Bridge, aluminium

While the isolation of ClMeAl[2,6-(t-Bu)-OC6H3] from tert-butylamine has already been reported to result in the simple, monomeric mono-solvate [132], the incorporation of Group 17 elements as inter-aluminium bridges has been revealed in the (AlCl)2-based dimers [ArO(Me)Al(/r-Cl)]2 Ar = 2,6-(t-Bu)2-C6H3 [132], 2,6-(t-Bu)2-4-Me-C6H2 [129]. ... 

Kleinschmidt proposed an alternative structure for the trimer (2-XI) involving a central five-coordinated aluminium bridged to two four-coordinated aluminium atoms. 

A novel molecular species containing an Al-Ni bond has been prepared from (Cp Al)4 and Cp2Ni. The product, (CpNi)2(Cp Al)2, which adopts a butterfly arrangement with each aluminium bridging a Ni-Ni bond, represents the first crystallographic characterisation of the Al-Ni bond in a discrete species. 

Aluminium tetrahydridoborate is a volatile liquid. It is the most volatile aluminium compound known. It is covalent and does not contain ions but has a hydrogen-bridge structure like that of diborane, i.e. each boron atom is attached to the aluminium by two hydrogen bridges ... 

The solid anhydrous halides of some of the transition metals are often intermediate in character between ionic and covalent their structures are complicated by (a) the tendency of the central metal ion to coordinate the halide ions around it, to form an essentially covalent complex, (b) the tendency of halide ions to bridge, or link, two metal ions, again tending to covalency (cf. aluminium chloride, p. 153 and iron(III) chloride, p. 394). 

The Schwerdtfeger polarisation break and the polarisation resistance methods have been studied by Jones and Lowe " in relation to their effectiveness in evaluating corrosion rates of buried metals. A Holler bridge circuit was used to remove IR contributions during the measurement of the polarised potential. Jones and Lowe, on the basis of their studies of buried steel and aluminium specimens, concluded that the polarisation resistance was the most useful, and that the polarisation break had the serious limitation that it was difficult to identify the breaks in the curve. 

Although this account of gelation is made with reference to organic polyelectrolytes, it is of wider application and may be applied to phosphoric acid cements. Orthophosphoric acid solutions used in these cements contain aluminium, and soluble aluminophosphate complexes are formed. Some appear to be multinuclear and there is evidence for polymers based on the bridging Al-O-P unit. These could be termed polyelectrolytes (Akitt, Greenwood Lester, 1971 Wilson et al., 1972 O Neill et al., 1982). 

A trivalent cation, for example AF, has the potential to link three chains. Sterically, this is improbable Mehrotra Bohra (1983) assert that simple aluminium tricarboxylates are not known in solution. Nevertheless we consider it probable that a small proportion of AF ions link three chains, in which all three charged ligands are COO". More probable molecular structures would contain one or two F" ions with a single F", an [A1F(H20)3] unit could bridge two polyanion chains, while an [A1F2(H20)2] would have no crosslinking ability. 

Natta s bimetallic mechanism stipulates that when the catalyst and cocatalyst components are mixed, the chemisorption of the aluminium alkyl (electropositive in nature) occurs on the titanium chloride solid surface which results in the formation of an electron-deficient bridge complex of the structure shown... 

This type of mechanism is likely to be partly operative in systems containing inorganic electrolytes as, for example, in the case of aluminium species. Some polyelectrolytes may also induce flocculation by charge neutralisation but the adsorbed polymer may also be able to bridge from one particle surface to another ( polymer bridging ). 

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