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Halonium ion

A halonium ion is a positively charged onium species in which a halogen atom (typically chlorine, bromine, or iodine) bears the formal positive charge and is bridged between two carbon atoms via a three-center, two-electron bond, often manifesting as a three-membered cyclic structure.^[1] These ions serve as crucial reactive intermediates in organic chemistry, particularly in the electrophilic addition of halogens to alkenes, where they enforce stereospecific anti addition by shielding one face of the double bond.^[2] Halonium ions can be classified into cyclic variants, such as the bromonium ion formed from ethylene and bromine, and acyclic bridged forms like the dimethylbromonium ion, both of which have been characterized through NMR spectroscopy and superacid media.^[1] Pioneering work by George A. Olah in the 1970s enabled the isolation and direct observation of stable halonium salts using superacid conditions, confirming their structures and distinguishing them from open carbenium ion alternatives.^[3] In addition to carbon-bridged forms, halonium ions can also form symmetric linear complexes [D···X···D]⁺ with two Lewis base donors (D), exhibiting strong halogen bonding interactions with energies up to 45 kcal/mol, which enhances their utility in supramolecular assemblies and as synthons in crystal engineering.^[4] In synthetic applications, halonium ions drive regioselective halocyclizations, oxidations, and arylation reactions, with anion effects modulating their reactivity and product distribution.^[5] Recent advances, including gas-phase ultrafast electron diffraction, have captured their transient structures in real time, revealing bond lengths (e.g., C-Br at 1.96 Å in bromonium ions) and dynamic transformations on picosecond timescales, bridging the gap between theoretical models and experimental validation.^[2] As of 2025, new syntheses of stable acyclic dialkyl halonium salts, including chloronium ions via fluoroalkylation, have expanded their accessibility for reactivity studies.^[6] Their electron-deficient nature positions them as potent electrophiles, influencing fields from asymmetric synthesis to materials design, though their high reactivity often limits isolation to specialized conditions.

Fundamentals

Definition and Properties

A halonium ion is a positively charged species in which a halogen atom (X) serves as the central atom in a three-center, two-electron bonding arrangement, typically represented by the general formula R-X^+-R', where X is a halogen (F, Cl, Br, or I) and R and R' are organic groups, hydrogen atoms, or other substituents. These ions exhibit a bridged structure where the halogen shares its positive charge with the adjacent groups, distinguishing them from simple haloalkyl cations.^[7]^[8] Halonium ions are classified into cyclic and acyclic forms. Cyclic halonium ions, such as haliranium ions, feature a three-membered ring involving the halogen and two carbon atoms, often from alkene addition, and can exhibit symmetric or asymmetric bridging depending on the substituents. Acyclic forms involve linear or open-chain arrangements without ring closure, commonly stabilized by donor atoms like nitrogen.^[7]^[4] Stability of halonium ions decreases across the halogen series from iodonium > bromonium > chloronium > fluoronium, primarily due to increasing electronegativity and decreasing atomic size, which weaken the bridging interactions; fluoronium ions, in particular, are highly unstable and rarely isolated. Most halonium ions are transient intermediates with short lifetimes in solution, except for certain iodonium salts that can persist for days or longer under dry, aprotic conditions. These ions display high electrophilicity, making them potent reagents in organic synthesis, and exhibit solubility in aprotic polar solvents such as dichloromethane and acetonitrile, while being insoluble in nonpolar media or decomposing in protic solvents. A prototypical example is the ethylene chloronium ion (C_2H_4Cl^+), a cyclic species formed during chlorination of ethylene, illustrating the bridged nature central to halonium reactivity.^[7]^[8]^[9]

