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. 2014 Sep 5;3(5):199–205. doi: 10.1002/open.201402021

Figure 5.

Figure 5

a) Change in excimer emission of deaerated CS@Py sample versus time under an air atmosphere, monitored for hexane (A), dichloromethane (B), ethyl acetate (C), tetrahydrofuran (D), chloroform (E), toluene (F) and dioxane (G). b) Regression between the Ln K and Ln cP for the pyrene excimer of CS@Py in the different solvents employed in this study.