# Electronic Supplementary Material (ESI) for Dalton Transactions.
# This journal is © The Royal Society of Chemistry 2023

####################################################################### 
# 
# 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_arca-1-2
_database_code_depnum_ccdc_archive 'CCDC 2249965'
loop_
_audit_author_name
_audit_author_address
'Enrico Podda'
;Centro Servizi di Ateneo per la Ricerca CeSAR Universita degli Studi di Cagliari 
Italy
;
_audit_update_record             
;
2023-03-20 deposited with the CCDC.	2023-06-20 downloaded from the CCDC.
;
_audit_creation_date             2021-05-07
_audit_creation_method           
;
Olex2 1.3
(compiled 2020.11.12 svn.r5f609507 for OlexSys, GUI svn.r6272)
;
_shelx_SHELXL_version_number     2018/3
_chemical_name_common            ?
_chemical_name_systematic        ?
_chemical_formula_moiety         'C14 H12 N2 Pt S4'
_chemical_formula_sum            'C14 H12 N2 Pt S4'
_chemical_formula_weight         531.59
_chemical_melting_point          ?
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'
Pt Pt -1.7033 8.3905 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
S S 0.1246 0.1234 '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      orthorhombic
_space_group_IT_number           62
_space_group_name_H-M_alt        'P n m a'
_space_group_name_Hall           '-P 2ac 2n'
loop_
_space_group_symop_operation_xyz
'x, y, z'
'-x+1/2, -y, z+1/2'
'x+1/2, -y+1/2, -z+1/2'
'-x, y+1/2, -z'
'-x, -y, -z'
'x-1/2, y, -z-1/2'
'-x-1/2, y-1/2, z-1/2'
'x, -y-1/2, z'

_cell_length_a                   7.8675(17)
_cell_length_b                   14.825(4)
_cell_length_c                   12.827(3)
_cell_angle_alpha                90
_cell_angle_beta                 90
_cell_angle_gamma                90
_cell_volume                     1496.1(6)
_cell_formula_units_Z            4
_cell_measurement_reflns_used    6142
_cell_measurement_temperature    125(2)
_cell_measurement_theta_max      1.59
_cell_measurement_theta_min      26.37
_shelx_estimated_absorpt_T_max   0.826
_shelx_estimated_absorpt_T_min   0.230
_exptl_absorpt_coefficient_mu    9.929
_exptl_absorpt_correction_T_max  0.821
_exptl_absorpt_correction_T_min  0.636
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   'REQAB (Rigaku, 1998)'
_exptl_crystal_colour            black
_exptl_crystal_colour_primary    black
_exptl_crystal_density_diffrn    2.360
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    'not measured'
_exptl_crystal_description       plate
_exptl_crystal_F_000             1008
_exptl_crystal_size_max          0.21
_exptl_crystal_size_mid          0.06
_exptl_crystal_size_min          0.02
_exptl_transmission_factor_max   ?
_exptl_transmission_factor_min   ?
_diffrn_ambient_temperature      125
_diffrn_radiation_type           'Mo K\a'
_diffrn_radiation_wavelength     0.71075
_diffrn_measurement_device_type  'Rigaku Saturn724'
_diffrn_measurement_method       ω
_diffrn_detector_area_resol_mean 28.944
_diffrn_reflns_number            8678
_diffrn_reflns_av_R_equivalents  0.0409
_diffrn_reflns_theta_max         25.00
_diffrn_reflns_theta_full        25.00
_diffrn_measured_fraction_theta_max 0.975
_diffrn_measured_fraction_theta_full 0.975
_diffrn_reflns_limit_h_min       -9
_diffrn_reflns_limit_h_max       8
_diffrn_reflns_limit_k_min       -17
_diffrn_reflns_limit_k_max       17
_diffrn_reflns_limit_l_min       -15
_diffrn_reflns_limit_l_max       13
_diffrn_standards_number         0
_diffrn_standards_interval_count .
_diffrn_standards_decay_%        ?
_reflns_Friedel_coverage         0.000
_reflns_Friedel_fraction_full    .
_reflns_Friedel_fraction_max     .
_reflns_number_gt                1323
_reflns_number_total             1338
_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       ?
_computing_data_collection       ?
_computing_data_reduction        ?
_computing_molecular_graphics    'Olex2 1.3 (Dolomanov et al., 2009)'
_computing_publication_material  'Olex2 1.3 (Dolomanov et al., 2009)'
_computing_structure_refinement  'SHELXL 2018/3 (Sheldrick, 2015)'
_computing_structure_solution    'SHELXT 2018/2 (Sheldrick, 2018)'
_refine_diff_density_max         1.128
_refine_diff_density_min         -0.834
_refine_diff_density_rms         0.145
_refine_ls_extinction_coef       .
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.131
_refine_ls_hydrogen_treatment    constr
_refine_ls_matrix_type           full
_refine_ls_number_parameters     107
_refine_ls_number_reflns         1338
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.0254
_refine_ls_R_factor_gt           0.0251
_refine_ls_restrained_S_all      1.131
_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)+(0.0346P)²+5.7610P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.0656
_refine_ls_wR_factor_ref         0.0657
_refine_special_details          ?
_olex2_refinement_description    
;
1. Fixed Uiso
 At 1.2 times of:
  All C(H,H) groups
2. Others
 Sof(C1A)=Sof(H1AA)=Sof(H1AB)=1-FVAR(1)
 Sof(C1)=Sof(H1A)=Sof(H1B)=FVAR(1)
 Fixed U12: Pt1(0)
 Fixed U23: Pt1(0)
 Fixed Uiso: H3(0.0336) H4(0.0397) H5(0.0338) H6(0.0295)
 Fixed X: H3(-0.372799) H4(-0.350699) H5(-0.0894) H6(0.1384)
 Fixed Y: Pt1(0.75) H3(0.6758) H4(0.518801) H5(0.452499) H6(0.5439)
 Fixed Z: H3(0.181901) H4(0.177) H5(0.1328) H6(0.088201)
3.a Secondary CH2 refined with riding coordinates:
 C1(H1A,H1B), C1A(H1AA,H1AB)
;
_atom_sites_solution_hydrogens   mixed
_atom_sites_solution_primary     direct
_atom_sites_solution_secondary   difmap
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
Pt1 Pt 0.20181(3) 0.750000 0.05303(2) 0.01827(13) Uani 1 2 d S T P . .
S2 S 0.38132(14) 0.85620(8) -0.00629(10) 0.0244(3) Uani 1 1 d . . . . .
S3 S 0.69588(14) 0.86799(9) -0.12478(11) 0.0272(3) Uani 1 1 d . . . . .
N1 N 0.0193(5) 0.6620(3) 0.1049(3) 0.0218(8) Uani 1 1 d . . . . .
C1 C 0.793(2) 0.7926(8) -0.2190(15) 0.028(4) Uani 0.49(3) 1 d . . P A 1
H1A H 0.707766 0.776479 -0.272646 0.034 Uiso 0.49(3) 1 calc R U P A 1
H1B H 0.887359 0.824536 -0.254354 0.034 Uiso 0.49(3) 1 calc R U P A 1
C1A C 0.861(2) 0.7932(8) -0.1700(17) 0.038(4) Uani 0.51(3) 1 d . . P A .
H1AA H 0.931999 0.825401 -0.221872 0.046 Uiso 0.51(3) 1 calc R U P . .
H1AB H 0.935266 0.776997 -0.110456 0.046 Uiso 0.51(3) 1 calc R U P . .
C2 C -0.1290(6) 0.7003(3) 0.1333(4) 0.0232(10) Uani 1 1 d . . . . .
C3 C -0.2699(7) 0.6480(4) 0.1618(4) 0.0276(11) Uani 1 1 d . . . . .
H3 H -0.372799 0.675800 0.181901 0.034 Uiso 1 1 d . U . . .
C4 C -0.2559(8) 0.5553(4) 0.1600(4) 0.0331(12) Uani 1 1 d . . . . .
