Triphenylmethane Dyes Research Articles

Albumin-Chaperoned Deep-NIR Triarylmethane Dyes for High-Contrast In Vivo Imaging and Photothermal Therapy.

Fluorophores absorbing/emitting in the deep near-infrared (deep NIR) spectral region, that is, 800 nm and beyond, hold great promise for in vivo bioimaging, diagnosis, and phototherapy due to deeper tissue penetration. The bottleneck is the lack of bright, stable, and readily synthesized deep NIR fluorophores. Here, it is reported that the albumin-chaperon strategy is a viable one-for-all strategy to address these difficulties. A focused library of deep-NIR absorbing dyes (EA5) is easily synthesized via a two-step cascade. They are neither very stable nor bright in phosphate bufferdue to a propeller-type flexible scaffold. Through screening, EA5_c3 is found to exhibit a high affinity toward bovine serum albumin (BSA). Binding-associated structural rigidification resulted in a gigantic 26-fold fluorescence enhancement. The albumin chaperone also greatly improved the stability of EA5_c3 by shielding the bisbenzannulated triarylmethane core from nucleophilic or oxidative species. The resulting EA5_c3@BSA exhibits high biocompatibility. It offered high-resolution vasculature, lymph systems, tumors, and other tissue imaging with its bright deep NIR emission. At the same time, it exhibits prominent potential in photoacoustic imaging and photothermal treatment of subcutaneous and orthotopic breast tumors. These findings provide insights into robust and high-performance fluorophores with deep NIR regions for theranostic against aggressive cancers.

Influence of symmetry breaking on the absorption spectrum of crystal violet: from isolated cations at 5 K to room temperature solutions.

We report the resolution of a long-standing puzzle in molecular spectroscopy: the origin of the shoulder in the room temperature solution absorption spectrum of crystal violet (CV) - an archetypal cationic triphenylmethane dye. This was achieved by comparing experimental and theoretical results for CV in solution at room temperature and as an isolated cation in gas-phase at 5 K. The two lowest energy electronically excited states involved in the visible region absorption are degenerate and coupled via a Jahn-Teller (JT) mechanism involving phenyl torsions, making CV particularly sensitive to environmental perturbations. The shoulder is absent in the low-temperature isolated cation spectrum, and vibronic simulations based on time dependent density functional theory (TD-DFT) indicate negligible JT effects under these conditions. Combining vibronic simulations with molecular dynamics, demonstrates that in water and toluene solution at room temperature the shoulder arises mainly from an intermolecular, Jahn-Teller-like symmetry-breaking effect induced by the fluctuating electrostatic potential of the disordered solvent environment, rather than from molecular distortions.

A hapten design strategy to enhance the selectivity of monoclonal antibodies against malachite green

Malachite green (MG), a triphenylmethane dye, is used in the aquaculture industry as a disinfectant and insect repellent due to its potent bactericidal and pesticidal properties. However, its use poses potential environmental and health risks. This study analyzed and designed two haptens using computer simulation. Serum data confirmed the feasibility of introducing an arm at the dimethylamine group. Subsequently, a highly selective monoclonal antibody strain was successfully prepared based on the hapten. After optimizing the working conditions of indirect competitive enzyme-linked immunosorbent assay (IC-ELISA), the IC50 value was 0.83 ng/mL, with a detection limit (IC10) of 0.08 ng/mL and a linear range of 0.19–3.52 ng/mL. The developed monoclonal antibody exhibited a crossover rate of less than 0.1% with other similar structures and can be used to establish an immunoassay.

Plasmonic hemispherical Ag nanoparticles on silicon substrate: A comprehensive study of optical properties

In this work, we demonstrate a comprehensive study of the optical properties of hemispherical Ag nanoparticles (AgNPs) on a single-crystal (c-Si) wafer. The fabricated method involves a galvanic displacement reaction of Ag on c-Si and annealing in oxygen atmosphere at 500 °C. Substrates with different morphological parameters of AgNPs were obtained by varying the volume ratio of Ag in the deposition solution. Using the quasinormal modes (QNMs) theory formalism, the localized surface plasmon resonance (LSPR) multipole positions were determined as a function of the AgNP size and incidence angle. Also, the effective field approximation and QNMs methods were used to calculate the specular reflectance of the disordered hemispherical array on c-Si. Thus, the experimentally obtained LSPR positions in the reflectance spectra were described. Finally, surface-enhanced Raman scattering (SERS) demonstrated reliable detection of brilliant green triphenylmethane dye (1 nM), methyl red dye (10 nM) and hemoglobin from bovine blood (1 mM). The dependence of the SERS enhancement factor on the LSPR position and the absorption band of the analyte was established, the maximum value of which was 1.1 × 107. In summary, this study suggests that the numerical and experimental investigation of the optical properties of hemispherical AgNPs on c-Si contributes to the field of optical sensing.

