901409
[Ir(dF(Me)ppy)2(dtbbpy)]PF6
Sinonimo/i:
Iridium(III) bis[2-(2,4-difluorophenyl)-5-methylpyridine-N,C20]-4,40-di-tert-butyl-2,20-bipyridine hexafluorophosphate
Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Scegli un formato
100 MG
CHF 253.00
Scegli un formato
Cambia visualizzazione
100 MG
CHF 253.00
About This Item
Formula empirica (notazione di Hill):
C42H40F10IrN4P
Numero CAS:
Peso molecolare:
1013.97
Numero MDL:
Codice UNSPSC:
12161600
NACRES:
NA.22
Prodotti consigliati
![(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)
Stato
solid
Livello qualitativo
Impiego in reazioni chimiche
core: iridium
reaction type: Photocatalysis
reagent type: catalyst
Attivazione fotocatalizzatore
450 nm
InChI
XAJPUJWOMJJPNU-UHFFFAOYSA-N
Applicazioni
[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)
Altre note
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
Prodotti correlati
N° Catalogo
Descrizione
Determinazione del prezzo
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Scegli una delle versioni più recenti:
Certificati d'analisi (COA)
Lot/Batch Number
Non trovi la versione di tuo interesse?
Se hai bisogno di una versione specifica, puoi cercare il certificato tramite il numero di lotto.
Possiedi già questo prodotto?
I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.
I clienti hanno visto anche
![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)
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
Correlating electronic structures to electrochemiluminescence of cationic Ir complexes.
Swanick KN, et al.
Royal Society of Chemistry Advances, 43, 19961-19964 (2013)
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
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)
Sébastien Ladouceur et al.
Inorganic chemistry, 50(22), 11514-11526 (2011-10-04)
Herein we report the synthesis of 4-aryl-1-benzyl-1H-1,2,3-triazoles (atl), made via "Click chemistry" and their incorporation as cyclometallating ligands into new heteroleptic iridium(III) complexes containing diimine (N(^)N) ancillary ligands 2,2'-bipyridine (bpy) and 4,4'-di-tert-butyl-2,2'-bipyridine (dtBubpy). Depending on decoration, these complexes emit from
Active Filters
Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..
Contatta l'Assistenza Tecnica.
