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Glucose, an abundant and renewable form of biomass, has garnered significant attention in research for its conversion into high‐value chemicals such as gluconic acid. Traditional methods for biomass transformation typically involve high energy input, elevated temperature, pressure, and costly systems. In contrast, photocatalysis emerges as a promising approach to produce organic molecules under mild conditions, harnessing energy from natural sunlight or lamps. This study presents the nitrogen‐enriched graphene with zeolite second Mobil–5 (NenG/ZSM‐5) photocatalyst, evaluated for generating high‐value chemicals (gluconic acid and leucodopaminechrome) under solar light irradiation. The NenG/ZSM‐5 photocatalyst, synthesized from nitrogen‐doped graphene and ZSM‐5, successfully converted dopamine into leucodopaminechrome (71.54 %) — a critical step in dopamine regeneration and transformed glucose into gluconic acid (85 %). The addition of ZSM‐5 to NenG provided stability and enhanced product selectivity. The outstanding performance of the NenG/ZSM‐5 photocatalyst can be attributed to its heightened solar light harvesting potential, appropriate energy band gap, and uniformly arranged π‐electron channels. This research focuses on solar conversion of glucose to gluconic acid and dopamine regeneration, with potential for further exploration in the research domain. [ABSTRACT FROM AUTHOR]

The ultimate objective is to create strategies for glycol acetalization that are both economically and ecologically benign. The product cyclic dioxolane formed by acetalization of glycol shows excellent solvent properties as it is non-carcinogenic and causes no ozone related problems. It is used as a component of solvent in batteries and also finds application in the fragrance, flavour, pharmaceutical, polymers and textile industries. Herein we report a highly promising and environmentally benign process for converting glycol into 2,2 dimethyl 1,3 dioxolane via acetalization through NiO@B@GCN nanocubes catalys. Comprehensive analysis shows that the high catalytic performance of NiO@B@GCN nanocubes is the result of the cooperation of band gap engineering and efficient charge transfer capabilities. This work demonstrates the use of a synergistic strategy to effectively synthesize soft NiO@B@GCN nanocubes as a promising catalyst that exhibit excellent product yield. [ABSTRACT FROM AUTHOR]

Elevated global pollution level is the prime reason that contributes to the onset of various harmful health diseases. The products of Biginelli reaction are enormously used in the pharmaceutical industry as they have antiviral, antibacterial, and calcium channel modulation abilities. This work reports a novel eosin Y sensitized boron graphitic carbon nitride (EY‐Ben‐g‐C3N4) as a photocatalyst that efficiently produced 3,4‐dihydropyrimidine‐2‐(1H)‐one by the Biginelli reaction of benzaldehyde, urea, and methyl acetoacetate. The photocatalyst EY‐Ben‐g‐C3N4 showed a successful generation of 3,4‐dihydropyrimidine‐2‐(1H)‐one (Biginelli product) in good yield via photocatalysis which is an eco‐friendly method and has facile operational process. In addition to the production of Biginelli products, the photocatalyst also showed a remarkable NADH regeneration of 81.18%. The incorporation of g‐C3N4 with boron helps increase the surface area and the incorporation of eosin Y which is an inexpensive and non‐toxic dye, and in Ben‐g‐C3N4, enhanced the light‐harvesting capacity of the photocatalyst. The production of 3,4‐dihydropyrimidine‐2‐(1H)‐one and NADH by the EY‐Ben‐g‐C3N4 photocatalyst is attributed to the requisite band gap, high molar absorbance, low rate of charge recombination, and increased capacity of the photocatalyst to harvest solar light energy. [ABSTRACT FROM AUTHOR]

A schematic strategy is presented to overcome the problem of low photocatalytic performance of graphene. Herein, we synthesized nitrogen-doped graphene (NDG)-coupled acid fuchsin (AF) photocatalyst, i.e.; NDGCAF photocatalyst. The NDGCAF photocatalyst has excellent solar light harvesting ability, band gap suitability, and high molar extinction coefficient than the NDG photocatalyst. Due to these properties, the NDGCAF photocatalyst has the ability to oxidize aryl-vinyl into aryl-vinyl-aldehyde under the irradiation of visible light. In this context, it exhibited the utmost conversion efficiency of aryl-vinyl to aryl-vinyl-aldehyde with a good yield of 98.15%. Current research highlights the significant application of NDGCAF light-harvesting photocatalysts in the research field of organic transformations. [ABSTRACT FROM AUTHOR]

