Abstract
A novel synthetic pathway involving the desilylation of a tin trimethylsilyl species (Ph2Sn(SiMe3)2) towards nonprotected di(3-aminopropyl)tin dichloride ((H2N(CH2)3)2SnCl2) is described. Di(3-aminopropyl)tin dichloride is then converted to the respective dicarboxylates species (H2N(CH2)3)2Sn(OCOR)2 containing carboxylic acids of different lengths (R = –CH3, –(CH2)10CH3). Depending on the nature of R, discrete packing effects are observed in the solid state of di(3-aminopropyl)tin dicarboxylate derivatives. All the synthesized substances were characterized by 1H, 13C, and 119Sn nuclear magnetic resonance data and also single crystal X-ray analysis. These compounds are a promising class of substances for biological, pharmaceutical, and technical applications.
Originalsprache | englisch |
---|---|
Seiten (von - bis) | 411 |
Seitenumfang | 418 |
Fachzeitschrift | Canadian Journal of Chemistry |
Jahrgang | 96 |
Ausgabenummer | 4 |
DOIs | |
Publikationsstatus | Veröffentlicht - 8 Feb. 2018 |
Fields of Expertise
- Advanced Materials Science