
data_CB2210

_audit_creation_method            'SHELXL-2018/3'
_shelx_SHELXL_version_number      '2018/3'
_chemical_name_systematic         ?
_chemical_name_common             ?
_chemical_melting_point           ?
_chemical_formula_moiety
 'C11 H14 Br N O'
_chemical_formula_sum
 'C11 H14 Br N O'
_chemical_formula_weight          256.14

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'
 'Br'  'Br'  -0.6763   1.2805
 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
 'N'  'N'   0.0311   0.0180
 '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'

_space_group_crystal_system       monoclinic
_space_group_IT_number            14
_space_group_name_H-M_alt         'P 21/c'
_space_group_name_Hall            '-P 2ybc'

_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.
;

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                    16.5949(6)
_cell_length_b                    6.7477(2)
_cell_length_c                    10.2051(4)
_cell_angle_alpha                 90
_cell_angle_beta                  101.319(4)
_cell_angle_gamma                 90
_cell_volume                      1120.50(7)
_cell_formula_units_Z             4
_cell_measurement_temperature     173(2)
_cell_measurement_reflns_used     1406
_cell_measurement_theta_min       5.4280
_cell_measurement_theta_max       72.5620

_exptl_crystal_description        plates
_exptl_crystal_colour             'Pale yellow'
_exptl_crystal_density_meas       ?
_exptl_crystal_density_method     ?
_exptl_crystal_density_diffrn     1.518
_exptl_crystal_F_000              520
_exptl_transmission_factor_min    ?
_exptl_transmission_factor_max    ?
_exptl_crystal_size_max           0.184
_exptl_crystal_size_mid           0.114
_exptl_crystal_size_min           0.032
_exptl_absorpt_coefficient_mu     4.739
_shelx_estimated_absorpt_T_min    ?
_shelx_estimated_absorpt_T_max    ?
_exptl_absorpt_correction_type    analytical
_exptl_absorpt_correction_T_min   0.583
_exptl_absorpt_correction_T_max   0.874
_exptl_absorpt_process_details
;
CrysAlisPro 1.171.38.46 (Rigaku Oxford Diffraction, 2015)
Analytical numeric absorption correction using a multifaceted crystal
model based on expressions derived by R.C. Clark & J.S. Reid.
(Clark, R. C. & Reid, J. S. (1995). Acta Cryst. A51, 887-897)
Empirical absorption correction using spherical harmonics,
implemented in SCALE3 ABSPACK scaling algorithm.
;
_exptl_absorpt_special_details    ?
_diffrn_ambient_temperature       173(2)
_diffrn_radiation_wavelength      1.54184
_diffrn_radiation_type            CuK\a
_diffrn_source                    'Enhance Ultra (Cu) X-ray Source'
_diffrn_measurement_device_type   'Agilent Xcalibur PX Ultra A'
_diffrn_measurement_method        'omega scans'
_diffrn_detector_area_resol_mean  10.4115
_diffrn_reflns_number             3642
_diffrn_reflns_av_unetI/netI      0.0614
_diffrn_reflns_av_R_equivalents   0.0429
_diffrn_reflns_limit_h_min        -17
_diffrn_reflns_limit_h_max        20
_diffrn_reflns_limit_k_min        -5
_diffrn_reflns_limit_k_max        8
_diffrn_reflns_limit_l_min        -12
_diffrn_reflns_limit_l_max        12
_diffrn_reflns_theta_min          5.437
_diffrn_reflns_theta_max          73.773
_diffrn_reflns_theta_full         67.684
_diffrn_measured_fraction_theta_max   0.952
_diffrn_measured_fraction_theta_full  0.984
_diffrn_reflns_Laue_measured_fraction_max    0.952
_diffrn_reflns_Laue_measured_fraction_full   0.984
_diffrn_reflns_point_group_measured_fraction_max   0.952
_diffrn_reflns_point_group_measured_fraction_full  0.984
_reflns_number_total              2165
_reflns_number_gt                 1661
_reflns_threshold_expression      'I > 2σ(I)'
_reflns_Friedel_coverage          0.000
_reflns_Friedel_fraction_max      .
_reflns_Friedel_fraction_full     .

