Diethylaluminium chloride

Last updated
Diethylaluminium chloride
Et2AlCldimer.svg
Names
IUPAC name
Chlorodiethylalumane
Other names
Chlorodiethylaluminium
Identifiers
3D model (JSmol)
4123259
ChemSpider
ECHA InfoCard 100.002.253 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 202-477-2
PubChem CID
RTECS number
  • BD0558000
UNII
UN number 3394
  • InChI=1S/2C2H5.Al.ClH/c2*1-2;;/h2*1H2,2H3;;1H/q;;+1;/p-1 Yes check.svgY
    Key: YNLAOSYQHBDIKW-UHFFFAOYSA-M Yes check.svgY
  • CC[Al](Cl)CC
Properties
C8H20Al2Cl2
Molar mass 241.11 g·mol−1
AppearanceColorless liquid [1]
Density 0.96 g/cm3 [1]
Melting point −74 °C (−101 °F; 199 K) [1]
Boiling point 125 to 126 °C (257 to 259 °F; 398 to 399 K) at 50 mmHg
Reacts [1]
Vapor pressure 3 mmHg (at 60 °C)
Hazards
GHS labelling:
GHS-pictogram-flamme.svg GHS-pictogram-acid.svg
Danger
H225, H250, H260, H261, H314
P210, P222, P223, P231+P232, P233, P240, P241, P242, P243, P260, P264, P280, P301+P330+P331, P302+P334, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P335+P334, P363, P370+P378, P402+P404, P403+P235, P405, P422, P501
NFPA 704 (fire diamond)
NFPA 704.svgHealth 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gasFlammability 4: Will rapidly or completely vaporize at normal atmospheric pressure and temperature, or is readily dispersed in air and will burn readily. Flash point below 23 °C (73 °F). E.g. propaneInstability 2: Undergoes violent chemical change at elevated temperatures and pressures, reacts violently with water, or may form explosive mixtures with water. E.g. white phosphorusSpecial hazard W: Reacts with water in an unusual or dangerous manner. E.g. sodium, sulfuric acid
3
4
2
W
Flash point −18 °C (0 °F; 255 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Diethylaluminium chloride, abbreviated DEAC, is an organoaluminium compound. Although often given the chemical formula (C2H5)2AlCl, it exists as a dimer, [(C2H5)2AlCl]2 It is a precursor to Ziegler-Natta catalysts employed for the production of polyolefins. The compound is also a Lewis acid, useful in organic synthesis. The compound is a colorless waxy solid, but is usually handled as a solution in hydrocarbon solvents. It is highly reactive, even pyrophoric. [2]

Contents

Structure and bonding

Compounds of the empirical formula AlR2Cl (R = alkyl, aryl) usually exist as dimers with the formula (R2Al)2(μ-Cl)2. The bridging ligands (indicated by "μ-") are halides, not the organic substituents. The aluminium adopts a tetrahedral geometry. Each Al(III) center follows the octet rule. [3] [4] In contrast, triethylaluminium and trimethylaluminium feature bridging alkyl groups and these compounds violate the octet rule.

Production

Diethylaluminium chloride can be produced from ethylaluminium sesquichloride, (C2H5)3Al2Cl3, by reduction with sodium: [5]

2 (C2H5)3Al2Cl3 + 3 Na → 3 (C2H5)2AlCl + Al + 3 NaCl

It is also obtained from the reaction of triethylaluminium with hydrochloric acid:

(C2H5)3Al + HCl → (C2H5)2AlCl + C2H6

Reproportionation reactions can also be used:

2 (C2H5)3Al + AlCl3 → 3 (C2H5)2AlCl
(C2H5)3Al2Cl3 + (C2H5)3Al → 3 (C2H5)2AlCl

Uses

Diethylaluminium chloride and other organoaluminium compounds are used in combination with transition metal compounds as Ziegler–Natta catalysts for the polymerization of various alkenes. [6]

As a Lewis acid, diethylaluminium chloride also has uses in organic synthesis. For example, it is used to catalyze the Diels–Alder and ene reactions. Alternatively, it can react as a nucleophile or a proton scavenger. [2]

Safety

Diethylaluminium chloride is not only flammable but pyrophoric.

