SU386656A1 - CATALYST FOR HYDRATION AND / OR ISOMERIZATION OF UNLIMITED ORGANIC COMPOUNDS - Google Patents

CATALYST FOR HYDRATION AND / OR ISOMERIZATION OF UNLIMITED ORGANIC COMPOUNDS

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Publication number
SU386656A1
SU386656A1 SU1663320A SU1663320A SU386656A1 SU 386656 A1 SU386656 A1 SU 386656A1 SU 1663320 A SU1663320 A SU 1663320A SU 1663320 A SU1663320 A SU 1663320A SU 386656 A1 SU386656 A1 SU 386656A1
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USSR - Soviet Union
Prior art keywords
catalyst
organic compounds
isomerization
hydration
unlimited
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SU1663320A
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Russian (ru)
Inventor
изобретени Авторы
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Л. Фрейдлин, Н. М. Назарова , Ю. А. Копытцев Институт органической химии Н. Д. Зелинского
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Application filed by Л. Фрейдлин, Н. М. Назарова , Ю. А. Копытцев Институт органической химии Н. Д. Зелинского filed Critical Л. Фрейдлин, Н. М. Назарова , Ю. А. Копытцев Институт органической химии Н. Д. Зелинского
Priority to SU1663320A priority Critical patent/SU386656A1/en
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Publication of SU386656A1 publication Critical patent/SU386656A1/en

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Description

;ii Изобретение относитс  к производству катализаторов , в частности к катализатору на основе комплексов металлов платиновой группы дл  гидрировани  и/или изомеризации непредельных органических соединений.; ii The invention relates to the production of catalysts, in particular to a catalyst based on platinum-group metal complexes for the hydrogenation and / or isomerization of unsaturated organic compounds.

Известен катализатор, например, дл  гидрировани  непредельных органических соединений , представл ющий СОбой комплексное соединение металла платиновой группы, лигандом которого  вл етс  соединение, склонное к бензоидно-хиноидной мезомерии, например флуоросцеин.A catalyst is known, for example, for the hydrogenation of unsaturated organic compounds, which is a SOBY complex compound of a platinum group metal whose ligand is a compound prone to benzoid-quinoid mesomerism, such as fluorocein.

Однако этот катализатор не обладает до Ётаточно высокой активностью.However, this catalyst does not have high activity.

Предлагаетс  в качестве катализатора примен ть диалкилсульфоксидные комплексы металлов платиновой группы в восстановленной форме.It is proposed to use dialkyl sulfoxide complexes of platinum group metals in reduced form as a catalyst.

Этот катализатор обладает высокой аКтивНоетью не только при гидрировании, но и при изомеризации непредельных органических соединений .This catalyst has a high level of activity not only in hydrogenation, but also in the isomerization of unsaturated organic compounds.

Элементарный состав комплесного диметилсульфоксидного катализатора, например палладиевого, следующий:The elemental composition of the complex dimethyl sulfoxide catalyst, for example, palladium, is as follows:

ВМС ОNavy O

DTICODTICO

где п - равно приблизительно 6.where n is about 6.

В ИК-спектре этого комплекса наблюдаетс  очень интенсивна  полоса поглощени  валентных колебаний S-О около 1100 см, котора  сдвинута в область более высоких частот по сравнению со свободным диметилсульфоксидом (v5-0 1000 еж-). Это свидетельствует о том, что молекула диметилсульфоксида координирована на атоме паллади  через атом серы.In the IR spectrum of this complex, a very intense absorption band of S-O oscillations around 1100 cm is observed, which is shifted to higher frequencies compared to free dimethyl sulfoxide (v5-0 1000 hedgehog). This suggests that the dimethyl sulfoxide molecule is coordinated on the palladium atom through the sulfur atom.

Пример 1. Деметилсульфоксидные комплексы готов т по следующей методике: на пример, 1 г Pd Cl2 растирают с 2 г диметйлсульфоксида . Образующийс  желтый кристаллический осадок фильтруют и промывают этиловым спиртом,Example 1. Demethylsulfoxide complexes are prepared according to the following procedure: for example, 1 g of Pd Cl2 is triturated with 2 g of dimethyl sulfoxide. The resulting yellow crystalline precipitate is filtered and washed with ethyl alcohol,

Пример 2. 0,03 г диметилсульфоксйдНбго комплекса паллади  или рутени  раствор ют в 20 мл диметилсульфоксида и в течение 5-30 мин обрабатывают 0,1 г гидрида лити  в инертной атмосфере (азот или аргон) при 5-40°С. Раствор катализатора хран т в атмосфере инертного газа.Example 2. 0.03 g of dimethylsulfoxide-dyed palladium or ruthenium complex is dissolved in 20 ml of dimethyl sulfoxide and treated with 5 g of lithium hydride in an inert atmosphere (nitrogen or argon) for 5-30 minutes at 5-40 ° C. The catalyst solution is stored in an inert gas atmosphere.

При м е р 3. 0,03 г диметилсульфоксидного комплекса роди  или платины раствор ют в 30 мл смеси спирта с диметилсульфоксидом (1:1). Раствор в течение 15-20 мин обрабатывают 1,0 г гидразина при 10-40°С в инерт-ной атмосфере. iPacTBop катализатора хран т в атмосфере инертного газа.Example 3. 0.03 g of dimethyl sulfoxide complex of rhodium or platinum is dissolved in 30 ml of a mixture of alcohol and dimethyl sulfoxide (1: 1). Within 15-20 minutes, the solution is treated with 1.0 g of hydrazine at 10-40 ° C in an inert atmosphere. iPacTBop catalysts are stored in an inert gas atmosphere.

П р и м е р 4. 0,05 г диметилсульфоксндного комплекса ириди  или роди  раствор ют в 30 мл N-метилпирролидона, и в течение 10-EXAMPLE 4: 0.05 g of the dimethyl sulfox complex of the iridium or rhodium complex is dissolved in 30 ml of N-methylpyrrolidone and within 10 to

SU1663320A 1971-05-28 1971-05-28 CATALYST FOR HYDRATION AND / OR ISOMERIZATION OF UNLIMITED ORGANIC COMPOUNDS SU386656A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU1663320A SU386656A1 (en) 1971-05-28 1971-05-28 CATALYST FOR HYDRATION AND / OR ISOMERIZATION OF UNLIMITED ORGANIC COMPOUNDS

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU1663320A SU386656A1 (en) 1971-05-28 1971-05-28 CATALYST FOR HYDRATION AND / OR ISOMERIZATION OF UNLIMITED ORGANIC COMPOUNDS

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SU386656A1 true SU386656A1 (en) 1973-06-21

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