High Yield Research Articles

Preparation of Silver Nanoparticles in a Water-in-Oil Microemulsion Stabilized by Ecosurf EH3 and Determination of Their Electrophoretic Mobility.

This work describes a study on the electrophoresis of silver nanoparticles in reverse microemulsions with varying water content. The microemulsion was stabilized using a nonionic ethoxylated surfactant, 2-ethylhexanol triethoxylate (Ecosurf EH3). This study represents the second example of electrophoresis research conducted in media with a low dielectric constant for etoxylated surfactants. The study also determined the boundaries of thermodynamic stability and the conditions required to obtain nanoparticles with a high yield. The hydrodynamic diameter and electrophoretic mobility of nanoparticles were measured using dynamic light scattering and laser Doppler electrophoresis. The study determined the boundary conditions for applying these methods to laser-absorbing samples. The electrophoretic mobility of nanoparticles was found to be dependent on the fraction of water in the range of 2-5%vol. (equivalent to a metal content of 10-25mM), as determined by electrophoresis in a free medium. The increase in volume fraction of water leads to agglomeration of micelles, which causes a decrease in the electrokinetic potential of nanoparticles, likely due to the blurring of the diffuse part of the electrical double layer.

Synthesis of Naphthalenones Via Photo‐Induced Radical Cascade Fluoroalkylation/Cyclization of Alkenes

AbstractHerein, we report a photoredox‐catalyzed fluoroalkylation of activated alkenes via fluorinated alkyl‐centered radical induced radical addition/annulation/SET/deprotonation in a domino fashion using 4CzIPN as photocatalyst. The protocol features room temperature, transition metal free, high yields and simple operation, affording a facile and efficient strategy to access fluorine‐containing naphthalenone.

Long-Term Effects of Nitrogen Sources on Yields, Nitrogen Use Efficiencies, and Soil of Tilled and Irrigated Corn

Although corn is the most important and nitrogen (N)-fertilized crop, there is a lack of long-term data on the effects of organic and inorganic N fertilizers on the N balance and losses for corn systems under different tillage approaches. From 2012 to 2023, we assessed the effects of the N source on the grain yields from cultivated continuous corn receiving irrigation at a site with minimal erosion in Fort Collins, Colorado, USA, and compared these effects to no-till (NT) and strip till (ST) systems receiving inorganic N. An N balance accounting for N and carbon (C) sequestration found a system nitrogen use efficiency (NUESys) for organic N fertilizer (manure) with a tillage of 86.6%, which was higher than the NUESys of 62.6% with inorganic N fertilizer (enhanced efficiency fertilizer, EEF). Conventional tillage with manure use is a good management practice that contributed to higher grain yields (2 of 11 years), C sequestration (p < 0.05), soil organic N content (p < 0.05), and soil phosphorus (P) content than inorganic N fertilizer with tillage (p < 0.05). The tilled systems, whether receiving organic or inorganic N fertilizer, had higher yields and grain N content than the NT and ST systems receiving inorganic N fertilizer (p < 0.05). The grain production of the cultivated system receiving organic N fertilizer did not decrease with time, while the yields of the cultivated system receiving inorganic N fertilizer decreased with time (p < 0.05), suggesting that cultivated systems receiving organic N fertilizer may be more sustainable and better able to adapt to a changing climate. Additionally, a combination of manure (30% of N input) with EEF (70% of N input) contributed to a synergistic effect that increased the agronomic productivity (harvested grain yields).

Assessment of Genetic Diversity in Greengram (Vigna radiata L.) Using Metroglyph Analysis

