Fluorescent Macrocyclic Arenes: Synthesis and Applications.

Fluorescent macrocyclic arenes have attracted increasing interest in macrocyclic and supramolecular chemistry due to their exceptional photophysical properties and versatile applications. Classical macrocyclic arenes modified with fluorescent groups at the upper or bottom rims have long provided valuable platforms across various fields. Recently, a large number of novel fluorescent macrocyclic arenes directly composed of polycyclic aromatic or heteroaromatic building blocks including naphthalene, anthracene, tetraphenylethene, pyrene, fluorene, carbazole, acridan, phenothiazine, coumarin, triphenylamine, benzothiadiazole and so on, have been reported, and they have shown specific fluorescent property, and also exhibited broad applications in molecular recognition, sensing, bioimaging and functional materials.

One-step Macrocycle-to-Macrocycle Conversion Towards Two New Macrocyclic Arenes with Different Structures and Properties.

Two new macrocyclic arenes H1 and H2 were conveniently synthesized by the one-step reaction of carboxylic acid substituted octopus[3]arene. It was found that H1 was composed of three ethenoanthracene subunits with a rigid hexagonal structure and H2 contained two ethenoanthracene subunits and one anthracene subunit with a rigid house-shaped structure. Among them, H2 exhibited strong blue fluorescence due to the existence of an anthracene subunit.

Metal-Free Peroxidase-Mimetic Nanocatalysts for Chemodynamic Vascular-Disrupting Cancer Therapy.

Metal ion-facilitated chemodynamic therapy (CDT) is an emerging method for treating cancer. However, its potential is hindered by its low catalytic performance in weakly acidic tumor microenvironments (TMEs) and the severe toxicity of free metal ions. A new approach to tumor therapy, chemodynamic vascular disruption (CVD), is introduced using metal-free, peroxidase (POD)-mimetic multihydroxylated [70] fullerene (MHF) nanocatalysts.

Hepatic oxidative stress and neurotoxicity in Pelophylax kl. esculentus frogs: Influence of long-term exposure to a cyanobacterial bloom.

Although the long-term exposure of aquatic organisms to cyanobacterial blooms is a regular occurrence in the environment, the prooxidant and neurotoxic effects of such conditions are still insufficiently investigated in situ. We examined the temporal dynamics of the biochemical parameters in the liver of Pelophylax kl. esculentus frogs that inhabit the northern (N) side of Lake Ludaš (Serbia) with microcystins (MCs) produced in a cyanobacterial bloom over three summer months.

Biochemical parameters in skin and muscle of Pelophylax kl. esculentus frogs: Influence of a cyanobacterial bloom in situ.

There is little information in scientific literature as to how conditions created by a microcystin (MC) producing cyanobacterial bloom affect the oxidant/antioxidant, biotransformation and neurotoxicity parameters in adult frogs in situ. We investigated biochemical parameters in the skin and muscle of Pelophylax kl. esculentus from Lake Ludaš (Serbia) by comparing frogs that live on the northern bloom side (BS) of the lake with those that inhabit the southern no-bloom side (NBS).

Intramolecular Singlet Fission in an Antiaromatic Polycyclic Hydrocarbon.

Singlet fission (SF), in which one singlet exciton (S ) splits into two triplets (T ) on adjacent molecules through a correlated triplet-pair (TT) state, requires precise but difficult tuning of exciton energetics and intermolecular electronic couplings in the solid state. Antiaromatic 4nπ dibenzopentalenes (DPs) are demonstrated as a new class of single-chromophore-based intramolecular SF materials that exhibit an optically allowed S state with E(S )>2×E(T ) and an optically forbidden S state. Ultrafast population transfer from a high-lying S state to a (TT) state was observed in monomeric solution of styryl-substituted DP (SDP) on a sub-picosecond timescale.

Photocatalytic activation of pyridine for addition reactions: an unconventional reaction feature between a photo-induced hole and electron on TiO2.

TiO2 photocatalysis can be performed for the addition of pyridines to vinylarenes in an anti-Markovnikov manner. Seven examples with considerable yields (56-91%) and selectivity were demonstrated. A comparative survey of the involved process through ESR revealed a novel concerted two electron transfer pathway for these photocatalytic bimolecular addition reactions.

H2O-involved two-electron pathway for photooxidation of aldehydes on TiO2: an isotope labeling study.

Aldehyde pollution has been receiving increasing environmental concern recently. In this study, the photooxidation of aldehydes to carboxylates on the TiO2 surface was studied by an oxygen-isotope-labeling method. The solvent H2O was found to contribute much to the oxygen source of the formed carboxylate, which cannot be explained if the conventional O2-involved free radical chain reaction is the only mechanism for the photocatalytic oxidation of aldehydes.