# Electronic Supplementary Material (ESI) for Organic & Biomolecular Chemistry.
# This journal is © The Royal Society of Chemistry 2022

####################################################################### 
# 
# 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_DATAM_a
_database_code_depnum_ccdc_archive 'CCDC 2155832'
loop_
_audit_author_name
_audit_author_address
'Rambabu Dandela'
;Institute of Chemical Technology IOC Bhubaneswar
India
;
_audit_update_record             
;
2022-03-02 deposited with the CCDC.	2022-04-20 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         'C13 H15 N O2'
_chemical_formula_sum            'C13 H15 N O2'
_chemical_formula_weight         217.26

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      monoclinic
_space_group_IT_number           14
_space_group_name_H-M_alt        'P 21/c'
_space_group_name_Hall           '-P 2ybc'

_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+1/2, -z+1/2'
'-x, -y, -z'
'x, -y-1/2, z-1/2'

_cell_length_a                   9.581(1)
_cell_length_b                   11.381(1)
_cell_length_c                   10.941(1)
_cell_angle_alpha                90
_cell_angle_beta                 103.15(2)
_cell_angle_gamma                90
_cell_volume                     1161.9(1)
_cell_formula_units_Z            4
_cell_measurement_temperature    273(2)
_cell_measurement_reflns_used    1832
_cell_measurement_theta_min      0.980
_cell_measurement_theta_max      0.987

