Photoluminescence Quenching of Hydrophobic Ag29 Nanoclusters Caused by Molecular Decoupling during Aqueous Phase Transfer and EmissionRecovery through Supramolecular Recoupling.

Exploiting emissive hydrophobic nanoclusters for hydrophilic applications remains a challenge because of photoluminescence (PL) quenching during phase transfer. In addition, the mechanism underlying PL quenching remains unclear. In this study, the PL-quenching mechanism was examined by analyzing the atomically precise structures and optical properties of a surface-engineered Ag29 nanocluster with an all-around-carboxyl-functionalized surface. Specifically, phase-transfer-triggered PL quenching was justified as molecular decoupling, which directed an unfixed cluster surface and weakened the radiative transition. Furthermore, emission recovery of the quenched nanoclusters was accomplished by using a supramolecular recoupling approach through the glutathione-addition-induced aggregation of cluster molecules, wherein the restriction of intracluster motion and intercluster rotation strengthened the radiative transition of the clusters. The results of this work offer a new perspective on structure-emission correlations for atomically precise nanoclusters and hopefully provide insight into the fabrication of highly emissive cluster-based nanomaterials for downstream hydrophilic applications.

Stepwise construction of Ag29 nanocluster-based hydrogen evolution electrocatalysts.

Although several silver-based nanoclusters have been controllably prepared and structurally determined, their electrochemical catalytic performances have been relatively unexplored (or showed relatively weak ability towards electro-catalysis). In this work, we accomplished the step-by-step enhancement of the electrocatalytic hydrogen evolution reaction (HER) efficiency based on an Ag29 cluster template. A combination of atomically precise operations, including the kernel alloying, ligand engineering, and surface activation, was exploited to produce a highly efficient Pt1Ag28-BTT-Mn(10) nano-catalyst towards HER, derived from both experimental characterization and theoretical modelling. The precision characteristic of the Ag29-based cluster system enables us to understanding the correlations between nanocluster structures and HER performances at the atomic level. Overall, the findings of this work will hopefully provide more opportunities for the customization of new cluster-based nano-catalysts with enhanced electrocatalytic capacities.

Probing the surface-active sites of metal nanoclusters with atomic precision: a case study of Au5Ag11.

The determination of surface-active sites in metal nanoclusters is of great significance for the in-depth understanding of structural evolutions and physicochemical property mechanisms. In this work, the surface-active sites of the Au5Ag11(DMBT)8(DPPOE)2 cluster template towards metal-/ligand-exchange reactions were unambiguously identified at the atomic level. The active-site tailoring of this nanocluster gave rise to three derivative nanoclusters, Au5Ag9Cu2(DMBT)8(DPPOE)2, Au5Ag11(DMBT)6(DCBT)2(DPPOE)2, and Au5Ag11(DCBT)8(DPPOE)2. The single-crystal structural analysis revealed that all these M16 (M = Au/Ag/Cu) clusters exhibited almost the same framework. Besides, the surface-active site tailoring contributed to significant changes in optical absorptions and emissions of these metal nanoclusters. The findings in this work not only provide an in-depth understanding of the active-site tailoring of cluster surface structures but also develop an intriguing template that enables us to grasp the structure-property correlations at the atomic level.

Surface environment complication makes Ag29 nanoclusters more robust and leads to their unique packing in the supracrystal lattice.

Silver nanoclusters have received unprecedented attention in cluster science owing to their promising functionalities and intriguing physical/chemical properties. However, essential instability significantly impedes their extensive applications. We herein propose a strategy termed "surface environment complication" to endow Ag29 nanoclusters with high robustness. The Ag29(S-Adm)18(PPh3)4 nanocluster with monodentate PPh3 ligands was extremely unstable and uncrystallizable. By substituting PPh3 with bidentate PPh2py with dual coordination sites (i.e., P and N), the Ag29 cluster framework was twisted because of the generation of N-Ag interactions, and three NO3 ligands were further anchored onto the nanocluster surface, yielding a new Ag29(S-Adm)15(NO3)3(PPh2py)4 nanocluster with high stability. The metal-control or ligand-control effects on stabilizing the Ag29 nanocluster were further evaluated. Besides, Ag29(S-Adm)15(NO3)3(PPh2py)4 followed a unique packing mode in the supracrystal lattice with several intercluster channels, which has yet been observed in other M29 cluster crystals. Overall, this work presents a new approach (i.e., surface environment complication) for tailoring the surface environment and improving the stability of metal nanoclusters.

Ligand Effects on Intramolecular Configuration, Intermolecular Packing, and Optical Properties of Metal Nanoclusters.

