#------------------------------------------------------------------------------
#$Date: 2018-01-05 07:53:19 +0200 (Fri, 05 Jan 2018) $
#$Revision: 204738 $
#$URL: svn://www.crystallography.net/cod/cif/7/22/98/7229876.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_7229876
loop_
_publ_author_name
'Kalaiarasi, G.'
'Jeya Rajkumar, S. Rex'
'Dharani, S.'
'Małecki, J. G.'
'Prabhakaran, R.'
_publ_section_title
;
 An investigation on 3-acetyl-7-methoxy-coumarin Schiff bases and their
 Ru(ii) metallates with potent antiproliferative activity and enhanced LDH
 and NO release
;
_journal_issue                   3
_journal_name_full               'RSC Advances'
_journal_page_first              1539
_journal_paper_doi               10.1039/C7RA12104K
_journal_volume                  8
_journal_year                    2018
_chemical_formula_moiety         'C13 H13 N3 O3 S, C H4 O'
_chemical_formula_sum            'C14 H17 N3 O4 S'
_chemical_formula_weight         323.36
_chemical_name_systematic
;
 ?
;
_space_group_crystal_system      triclinic
_space_group_IT_number           2
_space_group_name_Hall           '-P 1'
_space_group_name_H-M_alt        'P -1'
_symmetry_space_group_name_Hall  '-P 1'
_symmetry_space_group_name_H-M   'P -1'
_atom_sites_solution_hydrogens   mixed
_atom_sites_solution_primary     direct
_audit_creation_date             2017-04-01
_audit_creation_method
;
Olex2 1.2
(compiled 2017.03.28 svn.r3405 for OlexSys, GUI svn.r5335)
;
_audit_update_record
;
2017-10-16 deposited with the CCDC.
2017-12-18 downloaded from the CCDC.
;
_cell_angle_alpha                97.411(7)
_cell_angle_beta                 106.008(6)
_cell_angle_gamma                113.670(8)
_cell_formula_units_Z            2
_cell_length_a                   8.3702(6)
_cell_length_b                   8.8979(8)
_cell_length_c                   12.4669(9)
_cell_measurement_reflns_used    2611
_cell_measurement_temperature    295(2)
_cell_measurement_theta_max      27.4240
_cell_measurement_theta_min      4.2230
_cell_volume                     786.53(13)
_computing_cell_refinement       'CrysAlisPro 1.171.38.46 (Rigaku OD, 2015)'
_computing_data_collection       'CrysAlisPro 1.171.38.46 (Rigaku OD, 2015)'
_computing_data_reduction        'CrysAlisPro 1.171.38.46 (Rigaku OD, 2015)'
_computing_molecular_graphics    'Olex2 (Dolomanov et al., 2009)'
_computing_publication_material  'Olex2 (Dolomanov et al., 2009)'
_computing_structure_refinement  'ShelXL (Sheldrick, 2015)'
_computing_structure_solution    'ShelXS (Sheldrick, 2008)'
_diffrn_ambient_temperature      295(2)
_diffrn_detector                 'CCD plate'
_diffrn_detector_area_resol_mean 10.4015
_diffrn_detector_type            Atlas
_diffrn_measured_fraction_theta_full 0.995
_diffrn_measured_fraction_theta_max 0.859
_diffrn_measurement_details
;
List of Runs (angles in degrees, time in seconds):

  # Type    Start    End  Width  tₑₓₚ   ω     θ     κ     φ   Frames
#--------------------------------------------------------------------------
  1  ω    -63.00  38.00   1.00   22.40    --    9.75 -57.00  60.00  101
  2  ω    -18.00  83.00   1.00   22.40    --    9.75  57.00-150.00  101
  3  ω    -79.00 -34.00   1.00   22.40    --    9.75-179.00-180.00   45
  4  ω   -100.00 -34.00   1.00   22.40    --  -11.62-179.00-150.00   66
  5  ω    -18.00   7.00   1.00   22.40    --    9.75  57.00  30.00   25
