Enantioconvergent synthesis of chiral fluorenols from racemic secondary alcohols via Pd(ii)/chiral norbornene cooperative catalysis.

An efficient protocol for the asymmetric synthesis of fluorenols has been developed through an enantioconvergent process enabled by Pd(ii)/chiral norbornene cooperative catalysis. This approach allows facile access to diverse functionalized chiral fluorenols with constantly excellent enantioselectivities, applying readily available racemic secondary ortho-bromobenzyl alcohols and aryl iodides as the starting materials.

A mini-review on building insulation materials from perspective of plastic pollution: Current issues and natural fibres as a possible solution.

As plastic pollution is eroding our ecological environment at an alarming rate around the world, tracking the origins is a necessity for putting forward effective measures to prevent it. The building industry, as an important sector consuming plastic products and producing plastic wastes, is increasing application of thermal insulations to improve energy efficiency. However, most insulation materials have negative impact on the environment. With the strategies to boost sustainability of buildings, natural fibres have occurred in the market as promising raw materials for thermal insulations. This mini-review aims to describe the extent building insulations contributed to plastic pollution, and a possible solution to plastic pollution from natural fibres and their current shortcomings. Hopefully, the mini-review could advance the current knowledge on contribution of building materials, especially thermal insulations to the ubiquitous plastic pollution, and the potential of natural fibres for replacing the plastic insulations, which could accordingly help future development of sustainable green insulations.

Two-dimensional type-II g-C3N4/SiP-GaS heterojunctions as water splitting photocatalysts: first-principles predictions.

Hydrogen production from water splitting by sunlight is a promising approach to solve the increasing energy and environmental crises, and the two-dimensional (2D) g-C3N4 monolayer is a red star in this realm. However, it suffers from low quantum efficiency caused by the fast combination of photogenerated electrons and holes. In this work, we investigate the electronic and photocatalytic properties of three newly proposed g-C3N4/SiP-GaS-α, -ß and -γ heterojunctions via first principles predictions. Theoretical results demonstrate that the three g-C3N4/SiP-GaS heterojunctions exhibit direct bandgaps of ∼2.2 eV, and have a type-II band alignment with the valence band maximum (VBM) located at the g-C3N4 layer and the conduction band minimum (CBM) at the SiP-GaS layer. Furthermore, their band edges straddle the redox potential of water in a wide range of biaxial strain. Their absorption coefficients are several times larger than that of most previously discovered 2D heterojunctions. Moreover, the in-built electric field adds a driving force to separate photogenerated electrons and holes. The oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) successfully take place on the g-C3N4 and SiP-GaS layers, respectively. Briefly, separated charge carriers, suitable band edges and strong visible-light absorbance, successful OER and HER enable the three g-C3N4/SiP-GaS heterojunctions to be promising water-splitting photocatalysts.

Structural Engineering of Two-Dimensional Covalent Organic Frameworks for Visible-Light-Driven Organic Transformations.

Covalent organic frameworks (COFs) emerging as a novel kind of visible light-responsive organic semiconductor have attracted extensive research attention in the field of photocatalytic organic transformations. However, the key parameters affecting their photocatalytic properties are still not clear. In this work, a series of [3 + 3] COFs with similar two-dimensional hexagonal structure but different compositions are synthesized and employed as model materials for investigating the key factors affecting the photocatalytic properties in the visible-light-driven reductive dehalogenation reaction and the aerobic cross-dehydrogenative coupling reaction. In comparison with -H and -CF3, the -OH substituent in the aromatic ring could narrow the band gap of the COFs. The COFs with a triazine skeleton in the framework usually boost the photocatalytic activity, possibly because of the enhanced charge separation efficiency by the formation of a donor-acceptor domain. As a combined result of the narrow band gap, efficient charge separation, and high conductivity, the COF possessing both a -OH group and triazine skeleton shows the highest activity in the photocatalytic reductive dehalogenation reaction. Notably, COFs could be easily recovered and reused several times without the loss of crystallinity. Our primary results may shed light on the design of efficient COF-based semiconductors for photocatalytic organic transformations.

Planar graphitic ZnS, buckling ZnS monolayers and rolled-up nanotubes as nonlinear optical materials: first-principles simulation.

