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Dalton Trans ; 45(31): 12548-58, 2016 Aug 02.
Artigo em Inglês | MEDLINE | ID: mdl-27435308

RESUMO

N-Substituted-9-aza-3,6,12,15-tetrathiaheptadecanes having Ph-C-N frameworks (N-R-ATH; R = benzyl (N-Bn-ATH), 4-nitrobenzyl (N-NO2Bn-ATH), and diphenylmethyl (N-Ph2CH-ATH)) were synthesized, and their Ag(i) complexes were structurally characterized. X-Ray crystal structure analyses of [Ag(N-R-ATH)](BF4) (R = Bn and Ph2CH) revealed monomeric tetra-S-coordinated complex cation structures without the N-coordination, and a benzene ring of the N-R group covered over the amine nitrogen atom. The precise extraction analyses of a Ag(i) ion with ATH derivatives (L = N-R-ATHs and N-H-ATH) associated with the (1)H NMR analyses of the [Ag(L)](+) complexes in polar and non-polar solvents revealed that the introduction of the N-substituent significantly enhanced the extractability of Ag(+), due to the "hydrophobic cover" effect by the Ph-C-N framework in the [Ag(N-R-ATH)](+) complexes.

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