#------------------------------------------------------------------------------ #$Date: 2008-01-26 13:05:32 +0000 (Sat, 26 Jan 2008) $ #$Revision: 19 $ #$URL: svn://www.crystallography.net/cod/cif/2/2003525.cif $ #------------------------------------------------------------------------------ # # This file is available in the Crystallography Open Database (COD), # http://www.crystallography.net/ # # All data on this site have been placed in the public domain by the # contributors. # data_2003525 _journal_name_full 'Acta Crystallographica' _journal_year 1995 _journal_volume C51 _journal_page_first 1160 _journal_page_last 1164 _publ_section_title ; Conformationally Defined Cyclohexyl Carnitine Analogs ; _chemical_formula_sum 'C10 H20 Cl1 N1 O3' _chemical_formula_weight 237.73 _symmetry_space_group_name_H-M 'C c' _cell_length_a 12.390(1) _cell_length_b 8.245(2) _cell_length_c 13.732(1) _cell_angle_alpha 90 _cell_angle_beta 121.543(9) _cell_angle_gamma 90 _cell_volume 1195.6(3) _cell_formula_units_Z 4 _exptl_crystal_density_diffrn 1.321 _exptl_crystal_density_meas ? _diffrn_radiation_type 'CuK\a' _diffrn_radiation_wavelength 1.5418 _cell_measurement_reflns_used 25 _cell_measurement_theta_min 25 _cell_measurement_theta_max 35 _exptl_absorpt_coefficient_mu 2.79 _cell_measurement_temperature 295 _exptl_crystal_description 'Needles cut into blocks' _exptl_crystal_size_max 0.65 _exptl_crystal_size_mid 0.62 _exptl_crystal_size_min 0.46 _exptl_crystal_size_rad ? _exptl_crystal_colour 'Colorless' _chemical_compound_source 'Prepared by authors' _diffrn_measurement_device 'Enraf-Nonius CAD-4' _diffrn_measurement_method '\w-2\q' _exptl_absorpt_correction_type 'empirical' _exptl_absorpt_correction_T_min 0.899 _exptl_absorpt_correction_T_max 0.998 _diffrn_reflns_number 1301 _reflns_number_total 1272 _reflns_number_observed 1242 _reflns_observed_criterion I>=3\s(I) _diffrn_reflns_av_R_equivalents notaveraged _diffrn_reflns_theta_max 74 _diffrn_reflns_limit_h_min -15 _diffrn_reflns_limit_h_max 0 _diffrn_reflns_limit_k_min 0 _diffrn_reflns_limit_k_max 10 _diffrn_reflns_limit_l_min -17 _diffrn_reflns_limit_l_max 17 _diffrn_standards_number 3 _diffrn_standards_interval_count ? _diffrn_standards_interval_time 60 _diffrn_standards_decay_% -0.1 _refine_ls_structure_factor_coef F _refine_ls_R_factor_obs '0.025 (or 0.034)' _refine_ls_wR_factor_obs '0.0332 (or 0.054)' _refine_ls_goodness_of_fit_obs '1.415 (or 1.21)' _refine_ls_number_reflns 1242 _refine_ls_number_parameters 197 _refine_ls_hydrogen_treatment 'refxyz (O-H 0.76-0.79; C-H 0.89-1.14\%A)' _refine_ls_weighting_scheme 'w=1/\s^2^(F~o~)' _refine_ls_shift/esd_max 0.01 _refine_diff_density_max 0.111 _refine_diff_density_min -0.043 _refine_ls_extinction_method 'Zachariasen (1963)' _refine_ls_extinction_coef 9.1(7)E-6 _atom_type_scat_source 'Cromer & Waber (1974)' loop_ _atom_site_label _atom_site_fract_x _atom_site_fract_y _atom_site_fract_z _atom_site_B_iso_or_equiv Cl .800 .55262(7) .800 3.93(1) O1 .4919(2) 1.1395(2) .7411(1) 4.55(3) O2 .4699(2) .9042(2) .6537(1) 4.54(4) O3 .4059(1) 1.2318(2) .4771(1) 3.36(3) N1 .5599(1) 1.4934(2) .4574(1) 2.72(3) C1 .5988(2) 1.1143(3) .6419(2) 2.89(4) C2 .5312(2) 1.2633(2) .5667(1) 2.54(4) C3 .6153(2) 1.3355(2) .5259(1) 2.44(4) C4 .6464(2) 1.2127(3) .4617(2) 3.08(4) C5 .7172(2) 1.0703(3) .5410(2) 3.46(4) C6 .6372(2) .9907(3) .5826(2) 3.32(4) C7 .5141(2) 1.0381(3) .6784(2) 3.11(4) C8 .4944(2) 1.5919(3) .5029(2) 3.83(5) C9 .6686(2) 1.5922(3) .4698(2) 3.38(4) C10 .4696(3) 1.4628(3) .3326(2) 4.49(6) H1 .671(2) 1.152(3) .707(2) 3.8 H2 .528(2) 1.343(3) .621(2) 3.3 H3 .692(2) 1.369(3) .591(2) 3.2 H4 .567(2) 1.171(3) .396(2) 3.9 H4' .699(2) 1.261(3) .436(2) 3.9 H5 .731(3) .984(4) .499(2) 4.4 H5' .799(2) 1.124(4) .607(2) 4.4 H6 .679(3) .902(4) .633(2) 4.4 H6' .560(2) .942(3) .517(2) 4.4 H8 .469(3) 1.690(4) .459(2) 5.2 H8' .556(3) 1.609(4) .581(2) 5.2 H8" .412(3) 1.533(4) .489(3) 5.2 H9 .624(3) 1.696(3) .425(2) 4.6 H9' .707(3) 1.535(3) .440(2) 4.6 H9" .720(3) 1.626(4) .556(2) 4.6 H10 .444(3) 1.562(4) .304(3) 6.1 H10' .408(3) 1.380(4) .325(2) 6.1 H10" .531(3) 1.417(4) .299(3) 6.1 HO1 .444(2) 1.096(3) .751(2) 4.4 HO3 .404(3) 1.159(4) .439(2) 5.9