An anti-freeze fluorescent organogel with rapid shape-forming properties for constructing artificial light harvesting systems used in extremely cold environments.

Using polyvinyl alcohol (PVA) and perylene-3,9-dicarboxylic acid (PDA) as raw materials, a new anti-freeze (-50 °C) fluorescent organogel with rapid shape-forming (2 h) properties was synthesised based on a certain proportion of the binary solvent of ,-dimethylformamide (DMF) and dimethyl sulfoxide (DMSO). Then, an artificial light-harvesting system (ALHS) used in extremely cold environments was successfully constructed by mixing fluorescent dyes sulphorhodamine101 (SR101) and rhodamine 6G (R6G) into them as acceptors.

Construction of Artificial Light-Harvesting Systems Based on Aggregation-Induced Emission Type Supramolecular Self-Assembly Metallogels.

A method for preparing new artificial light-harvesting systems (ALHSs) based on supramolecular metallogels was proposed. Various metal ions were introduced into a solution of a bi-benzimidazole compound (P) in ethylene glycol, and P exhibited high selectivity toward Al, as indicated by the noticeable red shift (49 nm) observed in the fluorescence spectra of P after the addition of Al. Interestingly, the gelator, P, could self-assemble into a stable supramolecular gel (P-gel) that exhibits strong aggregation-induced emission in ethylene glycol.

Artificial light-harvesting systems based on supramolecular self-assembly multi-component metallogels.

This paper proposes a strategy for fabricating new artificial light-harvesting systems (ALHSs) based on supramolecular multi-component metallogels. Al was introduced into a solution of an acylhydrazone compound (L) in DMSO or DMF to form the L-Al assembly. After adding Al to the L solution, a noticeable blue shift appeared in the fluorescence spectra of L.

Preparation of a multifunctional organogel and its electrochemical properties.

A facile methodology to fabricate a highly elastic organogel for supercapacitors is demonstrated. A stable polymer organogel was obtained in DMSO by a simple esterification reaction. This organogel showed high mechanical performance, flexibility, high elasticity, luminous performance and conductivity, as well as high potential values for application in the energy sector.

Shape-controlled hollow CuO@CuS nanocubes with enhanced photocatalytic activities towards degradation of tetracycline.

In view of recent advances in photodegradation of antibiotics, low cost and stable photocatalyst remain rare. In this article, shape-controlled CuO@CuS nanocubes with the larger specific surface area were successfully prepared via a simple template-engaged strategy. CuO nanocubes were synthesized through a reduction method as original templates, the core-shelled CuO@CuS nanocubes were formed by sulphuration with NaS as sulphur source, and the CuO core can be incompletely removed by NaSO to generate the CuO@CuS nanoboxes.

Efficient artificial light-harvesting systems based on aggregation-induced emission in supramolecular gels.

Based on a new designed acyl hydrazone gelator (G2), we developed a supramolecular organogel in glycol with two different hydrophobic fluorescent dyes, namely rhodamine B (RhB) and acridine red, as acceptors. Both the G2@gel-RhB and G2@gel-acridine red systems showed high levels of energy-transfer efficiency and high fluorescence quantum yields.

A new strategy for constructing artificial light-harvesting systems: supramolecular self-assembly gels with AIE properties.

An artificial light-harvesting system (ALHS) has been designed and constructed based on supramolecular organogels made of a simple hydrazide-functionalized benzimidazole derivative (HB), as well as the fluorescent dye rhodamine B (RhB). RhB acted as a good acceptor to realize the energy-transfer process with good efficiency based on a HB/RhB assembly, which showed considerable fluorescence resonance energy transfer (FRET) efficiency of 53% for the energy transfer process. Remarkably, the obtained system showed superior color conversion abilities, converting blue light into orange light.

Intelligent writable material based on a supramolecular self-assembly gel.

