# 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 2019

####################################################################### 
# 
# 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_vijay01_0m_a
_database_code_depnum_ccdc_archive 'CCDC 1889051'
loop_
_audit_author_name
_audit_author_address
vijay
;Indian Institute of Technology Delhi
India
;
_audit_update_record             
;
2019-01-07 deposited with the CCDC.	2019-06-04 downloaded from the CCDC.
;

_audit_creation_method           SHELXL-2014/7
_shelx_SHELXL_version_number     2014/7
_chemical_name_systematic        ?
_chemical_name_common            ?
_chemical_melting_point          ?
_chemical_formula_moiety         'C16 H14 N2 O3'
_chemical_formula_sum            'C16 H14 N2 O3'
_chemical_formula_weight         282.29
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'

_space_group_crystal_system      triclinic
_space_group_IT_number           2
_space_group_name_H-M_alt        'P -1'
_space_group_name_Hall           '-P 1'

_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, -y, -z'

_cell_length_a                   6.158(5)
_cell_length_b                   7.899(6)
_cell_length_c                   14.325(10)
_cell_angle_alpha                79.963(15)
_cell_angle_beta                 87.426(16)
_cell_angle_gamma                86.68(2)
_cell_volume                     684.5(9)
_cell_formula_units_Z            2
_cell_measurement_temperature    305(2)
_cell_measurement_reflns_used    7075
_cell_measurement_theta_min      2.29
_cell_measurement_theta_max      20.61

_exptl_crystal_description       block
_exptl_crystal_colour            white
_exptl_crystal_density_meas      1.369
_exptl_crystal_density_method    'not measured'
_exptl_crystal_density_diffrn    1.369
_exptl_crystal_F_000             296.0
_exptl_transmission_factor_min   ?
_exptl_transmission_factor_max   ?
_exptl_crystal_size_max          0.19
_exptl_crystal_size_mid          0.17
_exptl_crystal_size_min          0.15
_exptl_absorpt_coefficient_mu    0.096
_shelx_estimated_absorpt_T_min   ?
_shelx_estimated_absorpt_T_max   ?
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_correction_T_min  0.982
_exptl_absorpt_correction_T_max  0.986
_exptl_absorpt_process_details   ?
_exptl_absorpt_special_details   ?
_diffrn_ambient_temperature      305(2)
_diffrn_radiation_wavelength     0.71073
_diffrn_radiation_type           MoK\a
_diffrn_source                   ?
_diffrn_measurement_device_type  'Bruker APEX-II CCD'
_diffrn_measurement_method       'φ and ω scans'
_diffrn_detector_area_resol_mean ?
_diffrn_reflns_number            21232
_diffrn_reflns_av_unetI/netI     0.0459
_diffrn_reflns_av_R_equivalents  0.0612
_diffrn_reflns_limit_h_min       -8
_diffrn_reflns_limit_h_max       8
_diffrn_reflns_limit_k_min       -10
_diffrn_reflns_limit_k_max       10
_diffrn_reflns_limit_l_min       -19
_diffrn_reflns_limit_l_max       19
_diffrn_reflns_theta_min         2.622
_diffrn_reflns_theta_max         28.458
_diffrn_reflns_theta_full        25.242
_diffrn_measured_fraction_theta_max 0.994
_diffrn_measured_fraction_theta_full 0.999
_diffrn_reflns_Laue_measured_fraction_max 0.994
_diffrn_reflns_Laue_measured_fraction_full 0.999
_diffrn_reflns_point_group_measured_fraction_max 0.994
_diffrn_reflns_point_group_measured_fraction_full 0.999
_reflns_number_total             3459
_reflns_number_gt                2315
_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-2014/7 (Sheldrick, 2014)'
_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)+(0.1000P)²+0.8875P] 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         3437
_refine_ls_number_parameters     192
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.1088
_refine_ls_R_factor_gt           0.0638
_refine_ls_wR_factor_ref         0.1934
_refine_ls_wR_factor_gt          0.1616
_refine_ls_goodness_of_fit_ref   0.830
_refine_ls_restrained_S_all      0.830
_refine_ls_shift/su_max          0.047
_refine_ls_shift/su_mean         0.004

