Titanium chloride complexes magnesium

Titanium lactate complexes, 25 88 Titanium magnesium alloys, 13 626 Titanium-magnesium chloride recycle magnesium manufacturing processes, 15 337-338... 

Okamoto et reported a catalytic system based on an aminetris(aiyl-oxide) titanium complex, which gives a low-valent titanium species in the presence of trimethylsilyl chloride and magnesium powder. This system was studied in radieal ring opening of epoxides and oxetanes to generate the corresponding aleohols. 

Excellent chelation control was observed using tributyl(2-propenyl)stannane and a-benzyloxy-cyclohexaneacetaldehyde with magnesium bromide or titanium(IV) chloride, whereas useful Cram selectivity was observed for boron trifluoride-diethyl ether complex induced reactions of the corresponding ferr-butyldimethylsilyl ether89. 

For a-benzyloxycyclohexaneacelaldehyde and 2-butenylstannanes, good chelation control was observed using zinc iodide and titanium(IV) chloride, but only weak synjanti selectivity. Better syn/anti selectivity was found using boron trifluoride-diethyl ether complex, but weak chelation control. Magnesium bromide gave excellent chelation control and acceptable syn/anli selectivity90. 

Plugging solution for low temperature wells—contains plugging cement, water and molten chloride melt obtained as waste from titanium-magnesium production as complex chloride additive. Patent RU 1091616-C, 1995. 

When the flowsheet is complex and involves numerous process steps, a low-energy efficiency will result. The metals titanium and magnesium are difficult to reduce, and their production involves chloride intermediates which are produced from the oxide raw materials. Titanium requires magnesium or sodium as the reducing agent, and these metals are themselves obtained by electrolytic processes which are energy-intensive. Another feature which may add to the complexity of the process flowsheet is the need to separate impurities and by-products using special processes this is the case with copper, lead, and nickel. 

The detail of the structure of the polymerisation centre present in suppported Ziegler-Natta catalysts for a-olefin polymerisation has been the subject of much research effort (e.g./-/2) The catalyst consists of a solid catalyst MgC /TiC /electron donor and a co-catalyst, an aluminium alkyl complexed with an electron donor. Proposed mechanisms for the polymerisation involve a titanium species attached to magnesium chloride with the olefin coordinated to titanium. The detail of the site at which the titanium species is attached is an important area of study in understanding the mechanism of catalysis and several recent papers 10-12) have investigated the surface structure of magnesium chloride and the attachment of TiCl4, in particular the interaction of titanium species with the 100 and 110 planes of a and (3- magnesium chloride. 

It may be interesting, in connection with the ethylene/propylene copolymers mentioned above, to present here some homogeneous Ziegler-Natta catalysts formed by soluble complexes of titanium and magnesium chlorides with alkyl phosphates as catalyst precursors and alkylaluminium compounds as activators (TiCl4)x.(MgCl2)r [0=P(0Bu)3]3-A1(/-Bu)3 and Cl3TiOMgCl-[0 = P(0Bu)3]3- A1(z -Bu)3 (Al/Ti molar ratio of ca 10 1). These catalysts have been used for random ethylene/propylene copolymerisation [73],... 

Active polymerization catalysts have been derived from organomagnesium compounds, for example by reaction with titanium (tv) chloride [7] the polymerization of various vinyl monomers has been initiated by organomagnesium compounds [8] and recently polymerization initiated by magnesium ate complexes has been described [9, 10]. 

The influence of Lewis acids on the diastereoselectivity of the cycloaddition of /f-alkoxyalde-hydes has also been studied35. Magnesium bromide, highly effective for a-alkoxyaldehydes, fails in the case of the cycloaddition of aldehyde 10 to diene 2 and the reaction does not exhibit any selectivity, probably due to a change of mechanism to Mukaiyama s aldol type. One reason may be the change of solvent from tetrahydrofuran to a mixture of benzene and diethyl ether. The additions of aldehyde 10 to other dienes are more selective but diastereoselectivity is still much lower than for the a-alkoxy aldehydes. Boron trifluoride-diethyl etherate complex also leads to a mixture of four possible products. Excellent selectivity is achieved for the titanium(IV) chloride catalyzed addition of aldehyde 10a to diene 2b, 11c is obtained as the only product. 

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