Polymer-bound Schiff-base ligand (PS-SalPhe) was prepared from polystyrene-bound salicylaldehyde and phenylalanine, and its complex (PS-SalPhe-M) (M ฯญ Co, Mn) was also synthesized. The polymer ligand and its complex were characterized by infrared spectra, small area X-ray photoelectron spectroscopy,
Hydrogenation of olefins by polymer-bound palladium(II) Schiff base catalyst
โ Scribed by S. Alexander; V. Udayakumar; V. Gayathri
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- English
- Weight
- 935 KB
- Volume
- 314
- Category
- Article
- ISSN
- 1381-1169
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โฆ Synopsis
Chloromethylated poly(styrene-divinylbenzene) was modified into coordinating Schiff base bearing ligand which was subsequently complexed with palladium chloride and activated by using sodium borohydride. The polymer-supported palladium complex and activated catalyst were characterized by various techniques such as elemental analysis, X-ray photoelectron spectroscopy, atomic absorption spectroscopy, IR, far IR spectral studies, SEM and thermogravimetric analysis. Surface area measurements by BET method and swelling studies with different solvents for the catalyst were also carried out. Catalytic activity towards hydrogenation of 1-hexene, 1-heptene, 1-octene, cyclohexene, norbornadiene (nbd) and 1,5-cyclooctadiene (1,5-cod) was assessed. The influence of variation in temperature, pressure, concentration of the catalyst as well as the substrate and the nature of the solvent on the rate of the reaction was studied for a few olefins. Recycling ability of the catalyst was also evaluated.
๐ SIMILAR VOLUMES
Two percent divinylbenzene (DVB) -crosslinked polystyrene was prepared and functionalized to obtain its aldehyde analog. Amino porphyrins were anchored on this polymer support by Schiff base condensation. The anchoring positions were adjusted so as to obtain ortho-, meta-, and para-isomeric systems.
A polymerizable unsymmetric tetradentate Schiff base with one vinyl group 3 was synthesized and copolymerized with styrene in toluene. Mn(III) ion was quantitatively incorporated into the copolymers by the functional moieties. The resulting linear polymer-bound manganese complexes ( 4a and 4b) were