1987
DOI: 10.1016/s0022-328x(00)99807-3
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13C and 119Sn NMR spectra of some tribenzyltin(IV) compounds

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Cited by 28 publications
(10 citation statements)
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“…The compound 1 in a non-coordinating solvent (deuterochloroform) exhibited the δ( 119 Sn) value as a sharp singlet at 0.82 ppm. The value found for 1 falls within the range + 55.0 to − 25.0 ppm specified for four-coordinate tribenzyltin species in solution [12]. This indicates that the five-coordinate dimeric structure of the solid (see X-ray discussion, vide infra) breaks up in solution.…”
Section: Synthetic and Spectroscopic Propertiessupporting
confidence: 57%
“…The compound 1 in a non-coordinating solvent (deuterochloroform) exhibited the δ( 119 Sn) value as a sharp singlet at 0.82 ppm. The value found for 1 falls within the range + 55.0 to − 25.0 ppm specified for four-coordinate tribenzyltin species in solution [12]. This indicates that the five-coordinate dimeric structure of the solid (see X-ray discussion, vide infra) breaks up in solution.…”
Section: Synthetic and Spectroscopic Propertiessupporting
confidence: 57%
“…[5][6][7][8][9][10][11] However, despite the large δ( 119 Sn) chemical shift range of organotin(IV) compounds, ca. 600 ppm ranging from tetra-to hexacoordinate tin, and the various factors [ influencing the 119 Sn chemical shift, e.g., solvent effects, self-association and temperature, the latter may not be sufficient for a full structural characterization.…”
Section: Introductionmentioning
confidence: 99%
“…However structural trends in these compounds could be inferred from the δ( 13 C) and the n J( 119 Sn, 13 C) (n = 1,2,3,4) couplings of the phenyl and benzyl groups and, only for the tribenzyltin(IV) derivatives, from the 2 J( 119 Sn, 1 H). [9,11] 3 J( 119 Sn, X) (X = 1 H, 2 H, 13 C) play a very important role in organotin(IV) conformational studies, somehow mirroring the distinctive role that the Karplus dependence of 3 J( 1 H, 1 H) on the dihedral angle holds in structure elucidation of organic molecules. Also in this case some empirical relationships have been reported.…”
Section: Introductionmentioning
confidence: 99%
“…In the methyltin(IV) derivative 3 the tin-proton coupling constants 2 J( 117 Sn, 1 H) and 2 J( 119 Sn, 1 H) are 73.0 and 77.0 Hz, falling in the range for five-or six-coordinated species [37]. The 119 Sn chemical shift of 3 falls at À472.4 ppm, providing an additional support for six-coordinated tin atom [38] (Fig. 2), with the donor acting as N,N 0 -bidentate chelating ligand [26].…”
Section: Resultsmentioning
confidence: 95%