# Electronic Supplementary Material (ESI) for New Journal of Chemistry.
# This journal is © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 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_shelx
_database_code_depnum_ccdc_archive 'CCDC 1911289'
loop_
_audit_author_name
_audit_author_address
'Yogesh Kumar G R'
;The Cambridge Crystallographic Data Centre
India
;
_audit_update_record             
;
2019-09-12 deposited with the CCDC.	2020-03-30 downloaded from the CCDC.
;

_audit_creation_method           SHELXL-2018/3
_shelx_SHELXL_version_number     2018/3
_chemical_name_systematic        ?
_chemical_name_common            ?
_chemical_melting_point          ?
_chemical_formula_moiety         ?
_chemical_formula_sum            'C11 H9 F N2 O3'
_chemical_formula_weight         236.20

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'
F F 0.0171 0.0103 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'

_space_group_crystal_system      monoclinic
_space_group_IT_number           14
_space_group_name_H-M_alt        'P 21/n'
_space_group_name_Hall           '-P 2yn'

_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.
;

loop_
_space_group_symop_operation_xyz
'x, y, z'
'-x+1/2, y+1/2, -z+1/2'
'-x, -y, -z'
'x-1/2, -y-1/2, z-1/2'

_cell_length_a                   10.8098(10)
_cell_length_b                   3.9789(4)
_cell_length_c                   24.250(2)
_cell_angle_alpha                90
_cell_angle_beta                 92.803(9)
_cell_angle_gamma                90
_cell_volume                     1041.75(17)
_cell_formula_units_Z            4
_cell_measurement_temperature    296(2)
_cell_measurement_reflns_used    1691
_cell_measurement_theta_min      4.0330
_cell_measurement_theta_max      27.3300

_exptl_crystal_description       BLOCK
_exptl_crystal_colour            COLORLESS
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    ?
_exptl_crystal_density_diffrn    1.506
_exptl_crystal_F_000             488
_exptl_transmission_factor_min   ?
_exptl_transmission_factor_max   ?
_exptl_crystal_size_max          ?
_exptl_crystal_size_mid          ?
_exptl_crystal_size_min          ?
_exptl_absorpt_coefficient_mu    0.123
_shelx_estimated_absorpt_T_min   ?
_shelx_estimated_absorpt_T_max   ?
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_correction_T_min  0.63556
_exptl_absorpt_correction_T_max  1.00000
_exptl_absorpt_process_details   CrysAlisPro
_exptl_absorpt_special_details   ?
_diffrn_ambient_temperature      296(2)
_diffrn_radiation_wavelength     0.71073
_diffrn_radiation_type           MoK\a
_diffrn_source                   'micro-focus sealed X-ray tube'
_diffrn_measurement_device_type  'Xcalibur, Eos, Nova'
_diffrn_measurement_method       'ω scans'
_diffrn_detector_area_resol_mean ?
_diffrn_reflns_number            7364
_diffrn_reflns_av_unetI/netI     0.0462
_diffrn_reflns_av_R_equivalents  0.0384
_diffrn_reflns_limit_h_min       -14
_diffrn_reflns_limit_h_max       11
_diffrn_reflns_limit_k_min       -5
_diffrn_reflns_limit_k_max       5
_diffrn_reflns_limit_l_min       -31
_diffrn_reflns_limit_l_max       29
_diffrn_reflns_theta_min         3.365
_diffrn_reflns_theta_max         27.482
_diffrn_reflns_theta_full        25.242
_diffrn_measured_fraction_theta_max 0.997
_diffrn_measured_fraction_theta_full 0.997
_diffrn_reflns_Laue_measured_fraction_max 0.997
_diffrn_reflns_Laue_measured_fraction_full 0.997
_diffrn_reflns_point_group_measured_fraction_max 0.997
_diffrn_reflns_point_group_measured_fraction_full 0.997
_reflns_number_total             2374
_reflns_number_gt                1575
_reflns_threshold_expression     'I > 2σ(I)'
_reflns_Friedel_coverage         0.000
_reflns_Friedel_fraction_max     .
_reflns_Friedel_fraction_full    .

_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.
;

_computing_data_collection       ?
_computing_cell_refinement       ?
_computing_data_reduction        ?
_computing_structure_solution    ?
_computing_structure_refinement  'SHELXL-2018/3 (Sheldrick, 2018)'
_computing_molecular_graphics    ?
_computing_publication_material  ?
_refine_special_details          ?
_refine_ls_structure_factor_coef Fsqd
_refine_ls_matrix_type           full
_refine_ls_weighting_scheme      calc
_refine_ls_weighting_details     
'w=1/[σ²(Fo²)+(0.0483P)²+0.2753P] where P=(Fo²+2Fc²)/3'
_atom_sites_solution_primary     ?
_atom_sites_solution_secondary   ?
_atom_sites_solution_hydrogens   geom
_refine_ls_hydrogen_treatment    constr
_refine_ls_extinction_method     none
_refine_ls_extinction_coef       .
_refine_ls_number_reflns         2374
_refine_ls_number_parameters     154
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.0937
_refine_ls_R_factor_gt           0.0597
_refine_ls_wR_factor_ref         0.1449
_refine_ls_wR_factor_gt          0.1263
_refine_ls_goodness_of_fit_ref   1.070
_refine_ls_restrained_S_all      1.070
_refine_ls_shift/su_max          0.000
_refine_ls_shift/su_mean         0.000

