792971-31-4Relevant articles and documents
Tri-n-butyltin carboxylate derivatives of para-substituted phenyl-ethanoic acids: Synthesis, characterization and X-ray structure determination
Angiolini, Luigi,Caretti, Daniele,Mazzocchetti, Laura,Salatelli, Elisabetta,Femoni, Cristina
, p. 3301 - 3307 (2007/10/03)
The tributyltin esters of 4-(ethyl)-phenyl-ethanoic acid and 4-(isopropyl)-phenyl-ethanoic acid have been prepared as model compounds of the repeating unit of the related stannylated polystyrenic derivatives. Both the products were fully characterized by proton and carbon NMR two-dimensional techniques. FT-IR spectra show in the solid state carboxylated moieties bridging R 3 Sn groups with the metal atom expanding its coordination number, this structure being destroyed in solution. The supramolecular arrangement of the products in the solid state has been investigated by X-ray diffraction, which confirms the pentacoordination at tin in both the products, and indicates a different spatial arrangement of the alkylated aryl groups, as evidenced also by the slightly different thermal properties.