Surface modification has served as an efficient approach to dictate nanocluster structures and properties. In this work, based on an Ag22 nanocluster template, the effects of surface modification on intracluster constructions and intercluster packing modes, as well as the properties of nanoclusters or cluster-based crystallographic assemblies have been investigated. On the molecular level, the Ag22 nanocluster with larger surface steric hindrance was inclined to absorb more small-steric chlorine but less bulky thiol ligands on its surface. On the supramolecular level, the regulation of intramolecular and intermolecular interactions in nanocluster crystallographic assemblies rendered them CIEE (crystallization-induced emission enhancement)-active or -inactive nanomaterials. This study has some innovation in the molecular and intramolecular tailoring of metal nanoclusters, which is significant for the preparation of new cluster-based nanomaterials with customized structures and enhanced performances.

Cocrystallization-driven stabilization of metastable nanoclusters: a case study of Pd1Au9.

The structural determination of metastable nanoclusters remains challenging, which impedes the in-depth understanding of their structural evolution. Herein, based on a case study of Pd1Au9, we present a "cocrystallization-driven stabilization" approach to stabilize the metastable nanocluster and then determine its atomically precise structure. The [Pd1Au9(TFPP)7Br2]+ nanocluster is unstable in solution and would spontaneously convert to Pd2Au23(TFPP)10Br7. The introduction of Au11(TFPP)7Br3 nanocluster to the crystallization process of [Pd1Au9(TFPP)7Br2]+ gives rise to the cocrystallized Pd1Au9(TFPP)6Br3@Au11(TFPP)7Br3, although the composition of Pd1Au9 changes from [Pd1Au9(TFPP)7Br2]+ to Pd1Au9(TFPP)6Br3 among this cocrystallization. With this approach, the overall structure of the metastable Pd1Au9 has been determined. Owing to the very similar cluster size and surface ligand environment between Au11 and Pd1Au9, the obtained Pd1Au9@Au11 cocrystal exhibits almost the same cell parameters as those of the single crystalized Au11. Overall, the proposed "cocrystallization-driven stabilization" approach hopefully sheds light on the structural determination of more metastable nanoclusters.

Ag48 and Ag50 Nanoclusters: Toward Active-Site Tailoring of Nanocluster Surface Structures.

The determination of active sites in metal nanoclusters is of great significance for the in-depth understanding of the structural evolution and the mechanism of physicochemical properties. In this work, the surface active Ag2(SR)3 units of the Ag48Cl14(S-Adm)30 nanocluster are determined, and the active-site tailoring of this nanocluster gives rise to two derivative nanoclusters, i.e., the structure-maintained Ag48Cl14(S-Adm)26(S-c-C6H11)4 and the structure-growth Ag50Cl16(S-Adm)28(DPPP)2. Both Ag48 and Ag50 nanoclusters exhibit almost the same cluster framework, but the Ag2(S-Adm)3 active units are regulated to Ag3(S-Adm)2(DPPP)1Cl1 with the transformation from Ag48 to Ag50. The surface active sites on Ag48 are rationalized by analyzing its crystal structure and the ligand-exchange-induced cluster transformation. This study provides some inspiration toward the active-site tailoring of nanocluster surface structures, which is significant for the preparation of new cluster-based nanomaterials with customized structures and enhanced performance.

Bioresolution production of (2R,3S)-ethyl-3-phenylglycidate for chemoenzymatic synthesis of the taxol C-13 side chain by Galactomyces geotrichum ZJUTZQ200, a new epoxide-hydrolase-producing strain.

A newly isolated Galactomyces geotrichum ZJUTZQ200 strain containing an epoxide hydrolase was used to resolve racemic ethyl 3-phenylglycidate (rac-EPG) for producing (2R,3S)-ethyl-3-phenylglycidate ((2R,3S)-EPG). G. geotrichum ZJUTZQ200 was verified to be able to afford high enantioselectivity in whole cell catalyzed synthesis of this chiral phenylglycidate synthon. After the optimization of the enzymatic production and bioresolution conditions, (2R,3S)-EPG was afforded with high enantioselectivity (e.e.S > 99%, E > 49) after a 8 h reaction. The co-solvents, pH buffer solutions and substrate/cell ratio were found to have significant influences on the bioresolution properties of G. geotrichum ZJUTZQ200. Based on the bioresolution product (2R,3S)-EPG, taxol's side chain ethyl (2R,3S)-3-benzoylamino-2-hydroxy-3-phenylpropionate was successfully synthesized by a chemoenzymatic route with high enantioselectivity (e.e.S > 95%).

Bioresolution of (R)-glycidyl azide by Aspergillus niger ZJUTZQ208: a new and concise synthon for chiral vicinal amino alcohols.

