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Fecl2.6h2o

Manufactured by Merck Group
Sourced in United States

FeCl2.6H2O is a chemical compound that consists of ferrous chloride and six water molecules. It is a crystalline solid that is typically used as a laboratory reagent and in various industrial applications. The core function of FeCl2.6H2O is to provide a source of ferrous (Fe2+) ions.

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3 protocols using fecl2.6h2o

1

Metal Chloride Synthesis and Purification

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FeCl3·6H2O, FeCl2·6H2O, and other chemicals were purchased from Sigma Aldrich (Sigma-Aldrich, St. Louis, MA, USA) unless noted otherwise. Stock solutions were prepared with ACS water. pH value and conductivity were measured using an inoLab Level 3 (Wissenschaftlich-Technische Werkstatten GmbH, Weilheim, Germany). Deionized water underwent demineralization by reverse osmosis using an Aqua Osmotic 02 (Aqua Osmotic, Tisnov, Czech Republic) and was subsequently purified using a Millipore RG (MiliQ water, 18 M Ω, Millipore Corp., Billerica, MA, USA). Deionized water was used for rinsing, washing, and buffer preparation.
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2

Synthesis of Metal-Organic Frameworks

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EXAMPLE 1

Chemicals and Materials

All reagents were used as purchased without further purification. 1,3,5-benzene tricarboxylic acid (BTC), Cu(NO3)2.3H2O, Co(NO3)2.6H2O, Ni(NO3)2.6H2O, Zn(NO3)2.6H2O, FeCl2.6H2O, N,N-dimethylformamide (DMF) and ethanol were obtained from Sigma-Aldrich. Acetonitrile was obtained from Sigma-Aldrich. Toluene, cyclohexane and methylcyclohexane were used as purchased from Sigma-Aldrich. New 10 mL and 20 mL kimble scintillation vials were used for the synthesis of various metal organic frameworks (MOFs).

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3

Synthesis of Metal-Organic Frameworks

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EXAMPLE 1

Chemicals and Materials

All reagents were used as purchased without further purification. 1,3,5-benzene tricarboxylic acid (BTC), Cu(NO3)2.3H2O, Co(NO3)2.6H2O, Ni(NO3)2.6H2O, Zn(NO3)2.6H2O, FeCl2.6H2O, N,N-dimethylformamide (DMF) and ethanol were obtained from Sigma-Aldrich. Acetonitrile was obtained from Sigma-Aldrich. Toluene, cyclohexane and methylcyclohexane were used as purchased from Sigma-Aldrich. New 10 mL and 20 mL kimble scintillation vials were used for the synthesis of various metal organic frameworks (MOFs).

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