Ruthenium carbenes supported on mesoporous silicas as highly active and selective hybrid catalysts for olefin metathesis reactions under continuous flow.

In the search for a highly active and selective heterogenized metathesis catalyst, we systematically varied the pore geometry and size of various silica-based mesoporous (i.e., MCM-41, MCM-48, and SBA-15) and microporous (ZSM-5 and MWW) versus macroporous materials (D11-10 and Aerosil 200), besides other process parameters (temperature, dilution, and mean residence time). The activity and, especially, selectivity of such "linker-free" supports for ruthenium metathesis catalysts were evaluated in the cyclodimerization of cis-cyclooctene to form 1,9-cyclohexadecadiene, a valuable intermediate in the flavor and fragrance industry. The optimized material showed not only exceptionally high selectivity to the valuable product, but also turned out to be a truly heterogeneous catalyst with superior activity relative to the unsupported homogeneous complex.

Linker-free, silica-bound olefin-metathesis catalysts: applications in heterogeneous catalysis.

A set of heterogenized olefin-metathesis catalysts, which consisted of Ru complexes with the H(2)ITap ligand (1,3-bis(2',6'-dimethyl-4'dimethyl aminophenyl)-4,5-dihydroimidazol-2-ylidene) that had been adsorbed onto a silica support, has been prepared. These complexes showed strong binding to the solid support without the need for tethering groups on the complex or functionalized silica. The catalysts were tested in the ring-opening-ring-closing-metathesis (RO-RCM) of cyclooctene (COE) and the self-metathesis of methyl oleate under continuous-flow conditions. The best complexes showed a TON>4000, which surpasses the previously reported materials that were either based on the Grubbs-Hoveyda II complex on silica or on the classical heterogeneous Re(2)O(7)/B(2)O(3) catalyst.

1-Phenyl-1,2-cyclohexadiene: generation, interception by activated olefins, dimerisation and trimerisation.

Four possible precursors of 1-phenyl-1,2-cyclohexadiene (2) were examined, namely, 6,6-dibromo-1-phenylbicyclo[3.1.0]hexane, (1alpha,5alpha,6alpha)-6-bromo-6-fluoro-1-phenylbicyclo[3.1.0]hexane, 1-bromo-2-phenylcyclohexene and 1-bromo-6-phenylcyclohexene. All four compounds could be converted into 2, as demonstrated by the products of the interception of 2 with activated olefins. Styrene, 1,1-diphenylethene, indene, furan and 2,5-dimethylfuran were employed as such. Whereas the first three gave [2+2] cycloadducts of 2, the last two provided one [4+2] cycloadduct each. To create the [2+2] cycloadducts, the pi bond of 2 that is more remote from the phenyl group reacted, whereas the pi bond of 2 conjugated with the phenyl group exclusively produced the [4+2] cycloadducts. The generation of 2 in the absence of a trapping reagent brought about relatively good yields of a dimer or a trimer of 2 depending on the mode of the liberation of 2. Being derivatives of triphenylene, the dimer as well as the trimer have unusual structures, thereby indicating that a phenyl group is participating in the formation of these compounds. The most surprising structure of the trimer was elucidated by X-ray crystal diffraction. As to the mechanisms, diradical intermediates are proposed both for the cycloadditions and for the dimerisation. The initial steps of the latter seem to proceed also in the trimerisation.

Access to new Janus head ligands: linking sulfur diimides and phosphanes for hemilabile tripodal scorpionates.

Reactions of lithium dialkyl/phenyl phosphanylmethylides, RR'PCH(X)Li (R, R' = Me, Et, Ph and R = Me, R' = Ph; X = H or Me), with sulfur diimides S(NR'')2 (R'' = (t)Bu or SiMe3) in an equimolar ratio yielded Janus head complexes with the structural motif [Li{RR'PCH(X)S(NR'')2}]2 (R'' = (t)Bu, SiMe3). The basic core of these dimeric complexes is composed of a (LiN)(2) four-membered ring containing two four-coordinated lithium atoms. A lithium complex of the new Janus head ligand with another structural motif [TMEDA·Li{Ph(2)PCH(2)S(NSiMe3)2}] (6) could be isolated from the reaction of [Ph2PCH2Li·TMEDA] with S(NSiMe3)2. Two monomeric complexes [Mg{Me2PCH2S(NR'')2}2] (7, 8) were synthesised by a straightforward reaction of [Li{Me2PCH2S(NR'')2}2] with MgCl2 in pentane. The magnesium atom is chelated by one phosphorus atom and two nitrogen atoms of each unit of the hemilabile ligand in a tripodal manner, leading to octahedral geometry around the magnesium cation. A complete analysis of [Ph2PCH2(SNSiMe3)(HNSiMe3)] (9) is also described in which one nitrogen atom of the imido moiety is protonated.

Unsymmetrical Ru-NHC catalysts: a key for the selective tandem ring opening-ring closing alkene metathesis (RO-RCM) of cyclooctene.

Dissymmetry for selectivity: NHC ligand with two different pendant group allows the selective formation of cyclic oligomers in place of polymers opening new strategy to generate macrocycles.

Terpenoid metabolism in wild-type and transgenic Arabidopsis plants.

Volatile components, such as terpenoids, are emitted from aerial parts of plants and play a major role in the interaction between plants and their environment. Analysis of the composition and emission pattern of volatiles in the model plant Arabidopsis showed that a range of volatile components are released, primarily from flowers. Most of the volatiles detected were monoterpenes and sesquiterpenes, which in contrast to other volatiles showed a diurnal emission pattern. The active terpenoid metabolism in wild-type Arabidopsis provoked us to conduct an additional set of experiments in which transgenic Arabidopsis overexpressing two different terpene synthases were generated. Leaves of transgenic plants constitutively expressing a dual linalool/nerolidol synthase in the plastids (FaNES1) produced linalool and its glycosylated and hydroxylated derivatives. The sum of glycosylated components was in some of the transgenic lines up to 40- to 60-fold higher than the sum of the corresponding free alcohols. Surprisingly, we also detected the production and emission of nerolidol, albeit at a low level, suggesting that a small pool of its precursor farnesyl diphosphate is present in the plastids. Transgenic lines with strong transgene expression showed growth retardation, possibly as a result of the depletion of isoprenoid precursors in the plastids. In dual-choice assays with Myzus persicae, the FaNES1-expressing lines significantly repelled the aphids. Overexpression of a typical cytosolic sesquiterpene synthase resulted in the production of only trace amounts of the expected sesquiterpene, suggesting tight control of the cytosolic pool of farnesyl diphosphate, the precursor for sesquiterpenoid biosynthesis. This study further demonstrates the value of Arabidopsis for studies of the biosynthesis and ecological role of terpenoids and provides new insights into their metabolism in wild-type and transgenic plants.