data_pna21
_publ_requested_journal          Chem.Mater.
_publ_contact_author_name        'Maksym V. Kovalenko'
_publ_contact_author_address     
;ETH Zurich,
Vladimir-Prelog-Weg, 1
8093 Zurich,
Switzerland
;
_publ_contact_author_email       mvkovalenko@ethz.ch
_publ_contact_author_phone       '+41 044 633 4156'
loop_
_publ_author_name
_publ_author_address
'Nazarenko, Olga'
;ETH Zurich,
Laboratory of Inorganic Chemistry,
Department of Chemistry and Applied Biosciences,
Vladimir-Prelog-Weg, 1
8093 Zurich,
Switzerland
;
'Kotyrba, Martin R.'
;ETH Zurich, 
Laboratory of Inorganic Chemistry,
Department of Chemistry and Applied Biosciences, 
Vladimir-Prelog-Weg, 1
8093 Zurich,
Switzerland
;
'Yakunin, Sergii'
;ETH Zurich, 
Laboratory of Inorganic Chemistry,
Department of Chemistry and Applied Biosciences, 
Vladimir-Prelog-Weg, 1
8093 Zurich,
Switzerland
;
'Wörle, Michael'
;ETH Zurich, 
Laboratory of Inorganic Chemistry,
Department of Chemistry and Applied Biosciences, 
Vladimir-Prelog-Weg, 1
8093 Zurich,
Switzerland
;
'Benin, Bogdan M.'
;ETH Zurich,
Laboratory of Inorganic Chemistry,
Department of Chemistry and Applied Biosciences, 
Vladimir-Prelog-Weg, 1
8093 Zurich,
Switzerland
;
'Raino, Gabriele '
;ETH Zurich, 
Laboratory of Inorganic Chemistry,
Department of Chemistry and Applied Biosciences,
Vladimir-Prelog-Weg, 1
8093 Zurich,
Switzerland
;
'Krumeich, Frank'
;ETH Zurich,
Laboratory of Inorganic Chemistry,
Department of Chemistry and Applied Biosciences,
Vladimir-Prelog-Weg, 1
8093 Zurich,
Switzerland
;
'Kepenekian, Mikael'
;Univ Rennes, ENSCR, 
INSA Rennes, CNRS, ISCR (Institut des Sciences Chimiques de Rennes) 
UMR 6226, F-35000 Rennes, 
France
;
'Even, Jacky'
;Univ Rennes, INSA Rennes, CNRS, Institut FOTON 
UMR 6082, F-35000 Rennes, 
France
;
'Katan, Claudine'
;Univ Rennes, ENSCR,
INSA Rennes, CNRS, ISCR (Institut des Sciences Chimiques de Rennes) 
UMR 6226, F-35000 Rennes, 
France
;
'Kovalenko, Maksym V.'
;ETH Zurich,
Laboratory of Inorganic Chemistry, 
Department of Chemistry and Applied Bioscience, 
Vladimir Prelog Weg, 1 
CH-8093 Zurich, 
Switzerland
;

_audit_update_record             
;
2018-02-25 # Formatted by publCIF

;

# publcif _publ_body_element loop start
loop_
_publ_body_element
_publ_body_title
_publ_body_contents


section
;
Introduction
;
;

;
section
;
Experimental
;
;

;
subsection
;
Synthesis and crystallization
;
;

;
subsection
;
Refinement
;
;
Crystal data, data collection and structure refinement details are summarized
in Table 1.
;
section
;
Results and discussion
;
;

;
# publcif _publ_body_element loop end
_audit_creation_date             2018-01-23
_audit_creation_method           
;
Olex2 1.2
(compiled 2017.08.10 svn.r3458 for OlexSys, GUI svn.r5381)
;
_shelx_SHELXL_version_number     2014/7
_publ_contact_author_id_orcid    ?
_publ_section_acknowledgements   
;
X-Ray services provided by SMoCC - The Small Molecule Crystallography Center of
ETH Zurich.
;
_publ_section_references         
;
Dolomanov, O. V., Bourhis, L. J., Gildea, R. J., Howard, J. A. K. & Puschmann,
H. (2009). J. Appl. Cryst. 42, 339--341.

