Against the flow? What factors dictate the relative merits of microflow reactors versus batch‐reaction flasks for homogeneous catalytic reactions? The optimal reaction protocol must be decided on a case‐by‐case basis. Flask reactors equipped with in situ detection devices provide a concise and information‐rich means of obtaining the intrinsic kinetic information required to make this decision.
Summary
Soil is a crucial component of the biosphere and is a major sink for organic carbon. Plant roots are known to release a wide range of carbon‐based compounds into soils, including polysaccharides, but the functions of these are not known in detail.Using a monoclonal antibody to plant cell wall xyloglucan, we show that this polysaccharide is secreted by a wide range of angiosperm roots, and relatively abundantly by grasses. It is also released from the rhizoids of liverworts, the earliest diverging lineage of land plants. Using analysis of water‐stable aggregate size, dry dispersion particle analysis and scanning electron microscopy, we show that xyloglucan is effective in increasing soil particle aggregation, a key factor in the formation and function of healthy soils.To study the possible roles of xyloglucan in the formation of soils, we analysed the xyloglucan contents of mineral soils of known age exposed upon the retreat of glaciers. These glacial forefield soils had significantly higher xyloglucan contents than detected in a UK grassland soil.We propose that xyloglucan released from plant rhizoids/roots is an effective soil particle aggregator and may, in this role, have been important in the initial colonization of land.
Acid-catalysed dehydration of 3-substituted benzene cis-l,2-di hydrodiols exhibits a Hammett plot with p = -8.2, consistent with reaction via a benzenonium ion-like intermediate; however, correlation of +M resonance substituents such as Me and Me0 by q, rather than (J+ constants indicates a marked imbalance between resonance and inductive stabilisation of the transition state.
Abstract. Modelling the development of soils in glacier forefields is necessary in order to assess how microbial and geochemical processes interact and shape soil development in response to glacier retreat. Furthermore, such models can help us predict microbial growth and the fate of Arctic soils in an increasingly ice-free future. Here, for the first time, we combined field sampling with laboratory analyses and numerical modelling to investigate microbial community dynamics in oligotrophic proglacial soils in Svalbard. We measured low bacterial growth rates and growth efficiencies (relative to estimates from Alpine glacier forefields) and high sensitivity of bacterial growth rates to soil temperature (relative to temperate soils). We used these laboratory measurements to inform parameter values in a new numerical model and significantly refined predictions of microbial and biogeochemical dynamics of soil development over a period of roughly 120 years. The model predicted the observed accumulation of autotrophic and heterotrophic biomass. Genomic data indicated that initial microbial communities were dominated by bacteria derived from the glacial environment, whereas older soils hosted a mixed community of autotrophic and heterotrophic bacteria. This finding was simulated by the numerical model, which showed that active microbial communities play key roles in fixing and recycling carbon and nutrients. We also demonstrated the role of allochthonous carbon and microbial necromass in sustaining a pool of organic material, despite high heterotrophic activity in older soils. This combined field, laboratory, and modelling approach demonstrates the value of integrated model–data studies to understand and quantify the functioning of the microbial community in an emerging High Arctic soil ecosystem.
The chiral rhodium complex pentamethylcyclopentadienylrhodium chloride dimer combined with the ligand 1R,2S-aminoindanol provides a superior catalyst for the rapid, high-yielding asymmetric transfer hydrogenation of acetophenone
with 2-propanol to produce (R)- and (S)-(1)-phenylethanol. The
effects of various reaction parameters such as reaction temperature, catalyst and substrate concentration, gaseous environment, and acetone concentration on conversion and enantioselectivity were investigated. The results indicate that catalyst
can be deactivated by high temperature and air atmosphere,
acetone reduces the reaction rate, and enantioselectivity decreases with conversion.
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