Synthesis Of Porphyrins Research Articles

Synthesis of novel zinc porphyrins with bioisosteric replacement of Sorafenib: Efficient theranostic agents for anti-cancer application

Novel zinc porphyrins (trans-A2B2 and A3B type) are reported containing pharmacophoric groups derived from Sorafenib at the meso-positions. The pharmacophoric and bioisosteric modification of Sorafenib was done with 2-methyl-4-nitro-N-phenylaniline. The in-vitro photo-cytotoxicity studies of zinc porphyrins on HeLa cells revealed excellent PDT based autophagy inhibition of cancer cells, with IC50 values between 6.2 to 15.4 μM. The trans-A2B2 type zinc porphyrin with two bioisosteric groups gave better cytotoxicity than A3B type. Molecular docking studies revealed excellent binding with mTOR protein kinase of the designed porphyrins. The confocal studies indicated significant ER localization of trans-A2B2 type zinc porphyrin in HeLa cells along with ROS generation. trans-A2B2 type zinc porphyrin induced ER stress in cancer cells, thereby causing elevation of Ca+2 ions in cytoplasm, which led to cancer cell death via autophagy pathway. The studies suggested that trans-A2B2 and A3B type zinc porphyrins can be developed as theranostic agents for anti-cancer applications.

Naphthodithiophene-Fused Porphyrins: Synthesis, Characterization, and Impact of Extended Conjugation on Aromaticity.

The fusion of tetrapyrroles with aromatic heterocycles constitutes a useful tool for manipulating their opto-electronic properties. In this work, the synthesis of naphthodithiophene-fused porphyrins was achieved through a Heck reaction-based cascade of steps followed by the Scholl reaction. The naphthodithiophene-fused porphyrins display a unique set of optical and electronic properties. Fusion of the naphtho[2,1-b:3,4-b']dithiophene to porphyrin (F2VTP) leads to a ~20% increase in the fluorescence lifetime, which is accompanied, unexpectedly, by a more than two-fold drop in the emission quantum yield (ϕ=0.018). In contrast, fusion of the isomeric naphtho[1,2-b:4,3-b']dithiophene to porphyrin (F3VPT) results in a ~1.5-fold increase in the fluorescence quantum yield (ϕ=0.13) with a concomitant ~30 % increase in the fluorescence lifetime. This behavior suggests that fusion of the porphyrin with the naphthodithiopheno-system mainly affects the radiative rate constant in the Q-state deactivation pathway, where the effects of the isomeric naphtho[2,1-b:3,4-b']dithiophene- versus naphtho[1,2-b:4,3-b']dithiophene-fusion are essentially the opposite. Interestingly, nucleus-independent chemical shifts analysis revealed a considerable difference between the aromaticities of these two isomeric systems. Our results demonstrate that subtle structural differences in the fused components of the porphyrin can be reflected in rather significant differences between the photophysical properties of the resulting systems.

Ring-Closing Reactions of Porphyrins on Noble Metal Surfaces

On-surface chemistry protocols provide elegant routes to individual molecular complexes, oligomers, and hybrid structures at confining interfaces, yielding distinct chemical, physical, and structural properties [1]. In this context, porphyrins and other tetrapyrroles represent versatile precursors that can undergo metalation, ring-opening, and ring-closing reactions. Furthermore, they are often used as functional tectons for self-assembled molecular films, metal-organic coordination networks, and covalent architectures at interfaces [2].We will report on temperature-induced ring-closing reactions of porphyrins on single crystalline Ag and Au surfaces in an ultrahigh vacuum environment. Examples covered include dehydrogenative homocoupling as well as intramolecular ring-closing. Specifically, distinct oligomers including square-type porphyrin tetramers featuring a planar, central antiaromatic cyclooctatetraene (COT) moiety were achieved on a Ag(100) support by employing unsubstituted Zn- and free-base porphines (see Figure) as precursors [3]. Low-temperature scanning tunnelling microscopy (STM), spectroscopy (STS), and bond-resolved atomic force microscopy (AFM) supported by complementary theoretical modelling were used to comprehensively characterize chemical structure and electronic properties of the square-type tetramers with sub-molecular resolution. Furthermore, the synthesis of π-extended oxygen-embedded porphyrins via O-annulation on Au(111) will be discussed. This surface chemical approach yields high selectivity and yield for planar porphyrin products with distinct symmetries and oxygen content that is not achieved by solution chemistry. The bond-resolved AFM characterization is complemented by X-ray photoelectron spectroscopy measurements. These studies thus give access, and insights, to novel porphyrinoids with distinct properties on noble metal supports.

