1-Trimethylsilylphosphirane as a ligand and as a stable masked reagent for phosphirane

Huw A. Tallis; Paul D. Newman; Peter G. Edwards; Liling Ooi; Andreas Stasch

doi:10.1039/b715327a

1-Trimethylsilylphosphirane as a ligand and as a stable masked reagent for phosphirane

Huw A. Tallis
, Paul D. Newman
, Peter G. Edwards^*
, Liling Ooi
, Andreas Stasch

^*Corresponding author for this work

School of Chemistry

Research output: Contribution to journal › Article › peer-review

Abstract

1-Trimethylsilylphosphirane, C₂H₄PSiMe₃, has been prepared on a multi gram scale from P(SiMe₃)₃ via ClCH₂CH₂P(SiMe₃)₂. C ₂H₄PSiMe₃ is readily susceptible to protonolysis forming the thermally unstable parent phosphirane, C ₂H₄PH, in good yields. Reaction of C₂H ₄PSiMe₃ with fac-M (CO)₃(CH₃CN) ₃ (M = Cr, Mo) or [Fe(η⁵-C₅H ₅)(η⁶-C₆H₆)](PF₆) give rise to fac-M(CO)₃(C₂H₄PSiMe ₃)₃ and [Fe(η⁵-C₅H ₅)(C₂H₄PSiMe₃)₃](PF ₆) respectively. Protonolysis of the free or coordinated 1-trimethylsilylphosphirane readily causes P-Si cleavage to give rise to the parent C₂H₄PH or the respective complexes, fac-M(CO) ₃(C₂H₄PH)₃ and fac- [Fe(η⁵-C₅H₅)(C₂H ₄PH)₃](PF₆) in situ. All new complexes are characterised by analytical and spectroscopic methods and the X-ray crystal structures of fac-Cr(CO)₃(C₂H₄PSiMe ₃)₃ and fac-Mo(CO)₃(C₂H ₄PH)₃ have also been determined.

Original language	English
Pages (from-to)	47-53
Number of pages	7
Journal	Dalton Transactions
Issue number	1
DOIs	https://doi.org/10.1039/b715327a
Publication status	Published - 2008

Access to Document

10.1039/b715327a

Handle.net

Persistent link to portal record

Cite this

@article{28365875ab2048358370616a4a2d44ea,

title = "1-Trimethylsilylphosphirane as a ligand and as a stable masked reagent for phosphirane",

abstract = "1-Trimethylsilylphosphirane, C2H4PSiMe3, has been prepared on a multi gram scale from P(SiMe3)3 via ClCH2CH2P(SiMe3)2. C 2H4PSiMe3 is readily susceptible to protonolysis forming the thermally unstable parent phosphirane, C 2H4PH, in good yields. Reaction of C2H 4PSiMe3 with fac-M (CO)3(CH3CN) 3 (M = Cr, Mo) or [Fe(η5-C5H 5)(η6-C6H6)](PF6) give rise to fac-M(CO)3(C2H4PSiMe 3)3 and [Fe(η5-C5H 5)(C2H4PSiMe3)3](PF 6) respectively. Protonolysis of the free or coordinated 1-trimethylsilylphosphirane readily causes P-Si cleavage to give rise to the parent C2H4PH or the respective complexes, fac-M(CO) 3(C2H4PH)3 and fac- [Fe(η5-C5H5)(C2H 4PH)3](PF6) in situ. All new complexes are characterised by analytical and spectroscopic methods and the X-ray crystal structures of fac-Cr(CO)3(C2H4PSiMe 3)3 and fac-Mo(CO)3(C2H 4PH)3 have also been determined.",

author = "Tallis, \{Huw A.\} and Newman, \{Paul D.\} and Edwards, \{Peter G.\} and Liling Ooi and Andreas Stasch",

year = "2008",

doi = "10.1039/b715327a",

language = "English",

pages = "47--53",

journal = "Dalton Transactions",

issn = "1477-9226",

publisher = "Royal Society of Chemistry",

number = "1",

}

TY - JOUR

T1 - 1-Trimethylsilylphosphirane as a ligand and as a stable masked reagent for phosphirane

AU - Tallis, Huw A.

AU - Newman, Paul D.

AU - Edwards, Peter G.

AU - Ooi, Liling

AU - Stasch, Andreas

PY - 2008

Y1 - 2008

N2 - 1-Trimethylsilylphosphirane, C2H4PSiMe3, has been prepared on a multi gram scale from P(SiMe3)3 via ClCH2CH2P(SiMe3)2. C 2H4PSiMe3 is readily susceptible to protonolysis forming the thermally unstable parent phosphirane, C 2H4PH, in good yields. Reaction of C2H 4PSiMe3 with fac-M (CO)3(CH3CN) 3 (M = Cr, Mo) or [Fe(η5-C5H 5)(η6-C6H6)](PF6) give rise to fac-M(CO)3(C2H4PSiMe 3)3 and [Fe(η5-C5H 5)(C2H4PSiMe3)3](PF 6) respectively. Protonolysis of the free or coordinated 1-trimethylsilylphosphirane readily causes P-Si cleavage to give rise to the parent C2H4PH or the respective complexes, fac-M(CO) 3(C2H4PH)3 and fac- [Fe(η5-C5H5)(C2H 4PH)3](PF6) in situ. All new complexes are characterised by analytical and spectroscopic methods and the X-ray crystal structures of fac-Cr(CO)3(C2H4PSiMe 3)3 and fac-Mo(CO)3(C2H 4PH)3 have also been determined.

AB - 1-Trimethylsilylphosphirane, C2H4PSiMe3, has been prepared on a multi gram scale from P(SiMe3)3 via ClCH2CH2P(SiMe3)2. C 2H4PSiMe3 is readily susceptible to protonolysis forming the thermally unstable parent phosphirane, C 2H4PH, in good yields. Reaction of C2H 4PSiMe3 with fac-M (CO)3(CH3CN) 3 (M = Cr, Mo) or [Fe(η5-C5H 5)(η6-C6H6)](PF6) give rise to fac-M(CO)3(C2H4PSiMe 3)3 and [Fe(η5-C5H 5)(C2H4PSiMe3)3](PF 6) respectively. Protonolysis of the free or coordinated 1-trimethylsilylphosphirane readily causes P-Si cleavage to give rise to the parent C2H4PH or the respective complexes, fac-M(CO) 3(C2H4PH)3 and fac- [Fe(η5-C5H5)(C2H 4PH)3](PF6) in situ. All new complexes are characterised by analytical and spectroscopic methods and the X-ray crystal structures of fac-Cr(CO)3(C2H4PSiMe 3)3 and fac-Mo(CO)3(C2H 4PH)3 have also been determined.

UR - https://www.scopus.com/pages/publications/37249058979

U2 - 10.1039/b715327a

DO - 10.1039/b715327a

M3 - Article

AN - SCOPUS:37249058979

SN - 1477-9226

SP - 47

EP - 53

JO - Dalton Transactions

JF - Dalton Transactions

IS - 1

ER -

1-Trimethylsilylphosphirane as a ligand and as a stable masked reagent for phosphirane

Abstract

Access to Document

Handle.net

Other files and links

Fingerprint

Cite this