Photothermal degradation of triphenylmethane dye wastewater by Fe3O4@C-laccase

The degradation of synthetic dye wastewater is important for green chemistry and cost-effectiveness. In this study, we developed Fe3O4@C-laccase (laccase immobilized on Fe3O4@C nanoparticles) for photothermal degradation of high concentration of triphenylmethane dye wastewater. The Fe3O4@C-laccase possessed superior pH and thermal stabilities, as well as excellent tolerance to organic solvents, inhibitors, and metal ions. Laccase activity assays revealed that the activity recovery was approximately 118.2 %. Furthermore, the Fe3O4@C-laccase presented rapid and sustainable photothermal degradation capabilities to triphenylmethane dye wastewater. The initial removal efficiencies of 400 mg/L malachite green (MG), 400 mg/L brilliant green (BG), 100 mg/L crystal violet (CV), and 600 mg/L mixed dye (MG:BG:CV = 1:1:1) wastewater were approximately 99.8 %, 99.9 %, 96.4 % and 99.2 % by 60 min treatment, respectively. After undergoing 10 batches of reuse, the photothermal degradation efficiencies of the triphenylmethane dye wastewater remained consistently high, at about 99.3 %, 97.4 %, 94.0 %, and 95.1 %, respectively. The excellent photothermal degradation properties indicate that the Fe3O4@C-laccase holds promise for addressing high concentration of textile wastewater in various applications.

Triarylmethanol Derivatives with Ultralong Organic Room-Temperature Phosphorescence.

Triphenylmethyl-based compounds such as rhodamines and fluoresceine representing an old and well-known class of triphenylmethane dyes, are widely used in fluorescent labeling of bioimaging. Inspired by ultralong room temperature phosphorescence of triphenylphosphine derivatives, herein we report a methoxy substituted triarylmethanol ((4-methoxyphenyl)diphenylmethanol, LJW-1) exhibits ultralong room temperature phosphorescence (RTP) under ambient condition with afterglows of about 7 seconds. Its multiple C-H···π intermolecular interactions, C-H···O intermolecular interactions, hydrogen bond and π-π interactions are beneficial for forming rigid environment in the aggregated state which is evidently an important factor in the appearance of excellent RTP. Different substituents on triarylmethanol result in compounds with different lifetimes varying from 7 µs to 818 ms. The substituent effects on the phosphorescence of triarylmethanol derivatives provide an efficient method for the design of organic RTP materials and may be enlightening the phosphorescence research of triarylmethanol derivatives.

Pea Pod–Derived Biochar–Zeolitic Imidazolate Framework Composite for the Photocatalytic Degradation of Two Organic Dyes Crystal Violet and Victoria Blue

ABSTRACTThe rapid increase of water pollution globally is a vital environmental concern that requires the immediate attention of researchers to find new innovative ways to remove unwanted environmental pollutants from our water sources. With the advances in the field of sustainable engineering, there is a high demand for the effective utilization of biomass resources for the removal of aqueous environmental contaminants. Biochar is carbon carbon‐enriched substance obtained by biomass pyrolysis; it is inexpensive and has received wide attention in the field of wastewater treatment. Herein, we describe the synthesis of pea pod (PO) biochar‐reinforced zeolitic imidazolate framework (ZIF‐8) nanocomposite (PO@ZIF‐8) through the in situ precipitation of ZIF‐8 onto the biochar surface. The crystal growth, morphology, chemical composition, and optical characteristics of fabricated PO@ZIF‐8 nanocomposite were scrutinized through PXRD, SEM, TEM, UV‐DRS, PL, and XPS analysis. The dodecahedral‐shaped PO@ZIF‐8 particles have an average size between 140 and 160 nm. The biochar‐reinforced ZIF‐8 nanocomposite showed significantly higher photocatalytic activity than the pure ZIF‐8 for the degradation of two commonly found organic dyes crystal violet (CV) and Victoria Blue (VB) in the presence of direct sunlight irradiation. The PO@ZIF‐8 nanocomposite showed the highest degradation efficiency of ~87% and ~80% within 50 min of irradiation time at a catalyst dosage of 20 mg for 30 ppm CV and VB dye solutions at pH 8. First‐order kinetics were obeyed during the photodegradation with 0.041 and 0.030 min−1 as the constant of degradation for the removal of CV and VB. The radical scavenger experiment and the photoluminescence analysis confirm the active participation of ·OH radical in the degradation of both dyes. LC–MS and TOC analysis was also performed to determine the degradation products and for evaluation of the degradation progress. Moreover, the synthesized PO@ZIF‐8 composite also exhibit good stability till the fourth cycle with high degradation efficiency thus making it a good choice of catalyst in the field of environmental decontamination.