Related Research Articles

<span class="mw-page-title-main">Organometallic chemistry</span> Study of organic compounds containing metal(s)

Organometallic chemistry is the study of organometallic compounds, chemical compounds containing at least one chemical bond between a carbon atom of an organic molecule and a metal, including alkali, alkaline earth, and transition metals, and sometimes broadened to include metalloids like boron, silicon, and selenium, as well. Aside from bonds to organyl fragments or molecules, bonds to 'inorganic' carbon, like carbon monoxide, cyanide, or carbide, are generally considered to be organometallic as well. Some related compounds such as transition metal hydrides and metal phosphine complexes are often included in discussions of organometallic compounds, though strictly speaking, they are not necessarily organometallic. The related but distinct term "metalorganic compound" refers to metal-containing compounds lacking direct metal-carbon bonds but which contain organic ligands. Metal β-diketonates, alkoxides, dialkylamides, and metal phosphine complexes are representative members of this class. The field of organometallic chemistry combines aspects of traditional inorganic and organic chemistry.

A Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, is a catalyst used in the synthesis of polymers of 1-alkenes (alpha-olefins). Two broad classes of Ziegler–Natta catalysts are employed, distinguished by their solubility:

<span class="mw-page-title-main">Acyl halide</span> Oxoacid compound with an –OH group replaced by a halogen

In organic chemistry, an acyl halide is a chemical compound derived from an oxoacid by replacing a hydroxyl group with a halide group.

<span class="mw-page-title-main">Aluminium chloride</span> Chemical compound

Aluminium chloride, also known as aluminium trichloride, is an inorganic compound with the formula AlCl3. It forms a hexahydrate with the formula [Al(H2O)6]Cl3, containing six water molecules of hydration. Both the anhydrous form and the hexahydrate are colourless crystals, but samples are often contaminated with iron(III) chloride, giving them a yellow colour.

<span class="mw-page-title-main">Trimethylaluminium</span> Chemical compound

Trimethylaluminium is one of the simplest examples of an organoaluminium compound. Despite its name it has the formula Al2(CH3)6 (abbreviated as Al2Me6 or TMA), as it exists as a dimer. This colorless liquid is pyrophoric. It is an industrially important compound, closely related to triethylaluminium.

<span class="mw-page-title-main">Rhodium(III) chloride</span> Chemical compound

Rhodium(III) chloride refers to inorganic compounds with the formula RhCl3(H2O)n, where n varies from 0 to 3. These are diamagnetic red-brown solids. The soluble trihydrated (n = 3) salt is the usual compound of commerce. It is widely used to prepare compounds used in homogeneous catalysis.

<span class="mw-page-title-main">Diisobutylaluminium hydride</span> Chemical compound

Diisobutylaluminium hydride (DIBALH, DIBAL, DIBAL-H or DIBAH) is a reducing agent with the formula (i-Bu2AlH)2, where i-Bu represents isobutyl (-CH2CH(CH3)2). This organoaluminium compound is a reagent in organic synthesis.

<span class="mw-page-title-main">Hafnium tetrachloride</span> Chemical compound

Hafnium(IV) chloride is the inorganic compound with the formula HfCl4. This colourless solid is the precursor to most hafnium organometallic compounds. It has a variety of highly specialized applications, mainly in materials science and as a catalyst.

Cycloocta-1,5-diene is a cyclic hydrocarbon with the chemical formula C8H12, specifically [−(CH2)2−CH=CH−]2.

<span class="mw-page-title-main">Aluminium iodide</span> Chemical compound

Aluminium iodide is a chemical compound containing aluminium and iodine. Invariably, the name refers to a compound of the composition AlI
3
, formed by the reaction of aluminium and iodine or the action of HI on Al metal. The hexahydrate is obtained from a reaction between metallic aluminum or aluminum hydroxide with hydrogen iodide or hydroiodic acid. Like the related chloride and bromide, AlI
3
is a strong Lewis acid and will absorb water from the atmosphere. It is employed as a reagent for the scission of certain kinds of C-O and N-O bonds. It cleaves aryl ethers and deoxygenates epoxides.

<span class="mw-page-title-main">Organotitanium chemistry</span>

Organotitanium chemistry is the science of organotitanium compounds describing their physical properties, synthesis, and reactions. Organotitanium compounds in organometallic chemistry contain carbon-titanium chemical bonds. They are reagents in organic chemistry and are involved in major industrial processes.

<span class="mw-page-title-main">Allylpalladium chloride dimer</span> Chemical compound

Allylpalladium(II) chloride dimer (APC) is a chemical compound with the formula [(η3-C3H5)PdCl]2. This yellow air-stable compound is an important catalyst used in organic synthesis. It is one of the most widely used transition metal allyl complexes.

