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The molecular geometry in the title compound, C19H21N, is as expected for a compound of this kind. The mol­ecules are interconnected to form layers by C—H...π interactions, some between edge-to-face mol­ecules in the manner characteristic of polycyclic hydro­carbon compounds and others involving H atoms of both methyl groups of the methyl­diethyl­amine substituent.

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The title 1,4-photoadduct, C21H19NO3, was formed on irra­diation of N-benzoyl­phthal­imide in di­chloro­methane con­tain­ing cyclo­hexene. The bond lengths and angles are generally within the normal ranges. A notable feature of the mol­ecule is the presence within it of four contiguous chiral centres.

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The mol­ecules of the title compound, C6H4ClNO2, are almost completely planar. Hydrogen bonds of the form O—H...N inter­connect the mol­ecules to form infinite chains, which are also planar and which are packed face-to-face to form well defined layers of mol­ecules.

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In the structure of the title compound, C17H17N, the two mol­ecules in the asymmetric unit are confined to distinct layers, one for each type of mol­ecule. The layers differ in the orientation, relative to the edges of the unit cell, of the mol­ecules within them.

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The title cocrystal, [PtCl(C4HF6)(C18H33P)2], contains mol­ecules with a random distribution of E and Z alkenyl isomers in essentially equal numbers. This is indicative of the isomerization of the E form of the Pt complex in the course of attempting to carry out a reaction between it and tricyclo­hexyl­tin 4-chloro­benzene­thiol­ate in acetone as solvent.

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The title compound, C14H8Cl4O2, has been isolated following irradiation of a dichloro­methane solution of N-acetyl­tetra­chloro­phthalimide and cyclo­hexene. The structure refinement is slightly compromised by the disorder over two positions of equal occupancy of a methyl­ene group β to the spiro C atom.

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A feature of the structure of the title compound, C17H17NO4, is the three-dimensional connectivity generated by inter­molecular hydrogen bonds.

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The cation and anion of the title salt, C7H10N+.C14H4N5-, are both bisected by a crystallographic mirror plane. Extensive hydrogen bonding, with the R66(28) graph-set motif, connects the ions into layers.

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The title compound, [Cu(C3H6NO3)2(H2O)2]·0.1H2O, is isostructural with the nickel analogue. The octa­hedral CuII ion lies on a twofold axis, with cis chelating O,N-serine groups and trans aqua ligands. Small amounts of a solvent water molecule form hydrogen bonds to link the mol­ecules along the [010] direction, while a number of strong hydrogen bonds combine to form sheets in the (110) plane.

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In the structure of the title salt, C12H10N3O+·Cl-·3H2O, the only species which do not coincide with the mirror plane in the space group P63/m are one complete water mol­ecule, one H atom of another water mol­ecule and two H atoms of the methyl group of the cation. Consequently, apart from the two H atoms of the methyl group, the cation is completely planar. The hydrogen bonding between the water mol­ecules and, through Cl- anions, to the cations, although extensive, can be modelled satisfactorily only by treating one H atom in each of the two types of water mol­ecules as disordered.
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