Site-Directed Mutagenesis of Two-Domain Laccase ScaSL for Obtaining a Biocatalyst with Improved Characteristics

Analysis of the structure of two-domain laccase ScaSL from Streptomyces carpinensis VKM Ac-1300 (with a middle-redox potential) revealed determinants that could affect the increased potential of ScaSL. Site-directed mutagenesis of the ScaSL laccase was carried out, and mutants H286A, H286T, H286W, and F232Y/F233Y were obtained. Replacement of His 286 with Ala led to a decrease in redox potential (0.45 V) and an increase in stability at pH 9 and 11; replacement with Thr led to an increase in redox potential (0.51 V) but to a decrease in the thermal stability of the protein; replacement with Trp did not affect the enzyme properties. Replacement of Phe residues 232 and 233 with Tyr led to a shift in enzyme activity to the acidic pH range without changing the redox potential and a decrease in the thermostability and pH stability of the enzyme. All mutants more efficiently oxidized phenolic substrate 2,6-DMP and were able to participate in direct electron transfer (DET) with MWCNT-modified electrodes. The F232Y/F233/Y mutant was unable to degrade triphenylmethane dyes without a mediator but showed a greater degree of decolorization of azo dyes in the presence of the mediator. The crystal structure of laccase with the highest potential was determined with high resolution.

Process optimization of victoria blue dye removal using polypyrrole-encapsulated zirconium oxide: Mechanistic pathway and economic assessment

In this study, an organometallic composite, namely a polypyrrole-encapsulated zirconium oxide (ZrO2/PPy) nanocomposite, was developed and used to eliminate Victoria blue dye (VB) from water system. Specific surface area of the ZrO2/PPy obtained from BET study was observed to be 61.822 m2/g. Solution pH of 7.0, ZrO2/PPy nanocomposite dose of 0.8 g/L, sonication period of 40 min and initial VB dye concentration of 50 mg/L were chosen as optimal test parameters, at which 86.23 (±1.15) % of VB dye elimination was observed. The VB dye uptake process follows pseudo-second-order kinetic model and Langmuir isotherm model, with the later providing the maximum VB dye adsorption capacity of ZrO2/PPy nanocomposite as 238.09 mg/g. Thermodynamics study suggests the spontaneous (ΔGo< 0) and endothermic (ΔHo> 0) nature of the adsorption study. Food processing wastewater causes maximum hindrance (∼20 (±0.90) % −25 (±1.03) %) in the VB dye uptake process while the presence of phosphate (PO43−) ions can create highest interference (∼17 (±0.93) % −19 (±1.08) %) in the VB dye uptake process. At the optimum test parameter values (adsorbent dose: 1.3 g/L, initial VB dye concentration: 20 mg/L, sonication period: 70 min) as suggested by response surface methodology (RSM), maximum VB dye elimination of ∼96 % was observed. Electrostatic attraction, π–π interaction and hydrogen bond formation are amongst the major uptake mechanisms. Regeneration study indicates ∼19 (±1.36) % of decrease in VB dye elimination (%) after fifth cycle of reuse. The lab scale and industrial scale fabrication expense of 1.0 kg of ZrO2/PPy nanocomposite were obtained as 75.74 and 22.20 USD, respectively. The findings of this study suggest the potential of ZrO2/PPy nanocomposite as an effective and economically viable adsorbent to eliminate VB dye from wastewater.

Characterization and Degradation of Triphenylmethane Dyes and Their Leuco-Derivatives by Heterologously Expressed Laccase From Coprinus cinerea.

