182359-52-0Relevant academic research and scientific papers
Effects of a sterically demanding P-aryl substituent in phosphole and 7-phosphanorbornene chemistry
Quin, Louis D.,Ionkin, Alexey S.,Kalgutkar, Rajdeep,Keglevich, Gyoergy
, p. 433 - 436 (2007/10/03)
The 2,4-di-tert-butyl-6-methylphenyl substituent was placed on phosphorus of a phosphole, causing restricted rotation about the P-C bond and flattening of the phosphorus pyramid. Electron delocalization was greater in this phosphole as a result of the fla
Phospholes with reduced pyramidal character from steric crowding. 1. Synthesis and NMR characterization of 1-(2,4-di-tert-butyl-6-methylphenyl)-3-methylphosphole
Quin, Louis D.,Keglevich, Gy?rgy,Ionkin, Alexey S.,Kalgutkar, Rajdeep,Szalontai, Gábor
, p. 7801 - 7807 (2007/10/03)
The sterically crowded 1-(2,4-di-tert-butyl-6-methylphenyl)-3-methylphosphole was synthesized by dehydrohalogenation of the corresponding 3,4-dibromophospholane, in order to probe the possibility that the steric congestion would cause some flattening of the phosphorus pyramid and an increase in electron delocalization. The phosphole was a recrystallizable solid with 31P NMR δ 1.8. Semiempirical calculations indicated that the pyramidal shape was retained but was noticeably flatter than in 1-phenylphosphole. In the low energy conformation, the phosphole and phenyl ring planes are approximately orthogonal, with the 2-tert-butyl group in the less crowded position that is syn to the lone pair on phosphorus. The 6-methyl group is positioned under the phosphole ring. This conformational prediction was amply confirmed by several chemical shift and coupling effects in the 13C NMR spectrum. The 1H NMR spectrum displayed an unusually large four-bond coupling (6 Hz) of 31P to the m-phenyl proton syn to the lone pair (and none to the anti-meta proton), consistent with the orthogonal conformation. The oxide of the phosphole showed more stability than that of less crowded phospholes and gave a 31P NMR signal that was detectable over a several hour period at room temperature. The oxide proceeded to give the usual Diels-Alder dimer and also formed a cycloadduct with N-phenylmaleimide. The phosphoryl group of the latter was reduced with trichlorosilane to give the phosphine. This new 7-phosphanorbornene derivative gave the most downfield 31P NMR shift (δ 153.3) of any member of this family, all of which are characterized by remarkable deshielding in the syn isomer.
