{SA}

Merck 14 ,3308

{SA}

Beil. 7 ,IV,1736

{SA}

Aldrich MSDS 1 , 824:B / Corp MSDS 1 (1), 1455:C / FT-IR 1 (2), 7:D / FT-IR 2 (2), 2365:B / FT-NMR 1 (2), 800:C / IR-Spectra (3), 853:B / IR-Spectra (2), 746:E / NMR-Reference 2 (2), 11:A / RegBook 1 (2), 1621:D / Structure Index 1 , 253:C:2

{ALFA} Undergoes [3 + 2] cycloadditions with phenylacetylenes and other alkynes, catalyzed by Tetracarbonyl­di-µ-chlorodirhodium(I)­, 10547, to give substituted cyclopentadienones: J. Am. Chem. Soc., 128, 14814 (2006).

{uni_hamburg} Short: III/35D2

Title: Nuclear Magnetic Resonance (NMR) Data: Chemical Shifts for Carbon-13, Part 2: Aromatic Compounds

Author: Mikhova, B.

Editor: Gupta, R.R.; Lechner, M.D.

Source: Landolt-Börnstein, New Series

Volume: III/35D2

Year: 2005

Keyword: aromatic compounds; carbon-13; chemical shift; coupling constant; molecular structure

ISBN: 978-3-540-20189-2

ISBN: 3-540-20189-0

Internet Resource: DOI:10.1007/b83345

RefComment: VIII, 291 p., Hardcover

RefComment: Written for Science and engineers in the fields of physics, chemistry and physical chemistry who inted to use NMR to study the structure and the binding of molecules

Abstract: Nuclear Magnetic Resonance (NMR) is based on the fact that certain nuclei exhibit a magnetic moment, orient by a magnetic field, and absorb characteristic frequencies in the radiofrequency part of the spectrum. The spectral lines of the nuclei are highly influenced by the chemical environment i.e. the structure and interaction of the molecules. NMR is now the leading technique and a powerful tool for the investigation of the structure and interaction of molecules. The present Landolt-Börnstein volume III/35 Nuclear Magnetic Resonance (NMR) Data is therefore of major interest to all scientists and engineers who intend to use NMR to study the structure and the binding of molecules. Volume III/35 "NMR-Data" is divided into s