hexafluorophosphate [5,10,15,20-tetrakis(3,5-di-tert-butylphenyl)porphyrinato]aurate(III)

Base Information

Chemical Name:hexafluorophosphate [5,10,15,20-tetrakis(3,5-di-tert-butylphenyl)porphyrinato]aurate(III)
CAS No.:136316-46-6
Molecular Formula:C₇₆H₉₂AuN₄*F₆P
Molecular Weight:1403.52
Hs Code.:

Synonyms:hexafluorophosphate [5,10,15,20-tetrakis(3,5-di-tert-butylphenyl)porphyrinato]aurate(III)

Suppliers and Price of hexafluorophosphate [5,10,15,20-tetrakis(3,5-di-tert-butylphenyl)porphyrinato]aurate(III)

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of hexafluorophosphate [5,10,15,20-tetrakis(3,5-di-tert-butylphenyl)porphyrinato]aurate(III)

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of hexafluorophosphate [5,10,15,20-tetrakis(3,5-di-tert-butylphenyl)porphyrinato]aurate(III)

There total 1 articles about hexafluorophosphate [5,10,15,20-tetrakis(3,5-di-tert-butylphenyl)porphyrinato]aurate(III) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 85.0%

: 17084-13-8
potassium hexafluorophosphate

: 13682-61-6
potassium tetrachloroaurate(III)

: 5,10,15,20-tetrakis[(3,5-di-tert-butylphenyl)]porphyrin

: 136316-46-6
hexafluorophosphate [5,10,15,20-tetrakis(3,5-di-tert-butylphenyl)porphyrinato]aurate(III)

Guidance literature:: With sodium acetate; In dichloromethane; acetic acid; soln. porphyrin, K(AuCl4), and AcONa in CH2Cl-AcOH heated at reflux for 24 h, diluted with CHCl3, washed with water, aq. Na2CO3, and water, dried over Na2SO4, filtered, evapd., dissolved in CH2Cl2, aq. soln. KPF6 wasadded and stirred for 24 h; react. mixt. was diluted with CH2Cl2, washed with water, and dried over Na2SO4, soln. was evapd. in vacuo, residue was chromed. on silica (CHCl3-MeOH 50:1); elem. anal.;
DOI:10.1021/ic035070w