  6  ω   -100.00 -34.00   1.00   22.40    --  -11.62-179.00  90.00   66
;
_diffrn_measurement_device       'four-circle diffractometer'
_diffrn_measurement_device_type  'Xcalibur, Atlas, Gemini ultra'
_diffrn_measurement_method       'ω scans'
_diffrn_orient_matrix_type
'CrysAlisPro convention (1999,Acta A55,543-557)'
_diffrn_orient_matrix_UB_11      0.0952717000
_diffrn_orient_matrix_UB_12      0.0534543000
_diffrn_orient_matrix_UB_13      0.0351461000
_diffrn_orient_matrix_UB_21      -0.0182485000
_diffrn_orient_matrix_UB_22      -0.0245661000
_diffrn_orient_matrix_UB_23      0.0489836000
_diffrn_orient_matrix_UB_31      0.0207638000
_diffrn_orient_matrix_UB_32      -0.0687118000
_diffrn_orient_matrix_UB_33      -0.0122196000
_diffrn_radiation_monochromator  graphite
_diffrn_radiation_probe          x-ray
_diffrn_radiation_type           MoK\a
_diffrn_radiation_wavelength     0.71073
_diffrn_reflns_av_R_equivalents  0.0307
_diffrn_reflns_av_unetI/netI     0.0464
_diffrn_reflns_Laue_measured_fraction_full 0.995
_diffrn_reflns_Laue_measured_fraction_max 0.859
_diffrn_reflns_limit_h_max       11
_diffrn_reflns_limit_h_min       -11
_diffrn_reflns_limit_k_max       12
_diffrn_reflns_limit_k_min       -12
_diffrn_reflns_limit_l_max       17
_diffrn_reflns_limit_l_min       -16
_diffrn_reflns_number            8659
_diffrn_reflns_point_group_measured_fraction_full 0.995
_diffrn_reflns_point_group_measured_fraction_max 0.859
_diffrn_reflns_theta_full        25.242
_diffrn_reflns_theta_max         29.376
_diffrn_reflns_theta_min         3.512
_diffrn_source                   'fine-focus sealed X-ray tube'
_diffrn_source_type              'Enhance (Mo) X-ray Source'
_exptl_absorpt_coefficient_mu    0.227
_exptl_absorpt_correction_T_max  1.00000
_exptl_absorpt_correction_T_min  0.67171
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details
;
CrysAlisPro 1.171.38.46 (Rigaku Oxford Diffraction, 2015)
Empirical absorption correction using spherical harmonics,
 implemented in SCALE3 ABSPACK scaling algorithm.
;
_exptl_crystal_colour            yellow
_exptl_crystal_density_diffrn    1.365
_exptl_crystal_description       needle
_exptl_crystal_F_000             340
_exptl_crystal_size_max          0.34
_exptl_crystal_size_mid          0.08
_exptl_crystal_size_min          0.02
_refine_diff_density_max         0.511
_refine_diff_density_min         -0.438
_refine_diff_density_rms         0.071
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.042
_refine_ls_hydrogen_treatment    mixed
_refine_ls_matrix_type           full
_refine_ls_number_parameters     215
_refine_ls_number_reflns         3726
_refine_ls_number_restraints     0
_refine_ls_restrained_S_all      1.042
_refine_ls_R_factor_all          0.0984
_refine_ls_R_factor_gt           0.0641
_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)+(0.0940P)²+0.2260P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.1760
_refine_ls_wR_factor_ref         0.2032
_reflns_Friedel_coverage         0.000
_reflns_number_gt                2480
_reflns_number_total             3726
_reflns_threshold_expression     'I > 2σ(I)'
_cod_data_source_file            c7ra12104k2.cif
_cod_data_source_block           7a2
_cod_original_cell_volume        786.53(12)
_cod_database_code               7229876
_shelxl_version_number           2014-3
_chemical_oxdiff_formula         'C12 H10 N3 O3 S1'
_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.
