推荐产品
品質等級
化驗
99%
形狀
liquid
反應適用性
reagent type: ligand
reaction type: Arylations
折射率
n20/D 1.456 (lit.)
bp
127-128 °C (lit.)
密度
0.802 g/mL at 20 °C (lit.)
官能基
phosphine
SMILES 字串
CCP(CC)CC
InChI
1S/C6H15P/c1-4-7(5-2)6-3/h4-6H2,1-3H3
InChI 密鑰
RXJKFRMDXUJTEX-UHFFFAOYSA-N
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應用
Triethylphosphine is generally used as a ligand in the organometallic chemistry. It can be used in:
- Synthesis of the tetrahedrally coordinated L3Fe-Nx complex with a terminal nitride group.
- Synthesis of (PEt3)2Ni(η2-C14H10), a source of the reactive Ni(PEt3)2 moiety.
- Synthesis of dinuclear rhodium complexes with triethyllphosphane bridges.
其他說明
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訊號詞
Danger
危險聲明
危險分類
Eye Dam. 1 - Pyr. Liq. 1 - Skin Corr. 1B
儲存類別代碼
4.2 - Pyrophoric and self-heating hazardous materials
水污染物質分類（WGK）
WGK 3
個人防護裝備
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
A Tetrahedrally Coordinated L3Fe? N x Platform that Accommodates Terminal Nitride (FeIV? N) and Dinitrogen (FeI? N2? FeI) Ligands.
Betley T A and Peters J C
Journal of the American Chemical Society, 126(20), 6252-6254 (2004)
Unexpected Intermediates and Products in the C? F Bond Activation of Tetrafluorobenzenes with a Bis (triethylphosphine) Nickel Synthon: Direct Evidence of a Rapid and Reversible C? H Bond Activation by Ni (0).
Johnson S A, et al.
Journal of the American Chemical Society, 130(51), 17278-17280 (2008)
Breaking the Rule: Synthesis and Molecular Structure of Dinuclear Rhodium Complexes with Bridging and Semibridging Trialkylphosphane Ligands.
Pechmann T, et al.
Angewandte Chemie (International Edition in English), 39(21), 3909-3911 (2000)
Quintin R Sheridan et al.
The journal of physical chemistry. B, 120(46), 11951-11960 (2016-10-27)
A combination of X-ray scattering experiments and molecular dynamics simulations were conducted to investigate the structure of ionic liquids (ILs) which chemically bind CO
Sarah A Weicker et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(37), 13027-13034 (2015-08-01)
Silyl triflates of the form R4-n Si(OTf)n (n=1, 2; OTf=OSO3 CF3 ) are shown to activate carbon dioxide when paired with bulky alkyl-substituted Group 15 bases. Combinations of silyl triflates and 2,2,6,6-tetramethylpiperidine react with CO2 to afford silyl carbamates via a
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