deuterium substitution on two ortho-substituted-och2-fragments in nitro-benzo-9-crown-3 induces low frequency shifts, positive mndcj, in all 13c nmr resonances which is an indication of the increased shielding in this crown ether. the magnitude of these shifts vary from 15dc7=716 to 54dc3=15 ppb for c7 and c3 cd3cocd3, and c6d6 on mndcj values were investigated. the mndcj values depended more o...

Deuterium substitution on two ortho-substituted-OCH2-fragments in Nitro-Benzo-9-Crown-3 induces low frequency shifts, positive mnDCj, in all 13C NMR resonances which is an indication of the increased shielding in this crown ether. The magnitude of these shifts vary from 15DC7=716 to 54D<...

By employing different diimine complexes and a naphthanoimidazolate (L(1)) or benzoimidazolate (L(2)) anion ligand as linker, a series of trimetallo-macrocycles have been synthesized through a directed self-assembly approach that involves spontaneous deprotonation of the ligands in aqueous solution. Some compounds, namely, [M(3)L(3)](NO(3))(3) (M = (18-crown-6-phen)Pt, 1 or 7; (15-crown-5-phen)...

Study of interaction between catechol and tetraethylene glycol dichloride in the n-butanol media, resulting with benzo-15-crown-5 production. Production of nitroand amino-derivatives of benzo-15-crown-5. Determination of their thermogravimetric characteristics. keywords: benzo-15-crown-5, catechol, tetraethylene glycol dichloride, crown ether, gas liquid chromatography, chromate-mass spectrometry

The title compound, [Sr(C(14)H(20)O(5))(2)](I(3))(2), obtained by slow evaporation of an ethanol/dichloro-methane solution (1:1) of SrCl(2), benzo-15-crown-5 and I(2), is built of sandwich-like [Sr(benzo-15-crown-5)(2)](2+) cations and isolated linear I(3) (-) anions which are arranged in alternating layers parallel to (010). The triiodide anions are located in general positions, whereas the ca...

Two procedures for the synthesis of benzo-21-crown-7 have been explored. The [1+1] macrocyclization with KBF₄ as the template was found to be more efficient than the intramolecular macrocyclization without template. Pseudorotaxanes form with secondary ammonium ions bearing at least one alkyl chain narrow enough to slip into the crown ether. Substitution on benzo-21-crown-7 or on the secondary a...

Substituted [1,4]thiazepino[2,3-h]quinolinecarboxylic acid 3 is prepared by PPA-catalyzed thermal lactamization of the respective 8-amino-7-[(2-carboxyethyl)thio]-1,4-dihydroquinoline-3-carboxylic acid 9. The latter synthon is obtained by reduction of the 8-nitro-1,4-dihydroquinoline precursor 8 which, in turn, is made accessible via interaction of 3-mercaptopropionic acid with 7-chloro-1-cyclo...

Condensation of either 2-bromobenzoic acid (4) or 2-chloro-3-nitrobenzoic acid (5) with suitable aminoquinolines 6-8 afforded phenylquinolylamines 9-13. Acid mediated cyclization gave the corresponding 12H-benzo[b][1,7]phenanthrolin-7-ones 14 and 15, and 12H-benzo[b][1,10]phenanthrolin-7-ones 16-18. Compounds 14, 16, and 17 were subsequently N-methylated to 6-demethoxyacronycine and acronycine ...