Scalar Cross-Relaxation Detected in the NOESY Spectra of Oxazolidines and Thiazolidines
Author(s) -
Tharindi Panduwawala,
Laia JosaCulleré,
Ilya Kuprov,
Barbara Odell,
Mark G. Moloney,
Timothy D. W. Claridge
Publication year - 2016
Publication title -
the journal of organic chemistry
Language(s) - English
Resource type - Journals
eISSN - 1520-6904
pISSN - 0022-3263
DOI - 10.1021/acs.joc.6b00458
Subject(s) - chemistry , two dimensional nuclear magnetic resonance spectroscopy , scalar (mathematics) , dipole , relaxation (psychology) , spectral line , proton , chemical physics , computational chemistry , stereochemistry , organic chemistry , quantum mechanics , physics , geometry , mathematics , psychology , social psychology
Anomalous cross-peaks observed in the NOESY spectra of 2,4-disubstituted thiazolidines and oxazolidines that cannot be attributed to classical dipolar NOE or chemical exchange peaks have been investigated experimentally and computationally and have been shown to arise from scalar cross-relaxation of the first kind. This process is stimulated by the relatively slow modulation of scalar couplings and, for the systems studied, arises from slow on-off proton exchange of the amino nitrogen, a process influenced by solution temperature, acidity, and concentration. The mechanism is likely to be significant for many systems in which proton exchange occurs on the millisecond time scale, and misinterpretation of these cross-peaks may lead to erroneous conclusions should their true origins not be recognized.
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