Boron Nitrate
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Boron Nitrate
Tetranitratoborate is an anion composed of boron with four nitrate groups. It has formula . It can form salts with large cations such as tetramethylammonium nitratoborate, or tetraethylammonium tetranitratoborate. The ion was first discovered by C. R. Guibert and M. D. Marshall in 1966 after failed attempts to make neutral (non-ionic) boron nitrate, , which has resisted attempts to make it; if it exists, it is unstable above −78 °C. Other related ions are the slightly more stable tetraperchloratoborates, with perchlorate groups instead of nitrate, and tetranitratoaluminate with the next atom down the periodic table, aluminium instead of boron (). Formation Tetramethylammonium chloride reacts with to make . Then the tetrachloroborate is reacted with at around −20 °C to form tetramethylammonium nitratoborate, and other gases such as and . Another mechanism to make tetranitratoborate salts is to shake a metal nitrate with in chloroform at 20 °C for ...
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Tetramethylammonium
Tetramethylammonium (TMA) or (Me4N+) is the simplest quaternary ammonium cation, consisting of four methyl groups attached to a central nitrogen atom, and is isoelectronic with neopentane. It is positively charged and can only be isolated in association with a counter-ion. Common salts include tetramethylammonium chloride and tetramethylammonium hydroxide. Tetramethylammonium salts are commonly used in chemical synthesis and are widely employed in pharmacological research. Common nomenclature In the toxicological literature, ''naturally occurring'' tetramethylammonium (anion unspecified) is often referred to by the name "tetramine". Unfortunately, this non-systematic or "trivial" name is also used for other chemical entities, including a toxic rodenticide (Tetramethylenedisulfotetramine). Similarly, the acronym "TMA", which is frequently used for tetramethylammonium in the pharmacological literature, may also refer to the investigational drug 3,4,5-trimethoxyamphetamine, which, ...
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