H4 H -0.350699 0.518801 0.177000 0.040 Uiso 1 1 d . U . . .
C5 C -0.1015(7) 0.5162(3) 0.1332(4) 0.0282(11) Uani 1 1 d . . . . .
H5 H -0.089400 0.452499 0.132800 0.034 Uiso 1 1 d . U . . .
C6 C 0.0329(6) 0.5709(3) 0.1062(4) 0.0245(10) Uani 1 1 d . . . . .
H6 H 0.138400 0.543900 0.088201 0.030 Uiso 1 1 d . U . . .
C14 C 0.5471(6) 0.7951(4) -0.0656(4) 0.0217(10) 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
Pt1 S2 2.2476(12) 8_575 ?
Pt1 S2 2.2476(12) . ?
Pt1 N1 2.052(4) 8_575 ?
Pt1 N1 2.052(4) . ?
S2 C14 1.761(5) . ?
S3 C1 1.816(13) . ?
S3 C1A 1.805(12) . ?
S3 C14 1.765(5) . ?
N1 C2 1.348(6) . ?
N1 C6 1.354(6) . ?
C1 H1A 0.990 . ?
C1 H1B 0.9900 . ?
C1 C1A 1.517(15) 8_575 ?
C1A H1AA 0.990 . ?
C1A H1AB 0.990 . ?
C2 C2 1.472(10) 8_575 ?
C2 C3 1.402(7) . ?
C3 C4 1.379(8) . ?
C4 H4 0.950 . ?
C4 C5 1.389(8) . ?
C5 H5 0.950 . ?
C5 C6 1.376(7) . ?
C6 H6 0.950 . ?
C14 C14 1.338(10) 8_575 ?

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
S2 Pt1 S2 88.93(6) 8_575 . ?
N1 Pt1 S2 95.98(11) 8_575 . ?
N1 Pt1 S2 174.42(11) 8_575 8_575 ?
N1 Pt1 S2 174.42(11) . . ?
N1 Pt1 S2 95.97(12) . 8_575 ?
N1 Pt1 N1 79.0(2) . 8_575 ?
C14 S2 Pt1 104.57(17) . . ?
C14 S3 C1 100.9(4) . . ?
C14 S3 C1A 103.9(4) . . ?
C2 N1 Pt1 115.2(3) . . ?
C2 N1 C6 119.1(4) . . ?
C6 N1 Pt1 125.6(3) . . ?
N1 C2 C2 115.0(3) . 8_575 ?
N1 C2 C3 121.4(5) . . ?
C3 C2 C2 123.6(3) . 8_575 ?
C4 C3 C2 119.0(5) . . ?
C3 C4 C5 119.3(5) . . ?
C6 C5 C4 119.2(5) . . ?
N1 C6 C5 122.0(5) . . ?
S2 C14 S3 111.3(3) . . ?
C14 C14 S2 120.95(17) 8_575 . ?
C14 C14 S3 127.75(17) 8_575 . ?

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
Pt1 S2 C14 S3 176.28(19) . . . . ?
Pt1 S2 C14 C14 -1.43(15) . . . 8_575 ?
Pt1 N1 C2 C2 -6.4(3) . . . 8_575 ?
Pt1 N1 C2 C3 174.5(4) . . . . ?
Pt1 N1 C6 C5 -173.8(4) . . . . ?
N1 C2 C3 C4 -0.4(8) . . . . ?
C1 S3 C14 S2 -157.9(7) . . . . ?
C1 S3 C14 C14 19.6(7) . . . 8_575 ?
C1A S3 C14 S2 175.2(8) . . . . ?
C1A S3 C14 C14 -7.2(8) . . . 8_575 ?
C2 N1 C6 C5 1.6(8) . . . . ?
C2 C2 C3 C4 -179.4(4) 8_575 . . . ?
C2 C3 C4 C5 2.0(9) . . . . ?
C3 C4 C5 C6 -1.8(8) . . . . ?
C4 C5 C6 N1 0.0(8) . . . . ?
