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DOI: 10.1016/S0022-328X(96)06734-4

Source and publish data:

Journal of Organometallic Chemistry p. 117 - 123 (1997)

Update date:2022-08-02

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Authors:

TillackTillack

PulstPulst

BaumannBaumann

BaudischBaudisch

KortusKortus

RosenthalRosenthal

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Article abstract of DOI:10.1016/S0022-328X(96)06734-4

The hydrosilatation of nPr-C≡C-nPr, Ph-C≡C-Ph, Me3Si-C≡C-SiMe3, Ph-C≡C-C≡C-Ph, tBu-C≡C-C≡C-tBu and Me3Si-C≡C-C≡C-SiMe3 with Ph2SiH2, PhMe2SiH and Et3SiH in the presence of L2Ni(0)-butadiyne catalysts [L = Ph3P, (o-Tol-O)3P] has been studied. In all cases the hydrosilylation proceeds via a via a cis-addition of the silanes. The disubstituted alkynes (nPr-C≡C-nPr, Ph-C≡C-Ph) give hydrosilylated ethene, butadiene and hexatriene derivatives as well as non-hydrosilylated benzene derivatives. In the case of Me3Si-C≡C-SiMe3 no reaction was observed. The hydrosilylation of disubstituted butadiynes proceeds stepwise to give at first the 1,2-adducts. In dependence on the butadiynes either a 1,4-addition (tBu-C≡C-C≡C-tBu, Me3Si-C≡C-C≡C-SiMe3) to the corresponding allene derivatives (11, 13, 15) or a 3,4-addition (Ph-C≡C-C≡C-Ph) to the 1,3-butadiene 19 takes place subsequently. The reaction products were characterized by mass spectrometry, IR and NMR spectroscopy.

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Full text of DOI:10.1016/S0022-328X(96)06734-4

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Product name:(E)-2-diphenylsilyl-1,4-bis(trimethylsilyl)-1-buten-3-yne

Cas No:103716-83-2

103716-83-2

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