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  • TITLE
  • CERTIFICATE
  • DECLARATION
  • ACKNOWLEDGEMENT
  • CONTENTS
  • LIST OF ABBREVIATIONSAND SYMBOLS
  • 1 . INTRODUCTION AND OBJECTIVES
  • 2 . METAL.COMPLEXATION BY POLYMERIC LIGANDS: CONCEPTUAL, SYNTHETIC, STRUCTURAL AND ANALYTICAL ASPECTS.
  • 11 -1. Polymeric Ligands: Synthesis
  • 11.3. Applications of Polymeric Ligands and Polymer-MetalComplexes
  • 11.4. Macromolecular Effects on Complexation
  • 3. N- (2-ETHYLENEDIAMINOETHYL) POLYACRYLAMIDES: SYNTHESIS., METAL COMPLEXATION AND CHARATERIZATION.
  • Results and Discussion
  • III.1. Preparation of Crosslinked Polyacrylamides
  • III 2. Preparation o f N- (2-Ethylenediaminoethyl) polyacrylamide
  • III 3. Complexation of N- (2-Ethylenediaminoethyl) polyacrylamides
  • III .4 Water Binding Studies
  • III - 5. Characterization of the Polymeric Ligands and the Polymer-Metal Complexes
  • Influence of the extent of crosslinking on morphology
  • Fig.III.29 and 30
  • Fig.III 31 and 32
  • Fig.III.33 and 34
  • DVB-cosslinked systems
  • TTEGDA- crosslinked Systems
  • Diffusion controlled reactions
  • III.6. Separation of Metal Ions
  • III. 7. Metal Ion Recognition
  • 4. N, N- BIS (2-AMINOETHYL) AMINOMETHYL POLYSTERENES
  • I V. 1 . Preparation o f Crosslinked Polystyrenes.
  • I V. 2 . Preparation of N, N-bis (2-Aminoethyl) aminomethyl styrenes
  • I V. 3 . Complexation of crosslinked N, N-bis (2-Aminoethyl) aminomethyl polystyrenes
  • IV.4. Equilibrium Water Content
  • IV.5. Characterization of N, N-bis (2-Aminethyl) aminomethyl-polystyrenes and the Polymer-Metal Complexes
  • IV.6. Recyclability of the Polymeric ligand.
  • 5 . N, N-BIS (SALICYLIDENE-2-AMINOETHYIL) AMINOMETHYL POLYSTERENES
  • Results and Discussion
  • V.1. Preparation of N.N-bis (Salicylidene-2-aminoethyl aminomethyl polystyrenes
  • V -2. Complexat ion Bahaviour of Schiff Base Functions Supported on crosslinked Polystyrenes.
  • V. 3 . Characterization of t h e Polymer-anchored Schiff Bases and Metal Complexes
  • V-4. Recyclability Studies.
  • 6. HDODA-CROSSLINKED POLYSTERENE- ANCHORED AMINO ACIDS AND PEPTIDES
  • Results and Discussion
  • VI.1. Preparation of HDODA-Crosslinked Polystyrenes.
  • VI. 2. Functionalization o f the Polystyrenes.
  • V I. 3 . Synthesis of Polymer-anchored Amino Acids and Paptides.
  • V I. 4 . Complexation Behaviour of Polymer-anchored Amino Acid and Peptide towards Ni (II) and cu (II)
  • V 1. 5 . Analysis and Charecterixation
  • 7. EXPERIMENTAL
  • VII.1 .General
  • VII 2 Preparation of Crosslinked Polacrylamides
  • VII.3. Transamidation of Polyacrylamides to N- (2-ethylanediaminoethyl) polyacrylamide
  • VII 5 Preparation of Crosslinked Polystyrenes by SolutionPolymer ization
  • VII.7 Preparation of N, N-bis (SaIicylidene-2-aminosthyl) aminomethyl polystyrenes
  • VII.8. Preparation of N, N-bis (2- Aminno ethyl) aminomethyl polystyrenes
  • VII.9. Chloromethylation of Crosslinked Polystyrene UsingAnhydrous ZnClp as the Lewis Acid
  • VII.10. Preparation of HDODA-crosslinked Aminomethyl Polystyrenes 347
  • VII-11. Estimation of Amino capacity by the Picric Acid Method
  • VI.12. Preparation of Polymer-Metal Complexes: General Procedure
  • VI.13. Estimation of Metal Ions
  • VII 14. Swelling Measurements
  • VII.15. Estimation of free- and bound-water content
  • VIII.16 Magnetic Sueceptibillty Measurements
  • VII -17. UV-Vis Spectra
  • VII -18 IR Spectra
  • VII. 19. EPR Spectra
  • VII.20. Cyclic Voltammetric Measurements
  • VII. 2 1. Matal Ion Separation using Column Technique
  • V II -21.a. Breakthrough Studies
  • VII.21 .b. Separation of Metal Ions
  • 8. CONCLUSION AND OUTLOOK
  • VIII. Conclusion and Outlook
  • REFERENCES