Accommodation of MnII, MnIII–N, O, O, O-donor Schiff base complexes in zeolite-Y: Synthesis, structural studies and CO adsorption

Physicochemical Studies and Heterogeneous Hydroxylation of Benzene on FeII, FeIII-Semicarbazone/Zeolite-Y Clathrates

“…[8] On the other hand, incorporation of metal complexes inside the zeolite enhances the chemical and thermal stability of the occluded complexes owing to the zeolite shielding. [9][10][11][12][13] In many cases, zeolite inclusion is applied to avoid the polymerization and to strongly reduce the self-oxidation tendency of the complexes. Literature survey in this trend referred to the encapsulation of different types of ligands, such as porphyrins, phthalocyanines, Schiff bases, (poly) pyridines, amidate, and polyaza macrocyclic models, and in addition we have recently published iron(II, III) complexes of hydrazone.…”

Crystal structure, characterization and magnetic properties of a 1D copper(II) polymer incorporating a Schiff base with carboxylate side arm

“…The structure was refined as an inversion twin, the refined ratio of the twin components obtained by the TWIN/BASF procedure 33 being 0.614 (17):0.386 (17). All calculations and graphical illustrations for the complex have been done using WinGX, 34 ORTEP, 35 and SCHAKAL 36 programs.…”

“…Amino acid-based Schiff bases, a class of the Schiff bases with carboxylate side arm, and their metal complexes were synthesized and studied extensively for their wide applications in biology, pharmacy and industry. [12][13][14][15][16][17][18][19][20][21][22][23][24][25] However, little focus has been given to the class of amino acid Schiff bases obtained by condensation of carbonyl compounds and aromatic amines with carboxylic acid side arm in spite of bearing similar free carboxylate end which is considerably flexible from the point of view of the steric orientation in the formation of less strained covalent bonds with the metal centers with potential to show versatile bridging modes.…”