Carboxylic Acid Groups Research Articles

In-Silico Analysis of Polyphenol Compounds in Pomegranate Fruit (Punica granatum L.) Peel Potential as type 2 Antidiabetes Mellitus

Diabetes mellitus is a disease characterized by increased blood sugar levels due to insulin resistance caused by the uncontrolled expression of the protein tyrosine phosphatase 1B (PTP1B). Several compounds that inhibit PTP1B have been studied, including polyphenol. Many studies have been conducted on diabetes medicines based on natural ingredients, including the pomegranate fruits (Punica granatum L). This study aims to test the inhibitory activity of polyphenolic compounds in pomegranate peel (gallic acid, caffeic acid, ellagic acid, chlorogenic acid, apigenin, quercetin, pelargonidin, and cyanidin) against PTP1B through molecular docking. The 3D structures of polyphenolic compounds were obtained from the PubChem database, while PTP1B was from the Protein Data Base. Molecular docking simulations were carried out using AutoDock Vina and several supporting softwares, such as Biovia Discovery Studio Client 4.1, AutoDockTools 1.5.6, PyMOL, and LigPlot. Molecular docking results showed that polyphenolic compounds from pomegranate peel have good inhibitory potential against PTP1B. It is proven by the binding affinity value for PTP1B, which is low and negative, namely in the range -6.4 to -8.4 kcal/mol, and the inhibition constant in the range 0.69 to 20,12 µM. The presence of phenol and carboxylic acid groups in polyphenol compounds can strengthen ligand-protein complexes through hydrogen bonds, especially with the amino acid residues Gln221 and Cys215. The potential of polyphenolic compounds as antidiabetics is also supported by van der Waals interactions and π-π stacking interactions with PTP1B. Based on the molecular docking test that has been carried out, it can be concluded that the polyphenolic compounds in pomegranate peel have the potential to act as type 2 anti-diabetes mellitus.

Bis(pyrazolyl)methane supported cobalt (II) complexes as sensitizers in dye-sensitized solar cells

A series of eight cobalt(II)-based dyes was synthesised using pyrazole and bis(pyrazolyl) methane derivatives. The new dyes were equipped with suitable anchoring functionalities, such as, carboxylic acid or thiocyanate groups, either on the ligand backbone or as a co-ligand to the metal center. All the synthesized compounds were characterized by various spectro-analytical techniques. The HOMO and LUMO energy gap of the dye molecules were determined theoretically by using B3LYP method. The opto-electronic and electrochemical properties of the dyes were analyzed by UV–visible spectroscopy and cyclic voltammetry studies respectively. The photo sensitizing capacity of all the synthesized cobalt-complexes was determined with a help of solar cell constructed using dye-TiO2 coated FTO anode, platinum coated FTO cathode and an iodine based redox mediator. Among the tested compounds, complexes C8 and C9 which contain carboxylic anchoring groups exhibited the best performance.

Resolution of trans-1,2-cyclohexanedicarboxylic acid containing two carboxylic groups by forming diastereomeric salts based on feeding molar ratio control.

To investigate the thermodynamic and molecular self-assembly mechanism of trans-1,2-cyclohexane dicarboxylic acid containing two carboxylic acid groups in the chiral resolution process, (S)-phenylethylamine was used as the chiral resolving agent. Two stoichiometric salts were formed when the raw materials were fed at different molar ratios: cyclohexane dicarboxylate monophenylethylamine salt and cyclohexane dicarboxylate diphenylethylamine salt. When the molar ratio of the (S)-phenylethylamine to trans-1,2-cyclohexane dicarboxylic acid was less than 3:1, trans-(1S,2S)-cyclohexane dicarboxylic acid was obtained with 97 e.e% purity. But when the molar ratio exceeded 3:1, the product was the racemic trans-(1,2)-cyclohexane dicarboxylic acid. In addition, single crystal structures of more soluble mono-salt, less soluble mono-salt, and less soluble di-salt were obtained. The weak intermolecular interactions and the way of the molecules packing in the crystals were analyzed. The hydrogen bond was stronger in the less soluble salt than that in the more soluble salt. And a "lock-and-key" structure in the hydrophobic layers makes it more tightly packed through the van der Waals interaction, which is responsible for the stability of less soluble salts.

