|
ChemicalBook Optimization Suppliers |
| 名前: |
LaaJoo Gold |
| 電話番号: |
021-60702684 18516024827 |
| 電子メール: |
huang.jiayi@sinocompound.com |
|
| | テトラキス(アセトニトリル)銅(I)ヘキサフルオロホスファート 製品概要 |
| 化学名: | テトラキス(アセトニトリル)銅(I)ヘキサフルオロホスファート | | 英語化学名: | TETRAKIS(ACETONITRILE)COPPER (I) HEXAFLUOROPHOSPHATE | | 别名: | tetrakis(acetonitrile)copper(I) hexa-fluorophosph;Tetrakis(acetonitrle)copper(I) Hexafluorophosphate;Tetrakis(acetonitrile)copper [Ⅰ] hexafluorophosphate;Tetrakis(acetonitrile)copper(I)hexafluorophosphate,98+%;tetrakis(acetonitrile)copper hexa-fluorophosph;Tetrakis(acetonitrile)copper [] hexafluorophosphate;Tetrakis(acetonitrile)copper(I) hexafluorophosphate 97%;Copper(I) tetrakis(acetonitrile) hexafluorophosphate | | CAS番号: | 64443-05-6 | | 分子式: | C8H12CuF6N4P | | 分子量: | 372.72 | | EINECS: | | | カテゴリ情報: | organometallic complex;Cu;Copper;Catalysis and Inorganic Chemistry;Chemical Synthesis | | Mol File: | 64443-05-6.mol |  |
| | テトラキス(アセトニトリル)銅(I)ヘキサフルオロホスファート 物理性質 |
| 融点 | 160 °C (dec.) (lit.) | | 貯蔵温度 | Inert atmosphere,Store in freezer, under -20°C | | 外見 | solid | | 色 | white to light blue | | Sensitive | air sensitive, moisture sensitive |
| | テトラキス(アセトニトリル)銅(I)ヘキサフルオロホスファート Usage And Synthesis |
| 外観 | 白色～ほとんど白色粉末～結晶 | | 使用 | Tetrakis(acetonitrile)copper(I) hexafluorophosphate can be employed as a catalyst for the synthesis of triazolo[1,2-a]indazole-1,3,8-trione and 2H-indazolo[2,1-b]phthalazine-trione derivatives by the reaction of aryl aldehydes, dimedone and urazole or phthalhydrazide, respectively.
It can also be used as a copper precursor:
- For the formation of Cu2S/CdS nanorod junctions by cationic exchange process.
- To synthesize monometallic copper macrocyclic biquinazoline ligand [Cu(Mabiq)].
- To prepare the cuprous complex [Cu(2-iQBO)(POP)]PF6]; where 2-iQBO=2-(1′-isoquinolyl)benzoxazole and POP=bis[2-(diphenylphosphino)phenyl]ether, which can form luminescent pseudo-polymorphs.
- For the synthesis of [Cu(NHC)2]PF6 complexes [(NHC = N-heterocyclic carbene] which can be further used in the hydrosilylation of carbonyl compounds.
|
|