2022
DOI: 10.1002/ejic.202200087
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Linear Phenylsilanes with PSi4P, PSi5P, and Si7 Backbones

Abstract: Linear α,ω‐diphosphaoligosilanes were prepared starting from 1,5‐dilithiodecaphenyl‐n‐pentasilane, Li(SiPh2)5Li, and chlorodiorganophosphanes. The compounds 1,5‐bis(diphenylphosphanyl)decaphenyl‐n‐pentasilane, (Ph2P)Si5Ph10(PPh2), 1,5‐bis(di‐iso‐propylphosphanyl)decaphenyl‐n‐pentasilane, (iPr2P)Si5Ph10(PiPr2), and 1,4‐bis(di‐iso‐propylphosphanyl)octaphenyl‐n‐tetrasilane, (iPr2P)Si4Ph8(PiPr2), were obtained in moderate to good yields and characterized with IR‐, Raman‐, UV‐, 31P‐, 29Si‐, and 1H‐NMR spectroscopy.… Show more

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Cited by 1 publication
(2 citation statements)
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“…[106,[125][126][127] Furthermore, it is possible to react the above-mentioned ring opening products with lithiated or halogenated boron or phosphorus compounds to produce linear and cyclic Si/B or Si/P compounds. [128][129][130][131][132][133][134][135] These could serve as precursors for "doped" silicon precursors for the direct deposition of doped silicon layers. However, it may be possible that the Si-B and Si-P bonds are also cleaved when the phenyl groups are removed.…”
Section: Wurtz Coupling Chlorination Hydrogenation -The Classical Met...mentioning
confidence: 99%
See 1 more Smart Citation
“…[106,[125][126][127] Furthermore, it is possible to react the above-mentioned ring opening products with lithiated or halogenated boron or phosphorus compounds to produce linear and cyclic Si/B or Si/P compounds. [128][129][130][131][132][133][134][135] These could serve as precursors for "doped" silicon precursors for the direct deposition of doped silicon layers. However, it may be possible that the Si-B and Si-P bonds are also cleaved when the phenyl groups are removed.…”
Section: Wurtz Coupling Chlorination Hydrogenation -The Classical Met...mentioning
confidence: 99%
“…In this case, the further reaction of the resulting terminally halogenated silicon chains is carried out with lithiated silicon compounds (Scheme 4). [106,125–127] Furthermore, it is possible to react the above‐mentioned ring opening products with lithiated or halogenated boron or phosphorus compounds to produce linear and cyclic Si/B or Si/P compounds [128–135] . These could serve as precursors for “doped” silicon precursors for the direct deposition of doped silicon layers.…”
Section: Synthesis Of Hydrogenated and Chlorinated Oligosilanesmentioning
confidence: 99%