Cobalt Phthalocyanine Research Articles

Effect of loading and pyrolysis of carbon-supported cobalt phthalocyanine on the electrocatalytic reduction of CO2

Understanding the structure-activity relationship of materials that are active for the CO2 electrochemical reduction reaction (CO2ERR) is crucial for developing stable, high-performance catalysts. In this research, it is first shown that ball-milling is a highly efficient way to disperse cobalt phthalocyanine (CoPC) onto carbon black without influencing the CO2 electroreduction performance of the resulting materials. Then, the link between the loadings of the CoPC precursor on the carbon support and the CO2ERR activity of the pyrolyzed materials is demonstrated. With CO current efficiencies higher than 45% and CO current densities as high as -20 mA cm−2 at -0.77 V vs. RHE, the materials with CoPC loadings of 7.9 wt% and higher were still surprisingly active after pyrolysis at 800 and 900 °C. On the other hand, the CO2ERR activity of the materials containing less than 6.1 wt% CoPC was drastically reduced after pyrolysis at these temperatures, with CO current efficiencies lower than 10 %. X-ray powder diffraction revealed that only the materials containing crystalline CoPC before pyrolysis showed good CO2ERR activity after pyrolysis at 800 and 900 °C. Furthermore, X-ray absorption spectroscopy showed that the loading of the CoPC precursor influenced the structure of the active sites in the pyrolyzed CoPC/C materials. Overall, this study highlights the importance of the dispersion of CoPC when forming a material that is catalytically active for CO2ERR after pyrolysis.

Tailored Local Electronic Environment of Co-N4 Sites in Cobalt Phthalocyanines for Enhanced CO2 Reduction Reaction.

Atomically dispersed Co-N4-based catalysts have been recently emerging as one of the most promising candidates for facilitating CO2 reduction reaction (CO2RR). The local electronic environment of Co-N4 sites in these catalysts is considered to play a critical role in adjusting the catalytic performance, the effort of which however is not yet clearly verified. Herein, a series of cobalt phthalocyanines with different peripheral substituents including unsubstituted phthalocyanine Co(II) (CoPc), 2,9,16,23-tetramethoxyphthalocyaninato Co(II) (CoPc-4OCH3), and 2,9,16,23-tetranitrophthalocyaninato Co(II) (CoPc-4NO2) are supported onto the surface of the multi-walled carbon nanotubes (CNTs), affording CoPc@CNTs, CoPc-4OCH3@CNTs, and CoPc-4NO2@CNTs. X-ray photoelectron spectroscopy and X-ray absorption near-edge structure measurements disclose the influence of the peripheral substituents on the local electronic structure of Co atoms in these three catalysts. Electrochemical tests indicate the higher CO2RR performance of CoPc-4OCH3@CNTs compared to CoPc@CNTs and CoPc-4NO2@CNTs as exemplified by the higher Faraday efficiency of CO, larger part current densities, and better stability displayed by CoPc-4OCH3@CNTs at the applied voltage range from -0.6 to -1.0V versus RHE in both H-cell and flow cell. These results highlight the effect of the electron-donating -OCH3 substituent on the enhanced catalytic activity of CoPc-4OCH3@CNTs, which will help develop Co-N4-based catalysts with promising catalytic performance toward CO2RR.

Insight into Impacts of π-π Assembly on Phthalocyanine Based Heterogeneous Molecular Electrocatalysis.

Electrochemical CO2 reduction (CO2R) to feedstocks competes with the hydrogen evolution reaction (HER). Cobalt phthalocyanine (CoPc) immobilized onto carbon driven by π-π interaction represents a classical type of heterogeneous molecular catalyst for CO2R. However, the impacts of π conjugation on the electrocatalysis have not been clarified. Herein, the electrochemical properties of CoPc were investigated by comparison of its analogue to 2,3-naphthalocyanine cobalt (NapCo) having extended π conjugation. It is found that CoPc is redox-active on carbon to provide low oxidized Co sites for improving the CO2R activity and selectivity, while NapCo on carbon turned out to be redox-inert leading to lower performance. In addition, the redox-mediated mechanism for CO2R on CoPc tends to operate with increasing electrolyte alkalinity, which further enhances the reaction selectivity. We speculated that moderate π conjugation allows the redox-mediated mechanism on CoPc, which is critical to promote CO2R performance while depressing the competing HER.

Superb bio-effectiveness of Cobalt (II) phthalocyanine and Ag NPs adorned Sm-doped ZnO nanorods/cuttlefish bone to annihilate Trichinella spiralis muscle larvae and adult worms: In-vitro evaluation

Herein, innovative biocides are designed for the treatment of Trichinella spiralis muscle larvae (ML) and adult worms. Samarium-doped ZnO nanorods (Sm-doped ZnO) are stabilized onto the laminar structure of cuttlefish bone (CB) matrix and adorned by either Ag NPs or cobalt phthalocyanine (CoPc) species. Physicochemical characteristics of such nanocomposites are scrutinised. Adorning of Sm-doped ZnO/CB with Ag NPs shortens rod-like shaped Sm-doped ZnO nanoparticles and accrues them, developing large-sized detached patches over CB moiety. Meanwhile, adorning of Sm-doped ZnO/CB by CoPc species degenerates CB lamellae forming semi-rounded platelets and encourages invading of Sm-doped ZnO nanorods deeply inside gallery spacings of CB. Both nanocomposites possess advanced parasiticidal activity, displaying quite intoxication for ML and adult worms (≥88% mortality) within an incubation period of <48 h at concentrations around 200 μg/ml. CoPc@Sm-doped ZnO/CB nanocomposite exhibits faster killing efficiency of adult worms than that of Ag@Sm-doped ZnO/CB at a concentration of ∼75 μg/ml showing entire destruction of parasite after 24 h incubation with the former nanocomposite and just 60% worm mortality after 36 h exposure to the later one. Morphological studies of the treated ML and adult worms show that CoPc@Sm-doped ZnO/CB exhibits a destructive impact on the parasite body, creating featureless and sloughed fragments enriched with intensive vacuoles. Hybridization of cuttlefish bone lamellae by CoPc species is considered a springboard for fabrication of futuristic aggressive drugs against various food- and water-borne parasites.

Coupling hole-transporting polyaniline layer with a cobalt phthalocyanine cocatalyst to boost photoelectrochemical water oxidation of bismuth vanadate photoanodes

Though bismuth vanadate (BiVO4) exhibits a promising potential as a semiconductor photoanode toward photoelectrochemical (PEC) water oxidation, its PEC performance is still limited by the poor charge carrier transport and sluggish oxygen evolution kinetics. Herein, the polyaniline (PANI) and cobalt coordinated-phthalocyanines (CoTcPc) were introduced onto the BiVO4 semiconductor substrate, constructing the integrated CoTcPc/nPANI/BiVO4 (n = 30, 60 and 90, n represents the deposition time for PANI with the unit of s) composite photoanodes. It is demonstrated that the PEC water oxidation activity of BiVO4 is significantly boosted by the incorporation of PANI and CoTcPc, stemming from the improved electron/hole transfer, enhanced charge separation efficiency, and accelerated carrier mobility and water oxidation kinetics. CoTcPc/60PANI/BiVO4 composite photoanode with the optimized compositions exhibits an enhanced photocurrent density of 4.03 mA/cm2 at 1.23 V vs. RHE under illumination, ranking among the best records reported recently. Furthermore, the roles of electrodeposition time to generate PANI are also distinguished through experimental studies. These results reveal the crucial role of engineering the hole transfer layer to optimize the semiconductor photoanodes toward efficient PEC water oxidation.

Hydrophilic phthalocyanine covalent organic frameworks for enhanced electrocatalytic H2O2 production

The electrocatalytic 2e− oxygen reduction reaction (ORR) is considered as a promising pathway to replace conditional anthraquinone process for hydrogen peroxide (H2O2) manufacture. However, the efficient electrocatalysts towards 2e− ORR remain urgently desired. Herein, hydrophilic two-dimensional cobalt phthalocyanine (CoPc) covalent organic frameworks (COFs), denoted as CoPc-2SO3H-COF and CoPc-SO3H-COF, were afforded via the imidization reaction of 2,3,9,10,16,17,23,24-octacarboxyphthalocyaninato cobalt(II) with hydrophilic building blocks 2,5-diaminobenzenesulfonic acid and 1,4-benzenedisulfonic acid, respectively. Powder X-ray diffraction, transmission electron microscope, and N2 sorption experiment results reveal the crystalline and porous structure of these two COFs. Moreover, the water contact angle and proton conduction measurements demonstrate the hydrophilic properties of these two COFs owing to the introduction of −SO3H into their skeleton. This, in combination with the high-efficiency active Co-N4 sites towards 2e− ORR, endows these two COFs with enhanced 2e− ORR activity in the aqueous electrolyte. In particular, CoPc-2SO3H-COF exhibits outstanding electrocatalytic H2O2 production performance with a stable H2O2 selectivity of 88.3 % under a high current density of 125 mA cm−2 for 20 h in a flow cell.

Cobalt Phthalocyanine Based Metal–Organic Framework as an Efficient Bifunctional Electrocatalyst for Water Electrolysis

Cobalt Phthalocyanine Based Metal–Organic Framework as an Efficient Bifunctional Electrocatalyst for Water Electrolysis

Directed Electron Delivery from a Pb-Free Halide Perovskite to a Co(II) Molecular Catalyst Boosts CO2 Photoreduction Coupled with Water Oxidation.

The development of high-performance photocatalytic systems for CO2 reduction is appealing to address energy and environmental issues, while it is challenging to avoid using toxic metals and organic sacrificial reagents. We here immobilize a family of cobalt phthalocyanine catalysts on Pb-free halide perovskite Cs2AgBiBr6 nanosheets with delicate control on the anchors of the cobalt catalysts. Among them, the molecular hybrid photocatalyst assembled by carboxyl anchors achieves the optimal performance with an electron consumption rate of 300±13 μmol g-1 h-1 for visible-light-driven CO2-to-CO conversion coupled with water oxidation to O2, over 8 times of the unmodified Cs2AgBiBr6 (36±8 μmol g-1 h-1), also far surpassing the documented systems (<150 μmol g-1 h-1). Besides the improved intrinsic activity, electrochemical, computational, ex-/in situ X-ray photoelectron and X-ray absorption spectroscopic results indicate that the electrons photogenerated at the Bi atoms of Cs2AgBiBr6 can be directionally transferred to the cobalt catalyst via the carboxyl anchors which strongly bind to the Bi atoms, substantially facilitating the interfacial electron transfer kinetics and thereby the photocatalysis.

Directed Electron Delivery from a Pb‐Free Halide Perovskite to a Co(II) Molecular Catalyst Boosts CO2 Photoreduction Coupled with Water Oxidation

AbstractThe development of high‐performance photocatalytic systems for CO2 reduction is appealing to address energy and environmental issues, while it is challenging to avoid using toxic metals and organic sacrificial reagents. We here immobilize a family of cobalt phthalocyanine catalysts on Pb‐free halide perovskite Cs2AgBiBr6 nanosheets with delicate control on the anchors of the cobalt catalysts. Among them, the molecular hybrid photocatalyst assembled by carboxyl anchors achieves the optimal performance with an electron consumption rate of 300±13 μmol g−1 h−1 for visible‐light‐driven CO2‐to‐CO conversion coupled with water oxidation to O2, over 8 times of the unmodified Cs2AgBiBr6 (36±8 μmol g−1 h−1), also far surpassing the documented systems (&lt;150 μmol g−1 h−1). Besides the improved intrinsic activity, electrochemical, computational, ex‐/in situ X‐ray photoelectron and X‐ray absorption spectroscopic results indicate that the electrons photogenerated at the Bi atoms of Cs2AgBiBr6 can be directionally transferred to the cobalt catalyst via the carboxyl anchors which strongly bind to the Bi atoms, substantially facilitating the interfacial electron transfer kinetics and thereby the photocatalysis.

Role of Mass Transport in Electrochemical CO2 Reduction to Methanol Using Immobilized Cobalt Phthalocyanine.

