78190-50-8Relevant academic research and scientific papers
Ditelluride-promoted diphosphene transfer from a cyclotriphosphane to 2,3-dimethylbutadiene: characterization of di(aryltelluro)diphosphanes
Meyer, H. U.,Severengiz, T.,Mont, W. W. du
, p. 691 - 694 (2007/10/02)
The cleavage of tri-tert-butylcyclotriphosphane 1 with di(4-methylphenyl)ditelluride 2 leads to 1,2-di-tert-butyl-1.2-di(4-methylphenyltelluro)diphosphane 3 and tetra-tert-butylcyclotetraphosphane.When 1 is heated with 2 in the presence of 2,3-dimethylbutadiene, the diphosphene trapping product 1,2-di-tert-butyl-4,5-dimethyl-1,2-diphosphacyclohex-4-ene 5 can be detected.The salt elimination reaction of tert-butyldichlorophosphane with 4-methylphenyltellurotelluromagnesium bromide leads mainly to 3 and ditelluride 2.Tellurophosphane 6 and 1,2-di-tert-butyl-1,2-di(aryltelluro)diphosphanes 3. 7 (7 : aryl = 2,4,6-triisopropylphenyl) are available in fair yields from di-tert-butylchlorophosphane or 1,2-di-tert-butyl-1,2-dichlorodiphosphane with metal tellurolates.At 90 deg C with 2,3-dimethylbutadiene, 7 acts as a source of 1,2-di-tert-butyldiphosphene trapped as cycloadduct 5. - Keywords: cyclophosphanes / phosphorus-carbon heterocycles / cleavage of phosphorus-phosphorus bonds / di(aryltelluro) diphosphanes / diphosphene transfer.