Evaluation of Rhodanine Indolinones as AANAT Inhibitors.

Circadian rhythm (CR) dysregulation negatively impacts health and contributes to mental disorders. The role of melatonin, a hormone intricately linked to CR, is still a subject of active study. The enzyme arylalkylamine N-acetyltransferase (AANAT) is responsible for melatonin synthesis, and it is a potential target for disorders that involve abnormally high melatonin levels, such as seasonal affective disorder (SAD). Current AANAT inhibitors suffer from poor cell permeability, selectivity, and/or potency. To address the latter, we have employed an X-ray crystal-based model to guide the modification of a previously described AANAT inhibitor, containing a rhodanine-indolinone core. We made various structural modifications to the core structure, including testing the importance of a carboxylic acid group thought to bind in the CoA site, and we evaluated these changes using MD simulations in conjunction with enzymatic assay data. Additionally, we tested three AANAT inhibitors in a zebrafish locomotion model to determine their effects in vivo. Key discoveries were that potency could be modestly improved by replacing a 5-carbon alkyl chain with rings and that the central rhodanine ring could be replaced by other heterocycles and maintain potency.

A3B type asymmetric metallo phthalocyanines bearing carboxylic acid and tert-butyl groups: Photophysical, photochemical and aggregation properties

In this study, A3B type asymmetric magnesium(II), zinc(II) and indium(III)chloro phthalocyanine derivatives bearing carboxylic acid and tert-butyl groups were synthesized and their photochemical, photophysical and aggregation properties for photodynamic therapy (PDT) application were investigated. In the first part of the study; phthalonitriles, which are the starting materials, were synthesized and then different phthalocyanine compounds were obtained from the synthesized phthalonitriles in the second part. The synthesized compounds were characterized using different techniques. At the same time, the photophysical and photochemical properties of the synthesized compounds were also investigated. The calculated singlet oxygen quantum values in DMSO are 0.30 for MgPc, 0.72 for ZnPc, and 0.62 for InPc in and these values in DMF are 0.25 for MgPc, 0.68 for ZnPc, and 0.60 for InPc after photochemical studies. The obtained results proved that the contribution of the substituents increased the therapeutic efficacy. Finally, our results show that all Pc derivatives have displayed desirable singlet oxygen, photodegradation, fluorescence and aggregation properties for PDT studies.

Study on inherent characteristics of asphalt regenerating agents: Insights from density functional theory calculations and molecular dynamics simulations

The asphalt mixtures containing reclaimed asphalt pavement (RAP) are gradually used in pavement. When the RAP content exceeds 25%, the influence of RAP properties on the performance of the asphalt mixture becomes more pronounced. To address this barrier, the incorporation of regenerating agents is adopted to soften RAP asphalt and ensure the performance of the asphalt mixture. Currently, research on the effect of regenerating agents is rapidly advancing, but there remains limited exploration of their inherent characteristics. This study employs advanced tools such as molecular dynamics (MD) simulations and density functional theory (DFT) to investigate the chemical properties and material attributes of regenerating agents. Fourteen common regenerating agents are selected, which can be classified into eight categories (A∼H) based on their structural features. The results reveal that linear alkanes and cycloalkanes are nonpolar surfaces due to their inherent structural characteristics, resulting in larger fraction free volume (FFV) values within the molecular structure. Considering the molecular weight and intermolecular interactions, these components exhibit a higher diffusion coefficient (D) value. In contrast, aromatics with benzene rings experience enhanced polarity and intermolecular interaction due to conjugated electron pairs forming π-π interactions, leading to reduced FFV values and D values. Moreover, the increase in molecular weight of aromatics significantly reduces both intermolecular interactions and D values. The carboxyl group in fatty acids leads to higher polarity, resulting in stronger intermolecular interactions and lower FFV values and D values. However, after esterification, the properties of fatty acid esters show improvement. Glycerol, with its hydroxyl group having the strongest polarity, exhibits a dense arrangement with the highest density and solubility parameters, which may exceed that of asphalt and may not be suitable as a rejuvenator. The investigation reveals that the polarity of regenerating agents is positively correlated with density, cohesive energy density, and solubility parameters.

