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  • TITLE
  • DEDICATION
  • CERTIFICATE
  • DECLARATION
  • ACKNOWLEDGEMENT
  • ABBREVIATIONS
  • COTNENTS
  • 1. INTRODUCTION AND OBJECTIVES
  • 1.1 Introduction
  • 1.2 Objectives of the Work
  • 1.3 Organisation of the Thesis
  • 2. POLAR SUPPORTED REACTIONS - AN OVERVIEW
  • 2.1 Introduction
  • 2.2 Characteristics of Functionalised Polymers
  • 2.2.1 Physical Properties
  • 2.2.1A Linear Polymers
  • 2.2.1 B Cross linked Polymers
  • a) Microporous or gel type resins
  • b) Macroporous resins and macroreticular resins
  • c) Popcorn polymers
  • d) Macronet polymers
  • e) Composite resins
  • 2.2.2 Reactivity of Functionalised Polymers
  • a) Molecular character and extent of crosslinking of the polymer matrix
  • b) Microenvironmental effects
  • c) Solvation and swelling
  • d) Spacer effect
  • 2.3 Characterisation of Functionalised Polymers
  • 2.4 Applications of Functionalised Polymers
  • 2.4.1 Organic Synthesis
  • 2.4.2 Enzyme Immobilization
  • 2.4.3 Mechanistic Studies Using Solid Supports
  • a) The Three Phase Test
  • b) Cyclobutadiene intermediates
  • c) Benzyne intermediate trapping
  • d) Fries rearrangement
  • e) Hoffmann rearrangement
  • f) Benzil-benzilic acid rearrangement
  • 2.4.4 Polymer Supported Halogen Containing Reagents
  • a) Polymeric halogen compounds as oxidising agents
  • b) As halogenating agents
  • 3. PREPARATION AND BECKMANN REARRANGEMENT REACTION OF POLYMER SUPPORTED KETOXIMES
  • 3.1 Syntnesis of DVB and HDODA Cross linked Polystyrene Supports
  • 3.1 1 Divinylbenzene (DVB) - Crosslinked Polystyrene
  • 3.1.2 Hexanediol Diacrylate (HDODA) -Cross linked Polystyrene
  • 3.2 Characterisation of the HDODA Crosslinked Polystyrene
  • 3.3 Preparation of DVB Crosslinked and HDODA Crosslinked Polystyrene bound Ketoximes
  • 3.4 Beckmann Rearrangement of the Polystyrene Bound Oximes
  • 3.5 Swelling Studies
  • 3.6 Influence of Different Structural Parameters on the Beckmann Rearrangement Rate
  • 3 6 1 Effect of the Nature of Cross linking
  • 3.6.2 Effect of the Degree of Cross linking
  • 3.6.3 Effect of Solvent
  • 3.6.4 Effect of Temperature
  • 3.6.5 Effect of Methylene Spacers
  • 3.66 Effect of Nonmigrating Group
  • 4. POLYMER-BOUND N-BROMOANILIDE- A POLYMERIC RECYCLABLE OXIDISING AND BROMINATING REAGENT
  • 4.1 Introduction
  • 4.2 Preparation of Polymer Bound N-bromoamides
  • 4.3 Characterisation of Polymer Bound N-bromoamides
  • 4.4 Swelling Studies
  • 4.5 Oxidation and Bromination Reactions Using the Polymeric N-bromoamide Reagents
  • 4 5 1 Oxidation of Alcohols
  • 4.5.2 Effect of Reaction Conditions on the Course of Oxidation Reactions Using Polymeric N-bromoamide
  • 4.5.2a Effect of Temperature
  • 4 5 2b Presence of Catalyst
  • 4.5.2c Effect of Solvent
  • 4.4.2d Effect of Concentration of Polymeric Reagents
  • 4.5.2e Effect of the Spacer Group
  • 4.5.3 Bromination Reactions Using Polymeric N-bromoamide
  • 4.5.4 Bromination of Toluene Under Radical Conditions
  • 4.5. 5 α-Bromination of Ketones
  • 4.6 Regeneration and Recyclability of the Polymer Supported N-bromoamides
  • 5. EXPERIMENTAL
  • 5.1 Source of Chemicals
  • 5.2 Physical Measurements
  • 5.3 Synthesis of Styrene-divinylbenzene Copolymer General Procedure
  • 5.4 Synthesis of Styrene-Hexanediol Diacrylate Copolymer
  • 5.5 Preparation of Polymer Supported Ketones: Friedel-Crafts Reaction of Polystyrene with Acid Chlorides or Acid Anhydrides
  • 5.5A Preparation of DVB Crosslinked and HDODA Crosslinked Polystyrene Supported Acetophenone and Benzophenones
  • 5.5B Preparation of Polymeric Ketones with Methylene Spacers between the Polymer Backbone and the Keto Functional Group
  • 5.6 Conversion of the Polymeric Ketones to Polymeric Oximes General Procedure
  • 5.7 Estimation of the N-hydroxyl Capacity of Polymeric Oximes; General Procedure
  • 5.8 Beckmann Rearrangement of the Polymeric Ketoximes
  • 5.9 Analysis of Rearranged Amide Products
  • 5.10 Determination of Amino Group Capacity of the Amino Polystyrene Resin-General Procedure
  • 5.11 Swelling Studies
  • 5 12 Effect of Various Parameters on the Beckmann Rearrangement of Polymer Bound Ketoximes
  • 5.12.1 Effect of Nature of Cross linking
  • 5.12.2 Effect of Degree of Cross linking
  • 5.12.3 Effect of Solvent
  • 5.12.4 Effect of Temperature
  • 5 12.5 Effect of Methylene Spacers
  • 5.12.6 Effect of Nonmigrating Group
  • 5.13 Preparation of Polymeric N-bromoamide Reagent
  • 5.14 Determination of the Bromine Capacities of the Polymer-bound N-bromoamides by lodometric Titration
  • 5.15 Oxidation of Alcohols-General Procedure
  • 5.16 Investigation of the Effect of the Reaction Conditions on Oxidation Reactions
  • 5.16.1 Effect of Temperature
  • 5.16.2 Effect of Acid Catalyst
  • 5.16.3 Effect of Solvent
  • 5.16.4 Effect of Concentration of the Polymeric Reagent
  • 5.16.5 Effect of Methylene Spacers
  • 5.17 Bromination Reactions Using Polymer-bound N-bromoanilide General Procedure
  • 5.18 α-Bromination of Ketones
  • 5.19 Recycling of the Spent Polymeric Reagent
  • 6. SUMMARY AND OUTLOOK
  • REFERENCES