Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ferrous Chloride | HCID 24458 | — |
| Reactant | Sodium Oleate | HCID 23665730 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Iron oleate | HCID 86605544 | — |
Reaction Steps
As the first exemplary example for demonstrating the method of synthesizing monodisperse nanoparticles according to the present invention, 10.8 g of iron chloride [FeCl3.6H2O, 40 mmol] and 36.5 g of sodium oleate (120 mmol) were dissolved in a mixture of solvents containing 80 mL of ethanol, 60 mL of distilled water, and 140 mL of hexane, and thereafter the resulting mixture was heated to 70° C. and kept at the same temperature for 4 hours to obtain an iron-oleate complex. During this process, the initial scarlet color in aqueous phase became clear, and the initial transparent organic phase turned to scarlet, indicating that iron-oleate complex was successfully synthesized. When the reaction was completed, the upper organic layer containing the metal-oleate complex was separated and thereafter the hexane was evaporated off, resulting in a waxy solid form. In FIG. 1, the FT-IR spectrum of the resulting iron-oleate complex shows a C═O stretching peak at 1700 cm−1, which is a unique characteristics for a metal-oleate complex.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07811545B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-c1eb4f727b624580a89410aae9ca844e |
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| Source note | uspto-grants-2010_10 |
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