Conclusions
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1.
We have prepared O-etbyl carboranylmethylphosphinites and studied their reactions with p-nitrophenyl azide, chlorine, dimethyl sulfate, methyl iodide, chloral, and water. The carboranylmethylphosphinites exhibit greater reactivity than carboranylphosphonites.
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2.
The carboranyl group attached to the phosphorus atom has a pronounced electron-acceptor effect, and substituents attached to the second carbon atom of the o-carboranyl nucleus have a weak influence on the overall electronic effect ofthe carboranyl group.
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N. N. Godovikov, A. N. Degtyarev, V. I. Bregadze, and M. I. Kabachnik, Izv. Akad. Nauk SSSR, Ser. Khim., 2568 (1975).
E. Steininger, Chem. Ber.,95, 2993 (1962).
N. N. Godovikov, A. N. Degtyarev, V. I. Bregadze, and M. I. Kabachnik, Izv. Akad. Nauk SSSR, Ser. Khim., 2797 (1975).
E. I. Matrosov, A. G. Kozachenko, and M. I. Kabachnik, Izv. Akad. Nauk SSSR, Ser. Khim., 1476 (1976).
I. N. Zhmurova, V. G. Yurchenko, V. P. Kukhar', and A. A. Zolotareva, Zh. Obshch. Khim.,42, 6256 (1972).
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 9, pp. 2099–2104, September, 1978.
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Degtyarev, A.N., Godovikov, N.N., Bregadze, V.I. et al. Synthesis and chemical properties of some carboranylmethylphosphinite esters. Russ Chem Bull 27, 1851–1857 (1978). https://doi.org/10.1007/BF00929237
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DOI: https://doi.org/10.1007/BF00929237