Selectivity of hexaphenylbenzene-based hydrocarbon stationary phase with propeller-like conformation for aromatic and aliphatic isomers.

Herein we report a propeller-like hexaphenylbenzene-based hydrocarbon material (denoted as BT) as the stationary phase for capillary gas chromatography (GC). The statically-coated BT capillary column showed a high column efficiency of 4340 plates m and weak polarity. Owing to its unique conformation, π-electron toroidal delocalization and intrinsic microporosity, the BT stationary phase exhibited interesting selectivity for aromatic compounds over alkanes.

Rational design of asymmetric red fluorescent probes for live cell imaging with high AIE effects and large two-photon absorption cross sections using tunable terminal groups.

In this work, we report the synthesis of a family of donor-acceptor (D-A) π-conjugated aggregation-induced red emission materials (, , and ) with the same core 2,2-(2,2-diphenylethene-1,1-diyl)dithiophene (DPDT) and different amounts and different strengths of electron-donating terminal moieties. Interestingly, and , which have asymmetric structures, give obviously higher solid fluorescence quantum efficiencies in comparison with those of the corresponding symmetric structures, and , respectively. In particular, the thin film of exhibited the highest fluorescence quantum efficiency of 38% with the highest .

Series of Multifluorine Substituted Oligomers for Organic Solar Cells with Efficiency over 9% and Fill Factor of 0.77 by Combination Thermal and Solvent Vapor Annealing.

We report the synthesis of a family of multifluorine substituted oligomers and the corresponding polymer that have the same backbones but different conjugation lengths and amounts of fluorine atoms on the backbone. The physical properties and photovoltaic performances of these materials were systematically investigated using optical absorption, charge mobility, atomic force microscopy, transmission electron microscopy, grazing incidence X-ray diffraction, resonant soft X-ray scattering methods, and photovoltaic devices. The power conversion efficiencies (PCEs) based on oligomers were much higher than that in the polymer.

Hexaphenylbenzene-Based, π-Conjugated Snowflake-Shaped Luminophores: Tunable Aggregation-Induced Emission Effect and Piezofluorochromism.

In this work, two rigid, multiple tetraphenylethene (TPE)-substituted, π-conjugated, snowflake-shaped luminophores BT and BPT were facilely synthesized by using a 6-fold Suzuki coupling reaction. These molecules are constructed based on the nonplanar structure of propeller-shaped hexaphenylbenzene (HPB) or benzene as core groups and TPE as end groups. As a result, they reserve the intrinsic aggregation-induced emission (AIE) property of the TPE moiety.

Aggregation-induced emission and efficient solid-state fluorescence from tetraphenylethene-based N,C-chelate four-coordinate organoborons.

In it together: Thermally stable N,C-chelate four-coordinate organoborons were attained by grafting intramolecular B⋅ ⋅ ⋅N coordination into tetraphenylethene-pyridine and -quinoline adducts. They exhibit aggregation-induced emission characteristics (see figure), and high fluorescence quantum yields approaching unity in solid films.

From tetraphenylethene to tetranaphthylethene: structural evolution in AIE luminogen continues.

Replacement of phenyl ring(s) in tetraphenylethene by naphthalene ring(s) generates a series of new luminogens with aggregation-induced emission (AIE) characteristics, demonstrating that bulky naphthalene rings can serve as a rotor to construct AIE luminogens.

Aggregation-enhanced emission and efficient electroluminescence of tetraphenylethene-cored luminogens.

A new design of luminescent materials by decorating a tetraphenylethene core with four aromatic chromophores is proposed. The generated luminogens exhibit aggregation-enhanced emission and excellent solid-state fluorescence efficiency (93-99%). Efficient non-doped OLEDs based on them afford remarkable efficiencies up to 11 cd A(-1).

Efficient electroluminescence from excimers of 1,3,6,8-tetrakis(3,5-dimethylphenyl)pyrene.

Excimers are generally considered as detrimental to OLEDs. For pyrene-based chromophores, however, this is not always true. In this contribution, two new methylated tetraphenylpyrenes, 1,3,6,8-tetra-o-tolylpyrene (TTPy) and 1,3,6,8-tetrakis(3,5-dimethylphenyl)pyrene (TDMPPy), were synthesized through Suzuki coupling reactions.

A fully substituted 3-silolene functions as promising building block for hyperbranched poly(silylenevinylene).

A 3-silolene derivative, 2,2,5,5-tetrakis(dimethylsilyl)-1,1-dimethyl-3,4-diphenyl-3-silolene (TDMSHS), is first synthesized and characterized by X-ray diffraction crystallography and spectroscopic methods. Hydrosilylation polymerization of TDMSHS with 1,1-dimethyl-2,5-bis(4-ethynylphenyl)-3,4-diphenylsilole in the presence of Karstedt's catalyst generates a stereoregular silole-containing hyperbranched poly(silylenevinylene) (hb-SPSV) with a high molecular weight (M(w) = 146,000, M(w)/M(n) = 1.5) in high yield (≈95%).