905100
Ir(p-tBu-ppy)3
powder
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A propos de cet article
Nom du produit
Ir(p-tBu-ppy)3,
form
powder
reaction suitability
reaction type: Photocatalysis, reagent type: catalyst
SMILES string
[Ir](c5c(ccc(c5)C(C)(C)C)c6ncccc6)(c3c(ccc(c3)C(C)(C)C)c4ncccc4)c1c(ccc(c1)C(C)(C)C)c2ncccc2
InChI
1S/3C15H16N.Ir/c3*1-15(2,3)13-9-7-12(8-10-13)14-6-4-5-11-16-14;/h3*4-7,9-11H,1-3H3;
InChI key
HVSYDKXCADBJCU-UHFFFAOYSA-N
Application
Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)
Other Notes
Photocatalytic Generation of 2-Azolyl Radicals: Intermediates for the Azolylation of Arenes and Heteroarenes via C–H Functionalization
Visible-Light Photocatalytic Decarboxylation of α,β-Unsaturated Carboxylic Acids: Facile Access to Stereoselective Difluoromethylated Styrenes in Batch and Flow
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Contenu apparenté
Organofluorine chemistry is an essential part of drug discovery programs as well as agrochemical programs and even plays a major role in materials chemistry. Despite the undeniable importance of fluorinated organic molecules, our ability to synthesize these substrates is lacking - though arguably it is better than that of Nature. Consequently, methods that allow facile access to fluorinated molecules are important especially when they provide unique access to fluorinated chemical space.