Polymers are essential to biology because they can have enough stable degrees of freedom to store the molecular code of heredity and to express the sequences needed to manufacture new molecules. Through these they perform or control virtually every function in life. Although some biopolymers are created and spend their entire career in the relatively large free space inside cells or organelles, many biopolymers must migrate through a narrow passageway to get to their targeted destination. This suggests the questions: How does confining a polymer affect its behavior and function? What does that tell us about the interactions between the monomers that comprise the polymer and the molecules that confine it? Can we design and build devices that mimic the functions of these nanoscale systems? The NATO Advanced Research Workshop brought together for four days in Bikal, Hungary over forty experts in experimental and theoretical biophysics, molecular biology, biophysical chemistry, and biochemistry interested in these questions. Their papers collected in this book provide insight on biological processes involving confinement and form a basis for new biotechnological applications using polymers. In his paper Edmund DiMarzio asks: What is so special about polymers? Why are polymers so prevalent in living things? The chemist says the reason is that a protein made of N amino acids can have any of 20 different kinds at each position along the chain, resulting in 20 N different polymers, and that the complexity of life lies in this variety.

This volume is based on lectures given at the NATO-Advanced Study Institute on Structure and Dynamics of Polymer and Colloid Systems held in Les Houches, France from September 14-24, 1999. The meeting arose from a perceived need to bring together scientists studying the polymer and colloid fields. Although these fields are intertwined and share many techniques (e. g. , light, neutron and x-ray scattering), it is remarkable how little the approaches and concepts used by the one field penetrate the other. For instance, the theory of spherical colloids is very highly developed and many of the concepts developed for these systems can be extended to those with non-spherical morphology, such as solutions of rigid rod polymers. In addition, mixtures of polymers and colloids, both in the bulk and at interfaces, are the basis for many industrial products. Methods are now rapidly being developed for understanding the structure and dynamics in polymer/colloid mixtures at the molecular level, but the point of view of the colloid scientist is often rather different from that of the polymer scientist. The NATO-ASI brought together polymer and colloid scientists, including many young researchers, who presented and discussed recent developments in these fields and the possibilities for cross-fertilization This volume contains articles on a wide variety of topics at the research forefront of the polymer and colloid fields by some of the world's foremost experts at a level accessible to graduate students, post-docs and researchers.

The theory presented in this book explains in a consistent manner all dynamics effects observed in very concentrated solutions and melts of linear polymers from a macromolecular point of view. The presentation is compact and self-contained.

Scattering is a very powerful tool to study the structure of polymers. Written by highly regarded and respected scientists in the field, this book presents the latest developments in the field of scattering in a uniform, systematic manner. This volume arms readers with both theoretical and experimental aspects of the intended area, offering much simplified theoretical explanations on the physics of scattering. The authors provide discussion on applications of experimental techniques. Han and Akcasu begin with a traditional treatment of light scattering from plane waves, followed by consistent application of density (in both real and Fourier space) correlation functions in both space and time. The authors do not distinguish among light, X-ray, and neutron, excepting their scattering length, q-range, coherence and detection differences. Readers can therefore concentrate on exactly the scattering tools they need to use, while theoretical explanation on the physics of scattering can be made much more simplified and uniform. Presents the latest development in the field of scattering in a uniform, systematic manner Arms readers with both theoretical and experimental aspects Gives a much simpler theoretical explanation on the physics of scattering Demonstrates application of experimental techniques

Conjugated polymers are a highly relevant class of materials due to their low processing cost and applicability in flexible electronic devices. A significant challenge in the field remains to relate the chemical structure of these materials with their morphology and dynamics, which in turn affect their charge transport characteristics. There are several experimental and computational methods that are commonly used when characterizing conjugated polymers. In this work, we attempt to synergistically apply these techniques so as to obtain a clear understanding of the properties that affect the structure and dynamics of conjugated polymers. A large experimental data set is used to validate molecular dynamics (MD) simulations of poly(3-hexylthiophene), a model conjugated polymer system. A sensitivity analysis of system and simulation parameters is performed, and the key factors affecting the conjugated polymer dynamics and configuration are found to be molecular weight, crystallinity, equilibration method, and force field parameters. Specifically, the atomistic partial charges are found to have the greatest influence on both properties. The identification of these key parameters will inform further studies of more complex conjugated polymer systems, elucidating the relationship between conjugated polymer chemistry and performance.

This text is the published version of many ofthe talks presented at two symposiums held as part of the Southeast Regional Meeting of the American Chemical Society (SERMACS) in Knoxville, TN in October, 1999. The Symposiums, entitled Solution Thermodynamics of Polymers and Computational Polymer Science and Nanotechnology, provided outlets to present and discuss problems of current interest to polymer scientists. It was, thus, decided to publish both proceedings in a single volume. The first part of this collection contains printed versions of six of the ten talks presented at the Symposium on Solution Thermodynamics of Polymers organized by Yuri B. Melnichenko and W. Alexander Van Hook. The two sessions, further described below, stimulated interesting and provocative discussions. Although not every author chose to contribute to the proceedings volume, the papers that are included faithfully represent the scope and quality of the symposium. The remaining two sections are based on the symposium on Computational Polymer Science and Nanotechnology organized by Mark D. Dadmun, Bobby G. Sumpter, and Don W. Noid. A diverse and distinguished group of polymer and materials scientists, biochemists, chemists and physicists met to discuss recent research in the broad field of computational polymer science and nanotechnology. The two-day oral session was also complemented by a number of poster presentations. The first article of this section is on the important subject of polymer blends. M. D.