N-(2-Thienylmethylene)naphthalen-1-amine
نویسندگان
چکیده
In the title compound, C(15)H(11)NS, the dihedral angle between the thio-phene and 1-naphthyl rings is 31.42 (11)°. The mol-ecule adopts a trans configuration about the central C=N bond. In the crystal, the mol-ecules are connected via weak C-H⋯π inter-actions.
منابع مشابه
[(Z)-1-({3-[(3-Aminopropyl)(2-nitrobenzyl)amino]propyl}iminomethyl)naphthalen-2-olato]copper(II) perchlorate
In the title compound, [Cu(C(24)H(27)N(4)O(3))]ClO(4), the Cu(II) atom has a distorted square-planar coordination geometry and is surrounded by an N(3)O donor set composed of a secondary amine N, a primary amine H, an imino N and a naphthalen-2-olate O atom. An intra-molecular N-H⋯O hydrogen bond occurs. In the crystal, mol-ecules are held together by inter-molecular N-H⋯O hydrogen bonds, leadi...
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The molecules in (E)-N-(3,4,5-trimethoxybenzylidene)naphthalen-1-amine, C20H19NO3, (I), and its reduction product N-(3,4,5-trimethoxybenzyl)naphthalen-1-amine, C20H21NO3, (II), are both conformationally chiral, but (I) crystallizes in a centrosymmetric space group, while (II) crystallizes with just one conformational enantiomer in each crystal. A combination of two C-H···O hydrogen bonds links ...
متن کامل2-(Naphthalen-1-ylamino)cyclohexanol
The title compound, C(16)H(19)NO, was synthesized under solvent-free conditions by reaction of 7-oxa-bicyclo-[4.1.0]heptane and naphthalen-1-amine in the presence of Ca(CF(3)COO)(2) as catalyst. The cyclo-hexane ring adopts a chair conformation. In the crystal, mol-ecules are linked by inter-molecular N-H⋯O hydrogen bonds and C-H⋯π inter-actions into chains parallel to the c axis.
متن کامل(E)-5-Phenyl-N-(2-thienylmethylene)-1,3,4-thiadiazole-2-amine
In the title compound, C(13)H(9)N(3)S(2), the thio-phene and phenyl rings are oriented at dihedral angles of 8.00 (7) and 6.31 (7)°, respectively, with respect to the central thia-diazole ring. No significant C-H⋯S and π-π inter-actions exist in the crystal structure.
متن کاملEstimation of the solvent reorganization energy and the absolute energy of solvation of charge-transfer states from their emission spectra.
We report herein the solvent and temperature effects on the emission of the intermolecular exciplexes 1-cyanonaphthalene/triethylamine and 1-methylnaphthalene/triethylamine and the intramolecular exciplexes formed by the bichromophoric compounds diethyl-(3-naphthalen-1-yl-propyl)-amine (I), diethyl-(2-naphthalen-1-yl-ethyl)-amine (II), 3-[ethyl-(2-naphthalen-1-yl-ethyl)-amino]-propionitrile (II...
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