The generation of a low HOMO-LUMO energy gap makes organic polymer-based composites an important class of materials with outstanding catalytic efficiency. The present work describes the simple and direct synthesis of an excellent photocatalyst, PC (C26H16NO7S)n via doping of erythrosine-B dye on sulfone infused poly(2-amino thiophenol) assembly (PA, (C6H4NO2S)n). The O 1 s spectrum displays peaks at 531.8 eV and 533.3 eV, representing the O=C and O–C groups of the in-situ generated fluorescein loaded on PA surface. Through absorption study (Tauc's plot), the optical band gap (Eg) for polymer PA (2.9 eV) and photocatalyst PC (2.1 eV) has been calculated. Further, due to the efficient absorbance in the range of 400–600 nm with a low optical band gap, the applicability of the catalyst, PC has been checked in photocatalytic C–H activation in thiophene, and the generation of C–C bond with p-nitro aryldiazonium salt. [ABSTRACT FROM AUTHOR]

The visible light-assisted photocatalysis approach allows more sustainable and atom-economical C–H bond arylation processes. The polymer-based photocatalysts are an attractive choice because of their variable design and development feasibility as well as effective catalytic applications. In the present work, by following the basic principles of green chemistry, we have chosen an environmentally friendly and biologically suitable chemical i.e. Erythrosine B as a unit molecule for the generation of photocatalyst EP (C20H8O5S4). The generation of EP has been performed via a one-pot solvothermal reaction of Erythrosine B with sulfur powder. The structural analysis of the EP evidence the generation of an interesting example 2D-polymeric assembly where disulfide (–S–S–) units are acting as linkers and show high thermal stability up to 800 °C (39.9% left as a residue). The low optical band gap of 2.08 eV and electrochemical band gap of 2.09 eV favors its catalytic applicability. The catalytic investigation reveals excellent applicability of EP in C–H arylation (yield 98.5% & selectivity 99%). [ABSTRACT FROM AUTHOR]

The combination of excellent electronic properties and thermal stability positions orange‐derived graphene quantum dots (GQDs) as promising materials for solar light‐based applications. Researchers are actively exploring their potential in fields such as photovoltaics, photocatalysis, optoelectronics, and energy storage. Their abundance, cost‐effectiveness, and eco‐friendly nature further contribute to their growing relevance in cutting‐edge scientific research. Furthermore, only GQDs are not much more effective in the UV‐visible region, therefore, required band gap engineering in GQDs material. In this context, we designed GQDs‐based light harvesting materials, which is active in UV‐visible region. Herein we synthesized GQDs coupled with 2,6‐diaminoanthrquninone (AQ), that is, GQDs@AQ light harvesting photocatalyst the first time for the oxidation of sulfide to sulfoxide under visible light. For the integrating reactions of sulfide in aerobic conditions under visible light by GQDs@AQ photocatalyst exhibit utmost higher photocatalytic activity than simple GQDs due to low molar extinction coefficient and slow recombination charges. The use of GQDs@AQ light harvesting photocatalyst, showed the excellent organic transformation efficiency of sulfide to sulfoxide with excellent yield (94%). The high efficiency and excellent yield of 94% indicate the effectiveness of GQDs@AQ as a photocatalyst for these specific organic transformations. [ABSTRACT FROM AUTHOR]

Photocatalytic processes triggered by graphene‐based photocatalysts under solar light have sparked interest as a new sort of instrument for solar chemical synthesis. Herein we investigated self‐assembled graphene quantum dots (GQDs)/NiSe‐NiO composite photocatalyst for organic transformation as well as dye degradation. The synthesized GQDs/NiSe‐NiO composite photocatalyst has an excellent suitable band gap, high molar extinction coefficient, low toxicity and chemical/thermal stability. The GQDs/NiSe‐NiO composite photocatalyst emerges as a new standard for sulfur oxidation and dye degradation reactions under homemade LED light with high yield. [ABSTRACT FROM AUTHOR]

