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This study reports the design of a donor‐acceptor (D‐A) molecule with two fluorene units on each side of a benzothiadiazole moiety, which allows multiple intermolecular interactions to compete with one another so as to induce the evolution of the metastable 2D platelets to the stable 2D platelets during the self‐assembly of the D‐A molecule. Importantly, the living seeded self‐assembly of metastable and stable 2D structures with precisely controlled sizes can be conveniently achieved using an appropriate supersaturated level of a solution of the D‐A molecule as the seeded growth medium that can temporarily hold the almost‐proceeding spontaneous nucleation from competing with the seeded growth. The stable 2D platelets with smaller area sizes exhibit higher sensitivity to gaseous dimethyl sulfide, illustrating that the novel living self‐assembly method provides more available functional structures with controlled sizes for practical applications. The key finding of this study is that the new living methodology is separated into two independent processes: the elaborate molecular design for various crystalline structures as seeds and the application of a supersaturated solution with appropriate levels as the growth medium to grow the uniform structures with controlled sizes; this would make convenient and possible the living seeded self‐assembly of rich 1D, 2D, and 3D architectures. [ABSTRACT FROM AUTHOR]

Constructing heterostructures have been demonstrated as an ideal strategy for boosting charge separation on plasmonic photocatalysts, but the detailed interface charge transfer mechanism remains elusive. Herein, that authors fabricate plasmonic Au and metal‐organic frameworks (MOFs, NH2−MIL‐125 and MIL‐125 used in this work) heterostructures and explore the interface charge transfer mechanism by in situ electron paramagnetic resonance (EPR) spectroscopy and electrochemical measurements. The plasmon‐excited hot electrons on Au can transfer across the Au/MOF interface and be captured by the coordinatively unsaturated sites of secondary building units (Ti8O8(OH)4 cluster) of the MOF structure, and the plasmon‐excited hot holes on Au tend to transfer to and be trapped at the functionalized organic ligand (1,4‐benzenedicarboxylate−NH2). The spatially separated hot electrons and holes exhibit boosted the photocatalytic activity for chromium (VI) reduction and selective benzyl alcohol oxidation. This work illustrates the advantage of the versatile functionalization of MOF structures enabling molecular‐level manipulation of interface charge transfer on plasmonic photocatalysts. [ABSTRACT FROM AUTHOR]

The controlled formation of complex and functional 1‐, 2‐, and 3D hierarchical assemblies from molecular building blocks represents a key current challenge. Herein, we report the use of a seeded growth approach for a series of perylenediimide‐based molecules (PDIs 1–4) to access otherwise inaccessible self‐assembly pathways that yield complex hierarchical structures. The key to the new approach is to use hetero‐seeds which possess a different composition and morphology from that of the molecular building block. For example, a nanotube seed (from PDI 3) and a microribbon seed (from PDI 4) were found to initiate different self‐assembly pathways for PDI 1, which normally assembles to yield nanocoils. This led to the formation of unprecedented 3D scroll‐like and scarf‐like hierarchical nanostructures, respectively. Also, the hetero‐seeds from PDI 3 initiate hidden self‐assembly pathways of PDI 2 to generate 1D tubular heterojunctions. Significantly, this new strategy offers new opportunities to create emergent and functional hierarchical and complex structures from small molecule precursors. [ABSTRACT FROM AUTHOR]

Manipulating the self‐assembly pathway is essentially important in the supramolecular synthesis of organic nano‐ and microarchitectures. Herein, we design a series of photoisomerizable chiral molecules, and realize precise control over pathway complexity with external light stimuli. The hidden single‐handed microcoils, rather than the straight microribbons through spontaneous assembly, are obtained through a kinetically controlled pathway. The competition between molecular interactions in metastable photostationary intermediates gives rise to a variety of molecular packing and thereby the possibility of chirality transfer from molecules to supramolecular assemblies. [ABSTRACT FROM AUTHOR]

Core-shell TiO2 microspheres possess a unique structure and interesting properties, and therefore, they have received much attention. The high-energy facets of TiO2 also are being widely studied for the high photocatalytic activities they are associated with. However, the synthesis of the core-shell structure is difficult to achieve and requires multiple-steps and/or is expensive. Hydrofluoric acid (HF), which is highly corrosive, is usually used in the controlling high-energy facet production. Therefore, it is still a significant challenge to develop low-temperature, template-free, shapecontrolled, and relative green self-assembly routes for the formation of core-shell-structured TiO2 microspheres with high-energy facets. Here, we report a template- and hydrofluoric acid free solvothermal self-assembly approach to synthesize core-shell TiO2 microspheres covered with high-energy {116}-facet-exposed nanosheets, an approach in which 1,4-butanediamine plays a key role in the formation of nanosheets with exposed {116} facets and the doping of nitrogen in situ. In the structure, nanoparticle aggregates and nanosheets with {116} high-energy facets exposed act as core and shell, respectively. The photocatalytic activity for degradation of 2,4,6-tribromophenol and Rhodamine B under visible irradiation and UV/Vis irradiation has been examined, and improved photocatalytic activity under visible light owing to the hierarchical core-shell structure, {116}-plane-oriented nanosheets, in situ N doping, and large surface areas has been found. [ABSTRACT FROM AUTHOR]

Titanium dioxide with surface-loaded palladium (Pd-TiO2) was able to easily remove all ten bromine atoms from decabromodiphenyl ether (BDE209) within 1 h under the irradiation of sunlight or an artificial light source. By contrast, fewer than three bromine atoms were eliminated on the pristine TiO2 even with prolonged irradiation (5 h). During the photocatalytic debromination, moreover, the formed BDE intermediates exhibited a significant difference between the Pd-TiO2 and pristine TiO2 systems, and much less position selectivity for the debromination on Pd-TiO2 was observed than that on the pristine TiO2 surface. For another polybrominated diphenyl ether (BDE15), pristine TiO2 was incapable of its photocatalytic reduction, whereas the loading of Pd enabled its debromination to diphenyl ether within 20 min. In addition, an evident induction period appeared in the photocatalytic debromination of BDE15 on Pd-TiO2. The experiments imply that the Pd-cocatalyzed effect changes significantly the photocatalytic reductive debromination pathways. [ABSTRACT FROM AUTHOR]

Epoxidation of olefins with H2O2 is one of the most important reactions in organic synthesis. We found that anatase TiO2 can be a good catalyst for the epoxidation of cyclooctene with H2O2 at room temperature. However, the catalyst deactivated quickly in the presence of excess amount of H2O2 because of the formation of inactive side-on Ti-η2-peroxide species on the surface of TiO2, the presence of which was confirmed by isotope-labelled resonance UV Raman spectroscopy and kinetics studies. Interestingly, the epoxidation reaction could be dramatically accelerated under irradiation of UV light with λ≥350 nm. This phenomenon is attributed to the photo-assisted removal of the inactive peroxide species, through which the active sites on the surface of anatase TiO2 are regenerated and the catalytic epoxidation of cyclooctene with H2O2 is resumed. This finding provides an alternative for sustained epoxidation reactions on TiO2 at room temperature. Moreover, it also has significant implications on the deactivation pathway and possible solutions in Ti-based heterogeneous catalysis or photocatalysis. [ABSTRACT FROM AUTHOR]

The degradation behaviours of five straight-chain dicarboxylic acids (from ethanedioic acid to hexanedioic acid) were compared in aqueous TiO2-based photocatalysis. When all other conditions were identical, the degradation rates were found to fluctuate regularly with the parity of the number of carbon atoms. Dicarboxylic acids with an even number of carbon atoms (e-DAs) always degraded more slowly than those acids with an odd number of carbon atoms (o-DAs). This unusual fluctuation in the reactivity for the degradation of dicarboxylic acids by TiO2-based photocatalysis is very closely related to the different pre-coordination modes of the acids with the photocatalyst. Attenuated total reflection FTIR (ATR-FTIR) of e-DAs labelled with 13C showed that both carboxyl groups of the acid coordinate to TiO2 through bidentate chelating forms. In contrast, only one carboxyl group of the o-DAs coordinated to TiO2 in a bidentate chelating manner, whereas the other formed a monodentate binding linkage. The bidentate chelating form with bilateral symmetric coordination did not favour degradation. Isotope-labelling experiments were performed with 18O2 to observe the different ways in which incorporated oxygen entered the initial decarboxylated products of e- and o-DAs. For the degradation of butanedioic acid, (45.9±0.5) % of the oxygen in the formed propanedioic acid came from H2O, whereas for pentanedioic acid, (97.4±0.2) % of the oxygen in the formed butanedioic acid came from H2O. Our results demonstrate that in TiO2-based photocatalysis, the reactivity of active species, such as .OH/hvb+, is far from non-selective and that the attacks of these active species on organic substrates are significantly affected by the coordination patterns of the substrates on the TiO2 surface. [ABSTRACT FROM AUTHOR]

Invited for the cover of this issue is the group of Professor Jincai Zhao at the Institute of Chemistry, CAS. The image shows that dicarboxylic acids with an even number of carbon atoms were degraded more slowly than those with an odd number of carbon atoms. This unusual fluctuation of the reactivity of dicarboxylic acids against the numbers of carbon atoms is very closely related to the different pre-coordination mode of the acids with the photocatalyst surface sites. Read the full text of the article at . [ABSTRACT FROM AUTHOR]

The degradation behavior…︁ of five straight ‐ chain dicarboxylic acids were compared in aqueous TiO2 ‐ based photocatalysis. The reactivity is found to be dependent on the number of carbon atoms. Dicarboxylic acids with an even number of carbon atoms were degraded more slowly than those with an odd number of carbon atoms. This unusual behavior is very closely related to the different pre ‐ coordination modes of the acids with the photocatalyst. For more details, see the Full Paper by J. C. Zhao et al. on page 1861 ff. [ABSTRACT FROM AUTHOR]