Laccase is a copper-containing polyphenol oxidase that can oxidize phenolic and non-phenolic organic substrates. In the past decades, laccases had received considerable attention because of the ability to degrade various organic substances. Based on the codon preference of the Pichia pastoris expression system, this study optimized the gene structure of the laccase gene Lcc1 from Coprius cinerea through synthetic biology methods. A new gene Lcc1I was synthesized and heterologously expressed in P. pastoris. After 3 days of cultivation in a shake flask at 30°C, the transformants produced at a yield of 890 mg L-1protein. The highest production level of the recombinant laccase was 2760 U L-1. The molecular mass of the recombinant laccase was estimated at 60 kDa. The enzyme showed highest activity at pH 3.4 and 45°C. It possessed better stability at higher pH and lower temperature condition. Using 2,2'-azino-bis-(3-ethylbenzothiazoline)-6-sulphonate (ABTS) as the substrate, the Km and Vmax values were 0.136 mM and 9778 μM min-1 mg-1, respectively. The recombinant laccase could directly oxidize some triphenylmethane dyes like leuco-crystal violet (LCV) and leuco-malachite green (LMG). With the help of ABTS mediator, it could oxidize and degrade 77.7% crystal violet (CV) and 79.2% malachite green (MG) within 1 h. Our results indicate that optimization of the laccase gene achieves good expression results in the host system. The dye degradation model constructed in this study may also be applied to the degradation of other organic pollutants and toxic substances, providing new solutions for environmental remediation against the increasingly severe environmental pollution.

Elucidation of radiation-induced molecular fragmentation in triphenylmethane aromatic dye using mass spectrometric tool

This study investigates the potential of triphenylmethane dye as a gamma radiation dosimeter using gas chromatography-mass spectrometry (GC-MS) through detection of radiation-induced derivatives produced at low concentrations in the irradiated material. Pristine triphenylmethane established a reference baseline for the dye’s dosimetric properties to establish a differentiated signature of the radiation-synthesized derivatives. The two key radiation-induced derivatives identified and quantified in the present work were 2-Propanone,1,1-diphenyl- and diphenylcarbinol Benzenemethanol, α, α-diphenyl- which was found in trace amounts in pristine material due to possible natural chemical or radiation processes. Gamma irradiation significantly accelerates their formation in which their relative concentration increases linearly with increasing radiation dose up to 100 kGy. Unavoidable radiation-induced synthesis of low-mass radiation fragments was observed at higher gas chromatography retention time; and also exhibit a linear increase with dose within the investigated range.

Hats Off to Modeling! Profiling Early Synthetic Dyes on Historic Woolen Samples with ATR-FTIR Spectroscopy and Multivariate Curve Resolution-Alternating Least Square Algorithm.

This research focuses on analyzing wool samples dyed with synthetic dyes from the early 20th century. A methodology to identify and distinguish wool fibers dyed with azo, triphenylmethane, and xanthene dyes, which are no longer in use, using the ATR-FTIR spectra, is presented. Firstly, the dataset was subjected to PCA, which revealed the similarities and differences among the samples, illustrating a distribution pattern based on dye classes. MCR-ALS was employed to extract the spectral profiles of the dyed fibers, thereby enhancing the efficacy of the analytical techniques and extracting the comprehensive information from a single instrument. The combination of ATR-FTIR spectroscopy with chemometric methods, such as PCA and MCR-ALS, has proven to be an effective strategy for identifying and differentiating wool fibers dyed with early azo, triphenylmethane, and xanthene dyes. This approach has demonstrated particular effectiveness in enabling rapid analysis without requiring sampling or pretreatment. Moreover, the analysis is supported by thorough bibliographic research on these no longer used colorants. In order to maximize the potential of non-destructive spectroscopic techniques, such as ATR-FTIR, the approach used has proven to be crucial. This study underscores how chemometric techniques expand the capabilities of spectroscopy, extracting extensive information from a single instrument and aligning with the goals of cultural heritage analysis.

Effect of molecular structure on membrane diffusion: Triphenylmethanes across Escherichia coli studied by second harmonic light scattering

