By Robert C. West, Anthony F. Hill, Mark J. Fink
Just about all branches of chemistry and fabric technological know-how now interface with organometallic chemistry - the learn of compounds containing carbon-metal bonds. This generally acclaimed serial includes authoritative studies that handle all points of organometallic chemistry, a box which has improved drastically because the book of quantity 1 in 1964.* offers an authoritative, definitive evaluation addressing all features of organometallic chemistry* invaluable to researchers inside this lively box and is a needs to for each sleek library of chemistry* top of the range study e-book inside of this quickly constructing box
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Additional info for Advances in Organometallic Chemistry, Vol. 55
Interestingly, only terminal (anti-Markovnikov) addition of SiH was observed for the polymers 45, as supported by NMR data, and it also appears that the hydrosilation was highly stereoselective towards one isomeric backbone structure. Flexible ﬁbers drawn from the Ph/Me polymer melt could be UV-crosslinked and pyrolyzed to yield ceramic ﬁbers. 152 All three polymers 46a–c exhibited similar UV–visible absorption proﬁles with lmax 260–270 nm. Fluorescence emissions were also observed, with an unusual red-shifted emission for 46a which the authors attribute to possible charge-transfer interaction between Si and the neighboring alkene group in each unit.
209 Over the last 10 years Ozawa and coworkers have investigated the catalytic aspects of hydrosilation in great and ﬁne detail. 211 The large body of mechanistic work with the less active catalytic transition metals has been instrumental to broadening understanding of not only hydrosilation but also the closely related and important reaction dehydrogenative silylation. 212 This was a stirring conclusion, backed also by further studies with colloidal Rh, Pt and other metals,213 that hurled enormous implications at homogeneous catalysis.
133 Several such substrates (acetyl pyridines, acetyl furan, acetyl thiazoles and others) provide high yields and very good to excellent stereoselectivity of the A Review of Recent Progress in Catalyzed Homogeneous Hydrosilation 29 corresponding chiral alcohols, in toluene or toluene–THF solvent at À78 to À35 1C and at 1 mol% catalyst. O R Ar MeO P MeO P Ar R' Ar = Ar Ar O P P O Ar R Ar Ar O R = t-Bu, R' = OMe; R = Me, R' = H 36 Ar 37 A Rh(III) complex 38 assembled from a bis-NHC-functionalized binaphthyl ligand was found to provide excellent asymmetric induction for the hydrosilation of aryl methyl ketones and dialkyl ketones with Ph2SiH2, affording yields and ee’s of 85–96% and 67–98%, respectively [Eq.
Advances in Organometallic Chemistry, Vol. 55 by Robert C. West, Anthony F. Hill, Mark J. Fink
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