Pulses like greengram are essential for sustainable agriculture and global food security due to their high protein, complex carbohydrates, fiber, vitamins, and minerals. However, their genetic diversity is underexplored, with existing studies mainly focusing on conventional methods. This study aims to estimate the variability parameters for 16 quantitative characters of greengram to classify the genotypes using Metroglyph analysis and assess genetic divergence to identify divergent parents for future hybridization programs using 45 greengram genotypes using Randomized Block Design replicated thrice. Among 45 genotypes of greengram on the basis of mean performance MGG-351(12.959) followed by MGG-347(43.16 q/ha), VBN -2 (41.12 q/ha), GM-3(40.8 q/ha) and MGG-385(39.8 q/ha) were found superior for grain yield. High GCV and PCV is recorded for Harvest Index and Number of primary branches. High heritability coupled with genetic advance as percent of mean are recorded for number of primary branches, harvest index (%), number of seeds per pod, biological yield per plant, seed index, number of pods per plant, number of clusters per plant. On the basis of Metroglyph analysis, the total index score was varied from 24 (SHAKTI) to 38 (SIKHA) with a mean of 31.84. Among the 45 germplasm lines, the genotypes GM-3, MGG-385, SML-1663 and MGG-371were observed as high yielder and identified for higher index score. Scatter diagram plotted with Plant Height and Harvest Index has revealed that 5 clusters could be distinguished on the basis of morphological variation. Cluster -1 was represented by 24 genotypes, Cluster -2 was represented by 10 genotypes, Cluster-3 was represented by 7 genotypes, Cluster-4 was represented by 3 genotype, Cluster -5 was represented by 1 genotype. From those complexes, the germplasm lines, SIKHA and MGG-371 recorded high index score and fell into different cluster, hence used as parents in hybridization for getting desirable transgressive segregants.

Green Synthesis of 2-Mercapto 5,6-Dihydro-4H-1,3-Thiazines via Sequential C–S Couplings

The six-membered N,S-heterocyclic 1,3-thiazines and their derivatives are widely acknowledged as pharmaceutical molecules with a wide range of biological activities. In this study, we developed a unique thiol-involved cascade reaction that enables the efficient construction of the 5,6-dihydro-4H-1,3-thiazine scaffold through consecutive intermolecular thiol-isothiocyanate and intramolecular thiol-halogen click reactions. Structurally diverse 2-mercapto dihydrothiazines including three antitumour candidates of bis-dihydrothiazines were readily obtained in high yields from the readily available thiols and 3-chloroisothiocyanate in the green solvent EtOH/H2O (1:1) using K2CO3 (0.6 equiv.) as the base. Between the two synthesis procedures investigated, the microwave-assisted reaction generally behaved more efficiently than that under routine heating conditions. Furthermore, DFT calculation confirmed the sequential addition–substitution mechanism. This cascade C–S coupling reaction methodology offers several advantages, including rapid completion, high reliability, easy purification, and benign conditions.

Selective Degradation of Polyethylene Terephthalate Plastic Waste Using Iron Salt Photocatalysts.

Plastic pollution poses a significant challenge to environmental conservation. Efficient recycling of plastic is a key strategy to address this issue. Polyethylene terephthalate (PET), commonly found in plastic bottles, represents a substantial portion of plastic waste. Consequently, the efficient degradation and recycling of PET is crucial for the sustainable development of society. However, the implementation of methods for PET depolymerization and recycling typically necessitates alkaline/acidic pre-treatment and significant energy input for heating. Here, we propose a gentle, and highly efficient photocatalysis approach for selectively degrading PET plastic waste into terephthalic acid (TPA) in high yield (up to 99%) using cost-effective iron salts. Notably, this method achieved excellent selectivity with high TON and TOF values, applying oxygen or air as environmentally friendly oxidants. In addition, the solvent can be recycled without compromising the TPA yield, and large-scale reactions can be performed smoothly.

Exploring advanced microwave strategy for the synthesis of two-dimensional energy materials

The rapid pace of technology and increasing energy demands underscore the urgent need for eco-friendly materials with exceptional energy conversion and storage capabilities. Two-dimensional (2D) energy materials, characterized by unique physicochemical properties, hold great promise in renewable energy conversion, catalysis, and electronics. Nevertheless, conventional synthesis methods often falter in balancing high quality, high yield, and cost-effectiveness, presenting substantial obstacles to their large-scale application. Microwave-assisted synthesis, characterized by its rapid and efficient process, emerges as a promising approach to surmount these limitations. This review meticulously examines the pivotal role of microwave-assisted synthesis in the preparation of 2D materials, highlighting its profound impact on enhancing material quality and production efficiency. By scrutinizing the unique physical properties of microwaves and their applications in material synthesis, the review elucidates the innovative contributions of microwave technology to materials science. Furthermore, it delves into the intricate influence of microwave parameter control on the synthesis process and resultant material properties, offering insight into the potential of microwave technology for the precise modulation of material structure and functionality. This comprehensive analysis underscores microwave-assisted synthesis as a viable solution for overcoming current challenges, thereby advancing the development of high-performance 2D energy materials.

