Novel Supramolecular Frameworks Self‐Assembled from a Two‐Dimensional Polymeric Network: Synthesis and Crystal Structure of a Macrocyclic Organotin(
<scp>IV</scp>
) Complex
作者:Chunlin Ma、Yinfeng Han、Rufen Zhang、Daqi Wang
DOI:10.1002/ejic.200401056
日期:2005.5
The two-dimensionalpolymer [nBu2Sn(O2CC6H4)]4 has been synthesized by the self-assembly of di-n-butyltin oxide and 4-carboxyphenylboronic acid. The X-ray crystal structure shows that the metal ions display a trigonal bipyramidal coordination geometry to bind the endocyclic oxygen atom. Intermolecular π–π stacking interactions between adjacent phenyl groups of the ligand cause the self-assembly into
Butyltin(IV) 5-sulfosalicylates: Structural characterization and their cytostatic activity
作者:Hanna Pruchnik、Małgorzata Latocha、Aleksandra Zielińska、Stanisław Ułaszewski、Florian P. Pruchnik
DOI:10.1016/j.poly.2012.10.025
日期:2013.1
Butyltin complexes with 5-sulfosalicylic acid (H(3)ssal) [Sn(C4H9)(3)O3SC6H3(OH)COOH}] (1), [Sn-2(C4H9)(6) (OOCC6H3OHSO3)] (2) and [Sn-3(C4H9)(6)(OOCC6H3(OH)SO3)(2)O] (3) have been synthesized and characterized by ESI-MS, IR and H-1, C-13 and Sn-119 NMR spectra. Their structures and properties in solid state and solutions were proposed on the basis of the spectroscopic data and density functional theory (DFT) calculations at B3LYP/3-21G** level. The complex 1 in solid state is a chain compound with bridging ligand O3SC6H3(OH)COOH- coordinated to two adjacent SnBu3 units via SO3 and COOH groups and complex 2 is a dinuclear compound with O3SC6H3(OH)COOH- bridging ligand bound to the SnBu3 moieties through SO3 and COO groups. The spectroscopic data indicate that 3 is probably a trinuclear complex containing bridging oxido and Hssal ligands containing two five-coordinate and one six-coordinate tin atoms. The complexes effectively interact with ATP and DAMP nucleotides forming Sn-OP bonds and O'-H'center dot center dot center dot O and N center dot center dot center dot H-O (nucleotide-Hssal) hydrogen bonds. All compounds are very effective cytotoxic agents against tumor cells. The cytotoxic activity changes in the order 2 > 1 > 3. Their activity toward non-tumor NHDF cells is much lower. They show also antibacterial and antifungal activity. (C) 2012 Elsevier Ltd. All rights reserved.