| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10570522 | Inorganic Chemistry Communications | 2005 | 7 Pages |
Abstract
31P NMR spectroscopic investigations of the products of sequential aminolysis with pyrrolidine (YH) of racemic trans-1,3-bisdibenzylamino-1,3,5,5-tetrachlorocyclotriphosphazene provide diastereoisomeric evidence that a racemisation reaction occurs for formation of the penta-amino derivative and is also most likely in the formation of the hexa-amino derivative.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Aylin Uslu,