✍ Scribed by Jens J Led; Steffen B Petersen
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract Deuterium isotope effects on ^13^C chemical shift of tetrabutylammonium salts of Schiff bases, derivatives of amino acids (glycine, L‐alanine, L‐phenylalanine, L‐valine, L‐leucine, L‐isoleucine and L‐methionine) and various ortho‐hydroxyaldehydes in CDCl~3~ have been measured. The resul
Deuterium isotope effects on I3C nuclear shielding, "AC(OD), were investigated for a series of enolic /3-diketones at different temperatures. The investigated enolic B-diketones cover a broad range of tautomeric equilibrium constants (K). The equilibrium constants were estimated from ''0 and I3C che
## Abstract The one‐ and two‐bond ^13^C isotope shifts, typically −1.5 to −2.5 ppb and −0.7 ppb respectively, in non‐cyclic aliphatic systems and up to −4.4 ppb and −1.0 ppb in glucose cause effects that need to be taken into account in the adaptive NMR spectral library‐based quantification of the
Deuterium-induced chemical shift differences on the 13C (DIS) are reported for a series of Schiff bases of salicylaldehydes, l-(phenyliminomethyl)naphthalen-2-ol and 4-chloro-1,7-phenanthrolin-l0-ol. Provided that corrections for the hydrogen donor atom and diamagnetic effects of the surrounding gro