A Multiresponsive Ferrocene‐Based Chiral Overcrowded Alkene Twisting Liquid Crystals

AbstractThe reversible modulation of chirality has gained significant attention not only for fundamental stereochemical studies but also for numerous applications ranging from liquid crystals (LCs) to molecular motors and machines. This requires the construction of switchable molecules with (multiple) chiral elements in a highly enantioselective manner, which is often a significant synthetic challenge. Here, we show that the dimerization of an easily accessible enantiopure planar chiral ferrocene‐indanone building block affords a multi‐stimuli‐responsive dimer (FcD) with pre‐determined double bond geometry, helical chirality, and relative orientation of the two ferrocene motifs in high yield. This intrinsically planar chiral switch can not only undergo thermal or photochemical E/Z isomerization but can also be reversibly and quantitatively oxidized to both a monocationic and a dicationic state which is associated with significant changes in its (chir)optical properties. Specifically, FcD acts as a chiral dopant for cholesteric LCs with a helical twisting power (HTP) of 13 μm−1 which, upon oxidation, drops to near zero, resulting in an unprecedently large redox‐tuning of the LC reflection color by up to 84 nm. Due to the straightforward stereoselective synthesis, FcD, and related chiral switches, are envisioned to be powerful building blocks for multi‐stimuli‐responsive molecular machines and in LC‐based materials.

Determinants of household participation in the cassava value-chain in South Africa

Cassava’s adaptability to different agroecological conditions, high yield, as well as its ability to thrive under harsh climatic conditions, makes it an essential food security crop. In South Africa, the cassava value chain is currently uncoordinated and underdeveloped, with a couple of smallholder farmers growing the crop for household consumption and as a source of income. Other farmers regard it as a secondary crop and hardly any producers grow it for industrial purposes. Hence, this study sought to analyze the determinants of household participation in the cassava value chain in South Africa. The study employed the multivariate probit model to analyze the determinants of household participation in the cassava value chain in South Africa, using a primary dataset collected through a simple sample method from smallholder farmers in KwaZulu-Natal, Mpumalanga, and Limpopo provinces. Results show that livestock ownership has a positive and significant effect on the likelihood of farmers participating in the value chain by growing cassava for household food consumption. Also, findings reveal that hiring labour in cassava production and an increase in the yield during the previous season increases the probability of farmers’ interest in selling cassava tubers along the value chain. Hence, the positive and statistically significant influence of hiring labour during cassava production in driving the farmers’ interest in selling cassava tubers and cuttings implies that the development of the cassava value chain presents great opportunities for creating jobs (employment) in the country. Also, policy interventions that ensure land tenure security and empower farmers to increase their cassava yields are bound to encourage further participation in the value chain with an interest in selling fresh tubers, among other derived products to generate income. Lastly, programmes that empower and encourage youth participation in the cassava value chain can increase the number of farmers interested in selling cassava products.

Assessing temporal variability in durum wheat performance and stability through multi-trait mean performance selection in Mediterranean climate

Durum wheat, a staple crop in Italy, faces substantial challenges due to increasing droughts and rising temperatures. This study examines the grain yield, agronomic traits, and quality of 41 durum wheat varieties over ten growing seasons in Southern Italy, utilizing a randomized complete block design. Notably, most varieties were not repeated between trials and 45% of the data was missing. The results indicate that the interaction between genotype and environment (GEI) significantly impacted all traits. High temperatures, elevated vapor pressure deficit (VPD), and water deficits severely affected yield and quality during warm years, while cooler years with favorable water availability promoted better growth and higher yields. Broad-sense heritability (H²) was generally low, suggesting that environmental factors played a major role in the observed traits. However, some traits, such as grain yield, ears per square meter, plant height, bleached wheat, thousand-grain weight, and hectoliter weight exhibited moderate to high heritability of the mean genotype (h²mg), indicating their potential for effective selection in breeding programs. Correlation analyses revealed strong connections between certain traits, such as protein content, and gluten index as well as between grain yield, and spike per square meter. Using the Multi-Trait Mean Performance Selection (MTMPS) index, the study identified six top-performing varieties. Among these, Antalis (G4) and Core (G18) consistently demonstrated strong adaptability and stability across different environments, particularly in hotter, drier conditions. Furio Camillo (G31) also exhibited valuable traits. This study highlights the challenges and complexities of breeding durum wheat for improved yield and quality in the face of climate change.

Mass transfer kinetics of ultrasonic- and vacuum-ultrasonic-assisted static brine of chicken breast (Pectoralis major).