Fabrication of carboxylic functionalized poly(methacrylic acid 2-(tert-butylamino)ethyl ester)-coated mesoporous silica nanoparticles and their application for removing ionic dyes from polluted water

The removal of dyes from wastewater that are released during industrial processes has become a significant concern in the environmental science in recent years. To tackle this issue, researchers are exploring the use of nanomaterials for designing new adsorbents. Another promising approach is to grow polymer brushes with high density functional groups via surface-initiated atom transfer radical polymerization (SI-ATRP), which can significantly enhance their ability to absorb dyes. The presence of carboxylic acid groups on the adsorbent material significantly contributes to its efficacy in dye removal by enhancing adsorption capacity, enabling selective adsorption, pH-dependent behavior, chelation, or complexation, and providing stability for repeated usage. In this work, a nanomaterial of carboxylic functionalized poly (methacrylic acid 2-(tert-butylamino)ethyl ester)-coated mesoporous silica nanoparticles (MSNPs–PMATBAE–COOH) was synthesized by the growth of PTBAEMA via surface-initiated atom-transfer radical polymerization, then reacted with succinic anhydride reaction. The chemical structure of MSNPs–PMATBAE–COOH was confirmed using multiple methods, including FT-IR and DLS, and the core-brush morphology was observed clearly using TEM. MSNPs–PMATBAE–COOH were subsequently employed to adsorb hazardous dyes efficiently. The anionic polymer brushes enabled the adsorption of methylene blue (MB) and tetraethylrhodamine (TER) at optimum pH value of 3. The results also indicated that MSNPs–PMATBAE–COOH possessed significant adsorption capacity (263.4 and 212.9 mg g−1 for MB and TER, respectively) and fast adsorption rate (within 15 min), which can be explained by the abundance of adsorptive polymer brushes and the small size of the nanoparticles. Overall, the findings indicate that MSNPs-PMATBAE-COOH is a highly effective adsorbent material for eliminating dye pollutants from wastewater.

PEO-b-PNBA in-situ functionalized mesoporous silica films and their light- and pH-controlled ionic mesopore accessibility

Multistimuli-responsive, in-situ functionalized mesoporous silica films were fabricated by evaporation-induced self-assembly through physical entrapment of the functional template poly(ethylene oxide)-b-poly(2-nitrobenzyl acrylate) (PEO-b-PNBA). The light-cleavable and pH-responsive block copolymer PEO-b-PNBA simultaneously serves as structure-directing agent and for in-situ polymer functionalization of the generated mesopore space. The use of different PEO-b-PNBA compositions results in highly filled hybrid mesoporous silica films with different pore sizes, porosity, and polymer chain sequence within the mesopores. Based on these structural variations and the polymer chain sequence the ionic permselectivity of the silica-polymer hybrid thin films is adjusted. The side chains of the template PNBA block can be deprotected upon irradiation, hereby releasing pH-responsive carboxylic acid groups. The irradiation energy and irradiation time-dependent deprotection allows gradually controlled charge regulation in mesopores. This approach of in-situ functionalization using multistimuli-responsive PEO-b-PNBA block copolymers facilitates the fabrication of multi-responsive hybrid mesoporous silica films and bears high potential for the production of complex, hierarchical, multifunctional mesoporous materials. This fabrication method including direct functionalization of mesoporous structures is of high interest for many applications based on controlled molecular transport in nanoscale pores, such as sensing, separation, or catalysis.

