# Electronic Supplementary Material (ESI) for RSC Advances.
# This journal is © The Royal Society of Chemistry 2016

####################################################################### 
# 
# 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_tempone
_database_code_depnum_ccdc_archive 'CCDC 1500661'
_audit_update_record             
;
2016-08-23 deposited with the CCDC.
2016-09-19 downloaded from the CCDC.
;

_audit_creation_method           SHELXL-2014/6
_chemical_name_systematic        ?
_chemical_name_common            ?
_chemical_melting_point          ?
_chemical_formula_moiety         'C9 H16 N O2'
_chemical_formula_sum            'C9 H16 N O2'
_chemical_formula_weight         170.23

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      orthorhombic
_space_group_IT_number           29
_space_group_name_H-M_alt        'P c a 21'
_space_group_name_Hall           'P 2c -2ac'

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

_cell_length_a                   7.8102(2)
_cell_length_b                   11.8025(3)
_cell_length_c                   10.2102(2)
_cell_angle_alpha                90
_cell_angle_beta                 90
_cell_angle_gamma                90
_cell_volume                     941.18(4)
_cell_formula_units_Z            4
_cell_measurement_temperature    100(2)
_cell_measurement_reflns_used    6066
_cell_measurement_theta_min      3
_cell_measurement_theta_max      30

_exptl_crystal_description       prism
_exptl_crystal_colour            colorless
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    ?
_exptl_crystal_density_diffrn    1.201
_exptl_crystal_F_000             372
_exptl_transmission_factor_min   ?
_exptl_transmission_factor_max   ?
_exptl_crystal_size_max          0.450
_exptl_crystal_size_mid          0.350
_exptl_crystal_size_min          0.320
_exptl_absorpt_coefficient_mu    0.084
_shelx_estimated_absorpt_T_min   0.963
_shelx_estimated_absorpt_T_max   0.974
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_correction_T_min  0.913
_exptl_absorpt_correction_T_max  0.989
_exptl_absorpt_process_details   'APEX2 (Bruker, 2005)'
_exptl_absorpt_special_details   ?
_diffrn_ambient_temperature      100(2)
_diffrn_radiation_wavelength     0.71073
_diffrn_radiation_type           MoK\a
_diffrn_source                   ?
_diffrn_measurement_device_type  'Bruker APEX2 CCD area detector'
_diffrn_measurement_method       'phi and omega scans'
_diffrn_detector_area_resol_mean ?
_diffrn_reflns_number            180671
_diffrn_reflns_av_unetI/netI     0.0152
_diffrn_reflns_av_R_equivalents  0.0351
_diffrn_reflns_limit_h_min       -18
_diffrn_reflns_limit_h_max       19
_diffrn_reflns_limit_k_min       -28
_diffrn_reflns_limit_k_max       28
_diffrn_reflns_limit_l_min       -24
_diffrn_reflns_limit_l_max       24
_diffrn_reflns_theta_min         1.725
_diffrn_reflns_theta_max         60.000
_diffrn_reflns_theta_full        25.242
_diffrn_measured_fraction_theta_max 1.000
_diffrn_measured_fraction_theta_full 0.999
_diffrn_reflns_Laue_measured_fraction_max 1.000
_diffrn_reflns_Laue_measured_fraction_full 0.999
_diffrn_reflns_point_group_measured_fraction_max 1.000
_diffrn_reflns_point_group_measured_fraction_full 0.999
_reflns_number_total             14287
_reflns_number_gt                12326
_reflns_threshold_expression     'I > 2σ(I)'
_reflns_Friedel_coverage         0.940
_reflns_Friedel_fraction_max     1.000
_reflns_Friedel_fraction_full    0.999