Electrochemical CO2 reduction (CO2R) using heterogenized molecular catalysts usually yields 2-electron reduction products (CO, formate). Recently, it has been reported that certain preparations of immobilized cobalt phthalocyanine (CoPc) produce methanol (MeOH), a 6-electron reduction product. Here, we demonstrate the significant role of intermediate mass transport in CoPc selectivity to methanol. We first developed a simple, physically mixed, polymer (and polyfluoroalkyl, PFAS)-free preparation of CoPc on multiwalled carbon nanotubes (MWCNTs) which can be integrated onto Au electrodes using a poly(3,4-ethylenedioxythiophene) polystyrenesulfonate (PEDOT:PSS) adhesion layer. After optimization of catalyst preparation and loading, methanol Faradaic efficiencies and partial current densities of 36% (±3%) and 3.8 (±0.5) mA cm-2, respectively, are achieved in the CO2-saturated aqueous electrolyte. The electrolyte flow rate has a large effect. A linear flow velocity of 8.5 cm/min produces the highest MeOH selectivity, with higher flow rates increasing CO selectivity and lower flow rates increasing the hydrogen evolution reaction, suggesting that CO is an unbound intermediate. Using a continuum multiphysics model assuming CO is the intermediate, we show qualitative agreement with the optimal inlet flow rate. Polymer binders were not required to achieve a high Faradaic efficiency for methanol using CoPc and MWCNTs. We also investigated the role of formaldehyde as an intermediate and the role of strain, but definitive conclusions could not be established.

Tuning the Interfacial Electronic Structure of MoS2 by Adsorption of Cobalt Phthalocyanine Derivatives

Tuning the Interfacial Electronic Structure of MoS₂ by Adsorption of Cobalt Phthalocyanine Derivatives

S-doped rich-defect cobalt-based carbon catalyst derived from cobalt phthalocyanine as catalysts of peroxymonosulfate for degradation of tetracycline hydrochloride from water

Organic pollution is a serious problem in the water environment. Peroxymonosulfat (PMS)- based advanced oxidation processes (AOPs) is the optimal way to treat such pollution. To better activate PMS, the S-doped cobalt-based carbon catalysts are attracting considerable attention. In this work, a mixture of cobalt phthalocyanine (CoPc) and thiourea was used as precursor to prepare CoPc-S-800 under Ar atmosphere at 800℃. Subsequently, CoPc-S-800 was used to activate PMS for degrading tetracycline hydrochloride (TC• HCl). In addition, experiments and X-ray photoelectron spectroscopy (XPS) showed that the introduction of S can promote the redox cycle of CO (III)/CO (II). Electron paramagnetic resonance (EPR) suggested that •OH, SO4• −, O2• − and 1O2 played important roles in TC• HCl degradation. This study investigated the influence of pH, different sources of water, and anions/cations/halogen ions on TC• HCl degradation. The results showed the CoPc-S-800/PMS system maintained excellent performance. This study provides a new strategy for TC• HCl degradation using cobalt-based carbon catalysts with CoPc as precursor. This work also elucidates the reaction mechanism of PMS activation by the catalyst.

Rational Design of Cobalt Phthalocyanine (CoPc)‐Anchored TiO2 Nanorods for High‐Efficiency Selective Catalytic Oxidation

AbstractQuinclorac is important precursor for pharmaceutical, agricultural, and synthetic chemistry. The state‐of‐art synthesis of quinclorac via condensation, chlorination and oxidative hydrolysis often uses homogeneous catalysts and strong acid oxidant agents to promote the catalytic oxidation, which requires huge manpower input for the late‐stage purification process and is usually environmentally unfriendly. In this work, we successfully fabricated a stable cobalt phthalocyanine (CoPc) Co‐based composite (CoPc/TiO2) by anchoring CoPc on the surface of TiO2 nanorods for the selective oxidation of 3,7‐dichloro‐8‐dichloro methyl quinoline (3,7‐D‐8‐DMQ) into quinclorac. More impressively, CoPc/TiO2‐2.5 %‐Mn‐Br exhibits a high selectivity of 91.9 % for the catalytic oxidation of 3,7‐D‐8‐DMQ to quinclorac in acetic acid, with a quinclorac yield of 86.4 %, which is approximately 2.43 times higher than that of pristine CoPc‐Mn‐Br. The obtained heterogeneous catalytic system shows good reusability. Detailed mechanistic investigations reveal that the system works through a free radical mechanism via the formation of Co2+/Co3+ redox cycles. This work provides a new understanding for the stabilization of reaction intermediates and facilitates the designs of catalysts for selective catalytic oxidation.

Closed-Loop Synthesis of Highly Dispersed Cobalt Phthalocyanine Catalysts for Efficient CO2 Electroreduction

Closed-Loop Synthesis of Highly Dispersed Cobalt Phthalocyanine Catalysts for Efficient CO₂ Electroreduction

Universal Sublimation Strategy to Stabilize Single-Metal Sites on Flexible Single-Wall Carbon-Nanotube Films with Strain-Enhanced Activities for Zinc-Air Batteries and Water Splitting.