C6 N1 C2 C2 177.7(3) . . . 8_575 ?
C6 N1 C2 C3 -1.4(7) . . . . ?

_olex2_submission_special_instructions 'No special instructions were received'
####################################################################### 
# 
# 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_2021cesar035r1_0m_a
_database_code_depnum_ccdc_archive 'CCDC 2249966'
loop_
_audit_author_name
_audit_author_address
'Enrico Podda'
;Centro Servizi di Ateneo per la Ricerca CeSAR Universita degli Studi di Cagliari 
Italy
;
_audit_update_record             
;
2023-03-20 deposited with the CCDC.	2023-06-20 downloaded from the CCDC.
;
_audit_creation_date             2021-07-15
_audit_creation_method           
;
Olex2 1.3
(compiled 2020.11.12 svn.r5f609507 for OlexSys, GUI svn.r6272)
;
_shelx_SHELXL_version_number     2018/3
loop_
_audit_author_email
''
?
_chemical_name_common            ?
_chemical_name_systematic        ?
_chemical_formula_moiety         'C16 H16 N2 Pt S4'
_chemical_formula_sum            'C16 H16 N2 Pt S4'
_chemical_formula_weight         559.64
_chemical_melting_point          ?
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'
Pt Pt -1.7033 8.3905 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
S S 0.1246 0.1234 '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                   10.451(5)
_cell_length_b                   21.309(9)
_cell_length_c                   8.335(4)
_cell_angle_alpha                90
_cell_angle_beta                 110.331(16)
_cell_angle_gamma                90
_cell_volume                     1740.5(14)
_cell_formula_units_Z            4
_cell_measurement_reflns_used    9906
_cell_measurement_temperature    298(2)
_cell_measurement_theta_max      27.50
_cell_measurement_theta_min      2.29
_shelx_estimated_absorpt_T_max   0.848
_shelx_estimated_absorpt_T_min   0.184
_exptl_absorpt_coefficient_mu    8.540
_exptl_absorpt_correction_T_max  0.7456
_exptl_absorpt_correction_T_min  0.5975
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   
;
SADABS-2016/2 (Bruker,2016/2) was used for absorption correction.
wR2(int) was 0.1091 before and 0.0661 after correction.
The Ratio of minimum to maximum transmission is 0.8014.
The λ/2 correction factor is Not present.
;
_exptl_absorpt_special_details   ?
_exptl_crystal_colour            blue
_exptl_crystal_colour_primary    blue
_exptl_crystal_density_diffrn    2.136
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    ?
_exptl_crystal_description       plate
_exptl_crystal_F_000             1072
_exptl_crystal_size_max          0.3
_exptl_crystal_size_mid          0.08
_exptl_crystal_size_min          0.02
_exptl_transmission_factor_max   ?
_exptl_transmission_factor_min   ?
_diffrn_reflns_av_R_equivalents  0.0542
_diffrn_reflns_av_unetI/netI     0.0252
_diffrn_reflns_Laue_measured_fraction_full 0.999
_diffrn_reflns_Laue_measured_fraction_max 0.996
_diffrn_reflns_limit_h_max       13
_diffrn_reflns_limit_h_min       -13
_diffrn_reflns_limit_k_max       27
_diffrn_reflns_limit_k_min       -27
_diffrn_reflns_limit_l_max       10
_diffrn_reflns_limit_l_min       -10
_diffrn_reflns_number            37262
_diffrn_reflns_point_group_measured_fraction_full 0.999
_diffrn_reflns_point_group_measured_fraction_max 0.996
_diffrn_reflns_theta_full        25.242
_diffrn_reflns_theta_max         27.490
_diffrn_reflns_theta_min         2.287
_diffrn_ambient_temperature      298(2)
_diffrn_detector                 'Bruker PHOTON II area detector'
_diffrn_detector_area_resol_mean 7.9
_diffrn_detector_type            'CPAD area detector'
_diffrn_measured_fraction_theta_full 0.999
_diffrn_measured_fraction_theta_max 0.996
_diffrn_measurement_device       'four-circle diffractometer'
_diffrn_measurement_device_type  'Bruker D8 VENTURE PHOTON II'
_diffrn_measurement_method       'ω and φ scans'
_diffrn_radiation_monochromator  'mirror optics'
_diffrn_radiation_probe          x-ray
_diffrn_radiation_type           MoK\a
_diffrn_radiation_wavelength     0.71073
_diffrn_source                   'microfocus sealed X-ray tube'
_diffrn_source_current           1.0
_diffrn_source_power             0.05
_diffrn_source_type              'Incoatec I\ms'
_diffrn_source_voltage           50.0
_diffrn_standards_number         0
_reflns_Friedel_coverage         0.000
_reflns_Friedel_fraction_full    .
