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Abstract: Copper sulfides were synthesized by using the low-molecular-mass hydrogel nanofibers self-assembled from a L-glutamic acid derivative. The as-prepared copper sulfides showed a nanoribbon structure with diameter of 30–70nm and lengths of 1–10μm. The investigation of FT-IR absorption spectra and XRD pattern for the neat hydrogel and composite gel suggested that H-bonding was the main driving force to help the formation of ordered nanofibers of the hydrogel and the composite gel. The resulted mineralization indicated that the inorganic ions (Cu2+) were firstly coordinated to the carboxylate anions (COO−). With the penetration of H2S, the preformed CuS nanoparticles on the surface of the fibers acted as the growing points for the continuous growth. [Copyright &y& Elsevier]

Abstract: Two-component organogelators based on a discotic H-bonding donor of 1,3,5-tris(4-amidobutanoic acid)phenyl benzene (2), and acceptors of 4-(4-alkoxybenzoyloxy)-4′-stilbazole derivatives were reported. These complexes showed good gelation ability for alcohols, which are known to be unfavorable for H-bonding formation. SEM study revealed that sheet-like network, nanotapes, and nanorods were gained from the self-assembling of the complexes with small difference of the carbon chain length. Based on XRD, IR, temperature-dependent 1H NMR, and UV–vis absorption investigations, the gel-phase materials were generated from 1D columnar-type packing of complexes facilitated by cooperative H-bonding, π-stacking, and van der Walls interactions. [Copyright &y& Elsevier]

Abstract: We report on the synthesis and self-assembly of a new discotic organogelator based on π-conjugated triphenylbenzene with three peripheral chiral substituents. It is found that the introduction of chiral groups to the C 3-symmetric molecule led to a hexagonal columnar chiral stacking of the molecules in a clockwise direction in the organogel fibers. And the fluorescent emission of the gel decreased significantly compared to the monomer state at the same concentration, as a result of the aggregation of the nonplanar triphenylbenzene core in the gel phase. [Copyright &y& Elsevier]

Four fluorescent low molecular weight gelators based on benzoxazole or benzothiazole functionalized pyrimidine were designed and synthesized. The ability of the target was tested, and all compounds could form stable supramolecular gels in an alcohol/water mixture and its fluorescence increased during gel formation. Photophysical spectra during gel formation, SEM, XRD, FT-IR study suggested that the self-assembly was driven by hydrogen bonding, van der Waals forces and weak π-π interaction. Interestingly, the gel collapsed after being illuminated by 365 nm UV light and 1H NMR of the gel before and after illumination proved that the [2 + 2]-cycloaddition between the double bond of pyrimidine was responsible for the light response. Furthermore, the fluorescent of xerogel film could be quenched by volatile acids while the fluorescent of the solution was enhanced after acid was added. The different phenomena were discussed. The nano-fiber assembled via gel formation could be used as fluorescent imaging material of latent fingerprints. [Display omitted] • Design and synthesis of novel uracil derivatives containing benzoxazole and benzothiazole. • Benzoxazole-modified uracil derivatives exhibit good gelation abilities and driving force of gel formation was investigated. • The gel could respond to light and acid. The response mechanism was studied. • The nano-materials assembled via gel formation could be used as fluorescent imaging material of latent fingerprints. [ABSTRACT FROM AUTHOR]

New β-diketone-boron difluoride complexes functionalized with tetraphenylethene ( TPEB , DTPEB and TTPEB ) which exhibit AIE (aggregation-induced emission) properties have been synthesized. It was found that only boomerang-shaped DTPEB without any traditional gelation groups could form organogel in specific organic solvents. It gave strong orange red fluorescence in organogel as well as in xerogel-based film although it was non-emissive in solution. It is interesting that the emission of DTPEB in xerogel-based film could be quenched significantly upon exposure to triethylamine (TEA) vapour, and the detection limit was as low as ca. 0.1 ppb. This work provides a strategy for the synthesis of a new rigid non-traditional π-gelator via the construction of a boomerang-shaped π-conjugated skeleton. In addition, the gelation of the π-gelators with AIE ability is a facile method for the fabrication of luminescent organic nanomaterials. [ABSTRACT FROM AUTHOR]

New triphenylvinyl substituted carbazole derivatives TPEICE , TPEC and TPECBr have been synthesized. They could self-assemble into nanofibers via organogelation processes in some organic solvents. Notably, the obtained xerogel-based films could emit strong fluorescence although the three compounds were non-emissive in solutions, indicating AIE in gel phases. The emission of TPEICE and TPEC in xerogel-based films could be quenched significantly upon exposed to gaseous DNT and TNT, while TPECBr could not sense nitro compounds on account of its poor electron donating ability. We also found that reversibility of the fluorescence response of TPEC was better than TPEICE because the photo-induced electron transfer would happen during the recognition of nitroaromatics for TPEICE and TPEC , except for the formation of charge–transfer complex between TPEICE and nitro compounds. Therefore, the different fluorescence response behaviors of TPEICE , TPEC and TPECBr towards nitroaromatics were resulted from their different electron donating abilities. [ABSTRACT FROM AUTHOR]

Four new D-π-A type N,O -chelated BF 2 complexes (TCBOB , TCBTB , TCQB and TCPB) were synthesized. It was found that TCPB bearing the ligand of N -(1-pyridinyl)benzoamide shows gelation ability in methylcyclohexane, DCM/peteroleum ether, etc. The time-dependent UV–vis absorption and fluorescent emission spectral changes during the gel formation revealed that π-π interactions play important roles in the self-assembling processes. Particularly, the emission of the xerogel-based film of TCPB can be quenched by TFA (trifluoroacetic acid) vapor, and it showed high performance in the detection of TFA compared with the spin-coating films of TCBOB , TCBTB and TCQB. In addition, the BF 2 complexes exhibited reversible mechanofluorochromic behavior under the treatment of grinding/fuming or heating, and TCPB gave high-contrast mechanofluorochromism compared with others. XRD patterns in different solid states demonstrated that the external mechanical forces can induce the transformation from the crystalline to the amorphous states. Powder of TCPB was also used to image latent fingerprints on surface of glasses, and distinct fluorescent images were obtained. [Display omitted] • New BF 2 complexes were synthesized. • Gelation abilities and MFC properties of them were studied. • They were first used to detect LFP. [ABSTRACT FROM AUTHOR]