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Each iron atom is bonded linearly to two NO + ligands and shares two bridging sulfidi ligands with the other iron atom. Roussin's black salt has a more complex cluster structure. The anion in this species has the formula [Fe 4 (NO) 7 S 3] −. It has C 3v symmetry. It consists of a tetrahedron of iron atoms with sulfide ions on three faces of ...
Iron(II) sulfide or ferrous sulfide (Br.E. sulphide) is one of a family of chemical compounds and minerals with the approximate formula Fe S. Iron sulfides are often iron-deficient non-stoichiometric .
Dibenzyl sulfide is a symmetrical thioether. It contains two C 6 H 5 CH 2 - (benzyl) groups linked by a sulfide bridge. It is a colorless or white solid that is soluble in nonpolar solvents.
The iron compounds produced on the largest scale in industry are iron(II) sulfate (FeSO 4 ·7H 2 O) and iron(III) chloride (FeCl 3). The former is one of the most readily available sources of iron(II), but is less stable to aerial oxidation than Mohr's salt ((NH 4) 2 Fe(SO 4) 2 ·6H 2 O). Iron(II) compounds tend to be oxidized to iron(III ...
Reactions of oxidation of sulfide to sulfate and elemental sulfur (incorrectly balanced). The electrons (e −) liberated from these oxidation reactions, which release chemical energy, are then used to fix carbon into organic molecules. The elements that become oxidized are shown in pink, those that become reduced in blue, and the electrons in ...
Three sulfide ions bridge two iron ions each, while the fourth sulfide bridges three iron ions. Their formal oxidation states may vary from [Fe 3 S 4] + (all-Fe 3+ form) to [Fe 3 S 4] 2− (all-Fe 2+ form). In a number of iron–sulfur proteins, the [Fe 4 S 4] cluster can be reversibly converted by oxidation and loss of one iron ion to a [Fe 3 ...
Iron–sulfur clusters are molecular ensembles of iron and sulfide. They are most often discussed in the context of the biological role for iron–sulfur proteins , which are pervasive. [ 2 ] Many Fe–S clusters are known in the area of organometallic chemistry and as precursors to synthetic analogues of the biological clusters.
In organic chemistry, the Swern oxidation, named after Daniel Swern, is a chemical reaction whereby a primary or secondary alcohol (−OH) is oxidized to an aldehyde (−CH=O) or ketone (>C=O) using oxalyl chloride, dimethyl sulfoxide (DMSO) and an organic base, such as triethylamine.