_reflns_Friedel_fraction_max     .
_reflns_number_gt                3419
_reflns_number_total             3985
_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       'SAINT v8.37A (Bruker, 2015)'
_computing_data_collection       ?
_computing_data_reduction        'SAINT v8.37A (Bruker, 2015)'
_computing_molecular_graphics    'Olex2 1.3 (Dolomanov et al., 2009)'
_computing_publication_material  'Olex2 1.3 (Dolomanov et al., 2009)'
_computing_structure_refinement  'SHELXL 2018/3 (Sheldrick, 2015)'
_computing_structure_solution    'SHELXT 2018/2 (Sheldrick, 2018)'
_refine_diff_density_max         1.365
_refine_diff_density_min         -0.684
_refine_diff_density_rms         0.120
_refine_ls_extinction_coef       .
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.103
_refine_ls_hydrogen_treatment    constr
_refine_ls_matrix_type           full
_refine_ls_number_parameters     210
_refine_ls_number_reflns         3985
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.0337
_refine_ls_R_factor_gt           0.0238
_refine_ls_restrained_S_all      1.103
_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)+(0.0101P)²+5.3260P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.0488
_refine_ls_wR_factor_ref         0.0554
_refine_special_details          ?
_olex2_refinement_description    
;
1. Fixed Uiso
 At 1.2 times of:
  All C(H) groups, All C(H,H) groups
 At 1.5 times of:
  All C(H,H,H) groups
2.a Secondary CH2 refined with riding coordinates:
 C15(H15A,H15B), C16(H16A,H16B)
2.b Aromatic/amide H refined with riding coordinates:
 C1(H1), C2(H2), C5(H5), C8(H8), C11(H11), C12(H12)
2.c Idealised Me refined as rotating group:
 C4(H4A,H4B,H4C), C10(H10A,H10B,H10C)
;
_atom_sites_solution_hydrogens   geom
_atom_sites_solution_primary     dual
_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
Pt1 Pt 0.40263(2) 0.44937(2) 0.60311(2) 0.02839(6) Uani 1 1 d . . . . .
S1 S 0.19953(12) 0.42097(5) 0.40953(15) 0.0369(2) Uani 1 1 d . . . . .
S2 S 0.49306(12) 0.36005(5) 0.54513(15) 0.0355(2) Uani 1 1 d . . . . .
S3 S 0.10176(15) 0.32441(6) 0.13980(19) 0.0529(3) Uani 1 1 d . . . . .
S4 S 0.40490(13) 0.26152(6) 0.27415(17) 0.0435(3) Uani 1 1 d . . . . .
N1 N 0.3398(4) 0.53491(16) 0.6668(5) 0.0304(8) Uani 1 1 d . . . . .
N2 N 0.5776(4) 0.47891(17) 0.7916(4) 0.0302(7) Uani 1 1 d . . . . .
C1 C 0.2179(5) 0.5610(2) 0.5946(6) 0.0411(11) Uani 1 1 d . . . . .
H1 H 0.151535 0.538980 0.509087 0.049 Uiso 1 1 calc R U . . .
C2 C 0.1853(5) 0.6193(2) 0.6409(7) 0.0431(11) Uani 1 1 d . . . . .