A newly isolated Aspergillus niger strain containing epoxide hydrolase was used to resolve racemic glycidyl azide and four derivatives to the (R)-enantiomers. After optimization of the biotransformation conditions, (R)-glycidyl azide was produced with good enantioselectivity (e.e.s > 95 %, E > 20). The substrate structure, pH, and reaction time were found to have profound influences on the catalytic property of A. niger ZJUTZQ208. Enantiopure glycidyl azide was further utilized to synthesize linezolid in good yield, indicating it is a new and concise synthon for chiral vicinal amino alcohols. Enzyme-substrate docking studies were carried out with glycidyl azide to study the selectivity of this strain.

Biocatalytic resolution of benzyl glycidyl ether and its derivates by Talaromyces flavus: effect of phenyl ring substituents on enantioselectivity.

Talaromyces flavus containing a constitutive epoxide hydrolase (EH) resolved racemic benzyl glycidyl ether and nine derivatives into their (R)-enantiomers. After optimization of the fermentation conditions, the specific EH activity and biomass concentration were improved from 13.5 U/g DCW and 14.8 g DCW/l to 26.2 U/g DCW and 31.3 g DCW/l, respectively, with final values for e.e. ( s ) of 96 % and E of 13 with (R)-benzyl glycidyl ether. Substituents on the phenyl ring, however, gave low enantioselectivities.

In vitro and in vivo antioxidant properties of the plant-based supplement greens+™.

Dietary antioxidants play an important role against oxidation, an underlying mechanism in the incidence of chronic diseases. Greens+ is a commercially available preparation containing a variety of plant-derived ingredients. The aim of the current study was to evaluate the antioxidant potential of the methanolic extract of greens+ powder using in vitro and in vivo techniques. In vitro studies were conducted using a liposome model system to simulate biological cell membranes. Total antioxidant potential and polyphenol content of the herbal preparation was measured. For in vivo analysis, 10 healthy human subjects consumed either three or six teaspoons of greens+ per day for four weeks. Blood samples were analyzed at baseline and at the conclusion of the treatment period for total antioxidant capacity, polyphenol content, protein, lipid and LDL oxidation, and the level of glutathione peroxidase. Results showed that greens+ supplementation was well tolerated and increased serum antioxidant potential at higher levels of intake in a dose-dependent manner. HPLC analysis showed the presence of quercetin, apigenin, kaempferol and luteolin in the supplement. Plasma analysis indicated the presence of kaempferol only. A statistically significant (p < 0.05) reduction in protein and lipid oxidation was observed. Based on its antioxidant properties, the results suggest that greens+ might play a role in reducing the risk of chronic diseases involving a burden of oxidative damage.

A BRCA1 mutation is not associated with increased indicators of oxidative stress.

BACKGROUND: Several functions have been attributed to the BRCA1 protein. A recent study suggests that BRCA1 is involved in the cellular antioxidant response by inducing the expression of genes involved in the antioxidant defense system and thus conferring resistance to oxidative stress. It is possible that individuals with a BRCA1 mutation might be susceptible to the effects of oxidative stress. The aim of this study was to evaluate whether women with a BRCA1 mutation exhibit increased indicators of oxidative stress. PATIENTS AND METHODS: We measured 3 markers of oxidative stress in vivo, the amounts of serum malondialdehyde and protein thiols, and 8-oxo-2'-deoxyguanosine (8-oxodG) levels in 25 unaffected BRCA1 mutation carriers and 25 noncarrier control subjects. RESULTS: There was no significant difference in serum malondialdehyde levels (P=.41), serum thiol levels (P=.85), or the number of 8-oxodG lesions (P=.49) in BRCA1 mutation carriers versus noncarriers. CONCLUSION: The results of this study suggest that the presence of a heterozygous BRCA1 mutation is not associated with increased levels of indicators of oxidative stress in serum or lymphocytes. Future studies are warranted to evaluate whether strategies aimed at minimizing oxidative stress might aid in the prevention of hereditary breast cancer.

Lycopene Content of Tomato Products: Its Stability, Bioavailability and In Vivo Antioxidant Properties.

Lycopene is a bioactive carotenoid present in many fruits and vegetables. Tomatoes constitute the major dietary source of lycopene. Recent evidence shows lycopene to be associated with several health benefits. However, very little information is available about the stability of lycopene and its bioavailability. Because tomatoes undergo extensive processing and storage before consumption, a study was conducted to evaluate the stability, isomeric form, bioavailability, and in vivo antioxidant properties of lycopene. Total lycopene and isomers were measured by spectrophotometry and high-performance liquid chromatography, respectively. Lycopene content of tomatoes remained unchanged during the multistep processing operations for the production of juice or paste and remained stable for up to 12 months of storage at ambient temperature. Moreover, subjecting tomato juice to cooking temperatures in the presence of corn oil resulted in the formation of the cis isomeric form, which was considered to be more bioavailable. Lycopene was absorbed readily from the dietary sources. Serum lipid and low-density lipoprotein oxidation were significantly reduced after the consumption of tomato products containing lycopene.