nitrosyl การใช้

• Nitrosyl fluoride ( NOF ) is colourless and a vigorous fluorinating agent.
• Nitrosyl chloride can further decompose into nitric oxide and chlorine.
• In this function, 種O is referred to as a nitrosyl ligand.
• In this function, NO is referred to as a nitrosyl ligand.
• Sometimes nitrosyl chloride NOCl also is considered as pseudohalogen.
• Dark red nitrosyl chloride is formed as a byproduct.
• Nitrosyl bromide can be formed by the reversible reaction of nitric oxide with bromine.
• Nitrosyl bromide ( NOBr ) is red.
• Nitrosyl fluoride reacts with water to form nitrous acid, which then forms nitric acid:
• It reacts with oxygen to give brown nitrogen dioxide and with halogens to give nitrosyl halides.
• The three step reaction begins with the regioselective addition of nitrosyl chloride across the trisubstituted double bond.
• It also reacts with transition metal compounds to give nitrosyl complexes, most of which are deeply coloured.
• Therefore, in addition to nitrosyl chloride and chlorine, the fumes over aqua regia contain nitric oxide.
• Related NO-delivery reagents include nitrosonium tetrafluoroborate ( [ NO ] BF 4 ) and nitrosyl chloride.
• Alternatively, a nonmetal example is the common reagent nitrosyl chloride ( Cl " N = O ).
• The reaction of nitrosyl chloride with aromatic alcohols generally yields nitroso compounds and other over-oxidation products.
• Nitrosyl chloride is produced as a by-product; it bubbles out of the solution as a gas.
• The results are exactly the same if the nitrosyl ligand were considered NO + or NO & minus;.
• Nitrosyl chloride ( NOCl ) behaves in much the same way and has often been used as an ionising solvent.
• Alternatively, another industrial route involves the reaction of cyclohexane with nitrosyl chloride, which is a free radical reaction.