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CAS RN: 864163-80-4 | 产品编码: B4944
(2,2'-Bipyridine)bis[2-(2,4-difluorophenyl)pyridine]iridium(III) Hexafluorophosphate
![(2,2'-Bipyridine)bis[2-(2,4-difluorophenyl)pyridine]iridium(III) Hexafluorophosphate No-Image](/medias/B4944.jpg?context=bWFzdGVyfHJvb3R8NjQzNTd8aW1hZ2UvanBlZ3xhR1F3TDJnNVlTODRPVEl3TXpNd056azNNRGcyTDBJME9UUTBMbXB3Wnd8ZWRmNTU1YWMzMmY4NGQ5MDM2ZDY2ZDFmMDcxMGEzY2E0MGJiZWQ2YjRjNWQ1ZTBhZjE2NjU2NjM3MzNkMDIzMQ)
产品编码 | B4944 |
纯度/分析方法 | >80.0%(HPLC) |
分子式/分子量 | C__3__2H__2__0F__1__0IrN__4P = 873.71 |
外观与形状(20°C) | 固体 |
储存温度 | 室温 (15°C以下阴凉干燥处) |
包装和容器 | 200MG-Glass Bottle with Plastic Insert (查看图片) |
CAS RN | 864163-80-4 |
Reaxys-RN | 20153920 |
PubChem物质ID | 354333555 |
Appearance | Light yellow to Brown powder to crystal |
Purity(HPLC) | min. 80.0 area% |
最大吸收波长 | 500 nm (CH__2Cl__2) |
象形图 |
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信号词 | Warning |
危险性说明 | H315 : Causes skin irritation. H319 : Causes serious eye irritation. |
防范说明 | P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ eye protection/ face protection. P302 + P352 : IF ON SKIN: Wash with plenty of water. P337 + P313 : If eye irritation persists: Get medical advice/ attention. P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P362 + P364 : Take off contaminated clothing and wash it before reuse. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. |
HS编码* | 2843.90-000 |
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Used Chemicals
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- Methyl Pentafluorobenzoate [P1418]
- (2,2'-Bipyridine)bis[2-(2,4-difluorophenyl)pyridine]iridium(III) Hexafluorophosphate (= Ir[(dFppy)2(bpy)]PF6) [B4944]
- Quinuclidine [Q0062]
- Tetrahydrofuran
- Dipotassium Hydrogenphosphate
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Procedure
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To a solution of quinuclidine (22.4 mg, 0.201 mmol, 0.20 eq), Ir[(dFppy)2(bpy)]PF6 (18.0 mg, 0.0165 mmol, 1.7 mol%), K2HPO4 (0.358 g, 2.07 mmol, 2.1 eq) in THF (10 mL) was added methyl pentafluorobenzoate (0.146 mL, 1.00 mmol, 1.0 eq) at rt under N2. The mixture was placed at a distance of 2-3 cm from Blue LED lamp. The orange solution was stirred at rt under visible light irradiation. After 4.5 hours of irradiation, the solvent was removed in vacuo. The residue was diluted with dichloromethane and filtered through a silica gel pad. The filtrate was concentrated and purified by column chromatography (hexane : ethyl acetate on silica gel, hexane : ethyl acetate = 9 : 1 → 20 : 3), giving compound 1 as a colorless oil (125 mg, y. 45%).
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Experimenter’s Comments
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Tetrahydrofuran was degassed with nitrogen for 1 hour before use.
Irradiation of visible light was performed with Kessil A160WE Tuna Blue 40W×2.
The reaction mixture was monitored by 1H NMR, TLC (hexane : ethyl acetate = 10 : 1, Rf = 0.26).
The reaction was performed at rt, however the internal temperature rose up to 40 ˚C due to the insufficient cooling. Neverthelss, the reaction proceeded without any problems.
Analytical Data(Compound 1)
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- 1H NMR (400 MHz, CDCl3); δ 5.27 (t, J = 7.8 Hz, 1H), 4.09 (q, J = 7.3 Hz, 1H), 3.97 (s, 3H), 3.99−3.90 (m, 1H), 2.40−2.31 (m, 1H), 2.24−2.15 (m, 1H), 2.11-2.06 (m, 2H).
13C NMR (101 MHz, CDCl3); δ 160.2, 145.8, 143.4, 124.8, 104.5, 71.7, 69.4, 53.3, 32.4, 27.0.
19F NMR (376.5 MHz, CDCl3); δ −140.34 (d, J = 23 Hz, 2F), −142.95 (d, J = 23 Hz, 2F).
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Lead Reference
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- Direct C-H Multifluoroarylation of Ethers through Hydrogen Atom Transfer Using Photoredox Catalysis
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Other References
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- A Retrosynthetic Approach for Photocatalysis
文章/手册
[TCI应用实例] 由光氧化还原催化剂催化的C(sp3)-H芳基化反应
[产品拾贝] 可用于化学修饰的可见光光氧化还原催化剂
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