Fluoride Anion Research Articles

Mineralogical insights into anion and cation dissolution behavior in calcium arsenic residue from copper smelting: Implications for safe disposal

This study investigates the dissolution behavior of calcium-arsenic residue (CAR) sourced from a copper smelter in China, crucial for its safe disposal. Using mineralogical analysis, we identified fine powders, medium particles, and varying crystallinity in lumps, with calcium arsenate oxides comprising 56.03 % of the total weight. Arsenic dissolution is predominantly influenced by arsenic-containing mineral phases, with calcium arsenate oxides serving as the primary controlling phase. Other cations, including copper, zinc, calcium, and lead, behave according to their respective mineral phases. At a leaching pH of 3, concentrations of heavy metal ions such as As, Zn, Cu, and Pb exceed permissible limits set by the United States Environmental Protection Agency (USEPA), reaching approximately 3500, 155, 30, and 7.5 mg/L, respectively. The release of fluoride and chloride anions remains consistent throughout the system, largely unaffected by pH variations, at approximately 10 and 200 mg/L, respectively. Additionally, the competitive interaction between SO42- and AsO43- for Ca2+ ions promote SO42- dissolution, leading to morphological changes in gypsum (CaSO4·2 H2O). Under acidic conditions (pH=3), there's an increase in gypsum volume, with SO42- leaching concentration around 1100 mg/L, while under alkaline conditions (pH=12), the SO42- leaching concentration increases to around 4400 mg/L due to the dominance of AsO43-. Kinetic analysis suggests that arsenic release involves a combination of diffusion and interfacial mass transfer. Overall, this study provides valuable insights into the characterization and dissolution behavior of CAR-related minerals, offering comprehensive data support for their safe disposal and landfilling.

Cyclic Azahelicene Dimers Showing Bright Circularly Polarized Luminescence and Selective Fluoride Recognition.

Although helicenes are promising molecules, the synthetic difficulty and tediousness have often been problems, and only small amounts of optically pure helicenes have been obtained by using chiral HPLC in most cases. Herein, aza[7]helicenes or closed-aza[7]helicenes with (1R)-menthyl substituents were selectively synthesized via the intramolecular Scholl reaction, and the diastereomeric pairs were separated by silica gel column chromatography. The optically pure helicenes were further transformed into the corresponding cyclic dimers, and the chiroptical properties were investigated. The rigid π-frameworks of the dimers led to the high molar extinction coefficients and fluorescence quantum yields, while the twisted helicene moieties induced clear Cotton effects and CPL in the visible region, and the high CPL brightness (BCPL) was achieved. Furthermore, the cyclic dimers were found to have the macrocyclic cavity with the two NH groups suitable for the selective binding of a fluoride anion, which induced significantly redshifted fluorescence and CPL in the red region.

Cyclic Azahelicene Dimers Showing Bright Circularly Polarized Luminescence and Selective Fluoride Recognition

AbstractAlthough helicenes are promising molecules, the synthetic difficulty and tediousness have often been problems, and only small amounts of optically pure helicenes have been obtained by using chiral HPLC in most cases. Herein, aza[7]helicenes or closed‐aza[7]helicenes with (1R)‐menthyl substituents were selectively synthesized via the intramolecular Scholl reaction, and the diastereomeric pairs were separated by silica gel column chromatography. The optically pure helicenes were further transformed into the corresponding cyclic dimers, and the chiroptical properties were investigated. The rigid π‐frameworks of the dimers led to the high molar extinction coefficients and fluorescence quantum yields, while the twisted helicene moieties induced clear Cotton effects and CPL in the visible region, and the high CPL brightness (BCPL) was achieved. Furthermore, the cyclic dimers were found to have the macrocyclic cavity with the two NH groups suitable for the selective binding of a fluoride anion, which induced significantly redshifted fluorescence and CPL in the red region.

Mechanism of the Low-Temperature Organic Removal from Imidazolium-Containing Zeolites by Ozone Treatment: Fluoride Retention in Double-4-Rings.

