The formation relationship between colloidal magic-size clusters (MSCs) and conventional quantum dots (QDs) has not been well established. Here, we report our systematic study on their formation pathways, using cadmium sulfide (CdS) as a model system. Two Cd precursors were prepared from CdO with branched 2-methyloctadecanoic acid (CHCH(CH)-COOH) and linear oleic acid (CHCH-COOH), reacting with elemental S powder in 1-octadecene (ODE). We show that the presence of MSC-311 (exhibiting a sharp absorption peaking at 311 nm) is regulated by the growth of conventional QDs. We demonstrate that MSC-311 cannot directly convert into conventional QDs but to its immediate precursor (IP-311), which is transparent in optical absorption (>310 nm). We propose that there are two individual pathways for the formation of MSCs and conventional QDs, linked by an intrinsic pathway from MSCs to IPs to fragments to QDs. The present study introduces new avenues to precisely control their formation.

The nature of the active aluminum species and their interaction with glucose in water are studied to establish a detailed mechanism for understanding the AlCl3-catalyzed glucose-tofructose isomerization. The combination of activity results with electrospray ionization tandem mass spectrometry (ESI-MS/MS) reveal that [Al(OH)2(aq)] + species contributes a lot to the isomerization. Attenuated total reflection infrared spectroscopy (ATR-IR) results show that glucose undergoes a ring-opening process which is accelerated by the [Al(OH)2(aq)] + species. The binding of acyclic glucose with [Al(OH)2(aq)] + species occurs at the C1-O and C2-O positions of glucose, which initiates the hydride shift of the aldose-to-ketose isomerization. The in-situ 27 Al NMR data elucidate the maintenance of the hexa-coordinated form of Al species throughout the reaction. An obvious kinetic isotope effect (KIE) occurs with the C2 deuterium-labeled glucose, confirming that the intramolecular hydride shift from the C2 to C1 positions of glucose is the ratelimiting step for the isomerization. The apparent activation energy (Ea) of the AlCl3-catalyzed glucose-to-fructose isomerization reaction is estimated to be 110 ± 2 kJ·mol -1 .

The efficient valorization of lignin could dictate the success of the 2nd generation biorefinery. Lignin, accounting for on average a third of the lignocellulosic biomass, is the most promising candidate for sustainable production of value‐added phenolics. However, the structural alteration induced during lignin isolation is often depleting its potential for value‐added chemicals. Recently, catalytic reductive depolymerization of lignin has appeared to be a promising and effective method for its valorization to obtain phenolic monomers. The present study systematically summarizes the far‐reaching and state‐of‐the‐art lignin valorization strategies during different stages, including conventional catalytic depolymerization of technical lignin, emerging reductive catalytic fractionation of protolignin, stabilization strategies to inhibit the undesired condensation reactions, and further catalytic upgrading of lignin‐derived monomers. Finally, the potential challenges for the future researches on the efficient valorization of lignin and possible solutions are proposed.

No abstract

Furfural was prepared in high yields (75 %) from the reaction of xylose in a water-tetrahydrofuran biphasic medium containing AlCl(3)·6H2O and NaCl under microwave heating at 140 °C. The reaction profile revealed the formation of xylulose as an intermediate en route to the dehydration product (furfural). The reaction under these conditions reached completion in 45 min. The aqueous phase containing AlCl(3)·6H(2)O and NaCl could be recycled multiple times (>5) without any loss of activity or selectivity for furfural. Extension of this biphasic reaction system to include xylan as the starting material afforded furfural in 64 % yield. The use of corn stover, pinewood, switchgrass, and poplar gave furfural in 55, 38, 56, and 64 % yield, respectively, at 160 °C. Even though AlCl(3)·6H(2)O did not affect the conversion of crystalline cellulose, moderate yields of the by-product 5-hydroxymethylfurfural (HMF) were noted. The highest HMF yield of 42 % was obtained from pinewood. The coproduction of HMF and furfural from biomass was attributed to the weakening of the cellulose network in the biomass, as a result of hemicellulose hydrolysis. The multifunctional capacity of AlCl(3)·6H(2)O (hemicellulose hydrolysis, xylose isomerization, and xylulose dehydration) in combination with its ease of recyclability make it an attractive candidate/catalyst for the selective synthesis of furfural from various biomass feedstocks.