Understanding how the structure of molecules affects their permeability across cell membranes is crucial for many topics in biomedical research, including the development of drugs. In this work, we examine the transport rates of structurally similar triphenylmethane dyes, malachite green (MG) and brilliant green (BG), across the membranes of living Escherichia coli (E. coli) cells and biomimetic liposomes. Using the time-resolved second harmonic light scattering technique, we found that BG passively diffuses across the E. coli cytoplasmic membrane (CM) 3.8 times faster than MG. In addition, BG exhibits a diffusion rate 3.1 times higher than MG across the membranes of liposomes made from E. coli polar lipid extracts. Measurements on these two molecules, alongside previously studied crystal violet (CV), another triphenylmethane molecule, are compared against the set of propensity rules developed by Lipinski and co-workers for assessing the permeability of hydrophobic ion-like drug molecules through biomembranes. It indicates that BG’s increased diffusion rate is due to its higher lipophilicity, with a distribution coefficient 25 times greater than MG. In contrast, CV, despite having similar lipophilicity to MG, shows negligible permeation through the E. coli CM on the observation scale, attributed to its more hydrogen bonding sites and larger polar surface area. Importantly, cell viability tests revealed that BG’s antimicrobial efficacy is ∼2.4 times greater than that of MG, which aligns well with its enhanced diffusion into the E. coli cytosol. These findings offer valuable insights for drug design and development, especially for improving the permeability of poorly permeable drug molecules.

Discoloration of triphenylmethane dyes in ethylene glycol-water coolant medium

Discoloration of triphenylmethane dyes in ethylene glycol-water coolant medium

Optimization of the Decolorization of Triphenylmethane Dyes by Bacterial Monoculture and Consortium Screened from Textile Wastewater

Optimization of the Decolorization of Triphenylmethane Dyes by Bacterial Monoculture and Consortium Screened from Textile Wastewater

Toxicological Impact of Malachite Green on Freshwater Fish: A Comprehensive Review

Triarylmethane dyes, such as malachite green, are widely used in the culinary, pharmaceutical, textile, and other sectors for a variety of purposes, including aquaculture parasiticides. It controls fungal attacks, protozoan infections, and some other diseases caused by helminthes on a wide range of fish and aquatic organisms. Nonetheless, the dye's purportedly harmful effects have raised a lot more questions about its usage. The exposure time, temperature and the concentration all raise the dye's toxicity. It has been linked to chromosomal breaks, mutagenesis, cancer,teratogeneity, and pulmonary toxicity. Multi-organ tissue damage is one of malachite green's histopathological consequences. Fish exposed to malachite green have notable changes in their blood's biochemical characteristics. Malachite green and its reduced form, leucomalachite green, have been found in a variety of tissues, including eggs and fries, as well as serum, liver, kidney, and muscles. Despite a wealth of information about malachite green's toxicity, several developing countries still utilize it as a parasiticide in aquaculture and other industries. Hence, there is a significant likelihood of malachite green disposition in the food chain. To counteract its toxicological effect, it is crucial to identify a substitute because of its high toxicity.

Ordered Mesoporous Carbon as Adsorbent for the Removal of a Triphenylmethane Dye from Its Aqueous Solutions.

A nanostructured material, ordered mesoporous carbon (OMC), was synthesised in metal- and halide-free form and its use for the sequestration of crystal violet, a hazardous triphenylmethane dye, is reported for the first time. The OMC material is characterised using scanning transmission electron microscopy with energy-dispersive spectroscopy for chemical analysis, by Fourier-transform infrared spectroscopy, and by nitrogen gas physisorption. The ideal conditions for the uptake of crystal violet dye were determined in batch experiments covering the standard parameters: pH, concentration, contact time, and adsorbent dosage. Experimental data are validated by applying Langmuir, Freundlich, Dubinin-Radushkevich, and Temkin isotherms. The thermodynamic parameters, ΔH°, ΔG°, and ΔS°, are calculated and it has been found that the adsorption process is spontaneous and endothermic with increasing disorder. An in-depth analysis of the kinetics of the adsorption process, order of the reaction and corresponding values of the rate constants was performed. The adsorption of crystal violet over OMC has been found to follow pseudo-second-order kinetics through a film diffusion process at all temperatures studied. Continuous flow column operations were performed using fixed bed adsorption. Parameters including percentage saturation of the OMC bed are evaluated. The exhausted column was regenerated through a desorption process and column efficiency was determined.

Remediation of cationic dye from aqueous solution through adsorption utilizing natural Haloxylon salicornicum: An integrated experimental, physical statistics and molecular modeling investigation