For zeolites synthesized using imidazolium cations, the organic matter can be extracted at very low temperatures (100 °C) using ozone. This is possible for zeolites with 12-ring or larger pores but requires higher temperatures in medium-pore zeolites. The first chemical events in this process occur fast, even at room temperature, and imply the loss of aromaticity likely by the formation of an adduct between ozone and the imidazole ring through carbons C4 and C5. Subsequent rupture of the imidazole ring provides smaller and more flexible fragments that can desorb more readily. This process has been studied experimentally, mainly through infrared spectroscopy, and theoretically by density functional theory. Amazingly, fluoride anions occluded in the small double-four-ring units (d4r) during the synthesis remain inside the cage throughout the whole process when the temperature is not too high (≤150 °C). However, fluoride in larger cages in MFI ends up bonded to silicon in penta or hexacoordinated units, likely out of the cages, after ozone treatment at 150 °C. For several germanosilicate zeolites, the process allows their subsequent degermanation to yield stable high-silica zeolites. Quaternary ammonium cations require harsher conditions that eventually also extract fluoride from zeolite cages, including the d4r unit.

Order-to-Disorder Transition and Hydrogen Bonding in the Jahn-Teller Active NH4CrF3 Fluoroperovskite.

Large quantities of high-purity NH4CrF3 have been synthesized using a wet-chemical method, and its structural chemistry and magnetic properties are investigated in detail for the first time. NH4CrF3 is a tetragonal fluoroperovskite that displays an ordering of the ammonium (NH4+) groups at room temperature and C-type orbital ordering. The ammonium groups order and display distinct signs of hydrogen bonds to nearby fluoride anions by buckling the Cr-F-Cr angle away from 180°. The ammonium ordering remains up to 405 K, much higher than in other ammonium fluoroperovskites, indicating a correlation between the flexibility of the Jahn-Teller ion, the hydrogen bond formation, and the ammonium ordering. At 405 K, an order-to-disorder transition occurs, where the ammonium groups disorder, corresponding to a transition to higher symmetry. This is accompanied by a contraction of the unit cell from breaking hydrogen bonds, similar to the phenomenon observed in water ice melting. The compound orders antiferromagnetically with a Neél temperature of 60 K, an effective paramagnetic moment of 4.3 μB, and a Weiss temperature of -33 K. An A-type antiferromagnetic structure is identified by neutron diffraction, with an ordered moment of 3.72(2) μB.

Fluoride-Ion-Responsive Sol-Gel Transition in an L-Cysteine/AgNO3 System: Self-Assembly Peculiarities and Anticancer Activity.

Supramolecular hydrogels based on low-molecular-weight compounds are a unique class of so-called "soft" materials, formed by weak non-covalent interactions between precursors at their millimolar concentrations. Due to the variety of structures that can be formed using different low-molecular-weight gelators, they are widely used in various fields of technology and medicine. In this study, we report for the first time an unusual self-assembly process of mixing a hydrosol obtained from L-cysteine and silver nitrate (cysteine-silver sol-CSS) with sodium halides. Modern instrumental techniques such as viscosimetry, UV spectroscopy, dynamic light scattering, zeta potential measurements, SEM and EDS identified that adding fluoride anions to CSS is able to form stable hydrogels of a thixotropic nature, while Cl-, Br- and I- lead to precipitation. The self-assembly process proceeds using a narrow concentration range of F-. An increase in the fluoride anion content in the system leads to a change in the gel network morphology from elongated structures to spherical ones. This fact is reflected in a decrease in the gel viscosity and a number of gel-sol-gel transition cycles. The mechanism of F-'s interaction with hydrosol includes the condensation of anions on the positive surface of the CSS nanoparticles, their binding via electrostatic forces and the formation of a resulting gel carcass. In vitro analysis showed that the hydrogels suppressed human squamous carcinoma cells at a micromolar sample concentration. The obtained soft gels could have potential applications against cutaneous malignancy and as carriers for fluoride anion and other bioactive substance delivery.

G-C3N4-Catalyzed photochemical synthesis of trifluoromethylated gem-difluoroalkenes from α-trifluoromethyl styrenes and CF3SO2Na

Trifluoromethyl-substituted gem-difluoroalkenes were synthesized via the reaction of α-trifluoromethyl styrenes with trifluoromethyl radical derived from sodium trifluoromethylsulfinate under the visible light induced graphitic carbon nitride-mediated heterogeneous photocatalysis. The disclosed process is based on the sequential radical/ionic transformations of α-trifluoromethyl alkenes. The developed approach exploits the dual role of g-C3N4 as a photocatalyst. g-C3N4 acts as an electron acceptor for the generation of CF3 radicals and participates in the reduction of intermediate carbon-centered radical with β-elimination of fluoride anion and formation of the target products.

