The isolation from diethyl ether of ionic [(Me2N)3PI]I and [(CH2
CHCH2)2PhPI]I, and the crystallographically characterised molecular ‘spoke’ structure PhMe2PI2
Abstract
Ten new compounds of stoichiometry R3PI2[R3=(o-MeOC6H4)3, (o-MeOC6H4)2Ph, (o-MeOC6H4)Ph2, (p-FC6H4)2Ph, (p-FC6H4)Ph2, (p-CH2CHC6H4)Ph2, (CH2
CHCH2)2Ph, (C6H11)Ph2, (PhCH2CH2)3 or (Me2N)3] have been prepared by the direct reaction of PR3 and I2 in diethyl ether solution. The compounds have been characterised by Raman and solid-state 31P-{H} magic angle spinning (MAS) and solution NMR spectroscopy. Solid-state 31P-{H} MAS NMR studies indicate that the predominant solid-state species is the molecular ‘spoke’ structure R3P–I–I; however, in some cases a minor peak was also assignable to the ionic species, [R3PI]I. Additionally, solid-state 31P-{H} MAS NMR studies of (Me2N)3PI2 and (CH2
CHCH2)2PhPI2 indicate that, in contrast to all other compounds of stoichiometry R3PI2 prepared in diethyl ether, they are exclusively ionic, [R3PI]I. The crystal structure of PhMe2PI2 shows it to have the molecular ‘spoke’ geometry, PhMe2P–I–I, d(I–I)= 3.408 Å, previously observed for Ph3PI2, in agreement with solid-state 31P-{H} MAS NMR results.