Diethylaluminium chloride

Visit ChemicalBook To find more DIETHYLALUMINUM CHLORIDE(96-10-6) information like chemical properties Structure melting point boiling point density molecular formula molecular weight physical properties toxicity information customs codes You can also browse global suppliers vendor prices Price manufacturers of DIETHYLALUMINUM CHLORIDE(96-10-6) Abstract Controlled cyclization of styrene-butadiene rubber (SBR) was achieved with the aid of cationic catalyst system based on diethylaluminium chloride (AIEt(2)Cl) and benzyl chloride (C6H5CH2Cl) and by working in xylene solution at high temperature (T 100 degreesC)

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S7 Diethylaluminium chloride solution (0 9 M in MePh 4 10 mL 3 69 mmol) was added dropwise via syringe to a solution of (R R)-N N ′-bis(3 5-di-tert-butylsalicylidene)-1 2-cyclohexanediamine (2 00 g 3 66 mmol) in dry MePh The resulting solution was stirred under nitrogen for 24 h Solvent was removed

Diethylaluminum chloride 97% Synonym: Chloro diethyl aluminum CAS Number 96-10-6 Linear Formula (C 2 H 5) 2 AlCl Molecular Weight 120 56 Beilstein/REAXYS Number 4123259 EC Number 202-477-2 MDL number MFCD00000459 PubChem Substance ID 24855548 NACRES NA 22

A kinetic study of propylene dimerization by binuclear nickel—ylide complexes in presence of diethylaluminium chloride as cocatalyst Journal of Molecular Catalysis A: Chemical 1996 110 (1) 25-32 DOI: 10 1016/1381-1169(96)00025-8

) and diethylaluminium chloride [(C 2 H 5) 2 AlCl] as a co-catalyst for the polymerization of ethylene [4 5] into high molecular weight HDPE (high density polyethylene) at room temperature (Figure 1 shows a photo of the original equipment employed by Ziegler) [3–7]

The aluminium–salen complexes were prepared by treating 8a and 8b with diethylaluminium chloride affording complexes 1 and 2 in 96% and 91% yields respectively These complexes could be used without any additional purification Scheme 2: Synthesis of salen ligands 8a and 8b

Free radical reactions to generate alkenes and/or ionic

-Nitrostyrenes l react with triethylaluminium or diethylaluminium chloride in diethyl ether solution and under nitrogen or argon to generate the alkenes 2 and the hydroximoyl chlorides 3 after work-up with ice-cold cone hydrochloric acid

The aluminium–salen complexes were prepared by treating 8a and 8b with diethylaluminium chloride affording complexes 1 and 2 in 96% and 91% yields respectively These complexes could be used without any additional purification Scheme 2: Synthesis of salen ligands 8a and 8b

) and diethylaluminium chloride [(C 2 H 5) 2 AlCl] as a co-catalyst for the polymerization of ethylene [4 5] into high molecular weight HDPE (high density polyethylene) at room temperature (Figure 1 shows a photo of the original equipment employed by Ziegler) [3–7]

2011-09-07The catalytic systems using the co-catalysts diethylaluminium chloride (Et(2)AlCl) or methylaluminoxane (MAO) were investigated in detail and the molecular weights and distributions of the PEs obtained were found to significantly rely on the nature of the different ligands present and reaction parameters such as the molar ratios of Al/Ni reaction temperature and reaction time

N2 - Dicyclopentadiene was polymerized by reaction injection molding (RIM) using a catalyst system based on WCl6 and diethylaluminium chloride Ring opening polymerization results in formation of a crosslinked polymer with a high crosslink density The kinetics of the fast exothermic reaction was followed by the adiabatic temperature rise method

Diethylaluminium cyanide Names IUPAC name diethylalumanylformonitrile Other names Cyanodiethyl Aluminum (cyano-κC)diethyl-Aluminum (cyano-C)diethyl-Aluminum Cyanodiethyl-(7CI 8CI) Aluminum Cyanodiethylallane Cyanodiethylaluminum Diethylaluminum Cyanide Identifiers CAS Number

A kinetic study of propylene dimerization by binuclear nickel—ylide complexes in presence of diethylaluminium chloride as cocatalyst Journal of Molecular Catalysis A: Chemical 1996 110 (1) 25-32 DOI: 10 1016/1381-1169(96)00025-8

The 'Global and Chinese Diethylaluminium chloride Industry 2012-2022 Market Research Report' is a professional and in-depth study on the current state of the global Diethylaluminium chloride industry with a focus on the Chinese market The report provides key statistics on the market status of the Diethylaluminium chloride manufacturers and is a valuable source of guidance and direction for

دی‌اتیل‌آلومینیم کلرید

دی‌اتیل‌آلومینیم کلرید (به انگلیسی: Diethylaluminium chloride) یک ترکیب شیمیایی با شناسه پاب‌کم ۷۲۷۷ است این ماده یک ترکیب شیمیایی خطرناک است که به عنوان اسید لوییس استفاده می شود فرمول شیمیایی آن C4H10AlCl است

The unique properties of diethylaluminium azide arising from the Lewis acid aluminium and the nucleophilicity of the azide make it a versatile reagent in organic synthesis Ring-opening of epoxides Michael-type additions synthesis of acyl azides and functionalizations of fullerene C60 will be discussed Among the recently described uses of the reagent particular attention will be devoted

-Nitrostyrenes l react with triethylaluminium or diethylaluminium chloride in diethyl ether solution and under nitrogen or argon to generate the alkenes 2 and the hydroximoyl chlorides 3 after work-up with ice-cold cone hydrochloric acid

) and diethylaluminium chloride [(C 2 H 5) 2 AlCl] as a co-catalyst for the polymerization of ethylene [4 5] into high molecular weight HDPE (high density polyethylene) at room temperature (Figure 1 shows a photo of the original equipment employed by Ziegler) [3–7]

When diethylaluminium chloride was employed as catalyst the selectivity of 87 increased to 4:1 and that of the 101 increased to 6:1 Only 102 showed almost complete selectivity using this catalyse The dienophile 87 reacted with isoprene to give a 2:1 mixture of products using titanium catalysts and 5:1 using diethylaluminium chloride catalyst

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