Sheldrick, G. M. (2008). Acta Cryst. A64, 112--122.
;
_chemical_name_systematic        ?
_chemical_name_common            ?
_chemical_formula_moiety         '0.5(Br8 Sn2), 2(C H6 N3)'
_chemical_formula_sum            'C2 H12 N6 Sn Br4 '
_chemical_formula_weight         558.51
_space_group_crystal_system      orthorhombic
_space_group_IT_number           33
_space_group_name_H-M_alt        'P n a 21'
_space_group_name_Hall           'P 2c -2n'
_chemical_absolute_configuration ?
loop_
_space_group_symop_operation_xyz
'x, y, z'
'-x, -y, z+1/2'
'-x+1/2, y+1/2, z+1/2'
'x+1/2, -y+1/2, z'
_exptl_crystal_recrystallization_method 
'crystallized from hydrobromic acid (48 percent water solution)'
_chemical_melting_point          ?
_exptl_crystal_description       needle
_exptl_crystal_colour            colourless
_diffrn_ambient_temperature      298
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'
Br Br -0.2901 2.4595 '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'

_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.
;

_cell_length_a                   32.082(3)
_cell_length_b                   8.3226(6)
_cell_length_c                   10.4238(8)
_cell_angle_alpha                90
_cell_angle_beta                 90
_cell_angle_gamma                90
_cell_volume                     2783.2(4)
_cell_formula_units_Z            8
_cell_measurement_reflns_used    5575
_cell_measurement_temperature    298
_cell_measurement_theta_max      25.855
_cell_measurement_theta_min      2.330
_shelx_estimated_absorpt_T_max   0.109
_shelx_estimated_absorpt_T_min   0.093
_exptl_absorpt_coefficient_mu    13.296
_exptl_absorpt_correction_T_max  0.1291
_exptl_absorpt_correction_T_min  0.0651
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   
'SADABS-2014/5 (Bruker,2014/5) was used for absorption correction. wR2(int) was 0.1579 before and 0.0526 after correction. The Ratio of minimum to maximum transmission is 0.5043. The λ/2 correction factor is 0.00150.'
_exptl_absorpt_special_details   ?
_exptl_crystal_colour_lustre     ?
_exptl_crystal_colour_primary    colourless
_exptl_crystal_density_diffrn    2.666
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    ?
_exptl_crystal_F_000             2048
_exptl_crystal_size_max          0.34
_exptl_crystal_size_mid          0.34
_exptl_crystal_size_min          0.3
_exptl_special_details           
'The data collection nominally covered a full sphere of reciprocal space by a combination of 4 sets of ω scans each set at different φ and/or 2θ angles and each scan (10 s exposure) covering -0.300° degrees in ω. The crystal to detector distance was 4.956 cm.'
_exptl_transmission_factor_max   ?
_exptl_transmission_factor_min   ?
_diffrn_reflns_av_R_equivalents  0.0477
_diffrn_reflns_av_unetI/netI     0.0444
_diffrn_reflns_Laue_measured_fraction_full 0.999
_diffrn_reflns_Laue_measured_fraction_max 0.998
_diffrn_reflns_limit_h_max       43
_diffrn_reflns_limit_h_min       -43
_diffrn_reflns_limit_k_max       11
