The air tolerant precatalyst, [Rh­(L)­(NBD)]Cl ([1]­Cl) [L = κ3-( i Pr2PCH2CH2)2NH, NBD = norbornadiene], mediates the selective synthesis of N-methylpolyaminoborane, (H2BNMeH) n , by dehydropolymerization of H3B·NMeH2. Kinetic, speciation, and DFT studies show an induction period in which the active catalyst, Rh­(L)­H3 (3), forms, which sits as an outer-sphere adduct 3·H 3 BNMeH 2 as the resting state. At the end of catalysis, dormant Rh­(L)­H2Cl (2) is formed. Reaction of 2 with H3B·NMeH2 returns 3, alongside the proposed formation of boronium [H2B­(NMeH2)2]­Cl. Aided by isotopic labeling, Eyring analysis, and DFT calculations, a mechanism is proposed in which the cooperative “PNHP” ligand templates dehydrogenation, releasing H2BNMeH (ΔG ‡ calc = 19.6 kcal mol–1). H2BNMeH is proposed to undergo rapid, low barrier, head-to-tail chain propagation for which 3 is the catalyst/initiator. A high molecular weight polymer is formed that is relatively insensitive to catalyst loading (M n ∼71 000 g mol–1; Đ, of ∼ 1.6). The molecular weight can be controlled using [H2B­(NMe2H)2]Cl as a chain transfer agent, M n = 37 900–78 100 g mol–1. This polymerization is suggested to arise from an ensemble of processes (catalyst speciation, dehydrogenation, propagation, chain transfer) that are geared around the concentration of H3B·NMeH2. TGA and DSC thermal analysis of polymer produced on scale (10 g, 0.01 mol % [1]­Cl) show a processing window that allows for melt extrusion of polyaminoborane strands, as well as hot pressing, drop casting, and electrospray deposition. By variation of conditions in the latter, smooth or porous microstructured films or spherical polyaminoboranes beads (∼100 nm) result.

Metal organic framework UiO-66 is studied as an adaptable heterogeneous catalyst for glucose conversion. UiO-66 was modified by; i) partial linker substitution, ii) particle size modulation and iii) linker defects. We studied the effect of crystallinity and functional groups on the glucose conversion and product yields. The main products are: i) fructose from the isomerisation of glucose, ii) mannose from the epimerisation of glucose and iii) 5-hydroxymethyl furfural from the dehydration of fructose. We found that defective and nano crystalline UiO-66 catalyst performs best for isomerisation. When 50 % of the linkers of UiO-66 are replaced by a sulfonate-containing linker, the catalyst shows higher isomerisation activity than other UiO-66 catalysts. Naphthalene-dicarboxylate linkers were introduced to induce hydrophobicity and this catalyst further increased isomerisation activity showing 31 % fructose selectivity. Finally, the promising catalysts were tested in a flow reactor and a bifunctional mixed linker catalyst possessing both hydrophobic and acidic functional groups is shown to be stable in a time-onstream study.

with a useful lifetime of decades. Tin perovskites also offer narrower bandgaps than their lead analogues, enabling a greater proportion of the solar spectrum to be harvested. [4] The Achilles' heel of tin perovskites for PV applications is their higher susceptibility to oxidation in air which stems from the tendency of Sn 2+ to convert to the more thermodynamically stable +4 oxidation state upon exposure to ambient air. [5] The intrinsic resistance of the device stack to air ingress dictates the degree of packaging required for practical applications, and thus the packaging cost, so there is a need to identify ways to make tin perovskite PVs more intrinsically stable. [1,2] Strategies to achieving this goal include making the perovskite more stable by compositional engineering or defect passivation [6] and/or making the other

The composition of atmospheric aerosols varies with time, season, location, and environment. This affects key aerosol properties such as hygroscopicity and reactivity, influencing the aerosol’s impact on the climate and air quality. The organic fraction of atmospheric aerosol emissions often contains surfactant material, such as fatty acids. These molecules are known to form three-dimensional nanostructures in contact with water. Different nanostructures have marked differences in viscosity and diffusivity that are properties whose understanding is essential when considering an aerosol’s atmospheric impact. We have explored a range of nanostructures accessible to the organic surfactant oleic acid (commonly found in cooking emissions), simulating variation that is likely to happen in the atmosphere. This was achieved by changing the amount of water, aqueous phase salinity and by addition of other commonly coemitted compounds: sugars and stearic acid (the saturated analogue of oleic acid). The nanostructure was observed by both synchrotron and laboratory small/wide angle X-ray scattering (SAXS/WAXS) and found to be sensitive to the proxy composition. Additionally, the spacing between repeat units in these nanostructures was water content dependent (i.e., an increase from 41 to 54 Å in inverse hexagonal phase d-spacing when increasing the water content from 30 to 50 wt %), suggesting incorporation of water within the nanostructure. A significant decrease in mixture viscosity was also observed with increasing water content from ∼104 to ∼102 Pa s when increasing the water content from 30 to 60 wt %. Time-resolved SAXS experiments on levitated droplets of this proxy confirm the phase changes observed in bulk phase mixtures and demonstrate that coexistent nanostructures can form in droplets. Aerosol compositional and subsequent nanostructural changes could affect aerosol processes, leading to an impact on the climate and urban air pollution.