 C17 C11 122.8(4) . . ?
O6 C17 C11 111.5(4) . . ?
O6 C18 C19 111.9(4) . . ?
O6 C18 H18A 109.2 . . ?
C19 C18 H18A 109.2 . . ?
O6 C18 H18B 109.2 . . ?
C19 C18 H18B 109.2 . . ?
H18A C18 H18B 107.9 . . ?
C18 C19 H19A 109.5 . . ?
C18 C19 H19B 109.5 . . ?
H19A C19 H19B 109.5 . . ?
C18 C19 H19C 109.5 . . ?
H19A C19 H19C 109.5 . . ?
H19B C19 H19C 109.5 . . ?
C4 N1 C8 118.7(4) . . ?
C4 N1 Re1 124.8(3) . . ?
C8 N1 Re1 116.4(3) . . ?
C13 N2 C9 118.4(4) . . ?
C13 N2 Re1 124.3(3) . . ?
C9 N2 Re1 117.2(3) . . ?
C17 O6 C18 116.6(4) . . ?
C2 Re1 C1 90.7(2) . . ?
C2 Re1 C3' 85.7(4) . . ?
C1 Re1 C3' 87.8(3) . . ?
C2 Re1 C3 87.1(4) . . ?
C1 Re1 C3 85.9(5) . . ?
C3' Re1 C3 170.4(5) . . ?
C2 Re1 N2 97.31(18) . . ?
C1 Re1 N2 171.64(17) . . ?
C3' Re1 N2 95.1(3) . . ?
C3 Re1 N2 92.2(5) . . ?
C2 Re1 N1 172.12(18) . . ?
C1 Re1 N1 97.14(18) . . ?
C3' Re1 N1 94.8(3) . . ?
C3 Re1 N1 93.2(4) . . ?
N2 Re1 N1 74.81(13) . . ?
C2 Re1 Br1 92.91(16) . . ?
C1 Re1 Br1 90.88(15) . . ?
C3' Re1 Br1 7.9(3) . . ?
C3 Re1 Br1 176.8(5) . . ?
N2 Re1 Br1 90.99(9) . . ?
N1 Re1 Br1 87.24(9) . . ?
C2 Re1 Br1' 89.79(15) . . ?
C1 Re1 Br1' 93.40(15) . . ?
C3' Re1 Br1' 175.4(3) . . ?
C3 Re1 Br1' 8.0(5) . . ?
N2 Re1 Br1' 84.38(9) . . ?
N1 Re1 Br1' 89.48(9) . . ?
Br1 Re1 Br1' 174.90(4) . . ?
O3 C3 Re1 176.3(13) . . ?
O3' C3' Re1 174.9(9) . . ?
O5 C14 O4 125.8(5) . . ?
O5 C14 C6 122.7(5) . . ?
O4 C14 C6 111.6(4) . . ?
C5 C6 C7 119.4(4) . . ?
C5 C6 C14 119.0(4) . . ?
C7 C6 C14 121.6(4) . . ?
C14 O4 C15 117.9(5) . . ?
C16 C15 O4 109.2(7) . . ?
C16 C15 H15A 109.8 . . ?
O4 C15 H15A 109.8 . . ?
C16 C15 H15B 109.8 . . ?
O4 C15 H15B 109.8 . . ?
H15A C15 H15B 108.3 . . ?
C15 C16 H16A 109.5 . . ?
C15 C16 H16B 109.5 . . ?
H16A C16 H16B 109.5 . . ?
C15 C16 H16C 109.5 . . ?
H16A C16 H16C 109.5 . . ?
H16B C16 H16C 109.5 . . ?

#===END