Turn-on Coumarin Precursor: From Hydrazine Sensor to Covalent Inhibition and Fluorescence Detection of Rabbit Muscle Aldolase.

Hydrazine, a highly toxic compound, demands sensitive and selective detection methods. Building upon our previous studies with pre-coumarin OFF-ON sensors for fluoride anions, we extended our strategy to hydrazine sensing by adapting phenol protecting groups (propionate, levulinate, and γ-bromobutanoate) to our pre-coumarin scaffold. These probes reacted with hydrazine, yielding a fluorescent signal with low micromolar limits of detection. Mechanistic studies revealed that hydrazine deprotection may be outperformed by a retro-Knoevenagel reaction, where hydrazine acts as a nucleophile and a base yielding a fluorescent diimide compound (6,6'-((1E,1'E)-hydrazine-1,2diylidenebis(methaneylylidene))bis(3(diethylamino)phenol, 7). Additionally, our pre-coumarins unexpectedly reacted with primary amines, generating a fluorescent signal corresponding to phenol deprotection followed by cyclization and coumarin formation. The potential of compound 3 as a theranostic Turn-On coumarin precursor was also explored. We propose that its reaction with ALDOA produced a γ-lactam, blocking the catalytic nucleophilic amine in the enzyme's binding site. The cleavage of the ester group in compound 3 induced the formation of fluorescent coumarin 4. This fluorescent signal was proportional to ALDOA concentration, demonstrating the potential of compound 3 for future theranostic studies in vivo.

Optoelectronic Response to the Fluor Ion Bond on 4-(4,4,5,5-Tetramethyl-1,3,2-dioxoborolan-2-yl)benzaldehyde.

Boronate esters are a class of compounds containing a boron atom bonded to two oxygen atoms in an ester group, often being used as precursors in the synthesis of other materials. The characterization of the structure and properties of esters is usually carried out by UV-visible, infrared, and nuclear magnetic resonance (NMR) spectroscopic techniques. With the aim to better understand our experimental data, in this article, the density functional theory (DFT) is used to analyze the UV-visible and infrared spectra, as well as the isotropic shielding and chemical shifts of the hydrogen atoms 1H, carbon 13C and boron 11B in the compound 4-(4,4,5,5-tetramethyl-1,3,2-dioxoborolan-2-yl)benzaldehyde. Furthermore, this study considers the change in its electronic and spectroscopic properties of this particular ester, when its boron atom is coordinated with a fluoride anion. The calculations were carried out using the LSDA and B3LYP functionals in Gaussian-16, and PBE in CASTEP. The results show that the B3LYP functional gives the best approximation to the experimental data. The formation of a coordinated covalent B-F bond highlights the remarkable sensitivity of the NMR chemical shifts of carbon, oxygen, and boron atoms and their surroundings. Furthermore, this bond also highlights the changes in the electron transitions bands n → π* and π → π* during the absorption and emission of a photon in the UV-vis, and in the stretching bands of the C=C bonds, and bending of BO2 in the infrared spectrum. This study not only contributes to the understanding of the properties of boronate esters but also provides important information on the interactions and responses optoelectronic of the compound when is bonded to a fluorine atom.

Redox transformation of bismuth active units encapsulated on carbon nanorods for efficient fluoride Electrosorption: Synergistic roles of Faradaic effect and EDL capacitance

Remediation of fluoride in groundwater through electrosorption to cope with its high charge density and the smallest anion radius remains a promising strategy. Composite carbon materials obtained by calcining metal–organic frameworks contribute to the performance of conventional fluoride electrosorption systems. This study provides a redox-active electrode (MBiC@tE) that incorporates the Faradaic ion trapping effect for fluoride removal. Under potential control, MBiC@tE reversibly traps/releases fluoride anions from the aqueous solution through the combined roles of Faradaic pseudocapacitance and electrical double layer capacitance, with an electrosorption capacity of approximately 37.9 mgF- gelectrode-1. The target contaminant anions are directly involved in the Faradaic reaction on the bismuth sites, with the formation of Bi-F bond excited by an electric field, thus resulting in the removal of fluoride as a consequence of the generation of insoluble substance (BiF3). Furthermore, as expected (Bi0 + 3F- ⇌ BiF3 + 3e-), the working electrode exhibits good reversibility and maintains a high fluoride removal capacity even after multiple cycles. This study presents a comprehensive elucidation on the synergistic roles of Faradaic effect and electrical double layer capacitance induced by the electric field, and offers profound insights into the phase transition of bismuth and its affinity for fluoride during the electrosorption.

