A Stabilized Phosphinothioylidene Generated by Deselenation of a Selenoxothioxophosphorane

A Stabilized Phosphinothioylidene Generated by Deselenation of a Selenoxothioxophosphorane
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硒氧硫代正膦脱硒产生的稳定亚膦基硫代膦

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发表时间:
1993
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通讯作者:
Kozo Toyota
Kozo Toyota
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作者:
M. Yoshifuji;S. Sangu;Masaru Hirano;Kozo Toyota

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合成了硒氧硫代(2,4-二叔丁基-6-二甲氨基苯基)正膦,并与三二甲氨基膦脱硒,首次得到相应的硫代亚膦(硫代膦、硫代膦或硫代亚膦),它是一种热稳定的化合物,被认为是由邻二甲氨基的孤对电子稳定的。
Selenoxothioxo(2,4-di-t-butyl-6-dimethylaminophenyl)phosphorane was prepared and was deselenated with tris(dimethylamino)phosphine to give the corresponding phosphinothioylidene (thioxophosphine, thionophosphine, or phosphinidene sulfide), for the first time, as a thermally stable compound, which is considered to be stabilized with the lone pair electrons of the o-dimethylamino group.