Historical Development

The concept of the halonium ion was first proposed in 1937 by Irving Roberts and George E. Kimball to rationalize the stereospecific anti addition of halogens to alkenes, invoking a bridged three-center two-electron bond that preserved Markovnikov regioselectivity while accounting for the observed diastereoselectivity. This theoretical construct addressed longstanding discrepancies in halogenation mechanisms, suggesting an ionic intermediate rather than a simple open carbocation. During the 1950s and 1960s, accumulating theoretical and experimental evidence bolstered the bridged halonium model. Quantum mechanical calculations, including Hückel molecular orbital approaches, demonstrated the stability of three-center two-electron bonds in such systems, providing a conceptual framework for hypervalent halogen species. Spectroscopic studies, particularly NMR investigations in the mid-1960s, offered direct support by revealing symmetric bridged structures in halonium-like intermediates generated under acidic conditions. A major milestone occurred in 1970 when George A. Olah achieved the first isolation and characterization of stable halonium ions using superacid media, such as SbF₅ in SO₂ClF, enabling low-temperature NMR spectroscopy of species like the ethylchloronium ion.^[3] This breakthrough, part of Olah's pioneering "stable ion" technique for reactive intermediates, confirmed the bridged geometry and earned him the 1994 Nobel Prize in Chemistry for contributions to carbocation chemistry. In the 1980s, structural confirmation advanced with X-ray crystallography, exemplified by the 1985 determination of the biadamantylidene-bromonium ion, which revealed a symmetric three-membered ring with Br–C bond lengths of approximately 1.98 Å, validating the cyclic model in solid state.^[10] By the early 2000s, research shifted toward practical applications, emphasizing iodonium salts as thermally stable, non-metal alternatives for arylation reactions due to their tunable reactivity and ease of handling.

Structure and Bonding

Cyclic Structures

Cyclic halonium ions, particularly the prototypical three-membered ring species, are characterized by a three-center two-electron (3c-2e) bonding model in which the halogen atom bridges two adjacent carbon atoms, forming partial bonds with each. In this arrangement, the halogen utilizes its p-orbitals to interact with the carbon-carbon π-system, resulting in a delocalized positive charge distributed across the C-X-C framework, where X represents chlorine or bromine. The idealized symmetric structure for the ethylene halonium ion is represented as [\ce{CH2-CH2-X}]^{+}, with X = Cl or Br, featuring equivalent C-X distances typically in the range of 2.0–2.2 Å for bromonium ions based on ab initio calculations. The C-X-C bond angle at the halogen is approximately 60°, reflecting the severe ring strain inherent to the three-membered geometry.^[1] In symmetric cases like the ethylene bromonium ion, the bridging is equitable, with both C-X bonds identical and the halogen positioned equidistant from the carbons, minimizing electronic asymmetry. However, substitution on the alkene carbons introduces steric or electronic perturbations, leading to unsymmetric rings where the halogen shifts toward the less substituted or more electron-rich carbon, resulting in disparate C-X bond lengths (e.g., one shortened to ~1.99 Å and the other elongated to ~2.39 Å in certain propylene derivatives).^[11] This asymmetry arises from differential charge stabilization, as confirmed by NMR studies of stable cyclic halonium ions.^[1] Representative examples include the ethylene bromonium ion, a cornerstone intermediate in alkene bromination reactions, where the 3c-2e bond enforces anti addition stereochemistry. In carbohydrate chemistry, chloronium ions form bridged structures with glycals, facilitating stereoselective glycosylations and highlighting the role of these species in natural product synthesis.^[12] The pronounced ring strain in these cyclic halonium ions, exacerbated by the small C-X-C angle and compressed geometry, enhances their electrophilicity, with chloronium ions exhibiting greater reactivity than bromonium counterparts due to the smaller chlorine atom imposing higher angular distortion (~60° vs. slightly larger for Br).^[11] This strain contributes to their transient nature and propensity for nucleophilic ring opening, though isolated examples persist under superacid conditions.^[1]