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
O3 O 0.2401(3) 0.1480(2) 0.28642(12) 0.0455(5) Uani 1 1 d . . . . .
O2 O 0.6695(3) 0.6037(2) 0.25014(11) 0.0433(4) Uani 1 1 d . . . . .
O1 O 0.8895(4) 0.8166(3) 0.24010(15) 0.0619(6) Uani 1 1 d . . . . .
N2 N 0.2207(4) 0.0401(3) 0.15532(17) 0.0578(7) Uani 1 1 d . . . . .
H2A H 0.0945 0.0090 0.1777 0.069 Uiso 1 1 calc R U . . .
H2B H 0.2679 0.0169 0.1013 0.069 Uiso 1 1 calc R U . . .
N1 N 0.7197(4) 0.1120(4) 0.02581(16) 0.0565(6) Uani 1 1 d . . . . .
C6 C 0.5618(4) 0.2675(3) 0.33352(15) 0.0349(5) Uani 1 1 d . . . . .
C9 C 0.5405(4) 0.1863(3) 0.17747(16) 0.0365(5) Uani 1 1 d . . . . .
C5 C 0.3648(4) 0.1961(3) 0.35557(16) 0.0382(5) Uani 1 1 d . . . . .
C10 C 0.6403(4) 0.1457(3) 0.09394(16) 0.0403(5) Uani 1 1 d . . . . .
C7 C 0.6788(4) 0.3044(3) 0.40740(16) 0.0400(5) Uani 1 1 d . . . . .
H7 H 0.8144 0.3508 0.3941 0.048 Uiso 1 1 calc R U . . .
C11 C 0.3424(4) 0.1241(3) 0.20405(17) 0.0398(5) Uani 1 1 d . . . . .
C8 C 0.6420(4) 0.3058(3) 0.23225(15) 0.0344(5) Uani 1 1 d . . . . .
H8 H 0.8004 0.2849 0.2297 0.041 Uiso 1 1 calc R U . . .
C12 C 0.5858(4) 0.4980(3) 0.18861(16) 0.0386(5) Uani 1 1 d . . . . .
C2 C 0.5997(5) 0.2740(3) 0.50001(17) 0.0463(6) Uani 1 1 d . . . . .
C14 C 0.7077(4) 0.5525(4) 0.09726(17) 0.0454(6) Uani 1 1 d . . . . .
H14 H 0.6967 0.5047 0.0428 0.054 Uiso 1 1 calc R U . . .
C16 C 0.8079(4) 0.7128(3) 0.20265(19) 0.0461(6) Uani 1 1 d . . . . .
C4 C 0.2789(5) 0.1664(4) 0.44706(18) 0.0476(6) Uani 1 1 d . . . . .
H4 H 0.1438 0.1192 0.4603 0.057 Uiso 1 1 calc R U . . .
C13 C 0.3440(4) 0.5420(4) 0.18081(19) 0.0464(6) Uani 1 1 d . . . . .
H13A H 0.2720 0.5073 0.2414 0.070 Uiso 1 1 calc R U . . .
H13B H 0.2867 0.4826 0.1350 0.070 Uiso 1 1 calc R U . . .
H13C H 0.3200 0.6639 0.1610 0.070 Uiso 1 1 calc R U . . .
C15 C 0.8330(5) 0.6778(4) 0.10476(19) 0.0497(6) Uani 1 1 d . . . . .
H15 H 0.9222 0.7347 0.0567 0.060 Uiso 1 1 calc R U . . .
C3 C 0.3966(5) 0.2077(4) 0.51843(18) 0.0524(7) Uani 1 1 d . . . . .
H3 H 0.3385 0.1906 0.5802 0.063 Uiso 1 1 calc R U . . .
C1 C 0.7333(6) 0.3128(5) 0.57822(19) 0.0628(8) Uani 1 1 d . . . . .
H1A H 0.6806 0.4200 0.5958 0.094 Uiso 1 1 calc R U . . .
H1B H 0.8829 0.3208 0.5567 0.094 Uiso 1 1 calc R U . . .
H1C H 0.7219 0.2223 0.6322 0.094 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
O3 C11 1.350(3) . ?
O3 C5 1.396(3) . ?
O2 C16 1.327(3) . ?
O2 C12 1.445(3) . ?
O1 C16 1.199(3) . ?
N2 C11 1.325(3) . ?
N2 H2A 0.8600 . ?
N2 H2B 0.8600 . ?
N1 C10 1.138(3) . ?
C6 C5 1.368(3) . ?
C6 C7 1.387(3) . ?
C6 C8 1.497(3) . ?
C9 C11 1.355(3) . ?
C9 C10 1.399(3) . ?
C9 C8 1.506(3) . ?
C5 C4 1.377(3) . ?
C7 C2 1.378(3) . ?
C7 H7 0.9300 . ?
C8 C12 1.563(4) . ?
C8 H8 0.9800 . ?
C12 C14 1.488(3) . ?
C12 C13 1.514(4) . ?
C2 C3 1.381(4) . ?
C2 C1 1.502(4) . ?
C14 C15 1.311(4) . ?
C14 H14 0.9300 . ?
C16 C15 1.476(4) . ?
C4 C3 1.374(4) . ?
C4 H4 0.9300 . ?
C13 H13A 0.9600 . ?
C13 H13B 0.9600 . ?
C13 H13C 0.9600 . ?
C15 H15 0.9300 . ?
C3 H3 0.9300 . ?
C1 H1A 0.9600 . ?
C1 H1B 0.9600 . ?
C1 H1C 0.9600 . ?

