Polynuclear palladium clusters for catalytic hydrolysis of carbon disulfide and carbonyl sulfide
A carbon disulfide, catalytic hydrolysis technology, applied in the preparation/purification of sulfur, chemical instruments and methods, chemical/physical processes, etc., can solve the problem of low recovery rate, catalytic hydrolysis conversion rate of organic sulfides difficult to reach 100%, very difficult Significant improvement and other problems to achieve the effect of high-efficiency catalytic cycle process
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Embodiment 1
[0067] Embodiment 1: the synthesis of (2,2'-bipyridine) palladium nitrate (1a)
[0068] Synthesis of S1(2,2'-bipyridyl)palladium chloride
[0069] 1.0g (5.64mmol) PdCl 2 Dissolve in 150ml of hot acetonitrile at 60°C and add to a 250ml single-necked bottle. Under electromagnetic stirring, 880.9mg (5.64mmol) of 2,2’-bipyridine was dissolved in a small amount of methanol (3mL) and added dropwise to the reaction flask, immediately forming yellow needle-like crystals, which continued to reflux for 2h. Then it was cooled to room temperature, filtered, washed with a small amount of acetonitrile and acetone, and dried to obtain 1.67 g of the product with a yield of 88.3%.
[0070] Synthesis of S2(2,2'-bipyridyl)palladium nitrate
[0071] 1.67g (5.0mmol) bpyPdCl 2 Suspend in 200ml water, add 1.70g (5.0mmol) AgNO dropwise under electromagnetic stirring 3 A small amount of deionized aqueous solution was reacted at 60°C in the dark for 3h. Let stand for 2 hours, filter, and concentr...
Embodiment 2
[0072] Synthesis of Example 2 (4,4'-dimethyl-2,2'-bipyridyl) palladium nitrate (2a)
[0073] Synthesis of S1(4,4'-dimethyl-2,2'-bipyridyl)palladium chloride
[0074] 1.0g (5.64mmol) PdCl 2 Dissolve in 150ml of acetonitrile at 60°C and add to a 250ml single-necked bottle. Under electromagnetic stirring, 5.6 mmol of 4,4'-dimethyl-2,2'-bipyridine was dissolved in a small amount of methanol (3 mL), and added dropwise to the reaction flask, yellow needle-like crystals were formed immediately, and the reflux was continued for 2 h. Then cool to room temperature, filter, wash with a small amount of acetonitrile and acetone, and dry to obtain the product.
[0075] Step S2 is the same as in Embodiment 1. The product is a yellow powder with a yield of 90%.
Embodiment 3
[0076] The synthesis of embodiment 3 (1,10-phenanthroline) palladium nitrate (3a)
[0077] Synthesis of S1(1,10-phenanthroline)palladium chloride
[0078] 1.0g (5.64mmol) PdCl 2 Dissolve in 150ml of acetonitrile at 60°C and add to a 250ml single-necked bottle. Under electromagnetic stirring, 5.5 mmol of 1,10-phenanthroline was dissolved in a small amount of methanol (3 mL), and added dropwise to the reaction flask, yellow needle-like crystals were formed immediately, and the reflux was continued for 2 h. Then cool to room temperature, filter, wash with a small amount of acetonitrile and acetone, and dry to obtain the product.
[0079] Step S2 is the same as in Embodiment 1. The product is a yellow powder with a yield of 91%.
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