1,3-Dichloro-1,1,2,2,3,3-hexa-tert-butyltristannane: Thermolysis involving trapping of stannylene, Bu2Sn: and reactivity with various nucleophiles
Autor: | Hemant K. Sharma, Keith H. Pannell, Alejandro J. Metta-Magaña |
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Rok vydání: | 2018 |
Předmět: |
010405 organic chemistry
Thermal decomposition Catenane 010402 general chemistry HEXA 01 natural sciences Medicinal chemistry 0104 chemical sciences Inorganic Chemistry chemistry.chemical_compound chemistry Nucleophile Reagent Materials Chemistry Nucleophilic substitution Organic chemistry Reactivity (chemistry) Physical and Theoretical Chemistry Bifunctional |
Zdroj: | Inorganica Chimica Acta. 475:3-7 |
ISSN: | 0020-1693 |
DOI: | 10.1016/j.ica.2017.03.045 |
Popis: | The bifunctional 1,3-dichloro-tristannane CltBu2Sn-SntBu2-SntBu2Cl, 1, has been investigated with respect to thermolysis and nucleophilic substitution. Thermolysis of 1 leads to slow elimination of the stannylene which may be trapped by elemental sulphur, PhSSPh and 2,3-dimethylbutadiene. Reactions of 1 with the silyllithium reagent PhMe2SiLi, lead to new group 14 catenanes PhMe2Si-SntBu2-tBu2Sn-SntBu2-Cl, 9, and PhMe2Si-SntBu2-tBu2Sn-SntBu2-SntBu2-SiPhMe2, 10. Both 9 and 10 have been characterized by single crystal X-ray diffraction. Overall the new chemistry illustrates the significance of tBu2Sn: during such reactions, either loss or addition! |
Databáze: | OpenAIRE |
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