Crosslinked bis(triphenylphosphine)iminium chlorides are recyclable catalysts for small molecule CO 2 and CO insertions and polymerisations.

Oral squamous cell carcinoma (OSCC) is a major health concern in high-risk regions globally, with rising mortality rates indicating the urgent need for early detection tools. This study presents an innovative point-of-care (POC) diagnostic tool using disposable microelectrodes to detect cholic acid, a crucial OSCC biomarker, in human saliva. By combining a poly(methacrylic acid-co-acrylamide) copolymer (CoP) with polythiophene (PTh) nanofibers as selective coatings for disposable, screen-printed carbon electrodes (SPCE), the developed CoP-PTh/SPCE sensors demonstrate exceptional performance. Using impedance spectroscopy and voltammetric techniques, the electrochemical oxidation of cholic acid in solution and saliva samples is investigated. The CoP-PTh/SPCE sensors exhibit an outstanding sensitivity of 1.05µAcm-2nm-1 (74.2µA µm-1), a detection limit (LOD) of 0.240nm, and a quantification limit (LOQ) of 0.727nm, demonstrating their superior capabilities. Additionally, these sensors exhibit remarkable selectivity against structurally similar compounds such as cholesterol and various salivary analytes. The practical application of CoP-PTh/SPCE sensors is realized through a 97.67±1.08% recovery of spiked cholic acid concentrations in human saliva samples. This study highlights the potential of CoP-PTh/SPCE sensors for reliable, efficient, and non-invasive POC testing, offering a promising solution for the early diagnosis of poorly differentiated OSCC.

This study investigates the development of bio-based polymers derived from plantain peels (Musa paradisiaca L.) (PPB) and arrowroot peels (Maranta arundinacea) (APB), as well as their copolymers (COP), as sustainable alternatives to non-degradable synthetic polymers. Biodegradable polymers offer unique physical, chemical, biological, biomechanical, and degradative properties, making them highly relevant for environmentally friendly applications. In this work, PPB, APB, and COP were synthesized and characterized through physico- chemical analysis, including moisture content determination, soil burial degradability tests, and various instrumental techniques: X-ray Diffraction (XRD), Fourier Transform Infrared (FTIR), Scanning Electron Microscopy (SEM) and Thermogravimetric Analysis (TGA). By varying glycerol content across samples (20, 15, 10, and 5 cm³), a reduction in moisture content was observed, with values ranging from 35.70% to 20.13%. A 30-day soil burial test revealed significant weight loss for PPB (100%), with moderate degradation for APB (2.17%) and COP (1.51%). XRD analysis indicated an amorphous phase across all samples, while FTIR spectra confirmed characteristic functional groups (OH, C-H, C=O, C=C, -CH3, and C-O) consistent with successful polymer formation. TGA results showed that thermal stability decreased with glycerol content in the order of APB > PPB > COP. SEM images of samples with 5 cm³ glycerol displayed voids and cracks in APB and PPB, whereas COP exhibited a smoother and more uniform surface, depicting enhanced interfacial interaction and compatibility. These findings demonstrate that bio-copolymers COP offer increased moisture absorption and superior surface characteristics and also enhance biodegradability, making it promising candidate for eco-friendly applications in industries where sustainable and degradable materials are required.

A green and efficient strategy for synthesizing bio-based polyfurans with mechanical properties and nonconventional fluorescence from CO2 and 5-hydroxymethylfurfural derivatives.

Ureate anions rapidly polymerize CO 2 -derived lactones to high molar mass polyesters. A key carboxylic acid impurity from the lactone synthesis inhibits polymerization, highlighting the need for rigorous purification to achieve fast catalysis.