Single-metal-site catalysts have recently aroused extensive research in electrochemical energy fields such as zinc-air batteries and water splitting, but their preparation is still a huge challenge, especially in flexible catalyst films. Herein, we propose a sublimation strategy in which metal phthalocyanine molecules with defined isolated metal-N4 sites are gasified by sublimation and then deposited on flexible single-wall carbon nanotube (SWCNT) films by means of π-π coupling interactions. Specifically, iron phthalocyanine anchored on the SWCNT film prepared was directly used to boost the cathodic oxygen reduction reaction of the zinc-air battery, showing a high peak power density of 247 mW cm-2. Nickel phthalocyanine and cobalt phthalocyanine were, respectively, stabilized on SWCNT films as the anodic and cathodic electrocatalysts for water splitting, showing a low potential of 1.655 V at 10 mA cm-2. In situ Raman spectra and theoretical studies demonstrate that highly efficient activities originate from strain-induced metal phthalocyanine on SWCNTs. This work provides a universal preparation method for single-metal-site catalysts and innovative insights for electrocatalytic mechanisms.

Interface transformation strategy to 1D hierarchically porous carbon with enhanced bifunctional oxygen electrocatalytic performance

Developing efficient oxygen electrocatalysts is considered a key step to advancing renewable energy technologies, especially in fuel cells and metal-air batteries. Herein, an interface transformation strategy is proposed to prepare a one-dimensional cobalt (Co)/nitrogen (N) co-doped porous carbon material (Co/N-PCM). Polydopamine nanotubes (PDA NT) and cobalt phthalocyanine (CoPc) were used as precursors for the controlled formation of Co/N-PCM. Immobilized CoPc molecules on PDA NT formed Co/N-PCM with evenly distributed Co/Co-N-C sites and a hierarchical micro-/mesoporous structure. Theoretical calculations revealed that the electronic modulation of the substrate by Co(111) played a pivotal role in establishing the d-band center of active Co sites on the monatomic Co-N-C layer. The surface-active Co sites provided an optimum adsorption strength between the Co/N-PCM and oxygenated intermediates, leading to significantly enhanced intrinsic oxygen reduction/evolution reaction (ORR/OER) activities. The engineered Co/N-PCM catalyst displayed high activity towards bifunctional oxygen electrocatalysis and delivered outstanding rechargeable zinc-air battery (ZAB) performance.

Electrocatalytic detection of Hg(II) using a platinum electrode modified with composite film of cobalt(II) phthalocyanine tetra-substituted with 1-(methoxymethyl)-benzotriazole groups and co-electropolymerized polypyrrole

The presence of mercury adversely affects the daily lives of humankind due to its acute toxicity and environmental persistence. Therefore, the development of cost-effective smart materials which can allow the real time, ultrasensitive and discriminatory monitoring of mercury concentrations in industrial and municipal water treatment plants is an imperative. It is foreseen that this proposed water quality assurance measure will be of utmost importance to identify the culprits for the wide prevalence of this heavy metal ion in the environment. Herein, a platinum electrode (Pt) was modified via the simultaneous electropolymerization of polypyrrole (PPy) and the co-electrodeposition of tetra-[4-((1H-benzotriazole)methoxy)phthalocyaninato]cobalt(II) (CoPc-Bzt, 2, (Btz = benzotriazole)). The complementary electrode modification processes were performed in a 1:1 (v: v) DMF: acetonitrile containing 1 M tetrabutylammonium hexafluorophosphate electrolyte solution over 20 cycles using cyclic voltammetry to afford the chemically modified electrode (CME), Pt|PPy/2. Differential pulse anodic stripping voltammetry (DPASV) was used to detect Hg(II) ions using the CME within a 10 µM to 100 µM linear range while calculated limits of detection and quantification (LOD and LOQ) were determined as 3.11 and 10.00 µM, respectively. The analytical performance of the CME rendered a statistically accepted percentage recovery (97.4%) whereas that of Inductively Coupled Plasma – Optical Emission Spectroscopy (ICP-OES) is 112.3%.

Insights into the G-quadruplex DNA interaction landscape: Comparative analysis of anionic Zn(II) and Co(II) phthalocyanine-tetrasulfonate complexes.