The aim of this study was to investigate the effect of different ultrasound treatment (UT) conditions (Control, UT-150, UT-300, UT-450, Vacuum-UT-150, Vacuum-UT-300, Vacuum-UT-450) on the brining kinetics and meat quality of chicken breast. The results showed that vacuum-ultrasonic-assisted treatment greatly accelerated the transfer of moisture and NaCl, and the highest yield was obtained by ultrasonic power of 450W. The mass transfer kinetics (k1 and k2) were significantly related to vacuum pretreatment and ultrasonic power. The values of k1 for total and moisture weight changes decreased with the increase of ultrasonic power, whereas the values of k2 increased with vacuum pretreatment. The application of ultrasound treatment with vacuum improved the NaCl effective diffusion coefficients (De) from 1.189×10-9 to 1.308-1.449×10-9 m2/s, and the highest De was found with Vacuum-UT-450. The treatment of ultrasound and vacuum can reduce shear force and enhance the water-holding capacity (WHC). According to the analysis of water distribution, vacuum and ultrasound could decrease the T23 values, indicating that the mobility of water decreased. The result of microscopic observation further supported that the disruption of myofibrils was related to the tenderness and WHC changes, which was caused by vacuum and ultrasound treatment. Thus, Vacuum-UT brining could be employed as an emerging technology for improving the efficiency of brining and meat quality of other meat. PRACTICAL APPLICATION: Vacuum-ultrasonic-assisted static brine is an effective and feasible treatment to replace tumbling treatment for maintaining the integrity of the muscle bundles and accelerating the brining rate.

Effect of Spacing and Ratooning on Growth and Yield of Okra (Abelmoschus esculentus L. Moench) Var. Lal Bhendi No. 533

The experiment was laid down in Factorial Randomized Block Design (FRBD) with nine treatment combinations and four replications during year 2023. The experiment consists of two factors, factor A: Spacings (S1- 60 cm x 30 cm, S2- 90 cm x 30 cm and S3- 120 cm x 30 cm) and factor B: Stages of ratooning (R1- Ratooning at 90 DAS, R2- Ratooning at 105 DAS and R3- No ratooning). Among the three spacings, 120 cm x 30 cm (S3) revealed higher values for growth parameters such as number of leaves (33.96), nodes (17.25), branches (1.42), yield parameters like number of fruits (24.37), yield per plant (304.31 g). The highest yield per hectare (15.07 t/ha) was obtained under closer spacing S1 - 60 cm x 30 cm. Among various ratooning treatments, number of fruits (25.33), yield per plant (315.98 g) and total yield (12.51 t/ha) was significantly higher in control (R3-No ratooning), the number of fruits (22.93), yield per plant (277.54 g) and total yield (10.99 t/ha) was greater in R1 than R2. Among ratooning treatment, R1 was better than R2 in terms of growth and yield characters. In interaction, spacing of 120 cm x 30 cm without ratooning (S3R3) was found better with respect to growth and yield of okra, whereas overall yield per hectare (16.53 t/ha) was greater in (S1R3) spacing 60 cm x 30 cm without ratooning. The data recorded in present investigation revealed that spacing and ratooning influenced the growth and yield parameters of okra. Thus, considering the yield of okra, spacing of 60 cm x 30 cm without ratooning found to be beneficial for Konkan agro-climatic conditions.

Chiral Rare-Earth (Ce, Eu) Metal Halides with Bright Circularly Polarized Luminescence.

Chiral metal halide materials are emerging chiroptical materials that are easy to synthesize and have a wide tunability. Rare-earth (RE) metals are desirable components to be incorporated in the hybrid regime; however, they are typically difficult to handle for solution-based halide chemistry. Here, we report two new examples of chiral RE metal halides with Ce(III) and Eu(III) with chiral alkanolammonium cations (R/S-3-hydroxyquinuclidium). These compounds crystallize in the non-centrosymmetric space group R3, where their mirror-like symmetric circular dichroism (CD) and circularly polarized luminescence (CPL) further witness the chiral nature. The superior emission properties, including the high photoluminescence quantum yield of the Ce-based materials (84-90%) and Eu-based materials (27-29%), have led to distinct and sharp symmetrical CPL in the ultraviolet and visible regions, with dissymmetry factors (glum) of ∼2 × 10-3 and ∼4 × 10-3, respectively. This work has established and expanded the materials space for chiral RE metal halides and demonstrated their potential for chiroptical and spintronic applications.

