Rhodium (II) Acetate Dimer CAS 15956-28-2 Rh 43.0 ~ 46.6%

Takaitaccen Bayani:

Sunan Sinadari: Rhodium (II) Acetate Dimer

Saukewa: 15956-28-2

Rh: 46.5%

Tsafta: ≥99.95% Tushen Karfe

Bayyanar: Green Foda

Kyakkyawan inganci, Samar da Kasuwanci

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Abubuwan Sinadarai:

Sunan Sinadari Rhodium (II) Acetate Dimer
Makamantu Dirhodium (II) Tetraacetate;Tetrakis (acetato) dirhodium (II);Tetrakis [micron-(acetato-O: O')] dirhodium;Tetrakis (μ-acetato) di-rhodium (Rh-Rh);Tetrakis[μ- (acetato-O: O')] di-Rhodium(Rh-Rh)
Lambar CAS 15956-28-2
Lambar CAT Saukewa: RF2727
Matsayin Hannun jari A cikin Hannun jari, Ma'aunin samarwa Har zuwa Ton
Tsarin kwayoyin halitta Saukewa: C8H12O8Rh2
Nauyin Kwayoyin Halitta 441.99
Matsayin narkewa 205 ℃
Yawan yawa 1.126 g/cm 3
Kwanciyar hankali Hygroscopic
Solubility Mai narkewa a Magani Mai Ruwa Kamar Ruwa.Dan Soluble a cikin Ethanol
Alamar Ruifu Chemical

Ƙayyadaddun bayanai:

Abu Ƙayyadaddun bayanai
Bayyanar Koren Foda
Rh (Binciken Gravimetric) 43.0 ~ 46.6%
ICP Ya Tabbatar da Tabbatar da Abubuwan Rhodium
Infrared Spectrum Yayi daidai da Tsarin
X-ray Diffraction Yayi daidai da Tsarin
Matsayin Gwaji Matsayin Kasuwanci

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Aikace-aikace:

Rhodium (II) Acetate Dimer (CAS: 15956-28-2), CH Bond Activation Reaction, Transition Metal Catalysts, Binuclear Rhodium Complexes Tasiri don Ƙirƙirar Ƙarami da Matsakaici-zobe.Rhodium (II) Acetate Dimer yana da tasiri mai tasiri don samar da ylide kuma yana haifar da cyclopropanation na alkenes, oxidation na alcohols, halayen cyclization da suka shafi -diazo carbonyl kungiyoyin, sakawa cikin CH da XH shaidu (XH shine NH ko SH ko OH) .Ƙarin amsawa da amfani a bambance ribonucleosides da deoxynucleosides.Hakanan ana amfani dashi a cikin aikin fullerenes cikin polymers.Ingantacciyar mai haɓakawa don canja wurin hydrogen daga 2-propanol zuwa cyclohexanone da sauran mahadi marasa ƙarfi.Mai haɓakawa don sakawa cikin haɗin CH da XH.Mai kara kuzari ga tsarar Ylide.Doyle Kirmse Reaction na Allylic Sulfides tare da Diazoalkane.Claisen sake tsarawa.Epoxides daga aldehydes.Maganar aziridines daga allylic N-tosyloxycarbamates.Rh/NHC catalyzed kai tsaye intermolecular arylation na CH bond.Chiral Bronsted acid-Rh ya haifar da halayen sassa uku na mahadi na diazo tare da barasa da imines.Rh-catalyzed cyclopropenations na ynamides.Tandem asymmetric aza-Darzens/maganin buɗe ido.

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