Acyclic and Hypervalent Structures

Acyclic halonium ions feature a linear, open-chain structure of the form R–X⁺–R', where X is a halogen and R, R' are alkyl or aryl groups bound directly to the central halogen via two-coordinate sigma bonds, without bridging or ring formation. These species are less common than their cyclic counterparts due to their inherent instability, as the positive charge on the halogen leads to rapid decomposition or rearrangement, particularly for lighter halogens like chlorine. For instance, dialkylchloronium ions such as [Cl(CH₃)₂]⁺ are highly reactive and thermally unstable, decomposing rapidly even at low temperatures, while fluorinated analogs like [Cl(CH₂CF₃)₂]⁺ exhibit slightly improved stability but still require low-temperature conditions for isolation.^[13] In these open-chain forms, the C–X–C bond angles are typically around 100–102°, as observed in crystal structures of [Br(CH₂CF₃)₂]⁺ with C–Br bond lengths of approximately 1.96 Å.^[13] Hypervalent halonium ions, particularly iodonium species, represent a distinct class where the central halogen exceeds the octet rule, accommodating two ligands with 10 valence electrons in a bent geometry. Diaryliodonium salts, such as Ph₂I⁺ (diphenyliodonium), exemplify this hypervalency and are notably stable as air- and moisture-resistant crystalline solids, unlike simpler acyclic forms. The bonding in these hypervalent ions is best described by the three-center four-electron (3c-4e) model, involving hypervalent interactions that utilize s and p orbitals on the iodine without significant d-orbital participation, though earlier interpretations invoked d-orbital involvement for the expanded octet.^[14] A representative structure for diaryliodonium ions is Ar–I⁺–Ar', where the I–C bond lengths are approximately 2.1 Å, as measured in various salts like diphenyliodonium fluoborate (I–C ≈ 2.02 Å, C–I–C angle ≈ 94°). Fluoronium analogs of hypervalent halonium ions are rare due to fluorine's poor ability to support hypervalency, stemming from its high electronegativity and limited capacity for expanded coordination. These hypervalent structures contrast with simpler acyclic ions by leveraging the larger size and lower electronegativity of iodine to stabilize the 10-electron configuration.^[15]

Synthesis and Characterization

Generation Methods

Halonium ions are commonly generated through the electrophilic addition of halogens or interhalogens to alkenes, forming cyclic three-membered ring intermediates. In this process, a halogen molecule such as Br₂ approaches the π-bond of the alkene, leading to heterolytic cleavage and formation of a bromonium ion with the bromide counterion. For example, the reaction of ethylene with Br₂ produces the ethylenebromonium ion, which can be represented as:

\ce{CH2=CH2 + Br2 -> [CH2-CH2-Br]+ Br-}

This method is widely used in organic synthesis for anti addition reactions, with conditions typically involving non-nucleophilic solvents like dichloromethane at room temperature.^[16] Stable halonium ions, including both cyclic and acyclic variants, can be generated and isolated in superacid media, pioneered by George A. Olah. Using Magic Acid (a mixture of fluorosulfuric acid, FSO₃H, and antimony pentafluoride, SbF₅), alkyl halides or dihalides are ionized at low temperatures (e.g., -60°C) to form long-lived halonium ions with weakly coordinating anions like Sb₂F₁₁⁻. For instance, 1,2-dibromoethane in Magic Acid yields the ethylenepromonium ion, allowing spectroscopic study without decomposition. This approach has been instrumental in characterizing hypervalent and bridged structures.^[3]^[1] Hypervalent halonium ions, particularly diaryliodonium salts, are synthesized via oxidation of aryl iodides with arenes in the presence of peroxides. A common one-pot protocol involves treating an iodoarene (e.g., iodobenzene) with an arene (e.g., toluene) and m-chloroperbenzoic acid (mCPBA) in dichloromethane, followed by addition of triflic acid (TfOH) to form the iodonium triflate with yields often exceeding 70%. The reaction proceeds through hypervalent iodine(III) intermediates, such as (diacetoxyiodo)benzene, oxidized to the dicationic species. Persulfate oxidants like Oxone® offer sustainable alternatives, enabling scalable synthesis under mild conditions. These salts serve as transferable aryl cation equivalents, isolable with counterions like BF₄⁻ or OTf⁻.^[17]^[18] Halonium ions also form via neighboring group participation, particularly in halocyclization reactions leading to five-membered rings. For example, allylic halides or alcohols undergo intramolecular cyclization with electrophilic halogen sources like N-bromosuccinimide (NBS) in aqueous media, where the halogen migrates to form a bromonium ion intermediate, facilitating stereospecific ring closure. Olah demonstrated this in the ionization of vicinal dihalides, such as 1,3-dibromopropane in superacid, yielding propylenebromonium ions through 1,3-halogen shift. This method is prevalent in synthesizing tetrahydrofurans or pyrrolidines from unsaturated precursors, with conditions tuned to pH and solvent for selectivity.^[16]^[19]

