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HRID 2305248作成日:2026年10月25日

2-Methoxyethanol → Gadolinium (III) isopropoxide

https://huagongshe.com/reaction/2305248

反応式

関与物質

役割名称HCID仕込み量
反応物2-MethoxyethanolHCID 8019—
反応物Gadolinium (III) isopropoxideHCID 15047187—
生成物Gadolinium (III) isopropoxideHCID 15047187—
生成物Gadolinium(3+);tris(1-methoxyethanolate)HCID 131723452—

反応手順

Gadolinium isopropoxide was synthesized using the method of Brown et al. The Gd2O3 precursor solution was prepared by reacting 4.85 g (15 mmole) of gadolinium isopropoxide with 50 ml of 2-methoxyethanol under an inert atmosphere. After refluxing for approximately 1 hour, two-thirds of the solution (isopropanol and 2-methoxyethanol) was removed by distillation. The flask was allowed to cool, and 20 ml of 2-methoxyethanol was added. The flask was refluxed for 1 hour, and ⅔ of the solution was then removed by distillation. This process of dilution, reflux, and distillation was repeated for a total of three cycles to ensure the complete exchange of the methoxyethoxide ligand for the isopropoxide ligand. It was estimated that this occurs when the boiling point of the solution reaches 124° C. The final concentration of the solution was adjusted to obtain a 0.5 M solution of gadolinium methoxyethoxide in 2-methoxyethanol. A partially hydrolyzed solution suitable for spin coating or dip-coating was prepared by reacting 1 part of a 1.0 molar solution of water in 2-methoxyethanol with 4 parts of the 0.5 M gadolinium methoxyethoxide solution.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06440211B1
出典データセットuspto-grants-2002_08
ORD IDord-be7b3a1a1fae4746a680fedc48183b2d
出典メモuspto-grants-2002_08