A Butterfly-Shaped Pyrene Derivative Of Cholesterol And Its Uses As A Fluorescent Probe

A butterfly-shaped pyrene derivative of cholesterol, namely, N,N′-(ethane-1,2-diyl)-bis(N-(2-(chol-amino)ethyl)pyrene-1-sulfonamide) (ECPS), has been designed and synthesized. Solvent effect studies revealed that in good solvents such as n-hexane, benzene, and 1,4-dioxane, the profile of the fluorescence emission of the compound is characterized by pyrene monomer emission, but in poor solvent such as water, the emission is dominated by pyrene excimer emission. Quantitatively speaking, the ratio of the excimer emission to monomer emission changes from 50 to 0 when ECPS is dissolved in water and n-hexane, respectively. In contrast, for a commonly used polarity probe pyrene, the ratio of I3/I1 varies only from ∼0.6 to ∼1.7, where I3 and I1 stand for the intensities of the fluorescence emission at peak 3 and peak 1, respectively. This value suggests that a more powerful discriminating ability of the new compound in polarity sensing. Furthermore, unlike the main components of the compound, pyrene and cholesterol, its main chain is composed of multiple hydrophilic structures, and it is this structure that makes the emission of the compound in organic solvents sensitive to the presence of water. Accordingly, the applicability of the compound in determination of the trace amount of water in some organic solvents was evaluated. As expected, the detection limit of the compound toward water in acetonitrile reaches 7 ppm, a result never reached before. Furthermore, the fluorescence emission of the compound is also sensitive to viscosity variation. Therefore, it is assumed that ECPS may be used both as a polarity probe and a viscosity probe. On the bases of a series of steady-state and time-resolved fluorescence, as well as dynamic light scattering studies, a structural model was proposed to rationalize the fluorescence behavior of the compound in different solvents and its polarity and viscosity probing performances. © 2013 American Chemical Society

Formation of An Ionic PTCA-β-CDNH₂ Complex and Its Application for Phenol Sensing in Aqueous Phase

On the basis of proton transfer in aqueous phase, we prepared a water-soluble and highly fluorescent ionic complex of 3,4,9,10-perylene tetracarboxylic acid (PTCA) and 6-deoxy-6-amino-β-CD (β-CDNH₂) and studied its fluorescence behavior. It was found that the fluorescence emission of the complex is sensitive and selective to the presence of trace amount of toxic phenolic compounds, in particular phenol, which is crucial for water quality control. The detection limit (DL) of the method to the analyte is ∼0.03 μM, a lowest value reported in literatures for similar techniques. Interestingly, the detection at an unprecedented subnanogram (DL, ∼0.12 ng/cm²) level can also be conducted in a visualized manner, which may provide a simple and low-cost protocol for on-site and real-time detection of the analyte. Moreover, the complex is humidity sensitive in dry state, and its color changes from bright yellow to bright green when exposed to wet vapor. Unlike other PTCA bisimide derivatives, preparation of the ionic complex of PTCA/β-CDNH₂ is simple and avoids complicated synthetic burden. Furthermore, introduction of methanol into the aqueous solution of the complex resulted in aggregation as indicated by solution color change and proved by transmission electron microscopy and dynamic light scattering studies, which explains why the compound in dry state is sensitive to the presence of water and water vapor. X-ray diffraction, UV–vis, and fluorescence studies uncovered the H-packing nature of the structure of the aggregate

A Butterfly-Shaped Pyrene Derivative of Cholesterol and Its Uses as a Fluorescent Probe

A butterfly-shaped pyrene derivative of cholesterol, namely, <i>N</i>,<i>N</i>′-(ethane-1,2-diyl)-bis­(<i>N</i>-(2-(chol-amino)­ethyl)­pyrene-1-sulfonamide) (ECPS), has been designed and synthesized. Solvent effect studies revealed that in good solvents such as <i>n</i>-hexane, benzene, and 1,4-dioxane, the profile of the fluorescence emission of the compound is characterized by pyrene monomer emission, but in poor solvent such as water, the emission is dominated by pyrene excimer emission. Quantitatively speaking, the ratio of the excimer emission to monomer emission changes from 50 to 0 when ECPS is dissolved in water and <i>n</i>-hexane, respectively. In contrast, for a commonly used polarity probe pyrene, the ratio of I₃/I₁ varies only from ∼0.6 to ∼1.7, where I₃ and I₁ stand for the intensities of the fluorescence emission at peak 3 and peak 1, respectively. This value suggests that a more powerful discriminating ability of the new compound in polarity sensing. Furthermore, unlike the main components of the compound, pyrene and cholesterol, its main chain is composed of multiple hydrophilic structures, and it is this structure that makes the emission of the compound in organic solvents sensitive to the presence of water. Accordingly, the applicability of the compound in determination of the trace amount of water in some organic solvents was evaluated. As expected, the detection limit of the compound toward water in acetonitrile reaches 7 ppm, a result never reached before. Furthermore, the fluorescence emission of the compound is also sensitive to viscosity variation. Therefore, it is assumed that ECPS may be used both as a polarity probe and a viscosity probe. On the bases of a series of steady-state and time-resolved fluorescence, as well as dynamic light scattering studies, a structural model was proposed to rationalize the fluorescence behavior of the compound in different solvents and its polarity and viscosity probing performances