Engineering Clock Transitions in Molecular Lanthanide Complexes.

Molecular lanthanide (Ln) complexes are promising candidates for the development of next-generation quantum technologies. High-symmetry structures incorporating integer spin Ln ions can give rise to well-isolated crystal field quasi-doublet ground states, i.e., quantum two-level systems that may serve as the basis for magnetic qubits. Recent work has shown that symmetry lowering of the coordination environment around the Ln ion can produce an avoided crossing or clock transition within the ground doublet, leading to significantly enhanced coherence. Here, we employ single-crystal high-frequency electron paramagnetic resonance spectroscopy and high-level ab initio calculations to carry out a detailed investigation of the nine-coordinate complexes, [HoIIIL1L2], where L1 = 1,4,7,10-tetrakis(2-pyridylmethyl)-1,4,7,10-tetraaza-cyclododecane and L2 = F- (1) or [MeCN]0 (2). The pseudo-4-fold symmetry imposed by the neutral organic ligand scaffold (L1) and the apical anionic fluoride ion generates a strong axial anisotropy with an mJ = ±8 ground-state quasi-doublet in 1, where mJ denotes the projection of the J = 8 spin-orbital moment onto the ∼C4 axis. Meanwhile, off-diagonal crystal field interactions give rise to a giant 116.4 ± 1.0 GHz clock transition within this doublet. We then demonstrate targeted crystal field engineering of the clock transition by replacing F- with neutral MeCN (2), resulting in an increase in the clock transition frequency by a factor of 2.2. The experimental results are in broad agreement with quantum chemical calculations. This tunability is highly desirable because decoherence caused by second-order sensitivity to magnetic noise scales inversely with the clock transition frequency.

The effect of pseudoknot base pairing on cotranscriptional structural switching of the fluoride riboswitch.

A central question in biology is how RNA sequence changes influence dynamic conformational changes during cotranscriptional folding. Here we investigated this question through the study of transcriptional fluoride riboswitches, non-coding RNAs that sense the fluoride anion through the coordinated folding and rearrangement of a pseudoknotted aptamer domain and a downstream intrinsic terminator expression platform. Using a combination of Escherichia coli RNA polymerase in vitro transcription and cellular gene expression assays, we characterized the function of mesophilic and thermophilic fluoride riboswitch variants. We showed that only variants containing the mesophilic pseudoknot function at 37°C. We next systematically varied the pseudoknot sequence and found that a single wobble base pair is critical for function. Characterizing thermophilic variants at 65°C through Thermus aquaticus RNA polymerase in vitro transcription showed the importance of this wobble pair for function even at elevated temperatures. Finally, we performed all-atom molecular dynamics simulations which supported the experimental findings, visualized the RNA structure switching process, and provided insight into the important role of magnesium ions. Together these studies provide deeper insights into the role of riboswitch sequence in influencing folding and function that will be important for understanding of RNA-based gene regulation and for synthetic biology applications.

Defluoridation of tap water by electrocoagulation and fluoride adsorption on aluminum hydroxide flocs

ABSTRACT Overload of fluoride ions in water is observed in several regions of southern Tunisia, mainly the regions close to the mining basin of Gafsa: Metlaoui, Omlarayes and Redayef. This study concerns fluoride removal from Metlaoui's tap water by electrocoagulation (EC) using aluminum electrodes in a batch reactor. This water contains 3.5 mg·L−1 of fluoride, the highest concentration observed in these basins. The effect of the operating conditions of EC treatment on tap water defluoridation was analyzed, namely, current density, temperature and interelectrode distance. Hydroxide aluminum flocs, formed with different durations of EC, were used as sorbents in fluorinated deionized water ([F−] = 3.5 mg·L−1) and Metlaoui's tap water. Flocs formed after 30 min of EC, produced by dissolving (79 ± 1) mg·L−1 of aluminum and adjusted at pH = 6.5, allowed the adsorption of (98 ± 1)% of fluoride ions from deionized fluorinated water. Flocs adjusted at different pH, from 5 to 9, were used as sorbents in fluorinated deionized water and Metlaoui's tap water. Acidic and neutral flocs allowed the best yields of fluoride adsorption. Contrary to the literature, this work highlighted the absence of ion exchange of hydroxide anion by fluoride anion in water, highlighting a mechanism of physical adsorption on aluminum hydroxide flocs.