<span class="mw-page-title-main">Organoaluminium chemistry</span>

Organoaluminium chemistry is the study of compounds containing bonds between carbon and aluminium. It is one of the major themes within organometallic chemistry. Illustrative organoaluminium compounds are the dimer trimethylaluminium, the monomer triisobutylaluminium, and the titanium-aluminium compound called Tebbe's reagent. The behavior of organoaluminium compounds can be understood in terms of the polarity of the C−Al bond and the high Lewis acidity of the three-coordinated species. Industrially, these compounds are mainly used for the production of polyolefins.

<span class="mw-page-title-main">Triethylaluminium</span> Chemical compound

Triethylaluminium is one of the simplest examples of an organoaluminium compound. Despite its name the compound has the formula Al2(C2H5)6 (abbreviated as Al2Et6 or TEA). This colorless liquid is pyrophoric. It is an industrially important compound, closely related to trimethylaluminium.

<span class="mw-page-title-main">Diethylaluminium cyanide</span> Chemical compound

Diethylaluminium cyanide is the organoaluminium compound with formula ( 2AlCN)n. This colorless compound is usually handled as a solution in toluene. It is a reagent for the hydrocyanation of α,β-unsaturated ketones.

<span class="mw-page-title-main">Ethylaluminium sesquichloride</span> Chemical compound

Ethylaluminium sesquichloride, also called EASC, is an industrially important organoaluminium compound used primarily as a precursor to triethylaluminium and as a catalyst component in Ziegler–Natta type systems for olefin and diene polymerizations. Other applications include use in alkylation reactions and as a catalyst component in linear oligomerization and cyclization of unsaturated hydrocarbons. EASC is a colourless liquid, spontaneously combustible in air and reacts violently when in contact with water and many other compounds.

<span class="mw-page-title-main">Triisobutylaluminium</span> Chemical compound

Triisobutylaluminium (TiBA) is an organoaluminium compound with the formula Al(CH2CH(CH3)2)3. This colorless pyrophoric liquid is mainly used to make linear primary alcohols and α-olefins.

In organic chemistry, the Ziegler process is a method for producing fatty alcohols from ethylene using an organoaluminium compound. The reaction produces linear primary alcohols with an even numbered carbon chain. The process uses an aluminum compound to oligomerize ethylene and allow the resulting alkyl group to be oxygenated. The usually targeted products are fatty alcohols, which are otherwise derived from natural fats and oils. Fatty alcohols are used in food and chemical processing. They are useful due to their amphipathic nature. The synthesis route is named after Karl Ziegler, who described the process in 1955.

<span class="mw-page-title-main">Dimethylaluminium chloride</span> Chemical compound

Dimethylaluminium chloride is an organoaluminium compound with the chemical formula [(CH3)2AlCl]2. It behaves similarly to diethylaluminium chloride but is more expensive. Hence, it is less commonly used.

<span class="mw-page-title-main">Main group organometallic chemistry</span>

Main group organometallic chemistry concerns the preparation and properties of main-group elements directly bonded to carbon. The inventory is large. The compounds exhibit a wide range of properties, including ones that are water-stable and others that are pyrophoric. Many are very useful themselves, as chemical reagents, or as catalysts.

References

  1. 1 2 3 4 John Rumble (June 18, 2018). CRC Handbook of Chemistry and Physics (99th ed.). CRC Press. pp. 4–40. ISBN   978-1138561632.
  2. 1 2 Snider, Barry B. (2001). "Diethylaluminum Chloride". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rd165. ISBN   0-471-93623-5.
  3. Brendhaugen, Kristen; Haaland, Arne; Novak, David P.; Østvold, Terje; Bjørseth, Alf; Powell, D. L. (1974). "The Molecular Structure of Dimethylaluminium Chloride Dimer, [(CH3)2AlCl]2 Redetermined by Gas Phase Electron Diffraction". Acta Chemica Scandinavica. 28a: 45–47. doi: 10.3891/acta.chem.scand.28a-0045 .
  4. McMahon, C. Niamh; Francis, Julie A.; Barron, Andrew R. (1997). "Molecular Atructure of [(t Bu)2Al(μ-Cl)]2". Journal of Chemical Crystallography. 27 (3): 191–194. doi:10.1007/BF02575988. S2CID   195242291.
  5. Krause, Michael J.; Orlandi, Frank; Saurage, Alfred T.; Zietz, Joseph R. (2000), "Aluminum Compounds, Organic", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, pp. 592–593, doi:10.1002/14356007.a01_543, ISBN   978-3-527-30673-2
  6. Fisch, A. G. (2000). "Ziegler–Natta Catalysts". Kirk-Othmer Encyclopedia of Chemical Technology. Wiley. pp. 1–22. doi:10.1002/0471238961.2609050703050303.a01.pub2. ISBN   978-0-471-48494-3. S2CID   213111515.