# Electronic Supplementary Material (ESI) for RSC Advances.
# This journal is © The Royal Society of Chemistry 2020

####################################################################### 
# 
# 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_mo_gb2018_3_0m
_database_code_depnum_ccdc_archive 'CCDC 1997399'
loop_
_audit_author_name
_audit_author_address
'Hamilton Napolitano'
;State University of Goias
Brazil
;
_audit_update_record             
;
2020-04-16 deposited with the CCDC.	2020-05-28 downloaded from the CCDC.
;
_audit_creation_date             2019-10-04
_audit_creation_method           
;
Olex2 1.2
(compiled 2018.05.29 svn.r3508 for OlexSys, GUI svn.r5506)
;
_shelx_SHELXL_version_number     2018/3
_chemical_name_common            'fluorinated chalcone'
_chemical_name_systematic        
(E)-3-(2,6-difluorophenyl)-1-(4-fluorophenyl)prop-2-en-1-one
_chemical_formula_moiety         'C15 H9 F3 O'
_chemical_formula_sum            'C15 H9 F3 O'
_chemical_formula_weight         262.22
_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'
O O 0.0106 0.0060 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
F F 0.0171 0.0103 '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                   11.2133(5)
_cell_length_b                   9.1206(4)
_cell_length_c                   12.1021(5)
_cell_angle_alpha                90
_cell_angle_beta                 100.356(2)
_cell_angle_gamma                90
_cell_volume                     1217.54(9)
_cell_formula_units_Z            4
_cell_measurement_reflns_used    9864
_cell_measurement_temperature    296(2)
_cell_measurement_theta_max      25.94
_cell_measurement_theta_min      2.81
_shelx_estimated_absorpt_T_max   0.973
_shelx_estimated_absorpt_T_min   0.945
_exptl_absorpt_coefficient_mu    0.120
_exptl_absorpt_correction_T_max  ?
_exptl_absorpt_correction_T_min  ?
_exptl_absorpt_correction_type   none
_exptl_absorpt_process_details   ?
_exptl_absorpt_special_details   ?
_exptl_crystal_colour            colourless
_exptl_crystal_colour_primary    colourless
_exptl_crystal_density_diffrn    1.431
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    ?
_exptl_crystal_description       prism
_exptl_crystal_F_000             536
_exptl_crystal_size_max          0.475
_exptl_crystal_size_mid          0.343
_exptl_crystal_size_min          0.231
_exptl_transmission_factor_max   ?
_exptl_transmission_factor_min   ?
_diffrn_reflns_av_R_equivalents  0.0334
_diffrn_reflns_av_unetI/netI     0.0098
_diffrn_reflns_Laue_measured_fraction_full 0.999
_diffrn_reflns_Laue_measured_fraction_max 0.996
_diffrn_reflns_limit_h_max       14
_diffrn_reflns_limit_h_min       -14
_diffrn_reflns_limit_k_max       11
_diffrn_reflns_limit_k_min       -11
_diffrn_reflns_limit_l_max       13
_diffrn_reflns_limit_l_min       -15
_diffrn_reflns_number            41914
_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         26.422
_diffrn_reflns_theta_min         1.846
_diffrn_ambient_temperature      296.15
_diffrn_detector_area_resol_mean ?
_diffrn_measured_fraction_theta_full 0.999
_diffrn_measured_fraction_theta_max 0.996
_diffrn_measurement_device_type  'Bruker APEX-II CCD'
_diffrn_measurement_method       'φ and ω scans'
_diffrn_radiation_type           MoK\a
_diffrn_radiation_wavelength     0.71073
_diffrn_source                   ?
_reflns_Friedel_coverage         0.000
_reflns_Friedel_fraction_full    .
_reflns_Friedel_fraction_max     .