On characterization of entropy measure using logarithmic regression model for Copper(II) Fluoride.

The versatile uses of Copper(II) Fluoride (CuF2) are well known; these include its usage as a precursor in chemical synthesis as well as its contribution to the creation of sophisticated materials and electronics. There are interesting opportunities to study the interactions between these elements because of their unique crystal structure, which contains copper ions and fluoride anions. Its potential in optoelectronic devices and conductive qualities also make it a viable material for next-generation technologies. To better understand the structural properties of CuF2 and how they affect its entropy, we present new Zagreb indices in this study and use them to calculate entropy measures. We also build a regression model to clarify the relationship between the calculated indices and entropy levels. The findings of our investigation offer significant understanding regarding the ability of the suggested Zagreb indices to extract meaningful content and their correlation with entropy in the context of CuF2. This information is important for understanding CuF2 alloys and for exploring related complex materials.

Sodium fluoride enables room-temperature synthesis of dimethyl carbonate

Carbon dioxide (CO2) in the atmosphere of the Earth represents an abundant and largely free source of carbon, which remains heavily underestimated nowadays. The disbalance between the emission and utilization of CO2 puts the sustainable development of humanity at risk because of its possible correlation with global climate change. The valorization of CO2 is an important strategy to attend to the above-mentioned challenges. CO2 can be converted to dimethyl carbonate by grafting to methanol (CH3OH) in the presence of the catalyst. The presently known catalytic solutions require high temperatures and pressures to be employed. Herein, we report sodium fluoride as a new catalyst offering an unprecedentedly low activation barrier, 23 kJ/mol, for the carboxylation of CH3OH. The fluoride anion coordinates the hydroxyl hydrogen of CH3OH thanks to forming a very strong H-bond. Upon the collision with CO2, the proton detaches, and CO2 grafts to CH3O* while becoming the carboxyl group. The reaction finishes by methylating CH3OC(O)O– via the methyl radical originating from another CH3OH molecule (esterification stage). The hydrogen fluoride molecule is an intermediate in this reaction providing the proton and fostering esterification. The subsequent in-lab experiments showed that much milder conditions can be used to synthesize DMC out of CH3OH. Under 80 °C and 40 bar, we obtained an outstanding DMC yield of 21.1 %. However, the synthesis was also possible at lower temperatures giving DMC yields of 16.3 % at 65 °C, 14.7 % at 55 °C, and 10.8 % at 25 °C. The unprecedented possibility to obtain a non-negligible production of an organic carbonate at room temperature represents a cornerstone advance in the field of CO2 valorization and promises huge energy savings. Given the current global amount of the yearly prepared DMC amounting to over one million tons and the demand for this chemical by emerging chemical technologies, the achieved result is deemed to be of paramount importance. The exemplified catalytic mechanism is also interesting in the context of other syntheses, in which a low-energetic production of the methoxy moieties is a cornerstone.

Sequence closed-loop recovery of fluoride, phosphate, and sulfate anions from phosphogypsum leachate via precipitation-electrodialysis-crystallization approaches

Phosphogypsum (PG) is a large-scale industrial by-product generated during the production of phosphoric acid, typically being deposited in landfills worldwide. The leaching of fluoride (F−), phosphate (PO43−), and sulfate (SO42−) anions from PG into water bodies through rainfall results in significant environmental pollution. Herein, we propose a stepwise precipitation combined with electrodialysis and crystallization strategy for efficient recovery and valorization of multiple anions from PG leachate. Our method demonstrates effectiveness both theoretically and practically. Consequently, fluoride anions were precipitated as CaF2 and Ca5(PO4)3F at pH 4.7, with a recovery rate of 98.80 %; phosphate anions as MgNH4PO4·H2O at pH 8.5, with a recovery rate of 99.91 %; and sulfate anions through electrodialysis and crystallization with a recovery efficiency of 99.89 %, ensuring effluent met discharge standards. In addition, the concentrated sulfate-rich solution was employed for electrochemical production of persulfate, yielding ammonium persulfate salts after cooling crystallization. Our integrated approach for multiple anion recovery from PG leachate offers significant environmental and economic benefits, providing valuable insights and references for future research and practical production.

A Chromogenic Probe for Detection of Biologically Important Anions and its Implications for Designing Molecular Logic Gates.

