1362855-82-0Relevant academic research and scientific papers
Addition of Lappert's stannylenes to carbodiimides, providing a new class of tin(II) guanidinates
Chlupaty, Tomas,Padelkova, Zdenka,Deproft, Frank,Willem, Rudolph,Ruzicka, Ales
, p. 2203 - 2211 (2012/06/04)
Reactions of bis[bis(trimethylsilyl)amino]tin and the dimer of [bis(trimethylsilyl)amino]tin chloride with various carbodiimides give pure corresponding tin(II) guanidinates in essentially quantitative yields. Heteroleptic bis(trimethylsilyl)amido ({R-NC[N(SiMe3) 2]N-R}SnN(SiMe3)2)- and chloro-substituted ({R-NC[N(SiMe3)2]N-R}SnCl) tin(II) guanidinates were obtained from reactions of N,N′-diisopropyl-, N,N′-dicyclohexyl-, N,N′-bis(4-methylphenyl)-, and N-[3-(dimethylamino)propyl]-N′- ethylcarbodiimides, respectively. Homoleptic tin(II) guanidinates {R-NC[N(SiMe3)2]N-R}2Sn were obtained from the N,N′-bis(4-methylphenyl)- and N-[3-(dimethylamino)propyl]-N′-ethyl- substituted carbodiimides. Similar reactions of N,N′-bis(2,6- diisopropylphenyl)- and N,N′-bis(trimethylsilyl)carbodiimide, respectively, having the bulkiest substituents of the series, failed to take place under various conditions. The complexes prepared were characterized as monomers in solution by 1H, 13C, and 119Sn NMR spectroscopy in C6D6 and THF-d8. The solid-state NMR spectra were recorded for structure comparison. X-ray diffraction studies of one homoleptic monomer, two heteroleptic chloro complexes with the structures of two different types of dimers, and the oxidation product of the heteroleptic bis(trimethylsilyl)amido-substituted guanidinate-a centrosymmetric (guanidinato)tin(IV) oxide-were performed on appropriate crystals. Attempts to prepare homoleptic types of isopropyl- and cyclohexyl-substituted tin(II) guanidinate complexes were unsuccessful. The structures were also evaluated by DFT methods.