_diffrn_reflns_limit_k_min       -11
_diffrn_reflns_limit_l_max       14
_diffrn_reflns_limit_l_min       -14
_diffrn_reflns_number            29756
_diffrn_reflns_point_group_measured_fraction_full 0.999
_diffrn_reflns_point_group_measured_fraction_max 0.999
_diffrn_reflns_theta_full        25.242
_diffrn_reflns_theta_max         29.026
_diffrn_reflns_theta_min         2.330
_diffrn_detector                 'Bruker SMART CCD 1K area detector'
_diffrn_detector_area_resol_mean 7.9
_diffrn_detector_type            'CCD area detector'
_diffrn_measured_fraction_theta_full 0.999
_diffrn_measured_fraction_theta_max 0.998
_diffrn_measurement_device       'fixed chi three-circle diffractometer'
_diffrn_measurement_device_type  'Bruker SMART CCD'
_diffrn_measurement_method       'ω scans'
_diffrn_radiation_monochromator  Parallel,graphite
_diffrn_radiation_probe          x-ray
_diffrn_radiation_type           MoK\a
_diffrn_radiation_wavelength     0.71073
_diffrn_source                   'sealed X-ray tube'
_diffrn_source_current           35.0
_diffrn_source_power             1.575
_diffrn_source_target            Mo
_diffrn_source_voltage           45.0
_diffrn_special_details          ?
_diffrn_standards_number         0
_reflns_Friedel_coverage         0.900
_reflns_Friedel_fraction_full    1.000
_reflns_Friedel_fraction_max     0.999
_reflns_number_gt                5460
_reflns_number_total             7393
_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       'Bruker SAINT'
_computing_data_collection       'Bruker SAINT'
_computing_data_reduction        'Bruker SAINT'
_computing_molecular_graphics    'Olex2 (Dolomanov et al., 2009)'
_computing_publication_material  'Olex2 (Dolomanov et al., 2009)'
_computing_structure_refinement  'XL (Sheldrick, 2008)'
_computing_structure_solution    'XS (Sheldrick, 2008)'
_refine_diff_density_max         0.521
_refine_diff_density_min         -0.550
_refine_diff_density_rms         0.125
_refine_ls_abs_structure_details 
;
 Refined as an inversion twin.
;
_refine_ls_abs_structure_Flack   0.10(2)
_refine_ls_extinction_coef       0.00185(8)
_refine_ls_extinction_expression Fc^*^=kFc[1+0.001xFc²λ³/sin(2θ)]^-1/4^
_refine_ls_extinction_method     'SHELXL-2014/7 (Sheldrick 2014'
_refine_ls_goodness_of_fit_ref   1.013
_refine_ls_hydrogen_treatment    constr
_refine_ls_matrix_type           full
_refine_ls_number_parameters     237
_refine_ls_number_reflns         7393
_refine_ls_number_restraints     1
_refine_ls_R_factor_all          0.0574
_refine_ls_R_factor_gt           0.0348
_refine_ls_restrained_S_all      1.013
_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)+(0.0287P)²] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.0674
_refine_ls_wR_factor_ref         0.0738
_refine_special_details          
;
An examination of the reconstructed reciprocal layer hk0 shows that only very few, weak reflections are responsible for the violation of a b-glide plane perpendicular to the c-axis (207 I/3s reflections from 825). 
