Gallium bromide iodide

The chalcogenide bromides and chlorides may be prepared by the reaction of the halide with the respective chalcogenide in a sealed ampoule. A mixture of gallium metal and chalcogen may be used, instead of the chalcogenide. The chalcogenide iodides are S3mthesized directly from the elements. The exact preparative conditions are listed in Table XVIII 160,165). 

The formation of molecular complexes between aluminum trihalides and pyridine or alkylpyridines has been the subject of systematic studies.35,36 Calorimetric data yield bond dissociation energies D(X3Al—py) of 323, 308 and 264 kJ mol-1 for X = C1, Br and I, respectively, and this same order is found for alkylpyridine adducts, although the A1—N bond is weakened in the case of lutidine by the effects of steric hindrance. For gallium halides the values of D(X3M—py) are smaller 248, 237 and 195 kJ mol-1 for chloride, bromide and iodide adducts, respectively. 

Aluminium, 0048 Ammonium phosphinate, 4549 Barium phosphinate, 0210 f Benzaldehyde, 2727 1,4-Benzenediol, 2326 Bis(hydrazine)tin(II) chloride, 4064 Calcium acetylide, 0582 Calcium phosphinate, 3925 Chromium(II) chloride, 4046 Chromium(II) oxide, 4235 Chromium(II) sulfate, 4238 Copper(I) bromide, 0264 Diacetatotetraaquocobalt, 1774 Diisobutylaluminium hydride, 3076 f 1,2-Dimethylhydrazine, 0951 1,2-Diphenylhydrazine, 3511 Dipotassium phosphinate, 4425 f Ethanedial, 0719 f Formaldehyde, 0415 Formic acid, 0417 Gallium(I) oxide, 4405 Glucose, 2513 f Hydrazine, 4515 Hydroxylamine, 4493 Hydroxylaminium phosphinate, 4550 Hyponitrous acid, 4464 Iron(II) chloride, 4055 Iron(II) hydroxide, 4386 Iron(II) sulfate, 4393 Fead(II) phosphinate, 4526 Fead(II) phosphite, 4530 Fithium dithionite, 4682 Magnesium, 4685 Magnesium phosphinate, 4512 Manganese(II) phosphinate, 4514 f Methylhydrazine, 0500 Phenylhydrazine, 2366 Phosphinic acid, 4498 Phosphonic acid, 4499 Phosphonium iodide, 4510 Potassium, 4640 Potassium hypoborate, 0163... 

Allylgallium and propargylgallium compounds can be prepared by the direct reaction of the corresponding bromides or iodides with gallium metal.402,403Gallium enolates are also prepared from a-halo carbonyl compounds with gallium.404... 

Lithium gallium hydride reduces effectively both primary and secondary alkyl bromides and iodides to the corresponding hydrocarbons (Table 41).435... 

The indium iodide complex [1-3] is > 99% extracted into diethyl ether from 0.5-2.5 M HI (6-30%). Gallium is not extracted under these conditions, but it is extracted from 6 M HCl. The hydriodic acid can be replaced by 0.5-3 M H2SO4 containing 15-20% of Kl. Chloride, bromide, fluoride, phosphate, and citrate do not interfere in the extraction of In from iodide media. Under the optimum conditions for the extraction, Tl, Cd, and Sn (and some Bi, Zn, Hg, and Sb) are extracted. Aluminium and Fe(II), like Ga, are not extracted. The indium iodide complex has also been extracted into chloroform containing N-benzylaniline [4,5]. 

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