Cationic Polymerization of Nonpolar Vinyl Monomers 3. Cationic Polymerization of Polar Monomers 3.
Anionic Polymerization of Nonpolar Monomers 3. Anionic Polymerization of Protected Functional Monomers 3. Anionic Polymerization of Polar Vinyl Monomers 3. Industrial Catalysts for Alkene Polymerization 3. Metallocene Alkene Polymerization Catalysts 3. Cycloolefin Polymerization 3. Alkyne Polymerization 3. Introduction 4.
Synthesis and Properties of Low- And High Molecular Compounds : Quantitative Level
Thermodynamic and Kinetic Polymerizability 4. Equilibrium Copolymerization in Ring-Opening Polymerization 4. Organocatalyzed Ring-Opening Polymerizations 4. Stereoselective Ring-Opening Polymerization of Epoxides 4. Ring-Opening Polymerization of Cyclic Acetals 4. ROP of Cyclic Esters. Mechanisms of Ionic and Coordination Processes 4. Polymerization of Oxazolines 4. Radical Ring-Opening Polymerization 4. High-Molecular-Weight Poly ethylene oxide 4. Nonlinear Macromolecules by Ring-Opening Polymerization 4. Chain Extension by Ring Opening 4. Ring-Opening Dispersion Polymerization 4.
Oligomeric Poly ethylene oxide s. Functionalized Poly ethylene glycol s. PEGylation 4. Polyphosphoesters 4. Ring-Opening Polymerization of Cyclic Esters 4. Template Polymerization 4. Mechanistic Aspects of Solid-State Polycondensation 4. Radical Polymerization at High Pressure 4. Electroinitiated Polymerization 4. Photopolymerization 4. Frontal Polymerization 4. Microwave-Assisted Polymerization 4. Polycondensation 5. Introduction and Overview 5. Sequence Control in One-Step Polycondensation 5. Nonstoichiometric Polycondensation 5.
Chain-Growth Condensation Polymerization 5. Oxidative Coupling Polymerization 5. Advances in Acyclic Diene Metathesis Polymerization 5. Enzymatic Polymerization 5. Nonlinear Polycondensates 5. Post-Polymerization Modification 5. Supramolecular Polymers 5. Chemistry and Technology of Step-Growth Polyesters 5.
Biodegradable Polyesters 5. Polycarbonates 5. Aromatic Polyethers, Polyetherketones, Polysulfides, and Polysulfones 5. Chemistry and Technology of Polyamides 5.officegoodlucks.com/order/33/1668-app-para-espiar.php
Macromolecule - Wikipedia
Lyotropic Polycondensation including Fibers 5. Polyimides 5. High-Performance Heterocyclic Polymers 5. Metal-Containing Macromolecules 5. Phosphorus-Containing Dendritic Architectures 5. Epoxy Resins and Phenol-Formaldehyde Resins 5. High-Temperature Thermosets 5. Macromolecular Architectures and Soft Nano-Objects 6. Introduction 6. Synthesis and Properties of Macrocyclic Polymers 6. Polymers with Star-Related Structures 6. Dendrimers 6. Hyperbranched Polymers 6. Molecular Brushes 6.
Spherical Polymer Brushes 6. Model Networks and Functional Conetworks 6. Polymer Nanogels and Microgels 6. Controlled Composition 6.
Synthesis & Properties of Low- & High-Molecular Compounds Quantitative Level Synopsis
Well-Defined Block Copolymers 6. Graft Copolymers and Comb-Shaped Homopolymers 6. Synthetic—Biological Hybrid Polymers 6. Dynamic Supramolecular Polymers 6. Stereocontrolled Chiral Polymers 6. Rigid—Flexible and Rod—Coil Copolymers 6. Nanostructured Polymer Materials and Thin Films 7. Introduction 7. Block Copolymers in the Condensed State 7.
Block Copolymer Thin Films 7. Block Copolymers under Confinement 7. Assemblies of Polymer-Based Nanoscopic Objects 7. Hybrid Polymer—Inorganic Nanostructures 7. Nanostructured Electrospun Fibers 7. Soft Lithographic Approaches to Nanofabrication 7. Nanoimprint Lithography of Polymers 7. Modeling Mixtures of Nanorods and Polymers 7. Sterically Stabilized Nanoparticles in Solutions and at Interfaces 7. Electrical Conductivity of Polymer Nanocomposites 7. Polymer Dynamics in Constrained Geometries 7. Polymer Nanomechanics 7. Polymers for Advanced Functional Materials 8.
Hydrogen bonds, with a strength of about 5 kilocalories 21 kilojoules per mole, are much weaker than normal covalent bonds , with bond energies of about 70 to kilocalories per mole. The amount of energy per mole that is required to break a given bond is called its bond energy. Water and alcohols have similar properties because water molecules contain hydroxyl groups that can form hydrogen bonds with other water molecules and with alcohol molecules, and likewise alcohol molecules can form hydrogen bonds with other alcohol molecules as well as with water.
Because alcohols form hydrogen bonds with water, they tend to be relatively soluble in water. Methanol, ethanol, n -propyl alcohol, isopropyl alcohol, and t - butyl alcohol are all miscible with water. Because they are strongly polar, alcohols are better solvents than hydrocarbons for ionic compounds and other polar substances. Article Media.
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