Spectroscopic and Structural Analysis

Nuclear magnetic resonance (NMR) spectroscopy provides key evidence for the bridged structure of halonium ions in solution, particularly through the equivalence of signals for symmetric cyclic systems. In the ethylene bromonium ion generated in superacid media, the ¹H NMR spectrum exhibits a symmetric CH₂ signal at approximately δ 5 ppm, reflecting the rapid bridging of the bromine atom and the resulting equivalence of the two protons. Similarly, the ¹³C NMR spectrum shows a single downfield-shifted signal for the bridged carbons at around δ 100-110 ppm, consistent with the three-center two-electron (3c-2e) bonding and lack of distinction between the two carbons. These observations, first reported by Olah and co-workers using carbon-13 NMR on various cyclic halonium ions, confirm the symmetric nature of the bridge and distinguish it from open-chain haloalkylcarbenium ion alternatives.^[1] Infrared (IR) and Raman spectroscopy further support the structural characterization of halonium ions by identifying characteristic vibrational modes associated with the C–X–C bridge. For bromonium ions, a prominent band at approximately 700 cm⁻¹ in the IR and Raman spectra corresponds to the asymmetric stretching of the C–Br–C unit, providing a diagnostic signature for the bridged geometry. These vibrational frequencies, observed in superacid solutions of cyclic halonium ions, align with the expected weakening of the C–X bonds due to the delocalized 3c-2e interaction and have been used to corroborate solution-phase structures. X-ray crystallography has provided definitive solid-state evidence for halonium ion structures, with the first reported crystal structure of a bromonium ion in 1985 by Olah and colleagues confirming the predicted 3c-2e bonding motif. In this structure, the bromine-carbon distances were measured at approximately 1.98 Å, longer than typical C–Br single bonds (1.94 Å) but indicative of partial bonding in the three-membered ring, while the C–C distance remained consistent with a single bond at about 1.50 Å. This seminal work on a stabilized bromonium ion derivative resolved long-standing debates about the intermediacy of such species in electrophilic additions and established benchmark geometric parameters for the class.^[10] Mass spectrometry techniques, particularly electrospray ionization mass spectrometry (ESI-MS), have enabled the observation of intact halonium ions in the gas phase, especially for more stable iodonium salts. For example, symmetric diaryliodonium ions appear as prominent molecular ions in ESI-MS spectra without fragmentation, allowing confirmation of their connectivity and stability under soft ionization conditions. These measurements, often coupled with collision-induced dissociation to probe bond strengths, complement solution studies by demonstrating the persistence of the bridged structure in isolated ions.^[20] Computational methods, such as density functional theory (DFT), have been employed to validate experimental spectroscopic and structural data for halonium ions. At the B3LYP/6-31G* level, calculated geometries for cyclic bromonium ions reproduce the observed Br–C distances of ~1.98 Å and C–C bond lengths, while predicted NMR chemical shifts match experimental ¹H (δ ~5 ppm) and ¹³C values within 5-10 ppm, supporting the symmetric bridged model. These simulations, benchmarked against Olah's experimental data, provide insights into the electronic structure and aid in interpreting subtle asymmetries in larger systems.^[21]

Reactivity and Mechanisms

Electrophilic Behavior

Halonium ions serve as potent electrophiles in the halogenation of alkenes, initiating the addition reaction by interacting with the π-electron density of the carbon-carbon double bond. The process begins when a dihalogen molecule (X₂, where X = Cl, Br, or I) approaches the alkene, forming a three-center cyclic halonium ion intermediate and releasing a halide anion (X⁻). This bridged structure, first proposed to explain the stereospecificity of halogen additions, positions the halogen atom above the plane of the double bond, shielding one face from further attack.^[22] The electrophilic nature of the halonium ion enforces strict anti addition stereochemistry in the overall reaction. The subsequent nucleophilic attack occurs from the opposite side of the bridged halogen, leading to trans delivery of the two substituents across the original double bond. This backside displacement mechanism was experimentally confirmed through the stereospecific conversion of cis- and trans-2-butene to the corresponding meso and racemic dibromides, respectively, without inversion or syn addition products. A representative example is the bromination of cyclohexene with Br₂, which proceeds via a bromonium ion intermediate to yield trans-1,2-dibromocyclohexane. In the presence of water, the bromide anion is displaced by H₂O as the nucleophile, forming a bromohydrin such as trans-2-bromocyclohexanol. The reaction can be summarized as:

\text{Alkene} + \ce{X2} \rightarrow [\text{halonium ion}]^{+} + \ce{X-} \quad \text{(followed by nucleophile attack)}

This pathway ensures stereospecific anti addition while avoiding carbocation rearrangements common in other electrophilic additions.^[22] In unsymmetrical alkenes, the halonium ion bridge is asymmetric, with the positive charge more localized on the carbon better able to stabilize it (typically the more substituted one). This partial charge distribution directs regioselectivity, where the nucleophile preferentially attacks the more substituted carbon, mimicking Markovnikov orientation without forming a free carbocation. For instance, in the aqueous bromination of propene, the bromonium ion leads predominantly to 1-bromopropan-2-ol, with the OH group at the secondary carbon.

Nucleophilic Reactions and Rearrangements

Halonium ions, particularly cyclic variants formed from alkenes, serve as highly electrophilic intermediates that undergo ring-opening reactions upon attack by nucleophiles. The nucleophilic attack typically proceeds in an anti fashion relative to the halogen bridge, resulting in stereospecific trans addition products. This mechanism combines features of SN1 and SN2 pathways, with the three-membered ring imparting partial carbocation character to the carbons while enforcing backside attack. In unsymmetrical halonium ions, the nucleophile preferentially targets the more substituted carbon atom, which bears greater positive charge density, thereby dictating regioselectivity.^[23] Common nucleophiles include water, which leads to halohydrin formation, as exemplified by the reaction of a bromonium ion with H₂O to yield a trans-2-bromohydrin. Similarly, halide ions such as Br⁻ or Cl⁻ attack to form vicinal dihalides, while alcohols like methanol produce β-halo ethers through crossed addition. These reactions are widely observed in alkene halogenation under aqueous or alcoholic conditions, maintaining the anti stereochemistry due to the bridged structure. For instance, the addition of Br₂ to cyclohexene in water generates trans-2-bromocyclohexanol as the major product.^[23] Rearrangements occur when the halonium bridge collapses to an open carbocation, a process facilitated in polar solvents where solvation stabilizes the dissociated form, or for less stable halonium ions such as chloronium or fluoronium species that exhibit greater open-ion character. This collapse enables carbocation migrations, including the Wagner-Meerwein rearrangement, observed in the halogenation of terpenes where skeletal reorganization leads to more stable polycyclic products. Temperature-dependent NMR studies reveal equilibria between cyclic halonium ions and open carbonium ions, with shifts indicating dynamic interconversion that promotes such rearrangements. In semipinacol-type processes, allylic alcohols undergo halonium-mediated 1,2-shifts to form β-halo carbonyl compounds.^[24]^[24]^[25] The simplified representation of nucleophilic ring-opening is given by:

[\ce{R2C-X-CR2}]^+ + \ce{Nu^-} \rightarrow \ce{R2C(Nu)-X-CR2}

where X denotes the halogen and Nu the nucleophile, highlighting the regioselective addition at the bridged carbons.^[23]

Applications and Recent Advances

Role in Organic Synthesis

Halonium ions play a pivotal role in organic synthesis by serving as electrophilic intermediates that enable stereoselective cyclizations and functionalizations under mild conditions. In halocyclization reactions, intramolecular formation of halonium ions from unsaturated alcohols facilitates the construction of oxygen-containing heterocycles such as tetrahydrofurans and tetrahydropyrans. For instance, treatment of homoallylic alcohols with N-bromosuccinimide (NBS) or iodine sources generates bromonium or iodonium intermediates, which are subsequently attacked by the pendant hydroxyl group, yielding exo- or endo-cyclized products with high regioselectivity. These transformations are particularly valuable for building fused ring systems, as the bridged halonium structure directs nucleophilic attack from the opposite face, ensuring anti stereochemistry.^[26] Asymmetric variants of halocyclization have advanced the field by incorporating chiral ligands or catalysts to achieve enantioselectivity. Chiral phosphoramidites or thioureas, often in catalytic amounts, coordinate with the halogen source to bias the formation of one enantiotopic face of the halonium ion, enabling stereocontrol in additions to alkenes. For example, Lewis base catalysis with chiral Brønsted acids promotes enantioselective bromocycloetherification of 4-penten-1-ols to tetrahydrofurans with up to 95% ee. These methods draw inspiration from earlier asymmetric dihydroxylation protocols but adapt them for halogen-mediated processes, providing access to enantioenriched heterocycles essential for pharmaceutical intermediates.^[27]^[28] Hypervalent iodine reagents, such as diaryliodonium salts, function as aryl cation equivalents akin to halonium ions, offering mild electrophiles for C–H activation and arylation. In palladium- or copper-catalyzed reactions, these salts transfer aryl groups to indoles or arenes via selective C–H functionalization, often in tandem with N–H arylation to form diarylated products in good yields (e.g., 65% for 1,3-diphenylindole). The mild conditions (60–110°C) and broad functional group tolerance make them superior to traditional cross-coupling methods. Similarly, Selectfluor acts as a fluoronium-like reagent for electrophilic fluorination, enabling regioselective introduction of fluorine into alkenes or aromatics under ambient conditions, as seen in the synthesis of fluorinated piperazines.^[29]^[30] In natural product synthesis, halonium-mediated cyclizations have been instrumental in assembling complex marine toxins. Bromocyclization of trans-(+)-laurediol derivatives using tetrabromocyclohexa-2,5-dien-1-one constructs the tetrahydrofuran ring in trans-(+)-deacetylkumausyne, a toxin from red algae Laurencia majuscula, with improved stereoselectivity (5:1 anti:syn) via epoxy ether intermediates. These approaches highlight the utility in forging polycyclic ethers found in ladder toxins. Compared to carbocation routes, halonium ion pathways offer superior stereocontrol through bridged intermediates that prevent rearrangements and enable diastereoselective anti additions (>15:1 dr in some cases), while operating under mild, neutral conditions compatible with sensitive substrates like polyenes in natural product scaffolds.^[31]^[19]