Loading Dyes into Chiral Cd/Zn‐Metal–Organic Frameworks for Efficient Full‐Color Circularly Polarized Luminescence

AbstractHost‐guest chemistry of chiral metal‐organic frameworks (MOFs) has endowed them with circularly polarized luminescence (CPL), it is still limited for MOFs to systematically tune full‐color CPL emissions and sizes. This work directionally assembles the chiral ligands, metal sites and organic dyes to prepare a series of crystalline enantiomeric D/L‐Cd/Zn‐n MOFs (n=1~5, representing the adding amount of dyes), where D/L‐Cd/Zn with the formula of Cd2(D/L–Cam)2(TPyPE) and Zn2(D/L–Cam)2(TPyPE) (D/L‐Cam=D/L‐camphoric acid, TPyPE=4,4’,4’’,4’’’‐(1,2‐henediidenetetra‐4,1‐phenylene)tetrakis[pyridine]) were used as the chiral platforms. The framework‐dye‐enabled emission and through‐space chirality transfer facilitate D/L‐Cd/Zn‐n bright full‐color CPL activity. The ideal yellow CPL of D‐Cd‐5 and D‐Zn‐4, with |glum| as 4.9 × 10−3 and 1.3×10−3 and relatively high photoluminescence quantum yield of 40.79 % and 45.40 %, are further assembled into a white CPL light‐emitting diode. The crystal sizes of D/L‐Cd/Zn‐n were found to be strongly correlated to the types and additional amounts of organic dyes, that the positive organic dyes allow for the preparation of > 7 mm bulks and negative dyes account for sub‐20 μm particles. This work opens a new avenue to fabricate full‐color emissive CPL composites and provides a potentially universal method for controlling the size of optical platforms.

Isolation of β-O-4-Rich Lignin From Birch in High Yields Enabled by Continuous-Flow Supercritical Water Treatment.

The continuous flow supercritical water (scH2O) treatment of Birch wood (T=372-382 °C; t=0.3-0.7 s; p=260 bar) followed by alkali extraction of lignin allowed for the isolation of lignin and lignin carbohydrate complexes (LCCs) with a high number of β-O-4 moieties in the range 29-57/100 Ar (evaluated by quantitative 13C NMR analysis) in yields ranging between 13-19 wt % with respect to the initial wood. A "lightning rod effect" of carbohydrates has been claimed to explain the low degradation of β-O-4 bonds during the process. The structure of the isolated lignin was thoroughly elucidated via comprehensive NMR studies (HSQC, 13C and 31P). A low degree of condensation (DC)<5 % was found for all the lignin samples, which was only slightly dependent on the reaction severity. The number of aliphatic -OH, phenolic -OH, and -COOH groups was in the range 3.37-5.25, 1.41-2.31 and 0.39-0.73 mmol/g, respectively. The number of -COOH groups increased with increased severity, suggesting that oxidation can occur during the scH2O treatment. Furthermore, by simply varying the reaction severity, it was possible to tune important lignin properties, like the molar mass and the glass transition temperature (Tg).

Evaluation of F2 Segregating Population of Chilli (Capsicum annuum L.) for Yield and Leaf Curl Virus Resistance

Chilli (Capsicum annuum L.) is an important vegetable crop, cultivated worldwide for its fruits which are valued for pungency, flavor, and nutritional benefits. However, chilli production is significantly restricted by various biotic stresses, especially the Chilli leaf curl virus (CLCV). The present study was conducted at the Department of Vegetable Science, College of Agriculture, Vellayani, Kerala Agricultural University during 2020-2021 to evaluate the F2 segregating population of chilli crosses viz., CHIVAR-6 x Sel-4 and CHIVAR-10 x Sel-3 for yield and leaf curl virus resistance. Evaluation of vegetative and yield related traits was conducted on these populations under the field conditions. Significant variability was observed for various traits such as plant height, fruits per plant, fruit length, yield per plant and resistance to leaf curl virus. The scoring for chilli leaf curl virus was done and based on the scoring the segregants were categorized into highly resistant, resistant, moderately resistant, moderately susceptible, susceptible and highly susceptible. Among the F2 population of the first cross, fruits per plant, plant height, fruit weight and fruit girth showed high and positive correlation with yield per plant. The segregants of the second cross recorded significant positive correlation for fruits per plant, plant height and fruit length with yield. The results of the study provide valuable insights into breeding for both high yield and leaf curl virus resistance, crucial for enhancing chilli production under the challenging situations.