H2 H 0.098484 0.635876 0.587474 0.052 Uiso 1 1 calc R U . . .
C3 C 0.2824(5) 0.6532(2) 0.7672(6) 0.0387(10) Uani 1 1 d . . . . .
C4 C 0.2522(6) 0.7177(3) 0.8202(9) 0.0611(16) Uani 1 1 d . . . . .
H4A H 0.239620 0.715053 0.928726 0.092 Uiso 1 1 calc R U . . .
H4B H 0.170639 0.733766 0.735862 0.092 Uiso 1 1 calc R U . . .
H4C H 0.327140 0.745252 0.829646 0.092 Uiso 1 1 calc R U . . .
C5 C 0.4088(5) 0.6257(2) 0.8431(6) 0.0355(10) Uani 1 1 d . . . . .
H5 H 0.475851 0.646712 0.930183 0.043 Uiso 1 1 calc R U . . .
C6 C 0.4368(4) 0.5673(2) 0.7909(5) 0.0300(9) Uani 1 1 d . . . . .
C7 C 0.5693(4) 0.5353(2) 0.8623(5) 0.0311(9) Uani 1 1 d . . . . .
C8 C 0.6797(4) 0.5601(2) 0.9923(6) 0.0353(10) Uani 1 1 d . . . . .
H8 H 0.672060 0.599250 1.037549 0.042 Uiso 1 1 calc R U . . .
C9 C 0.8012(5) 0.5274(2) 1.0557(6) 0.0355(10) Uani 1 1 d . . . . .
C10 C 0.9196(5) 0.5535(3) 1.1994(7) 0.0462(12) Uani 1 1 d . . . . .
H10A H 0.949430 0.591850 1.163175 0.069 Uiso 1 1 calc R U . . .
H10B H 0.993125 0.523689 1.230899 0.069 Uiso 1 1 calc R U . . .
H10C H 0.892237 0.561634 1.296011 0.069 Uiso 1 1 calc R U . . .
C11 C 0.8067(5) 0.4697(2) 0.9831(6) 0.0404(11) Uani 1 1 d . . . . .
H11 H 0.886082 0.445921 1.023245 0.049 Uiso 1 1 calc R U . . .
C12 C 0.6957(5) 0.4471(2) 0.8519(6) 0.0370(10) Uani 1 1 d . . . . .
H12 H 0.702652 0.408509 0.803441 0.044 Uiso 1 1 calc R U . . .
C13 C 0.2371(5) 0.3532(2) 0.3154(6) 0.0341(9) Uani 1 1 d . . . . .
C14 C 0.3628(5) 0.3280(2) 0.3713(6) 0.0351(10) Uani 1 1 d . . . . .
C15 C 0.1245(6) 0.2400(2) 0.1396(8) 0.0528(14) Uani 1 1 d . . . . .
H15A H 0.051787 0.220410 0.169011 0.063 Uiso 1 1 calc R U . . .
H15B H 0.113649 0.227086 0.023991 0.063 Uiso 1 1 calc R U . . .
C16 C 0.2585(5) 0.2147(2) 0.2582(7) 0.0433(11) Uani 1 1 d . . . . .
H16A H 0.271816 0.173042 0.219613 0.052 Uiso 1 1 calc R U . . .
H16B H 0.253128 0.210407 0.371556 0.052 Uiso 1 1 calc R U . . .


_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
Pt1 S1 2.2573(14) . ?
Pt1 S2 2.2509(13) . ?
Pt1 N1 2.068(4) . ?
Pt1 N2 2.052(4) . ?
S1 C13 1.751(5) . ?
S2 C14 1.746(5) . ?
S3 C13 1.755(5) . ?
S3 C15 1.815(6) . ?
S4 C14 1.761(5) . ?
S4 C16 1.792(5) . ?
N1 C1 1.328(6) . ?
N1 C6 1.358(5) . ?
N2 C7 1.354(6) . ?
N2 C12 1.343(6) . ?
C1 H1 0.9300 . ?
C1 C2 1.379(7) . ?
