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Hydrochloric Acid → Europium 2-thiophenecarboxylate

HRID 1589629
Notes
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Reaction equation

HRID 1589629 reaction equation
[Cl-].[Eu+3:2].[Cl-].[Cl-].[S:5]1[CH:9]=[CH:8][CH:7]=[C:6]1[C:10]([O-:12])=[O:11].[Na+].Cl>O>[S:5]1[CH:9]=[CH:8][CH:7]=[C:6]1[C:10]([O-:12])=[O:11].[Eu+3:2].[S:5]1[CH:9]=[CH:8][CH:7]=[C:6]1[C:10]([O-:12])=[O:11].[S:5]1[CH:9]=[CH:8][CH:7]=[C:6]1[C:10]([O-:12])=[O:11]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 9859933Europium chloride, anhydrous 99.9%HCID 23672340Sodium 2-thenoate

Product 1

HCID 86739360Europium 2-thiophenecarboxylate

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

A sodium 2-thiophenecarboxylate aqueous solution was obtained by dissolving 1.64 g of sodium hydroxide in 300 ml of purified water and then under stirring, adding 5.25 g of 2-thiophenecarboxylic acid (purity 99%; conjugate number=3) in the resultant aqueous solution until thorough solution. Then, a europium chloride aqueous solution obtained by thoroughly dissolving 5.0 g of europium chloride (EuCl3.6H2O; purity 99.99%) in 50 ml of purified water was gradually added while under stirring to the aforementioned sodium 2-thiophenecarboxylate aqueous solution at room temperature. The resultant reaction solution was adjusted to pH 5.0 with 0.1N hydrochloric acid and then stirred thoroughly. Subsequently, the aqueous solution was evaporated to afford europium 2-thiophenecarboxylate ##STR6## The europium 2-thiophenecarboxylate thus obtained was dried in vacuo at 80° to 100° C. for 20 to 24 hours. This salt had its maximum excitation wavelength at about 340 nm and strongly showed the red luminescence peculiar to europium at the main emission wavelength of about 616 nm. The luminescence efficiency was 31%. When it was tested for X-ray powder diffraction and DSC, it showed crystalline diffraction pattern and endothermic peaks.

Workup

  1. additionwas gradually added while
  2. customThe resultant reaction solution
  3. customSubsequently, the aqueous solution was evaporated

Sources & evidence

ORD record
ord-09b4f57d544b4a89b341670b3591f2ba
Source dataset
uspto-grants-1986_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04572803

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes