Simple basic ingredients are at the origin of the synthesis of Na(OCP), the phosphorus analogue of sodium cyanate. Na(OCP) is obtained from NaPH2 (made from Na, P, and a proton source) and CO (from carbon and air). This salt is remarkably stable, in complete contrast to HCP discovered 50 years ago.

Carbon dioxide and two equivalents of Na(OCP) form, in an equilibrium reaction, a CO2 adduct of the composition Na2(P2C3O4). The anion of this salt, [O2C-P(CO)2P](2-), is built up by a four-membered 1,3-diphosphetane-2,4-dione ring and a carboxylate unit attached to one of the phosphorus atoms. A remarkable π-delocalization was observed within the OCPCO moiety. The stepwise reaction mechanism leading to Na2(P2C3O4) was investigated with quantum chemical calculations. Accompanied by the release of CO2, Na2(P2C3O4) reacts with both 2-iodopropane and 4,4',4''-trimethoxytriphenylmethyl chloride to form four-membered cyclic anions. For comparison the analogous reactions were performed with Na(OCP) instead of Na2(P2C3O4) and the results are discussed in detail.

The reactivity of Na(OCP) was investigated towards triorganyl compounds of the heavier group 14 elements (R3EX R = Ph or (i)Pr; E = Si, Ge, Sn, Pb; X = Cl, OTf). In the case of E = Si two constitutional isomers were formed and characterised in situ: R3Si-O-C[triple bond, length as m-dash]P is the kinetic and R3Si-P[double bond, length as m-dash]C[double bond, length as m-dash]O is the thermodynamic product, representing experimental evidence of the ambident character of the (OCP)(-) anion. Applying theoretical calculations and spectroscopic methods, the compound previously reported as (i)Pr3Si-O-C[triple bond, length as m-dash]P can now unambiguously be identified as (i)Pr3Si-P[double bond, length as m-dash]C[double bond, length as m-dash]O. The heavier analogues form exclusively the phosphaketene isomer R3E-P[double bond, length as m-dash]C[double bond, length as m-dash]O (E = Ge, Sn, Pb). DFT calculations were performed to gain deeper insight into the bonding and thermodynamic stability of these compounds.

The terminal rhenium(I) phosphaethynolate complex [Re(PCO)(CO)(2)(triphos)] has been prepared in a salt metathesis reaction from Na(OCP) and [Re(OTf)(CO)(2)(triphos)]. The analogous isocyanato complex [Re(NCO)(CO)(2)(triphos)] has been likewise prepared for comparison. The structure of both complexes was elucidated by X-ray diffraction studies. While the isocyanato complex is linear, the phosphaethynolate complex is strongly bent around the pnictogen center. Computations including natural bond orbital (NBO) theory, natural resonance theory (NRT), and natural population analysis (NPA) indicate that the isocyanato complex can be viewed as a classic Werner-type complex, that is, with an electrostatic interaction between the Re(I) and the NCO group. The phosphaethynolate complex [Re(P=C=O)(CO)(2)(triphos)] is best described as a metallaphosphaketene with a Re(I)-phosphorus bond of highly covalent character.

Na(OCP) initiates the catalytic cyclo-trimerization of isocyanates involving the mutual formation of P-heterocycles and spiro phosphoranides (shown on the right) as reactive intermediates.