Australian Journal of Chemistry | 2019

Lithium: From Bipolar to Batteries

 

Abstract


Known as the lightestmetal in the periodic table, lithium’s natural existence is rare compared with its two siblings helium and hydrogen, all created during the Big Bang. It was discovered in its mineral form petalite (LiAlSi4O10) by the Brazilian Jozè Bonifácio Andralda e Silvia, who also first observed its crimson flame when the mineral was thrown into fire. Not surprising then that its name stems from the Greek word for stone: lithos. Swedish chemist Johan August Arfvedson deduced in 1817 that this new lighter alkalimetal (Nawas discovered first byHumphry Davy in 1807) was lithium, although he was unsuccessful in separating it from its ore. It was not until 1855 that an actual sample of lithium metal (Fig. 1) was able to be extracted by the chemists Robert Bunsen and Augustus Matthiessen through electrolysis of molten lithium chloride. Lithium represents 0.005% of the earth’s crust, making it the 25th most abundant element. It is primarily mined in Australia from the lithium aluminium inosilicate Spodumene [LiAl(SiO3)2] with over 1.5 million tonnes extracted in 2017 alone, with Chile and China following next as top producers. Due to its mass extraction, it is unsurprising to find lithium used in a variety of everyday materials; for instance, as an alloy with magnesium or aluminium allowing the production of strong lightweight aircraft, as lithium oxide in ceramics and glass manufacture, and as the vital component in high temperature grease (lithium stearate) that also works in Antarctic conditions (below 608C). Most catastrophically, it is the key element in hydrogen bombs – with lithium-deuteride, in which the i isotope is used as the fusion fuel. From a biological perspective, lithium is not considered an essential trace element. In fact, it was discovered to be moderately toxic when lithium chloride was substituted in place of common salt. However, possibly one of the most notable and life-changing discoveries in lithium salt chemistry of the 20th century is lithium carbonate, which has been used in the treatment of millions of sufferers of bipolar affective disorder. Discovered by Australian psychiatrist John Cade in 1948, he noticed considerable calming effects on normally active guinea pigs upon injection of a 0.5% solution of lithium carbonate. With no ethics committees in those days, Cade progressed to taking it himself for a week, to govern it was ‘safe’ before trialling it in one of his most manic patients at Bundoora Repatriation Mental Hospital. The extraordinary calming effects were so great that the patient was transferred out of psychiatric care and was soon able to return to work. Unpatentable due to it being a natural salt, it still remains the single most effective treatment for bipolar disorder today, making lithium the ‘penicillin of mental health’. Not only is lithium effective as a drug, but its use in organometallic chemistry has been fundamental. It is salient to recognise that Johanna Holtz and Wilhelm Schlenk discovered the now ubiquitous synthetic reagents, MeLi, EtLi, and PhLi, just over 100 years ago, in the process giving the organometallic chemist their lithium toolkit. With nearly 95% of drug syntheses relying upon lithium-based reagents at some point in their preparation, the value of their discovery cannot be underestimated. Reflecting its human health effects, the power of ‘salt effects’ in organometallic chemistry can have drastically different reactivity and selectivity outcomes compared with the analogous salt-free reactions. One of the most

Volume 72
Pages 931-932
DOI 10.1071/ch19596
Language English
Journal Australian Journal of Chemistry

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