Calix[3]Pyrrole and Related Macrocycles: Synthesis and Properties

Calix[4]pyrrole is a porphyrinogen-like macrocycle in which four pyrrole units are linked by four sp3-hybridized carbon atoms at the α-positions. While such tetrapyrrolic macrocycles are readily synthesized by acid-catalyzed condensation reactions of pyrrole monomer and carbonyl compound, analogous macrocycles composed of three pyrrole units are always not observed. Calix[3]pyrrole is a ring-contracted analogue of calix[4]pyrrole, and has been missing in porphyrin-related chemistry. In this presentation, the first synthesis of calix[3]pyrrole and its furan-embedded analogues is reported, and their unique reactivity derived from their macrocyclic ring strain will be discussed.Synthesis of calix[3]pyrrole started with a linear trimer of 3,3-dimethylpentane-2,5-dione. Intramolecular cyclization of the linear hexaketone was accomplished in 5 steps to give a cyclic hexaketone precursor. Paal–Knorr type pyrrole formation reaction of cyclic hexaketone gave calix[3]pyrrole in 41% yield (Scheme 1). Using similar strategies, analogous calix[3]-type macrocycles, namely, calix[1]furan[2]pyrrole, calix[2]furan[1]pyrrole, and calix[3]furan, were successfully synthesized. Single crystal X-ray diffraction analysis of calix[3]pyrrole revealed its strained structure, and the theoretical calculations showed the strain energy of calix[3]pyrrole is 22.1 kcal/mol per unit higher than that of calix[4]pyrrole. Such strain energy tends to decrease as the number of pyrrole unit decreased.Calix[3]pyrrole exhibited unique reactivity derived from macrocyclic ring strain under acidic (Rothemund–Lindsey) conditions that are frequently used for porphyrin synthesis. When calix[3]pyrrole was dissolved in 10 mM solution of trifluoroacetic acid in dichloromethane, calix[6]pyrrole was quantitatively formed within 30 seconds (Scheme 1). Similar strain-induced ring expansion was observed for calix[1]furan[2]pyrrole, but full conversion took approximately 5 minutes. On the other hand, calix[2]furan[1]pyrrole and calix[3]furan did not show ring expansion. Detailed mechanistic analysis revealed that protonation at a pyrrole unit in calix[3]pyrrole triggers irreversible ring-cleavage to give a linear tripyrrane moiety which undergoes cyclodimerization under acidic conditions.The strain-induced ring expansion reaction of calix[3]pyrrole solved a long-standing question in porphyrin-related chemistry. Tripyrrolic macrocycles such as calix[3]pyrrole are, even formed, not isolable from pyrrole condensation reaction using acid, because the strain-induced conversion to calix[6]pyrrole is too fast. Besides, this reaction provided a novel approach to ring-expanded calix-type macrocycles. Figure 1

Direct Synthesis of ABCD-porphyrin Platinum(II) Complexes via Dehydrative Aromatization.

Since the development of the first method for porphyrin synthesis by Rothemund in 1935, porphyrin derivatives have been widely investigated and have played an essential role in chemical sciences. Most synthetic routes of porphyrins involve oxidative aromatization. Herein, we present a synthetic method to produce ABCD-porphyrins, including chiral ones, through a one-pot reaction involving "coordination, cyclization, and dehydrative aromatization" using a mono-dipyrrinatoPt(II)Cl(COE) (COE = cyclooctene) complex as a platinum template.

