Novel triorganotin(IV) complexes of β-diketonates bearing two heterocycles in their structures

C. Pettinari, F. Marchetti, I. Timokhin, A. Marinelli, C. Di Nicola, Brian Skelton, Allan White

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Novel triorganotin(IV) derivatives of beta-diketonate Q ligands (HQ in general, in detail HQ(fur) = 1-phenyl-3-methyl-4-(2-furancarbonyl)-pyrazol-5-one, HQ(thi) = 1-phenyl-3-methyl-4-(2-thienylcarbonyl)-pyrazol-5one) of general formula (Q)SnR3 center dot xH(2)O (R = Ph, x = 0; R = Bu-n or Me, x = 1) have been synthesized and spectroscopically and thermally characterized. Triphenyltin(IV) complexes have been isolated as anhydrous compounds while trialkyltin(IV) are always monohydrated. The structures of (Q(fur))SnPh3 and (Q(thi))SnMe3(OH2) are recorded. The tin atoms are five-coordinate in both. In the first, the pyrazolonate ligand behaves as an O,O'-bidentate; there are two similar but independent molecules in the structure. In the quasi-trigonal-bipyramidal environments, Sn-O(acyl) are 2.478(3), 2.364(3), Sn-O(pyrazolonate) 2.050(2), 2.079(2), Sn-C 2.123(4)-2.162(3) angstrom with the longer O(acyl) and a phenyl group quasi-trans (O-Sn-C 162.5(1), 160.8(1)degrees). In (Q(thi)) SnMe3(OH2), the three methyl groups are equatorial (Sn-C 2.1259(9)-2.1380(8) angstrom); Sn-O(Qthi, OH2) are 2.2143(5), 2.3350(6) angstrom, O-Sn-O 175.36(2)degrees. Trimethyltin(IV) derivatives decompose on heating with release of H2O and SnMe4 and formation of (Q)(2)SnMe2. Decomposition occurs also within two days after dissolution of (Q) SnMe3(OH2) in chloroform. (C) 2010 Elsevier B.V. All rights reserved.
Original languageEnglish
Pages (from-to)98-107
JournalInorganica Chimica Acta
Volume367
DOIs
Publication statusPublished - 2011

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