C2 H2 0.9300 . ?
C2 C3 1.384(7) . ?
C3 C4 1.510(7) . ?
C3 C5 1.381(6) . ?
C4 H4A 0.9600 . ?
C4 H4B 0.9600 . ?
C4 H4C 0.9600 . ?
C5 H5 0.9300 . ?
C5 C6 1.383(6) . ?
C6 C7 1.471(6) . ?
C7 C8 1.384(6) . ?
C8 H8 0.9300 . ?
C8 C9 1.383(6) . ?
C9 C10 1.499(6) . ?
C9 C11 1.379(7) . ?
C10 H10A 0.9600 . ?
C10 H10B 0.9600 . ?
C10 H10C 0.9600 . ?
C11 H11 0.9300 . ?
C11 C12 1.375(7) . ?
C12 H12 0.9300 . ?
C13 C14 1.345(6) . ?
C15 H15A 0.9700 . ?
C15 H15B 0.9700 . ?
C15 C16 1.506(8) . ?
C16 H16A 0.9700 . ?
C16 H16B 0.9700 . ?

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
S2 Pt1 S1 88.88(5) . . ?
N1 Pt1 S1 96.68(10) . . ?
N1 Pt1 S2 174.11(10) . . ?
N2 Pt1 S1 174.80(10) . . ?
N2 Pt1 S2 95.44(11) . . ?
N2 Pt1 N1 79.11(14) . . ?
C13 S1 Pt1 103.88(16) . . ?
C14 S2 Pt1 104.16(16) . . ?
C13 S3 C15 106.2(2) . . ?
C14 S4 C16 98.0(2) . . ?
C1 N1 Pt1 126.4(3) . . ?
C1 N1 C6 118.5(4) . . ?
C6 N1 Pt1 115.1(3) . . ?
C7 N2 Pt1 115.5(3) . . ?
C12 N2 Pt1 126.2(3) . . ?
C12 N2 C7 118.3(4) . . ?
N1 C1 H1 118.6 . . ?
N1 C1 C2 122.8(4) . . ?
C2 C1 H1 118.6 . . ?
C1 C2 H2 120.1 . . ?
C1 C2 C3 119.7(4) . . ?
C3 C2 H2 120.1 . . ?
C2 C3 C4 121.6(4) . . ?
C5 C3 C2 117.3(4) . . ?
C5 C3 C4 121.1(4) . . ?
C3 C4 H4A 109.5 . . ?
C3 C4 H4B 109.5 . . ?
C3 C4 H4C 109.5 . . ?
H4A C4 H4B 109.5 . . ?
H4A C4 H4C 109.5 . . ?
H4B C4 H4C 109.5 . . ?
C3 C5 H5 119.6 . . ?
C3 C5 C6 120.8(4) . . ?
C6 C5 H5 119.6 . . ?
N1 C6 C5 120.8(4) . . ?
N1 C6 C7 114.9(4) . . ?
C5 C6 C7 124.2(4) . . ?
N2 C7 C6 115.4(4) . . ?
N2 C7 C8 121.2(4) . . ?
C8 C7 C6 123.4(4) . . ?
C7 C8 H8 119.6 . . ?
C9 C8 C7 120.7(4) . . ?
C9 C8 H8 119.6 . . ?
C8 C9 C10 120.8(4) . . ?
C11 C9 C8 117.0(4) . . ?
C11 C9 C10 122.2(4) . . ?
C9 C10 H10A 109.5 . . ?
C9 C10 H10B 109.5 . . ?
C9 C10 H10C 109.5 . . ?
H10A C10 H10B 109.5 . . ?
H10A C10 H10C 109.5 . . ?
H10B C10 H10C 109.5 . . ?
C9 C11 H11 119.7 . . ?
C12 C11 C9 120.6(4) . . ?
C12 C11 H11 119.7 . . ?
N2 C12 C11 122.1(4) . . ?
N2 C12 H12 118.9 . . ?
C11 C12 H12 118.9 . . ?
S1 C13 S3 114.9(3) . . ?
