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Counterintuitive deshielding on the 13 C NMR chemical shift for the trifluoromethyl anion
Author(s) -
Viesser Renan V.,
Tormena Cláudio F.
Publication year - 2020
Publication title -
magnetic resonance in chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0749-1581
DOI - 10.1002/mrc.4958
Subject(s) - chemistry , trifluoromethyl , chemical shift , ion , carbanion , carbon 13 nmr , fluorine 19 nmr , electromagnetic shielding , shielding effect , nuclear magnetic resonance spectroscopy , carbon 13 nmr satellite , paramagnetism , crystallography , computational chemistry , stereochemistry , organic chemistry , alkyl , physics , quantum mechanics , layer (electronics) , electrical engineering , engineering
The trifluoromethyl anion (CF 3 − ) displays 13 C NMR chemical shift (175.0 ppm) surprisingly larger than neutral (CHF 3 , 122.2 ppm) and cation (CF 3 + , 150.7 ppm) compounds. This unexpected deshielding effect for a carbanion is investigated by density functional theory calculations and decomposition analyses of the 13 C shielding tensor into localized molecular orbital contributions. The present work determines the shielding mechanisms involved in the observed behaviour of the fluorinated anion species, shedding light on the experimental NMR data and demystify the classical correlation between electron density and NMR chemical shift. The presence of fluorine atoms induces the carbon lone pair to create a paramagnetic shielding on the carbon nucleus.