The phosphaethynolate anion, also referred to as PCO, is the phosphorus-containing analogue of the cyanate anion with the chemical formula [PCO] or [OCP] . The anion has a linear geometry and is commonly isolated as a salt. When used as a ligand, the phosphaethynolate anion is ambidentate in nature meaning it … See more The first reported synthesis and characterisation of phosphaethynolate came from Becker et al. in 1992. They were able to isolate the anion as a lithium salt (in 87% yield) by reacting lithium bis(trimethylsilyl)phosphide … See more Extensive studies involving the phosphaethynolate anion have shown that it can react in a variety of ways. It has documented use in cycloadditions, as a phosphorus transfer agent, a synthetic building block and as pseudo halide ligands (as … See more The phosphaethynolate anion is the heavier isoelectronic congener of the cyanate anion. It has been shown that it behaves in a similar way to its lighter analogue, as an … See more The other analogues of the phosphaethynolate anion all obey the general formulae E-C-X and are made by varying E and X. When changing either atom, unique trends … See more WebJul 22, 2024 · In the last seven years, chemistry of the phosphaethynolate reagent, Na (OCP) (1,4-dioxane) 2.5, has seen a surge in organic and inorganic chemistry—A renaissance to …
The 2-phosphaethynolate anion: convenient synthesis and the …
WebApr 1, 2024 · Here we review the chemistry of the 2‐phosphaethynolate anion, a heavier phosphorus‐containing analogue of the cyanate anion, and describe the wide breadth of chemical transformations for which... WebAccompanied by the release of CO 2, Na 2 (P 2 C 3 O 4) 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 Na 2 (P 2 C 3 O 4) and the results are discussed in detail. how many times greater is 3.4 than 1.7
The Rise of Phosphaethynolate Chemistry in Early …
WebJan 22, 2014 · The straightforward synthesis of functionalized heterocycles on a larger scale remains a challenge. Herein, we report the use of the phosphaethynolate (OCP) − anion as a building block for various sterically unprotected and functionalized hydroxy substituted phosphorus heterocycles. WebSep 9, 2016 · In seeking to assess the influence of such factors, and thus potentially to elaborate means of control over reactivity, we report herein the synthesis and characterization of an extended range of these novel pyrazolylphosphaalkene complex. Scheme 1. Synthesis of [Ru {η 1 - N :η 2 - P, C -P (pz′)=CH (SiMe 2 R)} (CO) (PPh 3) 2] ( 2 – … WebIn organic chemistry, the oxy-Cope rearrangement is a chemical reaction.It involves reorganization of the skeleton of certain unsaturated alcohols. It is a variation of the Cope rearrangement in which 1,5-dien-3-ols are converted to unsaturated carbonyl compounds by a mechanism typical for such a [3,3]-sigmatropic rearrangement.. The reaction is highly … how many times greater is 2 than 1/8