|Molar mass||100.9494 g/mol|
|Appearance||greenish yellow powder|
|Melting point||approx. 1500°C|
|Safety data sheet||External MSDS|
|R-phrases (outdated)||R36, R37, R38|
|S-phrases (outdated)||S26, S36|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ‹See TfM› ?)(|
- By passing dry nitrogen over heated magnesium:
- or ammonia:
- Mg3N2(s) + 6 H2O(l) → 3 Mg(OH)2(aq) + 2 NH3(g)
In fact, when magnesium is burned in air, some magnesium nitride is formed in addition to the principal product, magnesium oxide.
Robert H. Wentorf, Jr. was trying to convert the hexagonal form of boron nitride into the cubic form by a combination of heat, pressure, and a catalyst. He had already tried all the logical catalysts (for instance, those that catalyze the synthesis of diamond), but with no success.
Out of desperation and curiosity (he called it the "make the maximum number of mistakes" approach), he added some magnesium wire to the hexagonal boron nitride and gave it the same pressure and heat treatment. When he examined the wire under a microscope, he found tiny dark lumps clinging to it. These lumps could scratch a polished block of boron carbide, something only diamond was known to do.
From the smell of ammonia, caused by the reaction of magnesium nitride with the moisture in the air, he deduced that the magnesium metal had reacted with the boron nitride to form magnesium nitride, which was the true catalyst.
- R. H. Wentorf, Jr. (March 1961). "Synthesis of the Cubic Form of Boron Nitride". Journal of Chemical Physics. 34 (3): 809–812. doi:10.1063/1.1731679.
- Robert H. Wentorf, Jr. (October 1993). "Discovering a Material That's Harder Than Diamond". R&D Innovator. Retrieved June 28, 2006.
Salts and covalent derivatives of the Nitride ion