#------------------------------------------------------------------------------
#$Date: 2019-11-28 20:47:58 +0100 (jue 28 de nov de 2019) $
#$Revision: 244721 $
#$URL: svn://www.crystallography.net/cod/cif/7/23/94/7239461.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_7239461
loop_
_publ_author_name
'Kalogirou, Andreas S.'
'Christoforou, Irene C.'
'Ioannidou, Heraklidia A.'
'Manos, Manolis J.'
'Koutentis, Panayiotis A.'
_publ_section_title
;
 Ring transformation of
 (4-chloro-5H-1,2,3-dithiazol-5-ylidene)acetonitriles to
 3-haloisothiazole-5-carbonitriles
;
_journal_issue                   15
_journal_name_full               'RSC Adv.'
_journal_page_first              7735
_journal_paper_doi               10.1039/C3RA47261B
_journal_volume                  4
_journal_year                    2014
_chemical_formula_moiety         'C4 H Cl N2 S2'
_chemical_formula_sum            'C4 H Cl N2 S2'
_chemical_formula_weight         176.64
_space_group_IT_number           14
_space_group_name_Hall           '-P 2ybc'
_space_group_name_H-M_alt        'P 1 21/c 1'
_symmetry_cell_setting           monoclinic
_symmetry_space_group_name_H-M   'P 1 21/c 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                 108.043(15)
_cell_angle_gamma                90.00
_cell_formula_units_Z            4
_cell_length_a                   7.5167(11)
_cell_length_b                   11.280(3)
_cell_length_c                   8.1382(16)
_cell_measurement_reflns_used    2459
_cell_measurement_temperature    100(2)
_cell_measurement_theta_max      33.4503
_cell_measurement_theta_min      3.5887
_cell_volume                     656.1(2)
_computing_cell_refinement       'CrysAlis RED'
_computing_data_collection       'CrysAlis CCD'
_computing_data_reduction        'CrysAlis RED'
_computing_molecular_graphics
;
 DIAMOND (Brandenburg, 2006)
 MERCURY (Bruno et al. 2002)
;
_computing_publication_material  'WINGX (Farrugia, 1999)'
_computing_structure_refinement  'SHELXL-97 (Sheldrick, 1997)'
_computing_structure_solution    'SHELXL-97 (Sheldrick, 1997)'
_diffrn_ambient_temperature      100(2)
_diffrn_detector_area_resol_mean 16.0288
_diffrn_measured_fraction_theta_full 0.960
_diffrn_measured_fraction_theta_max 0.960
_diffrn_measurement_device_type  'Xcalibur, Sapphire3'
_diffrn_measurement_method       'ω scans'
_diffrn_radiation_monochromator  graphite
_diffrn_radiation_source         'Enhance (Mo) X-ray Source'
_diffrn_radiation_type           MoK\a
_diffrn_radiation_wavelength     0.71073
_diffrn_reflns_av_R_equivalents  0.0291
_diffrn_reflns_av_sigmaI/netI    0.0279
_diffrn_reflns_limit_h_max       8
_diffrn_reflns_limit_h_min       -8
_diffrn_reflns_limit_k_max       13
_diffrn_reflns_limit_k_min       -13
_diffrn_reflns_limit_l_max       9
_diffrn_reflns_limit_l_min       -9
_diffrn_reflns_number            2781
_diffrn_reflns_theta_full        24.99
_diffrn_reflns_theta_max         24.99
_diffrn_reflns_theta_min         3.19
_exptl_absorpt_coefficient_mu    1.114
_exptl_absorpt_correction_T_max  1.00000
_exptl_absorpt_correction_T_min  0.26641
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details
'Empirical absorption correction (CrysAlis RED, Oxford Diffraction)'
_exptl_crystal_colour            yellow
_exptl_crystal_density_diffrn    1.788
_exptl_crystal_density_method    'not measured'
_exptl_crystal_description       needle
_exptl_crystal_F_000             352
_exptl_crystal_size_max          0.3
_exptl_crystal_size_mid          0.05
_exptl_crystal_size_min          0.03
_refine_diff_density_max         0.706
_refine_diff_density_min         -0.803
_refine_diff_density_rms         0.150
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.045
_refine_ls_hydrogen_treatment    mixed
_refine_ls_matrix_type           full
_refine_ls_number_parameters     86
_refine_ls_number_reflns         1102
_refine_ls_number_restraints     0
_refine_ls_restrained_S_all      1.045
_refine_ls_R_factor_all          0.0603
_refine_ls_R_factor_gt           0.0527
_refine_ls_shift/su_max          0.026
_refine_ls_shift/su_mean         0.004
_refine_ls_structure_factor_coef Fsqd
_refine_ls_weighting_details
'calc w=1/[σ²(Fo²)+(0.1227P)²+0.0000P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.1521
_refine_ls_wR_factor_ref         0.1555
_reflns_number_gt                905
_reflns_number_total             1102
_reflns_threshold_expression     >2sigma(I)
_cod_data_source_file            c3ra47261b.txt
_cod_data_source_block           shelxl
_cod_depositor_comments
;
The following automatic conversions were performed:

data item '_symmetry_cell_setting' value 'Monoclinic' was changed to
'monoclinic' in accordance with the
/home/saulius/struct/COD-crude-data/automatic-downloads/DataCite-retrospective/RSC/depositions/lib/dictionaries/cif_core.dic
dictionary named 'cif_core.dic' version 2.4.2 last updated on
2011-04-26.

