Über 2-Naphthol-6-mercaptan

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6-Bromo-2-naphthol–piperazine (2/1)

In the title compound, 2C(10)H(7)BrO·C(4)H(10)N(2), the piperazine (pip) mol-ecule displays a chair conformation and is linked to two mol-ecules of 6-bromo-2-naphthol (bno) via O-H⋯N hydrogen bonds. Weak N-H⋯O hydrogen bonds from pip to bno mol-ecules result in chains propagating in [100]. The chains inter-act via C-H⋯π inter-actions.

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1-(Hydroxy­imino­meth­yl)-2-naphthol

The title compound, C(11)H(9)NO(2), was prepared by a condens-ation reaction of 2-hydr-oxy-1-naphthaldehyde with hydroxyl-ammonium chloride in refluxing ethanol. An intra-molecular O-H⋯N hydrogen bond is observed. In the crystal structure, inter-molecular O-H⋯O and C-H⋯O hydrogen-bond inter-actions result in a two-dimensional network.

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2-(1,3-Benzothia­zol-2-ylimino­meth­yl)-2-naphthol

In the title mol-ecule, C(18)H(12)N(2)OS, the dihedral angle between the two fused-ring systems is 7.2 (1)°. The hydr-oxy group forms an intra-molecular hydrogen bond with the imino group.

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Photodegradation of 2-naphthol Using Nanocrystalline TiO2

The kinetics of the photocatalytic degradation of 2-naphthol has been investigated in aqueous suspensions of titanium dioxide (TiO2) under a variety of conditions, which is essential from application point of view. The degradation was studied using different parameters such as types of TiO2, catalyst concentration, substrate concentration, reaction pH and in the presence of different electron a...

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1-[Morpholino(phen­yl)meth­yl]-2-naphthol

There are two independent mol-ecules in the asymmetric unit of the title compound, C(21)H(21)NO(2), which was synthesized by the one-pot reaction of 2-naphthol, morpholine and benzaldehyde. The dihedral angles between the naphthalene ring systems and the benzene rings are 84.03 (7) and 75.76 (8)° in the two mol-ecules and an intra-molecular O-H⋯N hydrogen bond occurs in each independent mol-ecule.

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ژورنال

عنوان ژورنال: Berichte der deutschen chemischen Gesellschaft

سال: 1918

ISSN: 0365-9496,1099-0682

DOI: 10.1002/cber.19180510137