Rapid Determination of Wine Grape Maturity Level from pH, Titratable Acidity, and Sugar Content Using Non-Destructive In Situ Infrared Spectroscopy and Multi-Head Attention Convolutional Neural Networks.

In the pursuit of enhancing the wine production process through the utilization of new technologies in viticulture, this study presents a novel approach for the rapid assessment of wine grape maturity levels using non-destructive, in situ infrared spectroscopy and artificial intelligence techniques. Building upon our previous work focused on estimating sugar content (∘Brix) from the visible and near-infrared (VNIR) and short-wave infrared (SWIR) regions, this research expands its scope to encompass pH and titratable acidity, critical parameters determining the grape maturity degree, and in turn, wine quality, offering a more representative estimation pathway. Data were collected from four grape varieties-Chardonnay, Malagouzia, Sauvignon Blanc, and Syrah-during the 2023 harvest and pre-harvest phenological stages in the vineyards of Ktima Gerovassiliou, northern Greece. A comprehensive spectral library was developed, covering the VNIR-SWIR spectrum (350-2500 nm), with measurements performed in situ. Ground truth data for pH, titratable acidity, and sugar content were obtained using conventional laboratory methods: total soluble solids (TSS) (∘Brix) by refractometry, titratable acidity by titration (expressed as mg tartaric acid per liter of must) and pH by a pH meter, analyzed at different maturation stages in the must samples. The maturity indicators were predicted from the point hyperspectral data by employing machine learning algorithms, including Partial Least Squares regression (PLS), Random Forest regression (RF), Support Vector Regression (SVR), and Convolutional Neural Networks (CNN), in conjunction with various pre-processing techniques. Multi-output models were also considered to simultaneously predict all three indicators to exploit their intercorrelations. A novel multi-input-multi-output CNN model was also proposed, incorporating a multi-head attention mechanism and enabling the identification of the spectral regions it focuses on, and thus having a higher interpretability degree. Our results indicate high accuracy in the estimation of sugar content, pH, and titratable acidity, with the best models yielding mean R2 values of 0.84, 0.76, and 0.79, respectively, across all properties. The multi-output models did not improve the prediction results compared to the best single-output models, and the proposed CNN model was on par with the next best model. The interpretability analysis highlighted that the CNN model focused on spectral regions associated with the presence of sugars (i.e., glucose and fructose) and of the carboxylic acid group. This study underscores the potential of portable spectrometry for real-time, non-destructive assessments of wine grape maturity, thereby providing valuable tools for informed decision making in the wine production industry. By integrating pH and titratable acidity into the analysis, our approach offers a holistic view of grape quality, facilitating more comprehensive and efficient viticultural practices.

Exploring genetic landscape of low-density polyethylene degradation for sustainable troubleshooting of plastic pollution at landfills

