(E)-1-(4-Fluoro­phen­yl)-3-(4-methyl­phen­yl)prop-2-en-1-one

نویسندگان

  • Hoong-Kun Fun
  • Samuel Robinson Jebas
  • P. S. Patil
  • E. Deepak D’Silva
  • S. M. Dharmaprakash
چکیده

The title compound, C(16)H(13)FO, adopts an E configuration with respect to the C=C bond of the propenone unit. The dihedral angle between the two benzene rings is 47.0 (5)°. Intra-molecular C-H⋯O hydrogen bonds generate an S(5) ring motif. In the crystal structure, mol-ecules are packed into columns along the c axis and the structure is stabilized by weak intra-molecular C-H⋯O hydrogen bonds and inter-molecular C-H⋯π inter-actions involving both aromatic rings.

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منابع مشابه

(2E)-3-(3-Bromo-4-meth­oxy­phen­yl)-1-(4-fluoro­phen­yl)prop-2-en-1-one

In the title compound, C(16)H(12)BrFO(2), the dihedral angle between the aromatic rings is 23.75 (12)° and the dihedral angle between the prop-2-en-1-one fragment and the fluorobenzene ring is 20.9 (2)°. In the crystal, only van der Waals interactions occur.

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The C=C double-bond in the title compound, C(25)H(16)FN(3)O, has an E configuration. The dihedral angle between the fluoro-phenyl and triazole rings is 80.57 (2)°.

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(E)-1-{4-[Bis(4-meth­oxy­phen­yl)meth­yl]piperazin-1-yl}-3-(4-fluoro­phen­yl)prop-2-en-1-one

In the title compound, C(28)H(29)FN(2)O(3), the conformation about the ethene bond is E. The piperazine ring adopts a chair conformation. In the crystal, mol-ecules are linked by inter-molecular C-H⋯O hydrogen bonds.

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(E)-1-{4-[Bis(4-bromo­phen­yl)meth­yl]piperazin-1-yl}-3-(4-methyl­phen­yl)prop-2-en-1-one

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(2E)-3-[4-(Dimethyl­amino)­phen­yl]-1-(4-fluoro­phen­yl)prop-2-en-1-one

The mean planes of the two benzene rings in the title compound, C(17)H(16)FNO, are twisted slightly, making a dihedral angle of 7.8 (1)°. The prop-2-en-1-one group is also twisted slightly with a C-C-C-O torsion angle of -11.6 (3)°. In the crystal, weak inter-molecular C-H⋯O inter-actions link pairs of mol-ecules, forming centrosymmetric dimers.

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عنوان ژورنال:

دوره 64  شماره 

صفحات  -

تاریخ انتشار 2008