_reflns_number_gt                2087
_reflns_number_total             2490
_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 (Dolomanov et al., 2009)'
_computing_publication_material  'Olex2 (Dolomanov et al., 2009)'
_computing_structure_refinement  'ShelXL (Sheldrick, 2015)'
_computing_structure_solution    'olex2.solve (Bourhis et al., 2015)'
_refine_diff_density_max         0.178
_refine_diff_density_min         -0.195
_refine_diff_density_rms         0.041
_refine_ls_extinction_coef       .
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.122
_refine_ls_hydrogen_treatment    mixed
_refine_ls_matrix_type           full
_refine_ls_number_parameters     187
_refine_ls_number_reflns         2490
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.0554
_refine_ls_R_factor_gt           0.0460
_refine_ls_restrained_S_all      1.122
_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)+(0.0520P)²+0.4273P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.1251
_refine_ls_wR_factor_ref         0.1356
_refine_special_details          ?
_olex2_refinement_description    
;
1. Fixed Uiso
 At 1.2 times of:
  All C(H) groups
2.a Aromatic/amide H refined with riding coordinates:
 C1(H1), C12(H12), C2(H2), C13(H13)
;
_atom_sites_solution_hydrogens   mixed
_atom_sites_solution_primary     iterative
_atom_sites_solution_secondary   ?
_atom_sites_special_details      
;
The structure was solved using Direct Methods (ShelXS). RE = 0.2, Nqual =  -1, Ralpha = 0.030
;
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
F2 F 0.76035(11) 0.41503(15) 0.72038(9) 0.0731(4) Uani 1 1 d . . . . .
F3 F 0.88019(13) 0.65247(16) 0.41361(11) 0.0859(4) Uani 1 1 d . . . . .
F1 F 0.16635(13) -0.05616(18) 0.48170(13) 0.0979(5) Uani 1 1 d . . . . .
C10 C 0.81265(15) 0.52922(19) 0.56086(14) 0.0500(4) Uani 1 1 d . . . . .
C6 C 0.44310(16) 0.2130(2) 0.42907(13) 0.0513(4) Uani 1 1 d . . . . .
C11 C 0.83380(16) 0.5080(2) 0.67666(15) 0.0544(4) Uani 1 1 d . . . . .
O1 O 0.5461(2) 0.3435(3) 0.30823(13) 0.1253(9) Uani 1 1 d . . . . .
C9 C 0.71682(18) 0.4603(2) 0.48029(16) 0.0575(5) Uani 1 1 d . . . . .
H9 H 0.7183(18) 0.484(2) 0.4075(19) 0.069 Uiso 1 1 d R . . . .
C5 C 0.43313(17) 0.1700(2) 0.53736(15) 0.0554(4) Uani 1 1 d . . . . .
H5 H 0.4916(19) 0.203(2) 0.6013(18) 0.066 Uiso 1 1 d R . . . .
C8 C 0.63070(18) 0.3706(2) 0.49827(16) 0.0594(5) Uani 1 1 d . . . . .
H8 H 0.6203(19) 0.345(2) 0.5712(19) 0.071 Uiso 1 1 d R . . . .
C1 C 0.35765(19) 0.1616(2) 0.33957(15) 0.0643(5) Uani 1 1 d . . . . .
H1 H 0.363498 0.189116 0.266743 0.077 Uiso 1 1 calc R . . . .
C15 C 0.89414(18) 0.6257(2) 0.52484(18) 0.0608(5) Uani 1 1 d . . . . .
C4 C 0.34104(19) 0.0786(3) 0.55528(17) 0.0645(5) Uani 1 1 d . . . . .
H4 H 0.333(2) 0.049(3) 0.624(2) 0.077 Uiso 1 1 d R . . . .
C3 C 0.25902(18) 0.0321(2) 0.46435(18) 0.0638(5) Uani 1 1 d . . . . .
C7 C 0.54046(19) 0.3122(2) 0.40454(15) 0.0647(5) Uani 1 1 d . . . . .
C12 C 0.92479(19) 0.5742(2) 0.75035(18) 0.0672(5) Uani 1 1 d . . . . .
H12 H 0.934225 0.556331 0.827081 0.081 Uiso 1 1 calc R . . . .
C2 C 0.2652(2) 0.0713(3) 0.35667(17) 0.0701(6) Uani 1 1 d . . . . .
H2 H 0.208238 0.037546 0.296590 0.084 Uiso 1 1 calc R . . . .
C13 C 1.0015(2) 0.6674(2) 0.7087(2) 0.0753(6) Uani 1 1 d . . . . .
H13 H 1.063999 0.712922 0.757689 0.090 Uiso 1 1 calc R . . . .
C14 C 0.9874(2) 0.6944(2) 0.5954(2) 0.0733(6) Uani 1 1 d . . . . .
H14 H 1.039(2) 0.755(3) 0.562(2) 0.088 Uiso 1 1 d R . . . .