Plastic pollution increases globally due to the high volume of its production and inadequate mismanagement, leading to dumps in landfills affecting terrestrial and aquatic ecosystems. Landfills, as sink for plastics, leach various toxic chemicals and microplastics into the environment. We scrutinized the genetic expression for low-density polyethylene (LDPE) degradation via microorganisms to investigate cell viability and metabolic activities for biodegradation and genetic profiling. Samples were collected from the Pirana waste landfill at Ahmedabad, Gujarat, which is one of the largest and oldest municipal solid waste (MSW) dump sites in Asia. Results analyzed that isolated bacterial culture PN(A)1 (Bacillus cereus) is metabolically active on LDPE as carbon source during starvation conditions when incubated for up to 60 days, which was confirmed via 2,3,5-triphenyl-tetrazolium chloride (TTC) reduction test, reported cell viability and LDPE degradation. Abrasions, surface erosions, and cavity formations were analyzed via scanning electron microscopy (SEM), whereas the breakdown of high molecular polymers converted to low molecules, i.e., depolymerization, was also observed via Fourier-transform infrared (FTIR) spectroscopy over 90 days, along with changes in functional groups of carboxylic acids and aldehyde as well as the formation of polysulfide, aliphatic compounds, aromatic ethers, alcohols, and ether linkages. Further, transcriptomic analysis was performed via DESeq2 analysis to understand key gene expression patterns and pathways involved in LDPE degradation. During the initial phase of LDPE degradation, genes related to biological processes, like membrane transportation, ABC transporters, carbon and lipid metabolism, fatty acid degradation/oxidation, and TCA cycle, are likely to indicate pathways for stress response and molecular functions, like oxidoreductase, catalytic, lyase, transferase, and hydrolase activities were expressed. Interlinking between metabolic pathways indicates biodegradation process that mineralizes LDPE during subsequent incubation days. These pathways can be targeted for increasing the efficiency of LDPE degradation using microbes in future studies. Thus, considering microbial-mediated biodegradation as practical, eco-friendly, and low-cost alternatives, healthy biomes can degrade polymers in natural environments explored by understanding the genetic and enzymatic expression, connecting their role in the process to the likely metabolic pathways involved, thereby increasing the rate of their biodegradation.

Retention of Intrinsic Photophysical Properties of Porphyrin Building Blocks in 3D Organic Frameworks through Magic Angle Alignment.

Construction of three-dimensional (3D) frameworks maintaining intrinsic photophysical properties of monomeric building blocks is difficult and challenging due to the existence of various molecular interactions, such as metal-organic and π-π interactions. A 3D hydrogen-bonded organic framework (YSH-1Zn) with permanent porosity was constructed using a porphyrin having six carboxylic acid groups (1Zn). Brunauer-Emmett-Teller surface area measurement indicated that YSH-1Zn has a porous structure with a surface area of 392 m2/g. Single-crystal X-ray diffraction analysis revealed that 1Zn creates a 5-fold interwoven 3D network structure adopting a monoclinic system with a space group of P21/c. Each 1Zn within a single crystal exhibits parallel alignment with a slip-stack angle of 54.6°, in good agreement with the magic angle. Although the center-to-center distance of the nearest zinc atoms in YSH-1Zn is only 5.181 Å, the UV/vis absorption and fluorescence emission of YSH-1Zn are not different from those of 1Zn, indicating the absence of an interaction between excitons. Due to the magic angle alignment of 1Zn, the fluorescence lifetime, decay profiles, and quantum yield remained uniform even in the solid state.

Regenerable planting of multifunctional amine: Regeneration-enhanced antifouling/antiscaling properties and performance of thin film composite nanofiltration membrane

The problems of poly(piperazineamide)-based thin film composite (TFC) nanofiltration (NF) membrane are the fouling, scaling and poor separation performance of uncharged organics and heavy metal ions. Permanent surface modification lowers the fouling/scaling problems. However, these problems persist as the separation progresses. We address these issues by the on-demand regenerable planting of polyethyleneimine (PEI) into the polyamide (PA) layer of TFC NF membrane. The regenerable planting is based on the electrostatic interaction among the protonated amine groups of low molecular weight PEI and ionized carboxylic acid groups situated at the relatively inner sites (low dielectric constant) of the PA network. The incorporated PEI chains are stable at the pH range of 3–9. The PEI incorporated membrane exhibits significantly enhanced antifouling/antiscaling property, rejection of heavy metal ions (98–99%) and bisphenol A (BPA, 95%) without much negatively affecting the bivalent anion rejection (Na2SO4, 97.5%) and water permeance (11 L m−2 h−1 bar−1) as compared to the pristine and commercial membranes (55–82%, 50–76% and 98–99% rejections of heavy metal ions, BPA and Na2SO4). Advantageously, PEI chains are removable at pH ≤ 2 or pH ≥ 9.5 without affecting the main PA layer. The multiple removal and re-generation of the membrane have been achieved. The flux recovery of the membrane after antifouling/antiscaling tests significantly improved upon intentional removal and reincorporation of PEI. Inherent properties of the modified membrane channels couple with the on-demand regenerable ability show immense promises of the membrane in the separation applications.