Coordination-Driven Self-Assembled Metallacycles Incorporating Pyrene: Fluorescence Mutability, Tunability, and Aromatic Amine Sensing

Constructing polycyclic aromatics-based, highly emissive fluorophores with good solubility and tunable aggregated structures and properties is of great importance for film fabrication, solution processing, and relevant functionality studies. Herein, we describe a general strategy to endow conventional organic fluorophores with enhanced solubility and modulated fluorescent properties via their incorporation into coordination-driven self-assembled metallacycles. A widely used fluorophore, pyrene, was decorated with two pyridyl groups to yield functionalized pyrene 4. Mixing 4 with three aromatic dicarboxylates with different lengths and a 90° Pt(II) metal acceptor in a 2:2:4 stoichiometric ratio resulted in the formation of three metallacycles, 1, 2, and 3. The metallacycles display good solubility in polar organic solvents, highly aggregation-dependent fluorescence, and size-dependent emissions at higher concentrations. Moreover, metallacycle 2-based, silica-gel-supported film as fabricated not only is more emissive than the ligand 4-based one but also displays much improved sensing properties for amines in the vapor state, as demonstrated by significantly increased response speed and decreased recovery time. The enhanced solubility, unique fluorescence behavior, and multi-factor modulation character show that coordination-driven self-assembly can be utilized for the development of new fluorophores through simple modification of conventional fluorophores. The fluorophores synthesized this way possess not only complex topological structures but also good modularity and tunability in fluorescence behavior, which are important for grafting multi-stage energy-transfer systems necessary for the development of high-performance sensing materials

Noncovalent Immobilization of a Pyrene-Modified Cobalt Corrole on Carbon Supports for Enhanced Electrocatalytic Oxygen Reduction and Oxygen Evolution in Aqueous Solutions

Efficient oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) are the determinants of the realization of a hydrogen-based society, as sluggish OER and ORR are the bottlenecks for the production and utilization of H₂, respectively. A Co complex of 5,15-bis­(pentafluorophenyl)-10-(4)-(1-pyrenyl)­phenylcorrole (<b>1</b>) bearing a pyrene substituent was synthesized. When it was immobilized on multiwalled carbon nanotubes (MWCNTs), the <b>1</b>/MWCNT composite displayed very high electrocatalytic activity and durability for both OER and ORR in aqueous solutions: it catalyzed a direct four-electron reduction of O₂ to H₂O in 0.5 M H₂SO₄ with an onset potential of 0.75 V vs normal hydrogen electrode (NHE), and it catalyzed the oxidation of water to O₂ in neutral aqueous solution with an onset potential of 1.15 V (vs NHE, η = 330 mV). Control studies using a Co complex of 5,10,15-tris­(pentafluorophenyl)­corrole (<b>2</b>) demonstrated that the enhanced catalytic performance of <b>1</b> was due to the strong noncovalent π–π interactions between its pyrene moiety and MWCNTs, which were considered to facilitate the fast electron transfer from the electrode to <b>1</b> and also to increase the adhesion of <b>1</b> on carbon supports. The noncovalent immobilization of molecular complexes on carbon supports through strong π–π interactions appears to be a simple and straightforward strategy to prepare highly efficient electrocatalytic materials

Dynamic Chemistry-Based Sensing: A Molecular System for Detection of Saccharide, Formaldehyde, and the Silver Ion

Development of artificial complex molecular systems is of great importance in understanding complexity in natural processes and for achieving new functionalities. One of the strategies is to create them via optimized utilization of noncovalent interactions and dynamic covalent bonds. We report here on a new complex molecular system, which was constructed by integrating the multiple interactions containing a dynamic covalent interaction between 1,2-diol and boronic acid, a coordination interaction between the silver ion and pyridyl, and an easy accessible reaction between secondary amine and formaldehyde. By employing the three dynamic interactions, a pyrene (Py) labeled fluorophore, PPB, was designed and synthesized. The compound reacts with fructose (F), a monosaccharide, in aqueous phase and produces a fluorescent adduct, PPB-F, which can be further used as a sensing platform for formaldehyde (FA) and the silver ion. The respective dynamic interactions are accompanied with color changes due to the reversible switching between Py-monomer emission and excimer emission. The respective experimental detection limits (DLs) for the three analytes are much lower than 0.2 mM, 0.1 mM, and 2.5 μM, respectively. The presence of relevant compounds or ions shows little effect upon the sensing. No doubt, the results as presented show that the integration of supramolecular interactions including dynamic covalent bonds can be employed as a general strategy to develop new functional molecular systems or materials