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 O3 C5 117.67(19) . . ?
C16 O2 C12 110.72(19) . . ?
C11 N2 H2A 120.0 . . ?
C11 N2 H2B 120.0 . . ?
H2A N2 H2B 120.0 . . ?
C5 C6 C7 117.7(2) . . ?
C5 C6 C8 119.9(2) . . ?
C7 C6 C8 122.4(2) . . ?
C11 C9 C10 117.9(2) . . ?
C11 C9 C8 120.9(2) . . ?
C10 C9 C8 121.1(2) . . ?
C6 C5 C4 122.1(2) . . ?
C6 C5 O3 121.7(2) . . ?
C4 C5 O3 116.2(2) . . ?
N1 C10 C9 179.3(3) . . ?
C2 C7 C6 121.8(3) . . ?
C2 C7 H7 119.1 . . ?
C6 C7 H7 119.1 . . ?
N2 C11 O3 111.0(2) . . ?
N2 C11 C9 127.1(2) . . ?
O3 C11 C9 121.9(2) . . ?
C6 C8 C9 108.83(19) . . ?
C6 C8 C12 110.63(19) . . ?
C9 C8 C12 110.85(19) . . ?
C6 C8 H8 108.8 . . ?
C9 C8 H8 108.8 . . ?
C12 C8 H8 108.8 . . ?
O2 C12 C14 102.97(19) . . ?
O2 C12 C13 107.6(2) . . ?
C14 C12 C13 112.1(2) . . ?
O2 C12 C8 107.55(19) . . ?
C14 C12 C8 112.1(2) . . ?
C13 C12 C8 113.7(2) . . ?
C7 C2 C3 118.4(2) . . ?
C7 C2 C1 120.2(3) . . ?
C3 C2 C1 121.4(3) . . ?
C15 C14 C12 110.0(2) . . ?
C15 C14 H14 125.0 . . ?
C12 C14 H14 125.0 . . ?
O1 C16 O2 121.2(3) . . ?
O1 C16 C15 130.8(3) . . ?
O2 C16 C15 108.0(2) . . ?
C3 C4 C5 118.8(3) . . ?
C3 C4 H4 120.6 . . ?
C5 C4 H4 120.6 . . ?
C12 C13 H13A 109.5 . . ?
C12 C13 H13B 109.5 . . ?
H13A C13 H13B 109.5 . . ?
C12 C13 H13C 109.5 . . ?
H13A C13 H13C 109.5 . . ?
H13B C13 H13C 109.5 . . ?
C14 C15 C16 108.2(2) . . ?
C14 C15 H15 125.9 . . ?
C16 C15 H15 125.9 . . ?
C4 C3 C2 121.1(2) . . ?
C4 C3 H3 119.4 . . ?
C2 C3 H3 119.4 . . ?
C2 C1 H1A 109.5 . . ?
C2 C1 H1B 109.5 . . ?
H1A C1 H1B 109.5 . . ?
C2 C1 H1C 109.5 . . ?
H1A C1 H1C 109.5 . . ?
H1B C1 H1C 109.5 . . ?

_refine_diff_density_max         0.628
_refine_diff_density_min         -0.220
_refine_diff_density_rms         0.053

