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Ruthenium has four crystal modifications and does not tarnish at ambient conditions; it oxidizes upon heating to 800 °C (1,070 K). Ruthenium dissolves in fused alkalis to give ruthenates (RuO 2− 4). It is not attacked by acids (even aqua regia) but is attacked by sodium hypochlorite at room temperature, and halogens at high temperatures. [11]
Ruthenium(IV) oxide is the inorganic compound with the formula Ru O 2. This black solid is the most common oxide of ruthenium . It is widely used as an electrocatalyst for producing chlorine, chlorine oxides, and O 2 . [ 1 ]
The properties of ruthenium and osmium compounds are often similar. The +2, +3, and +4 states are the most common. The +2, +3, and +4 states are the most common. The most prevalent precursor is ruthenium trichloride , a red solid that is poorly defined chemically but versatile synthetically.
2 Properties. 3 Uses. ... Diruthenium phosphide is a binary inorganic compound of ruthenium metal and ... Diruthenium phosphide forms crystals of rhombic crystal ...
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Distrontium ruthenate, also known as strontium ruthenate, is an oxide of strontium and ruthenium with the chemical formula Sr 2 RuO 4.It was the first reported perovskite superconductor that did not contain copper.
The most important reagents for the introduction of ruthenium are ruthenium(III) chloride and triruthenium dodecacarbonyl. In its organometallic compounds, ruthenium is known to adopt oxidation states from -2 ([Ru(CO) 4] 2−) to +6 ([RuN(Me)4] −). Most common are those in the 2+ oxidation state, as illustrated below.
Tris(bipyridine)ruthenium(II) chloride is the chloride salt coordination complex with the formula [Ru(bpy) 3]Cl 2.This polypyridine complex is a red crystalline salt obtained as the hexahydrate, although all of the properties of interest are in the cation [Ru(bpy) 3] 2+, which has received much attention because of its distinctive optical properties.
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