Accordingly, during the refinement in the space group Pna21 (no. 33), large correlation matrix elements arise for parameters of atoms related by the b-pseudo-glide plane perpendicular to the c-axis (larger than 0.8 between displacement parameters of heavy atoms). Therefore, a refinement in the higher symmetric space group Pbcn (no. 60, which is the standard setting of Pnab, obtained when maintaining the setting given by the space group Pna21) has been tested. However, the second parameter of the empirical weighting scheme refines to an unusally high value of more than 20 and one of the two crystallographically independent guanidinium molecules had to be described as disordered over two positions. Therefore, for the final refinement, the space group Pna21 has been chosen. A refinement as an inversion twin yields a contribution of 10(2)% of an inverted domain, which is just slightly above the significance criterion of 3*sigma. There are also very few reflections originating from a small, randomly oriented crystal. The weak reflections 4 1 0, 3 1 0 were larger observed than calculated with an error/esd larger than 8 times the standard uncertainty. It was assumed that these reflections are affected by a contribution from reflections of the small randomly oriented domain, and were subsequently excluded from the refinement. The reflection 2 0 0, has been omitted from the refinement too, since its intensity is biased by the beamstop.
;
_olex2_refinement_description    
;
1. Twinned data refinement
 Scales: 0.90(2)
 0.10(2)
2. Fixed Uiso
 At 1.2 times of:
  All N(H,H) groups
3.a X=CH2 refined with riding coordinates:
 N1(H1A,H1B), N2(H2A,H2B), N3(H3A,H3B), N4(H4A,H4B), N5(H5A,H5B), N6(H6A,H6B),
 N7(H7A,H7B), N8(H8A,H8B), N9(H9A,H9B), N10(H10A,H10B), N11(H11A,H11B),
 N12(H12A,H12B)
;
_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
Sn1 Sn 0.62067(2) 0.04517(8) 0.41578(9) 0.0385(3) Uani 1 1 d . . . . .
Sn2 Sn 0.62186(2) 0.54671(7) 0.25611(9) 0.0380(3) Uani 1 1 d . . . . .
Br1 Br 0.66976(4) -0.21157(13) 0.53744(17) 0.0513(4) Uani 1 1 d . . . . .
Br2 Br 0.55581(3) -0.20011(16) 0.34115(18) 0.0479(3) Uani 1 1 d . . . . .
Br3 Br 0.58258(4) 0.06514(12) 0.64880(16) 0.0486(4) Uani 1 1 d . . . . .
Br4 Br 0.67370(4) 0.29787(14) 0.5100(2) 0.0575(4) Uani 1 1 d . . . . .
Br5 Br 0.55849(3) 0.30095(16) 0.33406(18) 0.0468(3) Uani 1 1 d . . . . .
Br6 Br 0.58170(5) 0.57547(13) 0.02709(16) 0.0473(4) Uani 1 1 d . . . . .
Br7 Br 0.67658(4) 0.80806(13) 0.16236(18) 0.0534(4) Uani 1 1 d . . . . .
Br8 Br 0.66722(4) 0.29759(13) 0.13147(18) 0.0530(4) Uani 1 1 d . . . . .
N1 N 0.5373(3) 0.6949(11) 0.6849(13) 0.066(4) Uani 1 1 d . . . . .
H1A H 0.5535 0.7748 0.6700 0.079 Uiso 1 1 calc R . . . .
H1B H 0.5121 0.7115 0.7101 0.079 Uiso 1 1 calc R . . . .
N2 N 0.5271(3) 0.4231(11) 0.6990(16) 0.059(4) Uani 1 1 d . . . . .
H2A H 0.5367 0.3268 0.6935 0.071 Uiso 1 1 calc R . . . .
H2B H 0.5020 0.4393 0.7242 0.071 Uiso 1 1 calc R . . . .