_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
F2 C11 1.354(2) . ?
F3 C15 1.349(2) . ?
F1 C3 1.360(2) . ?
C10 C11 1.392(2) . ?
C10 C9 1.458(3) . ?
C10 C15 1.394(3) . ?
C6 C5 1.392(2) . ?
C6 C1 1.392(2) . ?
C6 C7 1.488(3) . ?
C11 C12 1.369(3) . ?
O1 C7 1.212(2) . ?
C9 H9 0.91(2) . ?
C9 C8 1.313(3) . ?
C5 H5 0.97(2) . ?
C5 C4 1.375(3) . ?
C8 H8 0.94(2) . ?
C8 C7 1.477(3) . ?
C1 H1 0.9300 . ?
C1 C2 1.368(3) . ?
C15 C14 1.377(3) . ?
C4 H4 0.90(2) . ?
C4 C3 1.368(3) . ?
C3 C2 1.365(3) . ?
C12 H12 0.9300 . ?
C12 C13 1.368(3) . ?
C2 H2 0.9300 . ?
C13 H13 0.9300 . ?
C13 C14 1.374(4) . ?
C14 H14 0.95(3) . ?

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
C11 C10 C9 125.80(17) . . ?
C11 C10 C15 113.59(17) . . ?
C15 C10 C9 120.61(17) . . ?
C5 C6 C1 118.50(18) . . ?
C5 C6 C7 123.04(16) . . ?
C1 C6 C7 118.46(16) . . ?
F2 C11 C10 118.36(16) . . ?
F2 C11 C12 117.15(17) . . ?
C12 C11 C10 124.49(19) . . ?
C10 C9 H9 114.0(13) . . ?
C8 C9 C10 129.32(18) . . ?
C8 C9 H9 116.7(13) . . ?
C6 C5 H5 120.5(13) . . ?
C4 C5 C6 120.63(17) . . ?
C4 C5 H5 118.8(13) . . ?
C9 C8 H8 122.1(13) . . ?
C9 C8 C7 121.34(18) . . ?
C7 C8 H8 116.5(13) . . ?
C6 C1 H1 119.4 . . ?
C2 C1 C6 121.28(18) . . ?
C2 C1 H1 119.4 . . ?
F3 C15 C10 117.48(18) . . ?
F3 C15 C14 118.40(19) . . ?
C14 C15 C10 124.1(2) . . ?
C5 C4 H4 122.3(15) . . ?
C3 C4 C5 118.45(18) . . ?
C3 C4 H4 119.3(15) . . ?
F1 C3 C4 118.74(18) . . ?
F1 C3 C2 118.28(19) . . ?
C2 C3 C4 122.98(19) . . ?
O1 C7 C6 120.10(17) . . ?
O1 C7 C8 120.44(19) . . ?
C8 C7 C6 119.46(16) . . ?
C11 C12 H12 120.7 . . ?
C13 C12 C11 118.6(2) . . ?
C13 C12 H12 120.7 . . ?
C1 C2 H2 120.9 . . ?
C3 C2 C1 118.17(18) . . ?
C3 C2 H2 120.9 . . ?
C12 C13 H13 119.6 . . ?
C12 C13 C14 120.8(2) . . ?
C14 C13 H13 119.6 . . ?
C15 C14 H14 117.4(16) . . ?
C13 C14 C15 118.4(2) . . ?
C13 C14 H14 124.1(16) . . ?

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
F2 C11 C12 C13 179.20(18) . . . . ?
F3 C15 C14 C13 179.89(19) . . . . ?
F1 C3 C2 C1 179.2(2) . . . . ?
C10 C11 C12 C13 -0.4(3) . . . . ?
C10 C9 C8 C7 179.66(19) . . . . ?
C10 C15 C14 C13 -0.3(3) . . . . ?
C6 C5 C4 C3 -0.6(3) . . . . ?
C6 C1 C2 C3 -0.2(3) . . . . ?
C11 C10 C9 C8 2.4(3) . . . . ?
C11 C10 C15 F3 179.96(16) . . . . ?
C11 C10 C15 C14 0.1(3) . . . . ?
C11 C12 C13 C14 0.3(3) . . . . ?
C9 C10 C11 F2 0.3(3) . . . . ?
C9 C10 C11 C12 179.91(19) . . . . ?
C9 C10 C15 F3 0.3(3) . . . . ?
C9 C10 C15 C14 -179.56(19) . . . . ?
C9 C8 C7 C6 -178.93(19) . . . . ?
C9 C8 C7 O1 1.8(4) . . . . ?
C5 C6 C1 C2 0.3(3) . . . . ?
C5 C6 C7 O1 178.4(2) . . . . ?
C5 C6 C7 C8 -0.8(3) . . . . ?
C5 C4 C3 F1 -178.78(19) . . . . ?
C5 C4 C3 C2 0.7(3) . . . . ?
C1 C6 C5 C4 0.1(3) . . . . ?
C1 C6 C7 O1 -1.9(3) . . . . ?
C1 C6 C7 C8 178.76(19) . . . . ?
C15 C10 C11 F2 -179.39(15) . . . . ?
C15 C10 C11 C12 0.2(3) . . . . ?
C15 C10 C9 C8 -178.0(2) . . . . ?
C4 C3 C2 C1 -0.3(4) . . . . ?
C7 C6 C5 C4 179.72(19) . . . . ?
C7 C6 C1 C2 -179.3(2) . . . . ?
C12 C13 C14 C15 0.1(3) . . . . ?

_olex2_submission_special_instructions 'No special instructions were received'