A simple dual acylhydrazone-functionalized gelator (G1) has been designed and synthesized, and it was found to form a supramolecular organogel (G1-gel) in a mixed solvent of DMF-H2O. The gelator solution shows brilliant blue light upon mixing with Mg2+; this blue light can be erased by saliva or CO32-. Owing to this characteristic, a smart erasable writable material was prepared.

Emissive intelligent supramolecular gel for highly selective sensing of Al and writable soft material.

A fluorine-containing acylhydrazone was newly designed and found to form gels in a mixed solvent of DMSO-ethylene glycol. The gelator could show brilliant blue light upon mixing with Al3+, which could be erased by F- ions and thus forming an erasable gel.

A novel thermo-responsive supramolecular organogel based on dual acylhydrazone: fluorescent detection for Al ions.

A new dual acylhydrazone-functionalized gelator (L) has been synthesized, which behaves as a thermal-responsive supramolecular organogel (L-gel) in DMSO. This L-gel exhibits very weak fluorescence based on the photoinduced electron transfer (PET) mechanism. The L-gel can recognize Al and assemble into an enhanced blue-light-emitting supramolecular metallogel (Al@gel).

A thermo-responsive supramolecular gel and its luminescence enhancement induced by rare earth Y.

A new acylhydrazone-functionalized dual benzimidazole derivative gelator (L) was synthesized. L can self-assemble in DMSO-EG (ethylene glycol) or DMF-water mixtures to form a thermo-responsive supramolecular organogel (L-gel). In order to increase the fluorescence intensity of L-gel (DMSO-EG system), L-gel slowly turned into a clear solution upon addition of one equivalent of RE (rare earth) Y.

A thermo-responsive supramolecular organogel: dual luminescence properties and luminescence conversion induced by Cd(2+).

A simple dual luminescent acylhydrazone-functionalized benzimidazole derivative (L) was blended with ethylene glycol affording a thermo-responsive green-light-emitting supramolecular gel (G-gel). This G-gel can convert to a blue-light-emitting gel (B-gel) by strongly increasing the luminescence of the benzimidazole moiety upon addition of one equivalent of Cd(2+).

Tb(3+)-containing supramolecular hydrogels: luminescence properties and reversible sol-gel transitions induced by external stimuli.

A dual-responsive green-light-emitting supramolecular metal hydrogel (G-gel) was prepared by the reaction of a simple hydrazide-functionalized benzimidazole ligand (L) with Tb(NO3)3. The green luminescence of gelator L is enhanced in the G-gel due to the coordination effect between L and Tb(3+). In addition, the G-gel shows different luminescence when in a semisolid state (gel) and in a solid state (xerogel).

Trinuclear and tetranuclear magnesium alkoxide clusters as highly active initiators for ring-opening polymerization of L-lactide.

Trinuclear and tetranuclear magnesium alkoxide clusters supported by bulky phenolates with triangular or rhombic structures were readily synthesized in acceptable yields via the reaction of 2-N,N-dimethylaminoethanol/methoxyethanol, different phenols, and dibutylmagnesium. These complexes have been characterized using (1)H and (13)C NMR, elemental analyses, and X-ray crystallography. The experimental results indicate that these clusters are efficient and excellent initiators for the ring-opening polymerizations (ROPs) of l-lactide (LA) and afford polylactides with desired molecular weights and narrow polydispersity indexes (PDIs).

[Fluorescence property of a chemical probe for naked-eye and detection of Fe3+].

A higher selective and sensitive probe for the detection of Fe(III) in aqueous media was made using 2,4-Diisocyanatotoluene (TDI) as a bridge to couple Fe3 O4 nanoparticles(NPs) and Rhodamine-6G hydrazide. The characterization of composite materials with Infrared spectra(IR), Thermal Gravimetric analysis(TGA) and Transmission Emission Microscopy(TEM) points to the graft of Rhodamine-6G hydrazide onto the surface of the Fe3O4. The obvious color change of the probe solution from light grey to pink upon the addition of Fe3+ demonstrated the probe could be used for "naked-eye" detection of Fe3+ in water at pH 7.