901409
[Ir(dF(Me)ppy)2(dtbbpy)]PF6
Synonym(s):
Iridium(III) bis[2-(2,4-difluorophenyl)-5-methylpyridine-N,C20]-4,40-di-tert-butyl-2,20-bipyridine hexafluorophosphate
Sign Into View Organizational & Contract Pricing
All Photos(2)
Select a Size
Change View
100 MG
CHF 253.00
About This Item
Empirical Formula (Hill Notation):
C42H40F10IrN4P
CAS Number:
Molecular Weight:
1013.97
MDL number:
UNSPSC Code:
12161600
NACRES:
NA.22
Recommended Products
![(Ir[dF(CF3)ppy]2(dtbpy))PF6](/deepweb/assets/sigmaaldrich/product/structures/982/913/02dd8ddd-6deb-40a0-ab9b-07b18f1abb09/640/02dd8ddd-6deb-40a0-ab9b-07b18f1abb09.png)
![[Ir{dFCF3ppy}2(bpy)]PF6](/deepweb/assets/sigmaaldrich/product/structures/180/924/79119ac4-7d62-429d-b23d-a14c012c6050/640/79119ac4-7d62-429d-b23d-a14c012c6050.png)
![[Ir(dtbbpy)(ppy)2]PF6](/deepweb/assets/sigmaaldrich/product/structures/158/329/2544d673-d267-4aa1-8f46-2652aad4bfa0/640/2544d673-d267-4aa1-8f46-2652aad4bfa0.png)
![[Ir(dFCF3ppy)2-(5,5’-dCF3bpy)]PF6 ≥95%](/deepweb/assets/sigmaaldrich/product/structures/422/901/e00f3148-fb86-4f94-9e79-21d064c3f327/640/e00f3148-fb86-4f94-9e79-21d064c3f327.png)
![Ir[dFFppy]2-(4,4′-dCF3bpy)PF6 ≥95%](/deepweb/assets/sigmaaldrich/product/structures/816/772/b116c17c-e6b2-4c95-be64-45a5a851d823/640/b116c17c-e6b2-4c95-be64-45a5a851d823.png)
![[4,4′-Bis(1,1-dimethylethyl)-2,2′-bipyridine] nickel (II) dichloride](/deepweb/assets/sigmaaldrich/product/structures/471/091/6faa29b1-bf8a-4d87-90b2-4cc55e082620/640/6faa29b1-bf8a-4d87-90b2-4cc55e082620.png)
![[Ir(p-F(Me)ppy)2-(4,4′-dtbbpy)]PF6 ≥95%](/deepweb/assets/sigmaaldrich/product/structures/231/079/a5445824-9d4b-4c84-9c5f-f3acbcc75fd4/640/a5445824-9d4b-4c84-9c5f-f3acbcc75fd4.png)
form
solid
Quality Level
reaction suitability
core: iridium
reaction type: Photocatalysis
reagent type: catalyst
photocatalyst activation
450 nm
Related Categories
Application
[Ir(dF(Me)ppy)2(dtbbpy)]PF6 is a photocatalyst readily facilitates hydroamination of olefins as well as the decarboxylative arylation and vinylation of carboxylic acids via metallaphotoredox catalysis.
Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)
Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)
Other Notes
Catalytic intermolecular hydroaminations of unactivated olefins with secondary alkyl amines
Merging photoredox and nickel catalysis: Decarboxylative cross-coupling of carboxylic acids with vinyl halides
Enhanced luminescent iridium(III) complexes bearing aryltriazole cyclometallated ligands
Site-Selective and Stereoselective C-H Alkylations of Carbohydrates via Combined Diarylborinic Acid and Photoredox Catalysis
Merging photoredox and nickel catalysis: Decarboxylative cross-coupling of carboxylic acids with vinyl halides
Enhanced luminescent iridium(III) complexes bearing aryltriazole cyclometallated ligands
Site-Selective and Stereoselective C-H Alkylations of Carbohydrates via Combined Diarylborinic Acid and Photoredox Catalysis
related product
Product No.
Description
Pricing
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Choose from one of the most recent versions:
Certificates of Analysis (COA)
Lot/Batch Number
Don't see the Right Version?
If you require a particular version, you can look up a specific certificate by the Lot or Batch number.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
![Ir[dF(t-Bu)-ppy]3](/deepweb/assets/sigmaaldrich/product/structures/254/294/d0fb19e5-05b2-4c1b-990b-a99fa60b3e73/640/d0fb19e5-05b2-4c1b-990b-a99fa60b3e73.png)
![Tris[2-phenylpyridinato-C2,N]iridium(III) 97%](/deepweb/assets/sigmaaldrich/product/structures/167/234/658d0b76-d31d-4fd5-8041-e04e207227c9/640/658d0b76-d31d-4fd5-8041-e04e207227c9.png)
Correlating electronic structures to electrochemiluminescence of cationic Ir complexes.
Swanick KN, et al.
Royal Society of Chemistry Advances, 43, 19961-19964 (2013)
Strongly Blue Luminescent Cationic Iridium(III) Complexes with an Electron-Rich Ancillary Ligand: Evaluation of Their Optoelectronic and Electrochemiluminescence Properties.
Ladouceur S, et al.
European Journal of Inorganic Chemistry, 2013(30), 5329-5343 (2013)
Victoria Dimakos et al.
Journal of the American Chemical Society, 141(13), 5149-5153 (2019-03-23)
Diphenylborinic acid serves as a cocatalyst for site- and stereoselective C-H alkylation reactions of carbohydrates under photoredox conditions using quinuclidine as the hydrogen atom transfer mediator. Products arising from selective abstraction of the equatorial hydrogens of cis-1,2-diol moieties, followed by
Andrew J Musacchio et al.
Science (New York, N.Y.), 355(6326), 727-730 (2017-02-18)
The intermolecular hydroamination of unactivated alkenes with simple dialkyl amines remains an unsolved problem in organic synthesis. We report a catalytic protocol for efficient additions of cyclic and acyclic secondary alkyl amines to a wide range of alkyl olefins with
Adam Noble et al.
Journal of the American Chemical Society, 137(2), 624-627 (2014-12-19)
Decarboxylative cross-coupling of alkyl carboxylic acids with vinyl halides has been accomplished through the synergistic merger of photoredox and nickel catalysis. This new methodology has been successfully applied to a variety of α-oxy and α-amino acids, as well as simple
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service
