Secure CheckoutPersonal information is secured with SSL technology.
Free ShippingFree global shipping
No minimum order.
Preface. 1. The Electron Paramagnetic Resonance Experiment. 2. Spin Doublets in an Applied Magnetic Field: A Qualitative Treatment. 3. The Quantitative Description of the Spectra from Spin Doublets Interacting with an Applied Magnetic Field Only. 4. The Spectra from Spin Doublets Interacting with a Nuclear Spin: A Qualitative Treatment. 5. Spectra of Spin Doublets Interacting with a Nuclear Spin: A Quantitative Treatment. 6. Nuclear Quadrupole and Nuclear Zeeman Effects in Spin Doublets. 7. Spectrum Simulation for Spin Doublets. 8. Metal Ions in Cubic and Axial Ligand Fields. 9. The Relationship between the Spin-Hamiltonian Parameters and the Electronic Structures of Spin Doublet Paramagnets. 10. Paramagnets with S 〉 1/2. 11. Monomeric Spin Triplets: Qualitative and Quantitative Aspects. 12. Monomeric Spin Quartet Paramagnets. 13. Monomeric Spin Quintets: Qualitative and Quantitative Aspects. 14. Monomeric Spin Sextet Paramagnets. 15. Polynuclear Transition Metal Compounds. 16. Simulation of Spectra for Paramagnets with Multiple Unpaired Electrons. 17. Extended Electron Exchange in Crystals. 18. Relaxation, Linewidths, Determination of Concentrations, and Microwave Power Saturation. Appendices. Some physical properties of selected solvents. Physical constants and conversion factors. Spin-Hamiltonians, operator equivalents and some relationships between angular momentum operators. Direction cosines and transformation of axes. Some useful mathematical relationships. Some properties of nuclei with non-zero nuclear spin and hyperfine interactions parameters. Polar coordinates, Cartesian coordinates, wavefunctions, orbitals. Determinantal wavefunctions. Inter-electron repulsion calculations. The effect of operators such as R&dgr;/&dgr;x. Dipole-dipole interactions and the point-dipole approximations. Expanded FIR diagrams for S=1, 1, 3/2, 2, 5/2, 3, 7/2, 4, 9/2. Mean values of functions and the methods of moments. Subject and Keyword Index. Chemical Index.
Electron paramagnetic resonance (epr) spectroscopy is a sensitive and versatile method of studying paramagnets, which is finding increasing use in chemistry, biochemistry, earth and materials sciences.
The technique is treated both qualitatively and quantitatively, with a progressive increase in sophistication in each succeeding chapter. Following a general introductory chapter, the first half of the book deals with single unpaired electron systems and considers both metal and ligand Zeeman, hyperfine and quadrupole interactions. The simulation of these spectra is discussed, followed by the relationship between spin-Hamiltonian parameters and models of the electronic structures of paramagnets. The second half of the book treats multiple unpaired electron systems using the same philosophy. An introduction to the epr properties of cluster compounds and of extended exchanging systems is also given. There is a chapter on linewidths and lineshapes, and an extensive appendix containing much additional information. A wide-ranging library of simulated and experimental spectra is given, as well as graphical data which should aid spectrum interpretation. Each chapter contains key references and there is a substantial subject and keyword index.
This book is designed to teach epr spectroscopy to students without any previous knowledge of the technique. However, it will also be extremely useful to researchers dealing with paramagnetic d transition metals.
- © Elsevier Science 1992
- 5th November 1992
- Elsevier Science
- eBook ISBN:
@qu:I recommend this excellent book to inorganic chemists and EPR spectroscopists for its commendable clarity, attention to detail and comprehensive coverage. @source:Spectroscopy Europe
Department of Chemistry, University of Manchester, Manchester, UK
Elsevier.com visitor survey
We are always looking for ways to improve customer experience on Elsevier.com.
We would like to ask you for a moment of your time to fill in a short questionnaire, at the end of your visit.
If you decide to participate, a new browser tab will open so you can complete the survey after you have completed your visit to this website.
Thanks in advance for your time.