1994
DOI: 10.1002/mrc.1260320906
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1H and 13C NMR structural studies in solution of oxotechnetium(V) complexes with N,N‐bis(2‐mercaptoethyl)‐N′,N′‐diethylethylenediamine and N,N‐bis(2‐mercaptoethyl)‐2‐ethylthioethylamine

Abstract: Institute of Radioisotopes-Radiodiagnostic

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Cited by 17 publications
(3 citation statements)
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“…These values were consistent with the coupling constants observed in the 1 H NMR, and on the basis of this consideration the signal at 3.83 ppm ( 3 J = 2.1) was assigned to the endo and the signal at 3.24 ppm ( 3 J = 7.9) to the exo proton. The assignments were in accordance with the literature-reported data on oxo−rhenium complexes, indicating that protons spatially close to the oxygen of the ReO are deshielded relative to those remote from the oxygen.…”
Section: Resultssupporting
confidence: 89%
“…These values were consistent with the coupling constants observed in the 1 H NMR, and on the basis of this consideration the signal at 3.83 ppm ( 3 J = 2.1) was assigned to the endo and the signal at 3.24 ppm ( 3 J = 7.9) to the exo proton. The assignments were in accordance with the literature-reported data on oxo−rhenium complexes, indicating that protons spatially close to the oxygen of the ReO are deshielded relative to those remote from the oxygen.…”
Section: Resultssupporting
confidence: 89%
“…The four protons of each moiety are diastereotopic each one resulting in a multiplet. The downfield overlapped multiplets (3.36−4.23 ppm) are assigned to the protons which are close (endo) to the TcO core, while the other two multiplets (2.61−3.42 ppm) are assigned to the protons which are remote (exo) . The protons attached to the C5 of the N-subtituent (Figure ) of the isolated major complexes are found in a deshielded environment at 3.87−4.06 ppm indicating that all have the same configuration ( syn ).…”
Section: Resultsmentioning
confidence: 99%
“…Chemical shifts ( δ , ppm) were referenced to TMS for samples run in CDCl 3 and to DSS for samples run in D 2 O. Parameters for the 2D experiments (COSY, HETCOR, NOESY, etc.) have been previously reported. ,,, Elemental analyses for C, H, N, and S were conducted on a Perkin-Elmer 2400/II Automatic Elemental Analyzer. HPLC analyses were performed on a Waters Chromatograph efficient with a 600 solvent delivery system and coupled to a Waters 996 Photodiode Array UV Detector.…”
Section: Methodsmentioning
confidence: 99%