Summary: Solar light active oxygenation reactions and coenzyme regenerations are play crucial role in the area of pharmaceutical industry. The highly selective and efficient synthesis of oxygen‐containing molecules in an environmental friendly manner is challenging at both industrial and laboratory level. Here, we proposed a new synthetic approach for oxygenation reactions along with coenzyme regenerations using flexible‐activated carbon cloth (FACC) oriented covalent (C) tetrakis(4‐carboxyphenyl) porphyrin (P) and thiourea (T)‐based framework (F), namely, CPTF@FACC photocatalyst. CPTF@FACC exhibits excellent solar light‐harvesting ability, well‐distinct photocatalytic centers, high molar extinction coefficient, excellent charge transport ability, and suitable optical band gap, which make the photocatalyst more efficient for oxygenation (sulfoxidation and epoxidation) reactions along with coenzyme regenerations. The oxygenation reactions were carried out in isopropyl alcohol via in situ production of hydrogen peroxide (H2O2) under solar light using CPTF@FACC photocatalyst with high yields (~97%‐98%). Finally, the CPTF@FACC photocatalyst also show a benchmark example in the coenzymes regeneration with high yields 81.1% and 73.1% for NADH and NADPH in 2 h, respectively. [ABSTRACT FROM AUTHOR]

Covalent triazine frameworks (CTFs), belonging to the super‐family of covalent organic frameworks, have attracted significant attention as a new type of photosensitizer due to the superb light‐harvesting ability and efficient charge transfer originating from the large surface area. However, the wide optical band gap in CTFs, which is larger than 3.0 eV, hinders the efficient light harvesting in the visible range. To overcome this limitation, we developed the new type CTFs photocatalyst based on the donor–acceptor conjugation scheme by using melamine (M) and 2,6‐diaminoanthraquinone (AQ) as monomeric units. The melamine‐2,6‐diaminoanthraquinone‐based covalent triazine frameworks (M‐AQ‐CTFs) photocatalyst shows the excellent light‐harvesting capacity with high molar extinction coefficient, and the suitable optical band gap involving the internal charge transfer character. Combination of M‐AQ‐CTFs and artificial photosynthetic system including the organometallic rhodium complex, acting as an electron mediator, exhibited the excellent photocatalytic efficiency for the regeneration of the nicotinamide cofactors such as NAD(P)H. In addition, this photocatalyst showed the high photocatalytic efficiency for the metal‐free aerobic oxidation of sulfide. This study demonstrates the high potential of CTFs photocatalyst with the donor–acceptor conjugated scheme can be actively used for artificial photosynthesis. [ABSTRACT FROM AUTHOR]

The dimethyl sulfite as an alkylating as well as alkoxylating reagent is well known in synthetic organic as well as organometallic chemistry for a long time. Herein, we have utilized dimethyl sulfite as an alkylating reagent and reacted with fluorescein derivative, N‐fluorescein‐lactam‐hydrazine (B). This reaction leads to the generation of tetramethylated fluorescein lactam hydrazine (A). The newly designed and synthesized molecule (A) has been characterized by 1H, 13C NMR and HRMS data. The antimicrobial activity of the synthesized alkylated fluorescein derivative has been tested against E. coli, P. aeruginosa, Salmonella typhimurium and S. aureus microbial agents. Time‐kill assay results also confirmed that fluorescein derivative is a potent antimicrobial agent and revealed that the time‐kill assay of fluorescein derivative is value‐added than the well‐known antibiotic. In addition, quantum chemical study was used to analyze its activity trend and correlated with the experimental data. The computed results of DFT revealed that the lipophilicity as well as the LUMO‐HOMO band gap (ΔELUMO‐HOMO = 4.75 eV) of compound A make it more suitable as an antimicrobial agent to match with in vitro antimicrobial experimental results. The MIC and MBC values of compound A were observed to be lower in contrast to fluorescein and ampicillin for all the tested bacterial strains, which were approximately 3‐ to 4‐fold lower than MIC and MBC values of the later. Results obtained from the study clearly indicate that compound A has better antimicrobial and bactericidal activity in comparison to ampicillin and fluorescein. Synthesized compound can be a better substitute of traditionally used antibiotics, Ampicillin. [ABSTRACT FROM AUTHOR]

