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The reaction of trans-[(C(6)F(5))(p-tol(3)P)(2)PtCl] (PtCl) and butadiyne (cat. CuI, HNEt(2)) gives trans-[(C(6)F(5))(p-tol(3)P)(2)Pt(Ctbond;C)(2)H] (PtC(4)H, 81 %), which reacts with excess HC(triple bond)CSiEt(3) under Hay coupling conditions (O(2), cat. CuCl/TMEDA, acetone) to yield PtC(6)Si (53 %). A solution of PtC(6)Si in acetone is treated with wet nBu(4)NF to generate PtC(6)H. The addition of ClSiMe(3) (F(-) scavenger) and then excess HC(triple bond)CSiEt(3) under Hay conditions gives PtC(8)Si (39 %). Hay homocouplings of PtC(4)H, PtC(6)H, and PtC(8)H (generated in situ analogously to PtC(6)H) yield PtC(8)Pt, PtC(12)Pt, and PtC(16)Pt (97-92 %). Reactions of PtC(4)H and PtC(6)H with PtCl (cat. CuCl, HNEt(2)) give PtC(4)Pt and PtC(6)Pt (69 %, 34 %). The attempted conversion of PtC(8)H to PtC(10)Si affords mainly PtC(16)Pt, with traces of PtC(20)Pt and PtC(24)Pt. The complexes PtC(x)Pt are exceedingly stable (dec pts 234 to 288 degrees C), and Et(3)P displaces p-tol(3)P to give the corresponding compounds Pt'C(8)Pt' and Pt'C(12)Pt' (94-90 %). The effect of carbon chain lengths upon IR nu(C(triple bond)C) patterns (progressively more bands), UV/Vis spectra (progressively red-shifted and more intense bands with epsilon >600 000 M(-1) cm(-1)), redox properties (progressively more difficult and less reversible oxidations), and NMR values are studied, and analyzed with respect to the polymeric sp carbon allotrope "carbyne". The crystal structure of PtC(12)Pt shows a dramatic, unprecedented degree of chain bending, whereas the chains in PtC(8)Pt, Pt'C(12)Pt', and PtC(16)Pt are nearly linear.

Reactions of the tertiary phosphines R(3)P (R = Me, Bu, Oct, Cy, Ph) with 35% aqueous H(2)O(2) gives the corresponding oxides as the H(2)O(2) adducts R(3)P=O·(H(2)O(2))(x) (x = 0.5-1.0). Air oxidation leads to a mixture of products due to the insertion of oxygen into one or more P-C bonds. (31)P NMR spectroscopy in solution and in the solid state, as well as IR spectroscopy reveal distinct features of the phosphine oxides as compared to their H(2)O(2) adducts. The single crystal X-ray analyses of Bu(3)P=O and [Cy(3)P=O·(H(2)O(2))](2) show a P=O stacking motif for the phosphine oxide and a cyclic structure, in which the six oxygen atoms exhibit a chair conformation for the dimeric H(2)O(2) adduct. Different methods for the decomposition of the bound H(2)O(2) and the removal of the ensuing strongly adsorbed H(2)O are evaluated. Treating R(3)P=O·(H(2)O(2))(x) with molecular sieves destroys the bound H(2)O(2) safely under mild conditions (room temperature, toluene) within one hour and quantitatively removes the adsorbed H(2)O from the hygroscopic phosphine oxides within four hours. At 60 °C the entire decomposition/drying process is complete within one hour.

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