Wastewater emanating from declining industrial processes often presents a vexing challenge due to its intricate composition replete with hazardous chemicals. The quest for environmentally sustainable methods to remediate such wastewater has led to the exploration of biomaterials as adsorbents and co-substrates within diverse treatment systems. In this study, we harnessed the abundant and cost-effective adsorbent, Haloxylon salicornicum (HS), as a potent agent for the removal of the pernicious triphenylmethane dye, crystal violet, from aqueous mediums. The adsorbent was characterised using Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and scanning electron microscopy (SEM), while Brunauer-Emmett-Teller (BET) analysis yielded a specific surface area (SBET) of 85.23 m2 g−1, highlighting its advantageous mesoporous structure for adsorption. Comprehensive investigations were conducted across various operational parameters, encompassing initial dye concentration, contact time, HS adsorbent dosage, initial pH, and temperature, with a keen focus on their influence on dye removal efficiency. The results unveiled several key trends, demonstrating that elevated initial dye concentration, prolonged contact time, and higher initial pH levels substantially enhanced the efficiency of dye removal, while ionic strength and temperature exhibited comparatively modest impacts. The kinetics of dye adsorption were rigorously examined, revealing a closer adherence to the pseudo-second-order model in comparison to the PFO model, thereby offering deeper insights into the adsorption dynamics. To further unravel the intricate mechanism underpinning the adsorption of CV on HS, we employed a single-layer model linked to SLMRG. In conjunction, DFT calculations, encompassing COSMO-RS, NCI, Molecular Dynamics (MD) simulations and QTAIM calculations, were applied to probe the interactions between adsorbed CV and the adsorbent-molecules, providing compelling evidence of robust binding interactions. These theoretical insights were subsequently aligned with empirical observations, affirming a significant relation between the theoretical and experimental data. This multifaceted study not only advances our understanding of CV removal using HS but also underscores the robustness of this adsorbent within the context of wastewater treatment. Furthermore, it demonstrates the synergy of empirical investigations and theoretical modeling in unraveling the intricacies of adsorption processes.

Novel amphipathic photoinitiating systems utilizing ethyl violet for acrylate and thiol-based click photopolymerization under 630 nm and 450 nm LED

We conducted the first-ever investigation on the use of amphipathic triphenylmethane dyes ethyl violet (EV), in combination with iodonium salts (Iod) and sodium tetraphenylborate (STPB), as novel visible light photoinitiating systems (PISs), for initiating oil-based photopolymerization of acrylate and thiol-ene, as well as water-based photopolymerization, under 630 nm and 450 nm light-emitting diodes (LED) irradiation. The polymerization kinetics verified the efficient initiation of the EV/STPB/Iod system under two light sources. Differential scanning calorimetry (DSC) and thermal imaging tests further confirmed the crucial role of light in the polymerization process. The potential photolysis mechanism of these systems containing EV was explored through steady-state photolysis, liquid chromatography-mass spectrometry (LC-MS), and electron spin resonance (ESR). This research not only offers a viable approach for developing PISs used for LED photopolymerization technology but also contributes to the development of water-based photopolymerization.

Co3O4–TiO2 supported into N-doped magnetic 3D porous microspheres as the “one stone with two birds” strategy for highly efficient removal of organic dyes via synergistic adsorption-photocatalysis

Constructing heterojunctions with rich porosity and unique microstructures is the main way to obtain efficient adsorption and photocatalysis. A ternary composite of Co3O4–TiO2 supported in N-doped magnetic 3D porous microspheres (Co3O4–TiO2/N-MCMs) was successfully constructed with hierarchical pore structures, large specific surface areas, and abundant active sites. The Co3O4–TiO2/N-MCMs possessed excellent adsorption and solar degradation capabilities for representative azo dye (methyl orange, MO) and triphenylmethane dye (rhodamine B, RhB), and the total removal rate of the two dyes with different initial concentration reached up to 99.0% and 99.2% within 2 h, respectively. MO and RhB were rapidly adsorbed and enrichment into Co3O4–TiO2/N-MCMs via pore filling, and then degraded by the nucleophilic reagents (•O– 2 and •OH). Characterizations and theoretical calculations demonstrated that Co3O4–TiO2/N-MCMs contained a sufficient amount of p-n type heterojunctions between Co3O4 and TiO2, which could effectively promote spatial separation of photogenerated e--h+ pairs to improve degradation ability and reduce band gap to extend visible-light absorption. Moreover, N-doping could further transfer photogenerated electrons from heterojunctions to reaction areas to effectively prolong the lifetime of photogenerated electrons. The LC-MS results showed that MO and RhB can be mineralized into H2O and CO2 without generating any secondary pollution. Furthermore, Co3O4–TiO2/N-MCMs exhibited excellent magnetic separation capability and reusability. This study designed a novel photocatalyst for highly efficient removal of organic dyes via “One stone with two birds” strategy of synergistic adsorption-photocatalysis, which could simplify the treating process and exhibit a highly promising in practical applications.