Since the first stimulated emission pumping (SEP) experiments more than a decade ago, this technique has proven powerful for studying vibrationally excited molecules. SEP is now widely used by increasing numbers of research groups to investigate fundamental problems in spectroscopy, intramolecular dynamics, intermolecular interactions, and even reactions. SEP provides rotationally pre-selected spectra of vibrationally highly excited molecules undergoing large amplitude motions. A unique feature of SEP is the ability to access systematically a wide variety of extreme excitations localized in various parts of a molecule, and to prepare populations in specific, high vibrational levels. SEP has made it possible to ask and answer specific questions about intramolecular vibrational redistribution and the role of vibrational excitation in chemical reactions.

Recent years have seen an explosion in the volume of work carried out using supersonic jets of molecules following the discovery that the technique could provide information on structure and dynamics of a very high quality otherwise impossible to obtain. Written and edited by a first class team of authors, acknowledged world leaders in their subjects, this book describes applications in detail along with analysis of data recorded and background theory. Physical chemists and chemical physicists will find this unique book an essential concentrated source of information and reference.

Molecular Spectroscopy and Quantum Dynamics, an exciting new work edited by Professors Martin Quack and Roberto Marquardt, contains comprehensive information on the current state-of-the-art experimental and theoretical methods and techniques used to unravel ultra-fast phenomena in atoms, molecules and condensed matter, along with future perspectives on the field. - Contains new insights into the quantum dynamics and spectroscopy of electronic and nuclear motion - Presents the most recent developments in the detection and interpretation of ultra-fast phenomena - Includes a discussion of the importance of these phenomena for the understanding of chemical reaction dynamics and kinetics in relation to molecular spectra and structure

Gas phase molecular spectroscopy is a powerful tool for obtaining information on the geometry and internal structure of isolated molecules and their interactions with others. It enables the understanding and description, through measurements and modeling, of the influence of pressure on light absorption, emission, and scattering by gas molecules, which must be taken into account for the correct analysis and prediction of the resulting spectra. Collisional Effects on Molecular Spectra: Laboratory Experiments and Models, Consequences for Applications, Second Edition provides an updated review of current experimental techniques, theoretical knowledge, and practical applications. After an introduction to collisional effects on molecular spectra, the book moves on by taking a threefold approach: it highlights key models, reviews available data, and discusses the consequences for applications. These include areas such as heat transfer, remote sensing, optical sounding, metrology, probing of gas media, and climate predictions. This second edition also contains, with respect to the first one, significant amounts of new information, including 23 figures, 8 tables, and around 700 references.Drawing on the extensive experience of its expert authors, Collisional Effects on Molecular Spectra: Laboratory Experiments and Models, Consequences for Applications, Second Edition, is a valuable guide for all those involved with sourcing, researching, interpreting, or applying gas phase molecular spectroscopy techniques across a range of fields. - Provides updated information on the latest advances in the field, including isolated line shapes, line-broadening and -shifting, line-mixing, the far wings and associated continua, and collision-induced absorption - Reviews recently developed experimental techniques of high accuracy and sensitivity - Highlights the latest practical applications in areas such as metrology, probing of gas media, and climate prediction

Spectroscopy and Computation of Hydrogen-Bonded Systems Comprehensive spectroscopic view of the state-of the-art in theoretical and experimental hydrogen bonding research Spectroscopy and Computation of Hydrogen-Bonded Systems includes diverse research efforts spanning the frontiers of hydrogen bonding as revealed through state-of-the-art spectroscopic and computational methods, covering a broad range of experimental and theoretical methodologies used to investigate and understand hydrogen bonding. The work explores the key quantitative relationships between fundamental vibrational frequencies and hydrogen-bond length/strength and provides an extensive reference for the advancement of scientific knowledge on hydrogen-bonded systems. Theoretical models of vibrational landscapes in hydrogen-bonded systems, as well as kindred studies designed to interpret intricate spectral features in gaseous complexes, liquids, crystals, ices, polymers, and nanocomposites, serve to elucidate the provenance of spectroscopic findings. Results of experimental and theoretical studies on multidimensional proton transfer are also presented. Edited by two highly qualified researchers in the field, sample topics covered in Spectroscopy and Computation of Hydrogen-Bonded Systems include: Quantum-mechanical treatments of tunneling-mediated pathways and molecular-dynamics simulations of structure and dynamics in hydrogen-bonded systems Mechanisms of multiple proton-transfer pathways in hydrogen-bonded clusters and modern spectroscopic tools with synergistic quantum-chemical analyses Mechanistic investigations of deuterium kinetic isotope effects, ab initio path integral methods, and molecular-dynamics simulations Key relationships that exist between fundamental vibrational frequencies and hydrogen-bond length/strength Analogous spectroscopic and semi-empirical computational techniques examining larger hydrogen-bonded systems Reflecting the polymorphic nature of hydrogen bonding and bringing together the latest experimental and computational work in the field, Spectroscopy and Computation of Hydrogen-Bonded Systems is an essential resource for chemists and other scientists involved in projects or research that intersects with the topics covered within.

The advent of laser-based sources of ultrafast infrared pulses has extended the study of very fast molecular dynamics to the observation of processes manifested through their effects on the vibrations of molecules. In addition, non-linear infrared spectroscopic techniques make it possible to examine intra- and intermolecular interactions and how su

High-Field EPR Spectroscopy on Proteins and their Model Systems: characterization of Transient Paramagnetic States offers a comprehensive overview of experimental techniques in, and paradigmatic examples of, the application of high-field EPR spectroscopy in biology and chemistry.

Molecular recognition, also known as biorecognition, is the heart of all biological interactions. Originating from protein stretching experiments, dynamic force spectroscopy (DFS) allows for the extraction of detailed information on the unbinding process of biomolecular complexes. It is becoming progressively more important in biochemical studies a

The second international conference on the subject of Picosecond Phenomena was held June 18-20, 1980, in Cape Cod, Massachusetts. Scientists from a broad range of disciplines were brought together to discuss their common interest in ultrafast processes. This meeting was organized as a Topical Meeting of the Optical Society of America and was attended by 250 partici pants. The conference reviewed the latest advances in the experimental and theo retical understanding of phenomena that occur on a picosecond timescale. New discoveries in electronics, chemical dynamics, solid state physics, and pico second optics highlighted the interactions between chemists, physicists, biologists,and engineers who attended the conference. The enthusia~m gener ated by the rapid progress in the last two years and the pleasant Cape Cod weather resulted in a successful and enjoyable conference. The conference owes a special thanks to Dr. Jarus Quinn, Joan Connon, and their colleagues at the Optical Society of America for doing a superb job in implementing the meeting arrangements and to the program committee for the selection and organization of the technical presentations. We gratefully acknowledge the financial support from the National Science Foundation, Office of Naval Research, the u.S. Army Research Office, and the AFOSR.