New insights from poly-lactic acid and ionomer films coupled with recombinant antibodies for processing sexed-sorting bovine sperm

In this study, the efficacy of ionomers and poly-lactic acid (PLA) as an alternative solid material combined with scFv antibodies specific to bovine Y-sperm (Y-scFv) was studied to create a novel method of sexing technology. The coupling efficiency of Y-scFv to the surface of PLA, Na+ and Zn2+ ionomer film was between 2 and 8 mg/mL. Fourier transform infrared spectra confirm that Y-scFv was bound with a carboxylic acid group in each film. Therefore, Na+, Zn2+ ionomers and PLA films conjugated with 4 and 8 mg/mL Y-scFv showed the highest concentration of Y-sperm in the eluted fraction. Considering that the elute fraction was enriched Y-sperm fraction, it contained 67.70–77.94 % of the Y-sperm ratio related to the produced supernatant fraction, which contained up to 69.31–76.01 % enriched X-sperm. In addition, the sperm quality after the sexing process was analyzed by CASA and imaging flow cytometry, which showed that each polymer did not have a negative effect on sperm motility and acrosome integrity for X-sperm. The capacity of ionomer and PLA combined with Y-scFv are used for bovine sperm sexing.

The Synergistic Effect of Phosphonic and Carboxyl Acid Groups for Efficient and Stable Perovskite Solar Cells

Reducing the interfacial defects between the perovskite/electron transport layer (ETL) is the key point to improving the efficient and stable performance of perovskite solar cells (PSCs). In this study, two self-assembled molecules ((aminomethyl)phosphonic acid and glycine) with different functional groups (phosphonic acid (-H2PO3) and carboxylic acid (-COOH)) were mixed to form the buried bottom interface of PSCs. The synergistic effect of -H2PO3 with its higher anchoring ability and -COOH with its fast carrier transport improved the performance of PSCs. Additionally, the SnO2 modified by mixed self-assembly molecules (M-SAM) showed a more appropriate energy level alignment, favoring charge transport and minimizing energy loss. In addition, the amine group (-NH2) on the two small molecules effectively interacted with uncoordinated Pb2+ in perovskite and improved the quality of the perovskite films. Consequently, the (FAPbI3)0.992(MAPbBr3)0.008 PSCs with M-SAM reached a PCE of 24.69% (0.08 cm2) and the perovskite modules achieved a champion efficiency of 18.57% (12.25 cm2 aperture area). Meanwhile, it still maintained more than 91% of its initial PCE after being placed in nitrogen atmosphere at 25 °C for 1500 h, which is better than that of the single-SAM and control devices. Further reference is provided for the future commercialization of perovskite with efficient and stable characteristics.

N,O‐Codoped Onion‐like Carbon Catalyzed Selective Oxidation of Methanol to Dimethoxymethane: Structure‐Activity Relationship

AbstractOne‐step synthesis of dimethoxymethane (DMM) via methanol oxidation under the catalysis of nanocarbon is a green and sustainable chemical industrial process. In this work, nitrogen, oxygen codoped onion‐like carbon (NOLC) were prepared via a simple thermal treatment method, which was applied to one‐step synthesis of DMM. The physicochemical characterization results revealed that nitrogen and oxygen elements were successfully introduced into the onion‐like carbon (OLC) catalyst. The proposed NOLC catalysts exhibited DMM selectivity of 75 % at relatively low reaction temperature (150 °C) and long stability over 10 h. In‐situ titration experiments revealed that the carboxylic acid groups on NOLC surface were the main acidic active sites. The Clemmensen reduction control experiment revealed that the carbonyl groups were the active sites for the formation of formaldehyde. The basic reaction kinetics and mechanism such as reaction orders, apparent activation energy and rate determining step etc. for one‐step synthesis of DMM via methanol were studied systematically. The present work shows an important structure‐function relation for designing highly efficient nanocarbon catalyzed methanol conversion reaction system that the appropriate redox/acid intensity on catalyst surface through the modulation of N and O elements would effectively improve the selectivity of DMM.

