Skip to Content
Merck
CN

747769

[Ir(dtbbpy)(ppy)2]PF6

powder

Synonym(s):

[Ir(dtbbpy)(ppy)2][PF6], Ir Photocatalyst, [4,4′-Bis(1,1-dimethylethyl)-2,2′-bipyridine-N1,N1′]bis[2-(2-pyridinyl-N)phenyl-C]iridium(III) hexafluorophosphate

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):
C40H40F6IrN4P
CAS Number:
Molecular Weight:
913.95
MDL number:
UNSPSC Code:
12161600
NACRES:
NA.22
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


Product Name

[Ir(dtbbpy)(ppy)2]PF6,

form

powder

Quality Level

reaction suitability

core: iridium, reaction type: Photocatalysis, reagent type: catalyst

photocatalyst activation

455 nm

storage temp.

2-8°C

SMILES string

CC(C1=CC=[N]([Ir]2([N]3=CC=C(C=C34)C(C)(C)C)([N]5=CC=CC=C5C6=CC=CC=C62)(C7=CC=CC=C78)[N]9=C8C=CC=C9)C4=C1)(C)C.FP(F)(F)(F)(F)F

InChI

1S/C18H24N2.2C11H8N.F6P.Ir/c1-17(2,3)13-7-9-19-15(11-13)16-12-14(8-10-20-16)18(4,5)6;2*1-2-6-10(7-3-1)11-8-4-5-9-12-11;1-7(2,3,4,5)6;/h7-12H,1-6H3;2*1-6,8-9H;;

InChI key

DZARMRZNOUWGQE-UHFFFAOYSA-N

Application

[Ir(dtbbpy)(ppy)2]PF6 is an iridium-based photocatalyst which is used to drive various photochemical reactions such as:
  • Coupling of N-arylamines and nitroalkanes via an oxidative aza-Henry reaction.
  • Atom transfer radical addition (ATRA) of haloalkanes to alkenes and alkynes.
  • Conversion of 2-bromoanilides to the corresponding 3,3-disubstituted oxindoles.
  • Aryl-alkyl C−C reductive cross-coupling reactions.
Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)


Storage Class

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.

Visit the Document Library


Related Content

Explore reliable, premium grade catalysis materials for your pharma or industrial project. Specialty chemicals and formulations are available in bulk quantities and volumes from a few grams to multi-metric tons with complete documentation to simplify your leap from development to commercialization.

Research in the Stephenson lab focuses upon the development of new chemical methods which enable the activation of chemical bonds under mild reaction conditions.


Synthesis of oxindoles via visible light photoredox catalysis.
Ju, Xuhui et al.
Organic & Biomolecular Chemistry, 10(3), 498-501 (2012)
Visible light-mediated atom transfer radical addition via oxidative and reductive quenching of photocatalysts.
Wallentin, Carl-Johan et al.
Journal of the American Chemical Society, 134(21), 8875-8884 (2012)
Visible-light photoredox catalysis: Aza-Henry reactions via C- H functionalization.
Condie, Allison G et al.
Journal of the American Chemical Society, 132(5), 1464-1465 (2010)



Global Trade Item Number

SKUGTIN
747769-100MG04061832891774
747769-50MG04061833241165