SU464596A1 - Method for preparing platinum nitroacetate - Google Patents
Method for preparing platinum nitroacetateInfo
- Publication number
- SU464596A1 SU464596A1 SU1902789A SU1902789A SU464596A1 SU 464596 A1 SU464596 A1 SU 464596A1 SU 1902789 A SU1902789 A SU 1902789A SU 1902789 A SU1902789 A SU 1902789A SU 464596 A1 SU464596 A1 SU 464596A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- nitroacetate
- preparing platinum
- platinum
- preparing
- potassium
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
(54) СПОСОБ ПОЛУЧЕНИЯ НИТРОАЦЕТАТА ПЛАТИНЫ(54) METHOD FOR PRODUCING PLATINUM NITROACETATE
форм, диметилформамид, ацетон) с образованием кнтенсивно окрашенных растворов. При нагревании с концентрированной сол ной кислотой нитроацетат платины раствор етс с образованием желтого раствора, из которого Пр-и добавлении хлористого кали выдел етс желтый Ооадок хлороплатината кали . Соединение весьма реа|КционноспособНо - легко реагирует с различными органическими и неорганическими аминамИ, образу соответствующие шродукты присоединени .forms, dimethylformamide, acetone) with the formation of intensely colored solutions. When heated with concentrated hydrochloric acid, platinum nitroacetate dissolves to form a yellow solution, from which Pr-and the addition of potassium chloride evolves yellow Potassium chloroplatinate ice. The compound is very reactive; it reacts readily with various organic and inorganic amines to form the corresponding addition products.
Предмет изобретени Subject invention
Способ получени нитроацетата платины, отличающийс тем, что, тетранитроплатоат кали подвергают взаимодействию с уксусной кислотой при нагревании, например до килени реакционной смеси, с последующи.м добавлением спирта и нагреванием смеси, например при 80° iC, до по влени буро-красной окраски и выделением целевого продукта известными Приемами.A method of producing platinum nitroacetate, characterized in that potassium tetranitroplate is reacted with acetic acid when heated, for example, until the reaction mixture is kiln, followed by adding alcohol and heating the mixture, for example, at 80 ° C, and the selection of the target product known techniques.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU1902789A SU464596A1 (en) | 1973-03-30 | 1973-03-30 | Method for preparing platinum nitroacetate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU1902789A SU464596A1 (en) | 1973-03-30 | 1973-03-30 | Method for preparing platinum nitroacetate |
Publications (1)
Publication Number | Publication Date |
---|---|
SU464596A1 true SU464596A1 (en) | 1975-03-25 |
Family
ID=20548130
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU1902789A SU464596A1 (en) | 1973-03-30 | 1973-03-30 | Method for preparing platinum nitroacetate |
Country Status (1)
Country | Link |
---|---|
SU (1) | SU464596A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2565423C1 (en) * | 2014-11-06 | 2015-10-20 | Федеральное государственное бюджетное учреждение науки Институт общей и неорганической химии им. Н.С. Курнакова Российской академии наук (ИОНХ РАН) | Platinum oxoacetate compounds for producing heterogeneous catalysts |
-
1973
- 1973-03-30 SU SU1902789A patent/SU464596A1/en active
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2565423C1 (en) * | 2014-11-06 | 2015-10-20 | Федеральное государственное бюджетное учреждение науки Институт общей и неорганической химии им. Н.С. Курнакова Российской академии наук (ИОНХ РАН) | Platinum oxoacetate compounds for producing heterogeneous catalysts |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
SU464596A1 (en) | Method for preparing platinum nitroacetate | |
SU549084A3 (en) | The method of obtaining piperazine derivatives or their salts | |
GB1436810A (en) | Preparation of iostoic anhydride and anthranilic acid | |
KR830009077A (en) | Method for preparing furan derivative | |
SU507042A1 (en) | Method of producing polybenzylpyridinium chloride | |
SU1130562A1 (en) | Process for preparing naphthalene thiols | |
SU427009A1 (en) | METHOD OF PREPARING TETRA- OR DECAHYDRO-CHIOLYL-N-METYL-2-TIOBEHNTHIIAZOLA | |
GB1363758A (en) | Process for the production of 1,2,4-oxa-diazoles and novel 1,2,4- oxadiazoles | |
SU502896A1 (en) | The method of obtaining bis (priortilsilyl) sulfates | |
SU374317A1 (en) | METHOD OF OBTAINING DISYLOXANE ISOCYANATES | |
GB1445674A (en) | Cyclohexanediol derivative and process for preparing the same | |
SU833959A1 (en) | Method of preparing 2-amino-6-choloro-3,4,5-tricyanopyridine | |
SU505644A1 (en) | The method of obtaining pyronilenebispirilievoy salt | |
SU434080A1 (en) | WAY OF OBTAINING 2-ALKIL-4-HALOID-2,4-DINITRO-1-ALKANOLOVV PT BFPMP ^^ tft ^ "^ 'f ^^ H-ujSA and" i-L: -:' '^ ;; | |
SU461925A1 (en) | The method of obtaining 3,3,8,8-tetramethyl 2,7-dioxaspiro (4,4) nonane-1,6 dione | |
JPS55122757A (en) | Production of thio-di-phthalic acid or anhydride | |
SU405895A1 (en) | METHOD OF OBTAINING IMIDAZO DERIVATIVES | |
SU374312A1 (en) | METHOD OF OBTAINING 3-OXISULFOLANE-4-SULPHONATE | |
SU455972A1 (en) | The method of obtaining dithioxy tetramethylene diphosphine | |
SU436819A1 (en) | Method for producing chloro derivatives of 2-aminoanthraquinone | |
US2802835A (en) | 3-benzyloxyphthalide | |
GB828746A (en) | Improved process for the preparation of organic phosphorus compounds | |
SU414262A1 (en) | ||
SU432143A1 (en) | METHOD OF OBTAINING TETRACHLOROHINOLIN | |
SU424857A1 (en) | METHOD OF OBTAINING pg ^ '- DISTILPHYME DYALYLIDE OF BUTYLMALONIC ACID |