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  • TITLE
  • CERTIFICATE
  • DECLARATION
  • ACKNOWLEDGEMENT
  • ABBREVIATIONS
  • CONTENTS
  • 1 Introduction and Objectives
  • 2 Polymer-Supported Reagents: An Overview
  • 2.1. Organic synthesis using polymer supports
  • 2.2. The polymer support
  • 2.3. Solvation behaviour of functionalised polymers
  • 2.4. Nature of the polymer backbone
  • 2.5. Functionalisation of polymer supports
  • 2.6. Characterisation of functional polymers
  • 2.7. Advantages and limitanions of polymer-supported reactions
  • 2.8. Characteristic effects of the polymer matrix on solid phase reactions
  • 2.8.1 Microenviournmental effects
  • 2.8.2 Effect of degree of crosslinking
  • 2.8.3 Effect of spacer handles
  • 2.9. Polymer-supported oxidising reagents
  • 2.10. Polymer-supported halogen containing reagents
  • 2.11. Miscellaneous polymeric oxidising reagents
  • 3 Experimental
  • 3.1. General
  • 3.2. Preparation of cross linked polyvinyl pyrrolidone) s (PVP) -General procedure
  • 3.3. Preparation of cross linked poly (vinyl pyrrolidone) --iodine complexes
  • 3.4. Determination of the capacity of the cross linked poly (vinyl pyrrolidone) iodine complex
  • 3.5. Oxidation and halogenation reactions using cross linked PVP iodine complexes
  • 3.6. Monitoring the course of oxidation reactions
  • 3.7. Investigation of the effect of cross linking on the extent of oxidation
  • 3.8. Effect of solvent
  • 3.9. Effect of molar concentration of the reagent
  • 3.10. Effect of temperature on oxidation reactions
  • 3.11. Effect of time
  • 3.12. Swelling studies of PVP-iodine complexes
  • 3.13. Recycling and reuse
  • 3.14. Preparation of polystyrene sulphonic acid resins
  • 3.15. Estimation of polystyrene sulphonic acid
  • 3.16. Polystyrene sulphonyl chloride
  • 3.17 Estimation of chlorine in polystyrene sulphonyl chloride
  • 3.18. Preparation of polystyrene sulphonamide
  • 3.19 N-chloro-N-sodio polystyrene sulphonamide resin
  • 3.20. N-Bromo-N-sodio polystyrene sulphonamide resin
  • 3.21. Estimation of the capacity of N-halo resins
  • 3.22. Halogenation reactions- general procedure
  • 3.23. Preparation of polystyrene with different cross link densities
  • 3.24. Functionalisation of polystyrene with different cross link densities
  • 3.25. Bromination of aqueous solution of phenol at different time intervals
  • 3.26. Effect of molar excess of the reagent
  • 3.27. Effect of temperature on halogenation of phenol
  • 3.28. Recyclability of the spent reagent
  • 3.29. Thermogravimetry
  • 3.30. 13C-CP MAS NMR
  • 4 Results and Discussion
  • SECTION A - POLY (VINYL PYRROLIDONE) SUPPORTED REAGENTS
  • 4.1. Poly (vinyl pvrrolidone) -general concept
  • 42. Poly (vinyl pyrrolidone) --iodine complexes
  • 4.3. Cross linked poly (vinyl pyrrolidone) - preparation and characterisation.
  • 4.3.1 Preparation and characterisation of DVB-crosslinked PW
  • 4.3.2 Preparation and characterisation of NNMBA-crosslinked PVP
  • 4.3.3 TEGDVE-crosslinked PVP-preparation and characterisation
  • 4.3.4 1, 6-HDODA-crosslinked PVPLpreparation and characterisation
  • 4.3.5 TTEGDA crosslinked PVP-preparation and characterisation
  • 4.4. Preparation of cross linked poly (vinyl pyrrolidone) -iodine complexes
  • 4.5. Characterisation of cross linked PGP-iodine complexes
  • 4.5.I DVEcrosslinked PVP-I complexes
  • 4.5.2 NNMBA-crosslinked PVP-I complex
  • 4.5.3 TTGDVE-crosslinked PVP-l complex
  • 4.5.4 1, 6 HDODA-crosslinked PVP-I complex
  • 4.5.5 TTEGDA-crosslinked PVP-I complex
  • 4.6. Reactions using cross linked poly (vinyl pyrrolidone) -iodine complexes.
  • 4.6.1 Oxidation of alcohols
  • 4.6.2 Halogenation of olefins
  • 4.6.3 Synthetic reactions using PVP-iodine complexes
  • 4.6.4 Selectivity of PW-iodine complexes
  • 4.7 Recyclability of the reagent
  • 4.8. Structure-reactivity correlation of PVP-iodine complexes
  • 4.8.1 Nature of the polymer support
  • 4.8.2 Effect of crosslink density
  • 4.8.3 Effect of solvent
  • 4.8.4 Effect of concentration of the reagent
  • 4.8.5 Effect of temperature on the oxidation reactions
  • 4.8.6 Hfect of time on mctiviiy of WPJ complexes
  • SECTION B - POLYSTYRENE-SUPPORTED REAGENTS
  • 4.9. Polystyrene-supported N-halosulphonamides
  • 4.9.1 N-haleN-sodio polysityrene sulphonamide resins-preparation andcharacterisation
  • 4.9.2 Synthetic reactions usin!g N-halo-N-sodio polystyrene sulphonamides
  • 4.9.3 E i M of various parameten on the extent of halogenation reaction
  • 4.9.4 Recycling and reuse of the reagent
  • Summary and Outlook
  • References