Porphyrins and porhyrin polymers: synthesis, structural features, prospects of application

The review covers works on the synthesis of porphyrins, including amphiphilic star-shaped ones, which are attracting more and more attention of synthetic scientists. The potential of various types of porphyrins, metalloporphyrins and their derivatives as photosensitizers in photodynamic therapy is discussed. The relationship between the structure of porphyrins and their antimicrobial activity is shown. Polymer-porphyrin systems based on biodegradable polyesters and tetraphenylporphyrins immobilized in their matrix are considered as promising composite materials with bactericidal properties.

Modification for Nitration of Halo-substituted meso-Tetraarylporphyrins: A Convenient Scale-up in Small Amount of Solvent

Abstract: The synthesis of porphyrins with halogens and nitro groups in meso-aryl rings is described. Halo-substituted meso-tetraarylporphyrin derivatives in the reaction with sodium nitrite in trifluoroacetic acid at 40°C (or room temperature) afford 5-(4-nitroaryl)-10,15,20- triarylporphyrins. The above mono-nitro products bearing halogens on meso-aryl rings (F, Cl, Br) are difficult to obtain selectively. The method elaborated herein allows to synthesize them with reasonable yield (of up to 57%), and the reaction can be easily scaled-up. By this route, the preparation of valuable substrates for further transformation to highly substituted ‘synthetic porphyrins’ was presented.

Highly effective self-assembled porphyrin MOCs nanomaterials for enhanced photodynamic therapy in tumor

Porphyrins and their derivatives are excellent photosensitizers in photodynamic therapy (PDT). The modification of porphyrin molecules into metal-organic cages (MOCs) is a viable strategy to improve their bioavailability. In this work, MOC C66 based on porphyrin was synthesised by a one-pot self-assembly method. The three-dimensional structure of the metal-organic cage ameliorated the aggregation and self-quenching of porphyrins and increased the molar absorption coefficient in the visible light region, which enhanced the reactive oxygen species (ROS) yield of porphyrins and effectively improved the efficiency of photodynamic therapy. ROS generation ability tests in solution confirmed the improved reactive oxygen capacity of the cage, which showed greater phototoxicity to HeLa and MCF-7 cells in vitro, suggesting a new strategy for future modifications of the simple synthesis of porphyrins as photosensitizers.

Synthesis of styrene, phenyl acrylate and allyloxyphenyl-functionalized porphyrins, and preliminary exploration of their utility for assembling multiple porphyrin units

Three free-base and two Zn(II) porphyrins carrying one alkene-substituted meso-aryl group and three solubilizing pentyl groups were prepared via mixed aldehyde-type syntheses. A meso [Formula: see text]-allyloxyphenyl porphyrin was obtained via the corresponding 5-([Formula: see text]-allyloxyphenyl) dipyrromethane. The porphyrins were fully characterized using a combination of NMR spectroscopy, high-resolution mass spectrometry, and UV-Vis absorption and emission spectroscopies. Two of the free-base porphyrins were heated in the presence of AIBN or benzoyl peroxide as the initiator. The major isolated products of these reactions contained two porphyrin units based on the results of MALDI-MS and 1H NMR analysis data, which was supported by the results of FTIR, UV-Vis absorption and emission spectroscopies, and gel permeation and liquid chromatographies. Additionally, the acrylamide-functionalized porphyrin could be attached to a polylysine scaffold under basic conditions. These results suggest that the olefinic handle can be used to assemble structures containing multiple porphyrinic macrocycles.

Synthesis of vanillin-based porphyrin for remarkably enhancing the toughness, UV-resistance and self-extinguishing properties of polylactic acid

To achieve high-performance polylactic acid (PLA) composites, the exploitation of multifunctional biomass additives derived from renewable resources are highly demanded. Herein, a vanillin-based porphyrin (VPR) was designed and synthesized to impart PLA with enhanced mechanical, anti-UV, and flame retardant properties. Multiple intermolecular interactions between VPR and PLA enabled significant toughening of the PLA/VPR biocomposites compared to PLA itself. The elongation at break and impact strength for PLA/3VPR were improved by 88.2 % and 104.2 %, respectively, without influence on their tensile strength. Furthermore, the PLA/VPR biocomposites exhibited improved anti-UV performance with only 1.5 % and 8.6 % decrease of the strength and elongation at break respectively after UV aging. More importantly, incorporation of only 3 wt% VPR loading within the PLA/3VPR composite allowed for excellent self-extinguishing with a UL-94 V-0 level, greatly improving the versatility of PLA composites. We envision that such bio-based PLA/VPR materials with multifunctional features will extensively broaden the usable range of PLA composites.

Exploring the reactivity of formylporphyrins with 3-(diethylamino)phenol. Synthesis, spectroscopic properties and singlet oxygen generation of a new porphyrin–rosamine conjugate

The design of novel molecular structures with tunable photophysical properties is an important research field for many applications including optoelectronics, sensing and bioimaging. Porphyrin and rhodamine/rosamine derivatives are among the most studied and relevant chemosensors and imaging probes due to their attractive photophysical properties, such as high absorption coefficients and long emission wavelengths. In this work, we present the synthesis and the structural characterization of a new porphyrin–rosamine conjugate H2P3 and its related triarylmethane precursors H2P1 and H2P2. The photophysical properties of H2P1, H2P2 and H2P3, and their ability to chelate iron(III) and copper(II) ions, were evaluated by absorption and emission spectroscopy. The formation of copper(II) complexes was confirmed by electron paramagnetic resonance (EPR), which also allowed the detection of an intense and stable radical signal for the free-base H2P3. Further studies involving the addition of the 2,2,6,6-tetramethylpiperidine spin trap to derivatives H2P1, H2P2 and H2P3, showed that only H2P3 gives rise to an EPR detectable signal due to a strong generation of singlet oxygen.

H-bonded acid-base type associates of sulfoheteryl substituted porphyrins and their influence on chromophoric properties

Directed synthesis of novel water-soluble asymmetric porphyrins containing in a molecule three sulfo-phenyl fragments and residues of small heterocyclic molecules (benzothiazole (S-spor), benzoxazole (O-spor) and benzo-N-methylimidazole (N-spor)) was performed using metal-complex catalysis method. The state of the synthesised porphyrins in water media was examined by spectrophotometric and potentiometric titration. It was shown that in the case of porphyrins with benzothiazole and benzoxazole residues two interconnected processes - protonation of the reaction centre and formation of self-associates from protonated O-spor and S-spor forms - occur in water. For the porphyrin with benzo-N-methylimidazole residual, the protonation processes dominate and revealed association was less evident compared to O-spor and S-spor. It was proved that formation of associates from protonated forms of anionic porphyrins does not result from π-π-interaction; the porphyrins under study form the H-bonded acid-base type associates’ stabilisation of which is due to specific bindings through direct participation of sulfo groups as well as monoheteryl substitutes in the case of O-spor and S-spor. Potentiometric and spectrophotopotentiometric titrations were conducted, the pKa values which reflect the protonation process of the porphyrin reaction centre were determined. Acid strength increased in the order O-spor < N-spor < S-spor and correlated with electronegativity of heteroatom in the peripheral porphyrin’s substitute.

Synthesis and antitumor study of novel porphyrin–coumarin derivatives for chemotherapy and photodynamic therapy

Photodynamic therapy (PDT) is attractive in cancer treatment because of its non-invasive and low side effects. In this study, we synthesized 20 porphyrin–coumarin compounds via condensation reactions of porphyrins with coumarin derivatives. In the singlet oxygen (1O2) assay, DPBF fluorescence was quenched by 85% after 10 s of light irradiation; the fluorescence of DPBF almost disappeared at 30 s by light irradiation. This indicates that the porphyrin–coumarin compounds have excellent 1O2 generation efficiency. Moreover, porphyrin–coumarin compounds showed different inhibitory effects on A549 and HepG2 cells under light irradiation. Whereas in dark conditions, compounds with shorter alkyl chains showed antitumor activity, the extension of branched and alkyl chains decreased the activity of the compounds. Therefore, accessing coumarin derivatives with shorter alkyl chains to porphyrins achieves PDT and chemotherapy. Additionally, the insertion of metal Zn into porphyrins also enhances the PDT effect of the compounds.

A New Strategy for the Synthesis of Porphyrin and Expanded Porphyrin Derivatives from Di‐ and Tripyrromethanes: Antioxidant, Cytotoxic Activity, and Molecular Docking Evaluation

AbstractWe present a novel and effective process for producing porphyrins in the absence of a solvent condition, in contrast to earlier procedures. An aldehyde and pyrrole were condensed by grinding in the presence of an acidic catalyst during the synthetic process. By adjusting reactant molar ratios and concentrations, dipyrromethane 3 and tripyrromethane 4 derivatives, the synthesis was improved at room temperature in 5–10 minutes with excellent yields. In this work, we successfully synthesized a number of novel porphyrin derivatives, 6 b–j. Here, we describe a method for reacting dipyrromethane 3a with various aryl aldehydes 5 b–j while using DMF as a capping agent. Moreover, expanding porphyrin derivatives 7 a, and 7 b were synthesized from the reaction of 4a with aldehydes 5a and 5b at 0 °C. Porphyrin derivatives 6 g and 6 h displayed good antioxidant potential. The cytotoxic activity of compounds 6 h, 6 b, and 6c against the human cell lines HePG‐2 and MCF‐7 were studied. The binding modes of the synthesized compounds were analyzed by docking studies that showed good binding scores against the diverse amino acids of the selected proteins (Bcl‐2). The conducted docking studies were found to be consistent with cytotoxic results.

Fascinating strategies of marine benthic organisms to cope with emerging pollutant: Titanium dioxide nanoparticles

Titanium dioxide nanoparticles (NPs) have numerous applications, and their demands have increased as an alternative for banned sunscreen filters. However, the underlying mechanisms of their toxicity, remain largely unknown. Here, we investigate the mechanism of TiO2 NP cytotoxicity and detoxification through time-course experiments (1, 6, and 24 h) based on cellular observations and single-cell transcriptome analyses in a marine benthic foraminifer strain, derived from a common unicellular eukaryotic organism worldwide. After exposure for 1 h, cells enhanced the production of reactive oxygen species (ROS) in acidic endosomes containing TiO2 NPs as well as in mitochondria. In acidic endosomes, ROS were produced through the Fenton reaction on the surface of charged TiO2 NPs. In mitochondria, ROS were associated with porphyrin synthesis that chelated metal ions. Glutathione peroxide and neutral lipids acted as a sink for free radicals, whereas lipid peroxides were excreted to prevent further radical chain reactions. By 24 h, aggregated TiO2 NPs were encapsulated in organic compounds, possibly ceramide, and excreted as mucus, thereby preventing their further uptake. Thus, we reveal that foraminifers can tolerate the toxicity of TiO2 NPs and even prevent their further phagocytosis and uptake by trapping TiO2 NPs inside mucus. This previously unknown strategy could be applied in bioremediation to sequester NPs from the marine environment and can guide management of TiO2 pollution.

Synthesis of New Amino-Functionalized Porphyrins:Preliminary Study of Their Organophotocatalytic Activity.

The design, synthesis, and initial study of amino-functionalized porphyrins as a new class of bifunctional catalysts for asymmetric organophotocatalysis is described. Two new types of amine-porphyrin hybrids derived from 5,10,15,20-tetraphenylporphyrin (TPPH2), in which a cyclic secondary amine moiety is covalently linked either to a β-pyrrolic position (Type A) or to the p-position of one of the meso phenyl groups (Type B), were prepared by condensation, reductive amination, or amidation reactions from the suitable porphyrins (either formyl or methanamine derivatives) with readily available chiral amines. A preliminary study of the possible use of Type A amine-porphyrin hybrids as asymmetric, bifunctional organophotocatalysts was performed using the chiral, imidazolidinone-catalyzed Diels-Alder cycloaddition between cyclopentadiene 28 and trans-cinnamaldehyde 29 as a benchmark reaction. The yield and the stereochemical outcome of this process, obtained under purely organocatalytic conditions, under dual organophocatalysis, and under bifunctional organophotocatalysis, were compared.

