Reaction of camphor hydrazone with TeCl4 under basic conditions gave an isomeric mixture of vinyl ditelluride and Wagner-Meerwein rearranged ditelluride. Initially formed tellurocamphor enolized and oxidized to give vinyl telluride, whereas tellurocamphor complexed with TeCl4 to afford carbocation, which rearranged in a Wagner-Meerwein manner to afford the rearranged ditelluride. Photolysis of ditelluride in methyl methacrylate solution gave the radical polymerization product, PMMA, in which ditelluride acted as a radical initiator.
YamagoS, NakamuraY. (2013) Recent progress in the use of photoirradiation in living radical polymerization. Polymer, 54, 981–994
2.
PintonS, LucheseC, NogueiraCW. (2011) Comparison of the antioxidant properties and the toxicity of p,p′-dichlorodiphenyl ditelluride with the parent compound, diphenyl ditelluride. Biological Trace Element Research, 139, 204–216
3.
Yamago S, UkaiY, MatsumotoA, NakamuraY. (2009) Organotellurium-mediated controlled/living radical polymerization by direct C-Te bond photolysis. Journal of the American Chemical Society, 131, 2100–2101
4.
KedarnathG, JainVK, WadawaleA, DeyGK. (2009) Bis(3-methyl-2-pyridyl)ditelluride and pyridyl tellurolate complexes of zinc, cadmium, mercury: Synthesis, characterization and their conversion to metal telluride nanoparticles. Journal of the Chemical Society, Dalton Transactions, 8378–8385;
5.
ChiversT, EislerD, RitchJ, TuononenH. (2005) An unusual ditelluride: Synthesis and molecular and electronic structures of the dimer of the tellurium-centered radical [TePiPr2NiPr2PTe]•Angewandte Chemie, International Edition, 44, 4953–4956
6.
YamagoS, IidaK, NakajimaM, YoshidaJ. (2003) Practical procedure for organotellurium mediated living radical polymerization by in situ generated initiations from AIBN and ditellurides. Macromolecules, 36, 3793–3796.
7.
SandhuA, BhasinKK, VermaRD. (1990) Preparation and characterization of ethyl aryl tellurides and their derivatives. Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 29A, 1178–81.
8.
LiJ, BaoW, LueP, ZhouX. (1991) Convenient method for the preparation of dialkyl ditellurides and dialky diselnides. Synthetic Communication, 21, 799–806
ShimadaK, AsakidaM, TakahashiK, SatoY, AoyagiS, TakikawaY, KabutoC. (1998) Synthesis of dialkyl dichalcogenides via alkenechalcogenolate ions generated by treating keton p-toluenesulfonylhydrazones with a base and elemental chalcogen. Chemistry Letters, 27, 513–514.
11.
OkumaK, MunakataK, TsubotaT, KantoM, NagahoraN, ShiojiK, YokomoriY. (2012) Synthesis and reaction of tricyclic tetrathiins and pentathiepins: novel formation of α-disulfines. Tetrahedron, 68, 6211–6217.
12.
OkumaK, MunakataK, MatsuiH, NagahoraN, ShiojiK. (2014) Reaction of fenchone hydrazone with diselenium dibromide: novel formation of bicyclic diselenide. Heterocycles, 89, 473–480.
13.
MinouraM, KawashimaT, OkazakiR. (1993) 1,1,3,3-Tetramethylindanetellone, the first telluroketone stable in solution. Journal of the American Chemical Society, 115, 7019–7020;
14.
MinouraM, KawashimaT, OkazakiR. (1997) A3-1,3,4-Telluradiazolines, a novel tellurium containing heterocycle: one-pot synthesis, structure, and reactivity. Tetrahedron, 53, 8138–8148.
15.
PotapovVA, AmosovaSV, NosyrevaVV, ZhnikinAR, ShestakovaVY, PetrovBV. (1996) The synthesis of diallyl telluride via intermediate diallyl ditelluride. Sulfur Letters, 20, 49–52.
16.
HartmannM, StuderA. (2014) Cyclizing radical carboiodination, carbotelluration and carboaminoxylation of aryl amines. Angewandte Chemie International Edition, 53, 8180–8183
17.
MitamuraT, TsuboiY, IwataK, TsuchiiK, NomotoA, SonodaM, OgawaA. (2007) Photoinduced thiotelluration of isocyanides by using a (PhS)2-(PhTe)2 mixed system, and its application to bisthiolation via radical cyclization. Tetrahedron Letters, 48, 5953–5957
18.
MohanB, HwangS, JangS, ParkKH. (2014) Ultrasound-assisted, transition-metal-free synthesis of diaryl tellurides from aryl boronic acids: a possible free-radical mechanism. SYNLETT, 25, 2078–2082.