C14 C13 S1 121.2(3) . . ?
C14 C13 S3 123.8(4) . . ?
S2 C14 S4 116.7(3) . . ?
C13 C14 S2 121.1(3) . . ?
C13 C14 S4 122.2(4) . . ?
S3 C15 H15A 108.2 . . ?
S3 C15 H15B 108.2 . . ?
H15A C15 H15B 107.3 . . ?
C16 C15 S3 116.5(4) . . ?
C16 C15 H15A 108.2 . . ?
C16 C15 H15B 108.2 . . ?
S4 C16 H16A 108.5 . . ?
S4 C16 H16B 108.5 . . ?
C15 C16 S4 115.1(4) . . ?
C15 C16 H16A 108.5 . . ?
C15 C16 H16B 108.5 . . ?
H16A C16 H16B 107.5 . . ?

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
Pt1 S1 C13 S3 -172.9(2) . . . . ?
Pt1 S1 C13 C14 4.1(4) . . . . ?
Pt1 S2 C14 S4 172.7(2) . . . . ?
Pt1 S2 C14 C13 -7.3(4) . . . . ?
Pt1 N1 C1 C2 -177.9(4) . . . . ?
Pt1 N1 C6 C5 178.7(3) . . . . ?
Pt1 N1 C6 C7 -1.4(5) . . . . ?
Pt1 N2 C7 C6 -1.0(5) . . . . ?
Pt1 N2 C7 C8 179.1(3) . . . . ?
Pt1 N2 C12 C11 -177.7(3) . . . . ?
S1 C13 C14 S2 2.2(6) . . . . ?
S1 C13 C14 S4 -177.7(3) . . . . ?
S3 C13 C14 S2 179.0(3) . . . . ?
S3 C13 C14 S4 -0.9(6) . . . . ?
S3 C15 C16 S4 -38.6(5) . . . . ?
N1 C1 C2 C3 0.3(8) . . . . ?
N1 C6 C7 N2 1.6(6) . . . . ?
N1 C6 C7 C8 -178.5(4) . . . . ?
N2 C7 C8 C9 -1.1(7) . . . . ?
C1 N1 C6 C5 1.0(6) . . . . ?
C1 N1 C6 C7 -179.2(4) . . . . ?
C1 C2 C3 C4 179.0(5) . . . . ?
C1 C2 C3 C5 -0.8(8) . . . . ?
C2 C3 C5 C6 1.4(7) . . . . ?
C3 C5 C6 N1 -1.5(7) . . . . ?
C3 C5 C6 C7 178.7(4) . . . . ?
C4 C3 C5 C6 -178.4(5) . . . . ?
C5 C6 C7 N2 -178.6(4) . . . . ?
C5 C6 C7 C8 1.3(7) . . . . ?
C6 N1 C1 C2 -0.4(7) . . . . ?
C6 C7 C8 C9 179.1(4) . . . . ?
C7 N2 C12 C11 0.6(7) . . . . ?
C7 C8 C9 C10 -178.5(4) . . . . ?
C7 C8 C9 C11 0.3(7) . . . . ?
C8 C9 C11 C12 0.9(7) . . . . ?
C9 C11 C12 N2 -1.4(7) . . . . ?
C10 C9 C11 C12 179.7(5) . . . . ?
C12 N2 C7 C6 -179.5(4) . . . . ?
C12 N2 C7 C8 0.6(6) . . . . ?
C13 S3 C15 C16 -11.0(5) . . . . ?
C14 S4 C16 C15 65.7(4) . . . . ?
C15 S3 C13 S1 -149.4(3) . . . . ?
C15 S3 C13 C14 33.6(5) . . . . ?
C16 S4 C14 S2 134.1(3) . . . . ?
C16 S4 C14 C13 -45.9(5) . . . . ?

_olex2_exptl_crystal_mounting_method 
'The crystal was mounted on a MITIGEN holder in perfluoroether oil'
_olex2_submission_original_sample_id 6A2
_olex2_submission_special_instructions 'No special instructions were received'