Facile Synthesis of β-Tetracyano Vanadyl Porphyrin from Its Tetrabromo Analogue and Its Excellent Catalytic Activity for Bromination and Epoxidation Reactions.

Complex 2,3,12,13-tetracyano-5,10,15,20-tetraphenylporphyrinatooxidovanadium(IV) {[VIVOTPP(CN)4], 2} has been prepared by nucleophilic substitution of β-bromo groups of the corresponding 2,3,12,13-tetrabromo-5,10,15,20-tetraphenylporphyrinatooxidovanadium(IV) {[VIVOTPP(Br)4], 1} using CuCN in quinoline. Both complexes show biomimetic catalytic activity similar to enzyme haloperoxidases and efficiently brominate various phenol derivatives in the presence of KBr, H2O2, and HClO4 in the aqueous medium. Between these two complexes, 2 exhibits excellent catalytic activity with high turnover frequency (35.5-43.3 s-1) due to the strong electron-withdrawing nature of the cyano groups attached at β-positions and its moderate nonplanar structure as compared to 1 (TOF = 22.1-27.4 s-1). Notably, this is the highest turnover frequency value observed for any porphyrin system. The selective epoxidation of various terminal alkenes using complex 2 has also been carried out, and the results are good, specifying the importance of electron-withdrawing cyano groups. Catalysts 1 and 2 are recyclable, and the catalytic activity proceeds through the corresponding [VVO(OH)TPP(Br)4] and [VVO(OH)TPP(CN)4] intermediates, respectively.

Vanadyl(IV) Porphyrin Dimers with Palladium(II) and Platinum(II) Linkages: Syntheses, Electronic Properties, and Magnetic Interactions between the Two Moieties

We report the synthesis of new vanadyl porphyrins bearing peripheral coordination sites. By using palladium(II) or platinum(II) as connecting ions, porphyrin dimers were isolated and characterized by X-ray crystallography. These paramagnetic species were studied by electronic spectroscopy and continuous wave electron paramagnetic resonance (CW EPR). Large bathochromic shifts were observed by comparing porphyrin monomers and dimers showing that electronic delocalization was present as demonstrated earlier for diamagnetic compounds. Despite the large distance (>14 Å) between the two vanadyl centers in these dimers, small dipolar interactions between the two paramagnetic ions could be determined.

Cellular Zinc Deficiency Impairs Heme Biosynthesis in Developing Erythroid Progenitors.

Anemia is the most prevalent nutrition-related disorder worldwide. Zinc is an essential trace element for various biological processes in the body, and zinc deficiency has been associated with anemia in humans. However, the molecular mechanisms by which zinc availability alters red blood cell development remain uncertain. The present study identifies the essentiality of zinc during erythroid development, particularly for normal heme biosynthesis. G1E-ER4 mouse cells were used as an in vitro model of terminal erythroid differentiation, which featured elevated cellular zinc content by development. Restriction of zinc import compromised the rate of heme and α-globin production and, thus, the hemoglobinization of the erythroid progenitors. Heme is synthesized by the incorporation of iron into protoporphyrin. The lower heme production under zinc restriction was not due to changes in iron but was attributable to less porphyrin synthesis. The requirement of adequate zinc for erythroid heme metabolism was confirmed in another erythropoietic cell model, MEL-DS19. Additionally, we found that a conventional marker of iron deficiency anemia, the ZnPP-to-heme ratio, responded to zinc restriction differently from iron deficiency. Collectively, our findings define zinc as an essential nutrient integral to erythroid heme biosynthesis and, thus, a potential therapeutic target for treating anemia and other erythrocyte-related disorders.

Synthesis of porphyrin and resorcinarene-based porous organic polymers for the superfast adsorption of bisphenol A and cationic herbicides

Porphyrin and resorcinarene-based POPs were synthesized via a post-modification strategy with a superfast removal rate towards bisphenol A and cationic herbicides.