By R. R. Gupta, M. D. Lechner, B. M. Gupta (auth.), R. R. Gupta, M. D. Lechner, V. Gupta (eds.)

The current quantity was once started through the overdue Dr. H.-O. Kalinowski, Justus-Liebig-Universität, Gießen, thirteen Germany who couldn't proceed the paintings on it. His books in regards to the idea and functions of C NMR are renowned and beneficial to many chemists. The authors and the editors commit the quantity to the reminiscence of Dr. H.-O. Kalinowski. Nuclear Magnetic Resonance (NMR) is predicated at the undeniable fact that sure nuclei express a magnetic second, orientated via a magnetic box, and take up attribute frequencies within the radiofrequency a part of the spectrum. The spectral traces of the nuclei are hugely motivated by way of the chemical atmosphere, i.e. the constitution and interplay of the molecules. Magnetic homes of nuclei were recognized considering the fact that 1924 and the 1st Nuclear Magnetic Resonance scan was once played in 1945. NMR is now the prime procedure and a strong instrument for the research of the constitution and interplay of molecules. the current Landolt-Börnstein quantity III/35 "Nuclear Magnetic Resonance (NMR) facts" is accordingly of significant curiosity to all scientists and engineers who intend to exploit NMR to review the constitution and the binding of molecules.

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Extra resources for Chemical Shifts and Coupling Constants for Carbon-13: Part 1: Aliphatic Compounds

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J. Magn. Reson. 18 (1975) 522. 1007/978-3-540-45285-0_4 © Springer 2010 Nuclear magnetic resonance data of CBr4 1 Nuclear magnetic resonance data of CBr4 Data extract from Landolt-Börnstein III/35 “Nuclear Magnetic Resonance Data”, Subvolume D “Chemical Shifts and Coupling Constants for Carbon-13”, Part 1 “Aliphatic Compounds” C chemical shifts δ [ppm] and coupling constants nJ [Hz], downfield from tetramethylsilane (TMS). All measurements refer to room temperature if not stated otherwise. 13 Gross formula Structure Solvent δC [ppm] / nJ [Hz] Ref.

J. Magn. Reson. 33 (3) (1979) 559.

Magn. Reson. 33 (3) (1979) 559. 1007/978-3-540-45285-0_5 © Springer 2010 Nuclear magnetic resonance data of CClF3 1 Nuclear magnetic resonance data of CClF3 Data extract from Landolt-Börnstein III/35 “Nuclear Magnetic Resonance Data”, Subvolume D “Chemical Shifts and Coupling Constants for Carbon-13”, Part 1 “Aliphatic Compounds” C chemical shifts δ [ppm] and coupling constants nJ [Hz], downfield from tetramethylsilane (TMS). All measurements refer to room temperature if not stated otherwise. 13 Gross formula Structure Solvent δC [ppm] / nJ [Hz] Ref.

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