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HRID 2181593作成日:2026年10月27日

Ethanol → Pyrene pyridine

https://huagongshe.com/reaction/2181593

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Pyridine-decanethiolHCID 22481273—
触媒Cobalt(II) chlorideHCID 24288—
触媒Cobalt dibromideHCID 24610—
触媒Copper bromide (CuBr2)HCID 24611—
触媒Iron bromide (FeBr2)HCID 425646—
溶媒AcetoneHCID 180—
溶媒MethanolHCID 887—
生成物Pyrene pyridineHCID 88002260—

反応手順

For multilayer film preparation, gold slides were purchased from Evaporated Metal Films (EMF). The slides have dimensions of 25 mm×75 mm×1 mm of float glass with cut edges and they are coated with 50 angstroms of chromium followed by 1000 angstroms of gold. The substrates were cut in different sizes according to experimental needs. Slides were immersed in a piranha solution (70% sulfuric acid/30% hydrogen peroxide) at 90° C. for 10-15 minutes in order to provide a clean surface. The slides were rinsed with water, ethanol and dried with nitrogen and used immediately. Monolayers were prepared by immersing the clean gold slides in a 1-2 mM ethanol solution of the desired compound. For pyridine-decanethiol the immersion time was 6-8 h. Copper bromide and iron bromide were used as the source of Cu(II) and Fe(III) ions in 1 mM solutions in ethanol. Immersion time for both solutions was less than 3 h. Cobalt bromide and cobalt chloride were used in 1 mM solutions in ethanol and acetone with immersion times of 24 h. Subsequent deposition of other organic ligands (bypyridine, pyrene-pyridine, disubstituted pyrene) required 12-30 hours immersion time and was obtained from 1 mM solutions in ethanol or methanol. The films were rinsed with ethanol and dried with nitrogen before changing from one solution to the next one in order to avoid the presence of physically adsorbed molecules on the surface.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06893716B2
出典データセットuspto-grants-2005_05
ORD IDord-576985157445432c996ec0829c610df8
出典メモuspto-grants-2005_05