Design of Cell-Adhesive Shellac Derivatives and Endowment of Photoswitchable Cell-Adhesion Properties.

The emergence of new biodegradable cell-adhesion materials is an attractive topic in biomaterial chemistry, particularly for the development of cell incubation scaffolds and drug encapsulation materials used in in situ regenerative therapy. Shellac is a natural resin with unique film-forming properties and high miscibility with various chemicals, in addition to being biodegradable and nontoxic to biological systems. However, since native shellac does not adhere to mammalian cells, there have been no reports of using shellac to develop cell-adhesive biomaterials. In this study, we report on the development of cell-adhesive shellac derivatives through slight chemical modification. Shellac is a mixture of oligoesters that consists of hydroxyl fatty acids and resin acids, and therefore, all oligomers have one carboxylic acid group at the terminal. We discovered that a simple modification of hydrophobic chemical groups, particularly those containing aromatic groups in the ester form, could dramatically improve cell-adhesion properties for mammalian cells. Furthermore, by using photocleavable esters containing aromatic groups, we successfully endowed photoswitchable properties in cell adhesion. Given that shellac is a low-cost, biodegradable, and nontoxic natural resin, the modified shellacs have the potential to become new and attractive biomaterials applicable to in situ regenerative therapy.

Cationic amino-acid functionalized polymethacrylamide vectors for siRNA transfection based on modification of poly(2-isopropenyl-2-oxazoline)

Poly(2-isopropenyl-2-oxazoline) (PiPOx) is a functional polymer showing great potential for the development of smart biomaterials. The straightforward synthesis and post-polymerization functionalization of PiPOx offers many opportunities for tailoring the properties of the polymer towards biomaterials. In this study we report for the first time PiPOx-based cationic charged polymethacrylamides with amino acid side chains that can complex siRNA and promote transfection in vitro. Therefore, PiPOx was fully modified via ring opening addition reactions with the carboxylic acid groups of a series of N-Boc-L-amino acids and their reaction kinetics were investigated. Based on the determined kinetic constants, another series of PiPOx-based copolymers with balanced hydrophilic/hydrophobic content of N-Boc-L-amino acids were obtained via one-pot modification reaction with two different N-Boc-L-amino acids. The N-Boc protected homopolymers and related copolymers were deprotected to obtain (co)polymers with the targeted side chain cationic charged units. The (co)polymers' structures were fully investigated via FT-IR and 1H NMR spectroscopy, size exclusion chromatography (SEC), and TGA–DSC–MS analysis. The polarimetry measurements revealed that the homopolymers retain their chiroptical properties after post-modification, and a sign inversion is noticed from (L) N-Boc-protected analogues to (D) for the TFA cationic charged homopolymers. Generally, cationically charged homopolymers with hydrophilic amino acids on the side chain showed efficient complexation of siRNA, but poor transfection while cationic copolymers having both tryptophan and valine or proline side chains revealed moderate siRNA binding, high transfection efficiency (> 90% of the cells) and potent gene silencing with IC50 values down to 5.5 nM. Particularly, these cationic copolymers showed higher gene silencing potency as compared to the commercial JetPRIME® reference, without reducing cell viability in the concentration range used for transfection, making this a very interesting system for in vitro siRNA transfection.

Functional-Group-Tolerant Pd-Catalyzed Carbonylative Negishi Coupling with Aryl Iodides.