Modern Developments and Examples

In 2018, researchers reported the first spectroscopic evidence for a [C–F–C]⁺ fluoronium ion in solution, characterized through extensive ¹⁹F, ¹H, and ¹³C NMR studies that revealed a symmetric cage-like structure with equivalent carbon atoms bridged by the central fluorine, confirming its elusive divalent fluoronium nature.^[32] This breakthrough addressed long-standing challenges in observing such hypervalent species in non-solid states, building on earlier gas-phase detections. Subsequent structural confirmation came in 2021 via X-ray crystallography of a modified double-norbornyl-type fluoronium cation, which displayed near-covalent F–C bonds and a symmetric geometry, resolving debates over its bonding and stability.^[33] During the 2020s, computational studies have provided deeper insights into halonium ion stability, particularly through quantum chemical modeling of halogen bonding interactions. For instance, density functional theory analyses in 2020 demonstrated the stabilization of iodonium ions in three-center, four-electron O–I–O bonds with oxygen ligands, revealing bond strengths comparable to hydrogen bonds and highlighting their potential in supramolecular assemblies.^[34] These models emphasize the role of electrostatic and charge-transfer contributions in enhancing stability within complex molecular environments. Recent examples illustrate the integration of halonium ions into advanced materials and synthetic protocols. Halogen-bonded organic frameworks (XOFs) based on iodonium-bridged N⋅⋅⋅I⁺⋅⋅⋅N interactions represent a type of periodic organic network, as reported in 2021.^[35] In 2025, stable chlorine(I)-bridged two-dimensional halogen-bonded organic frameworks (XOFs) were reported, demonstrating potential for advanced materials.^[36] Additionally, [N···X···N]⁺-based XOFs enabled ultrafast anhydrous proton conduction.^[37] Iodonium species continue to find applications in catalysis, including visible-light-mediated reactions with hypervalent iodine reagents for selective carbon-halogen couplings. These developments address gaps in green chemistry by promoting solvent-free halogenations, such as mechanochemical protocols using N-halosuccinimides for efficient, catalyst-free halogenation of phenols and anilines.^[38] Fluorine-substituted halide solid electrolytes have been explored for lithium-metal batteries, improving interfacial stability and reducing polarization during cycling, though with a slight decrease in ionic conductivity, as shown in 2023 studies (e.g., 2.1 × 10⁻⁴ S cm⁻¹ at room temperature for Li₂ZrCl₅.₅F₀.₅).^[39]

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[36]
Fluorine-Substituted Halide Solid Electrolytes with Enhanced ...
Aug 1, 2023 · The fluorine-substituted compound exhibits substantially lower polarization after 800 h of lithium stripping and plating owing to enhanced interfacial ...Missing: halonium | Show results with:halonium
[37]
Automated grindstone chemistry: a simple and facile way for PEG ...
Aug 9, 2022 · A simple electrical mortar–pestle was used for the development of a green and facile mechanochemical route for the catalyst-free halogenation of phenols and ...