Thallium Trinitrate (TTN)

Vieira, Tiago Oliveira

doi:10.1055/s-2002-31924

Cited by 3 publications

(1 citation statement)

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“…165 Finally, Tl() continues to find uses for organic chemistry synthesis: in the synthesis of chiral tricyclo[4.3.0.0(3.8)]-nonane-4.5-dione; 166 for oxidation of 3-alkenols giving cyclization or ring contraction depending on the substrate and conditions; 167a,167b and for the oxidative rearrangement of olefines. 168…”

Section: Thalliummentioning

confidence: 99%

4 Aluminium, gallium, indium, and thallium

Maher

2003

Annu. Rep. Prog. Chem., Sect. A: Inorg. Chem.

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The chemistry of metalloid cluster compounds for Al, Ga and In dominate current Group 13 chemistry; a review by Schnepf and Schnöckel summarizes the situation for Al and Ga. 13b The first direct observation of radicals by EPR in the activation of a Zeigler-Natta system is both interesting and important for our understanding of these catalysts. 50b For gallium and indium chemistry, a highlight very much in tune with the green chemistry movement, is the report of the first aqueous preparation of high yield, relatively monodisperse, well crystallized GaP and InP nanocrystallites, exhibiting pronounced quantum confinement. 59 Whilst they have had to be relegated to ESI, the increasing interest in indium for Barbier-Grignard type organic syntheses in aqueous media has a green complexion and there are the first signs of similar developments for aqueous gallium chemistry. 110b New work on the two-electron transfer for Tl aq 3ϩ /Tl aq ϩ with electrochemical evidence for [Tl()-Tl()] 4ϩ is a major highlight for thallium chemistry. 142 The synthesis and structure of [In()-In()] 4ϩ is also notable. 129 * Electronic supplementary information (ESI) available. See

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Section: Thalliummentioning

confidence: 99%