2011
DOI: 10.1016/j.jorganchem.2010.10.040
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Use of bis-aminoalcohol benzoquinones and dihydroxybenzoquinones in the formation of mono and polymeric structures of diorganotin(IV) derivatives

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Cited by 12 publications
(2 citation statements)
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“…This can indicate unique species or a fast exchanging equilibrium, on the NMR time scale. The chemical shifts are within the range of di-n-butyl (IV) hexacoordinated compounds [3][4][5][6][18][19][20][21][22]. Neverthelees, for compound 2a, the 119 Sn NMR spectrum show five signals in ca.…”
Section: Resultsmentioning
confidence: 99%
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“…This can indicate unique species or a fast exchanging equilibrium, on the NMR time scale. The chemical shifts are within the range of di-n-butyl (IV) hexacoordinated compounds [3][4][5][6][18][19][20][21][22]. Neverthelees, for compound 2a, the 119 Sn NMR spectrum show five signals in ca.…”
Section: Resultsmentioning
confidence: 99%
“…In particular, diorganotin (IV) compounds derived from ligands containing nitrogen and oxygen donor atoms present increasing number of reports, mainly derivates of aminoacids and analogues have been investigated [16,17]. Our current interest in the synthesis of organotin compounds and structural analysis [18][19][20][21][22], prompted us to extend our investigation in the synthesis of new organotin (IV) compounds, which could have corrosion inhibitors properties [23].…”
Section: Introductionmentioning
confidence: 99%