G-quadruplexes play a pivotal role in regulating various cellular processes, including gene expression and replication, making them essential structures in understanding, and manipulating cellular functions. The development of G-quadruplex ligands holds significant promise in therapeutic and research applications, offering targeted tools to modulate G-quadruplex structures and potentially influence critical biological pathways. An exciting frontier in G-quadruplex research lies in the exploration of anionic ligands, and their profound impact on stabilizing and modulating G-quadruplex DNA. In this study, the interaction of two anionic phthalocyanine compounds (Zinc (II) phthalocyanine 3,4',4″,4‴-tetrasulfonic acid, tetrasodium salt, ZnAPC; cobalt (II) phthalocyanine 3,4',4″,4‴-tetrasulfonic acid, tetrasodium salt, CoAPC) and three separate G-quadruplex-forming DNA sequences was investigated. Interactions were carried out by DNA polymerase stop studies along with spectroscopic studies. According to the results of experimental data, it was determined that ZnAPC actively interacts with the G-quadruplex DNA structures. On the other hand, it was thought that the interaction with CoAPC was less and even occurred in simple electrostatic interactions. KD constants and Bmax constants for the interaction with ZnAPC were calculated. The KD constants for ZnAPC were found to be (1.16 ± 0.07) × 10-5, (9.75 ± .24) × 10-6 and (1.00 ± 0.36) × 10-4 M for AS1411, Vegf, and Tel21, respectively. Accordingly, it was concluded that ZnAPC interacts with G-quadruplex DNA ligands effectively.

Non-enzymatic glucose sensor using mesoporous carbon screen-printed electrodes modified with cobalt phthalocyanine by phase inversion

The development of non-enzymatic glucose electrochemical sensors is still required to be used for the determination of glucose in complex biological media. This study presents a straightforward and remarkably efficient tool for the preparation of highly stable and sensitive glucose electrochemical sensors based on the deposition of cobalt phthalocyanine (CoPc) onto mesoporous carbon screen-printed electrodes (MCs). Results show that the MC electrochemical activation (aMC) followed by phase inversion (PI), which consisted of drop casting of CoPc in dimethylformamide onto a wetting electrolyte leading to the electrode aMC-CoPc/PI, enhanced sensitivity towards glucose determination in complex media. The beneficial need for MC surface activation and PI has been explored by scanning electron microscopy, energy dispersive X-ray spectroscopy, Raman spectroscopy, cyclic voltammetry and electrochemical impedance spectroscopy. The aMC-CoPc/PI electrode exhibited the highest electrocatalytic activity of the series (namely, MC-CoPc, MC-CoPc/PI and aMC-CoPc) towards glucose oxidation. By using square wave voltammetry technique, the aMC-CoPc/PI glucose electrochemical sensor demonstrated a sensitivity of 22.3 µA mM−1 and a low detection limit of 27.4 µM (S/N = 3) in a linear dynamic range of 0.1 to 3.5 mM. Additionally, it also displayed high selectivity, robust stability, repeatability and reproducibility toward the quantification of glucose concentration in complex samples such as horse serum, intravenous glucose saline solution and culture medium for sperm cells.

Synthesis and in vitro acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes activity of aldehyde and Schiff base substituted cobalt (II), copper (II), and zinc (II) phthalocyanines

In this work, a series of aldehyde‐substituted phthalocyanine compounds (1, 3, and 5) were prepared by the cyclotetramerization of the 4‐(5‐(diethylamino)‐2‐formylphenoxy) phthalonitrile (a) and the corresponding metal salts. Schiff base‐substituted phthalocyanines (2, 4, and 6) were derived from an aldehyde‐substituted phthalocyanine (1, 3, and 5) via the reaction of aldehyde‐substituted phthalocyanines with an amine reagent. The compounds that were obtained were characterized using FT‐IR, 1H {13C} NMR, UV–Vis, and MS spectra (a and 1–6). The inhibitory qualities of synthesized aldehyde and Schiff base‐substituted complexes against the enzymes butyrylcholinesterase (BChE) and acetylcholinesterase (AChE) were assessed. The majority of phthalocyanines exhibited strong enzyme‐inhibiting properties. Out of the six produced phthalocyanines, 3 and 4 displayed the most intriguing profiles as submicromolar selective AChE inhibitors (IC50 = 0.060 μM), whereas 1 demonstrated the most potent BChE inhibitor (IC50 = 0.024 μM). The aggregation studies of CoPcs, CuPcs, and ZnPcs (1–6) were also carried out in this work.