_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       'APEX2 (Bruker, 2005)'
_computing_cell_refinement       'APEX2 (Bruker, 2005)'
_computing_data_reduction        'APEX2 (Bruker, 2005)'
_computing_structure_solution    'APEX2 (Bruker, 2005)'
_computing_structure_refinement  'SHELXL-2014/6 (Sheldrick, 2014)'
_computing_molecular_graphics    'SHELXL-2014/6 (Sheldrick, 2014)'
_computing_publication_material  'SHELXL-2014/6 (Sheldrick, 2014)'
_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)+(0.0443P)²+0.0145P] where P=(Fo²+2Fc²)/3'
_atom_sites_solution_primary     ?
_atom_sites_solution_secondary   ?
_atom_sites_solution_hydrogens   difmap
_refine_ls_hydrogen_treatment    refall
_refine_ls_extinction_method     none
_refine_ls_extinction_coef       .
_refine_ls_abs_structure_details 
;
 Flack x determined using 5477 quotients [(I+)-(I-)]/[(I+)+(I-)]
 (Parsons, Flack and Wagner, Acta Cryst. B69 (2013) 249-259).
;
_chemical_absolute_configuration ?
_refine_ls_number_reflns         14287
_refine_ls_number_parameters     173
_refine_ls_number_restraints     1
_refine_ls_R_factor_all          0.0402
_refine_ls_R_factor_gt           0.0303
_refine_ls_wR_factor_ref         0.0809
_refine_ls_wR_factor_gt          0.0735
_refine_ls_goodness_of_fit_ref   1.048
_refine_ls_restrained_S_all      1.048
_refine_ls_shift/su_max          0.001
_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 0.22885(5) 0.68022(3) 0.91971(4) 0.02376(7) Uani 1 1 d . . . . .
O2 O -0.24751(5) 0.86597(3) 1.23859(4) 0.02076(5) Uani 1 1 d . . . . .
N1 N 0.11678(4) 0.72337(2) 0.99629(3) 0.01322(4) Uani 1 1 d . . . . .
C1 C -0.04647(4) 0.66069(3) 1.01731(3) 0.01273(4) Uani 1 1 d . . . . .
C2 C -0.18665(4) 0.74540(3) 1.05655(4) 0.01344(4) Uani 1 1 d . . . . .
C3 C -0.13932(4) 0.82299(3) 1.16831(3) 0.01282(4) Uani 1 1 d . . . . .
C4 C 0.04925(4) 0.84429(3) 1.18778(3) 0.01363(4) Uani 1 1 d . . . . .
C5 C 0.15853(4) 0.83210(3) 1.06335(3) 0.01220(4) Uani 1 1 d . . . . .
C6 C -0.09717(7) 0.60293(4) 0.88939(5) 0.02085(7) Uani 1 1 d . . . . .
C7 C -0.01708(6) 0.57132(4) 1.12424(5) 0.01950(6) Uani 1 1 d . . . . .
C8 C 0.12364(5) 0.92992(3) 0.96785(4) 0.01634(5) Uani 1 1 d . . . . .
C9 C 0.34762(5) 0.83043(4) 1.10212(5) 0.01983(6) Uani 1 1 d . . . . .
H2A H -0.2160(15) 0.7919(10) 0.9831(13) 0.024(2) Uiso 1 1 d . . . . .
H2B H -0.2898(17) 0.7085(11) 1.0764(14) 0.027(3) Uiso 1 1 d . . . . .
H4A H 0.0633(17) 0.9211(11) 1.2183(13) 0.027(3) Uiso 1 1 d . . . . .
H4B H 0.0891(16) 0.7908(11) 1.2517(13) 0.023(2) Uiso 1 1 d . . . . .
H6A H -0.106(2) 0.6584(15) 0.8168(19) 0.044(4) Uiso 1 1 d . . . . .
H6B H -0.018(2) 0.5476(13) 0.8617(16) 0.041(4) Uiso 1 1 d . . . . .
H6C H -0.2018(19) 0.5615(14) 0.9008(18) 0.042(4) Uiso 1 1 d . . . . .
H7A H 0.0725(19) 0.5200(11) 1.0967(13) 0.031(3) Uiso 1 1 d . . . . .
H7B H -0.1169(17) 0.5241(11) 1.1334(15) 0.031(3) Uiso 1 1 d . . . . .
H7C H 0.0158(17) 0.6027(13) 1.2081(15) 0.037(3) Uiso 1 1 d . . . . .
H8A H 0.0004(16) 0.9306(11) 0.9433(14) 0.029(3) Uiso 1 1 d . . . . .
H8B H 0.1922(16) 0.9245(11) 0.8909(14) 0.026(3) Uiso 1 1 d . . . . .
H8C H 0.1490(16) 1.0033(11) 1.0078(12) 0.025(3) Uiso 1 1 d . . . . .
H9C H 0.3772(16) 0.9006(12) 1.1481(13) 0.028(3) Uiso 1 1 d . . . . .
H9A H 0.4175(19) 0.8218(12) 1.0225(15) 0.031(3) Uiso 1 1 d . . . . .
H9B H 0.3668(16) 0.7667(11) 1.1571(13) 0.025(3) Uiso 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
O1 N1 1.2794(4) . ?
O2 C3 1.2191(4) . ?
N1 C1 1.4896(5) . ?
N1 C5 1.4907(4) . ?
C1 C6 1.5256(5) . ?
C1 C7 1.5353(5) . ?
C1 C2 1.5358(5) . ?
C2 C3 1.5090(5) . ?
C2 H2A 0.957(13) . ?
C2 H2B 0.938(13) . ?
C3 C4 1.5072(5) . ?
C4 C5 1.5373(5) . ?
C4 H4A 0.965(13) . ?
C4 H4B 0.960(13) . ?
C5 C9 1.5291(5) . ?
C5 C8 1.5355(5) . ?
C6 H6A 0.991(19) . ?
C6 H6B 0.941(15) . ?
C6 H6C 0.960(16) . ?
C7 H7A 0.967(14) . ?
C7 H7B 0.963(13) . ?
C7 H7C 0.968(16) . ?
C8 H8A 0.995(12) . ?
C8 H8B 0.953(14) . ?
C8 H8C 0.978(13) . ?
C9 H9C 0.980(14) . ?
C9 H9A 0.984(15) . ?
C9 H9B 0.950(13) . ?