N3 N 0.5890(3) 0.5215(13) 0.6307(13) 0.055(3) Uani 1 1 d . . . . .
H3A H 0.5986 0.4253 0.6251 0.066 Uiso 1 1 calc R . . . .
H3B H 0.6046 0.6019 0.6110 0.066 Uiso 1 1 calc R . . . .
C1 C 0.5510(3) 0.5453(12) 0.6688(16) 0.043(4) Uani 1 1 d . . . . .
N4 N 0.7680(4) 0.6207(15) 0.2437(11) 0.099(4) Uani 1 1 d . . . . .
H4A H 0.7834 0.6449 0.1788 0.119 Uiso 1 1 calc R . . . .
H4B H 0.7420 0.6443 0.2434 0.119 Uiso 1 1 calc R . . . .
N5 N 0.7616(3) 0.5126(14) 0.4422(11) 0.087(4) Uani 1 1 d . . . . .
H5A H 0.7724 0.4659 0.5079 0.105 Uiso 1 1 calc R . . . .
H5B H 0.7355 0.5364 0.4418 0.105 Uiso 1 1 calc R . . . .
N6 N 0.8229(3) 0.5090(14) 0.3506(15) 0.084(4) Uani 1 1 d . . . . .
H6A H 0.8324 0.4624 0.4181 0.101 Uiso 1 1 calc R . . . .
H6B H 0.8393 0.5298 0.2874 0.101 Uiso 1 1 calc R . . . .
C2 C 0.7846(4) 0.5471(15) 0.3441(18) 0.050(4) Uani 1 1 d . . . . .
N7 N 0.7592(3) 0.1298(14) 0.2517(10) 0.081(3) Uani 1 1 d . . . . .
H7A H 0.7324 0.1259 0.2526 0.097 Uiso 1 1 calc R . . . .
H7B H 0.7719 0.1778 0.1900 0.097 Uiso 1 1 calc R . . . .
N8 N 0.7620(3) -0.0105(14) 0.4389(10) 0.086(3) Uani 1 1 d . . . . .
H8A H 0.7353 -0.0157 0.4416 0.103 Uiso 1 1 calc R . . . .
H8B H 0.7766 -0.0537 0.4988 0.103 Uiso 1 1 calc R . . . .
N9 N 0.8213(3) 0.0635(12) 0.3414(13) 0.062(3) Uani 1 1 d . . . . .
H9A H 0.8343 0.1080 0.2786 0.075 Uiso 1 1 calc R . . . .
H9B H 0.8351 0.0192 0.4026 0.075 Uiso 1 1 calc R . . . .
C3 C 0.7805(4) 0.0632(14) 0.3438(16) 0.045(3) Uani 1 1 d . . . . .
N10 N 0.5901(3) 0.0184(12) 0.0463(15) 0.054(4) Uani 1 1 d . . . . .
H10A H 0.6072 0.0956 0.0611 0.065 Uiso 1 1 calc R . . . .
H10B H 0.5973 -0.0793 0.0613 0.065 Uiso 1 1 calc R . . . .
N11 N 0.5405(3) 0.1945(10) -0.0232(11) 0.052(3) Uani 1 1 d . . . . .
H11A H 0.5154 0.2128 -0.0484 0.063 Uiso 1 1 calc R . . . .
H11B H 0.5577 0.2729 -0.0138 0.063 Uiso 1 1 calc R . . . .
N12 N 0.5256(3) -0.0655(10) -0.0150(18) 0.064(4) Uani 1 1 d . . . . .
H12A H 0.5006 -0.0443 -0.0402 0.077 Uiso 1 1 calc R . . . .
H12B H 0.5328 -0.1632 0.0001 0.077 Uiso 1 1 calc R . . . .
C4 C 0.5523(4) 0.0501(11) 0.0002(14) 0.041(3) 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
Sn1 Br1 2.9418(15) . ?
Sn1 Br2 3.0170(15) . ?
Sn1 Br3 2.724(2) . ?
Sn1 Br4 2.8776(16) . ?
Sn1 Br5 3.0393(14) . ?
Sn2 Br5 2.9962(15) . ?
Sn2 Br6 2.7234(19) . ?
Sn2 Br7 2.9611(15) . ?
Sn2 Br8 2.8467(15) . ?
N1 H1A 0.8600 . ?
N1 H1B 0.8600 . ?
N1 C1 1.331(13) . ?
N2 H2A 0.8600 . ?
N2 H2B 0.8600 . ?
N2 C1 1.311(13) . ?
N3 H3A 0.8600 . ?
N3 H3B 0.8600 . ?
N3 C1 1.297(14) . ?
N4 H4A 0.8600 . ?
N4 H4B 0.8600 . ?
N4 C2 1.324(17) . ?
N5 H5A 0.8600 . ?
N5 H5B 0.8600 . ?
N5 C2 1.294(19) . ?
N6 H6A 0.8600 . ?
N6 H6B 0.8600 . ?
N6 C2 1.269(14) . ?
N7 H7A 0.8600 . ?
N7 H7B 0.8600 . ?
N7 C3 1.302(16) . ?
N8 H8A 0.8600 . ?
N8 H8B 0.8600 . ?
N8 C3 1.308(17) . ?
N9 H9A 0.8600 . ?
N9 H9B 0.8600 . ?
N9 C3 1.312(13) . ?
N10 H10A 0.8600 . ?
N10 H10B 0.8600 . ?
N10 C4 1.329(14) . ?
N11 H11A 0.8600 . ?
N11 H11B 0.8600 . ?
N11 C4 1.284(11) . ?
N12 H12A 0.8600 . ?
N12 H12B 0.8600 . ?
N12 C4 1.299(12) . ?