_exptl_crystal_description       plate
_exptl_crystal_colour            colorless
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    ?
_exptl_crystal_density_diffrn    1.242
_exptl_crystal_F_000             464
_exptl_transmission_factor_min   ?
_exptl_transmission_factor_max   ?
_exptl_crystal_size_max          0.25
_exptl_crystal_size_mid          0.20
_exptl_crystal_size_min          0.15
_exptl_absorpt_coefficient_mu    0.084
_shelx_estimated_absorpt_T_min   ?
_shelx_estimated_absorpt_T_max   ?
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_correction_T_min  0.980
_exptl_absorpt_correction_T_max  0.987
_exptl_absorpt_process_details   ?
_exptl_absorpt_special_details   ?
_diffrn_ambient_temperature      273(2)
_diffrn_radiation_wavelength     0.71073
_diffrn_radiation_type           MoK\a
_diffrn_source                   microfocus
_diffrn_measurement_device_type  'Bruker D8 Venture photon 100 CMOS detector'
_diffrn_measurement_method       'Omega and Phi scans'
_diffrn_detector_area_resol_mean ?
_diffrn_reflns_number            16343
_diffrn_reflns_av_unetI/netI     0.0368
_diffrn_reflns_av_R_equivalents  0.0611
_diffrn_reflns_limit_h_min       -11
_diffrn_reflns_limit_h_max       11
_diffrn_reflns_limit_k_min       -14
_diffrn_reflns_limit_k_max       14
_diffrn_reflns_limit_l_min       -13
_diffrn_reflns_limit_l_max       13
_diffrn_reflns_theta_min         2.619
_diffrn_reflns_theta_max         26.547
_diffrn_reflns_theta_full        25.242
_diffrn_measured_fraction_theta_max 0.983
_diffrn_measured_fraction_theta_full 0.984
_diffrn_reflns_Laue_measured_fraction_max 0.983
_diffrn_reflns_Laue_measured_fraction_full 0.984
_diffrn_reflns_point_group_measured_fraction_max 0.983
_diffrn_reflns_point_group_measured_fraction_full 0.984
_reflns_number_total             2377
_reflns_number_gt                1832
_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       'Bruker APEX3'
_computing_cell_refinement       'Bruker SHELXL'
_computing_data_reduction        'Bruker SAINT'
_computing_structure_solution    'SHELXT 2018/2 (Sheldrick, 2018)'
_computing_structure_refinement  'SHELXL-2018/3 (Sheldrick, 2018)'
_computing_molecular_graphics    'Bruker SHELXTL'
_computing_publication_material  'Bruker SHELXTL'
_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+0.3093P] 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         2377
_refine_ls_number_parameters     145
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.0690
_refine_ls_R_factor_gt           0.0510
_refine_ls_wR_factor_ref         0.1715
_refine_ls_wR_factor_gt          0.1508
_refine_ls_goodness_of_fit_ref   0.955
_refine_ls_restrained_S_all      0.955
_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
O1 O 0.31728(15) 0.12879(11) 0.45070(16) 0.0727(5) Uani 1 1 d . . . . .
O2 O 0.30976(16) 0.37571(13) 0.56101(12) 0.0694(4) Uani 1 1 d . . . . .
N1 N 0.50515(16) 0.23627(11) 0.41886(14) 0.0512(4) Uani 1 1 d . . . . .
C8 C 0.17751(16) 0.37338(13) 0.35062(15) 0.0437(4) Uani 1 1 d . . . . .
C9 C 0.16139(19) 0.32382(15) 0.23265(16) 0.0520(4) Uani 1 1 d . . . . .
H9 H 0.221594 0.263315 0.219600 0.062 Uiso 1 1 calc R U . . .
C6 C 0.37477(18) 0.22311(14) 0.43917(16) 0.0480(4) Uani 1 1 d . . . . .
C7 C 0.28977(17) 0.33196(14) 0.45694(15) 0.0464(4) Uani 1 1 d . . . . .
C5 C 0.5685(2) 0.35013(15) 0.40221(18) 0.0550(5) Uani 1 1 d . . . . .
H5A H 0.646995 0.366061 0.473560 0.066 Uiso 1 1 calc R U . . .
H5B H 0.497150 0.411311 0.398398 0.066 Uiso 1 1 calc R U . . .
C13 C 0.08840(19) 0.46501(17) 0.3689(2) 0.0590(5) Uani 1 1 d . . . . .
H13 H 0.099640 0.499361 0.447643 0.071 Uiso 1 1 calc R U . . .
C10 C 0.0550(2) 0.3650(2) 0.1342(2) 0.0681(6) Uani 1 1 d . . . . .
H10 H 0.043308 0.331565 0.054926 0.082 Uiso 1 1 calc R U . . .
C1 C 0.5964(2) 0.13413(16) 0.4139(2) 0.0632(5) Uani 1 1 d . . . . .
H1A H 0.541843 0.062827 0.416841 0.076 Uiso 1 1 calc R U . . .
H1B H 0.676355 0.134638 0.486558 0.076 Uiso 1 1 calc R U . . .
C11 C -0.0329(2) 0.4546(2) 0.1532(2) 0.0740(6) Uani 1 1 d . . . . .
H11 H -0.104242 0.481713 0.086722 0.089 Uiso 1 1 calc R U . . .
C12 C -0.0165(2) 0.50454(19) 0.2697(2) 0.0732(6) Uani 1 1 d . . . . .
H12 H -0.076641 0.565496 0.281708 0.088 Uiso 1 1 calc R U . . .
C2 C 0.6519(2) 0.13464(18) 0.2975(2) 0.0707(6) Uani 1 1 d . . . . .
H2A H 0.573209 0.121380 0.225620 0.085 Uiso 1 1 calc R U . . .
H2B H 0.720007 0.070944 0.301142 0.085 Uiso 1 1 calc R U . . .
C4 C 0.6229(3) 0.35167(18) 0.2838(2) 0.0684(6) Uani 1 1 d . . . . .
H4A H 0.672550 0.425101 0.278511 0.082 Uiso 1 1 calc R U . . .
H4B H 0.542543 0.346827 0.211783 0.082 Uiso 1 1 calc R U . . .
C3 C 0.7242(3) 0.2497(2) 0.2810(3) 0.0776(7) Uani 1 1 d . . . . .
H3A H 0.752968 0.249350 0.201517 0.093 Uiso 1 1 calc R U . . .
H3B H 0.809582 0.258994 0.347626 0.093 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
O1 C6 1.226(2) . ?
O2 C7 1.217(2) . ?
N1 C6 1.326(2) . ?
N1 C5 1.460(2) . ?
N1 C1 1.463(2) . ?
C8 C9 1.385(2) . ?
C8 C13 1.391(2) . ?
C8 C7 1.471(2) . ?
C9 C10 1.385(3) . ?
C6 C7 1.519(2) . ?
C5 C4 1.502(3) . ?
C13 C12 1.376(3) . ?
C10 C11 1.369(3) . ?
C1 C2 1.487(3) . ?
C11 C12 1.372(3) . ?
C2 C3 1.511(3) . ?
C4 C3 1.518(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
C6 N1 C5 123.73(14) . . ?
C6 N1 C1 120.68(14) . . ?
C5 N1 C1 115.58(14) . . ?
C9 C8 C13 119.83(16) . . ?
C9 C8 C7 120.87(15) . . ?
C13 C8 C7 119.29(15) . . ?
C8 C9 C10 119.57(18) . . ?
O1 C6 N1 125.35(16) . . ?
O1 C6 C7 115.74(15) . . ?
N1 C6 C7 118.83(13) . . ?
O2 C7 C8 122.67(16) . . ?
O2 C7 C6 118.59(15) . . ?
C8 C7 C6 118.49(14) . . ?
N1 C5 C4 110.71(15) . . ?
C12 C13 C8 119.61(19) . . ?
C11 C10 C9 120.2(2) . . ?
N1 C1 C2 111.20(15) . . ?
C10 C11 C12 120.38(19) . . ?
C11 C12 C13 120.38(19) . . ?
C1 C2 C3 111.64(17) . . ?
C5 C4 C3 110.97(17) . . ?
C2 C3 C4 110.34(18) . . ?

_refine_diff_density_max         0.213
_refine_diff_density_min         -0.141
_refine_diff_density_rms         0.029