;
_reflns_odcompleteness_completeness 99.78
_reflns_odcompleteness_iscentric 1
_reflns_odcompleteness_theta     26.32
_olex2_refinement_description
;
1. Fixed Uiso
 At 1.2 times of:
  All C(H) groups
 At 1.5 times of:
  All C(H,H,H) groups, All O(H) groups
2.a Aromatic/amide H refined with riding coordinates:
 C7(H7), C9(H9), C10(H10), C12(H12)
2.b Idealised Me refined as rotating group:
 C3(H3A,H3B,H3C), C13(H13A,H13B,H13C), C14(H14A,H14B,H14C)
2.c Idealised tetrahedral OH refined as rotating group:
 O4(H4)
;
_olex2_submission_special_instructions 'No special instructions were received'
_oxdiff_exptl_absorpt_empirical_details
;
Empirical correction (ABSPACK) includes:
- Absorption correction using spherical harmonics
- Frame scaling
;
_oxdiff_exptl_absorpt_empirical_full_max 1.296
_oxdiff_exptl_absorpt_empirical_full_min 0.698
loop_
_space_group_symop_operation_xyz
'x, y, z'
'-x, -y, -z'
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
S1 S 0.76668(11) 1.04008(12) 0.47801(7) 0.0575(3) Uani 1 1 d .
O1 O 1.2183(2) 0.8484(2) 1.12554(14) 0.0389(4) Uani 1 1 d .
O2 O 1.3652(3) 1.0790(3) 1.07739(17) 0.0537(5) Uani 1 1 d .
O3 O 0.8913(4) 0.4001(3) 1.2731(2) 0.0646(6) Uani 1 1 d .
N1 N 0.6237(4) 0.9113(4) 0.6302(2) 0.0520(7) Uani 1 1 d .
H1A H 0.631(5) 0.889(4) 0.692(3) 0.055(10) Uiso 1 1 d .
H1B H 0.532(5) 0.913(5) 0.590(3) 0.062(10) Uiso 1 1 d .
N2 N 0.9314(3) 0.9824(3) 0.66953(19) 0.0431(5) Uani 1 1 d .
H2 H 1.021(4) 1.012(4) 0.645(3) 0.050(9) Uiso 1 1 d .
N3 N 0.9313(3) 0.9256(3) 0.76699(18) 0.0394(5) Uani 1 1 d .
C1 C 0.7710(4) 0.9722(4) 0.5993(2) 0.0414(6) Uani 1 1 d .
C2 C 1.0881(3) 0.9485(3) 0.8392(2) 0.0366(6) Uani 1 1 d .
C3 C 1.2734(4) 1.0385(5) 0.8259(3) 0.0590(8) Uani 1 1 d .
H3A H 1.2640 0.9912 0.7494 0.088 Uiso 1 1 calc GR
H3B H 1.3667 1.0242 0.8823 0.088 Uiso 1 1 calc GR
H3C H 1.3079 1.1578 0.8374 0.088 Uiso 1 1 calc GR
C4 C 1.0722(3) 0.8700(3) 0.9355(2) 0.0341(5) Uani 1 1 d .
C5 C 1.2282(3) 0.9431(3) 1.0460(2) 0.0360(5) Uani 1 1 d .
C6 C 1.0578(3) 0.7082(3) 1.1135(2) 0.0358(5) Uani 1 1 d .
C7 C 1.0645(4) 0.6317(3) 1.2028(2) 0.0422(6) Uani 1 1 d .
H7 H 1.1733 0.6735 1.2676 0.051 Uiso 1 1 calc R
C8 C 0.9024(4) 0.4892(4) 1.1925(3) 0.0478(7) Uani 1 1 d .
C9 C 0.7401(4) 0.4280(4) 1.0956(3) 0.0539(8) Uani 1 1 d .
