| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1324499 | Journal of Organometallic Chemistry | 2009 | 6 Pages |
A straightforward method of synthesis of heteroleptic tin (II) alkoxides stabilized by one intramolecular coordination bond was developed. Addition of one equivalent of dimethylamino ethanol to diamide Sn(N(SiMe3)2)2 (5) yields alkoxy-amido derivative Sn(OCH2CH2NMe2)(N(SiMe3)2) (2). Further addition of alcohol leads to corresponding heteroleptic dialkoxides Sn(OCH2CH2NMe2)(OR) (R = Me (6), Et (7), iPr (8), tBu (9), Ph (10)). Catalytic activity of tin (II) compounds in polyurethane formation was tested.
Graphical abstractA straightforward method of synthesis of heteroleptic tin (II) alkoxides stabilized by one intramolecular coordination bond was developed. These compounds are active catalysts of polyurethane formation.Figure optionsDownload full-size imageDownload as PowerPoint slide
