Home Crystal structure of (E)-2-(1-((2-aminophenyl)imino)ethyl)-6-bromo-4-chlorophenol, C14H12BrClN2O
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Crystal structure of (E)-2-(1-((2-aminophenyl)imino)ethyl)-6-bromo-4-chlorophenol, C14H12BrClN2O

  • Yong Hong EMAIL logo and Wei Liu
Published/Copyright: June 29, 2018

Abstract

C14H12BrClN2O, monoclinic, P21/c (no. 14), a = 3.9454(10) Å, b = 24.189(6) Å, c = 13.728(3) Å, β = 90.07°, V = 643.99(7) Å3, Z = 4, Rgt(F) = 0.0589, wRref(F2) = 0.1584, T = 293(2) K.

CCDC no.: 1815144

The asymmetric unit of the title crystal structure is shown in the figure. Tables 1 and 2 contain details on crystal structure and measurement conditions and a list of the atoms including atomic coordinates and displacement parameters.

Table 1:

Data collection and handling.

Crystal:Colorless block
Wavelength:Mo Kα radiation (0.71073 Å)
μ:3.33 mm−1
Diffractometer, scan mode:Bruker SMART, φ and ω-scans
θmax, completeness:27.5°, >99%
N(hkl)measured, N(hkl)unique, Rint:11411, 3001, 0.188
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 2117
N(param)refined:175
Programs:Bruker programs [1], SHELX [2], OLEX2 [3]
Table 2:

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2).

AtomxyzUiso*/Ueq
Br1−0.29045(12)0.38586(2)−0.39960(3)0.0277(2)
Cl1−0.7092(3)0.44311(5)−0.02995(9)0.0332(3)
O1−0.5796(9)0.27468(14)−0.3354(2)0.0269(8)
H1−0.6362530.244189−0.3149520.040*
N1−1.1860(11)0.15480(19)−0.3723(3)0.0304(10)
H1B−1.3572430.139598−0.4016830.036*
H1A−1.2436160.187889−0.3543150.036*
N2−0.8479(10)0.20647(16)−0.2209(3)0.0223(8)
C1−1.0962(12)0.12366(19)−0.2914(4)0.0246(10)
C2−1.1520(12)0.0664(2)−0.2866(4)0.0292(11)
H2−1.2606220.048644−0.3379280.035*
C3−1.0476(12)0.0360(2)−0.2062(4)0.0318(12)
H3−1.087639−0.001907−0.2042330.038*
C4−0.8861(12)0.0613(2)−0.1299(4)0.0292(11)
H4−0.8169750.040701−0.0762200.035*
C5−0.8262(12)0.1177(2)−0.1330(4)0.0261(11)
H5−0.7146770.134561−0.0812670.031*
C6−0.9287(11)0.14928(19)−0.2114(3)0.0214(10)
C7−0.8896(11)0.24310(19)−0.1532(3)0.0202(9)
C8−1.0634(12)0.2315(2)−0.0589(3)0.0266(10)
H8B−0.8977950.228707−0.0078040.040*
H8A−1.1858530.197268−0.0637460.040*
H8C−1.2184390.260914−0.0443580.040*
C9−0.7633(11)0.29912(19)−0.1738(3)0.0197(9)
C10−0.7896(11)0.3403(2)−0.1022(3)0.0223(10)
H10−0.8906040.332307−0.0426240.027*
C11−0.6659(11)0.3925(2)−0.1201(3)0.0217(10)
C12−0.5146(11)0.4060(2)−0.2078(3)0.0222(10)
H12−0.4326760.441500−0.2184380.027*
C13−0.4867(11)0.3665(2)−0.2787(3)0.0207(9)
C14−0.6074(11)0.31188(19)−0.2641(3)0.0199(9)

Source of material

1,2-Diaminobenzene (1 mmol, 0.108 g) and 1-(3-bromo-5-chloro-2-hydroxyphenyl)ethanone (1 mmol, 0.249 g) were added to the solution of ethanol (10 mL), then the mixture was refluxed 2 h. After filtering the precipitate was disolved in mixed solvents of dichloromethane ethyl acetate and evaporated slowly at room temperature to obtain colorless prismatic crystals.

