Direct Functionalization of White Phosphorus to Cyclotetraphosphanes: Selective Formation of Four P–C Bonds

Converting elemental white phosphorus directly into organophosphorus or polyphosphorus is meaningful, challenging and attractive. The ate-complexes of aluminacyclopentadienes 1a, b react with P 4 to afford selectively the cyclotetraphosphanes 2a, b featuring four newly formed P–C bonds and a planar square cyclo -P 4 ring. Density functional theory calculations show that the conversion of tetrahedral P 4 to planar cyclo -P 4 moiety undergoes through an unexpected 1,1- P -insertion/Diels–Alder reaction/isomerization cascade process. The reaction of 2a with iodomethane or p -benzoquinone afforded the P -methylation product 3 and the metal-free cyclotetraphosphane 4, respectively. Interestingly, reduction of 4 generated the phospholyl anions 5 and 6 while treatment of 4 with iodomethane afforded the phospholyl cation 7 .