推薦產品
![(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)
![[Ni(dtbbpy)(H2O)4]Cl2](/deepweb/assets/sigmaaldrich/product/structures/777/629/15c13300-e874-4abd-8bd4-8b2bb4864570/640/15c13300-e874-4abd-8bd4-8b2bb4864570.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)
![[铱 (dF (Me) ppy)] 2 (dtbbpy) ] PF 6](/deepweb/assets/sigmaaldrich/product/structures/150/099/7c2dfa31-39f4-4cca-aee5-86d4a89fea78/640/7c2dfa31-39f4-4cca-aee5-86d4a89fea78.png)
形狀
powder or crystals
反應適用性
core: nickel
reaction type: Cross Couplings
reagent type: catalyst
mp
>300 °C
SMILES 字串
CC(C1=CC(C2=CC(C(C)(C)C)=CC=N2)=NC=C1)(C)C.Cl[Ni]Cl
InChI 密鑰
PCWIKFRTCXESOT-UHFFFAOYSA-L
相關類別
應用
[4,4′-双(1,1-二甲基乙基)-2,2′-联吡啶]二氯化镍(II)作为催化剂已用于：
- 含氧酸的脱羧芳基化。
- 醚的酰化。
- 芳基溴和醇的交叉偶联反应。
相關產品
產品號碼
描述
訂價
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
客戶也查看了
![双[(2-二甲氨基)苯基]胺氯化镍(II) ≥97% (AT)](/deepweb/assets/sigmaaldrich/product/structures/143/670/3d0cc911-c810-4324-914e-85c5c11b7dac/640/3d0cc911-c810-4324-914e-85c5c11b7dac.png)
![[(TMEDA)Ni(o-甲苯基)Cl] 95%](/deepweb/assets/sigmaaldrich/product/structures/236/439/768c916e-994f-47e3-a980-3ca0471317d7/640/768c916e-994f-47e3-a980-3ca0471317d7.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)
![[1,3-双(二苯基膦)丙烷]二氯化镍(II)](/deepweb/assets/sigmaaldrich/product/structures/844/065/af07f787-c6a3-4a6e-a22b-47a933c73978/640/af07f787-c6a3-4a6e-a22b-47a933c73978.png)
Wacharee Harnying et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(17), 4765-4773 (2011-03-23)
The roles of nickel and chromium catalysts in the coupling reaction of vinyl halides and aldehydes, the so-called Nozaki-Hiyama-Kishi (NHK) reaction, have been studied by UV/Vis spectroscopy, electrochemical, and spectroelectrochemical methods. Electrochemical studies revealed that nickel plays the central role
Lingling Chu et al.
Angewandte Chemie (International ed. in English), 54(27), 7929-7933 (2015-05-28)
The direct decarboxylative arylation of α-oxo acids has been achieved by synergistic visible-light-mediated photoredox and nickel catalysis. This method offers rapid entry to aryl and alkyl ketone architectures from simple α-oxo acid precursors via an acyl radical intermediate. Significant substrate
Photocatalytic α-Acylation of Ethers
Sun Z, et al.
Organic Letters, 19, 3727-3730 (2017)
Martins S Oderinde et al.
The Journal of organic chemistry, 80(15), 7642-7651 (2015-07-04)
In order to achieve reproducibility during iridium-photoredox and nickel dual-catalyzed sp(3)-sp(2) carbon-carbon bond-forming reactions, we investigated the role that molecular oxygen (O2), solvent and light-source (CF lamp or blue LED) play in a variety of Ir-photoredox mediated transformations. The presence
Aryl Ketones as Single-Electron-Transfer Photoredox Catalysts in Nickel-Catalyzed the Homocoupling of Aryl Halides
Masuda Y, et al.
European Journal of Organic Chemistry, 5822-5825 (2016)
我們的科學家團隊在所有研究領域都有豐富的經驗，包括生命科學、材料科學、化學合成、色譜、分析等.
聯絡技術服務