_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.
;

_computing_data_collection        'CrysAlisPro, Rigaku OD'
_computing_cell_refinement        'CrysAlisPro, Rigaku OD'
_computing_data_reduction         'CrysAlisPro, Rigaku OD'
_computing_structure_solution     'SHELXS-2014 (Sheldrick, 2017)'
_computing_structure_refinement 'SHELXL-2018/3 (Sheldrick, 2018)'
_computing_molecular_graphics     'Bruker SHELXTL'
_computing_publication_material   'CIFTAB-2014 (Sheldrick, 2017)'
_refine_special_details           ?
_refine_ls_structure_factor_coef  Fsqd
_refine_ls_matrix_type            full
_refine_ls_weighting_scheme       calc
_refine_ls_weighting_details
'w=1/[σ²(Fo²)+(0.0515P)²+0.1018P] where P=(Fo²+2Fc²)/3'
_atom_sites_solution_primary      ?
_atom_sites_solution_secondary    ?
_atom_sites_solution_hydrogens    geom
_refine_ls_hydrogen_treatment     constr
_refine_ls_extinction_method      none
_refine_ls_extinction_coef        .
_refine_ls_number_reflns          2165
_refine_ls_number_parameters      130
_refine_ls_number_restraints      0
_refine_ls_R_factor_all           0.0617
_refine_ls_R_factor_gt            0.0421
_refine_ls_wR_factor_ref          0.1151
_refine_ls_wR_factor_gt           0.1017
_refine_ls_goodness_of_fit_ref    1.039
_refine_ls_restrained_S_all       1.039
_refine_ls_shift/su_max           0.000
_refine_ls_shift/su_mean          0.000

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
N1 N 0.21951(19) 0.1470(5) 0.2184(3) 0.0258(7) Uani 1 1 d . . . . .
Br1 Br 0.30665(3) -0.03491(7) 0.22193(5) 0.03614(17) Uani 1 1 d . . . . .
C2 C 0.2460(2) 0.3219(6) 0.2852(4) 0.0297(9) Uani 1 1 d . . . . .
O2 O 0.2065(2) 0.4085(6) 0.3552(4) 0.0472(9) Uani 1 1 d . . . . .
C3 C 0.1393(3) 0.0517(7) 0.2307(4) 0.0307(9) Uani 1 1 d . . . . .
C4 C 0.1233(3) -0.1191(8) 0.1307(5) 0.0453(11) Uani 1 1 d . . . . .
H4A H 0.159546 -0.230407 0.163784 0.068 Uiso 1 1 calc R U . . .
H4B H 0.134140 -0.075071 0.044314 0.068 Uiso 1 1 calc R U . . .
H4C H 0.065850 -0.161531 0.119815 0.068 Uiso 1 1 calc R U . . .
C5 C 0.0715(3) 0.2054(9) 0.1893(6) 0.0485(13) Uani 1 1 d . . . . .
H5A H 0.017804 0.143407 0.187003 0.073 Uiso 1 1 calc R U . . .
H5B H 0.074015 0.256778 0.100355 0.073 Uiso 1 1 calc R U . . .
H5C H 0.079095 0.314541 0.253856 0.073 Uiso 1 1 calc R U . . .
C6 C 0.1423(3) -0.0234(9) 0.3720(5) 0.0452(12) Uani 1 1 d . . . . .
H6A H 0.157439 0.085687 0.435421 0.068 Uiso 1 1 calc R U . . .
H6B H 0.183331 -0.129307 0.391926 0.068 Uiso 1 1 calc R U . . .
H6C H 0.088266 -0.075003 0.379619 0.068 Uiso 1 1 calc R U . . .
C7 C 0.3233(2) 0.4119(6) 0.2563(4) 0.0255(8) Uani 1 1 d . . . . .
C8 C 0.3398(2) 0.4183(6) 0.1277(4) 0.0290(9) Uani 1 1 d . . . . .
H8A H 0.304677 0.351424 0.056747 0.035 Uiso 1 1 calc R U . . .
C9 C 0.4075(3) 0.5221(7) 0.1027(4) 0.0338(9) Uani 1 1 d . . . . .
H9A H 0.417512 0.529954 0.014331 0.041 Uiso 1 1 calc R U . . .
C10 C 0.4600(3) 0.6137(7) 0.2061(5) 0.0370(10) Uani 1 1 d . . . . .
H10A H 0.506763 0.682523 0.188872 0.044 Uiso 1 1 calc R U . . .
C11 C 0.4453(3) 0.6065(7) 0.3359(4) 0.0341(9) Uani 1 1 d . . . . .
H11A H 0.482474 0.667537 0.407089 0.041 Uiso 1 1 calc R U . . .
C12 C 0.3757(3) 0.5093(6) 0.3609(4) 0.0331(9) Uani 1 1 d . . . . .
H12A H 0.363889 0.509173 0.448253 0.040 Uiso 1 1 calc R U . . .