Nonlinear optical (NLO) materials have an ability to generate new coherent light. At the present stage, three dimensional (3D) mid-infrared NLO materials suffer from various deficiencies such as low laser damage thresholds (LDTs) for AgGaQ2 (Q = S, Se); the band gaps of most intensively studied two-dimensional (2D) NLO materials are not wide enough to avoid two-photon absorption (TPA); a steady NLO property regardless of diameter and chirality is absent in one-dimensional (1D) single-walled nanotubes (SWNTs). In this research, the electronic and second harmonic generation (SHG) properties of planar graphitic ZnS (g-ZnS) monolayer, buckling reconstructed ZnS (R-ZnS) monolayer which is synthesized in a recent experiment, and rolled-up SWNTs are investigated with first-principles simulations. Theoretical results suggest the SHG coefficients of planar g-ZnS, buckling R-ZnS and rolled-up SWNTs are comparable with that of AgGaS2 crystals. The band gaps of planar g-ZnS and ZnS SWNTs are ∼3.8 eV, and that of buckling R-ZnS is as wide as ∼4.0 eV, indicating high LDTs and reduced TPA as NLO materials. The TPA edges can be further blue shifted by using incident light beams with a polarized electric field perpendicular to buckling R-ZnS. On the other hand, the TPA edges of ZnS SWNTs are nearly not affected by diameter and chirality. The SHG coefficients of ZnS SWNTs are much less influenced by chirality and diameter than those of SiC, GeC and BN SWNTs. Therefore, they are superior ultrathin NLO materials, and especially have a potential application in the mid-infrared regime where high-quality NLO crystals are emergently needed.

Nickel-catalyzed cross-coupling of aldehydes with aryl halides via hydrazone intermediates.

Traditional cross-couplings require stoichiometric organometallic reagents. A novel nickel-catalyzed cross-coupling reaction between aldehydes and aryl halides via hydrazone intermediates has been developed, merging the Wolff-Kishner reduction and the classical cross-coupling reactions. Aromatic aldehydes, aryl iodides and aryl bromides are especially effective in this new cross-coupling chemistry.

A novel Ag3AsO4 visible-light-responsive photocatalyst: facile synthesis and exceptional photocatalytic performance.

A novel Ag3AsO4 photocatalyst has been prepared via a facile precipitation method. It exhibited higher activity than Ag3PO4 or AgI in degradation of rhodamine B or methyl orange. The excellent activity of Ag3AsO4 is attributed to its more separated photogenerated carriers and high absorption capacity of visible light.

Chirally functionalized hollow nanospheres containing L-prolinamide: synthesis and asymmetric catalysis.

Chirally functionalized hollow nanospheres with different surface properties were successfully synthesized by co-condensation of (2S,1'R,2'R)-N-tert-butyloxycarbonylpyrrolidine-2-carboxylic acid [2'-(4-trimethoxysilylbenzylamide)cyclohexyl] amide with 1,2-bis(trimethoxysilyl)ethane or tetramethoxysilane using F127 (EO(106)PO(70)EO(106)) as surfactant in water. The TEM and N(2) sorption characterizations show that the particle size of the hollow nanosphere is 15-21 nm with a core diameter of 10-16 nm. These L-prolinamide-functionalized hollow nanospheres are highly efficient solid catalysts for the direct asymmetric aldol reaction between cyclohexanone and aromatic aldehydes. It was found that the addition of water in the reaction system not only enhanced the catalytic activity but also increased the enantioselectivity, which is probably due to the enhanced hydrogen bond between the amide oxygen atom and the hydroxyl group of water. Moreover, the catalytic activity increases sharply as the surface hydrophobicity of the hollow nanospheres increases. These hollow nanospheres are quite stable and can be reused with almost the same enantioselectivity and only a slight decrease in catalytic activity.

Mesoporous titanosilicates with high loading of titanium synthesized in mild acidic buffer solution.

Mesoporous titanosilicates with high titanium content were synthesized under mild acidic conditions (pH=4.4, HAc-NaAc buffer solution) by co-condensation of acetylacetone-modified titanium isopropoxide (Ti(OBu(n))(3) (acac)) and mixture of sodium silicate with tetramethoxysilane (TMOS) or tetraethoxysilane (TEOS) or tetrakis(2-hydroxyethyl)orthosilicate (EGMS), using block copolymer Pluronic P123 as template. The combined results of XRD, N(2) sorption and TEM show that the highly regular structure of the mesoporous titanosilicates can still be obtained when Ti/Si molar ratio in the final product is as high as 0.059. The results of UV-vis diffuse reflectance spectra and UV resonance Raman spectra show that the framework titanium species are predominant in the mesoporous titanosilicates when Ti/Si molar ratio in the final product is less than 0.042. The mixture of sodium silicate and EGMS was proved to be the best silicon source for the synthesis of titanosilicates with ordered mesostructure and high titanium content. The efficiency of this synthetic method may be attributed to the mild acidic medium as well as the modified hydrolysis-condensation rate and hydrophility of the precursors.