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
C1 C 1.7534(2) 1.0763(8) 0.16896(11) 0.0665(8) Uani 1 1 d . . . . .
H1A H 1.809003 1.020890 0.140666 0.100 Uiso 1 1 calc R U . . .
H1B H 1.748071 1.316133 0.172451 0.100 Uiso 1 1 calc R U . . .
H1C H 1.783646 0.981448 0.203437 0.100 Uiso 1 1 calc R U . . .
C2 C 1.3542(2) 0.2239(7) -0.02624(9) 0.0613(7) Uani 1 1 d . . . . .
H2A H 1.432043 0.213497 -0.043603 0.092 Uiso 1 1 calc R U . . .
H2B H 1.322311 0.000598 -0.022079 0.092 Uiso 1 1 calc R U . . .
H2C H 1.296520 0.354295 -0.048706 0.092 Uiso 1 1 calc R U . . .
C3 C 1.0729(2) 0.5272(6) 0.12697(10) 0.0470(6) Uani 1 1 d . . . . .
H3 H 1.006180 0.561894 0.149104 0.056 Uiso 1 1 calc R U . . .
C4 C 1.19291(19) 0.6467(6) 0.14234(8) 0.0400(5) Uani 1 1 d . . . . .
C5 C 1.2193(2) 0.8320(6) 0.19104(9) 0.0462(6) Uani 1 1 d . . . . .
H5 H 1.154809 0.879492 0.213820 0.055 Uiso 1 1 calc R U . . .
C6 C 1.42045(19) 0.8648(6) 0.17071(8) 0.0408(5) Uani 1 1 d . . . . .
C7 C 1.06004(19) 0.3613(6) 0.07887(10) 0.0479(6) Uani 1 1 d . . . . .
C8 C 1.29348(18) 0.5894(5) 0.10880(8) 0.0368(5) Uani 1 1 d . . . . .
C9 C 1.2723(2) 0.4145(6) 0.05768(8) 0.0409(5) Uani 1 1 d . . . . .
C10 C 1.1551(2) 0.3014(6) 0.04346(9) 0.0469(6) Uani 1 1 d . . . . .
H10 H 1.139366 0.186066 0.010504 0.056 Uiso 1 1 calc R U . . .
C11 C 1.5459(2) 0.9993(6) 0.18991(9) 0.0476(6) Uani 1 1 d . . . . .
N1 N 1.33000(17) 0.9398(5) 0.20560(7) 0.0476(5) Uani 1 1 d . . . . .
N2 N 1.40958(15) 0.7016(5) 0.12382(7) 0.0398(4) Uani 1 1 d . . . . .
O1 O 1.63190(14) 0.9413(5) 0.15441(6) 0.0554(5) Uani 1 1 d . . . . .
O2 O 1.37175(14) 0.3783(5) 0.02711(6) 0.0527(5) Uani 1 1 d . . . . .
O3 O 1.56409(16) 1.1435(6) 0.23272(8) 0.0844(7) Uani 1 1 d . . . . .
F1 F 0.94618(12) 0.2401(4) 0.06225(6) 0.0718(5) 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
C1 O1 1.446(3) . ?
C2 O2 1.436(3) . ?
C3 C7 1.341(3) . ?
C3 C4 1.415(3) . ?
C4 C8 1.408(3) . ?
C4 C5 1.410(3) . ?
C5 N1 1.303(3) . ?
C6 N2 1.310(3) . ?
C6 N1 1.357(3) . ?
C6 C11 1.510(3) . ?
C7 F1 1.364(2) . ?
C7 C10 1.391(3) . ?
C8 N2 1.365(2) . ?
C8 C9 1.430(3) . ?
C9 O2 1.343(2) . ?
C9 C10 1.372(3) . ?
C11 O3 1.194(3) . ?
C11 O1 1.318(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
C7 C3 C4 116.7(2) . . ?
C8 C4 C5 115.99(19) . . ?
C8 C4 C3 121.2(2) . . ?
C5 C4 C3 122.8(2) . . ?
N1 C5 C4 123.0(2) . . ?
N2 C6 N1 127.8(2) . . ?
N2 C6 C11 118.98(19) . . ?
N1 C6 C11 113.17(19) . . ?
C3 C7 F1 119.0(2) . . ?
C3 C7 C10 124.9(2) . . ?
F1 C7 C10 116.1(2) . . ?
N2 C8 C4 121.26(19) . . ?
N2 C8 C9 119.79(18) . . ?
C4 C8 C9 118.94(18) . . ?
O2 C9 C10 125.5(2) . . ?
O2 C9 C8 115.59(18) . . ?
C10 C9 C8 118.9(2) . . ?
C9 C10 C7 119.3(2) . . ?
O3 C11 O1 124.1(2) . . ?
O3 C11 C6 123.1(2) . . ?
O1 C11 C6 112.85(19) . . ?
C5 N1 C6 116.02(19) . . ?
C6 N2 C8 115.87(18) . . ?
C11 O1 C1 115.90(19) . . ?
C9 O2 C2 117.96(17) . . ?

_refine_diff_density_max         0.179
_refine_diff_density_min         -0.203
_refine_diff_density_rms         0.043

