111655-80-2Relevant articles and documents
Synthesis and characterization of diacylgermanes: persistent derivatives with superior photoreactivity
Fischer, Roland C.,Frühwirt, Philipp,Gescheidt, Georg,Griesser, Thomas,Haas, Michael,Kelterer, Anne-Marie,Müller, Stefanie M.,Püschmann, Sabrina D.,Torvisco, Ana,Wagner, Stefan H.
, p. 11965 - 11974 (2021)
Acylgermanes are known as highly efficient photoinitiators. In this contribution, we present the synthesis of new diacylgermanes4a-eviaa multiple silyl abstraction methodology. The method outperforms the state-of-the-art approach (Corey-Seebach reaction)
3-Alkylidenethiagermiranes
Ando, Wataru,Tsumuraya, Takeshi
, p. 1467 - 1472 (2008/10/08)
Dimethyl- and diphenylgermylenes react with di-tert-butylthioketene to give 4-alkylidene-1,2,3-thiadigermetanes 2 and 4, the products of the insertion of germylenes into 3-alkylidenethiagermiranes. Dimesitylgermylene generated by the thermolysis of hexamesitylcyclotrigermane (12) at 80°C reacts with di-tert-butylthioketene to produce a stable 3-alkylidenethiagermirane, 13. Photolysis of 13 produces dimesitylgermylene and di-tert-butylthioketene via germathiocarbonyl ylide 17, which is intensely blue in color with a maximum band at 580 nm. 13 reacts with dimethylgermylene to yield the corresponding 4-alkylidene-1,2,3-thiadigermetane 22. Oxidation of 13 by m-chloroperbenzoic acid gives 3-alkylidene-1,2,4-oxathiagermetane S-oxide 23.