TY - JOUR
T1 - Metathesis of alkanes catalyzed by silica-supported transition metal hydrides
AU - Vidal, Véronique
AU - Théolier, Albert
AU - Thivolle-Cazat, Jean
AU - Basset, Jean-Marie Maurice
PY - 1997/4/4
Y1 - 1997/4/4
N2 - The silica-supported transition metal hydrides (≡Si-O-Si≡)(≡Si-O- )2Ta-H and (≡Si-O-)(x)M-H (M, chromium or tungsten) catalyze the metathesis reaction of linear or branched alkanes into the next higher and lower alkanes at moderate temperature (25°to 200°C). With (≡Si-O-Si≡)(≡Si-O-)2Ta-H, ethane was transformed at room temperature into an equimolar mixture of propane and methane. Higher and lower homologs were obtained from propane, butane, and pentane as well as from branched alkanes such as isobutane and isopentane. The mechanism of the step leading to carbon-carbon bond cleavage and formation likely involves a four-centered transition state between a tantalum-alkyl intermediate and a carbon-carbon σ-bond of a second molecule of alkane.
AB - The silica-supported transition metal hydrides (≡Si-O-Si≡)(≡Si-O- )2Ta-H and (≡Si-O-)(x)M-H (M, chromium or tungsten) catalyze the metathesis reaction of linear or branched alkanes into the next higher and lower alkanes at moderate temperature (25°to 200°C). With (≡Si-O-Si≡)(≡Si-O-)2Ta-H, ethane was transformed at room temperature into an equimolar mixture of propane and methane. Higher and lower homologs were obtained from propane, butane, and pentane as well as from branched alkanes such as isobutane and isopentane. The mechanism of the step leading to carbon-carbon bond cleavage and formation likely involves a four-centered transition state between a tantalum-alkyl intermediate and a carbon-carbon σ-bond of a second molecule of alkane.
UR - http://www.scopus.com/inward/record.url?scp=1842367896&partnerID=8YFLogxK
U2 - 10.1126/science.276.5309.99
DO - 10.1126/science.276.5309.99
M3 - Article
AN - SCOPUS:1842367896
SN - 0036-8075
VL - 276
SP - 99
EP - 102
JO - Science (New York, N.Y.)
JF - Science (New York, N.Y.)
IS - 5309
ER -