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Merck

481718

Sigma-Aldrich

五羰基铁

greener alternative

>99.99% trace metals basis

别名:

五羰基铁, 羰基铁

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About This Item

线性分子式:
Fe(CO)5
CAS号:
分子量:
195.90
EC號碼:
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.23

蒸汽密度

6.74 (vs air)

品質等級

蒸汽壓力

35 mmHg ( 25 °C)
40 mmHg ( 30.3 °C)

化驗

>99.99% trace metals basis

形狀

liquid

自燃溫度

122 °F

反應適用性

core: iron
reagent type: catalyst

環保替代產品特色

Catalysis
Learn more about the Principles of Green Chemistry.

sustainability

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折射率

n20/D 1.5196 (lit.)

bp

103 °C (lit.)

mp

−20 °C (lit.)

密度

1.49 g/mL at 25 °C (lit.)

環保替代類別

儲存溫度

2-8°C

SMILES 字串

[Fe].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+]

InChI

1S/5CO.Fe/c5*1-2;

InChI 密鑰

FYOFOKCECDGJBF-UHFFFAOYSA-N

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一般說明

Iron(0) pentacarbonyl is a straw-yellow to brilliant orange liquid soluble in organic solvents. It is widely used as a precursor for synthesizing iron oxide nanoparticles, which have applications in the field of energy conversion and storage due to their catalytic properties and ability to enhance electron transport.
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Green Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.

應用

用作以下过程的反应物:
  • 加成反应
  • 通过光解分解
  • 热分解法制备尺寸分布窄的铁洋葱状富勒烯磁性微粒
  • 碳酰胺氢硅烷还原反应中七核铁羰基簇合物的制备

  • 高碱性条件下制备光催化析氢 Fe 纳米粒子的前驱体
Iron(0) pentacarbonyl can be used:
  • To fabricate Fe-based anode materials for high-performance aqueous secondary Ni−Fe batteries. It helps to achieve good safety, high power density, long term-life cycle, and high energy density.
  • As a precursor to synthesize highly stable, colloidal magnetic iron nanoparticles with narrow size distribution. These nanoparticles are potential candidates for MRI contrasting agents and magnetically separable catalysts.
  • To synthesize zero valent sustainable iron nanocatalysts for reduction reactions.

象形圖

FlameSkull and crossbones

訊號詞

Danger

危險分類

Acute Tox. 1 Inhalation - Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Flam. Liq. 2

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

5.0 °F - closed cup

閃點(°C)

-15 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Kyoko Hibi et al.
Analytical and bioanalytical chemistry, 391(4), 1147-1152 (2008-04-29)
Bacterial cold water disease, caused by Flavobacterium psychrophilum, is a serious problem in the aquaculture industry worldwide. Several methods to prevent and treat cold water disease have been studied. Although detection at the early stage of F. psychrophilum infection is
Jianfeng Jin et al.
Applied microbiology and biotechnology, 89(6), 1831-1840 (2010-12-02)
A bifunctional hydratase/alcohol dehydrogenase was isolated from the cyclohexanol degrading bacterium Alicycliphilus denitrificans DSMZ 14773. The enzyme catalyzes the addition of water to α,β-unsaturated carbonyl compounds and the subsequent alcohol oxidation. The purified enzyme showed three subunits in SDS gel
John T Tsalavoutis et al.
Journal of computational chemistry, 31(10), 1969-1978 (2010-01-21)
The equilibrium structures and vibrational frequencies of the iron complexes [Fe(0)(CN)(n)(CO)(5-n)](n-) and [Fe(II)(CN)(n)(CO)(5-n)](2-n) (n = 0-5) have been calculated at the BP86 level of theory. The Fe(0) complexes adopt trigonal bipyramidal structures with the cyano ligands occupying the axial positions
Pro-oxidants or anti-oxidant defenses? Which one to blame in non-alcoholic steatohepatitis pathogenesis?
Isabelle A Leclercq
Journal of gastroenterology and hepatology, 27(11), 1651-1653 (2012-10-31)
Li Long et al.
Dalton transactions (Cambridge, England : 2003), 41(31), 9482-9492 (2012-07-04)
Reaction of Fe(3)(CO)(12) with pyridinyl thioester ligand PyCH(2)SCOCH(3) (L(1), Py = pyridin-2-yl) produced complex, [Fe(2)(κ-COCH(3))(μ-SCH(2)Py)(CO)(5)] (1) (PyCH(2)S = pyridin-2-ylmethanethiolate). When complex 1 reacted with PPh(3), a monosubstituted complex, [Fe(2)(κ-COCH(3))(μ-SCH(2)Py)(CO)(4)PPh(3)] (2), was derived. Reaction of the same precursor with analogous thioester

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