Organolanthanide-catalyzed dehydrogenative coupling of silanes. Mechanistic implications

Craig M. Forsyth; Steven P. Nolan; Tobin J Marks

Organolanthanide-catalyzed dehydrogenative coupling of silanes. Mechanistic implications

Craig M. Forsyth, Steven P. Nolan, Tobin J Marks

Northwestern University

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

99 Citations (Scopus)

Abstract

Organolanthanide complexes of the type Cp′₂LnR (Cp′ = η⁵-Me₅C₅; Ln = La, Nd, Sm, Y, Lu; R = H, CH(SiMe₃)₂), Me₂SiCp″₂LnR (Cp″ = η⁵-Me₄C₅; Ln = Nd; R = CH(SiMe₃)₂), Cp′₂Sm, and Cp′₂Sm(THF)₂ catalyze the rapid dehydrogenative oligomerization of PhSiH₃. Kinetic and mechanistic arguments exclude the importance of metal-centered redox processes in the catalytic cycle and support instead "four-center" "heterolytic" bond-scission/bond-forming sequences.

Original language	English
Pages (from-to)	2543-2545
Number of pages	3
Journal	Organometallics
Volume	10
Issue number	8
Publication status	Published - 1991

ASJC Scopus subject areas

Inorganic Chemistry
Organic Chemistry

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title = "Organolanthanide-catalyzed dehydrogenative coupling of silanes. Mechanistic implications",

abstract = "Organolanthanide complexes of the type Cp′2LnR (Cp′ = η5-Me5C5; Ln = La, Nd, Sm, Y, Lu; R = H, CH(SiMe3)2), Me2SiCp″2LnR (Cp″ = η5-Me4C5; Ln = Nd; R = CH(SiMe3)2), Cp′2Sm, and Cp′2Sm(THF)2 catalyze the rapid dehydrogenative oligomerization of PhSiH3. Kinetic and mechanistic arguments exclude the importance of metal-centered redox processes in the catalytic cycle and support instead {"}four-center{"} {"}heterolytic{"} bond-scission/bond-forming sequences.",

author = "Forsyth, {Craig M.} and Nolan, {Steven P.} and Marks, {Tobin J}",

year = "1991",

language = "English",

volume = "10",

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journal = "Organometallics",

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T1 - Organolanthanide-catalyzed dehydrogenative coupling of silanes. Mechanistic implications

AU - Forsyth, Craig M.

AU - Nolan, Steven P.

AU - Marks, Tobin J

PY - 1991

Y1 - 1991

N2 - Organolanthanide complexes of the type Cp′2LnR (Cp′ = η5-Me5C5; Ln = La, Nd, Sm, Y, Lu; R = H, CH(SiMe3)2), Me2SiCp″2LnR (Cp″ = η5-Me4C5; Ln = Nd; R = CH(SiMe3)2), Cp′2Sm, and Cp′2Sm(THF)2 catalyze the rapid dehydrogenative oligomerization of PhSiH3. Kinetic and mechanistic arguments exclude the importance of metal-centered redox processes in the catalytic cycle and support instead "four-center" "heterolytic" bond-scission/bond-forming sequences.

AB - Organolanthanide complexes of the type Cp′2LnR (Cp′ = η5-Me5C5; Ln = La, Nd, Sm, Y, Lu; R = H, CH(SiMe3)2), Me2SiCp″2LnR (Cp″ = η5-Me4C5; Ln = Nd; R = CH(SiMe3)2), Cp′2Sm, and Cp′2Sm(THF)2 catalyze the rapid dehydrogenative oligomerization of PhSiH3. Kinetic and mechanistic arguments exclude the importance of metal-centered redox processes in the catalytic cycle and support instead "four-center" "heterolytic" bond-scission/bond-forming sequences.

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M3 - Article

AN - SCOPUS:0001750853

VL - 10

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JO - Organometallics

JF - Organometallics

SN - 0276-7333

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ER -

Organolanthanide-catalyzed dehydrogenative coupling of silanes. Mechanistic implications

Abstract

ASJC Scopus subject areas

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