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
O1 N1 C1 118.42(3) . . ?
O1 N1 C5 118.28(3) . . ?
C1 N1 C5 123.27(3) . . ?
N1 C1 C6 108.70(3) . . ?
N1 C1 C7 108.40(3) . . ?
C6 C1 C7 109.91(3) . . ?
N1 C1 C2 108.93(3) . . ?
C6 C1 C2 109.22(3) . . ?
C7 C1 C2 111.61(3) . . ?
C3 C2 C1 114.69(3) . . ?
C3 C2 H2A 107.6(8) . . ?
C1 C2 H2A 109.9(7) . . ?
C3 C2 H2B 109.2(9) . . ?
C1 C2 H2B 111.5(8) . . ?
H2A C2 H2B 103.3(11) . . ?
O2 C3 C4 122.02(3) . . ?
O2 C3 C2 121.86(3) . . ?
C4 C3 C2 116.12(3) . . ?
C3 C4 C5 114.70(3) . . ?
C3 C4 H4A 108.1(8) . . ?
C5 C4 H4A 107.0(8) . . ?
C3 C4 H4B 107.3(7) . . ?
C5 C4 H4B 108.7(8) . . ?
H4A C4 H4B 111.2(11) . . ?
N1 C5 C9 108.61(3) . . ?
N1 C5 C8 108.47(3) . . ?
C9 C5 C8 110.21(3) . . ?
N1 C5 C4 109.80(3) . . ?
C9 C5 C4 108.87(3) . . ?
C8 C5 C4 110.85(3) . . ?
C1 C6 H6A 111.3(11) . . ?
C1 C6 H6B 113.4(10) . . ?
H6A C6 H6B 106.4(14) . . ?
C1 C6 H6C 110.2(11) . . ?
H6A C6 H6C 111.4(14) . . ?
H6B C6 H6C 103.9(14) . . ?
C1 C7 H7A 109.4(8) . . ?
C1 C7 H7B 110.2(8) . . ?
H7A C7 H7B 104.6(11) . . ?
C1 C7 H7C 113.9(9) . . ?
H7A C7 H7C 107.8(12) . . ?
H7B C7 H7C 110.5(13) . . ?
C5 C8 H8A 109.7(8) . . ?
C5 C8 H8B 111.9(8) . . ?
H8A C8 H8B 109.7(11) . . ?
C5 C8 H8C 111.4(7) . . ?
H8A C8 H8C 107.1(10) . . ?
H8B C8 H8C 106.8(11) . . ?
C5 C9 H9C 109.9(7) . . ?
C5 C9 H9A 108.9(9) . . ?
H9C C9 H9A 110.6(11) . . ?
C5 C9 H9B 108.4(8) . . ?
H9C C9 H9B 110.5(12) . . ?
H9A C9 H9B 108.5(11) . . ?

_refine_diff_density_max         0.389
_refine_diff_density_min         -0.222
_refine_diff_density_rms         0.051

_shelxl_version_number           2014/6

