Phosphaethynolate
WebMay 17, 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... WebAbstract. The reaction of the 2-phosphaethynolate anion and primary amines for the mechanochemical synthesis of phosphinecarboxamides was studied. The reaction has its …
Phosphaethynolate
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WebThe reaction of the pentaphenylborole [(PhC)4BPh] (1) with sodium phosphaethynolate·1,4-dioxane (NaOCP(1,4-dioxane)1.7) afforded the novel sodium salt of phosphaboraheterocycle 2. It comprises anionic fused tetracyclic P/B-heterocycles that arise from multiple bond activation between the borole backbone and [OCP]−anion. Density functional theory … WebOct 4, 2024 · Decarbonylation along with P-atom transfer from the phosphaethynolate anion, PCO −, to the Nb IV complex [(PNP)NbCl 2 (N t BuAr)] (1) (PNP=N[2-P i Pr 2-4-methylphenyl] 2 −; Ar=3,5-Me 2 C 6 H 3) results in its coupling with one of the phosphine arms of the pincer ligand to produce a phosphanylidene phosphorane complex [(PNPP)NbCl(N t BuAr)] …
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 WebSodium phosphaethynolate, Na(OCP), reacts as a P− transfer reagent with the imidazolium salt [DippNHC–H][Cl] [DippNHC = 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene] to give …
WebIntroduction. There is burgeoning interest in the emerging, fundamental chemistry of the 2-phosphaethynolate (OCP) − anion, not only because regular investigations of this anion became practicable only around a decade ago but also because it is a valence isoelectronic, P-analogue of the ubiquitous cyanate (OCN) − anion. 1 In terms of the fundamental redox … 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.
WebFrom 2-phosphaethynolate anion (− OC≡P) An actinide cyaphide complex can be prepared by C−O bond cleavage of the phosphaethynolate anion, the phosphorus analogue of …
erythropiotinWebMay 24, 2024 · The coordination mode of this trapped 2-phosphaethynolate is unique, and derives from an unprecedented highly reduced and highly bent form of this ligand with the most acute P-C-O angle in any complex to date (P-C-O ∡ ≈127°). The characterisation data support a mixed-valence diuranium(III/IV) formulation, ... erythropoese ablaufWebJan 18, 2024 · The reduction chemistry of the newly emerging 2-phosphaethynolate (OCP) - is not well explored, and many unanswered questions remain about this ligand in this … finger razor lawn mowerWebDec 8, 2024 · The phosphaethynolate anion, (OCP) −, may be regarded as the phosphorus analogue of cyanate, (OCN) −. 3 Natural Resonance Theory calculations have shown that (OCP) − has three major resonance structures: [O–C P] − (51.7%), [O C P] − (40.2%) and [O C → P] − (7.1%). 4 Recently, reactivity studies involving these salts has led to the formation … erythropoese woWebAccompanied 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. finger rash treatmentWebRecently, we have been exploring the chemistry of sodium phosphaethynolate, Na [OCP], which can be viewed as a hybrid of three resonance structures, a phosphaethynolate [O–C P] −, a phosphaketenide [O C P] − and a P-transfer reagent [O C→P] −. erythropoetin fachinformationWebHerein, we introduce sodium phosphaethynolate as an alternative, cheap and low-toxic phosphorus source for the synthesis of highly emitting InP-based QDs. The resulting QDs possess a size-tunable photoluminescence wavelength range between 465 and 620 nm and high emission quantum yield between 43 and 97%. erythropoietic protoporphyria genereviews