loop_
 _atom_site_aniso_label
 _atom_site_aniso_U_11
 _atom_site_aniso_U_22
 _atom_site_aniso_U_33
 _atom_site_aniso_U_23
 _atom_site_aniso_U_13
 _atom_site_aniso_U_12
N1 0.0237(15) 0.0233(17) 0.0314(16) -0.0016(14) 0.0081(13) 0.0016(13)
Br1 0.0355(2) 0.0252(2) 0.0484(3) -0.0001(2) 0.00999(18) 0.00443(18)
C2 0.0306(19) 0.028(2) 0.0305(19) -0.0017(17) 0.0067(16) 0.0020(16)
O2 0.0452(18) 0.044(2) 0.060(2) -0.0203(17) 0.0276(16) -0.0081(15)
C3 0.0281(18) 0.034(2) 0.0301(18) -0.0018(17) 0.0054(15) -0.0060(17)
C4 0.042(2) 0.049(3) 0.045(2) -0.009(2) 0.009(2) -0.015(2)
C5 0.025(2) 0.058(3) 0.064(3) 0.008(3) 0.009(2) 0.001(2)
C6 0.040(2) 0.059(3) 0.037(2) 0.008(2) 0.0089(19) -0.018(2)
C7 0.0290(19) 0.0165(19) 0.0311(19) 0.0035(15) 0.0064(15) 0.0017(14)
C8 0.0297(19) 0.029(2) 0.0278(18) -0.0005(16) 0.0045(15) 0.0043(15)
C9 0.035(2) 0.034(2) 0.034(2) 0.0060(18) 0.0101(17) -0.0005(18)
C10 0.035(2) 0.025(2) 0.053(3) 0.002(2) 0.0137(19) -0.0034(18)
C11 0.036(2) 0.024(2) 0.040(2) -0.0067(18) 0.0036(18) -0.0054(17)
C12 0.038(2) 0.027(2) 0.034(2) -0.0020(17) 0.0059(17) 0.0012(17)

_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
N1 C2 1.390(5) . ?
N1 C3 1.506(5) . ?
N1 Br1 1.892(3) . ?
C2 O2 1.211(5) . ?
C2 C7 1.501(6) . ?
C3 C6 1.519(6) . ?
C3 C5 1.527(6) . ?
C3 C4 1.528(7) . ?
C7 C8 1.393(6) . ?
C7 C12 1.401(6) . ?
C8 C9 1.388(6) . ?
C9 C10 1.376(7) . ?
C10 C11 1.395(7) . ?
C11 C12 1.393(6) . ?

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
C2 N1 C3 121.5(3) . . ?
C2 N1 Br1 112.0(3) . . ?
C3 N1 Br1 114.0(3) . . ?
O2 C2 N1 122.9(4) . . ?
O2 C2 C7 120.2(4) . . ?
N1 C2 C7 116.6(3) . . ?
N1 C3 C6 110.8(3) . . ?
N1 C3 C5 107.6(4) . . ?
C6 C3 C5 112.0(4) . . ?
N1 C3 C4 107.9(3) . . ?
C6 C3 C4 110.6(4) . . ?
C5 C3 C4 107.8(4) . . ?
C8 C7 C12 119.7(4) . . ?
C8 C7 C2 122.1(4) . . ?
C12 C7 C2 117.8(4) . . ?
C9 C8 C7 120.3(4) . . ?
C10 C9 C8 119.9(4) . . ?
C9 C10 C11 120.7(4) . . ?
C12 C11 C10 119.7(4) . . ?
C11 C12 C7 119.6(4) . . ?

_refine_diff_density_max    0.598
_refine_diff_density_min   -0.709
_refine_diff_density_rms    0.101



#===END
