The course is also offered to the students of the fields other than those the course is directly associated with.
Fields of study the course is directly associated with
there are 23 fields of study the course is directly associated with, display
Course objectives
Introduction to basic principles of NMR spectroscopy. Theoretical concepts of classical description using the vector model as well as of quantum mechanics needed for proper understanding of multi-dimensional NMR techniques are discussed. The product operator formalism is introduced to facilitate description of basic one and two-dimensional experiments frequently used in chemical research. The acquired knowledge enables students to understand the applications of NMR spectroscopy in organic and inorganic chemistry, biochemistry, strucutural biology and biophysics.
Syllabus
1. Introduction: NMR history and contemporary trends - applications of NMR to strcutural studies in liquids and solids, NMR tomography, expected developments, tour of NMR lab at NCBR
2. Basic principles: magnetic dipol, resonance condition, NMR spectrometer, Fourier spectroscopy, classical description - Bloch equations, relaxation - spin-lattice and spin- spin relaxation, Fourier transform, sensitvity
3. Spin system dynamics: basic properties of nuclear spin system, density matrix theory, matrix representaion, operators, spin Hamiltonia in Hilbert representation, average Hamiltonian theory.
4. Product operator formalism: basic principles, terminology, evolution of product operators, Hamiltnian in product basis, composite rotations, observables.
5. 1D Fourier spectroscopy: excitation sequences, spin-echo - principles, measurements of relaxtion times, polarization trasnfer, INEPT, DEPT, composite pulses, homo- and hetronuclear decoupling, plus filed gradients.
6. 2D Fourier spectroscopy: basic principles, formal theory of 2D detection, coherence pathways.
7. Basic methods of 2D spectroscopy: chemical shift correlation - COSY, dipol-dipol correlation - NOESY, phase cycles,methods for homo- and heteronuclear spin systems, spectral editing.
8. NMR apllications for structure determination of biomacromolecules: proteins and nucleic acids, structural parameters: proton distance determination, dihedral angles mesurements, mathematical reconstruction of 3D structures.
Literature
SANDERS, Jeremy K. M. Modern NMR spectroscopy :a workbook of chemical problems. 2nd ed. Oxford: Oxford University Press, 1993. 127 s. ISBN 0-19-855812-0. info
CAVANAGH, John and Wayne J. FAIRBROTHER. Protein NMR Spectroscopy. Principles and Practice. San Diego: Academic Press, 1996. 587 pp. ISBN 0-12-164490-1. info
NMR and the periodic table. Edited by Robin Kingsley Harris - Brian E. Mann. London: Academic Press, 1978. 459 s. ISBN 0-12-327650-0. info
VEN, Frank J. M. van de. Multidimensional NMR in Liquids :basic principles and experimental methods. New York: VCH Publishers, 1995. 399 s. ISBN 1-56081-665-1. info
RAHMAN, Atta-ur-. One and Two Dimensional NMR Spectroscopy. 1. vyd. Amsterdam: Elsevier Science Publishers B.V., 1989. 578 s. ISBN 0-444-87316-3. info
HOCH, Jeffrey C. and Alan S. STERN. NMR data processing. New York: Wiley-Liss, 1996. xi, 196 s. ISBN 0-471-03900-4. info
Two-dimensional NMR spectroscopy :applications for chemists and biochemists. Edited by William R. Croasmun - Robert M. K. Carlson. 2nd ed. New York: VCH Publishers, 1994. xxii, 958. ISBN 1-56081-664-3. info
Protein NMR spectroscopy principles and practice. San Diego: Academic Press, 1996. 587 s. ISBN 0-12-164490-1. info
EVANS, Jeremy N. S. Biomolecular NMR spectroscopy. Oxford: Oxford University Press, 1995. xvi, 444 s. ISBN 0-19-854766-8. info
HORE, Peter J., Jonathan A. JONES and Stephen WIMPERIS. NMR :the toolkit. 1st pub. Oxford: Oxford University Press, 2000. 85 s. ISBN 0-19-850415-2. info
Further Comments
The course can also be completed outside the examination period.
The course is taught annually.