4,4′-(Hexane-1,6-diyldi­oxy)dianiline

نویسندگان

  • Muhammad Saif Ullah Khan
  • Zareen Akhter
  • Michael Bolte
  • Amna Siraj
  • Humaira M. Siddiqi
چکیده

The complete molecule of the title compound, C(18)H(24)N(2)O(2), is generated by a crystallographic inversion centre. The torsion angles in the hexa-methyl-ene chain are consistent with an anti-periplanar conformation, whereas the conformation of the O-CH(2)-CH(2)-CH(2) unit is gauche. The three-dimensional crystal packing is stabilized by N-H⋯O and N-H⋯N hydrogen bonding.

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منابع مشابه

1,1′-[(Hexane-1,6-diyldi­oxy)bis­(nitrilo­methyl­idyne)]dinaphthalene

The title compound, C(28)H(28)N(2)O(2), was synthesized by condensation of 1-naphthaldehyde with 1,6-bis-(amino-oxy)hexane in ethanol. The mol-ecule is disposed about a crystallographic centre of symmetry. In the crystal structure, mol-ecules are linked through strong inter-molecular π-π stacking inter-actions [interplana distance = 2.986 (2) Å], forming a three-dimensional network.

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In the title compound, C(22)H(28)N(2)O(6), strong intra-molecular O-H⋯N hydrogen bonds and weak inter-molecular C-H⋯O hydrogen bonds stabilize the three-dimensional supra-molecular structure.

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3,3′-Dibromo-5,5′-bis­[(S)-l-menth­yloxy]-4,4′-(hexane-1,6-diyldiimino)difuran-2(5H)-one

The title compound, C(34)H(54)Br(2)N(2)O(6), was obtained by the Michael addition-elimination reaction of (5S)-5-(l-menthyl-oxy)-3,4-dibromo-furan-2(5H)-one with 1,6-hexa-nediamine in the presence of triethyl-amine. The crystal structure contains two chiral five-membered furan-one rings, in twist and envelope conformations, and two six-membered cyclo-hexane rings in chair conformations.

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عنوان ژورنال:

دوره 65  شماره 

صفحات  -

تاریخ انتشار 2009