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 all started by means of the past due Dr. H.-O. Kalinowski, Justus-Liebig-Universität, Gießen, thirteen Germany who couldn't proceed the paintings on it. His books in regards to the conception and purposes of C NMR are renowned and necessary to many chemists. The authors and the editors commit the quantity to the reminiscence of Dr. H.-O. Kalinowski. Nuclear Magnetic Resonance (NMR) relies at the proven fact that sure nuclei convey a magnetic second, orientated via a magnetic box, and take up attribute frequencies within the radiofrequency a part of the spectrum. The spectral strains of the nuclei are hugely inspired via the chemical surroundings, i.e. the constitution and interplay of the molecules. Magnetic homes of nuclei were recognized due to the fact that 1924 and the 1st Nuclear Magnetic Resonance test used to be played in 1945. NMR is now the best strategy and a strong device for the research of the constitution and interplay of molecules. the current Landolt-Börnstein quantity III/35 "Nuclear Magnetic Resonance (NMR) facts" is consequently of significant curiosity to all scientists and engineers who intend to exploit NMR to check the constitution and the binding of molecules.
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Additional resources for Chemical Shifts and Coupling Constants for Carbon-13: Part 1: Aliphatic Compounds
Example text
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.
J. Magn. Reson. 33 (3) (1979) 559. 1007/978-3-540-45285-0_16 © Springer 2010 Nuclear magnetic resonance data of CHCl2I 1 Nuclear magnetic resonance data of CHCl2I 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.
All measurements refer to room temperature if not stated otherwise. 13 Gross formula Structure Solvent δC [ppm] / nJ [Hz] Ref. : J. Magn. Reson. 18 (1975) 522. 1007/978-3-540-45285-0_6 © Springer 2010 Nuclear magnetic resonance data of CClI3 1 Nuclear magnetic resonance data of CClI3 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” 13 C chemical shifts δ [ppm] and coupling constants nJ [Hz], downfield from tetramethylsilane (TMS).