Main observation and conclusion: Photoredox C—H bond formation can proceed in aerobic environment under solar light and has therefore become attractive. Nowadays, different types of expensive novel metal complexes and nanomaterials have been urbanized as photocatalysts for direct C—H bond formation in between derivatives of heteroarenes (HAs) and aryl diazonium salts. These photocatalysts, however, still suffer from poor stability, high cost, and decay. Herein, a graphitic carbon nitride‐based fluorescein isothiocyanate (g‐C3N4–FITC) film photocatalyst has been reported, which shows excellent light harvesting ability, and band gap suitability to catalyze the metal free direct C—H arylation of HAs under solar light at ambient temperature. Moreover, the g‐C3N4–FITC film photocatalyst can be reused four times without significant loss of activity, confirming the excellent photocatalytic stability. The current strategy to construct a g‐C3N4–FITC film photocatalyst for direct C—H arylation opens a new path towards replacing metal‐based catalysts in fine chemical synthesis. [ABSTRACT FROM AUTHOR]

As most promising organic semiconductors, and polymeric materials have concentrated much attention due to their thermochemical stability, chemical inertness, non-toxicity, excellent photoelectrical properties, low cost, and abundance of raw materials. However, the light-harvesting polymeric material graphitic carbon nitride (g-C 3 N 4) has a limited ability to absorb light in the region below 420 nm because of its wide optical band gap. As one method to enhance the character of light harvesting and optical properties, such as EB-T (Eriochrome Black-T) has been used, and easy to prepare g-C 3 N 4 based EB-T (g-C 3 N 4 @EB-T) composite photocatalyst, which has tuned the energy gap of pristine g-C 3 N 4. In this article, we synthesized a new classic type of g-C 3 N 4 @EB-T composite photocatalyst by the copolymerization method. The EB-T moieties serve as external photosensitizing components in this composite photocatalyst. Compared to the initial materials, the g-C 3 N 4 @EB-T composite photocatalyst shows exceptional yields in the regeneration and formation of NADH and C(sp3) F bond. [Display omitted] • A novel photocatalytic system utilizing g-C 3 N 4 is proposed for the production and regeneration of the C(sp3)-F bond and NADH, crucial components in pharmaceutical synthesis. • The proposed system consists of a self-assembled g-C 3 N 4 composite that efficiently captures and utilizes sunlight to activate the reactions. • Ethylbenzene is used as a representative substrate for C(sp3)-F bond generation, while NAD+ serves as a model for NADH regeneration (65% yield). • The system exhibits remarkable selectivity and efficiency for both reactions and operates under mild conditions and at room temperature, making it suitable for large-scale synthesis. • This research highlights g-C 3 N 4 's potential as a versatile and environmentally friendly photocatalytic platform for various chemical transformations under sunlight. [ABSTRACT FROM AUTHOR]

[Display omitted] • Use of non-toxic/least toxic chemicals. • Generation of least studied ester-linked covalent organic polymer. • Crystalline nanosheet generation (average crystallite size = 43.5 nm, crystallinity = 90.5 %). • Excellent photocatalytic activity with high selectivity for C-H activation and C-C bond formation reaction. Among all polymeric materials, the chemistry of covalent organic polymers has been the least covered in the field of photocatalysis due to the rare availability of design and synthetic protocols. In the present work, we have come up with an efficient design of a one-dimensional Covalent Organic polymer (COP) (S-COP) through the ester-linked co-polymerization of Erythrosine B with 2,2′-Dithiodibenzoic acid (2,2′-DDB). The COP was synthesized via the facile one-pot solvothermal method. The XRD data analysis favors high crystalline nanoscale polymeric sheet generation (S-COP , 90.5 % & 43.5 nm). The HOMO-LUMO calculation through an electrochemical study as well as Tauc's plot showed 2.1 eV band gap. In this order, S-COP , a metal-free polymeric material was observed as an effective photocatalyst in the solar-driven photocatalytic reaction of heteroarenes with aryl diazonium salts via direct C-H arylation (High yield (∼98 %), and high selectivity (∼98 %)). [ABSTRACT FROM AUTHOR]