F. Bitterer et al., LINEAR OLIGOPHOSPHAALKANES .28.1. REDOX C YCLIZATION OF FUNCTIONAL METHYLENEBISPHOSPHANES XRP-CH2-PRX (X=H, CL) WITH CYCLOPOLYPHOSPHANES, Zeitschrift fur Naturforschung. B, A journal of chemical sciences, 50(10), 1995, pp. 1521-1526
Reaction of P-H or P-Cl functional methylenebisphosphanes X(R)P- CH2-P
(R)X (X = H, Cl; R = Ph, tBu) with cyclopolyphosphanes (R'P)(n) (R' =
Ph, tBu, Me; n = 4, 5) affords cyclocarbatetraphosphanes CH2(RP)(2)(R'
P)(2) (2-6). The cyclopolyphosphanes (R'P)(n) employed may be synthesi
zed in situ by reaction of chlorophosphanes R'PCl2 with primary phosph
anes R'PH2, LiH or magnesium, respectively, providing a single stage s
ynthesis for unsymme trically substituted cyclocarbatetraphosphanes.