A Selective Synthesis of the 1,3,4-Triphospholide Anion

Fish, Cheryl; Green, Michael; Jeffery, John C.; Kilby, Richard J.; Lynam, Jason M.; Russell, Christopher A.; Willans, Charlotte E.

doi:10.1021/om050766d

Cited by 40 publications

(19 citation statements)

References 16 publications

Supporting

Mentioning

Contrasting

Unclassified

Order By: Relevance

“…[22][23][24] Such mixtures can be separated by repeated fractional crystallisation of the sodium salts from thf. 1-Triorganylstannyl-1,2,4-triphospholes are accessible from the sodium salt Na5 upon treatment with the corresponding triorganyltin chloride (R 3 SnCl, 6).…”

Section: Resultsmentioning

confidence: 99%

Rock around the Ring: An Experimental and Theoretical Study of the Molecular Dynamics of Stannyltriphospholes with Chiral Tin Substituents

Hofmann

Clark²,

Heinemann

et al. 2008

Eur J Inorg Chem

View full text Add to dashboard Cite

The reaction of diphenyltin dichloride with enantiopure Grignard reagents prepared in situ leads to diphenyltin chlorides 7a-e, which contain chiral organyl substituents. The 2-bornyl derivative 7a forms a mixture of exo and endo isomers and the (-)-menthyl derivative 7b yields a mixture of epimers, whereas the cis-and trans-myrtanyl complexes 7c and 7d and the m-(2-bornyl-2-ene)phenyl species 7e form only one enantiomer as the tin atom is separated from the next stereogenic centre by a methylene or m-phenylene group. The target chirally modified 1-(triorganylstannyl)-1,2,4-triphospholes 2a-e are accessible from 7a-e by treatment of the latter with the salt (3,5-di-tert-butyl-1,2,4-triphospholyl)-sodium (Na5) in good yield. As for 7c-e, complexes 2c-e exhibit enantiopure organyl tin substituents that combine with the planar chiral 1,2,4-triphosphole moiety to form diastereomers. X-ray diffraction studies on crystalline phases of

show abstract

Section: Resultsmentioning

confidence: 99%

Rock around the Ring: An Experimental and Theoretical Study of the Molecular Dynamics of Stannyltriphospholes with Chiral Tin Substituents

Hofmann

Clark²,

Heinemann

et al. 2008

Eur J Inorg Chem

View full text Add to dashboard Cite

show abstract

“…The Mg-P (2.6224(7) Å ) and Mg-C (mean: 2.484 Å ) distances in that compound are markedly shorter than those in 1, again most probably because of the lesser steric bulk of its phosphorus heterocycle. The only other structurally characterized magnesium complex incorporating a phospholyl anion is [(THF) 3 Mg(l-Cl) 3 Mg(THF) 3 ][1,2,4-P 3 C 2 Bu 2 t ] [10], though this is a salt with a free triphospholyl anion that has no interaction with either Mg centre. We are currently exploring the use of 1 as a reagent for the transfer of its diphospholyl anion to less electropositive metals.…”

Section: Resultsmentioning

confidence: 99%

Synthesis and Crystal Structure of a Diphospholyl Magnesium(II) Chloride Complex

Jones

Schulten

2012

J Chem Crystallogr

View full text Add to dashboard Cite

The reaction of the diphospholyl anion, [1,3-P 2 C 3 Bu 3 t ] -(generated by reaction of the phosphaalkyne, P:CBu t , with sodium metal) with MgCl 2 has afforded the dimeric diphospholyl magnesium(II) chloride complex, [{Mg(g 5 -1,3-P 2 C 3 Bu 3 t )(THF)(l-Cl)} 2 ] 1. The cell parameters of compound 1Á(hexane) are: P-1, a = 10.792 (2) Å , b = 10.969(2) Å , c = 12.484(3) Å ; a = 64.38(3)°, b = 68.96(3)°, c = 83.10(3)°. The compound represents the first structurally characterized example of a group 2 metal diphospholyl.

show abstract

“…[13,14] In contrast, the all-phosphorus analogue of A, the tetraphosphacyclobutane complex C, which was synthesized in 1988 by Scherer et al, [15] has to date not been used for subsequent reactions. One reason might be its limited stability; it is only stable if Cp'' (Cp'' = h 5 -C 5 H 3 tBu 2 -1,3) is present as auxiliary ligand.…”

mentioning

confidence: 99%

Access to Phosphorus‐Rich Zirconium Complexes

et al. 2011

View full text Add to dashboard Cite

The missing member [Cp′′2Zr(η2‐P3CtBu)] (Cp′′=η5‐C5H3tBu2) of the phosphorus‐containing bicyclobutane zirconium complex family was synthesized by reaction between tetraphosphazirconocene derivative [Cp′′2Zr(η2‐P4)] and a phosphaalkyne with the release of a formal P2 unit. Synthetic evidence of another unknown isomer [Cp′′2Zr(η2‐P2(CtBu)2)] was found; according to DFT calculations, it is the stable form if a Cp′′2Zr moiety is used.

show abstract

A Selective Synthesis of the 1,3,4-Triphospholide Anion

Cited by 40 publications

References 16 publications

Rock around the Ring: An Experimental and Theoretical Study of the Molecular Dynamics of Stannyltriphospholes with Chiral Tin Substituents

Rock around the Ring: An Experimental and Theoretical Study of the Molecular Dynamics of Stannyltriphospholes with Chiral Tin Substituents

Synthesis and Crystal Structure of a Diphospholyl Magnesium(II) Chloride Complex

Access to Phosphorus‐Rich Zirconium Complexes

Contact Info

Product

Resources

About