Automatic conversion script
Id: cif_fix_values 6909 2019-04-08 15:41:33Z antanas 
;
_cod_original_sg_symbol_H-M      P2(1)/c
_cod_database_code               7239461
loop_
_symmetry_equiv_pos_as_xyz
'x, y, z'
'-x, y+1/2, -z+1/2'
'-x, -y, -z'
'x, -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
S1 S 0.12197(13) 0.23759(8) 0.89006(13) 0.0217(4) Uani 1 1 d
S2 S 0.21757(15) 0.06786(8) 0.97380(14) 0.0265(4) Uani 1 1 d
Cl1 Cl 0.61078(14) 0.26791(9) 1.32683(14) 0.0271(4) Uani 1 1 d
N1 N 0.3960(5) 0.1079(3) 1.1385(4) 0.0226(8) Uani 1 1 d
N2 N 0.0954(5) 0.5561(3) 0.8362(5) 0.0298(9) Uani 1 1 d
C1 C 0.4229(6) 0.2194(3) 1.1606(5) 0.0212(9) Uani 1 1 d
C2 C 0.3015(5) 0.3064(3) 1.0477(5) 0.0211(9) Uani 1 1 d
C3 C 0.3242(6) 0.4243(3) 1.0603(6) 0.0228(9) Uani 1 1 d
C4 C 0.1990(6) 0.4998(3) 0.9398(6) 0.0224(9) Uani 1 1 d
H1 H 0.418(7) 0.455(4) 1.150(7) 0.045(15) Uiso 1 1 d
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
S1 0.0149(6) 0.0217(6) 0.0200(8) -0.0006(4) -0.0069(5) -0.0009(4)
S2 0.0227(7) 0.0208(6) 0.0263(7) 0.0010(4) -0.0064(5) -0.0007(4)
Cl1 0.0150(6) 0.0333(6) 0.0226(7) 0.0040(4) -0.0093(5) -0.0021(4)
N1 0.0151(18) 0.0262(18) 0.021(2) 0.0047(14) -0.0022(16) 0.0025(14)
N2 0.023(2) 0.0292(19) 0.029(2) 0.0032(16) -0.0034(19) 0.0006(15)
C1 0.010(2) 0.025(2) 0.022(2) 0.0027(16) -0.0040(18) -0.0007(15)
C2 0.012(2) 0.026(2) 0.021(2) 0.0013(16) -0.0022(18) 0.0007(16)
C3 0.017(2) 0.026(2) 0.018(2) -0.0002(16) -0.007(2) 0.0010(16)
C4 0.018(2) 0.0184(19) 0.026(3) -0.0046(17) -0.0005(19) -0.0045(16)
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'
S S 0.1246 0.1234 '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
C2 S1 S2 93.38(14)
N1 S2 S1 97.24(12)
C1 N1 S2 116.1(3)
N1 C1 C2 122.3(4)
N1 C1 Cl1 118.8(3)
C2 C1 Cl1 119.0(3)
C3 C2 C1 125.5(4)
C3 C2 S1 123.6(3)
C1 C2 S1 110.9(3)
C2 C3 C4 120.2(4)
C2 C3 H1 119(3)
C4 C3 H1 121(3)
N2 C4 C3 176.4(4)
loop_
_geom_bond_atom_site_label_1
_geom_bond_atom_site_label_2
_geom_bond_distance
S1 C2 1.732(4)
S1 S2 2.0840(14)
S2 N1 1.639(4)
Cl1 C1 1.715(4)
N1 C1 1.277(5)
N2 C4 1.146(5)
C1 C2 1.456(6)
C2 C3 1.340(6)
C3 C4 1.414(6)
C3 H1 0.91(6)
