PEO Unsaturated Macromonomers ................... 21 PEO Saturated Macromonomers ..................... 24 PEO Block and Graft Copolymers .................... 25 Dispersion Polymerization of PEO Macromonomers ......... 27 Copolymerization of PEO Macromonomers with Styrene ...... 27 Copolymerization of PEO Macromonomers with Alkyl Acrylates and Methacrylates .................... 33 Emulsion Polymerization of PEO Macromonomers ......... 34 Homopolymerization of PEO Macromonomers ............ 34 Copolymerization of PEO Macromonomers with Styrene ...... 39 Copolymerization of PEO Macromonomers with Other Comonomers ............................ 45 Polymerization of PEO Macromonomers in Other Disperse Systems .......................... 48 Conclusion ................................. 50 References ................................. 52 List of Abbreviations and Symbols A acrylic group second virial coefficient A2 AA acrylic acid AVA 4,4'-azobis(4-cyanovaleric acide) AIBN 2,2'-azobiisobutyronitrile B A butyl acrylate BzMA benzyl methacrylate BMA butyl methacrylate CAC critical association concentration concentration of monomer in water cw concentration of polymer micelle concentration CMC critical CFC critical flocculation concentration CFT critical flocculation temperature chain length (CL) Radical Polymerization of Polyoxyethylene Macromonomers in Disperse Systems 3 methyl Cl t-butyl tC4 chain transfer constant to stabilizer cs chain transfer to solvent css chain transfer constant for transfer to polymeric stabilizer CSP D particle diameter DLS dynamic light scattering volume median diameter D50 final particle diameter " f DBP dibenzoyl peroxide number average degree of polymerization DPn diffusion coefficient of the radical in water " w overall activation energy EO activation energy for propagation E activation energy for termination E t activation energy for decomposition of initiator Ed EO ethylene oxide unit f initiator efficiency monomer feed composition fw graft available G a graft required G r HLB hydrofile-lipophile balance

-

PEO Unsaturated Macromonomers ................... 21 PEO Saturated Macromonomers ..................... 24 PEO Block and Graft Copolymers .................... 25 Dispersion Polymerization of PEO Macromonomers ......... 27 Copolymerization of PEO Macromonomers with Styrene ...... 27 Copolymerization of PEO Macromonomers with Alkyl Acrylates and Methacrylates .................... 33 Emulsion Polymerization of PEO Macromonomers ......... 34 Homopolymerization of PEO Macromonomers ............ 34 Copolymerization of PEO Macromonomers with Styrene ...... 39 Copolymerization of PEO Macromonomers with Other Comonomers ............................ 45 Polymerization of PEO Macromonomers in Other Disperse Systems .......................... 48 Conclusion ................................. 50 References ................................. 52 List of Abbreviations and Symbols A acrylic group second virial coefficient A2 AA acrylic acid AVA 4,4'-azobis(4-cyanovaleric acide) AIBN 2,2'-azobiisobutyronitrile B A butyl acrylate BzMA benzyl methacrylate BMA butyl methacrylate CAC critical association concentration concentration of monomer in water cw concentration of polymer micelle concentration CMC critical CFC critical flocculation concentration CFT critical flocculation temperature chain length (CL) Radical Polymerization of Polyoxyethylene Macromonomers in Disperse Systems 3 methyl Cl t-butyl tC4 chain transfer constant to stabilizer cs chain transfer to solvent css chain transfer constant for transfer to polymeric stabilizer CSP D particle diameter DLS dynamic light scattering volume median diameter D50 final particle diameter " f DBP dibenzoyl peroxide number average degree of polymerization DPn diffusion coefficient of the radical in water " w overall activation energy EO activation energy for propagation E activation energy for termination E t activation energy for decomposition of initiator Ed EO ethylene oxide unit f initiator efficiency monomer feed composition fw graft available G a graft required G r HLB hydrofile-lipophile balance

-

There is a growing interest in the use of nanoparticles modified with DNAs, viruses, peptides and proteins for the rational design of nanostructured functional materials and their use in biosensor applications. The challenge is to control the organization of biomolecules on nanoparticles while retaining their biological activity as potential chemical and gene therapeutics. These noble metal nanoparticles/biomolecules conjugates have specific properties and therefore they are attractive materials for nanotechnology in biochemistry and medicine.

In this book, the author review work performed dealing with the DNA structure and functionalities, interactions between DNA, noble metal nanoparticles, surface active agents, solvents and other additives. Particular attention is given to how the DNA's chain length and the DNA conformation affect the interaction and structure of the nanoconjugates and nanostructures that are formed. Also discussed are the recent advances in the preparation, characterization, and applications of noble metal nanoparticles that are conjugated with DNA aptamers and oligomers. The advantages and disadvantages of functionalized nanoparticles through various detection modes are highlighted, including colorimetry, fluorescence, electrochemistry, SPR, and, mass spectrometry for the detection of small molecules and biomolecules. The functionalized noble metal nanoparticles are selective and sensitive for the analytes, showing their great potential in biosensing. Furthermore, this book reviews recent progress in the area of DNA-noble metal nanoparticles based artificial nanostructures, that is, the preparation, collective properties, and applications of various DNA-based nanostructures are also described.