Detection of fluoride (F-), acetate (AcO-), and cyanide (CN-) anions is vital from the biological and environmental aspects. In the present contributions, we have introduced a simple Salen-type chromogenic sensor, BEN, to detect these biologically important anions. Changes in UV-visible absorption spectra and color of BEN solution from very pale yellow to pink color are similar for each of these anions and found to be reversible only in the case of F- ions in attendance of HSO4- ions. The estimated limit of detection of BEN solution for detecting F-, AcO-, and CN- anions is found to be below the micromolar (μM) concentration level. Our fabricated handy paper test kit is suitable for qualitatively naked-eye detection of the anions. An immediate quantitative estimation of these important anions is possible using our BEN employing a smartphone, avoiding any costly experimental setup.

Performance Enhancement of Tin-Based Perovskite Photodetectors through Bifunctional Cesium Fluoride Engineering.

Tin halide perovskites are rising as promising candidates for next-generation optoelectronic materials due to their good optoelectronic properties and relatively low toxicity. However, the high defect density and the easy oxidation of Sn2+ have limited their optoelectronic performance. Herein, we report the treatment of the FASnI3 (formamidinium tin, FA) perovskite film by a bifunctional cesium fluoride (CsF) additive, which improves the film quality and significantly enhances the photoelectric performance. The responsivity of the perovskite-based photodetector (PD) with an optimal CsF concentration of 15% is over 60 times larger than that of the PD without CsF. It indicates that both the Cs substitution and the fluoride anion additive from CsF inhibit the oxidation of Sn2+, optimize the crystal growth, and passivate the defects, demonstrating the dual roles of the CsF additive in improving the photoelectric performance. This work offers valuable insights into the additive selection for developing high-quality tin-based perovskite films and devices.

Dual-Responsive Near-Infrared BODIPY-Based Fluorescent Probe for the Detection of F- and HClO in Organisms.

Fluoride anions (F-) play a crucial role in human physiological processes. However, excessive intake of F- would affect oxygen metabolism and promote the generation of oxygen-free radicals. Hence, it is essential to develop a precise and efficient fluorescent probe for visualizing F--induced oxidative stress. In this work, we developed the first bifunctional BODIPY-based fluorescent probe dfBDP with p-tert-butyldimethylsilanolate benzyl thioether as the sensing site for the detection of F- and HClO via two distinct reactions, the self-immolative removal and the thioether oxidation, which generate the sensing products with two nonoverlap fluorescence bands: 800-1200 and 500-750 nm, respectively. The probe dfBDP displays rapid response, high specificity, and sensitivity for the detection of F- (LOD, 316.2 nM) and HClO (LOD, 33.9 nM) in vitro. Cellular imaging reveals a correlation between F--induced oxidative stress and the upregulation of HClO. Finally, probe dfBDP was employed to detect F- and HClO in mice under the stimulation of F-. The experimental results display that the level of HClO elevates in the liver of mice.

Template Assisted Formation of 32 and 34π Octaphyrins Embedded with Dithienopyrrole Cores: A New Scaffold to Unravel Proton Coupled Redox Switching and (Anti)Aromaticity.

Herein, we report two distinct octaphyrins obtained by the condensation of new dithieno[3,2-b:2',3'-d]pyrrole based tetrapyrrane under two different acidic conditions. Fourfold meso-substituted octaphyrin was the major product when the reaction was performed in the presence of an aryl aldehyde using trifluoroacetic acid. Whereas, the sixfold meso-substituted octaphyrin was obtained when the precursor was condensed with pentafluorobenzaldehyde using para-toluenesulfonic acid. Such a template effect of aryl aldehydes in oxidative coupling reactions is realized for the first time in literature. Experimental and theoretical studies suggested that the oxidized form of fourfold meso-substituted octaphyrin is 32π antiaromatic and undergoes proton-coupled electron transfer (PCET) to the protonated form of 34π aromatic congener upon treatment with protic acids. Furthermore, small organic molecules such as alcohols and amines were also found to promote chemical reduction. Single crystal X-ray structure revealed that the aromatic counterpart is highly planar and stabilized by several intermolecular H-bonding and F-F interactions, leading to a large 3D supramolecular arrangement and exhibited colorimetric sensing for fluoride and hydroxide anions. On the other hand, sixfold meso-substituted octaphyrin did not show (anti)aromatic features, PCET or anion sensing, but its intriguing absorption features associated with protonation could make it an ideal candidate for pH-dependent bioimaging.