Experimental details

The H atoms were positioned geometrically with d(C—H) = 0.93−0.98 Å and refined as riding with Uiso(H) = 1.2 Ueq(carrier) or 1.5 Ueq(methyl).

Discussion

Mono-imine with o-amino is a class of important tridentate ligands. Their complexes can be used for catalysis [4]. Mono-imine with o-amino is also a key intermediate for the synthesis of unsymmetrical tetradentate bis-Schiff base ligands [5].

In the crystal structure of the title compound, the dihedral angle between the two benzene rings (C1—C2—C3—C4—C5—C6 and C9—C10—C11—C12—C13—C14) is 48.25°. Bond lengths and angles are in the expected ranges and similar to a related structure [6]. There is an intramolecular O—H⋯N hydrogen bond (cf. the figure). The packing of crystal structure is via van der Waals forces.

Award Identifier / Grant number: 21461007

Funding statement: This work was financially supported by National Natural Science Foundation of China (Grant No.21461007) and Open Fund of Master Construction Discipline in Yunnan Province (Grant No. HXB1401).

References

Bruker, APEX2, SAINT and SADABS. Brucker AXS Inc., Madison, Wisconsin, USA (2009).Search in Google Scholar

Sheldrick, G. M.: A short history of SHELX. Acta Crystallogr. A64 (2008) 112–122.10.1107/S0108767307043930Search in Google Scholar

Dolomanov, O. V.; Bourhis, L. J.; Gildea, R. J.; Howard, J. A. K.; Puschmann, H.: OLEX2: a complete structure solution, refinement and analysis program. J. Appl. Crystallogr. 42 (2009) 339–341.10.1107/S0021889808042726Search in Google Scholar

Nozaki, H.; Takaya, H.; Moriuti, S.; Noyori, R.; Homogeneous catalysis in the decomposition of diazo compounds by copper chelates: asymmetric carbenoid reactions. Tetrahedron. 24 (1968) 3655–3669.10.1016/S0040-4020(01)91998-2Search in Google Scholar

Belmonte, M. M.; Wezenberg, S. J.; Haak, R. M.; Anselmo, D.; Escudero-Adán, E. C.; Benet-Buchholza, J.; Kleij, A. W.: Self-assembly of Zn(salphen) complexes: Steric regulation, stability studies and crystallographic analysis revealing an unexpected dimeric 3,3[prime or minute]-t-Bu-substituted Zn(salphen) complex. Dalton Transactions. 39 (2010) 4541–4550.10.1039/b925560eSearch in Google Scholar PubMed

Blagus, A.; Kaitner, B.: Two ketimine polymorphs of 2-{1-[(2-Aminophenyl)imino]ethyl}phenol. Acta. Chim. Slov. 58 (2011) 823–829.Search in Google Scholar

Received: 2018-03-12
Accepted: 2018-06-12
Published Online: 2018-06-29
Published in Print: 2018-08-28

©2018 Yong Hong et al., published by De Gruyter, Berlin/Boston

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

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  78. The crystal structure of 1-((5-chloro-3-methyl-1-phenyl-1H-pyrazole-4-yl)methyl)-1,3-diphenylurea, C24H21ClN4O
  79. Crystal structure of 6-(2-bromoacetamido)tetrahydro-2H-pyran-2,3,4,5-Tetrayl tetraacetate, C16H22BrNO10
  80. Crystal structure of 5-methylpyrazine-2-carbohydrazide, C6H8N4O
  81. Crystal structure of catena-poly[(μ2-5-(tert-butyl)isophthalato-κ4O,O′:O′′,O′′′)(-4′-(pyridin-4-yl)-2,2′:6′,2′′-terpyridine-κ3N,N′,N′′)manganese(II)], C32H28N4O5Mn
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