Synchronous photocatalytic benzimidazole formation and olefin reduction by magnetic separable visible-light-driven Pd-g-C3N4-Vanillin@γ-Fe2O3-TiO2 Nanocomposite.

A visible light-responsive magnetically separable photocatalyst Pd-g-C3N4-Vanillin@γ-Fe2O3-TiO2 is fabricated using vanillin as a natural junction under ultrasonic agitation. Structural, morphological, optical, thermal, and magnetic assessments of the as-prepared catalyst are carried out. The photocatalyst successfully drives the simultaneous benzimidazole formation, and olefin hydrogenation with high atom economy under blue LED light and mild conditions. The photocatalytic activity of Pd-g-C3N4-Vanillin@γ-Fe2O3-TiO2 is significantly affected by the γ-Fe2O3:TiO2 weight ratio. PL spectra revealed the effective separation of carriers in the fabricated catalyst promoting its photocatalytic activity. The action spectra using the apparent quantum efficiency (AQE) exhibited the maximum AQEs at 520 and 750nm in which the highest performance for styrene hydrogenation is observed. The title magnetically separable heterogeneous photocatalyst provides high yields of products under perfectly safe visible light, produces low/zero waste, and avoids using an external high-pressure hydrogen gas source, harmful solvents, undesirable additives, and reducing agents rendering green conditions for chemical reactions.

Synthesis of Bicyclo[3.2.0]heptanes by Organophotoredox Catalytic Diastereoselective Anion Radical [2+2] Photocycloadditions of Arylenones under Batch and Flow Conditions

AbstractIn this study, the anion radical [2+2] photocycloaddition of aryl‐enones was investigated under batch and flow conditions. The reaction was promoted by LiBr as a Lewis acid and catalyzed by Eosin Y under visible light irradiation. Symmetrical enones and asymmetrical unsaturated ketoesters were effectively cyclized to yield substituted bicyclo[3.2.0]heptanes in high yield and diastereoselectivity. Through the exploration of different experimental setups and reaction conditions, a precise control over the diastereoselectivity of the process was achieved, favoring the formation of either cis or trans substituted bicyclo[3.2.0]heptanes. In‐flow experiments allowed to further improve the efficiency of the methodology, leading to higher productivity and space time yields. Furthermore, DFT investigations were conducted in order to elucidate the reaction mechanism.

Synthesis of a Pd2L4 Hydrazone Molecular Cage Through Multiple Reaction Pathways

Molecular cages are preorganized molecules with a central cavity, typically formed through the reaction of their building blocks through chemical bonds. This requires, in most cases, forming and breaking reversible bonds during the cage formation reaction pathway for error correction to drive the reaction to the cage product. In this work, we focus on both Pd–ligand and hydrazone bonds implemented in the structure of a Pd2L4 hydrazone molecular cage. As the cage contains two different types of reversible bonds, we envisaged a cage formation comparative study by performing the synthesis of the cage through three different reaction pathways involving the formation of Pd–ligand bonds, hydrazone bonds, or a combination of both. The three reaction pathways produce the cage with yields ranging from 73% to 79%. Despite the complexity of the reaction, the cage is formed in a high yield, even for the reaction pathway that involves the formation of 16 bonds. This research paves the way for more sophisticated cage designs through complex reaction pathways.

Sequential Aerial Oxidation and Atom‐Economical C‐3 Chalcogenation of Indolines Facilitated by Potassium tert‐Butoxide

AbstractAn operationally straightforward and highly efficient potassium tert‐butoxide facilitated protocol for the C‐3 chalcogenation of indolines under catalyst and additive‐free conditions has been established under ambient temperature. The salient features of the process include the development of transition metal‐free, oxidant‐free and iodine‐free, atom‐economic and cost‐effective reaction conditions at room temperature in DMSO as solvent for regioselective generation of 3‐chalcogenyl indoles in high yields. The mechanistic interpretation through controlled experiments and analysis of intermediates suggests the prevalence of the ionic pathway. The reaction is scalable to gram‐scale without a significant decrease in product yield, indicating its potential for large‐scale applications. This protocol offers a practical and environment friendly approach to accessing a diverse range of 3‐arylthioindoles and 3‐arylselenylindoles withstanding electron releasing and withdrawing substituents in good to excellent yields. Interestingly, the biological evaluation of the 3‐arylselenylindole products exhibited significant activity against breast cancer and triple‐negative breast cancer cell lines MCF‐7, and MDA‐MB 231. These results indicate the derivatives to be potent candidates for further SAR study.