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State-Selected and State-to-State Ion-Molecule Reaction Dynamics Part 1: Experiment Edited by Cheuk-Yiu Ng and Michael Baer "It contains a wealth of technical detail and experience and is a ‘must’ for anyone using, or contemplating using, position-sensitive detection methods." —Chemical Engineering Science Illustrated with eight in-depth studies, which shed light on the key experimental work being done in the field today, Part 1 of State-Selected and State-to-State Ion-Molecule Reaction Dynamics is a well-organized look at the experimental side of this highly useful and emerging chemical specialty. Part 1’s progressive coverage includes: a comprehensive review of the theory and application of inhomogeneous rf fields; the application of multiphoton ionization for the preparation of reactant ion states; the conceptual and practical aspects of a multicoincidence technique; and the experimental results obtained using the photoionization and differential reactivity methods. 1992 (0-471-53258-4) 704 pp. State-Selected and State-to-State Ion-Molecule Reaction Dynamics Part 2: Theory Edited by Michael Baer and Cheuk-Yiu Ng Using clear illustrative examples culled from up-to-date research, Part 2: Theory makes the theory fundamental to state-to-state reaction dynamics not only understandable, but relevant to every day experimental work. Focusing exclusively on the theory of charge transfer processes during an atom (ion)-molecule (ion) collision, the book examines the different attitudes for treating the potential energy surfaces which govern the motion of the interacting atoms and ions and the reaction dynamics of these particles. The book also uses a variety of approaches, from the pure quantum mechanical approach, various semiclassical approaches to several statistical approaches, to address key issues in reaction dynamics. 1992 (0-471-53263-0) 576 pp. Advances in Chemical Physics Volume 84 Edited by I. Prigogine and Stuart A. Rice Volume 84 of this heralded series offers readers a detailed, up-to-date look at a host of important issues in chemical physics, including: the collisional time-correlation function approach to molecular energy transfer; molecular theory of liquid phase vibrational energy relaxation; electron degradation in molecular substances; and simulation of nonlinear electronic spectroscopy in the condensed phase. 1993 (0-471-58726-5) 560 pp.
Significant advances have occurred in the field since the previous edition, including advances in light squeezing, single photon optics, phase conjugation, and laser technology. The laser is essentially responsible for nonlinear effects and is extensively used in all branches of science, industry, and medicine.
6th European Conference on the Spectroscopy of Biological Molecules, 3--8 September 1995, Villeneuve d'Ascq, France
The Advances in Chemical Physics series provides the chemical physics and physical chemistry fields with a forum for critical, authoritative evaluations of advances in every area of the discipline. Filled with cutting-edge research reported in a cohesive manner not found elsewhere in the literature, each volume of the Advances in Chemical Physics series serves as the perfect supplement to any advanced graduate class devoted to the study of chemical physics.
A comprehensive discussion of the key role of modern spectroscopic investigations in interdisciplinary materials science and engineering, covering emerging materials that are either absolutely novel or well-known materials with recently discovered, exciting properties. The types of spectroscopy discussed include optical, electronic and magnetic, UV-visible absorption, Rayleigh scattering, photoluminescence, vibrational, magnetic resonance, electron energy loss, EXAFS, XANES, optical tomography, time-resolved spectroscopy, and point contact spectroscopy. The materials studied are highly topical, with a focus on carbon and silicon nanomaterials including nanotubes, fullerenes, nanoclusters, metallic superconducting phases, molecular materials, magnetic and charge-stripe oxides, and biomaterials. Theoretical treatments are presented of molecular vibrational dynamics, vibration-induced decay of electronic excited states, nanoscale spin-orbit coupling in 2D Si-based structures, and the growth of semiconductor clusters.
The Advances in Chemical Physics series provides the chemical physics and physical chemistry fields with a forum for critical, authoritative evaluations of advances in every area of the discipline. Filled with cutting-edge research reported in a cohesive manner not found elsewhere in the literature, each volume of the Advances in Chemical Physics series serves as the perfect supplement to any advanced graduate class devoted to the study of chemical physics.
The Advances in Chemical Physics series provides the chemical physics and physical chemistry fields with a forum for critical, authoritative evaluations of advances in every area of the discipline. Filled with cutting-edge research reported in a cohesive manner not found elsewhere in the literature, each volume of the Advances in Chemical Physics series serves as the perfect supplement to any advanced graduate class devoted to the study of chemical physics.
This first volume of this two-volume set deals with the important recent discovery of the photomagneton of electromagnetic radiation, a discovery which is fundamental in quantum field theory and in quantum mechanics in matter. The photomagneton is the elementary quantum of magnetic flux density carried by the individual photon in free space, and is generated directly by the intrinsic angular momentum of the free photon. The volume develops the theory of the photomagneton in a series of papers, which cover all the major aspects of the theory, from classical electrodynamics to the relativistic quantum field. Several suggestions are given for experimental tests, and the available experimental evidence is discussed in detail. The overall conclusion of the series of papers is that the photomagneton, which is observable experimentally in magneto-optical phenomena, indicates the presence in free space of a novel, longitudinal, magnetic flux density, linked ineluctably to the usual transverse components. If the photomagneton is not observed, then a paradox would have emerged at the most fundamental electrodynamical level, necessitating a modification of the Maxwell equations themselves.
Uniquely creates a strong bridge between molecular spectroscopy and quantum chemistry This two-volume book consists of many reviews reporting new applications of quantum chemistry to molecular spectroscopy (Raman, infrared, near-infrared, terahertz, far-ultraviolet, etc.). It contains brief introductions to quantum chemistry for spectroscopists, and to the recent progress on molecular spectroscopy for quantum chemists. Molecular Spectroscopy: A Quantum Chemistry Approach examines the recent progress made in the field of molecular spectroscopy; the state of the art of quantum chemistry for molecular spectroscopy; and more. It offers multiple chapters covering the application of quantum chemistry to: visible absorption and fluorescence, Raman spectroscopy, infrared spectroscopy, near-infrared spectroscopy, terahertz spectroscopy, and far-ultraviolet spectroscopy. It presents readers with hydrogen bonding studies by vibrational spectroscopy and quantum chemistry, as well as vibrational spectroscopy and quantum chemistry studies on both biological systems and nano science. The book also looks at vibrational anharmonicity and overtones, and nonlinear and time-resolved spectroscopy. -Comprehensively covers existing and recent applications of quantum chemistry to molecular spectroscopy -Introduces the quantum chemistry for the field of spectroscopy and the advancements being made on molecular spectroscopy for quantum chemistry -Edited by world leading experts who have long standing, extensive experience and international standing in the field Molecular Spectroscopy: A Quantum Chemistry Approach is an ideal book for analytical chemists, theoretical chemists, chemists, biochemists, materials scientists, biologists, and physicists interested in the subject.