Synthesis of 2,3- and 3,4-cyclopentenopyridines, 5,6,7,8-tetrahydroquinolines and 5,6,7,8-tetrahydroisoquinolines from 1,2,4-triazine derivatives is reported. Introduction of an alpha-functionalized methyl substituent (e.g. arylsulphonyl, sulphonamide, sulphonic acid ester) into position 3- or 6- of triazines by vicarious nucleophilic substitution of hydrogen and subsequent alkylation with alky...

Self-assembly of 2,4,6-tripyridyl-1,3,5-triazine (tpt) subunits with arene ruthenium building blocks and oxalato bridges affords cationic triangular metallo-prisms of the type [Ru6(arene)6(tpt)2(C2O4)3]6+ (arene = C6Me6 and p-Pr(i)C6H4Me); the unexpected double helical chirality of the metallo-prisms observed in the solid state persists in solution giving rise to two different stereodynamic pro...

A simple, specific and reproducible serum iron method is described using the recently synthesized and highly sensitive chromogen, tripyridyl-S-triazine. The absorbance of this chromogen is compared to other iron reagents. Procedural modifications are given for using the Ramsay iron-binding capacity method with this serum iron procedure. The normal values found agree with most of those in the li...

The properties relevant to pharmacokinetics and pharmacodynamics of four series of synthesized s-triazine derivatives have been studied by Quantitative structure-retention relationship (QSRR) approach. The chromatographic behavior of these compounds was investigated by using reversed-phase high performance thin-layer chromatography (RP-HPTLC). Chromatographic retention (R M (0)) was correlated ...

Two monopodal (2,4-dichloro-6-(3-hydroxytyramine)-1,3,5-triazine) and tripodal (2,4,6-(3-hydroxytyramine)-1,3,5-triazine) s-triazine derivatives were prepared through the reaction of cyanuric chloride (2,4,6-trichloro-1,3,5-triazine) and 3-hydroxytyramine hydrochloride (dopamine hydrochloride). The structures of the compounds were identified by FT-IR, 1H NMR, 13C NMR, thermal analysis and eleme...

Pesticides based on the s-triazine ring structure are widely used in cultivation of food crops. Cleavage of the s-triazine ring is an important step in the mineralization of s-triazine compounds and hence in their complete removal from the environment. Cyanuric acid amidohydrolase cleaves cyanuric acid (2,4,6-trihydroxy-s-triazine), which yields carbon dioxide and biuret; the biuret is subject ...

Hydrolysis of cyanuric acid, melamine, melem, atrazine and melamine-formaldehyde resin was found to be catalyzed by an A1203 catalyst. The reactions occur irreversibly with cleavage of the s-triazine ring between 240 and 450°C. The s-triazine-ring is hydrolyzed to ammonia and carbon dioxide, and the substituted groups to the corresponding molecules by addition of hydrogen.

Biodegradation of xenobiotic compounds is examined with s-triazines as an example and with biological treatment of wastewater containing striazines as an aim. s-Triazines have been termed recalcitrant, but examination of the literature indicates that a potential for biodegradation exists. Ni t rogenl imi ted enr ichment cultures yield organisms able to degrade by-products of the industrial synt...

Introduction The presence of certain heterocyclic rings with nitrogen atoms in an organic polymer may significantly improve its thermal stability. For typical polyurethane foams, the upper temperature range of save usage is usually considered to be 90-110°C [1, 2]. This limit can be improved by applying an oligoetherol component containing a thermostable heterocyclic ring with nitrogen atoms, s...