A chemoselective Pd-mediated carbonylative Negishi-type catalytic protocol for the synthesis of (hetero)aryl ketones is reported. The protocol employs the PEPPSI-IPr precatalyst and CO gas at atmospheric pressure (balloon) to foster the carbonylative coupling between diverse C(sp3)-hybridized organozinc reagents and a broad range of aryl iodides, including substrates carrying aldehyde, aniline, phenol, or carboxylic acid groups, and heteroaryls.

Versatile Surface Chemistry of Carbon-Based Nanoplatforms by Covalent Bonding, Non-Covalent Linking, Crosslinking, and Self-Assembling

This mini-review discussed the best-known chemical and synthetic methodologies used in the last years to modify carbon allotropes, with an interest in nanotechnology. In this perspective, chemistry with optoelectronics applications and recent trends within bio-applications focusing mainly on graphene and its derivatives were considered. So, the mini-review intended to focus on methodologies to add functional groups with varied reactivities, polymer chemistry, and nanoscale control. These methodologies provide insight for further developments. In this manner, traditional methods using strong acid media to convert simple carbon bonds into carboxylic acid and aldehydes organic functional groups were shown and discussed. Hence, chemical modifications in a variety of solvents could be developed. Notably, many organic chemical reactions, such as bimolecular nucleophilic substitution (SN2), click chemistry, and photochemical reactions, showed essential insights in designing the carbon-based material modifications and the bottom-up method. Moreover, incorporating atomic entities within graphene material defects led to interesting spectroscopic and quantum properties. The atomic change added blemishes to this homogeneous structure, which was tuned to modify optical properties. In addition, the review was also oriented towards the discussion on incorporating polymeric films, such as boron- and silicon-based monomers, to form polymeric-modified carbon-based slides. In this way, organoboranes and organosilanes permitted chemical functionalization because their chemical modification was more accessible on nanosurfaces. Moreover, emphasis was placed on exploiting non-covalent bonding with ions and polarized molecules with the highly electronic densities of graphene and its derivatives. In this manner, the manuscript intends to summarize the main types of reactions and synthetic pathways reported until today. Therefore, particular focus was given to chemical composition, 2D and 3D chemical structures, and their properties related to non-covalent interactions. Thus, based on the properties and reactivity of carbon allotropes, the review was intended to open the analysis and discussion, considering the design of new carbon-based materials, hybrid nanocomposites, and metamaterials.

Interfacial Behaviors of Giant Amphiphilic Molecules Composed of Hydrophobic Isobutyl POSS and Hydrophilic POSS Bearing Carboxylic Acid Groups at the Air-Water Interface.

The behavior of giant amphiphilic molecules at the air-water interface has become a subject of concern to researchers. Small changes in the molecular structure can cause obvious differences in the molecular arrangement and interfacial properties of the monolayer. In this study, we have systematically investigated the interfacial behaviors of the giant amphiphilic molecules with different number of hydrophobic BPOSS blocks and one hydrophilic ACPOSS block ((BPOSS)n-ACPOSS (n = 1-5)) at the air-water interface by the surface pressure-area (π-A) isotherm, Brewster angle microscopy (BAM), compression modulus measurement, and hysteresis measurement. We found that both the number of BPOSS blocks and the compression rate can significantly influence the interfacial behaviors of giant molecules. The π-A isotherms of giant molecules (BPOSS)n-ACPOSS (n = 2-5) exhibit a "cusp" phenomenon which can be attributed to the transition from monolayer to multilayer. However, the cusp is dramatically different from the "collapse" of the monolayer studied in other molecular systems, which is highly dependent on the compression rate of the monolayer. In addition, the compression modulus and hysteresis measurements reveal that the number of BPOSS blocks of (BPOSS)n-ACPOSS plays an important role in the static elasticity, stability, and reversibility of the Langmuir films.