H9 H 0.6323 0.3342 1.0906 0.065 Uiso 1 1 calc R
C10 C 0.7388(4) 0.5055(4) 1.0075(3) 0.0499(7) Uani 1 1 d .
H10 H 0.6301 0.4625 0.9425 0.060 Uiso 1 1 calc R
C11 C 0.8994(3) 0.6491(3) 1.0137(2) 0.0381(6) Uani 1 1 d .
C12 C 0.9135(3) 0.7301(3) 0.9241(2) 0.0374(6) Uani 1 1 d .
H12 H 0.8111 0.6867 0.8552 0.045 Uiso 1 1 calc R
C13 C 1.0579(6) 0.4484(5) 1.3704(3) 0.0708(10) Uani 1 1 d .
H13A H 1.1525 0.4419 1.3435 0.106 Uiso 1 1 calc GR
H13B H 1.0312 0.3725 1.4185 0.106 Uiso 1 1 calc GR
H13C H 1.1017 0.5630 1.4146 0.106 Uiso 1 1 calc GR
O4 O 0.4907(6) 0.6283(6) 0.3153(4) 0.1496(16) Uani 1 1 d .
H4 H 0.5266 0.7207 0.3605 0.224 Uiso 1 1 calc GR
C14 C 0.6108(9) 0.5587(9) 0.3564(6) 0.129(2) Uani 1 1 d .
H14A H 0.5644 0.4474 0.3060 0.194 Uiso 1 1 calc GR
H14B H 0.6170 0.5497 0.4332 0.194 Uiso 1 1 calc GR
H14C H 0.7334 0.6311 0.3583 0.194 Uiso 1 1 calc GR
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'
O O 0.0106 0.0060 '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'
loop_
_geom_angle_atom_site_label_1
_geom_angle_atom_site_label_2
_geom_angle_atom_site_label_3
_geom_angle
C6 O1 C5 122.79(19)
C8 O3 C13 118.3(3)
C1 N2 N3 118.5(2)
C2 N3 N2 118.4(2)
N1 C1 S1 123.0(2)
N1 C1 N2 117.4(3)
N2 C1 S1 119.5(2)
N3 C2 C3 124.2(2)
N3 C2 C4 114.6(2)
C4 C2 C3 121.1(2)
C5 C4 C2 119.8(2)
C12 C4 C2 121.5(2)
C12 C4 C5 118.7(2)
O1 C5 C4 117.0(2)
O2 C5 O1 115.5(2)
O2 C5 C4 127.5(2)
O1 C6 C7 116.7(2)
O1 C6 C11 119.8(2)
C7 C6 C11 123.5(2)
C6 C7 C8 117.6(3)
O3 C8 C7 123.5(3)
O3 C8 C9 115.6(3)
C9 C8 C7 120.9(3)
C10 C9 C8 120.1(3)
C9 C10 C11 121.1(3)
C6 C11 C10 116.8(3)
C6 C11 C12 118.3(2)
C10 C11 C12 124.7(2)
C4 C12 C11 122.1(2)
loop_
_geom_bond_atom_site_label_1
_geom_bond_atom_site_label_2
_geom_bond_distance
S1 C1 1.695(3)
O1 C5 1.381(3)
O1 C6 1.370(3)
O2 C5 1.203(3)
O3 C8 1.358(3)
O3 C13 1.433(5)
N1 C1 1.320(4)
N2 N3 1.375(3)
N2 C1 1.345(3)
N3 C2 1.288(3)
C2 C3 1.501(4)
C2 C4 1.476(4)
C4 C5 1.456(3)
C4 C12 1.363(3)
C6 C7 1.378(4)
C6 C11 1.395(4)
C7 C8 1.395(4)
C8 C9 1.390(5)
C9 C10 1.370(4)
C10 C11 1.408(4)
C11 C12 1.411(4)
O4 C14 1.398(7)