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
Br1 Sn1 Br2 89.37(4) . . ?
Br1 Sn1 Br5 168.80(6) . . ?
Br2 Sn1 Br5 87.07(5) . . ?
Br3 Sn1 Br1 84.27(6) . . ?
Br3 Sn1 Br2 87.81(5) . . ?
Br3 Sn1 Br4 85.21(6) . . ?
Br3 Sn1 Br5 84.99(5) . . ?
Br4 Sn1 Br1 93.86(5) . . ?
Br4 Sn1 Br2 171.97(6) . . ?
Br4 Sn1 Br5 88.38(4) . . ?
Br6 Sn2 Br5 88.66(5) . . ?
Br6 Sn2 Br7 85.79(5) . . ?
Br6 Sn2 Br8 84.59(6) . . ?
Br7 Sn2 Br5 173.34(5) . . ?
Br8 Sn2 Br5 88.48(4) . . ?
Br8 Sn2 Br7 94.66(5) . . ?
Sn2 Br5 Sn1 96.24(3) . . ?
H1A N1 H1B 120.0 . . ?
C1 N1 H1A 120.0 . . ?
C1 N1 H1B 120.0 . . ?
H2A N2 H2B 120.0 . . ?
C1 N2 H2A 120.0 . . ?
C1 N2 H2B 120.0 . . ?
H3A N3 H3B 120.0 . . ?
C1 N3 H3A 120.0 . . ?
C1 N3 H3B 120.0 . . ?
N2 C1 N1 120.1(12) . . ?
N3 C1 N1 119.5(11) . . ?
N3 C1 N2 120.2(10) . . ?
H4A N4 H4B 120.0 . . ?
C2 N4 H4A 120.0 . . ?
C2 N4 H4B 120.0 . . ?
H5A N5 H5B 120.0 . . ?
C2 N5 H5A 120.0 . . ?
C2 N5 H5B 120.0 . . ?
H6A N6 H6B 120.0 . . ?
C2 N6 H6A 120.0 . . ?
C2 N6 H6B 120.0 . . ?
N5 C2 N4 119.9(12) . . ?
N6 C2 N4 123.1(16) . . ?
N6 C2 N5 117.0(15) . . ?
H7A N7 H7B 120.0 . . ?
C3 N7 H7A 120.0 . . ?
C3 N7 H7B 120.0 . . ?
H8A N8 H8B 120.0 . . ?
C3 N8 H8A 120.0 . . ?
C3 N8 H8B 120.0 . . ?
H9A N9 H9B 120.0 . . ?
C3 N9 H9A 120.0 . . ?
C3 N9 H9B 120.0 . . ?
N7 C3 N8 121.4(11) . . ?
N7 C3 N9 120.7(14) . . ?
N8 C3 N9 117.9(13) . . ?
H10A N10 H10B 120.0 . . ?
C4 N10 H10A 120.0 . . ?
C4 N10 H10B 120.0 . . ?
H11A N11 H11B 120.0 . . ?
C4 N11 H11A 120.0 . . ?
C4 N11 H11B 120.0 . . ?
H12A N12 H12B 120.0 . . ?
C4 N12 H12A 120.0 . . ?
C4 N12 H12B 120.0 . . ?
N11 C4 N10 121.6(11) . . ?
N11 C4 N12 118.4(11) . . ?
N12 C4 N10 119.9(10) . . ?

_olex2_exptl_crystal_mounting_method tip-mounted
_olex2_submission_special_instructions 'No special instructions were received'
loop_
_twin_individual_id
_twin_individual_mass_fraction_refined
1 0.90(2)
2 0.10(2)
loop_
_publcif_info_cif.paper_type
?