Efficient electrochemical Li+ adsorption holds significant promise for lithium extraction, while the mismatched rate between Li+ diffusion and electron transport within the electrode material impedes the electrochemical activity and restricts the adsorption efficiency. To address this challenge, herein, we rationally design and integrate the ion and electron dual-conducting poly(vinyl alcohol)-polyaniline (PVA-PANI) copolymer (CP) within the H1.6Mn1.6O4 (HMO) electrode matrix to facilitate Li+ diffusion and electron transport. The Li+ diffusion coefficient (DLi+) increased from 3.03 × 10-10 to 5.92 × 10-10 cm2/s, while the charge transfer resistance (Rct) decreased from 53.73 to 29.57 ohm. Consequently, the HMO@CP electrode exhibits superior adsorption kinetics and a state-of-the-art high adsorption capacity of up to 49.48 mg/g. Comprehensive mechanistic studies reveal that the negatively charged hydroxyl groups (-OH) in PVA accelerate Li+ diffusion and that the conjugated structure and redox-active quinoid sites in PANI offer denser electron distribution and promote electron transport. This synergistic effect in CP significantly enhanced Li+ diffusion and electron transport, leading to electrochemical activity and adsorption efficiency. Our work highlights the critical role of simultaneously regulating the ion diffusion and electron transport dual pathways for optimizing Li+ adsorption performance and inspires development of the next generation electrochemical adsorption electrodes.

Abstract CO2 is an abundant C1 resource but a green‐house gas and chemically inert. Thus, its utilization has been a promising but challenging project. Herein, we report the unprecedented polymerization of CO2 and C6H4(SiMe2H)2 using B(C6F5)3 alone under mild conditions to give poly(silphenylene siloxane) accompanied by releasing CH4. The copolymerization can be extended to comonomers of phenylene silanes bearing functional groups. Moreover, it combines with Piers‐Rubinsztajn reaction to establish a tandem polymerization system to achieve super thermal resistant poly(siloxane‐co‐silphenylene siloxane)s. Density functional theory reveals that B(C6F5)3 is activated by silanes to form free HB(C6F5)2, which is the true active species for CO2 reducing to borylformate, the rate controlling step of the polymerization procedure. The subsequent multiple reductions of borylformate to CH4 and the step‐growth to poly(silphenylene siloxane)s can be fulfilled by both B(C6F5)3 and HB(C6F5)2, and the former shows a slightly higher activity. This work opens a new avenue of utilizing CO2 to fabricate polysiloxanes that is unable to access using current manners.

Development and validation study of compact biophotonic platform for detection of serum biomarkers

Conducting co-polymer derived N, S co-doped metal-free hierarchical nanoporous carbon for robust electrochemical capacitor

To formulate and characterize the chemical structure of a new dental composite with photodimerized cinnamyl methacrylate (PD-CMA) photo-crosslinking comonomer and to evaluate the monomer-to-polymer conversion (MPC) and glass transition temperature (Tg) of the new composite copolymers. CMA was PD by ultraviolet C-type (UVC) irradiation. The research groups were a control group C0 without PD-CMA and two trial groups: E10 (10 wt. % PD-CMA substituted in the base comonomers (B) and diluent (D) mixture); E20 (20 wt.% PD-CMA completely replacing the diluent (D) monomer). Infrared (FTIR) and nuclear magnetic resonance (NMR) spectroscopies were employed for ascertaining copolymerization (CP). The surface features and composition of the copolymers were explained by field-emission scanning electron microscopy (FESEM) and energy dispersive X-ray (EDX) spectroscopy, respectively. The MPC and Tg of the copolymers were assessed using FTIR and differential scanning calorimetry, respectively. Statistical tests were used to compare the groups. The configuration of the new copolymers P (BD-Co-CMA) and P(B-Co-CMA) was confirmed. The MPC% and T g of the copolymers were better than the control. PD-CMA at 20 wt. % in the P (B-Co-CMA) copolymer exhibited the highest MPC% and Tg. The incorporation of PD-CMA in the composite resin resulted in new P (BD-Co-CMA) and P (B-Co-CMA) copolymers with improved MPC% and Tg. The substitution with PD-CMA offset the shortcomings of the conventional BD comonomers concerning the mechanical properties and biocompatibility of the restorative composite resin. This might ameliorate the restorations in vivo longevity and serviceability.

Abstract The transition from lithium‐based energy storage to post lithium systems plays a crucial part in achieving an environmentally sustainable energy infrastructure. Prime candidates for the replacement of lithium are sodium and potassium batteries. Despite being critical to battery performance, the solid electrolyte interphase (SEI) formation process for Na and K batteries remains insufficiently understood, especially compared to the well‐established lithium systems. Using ab initio molecular dynamics (AIMD) simulations based on density functional theory (DFT) calculations, we study the first steps of SEI formation upon the decomposition of typical solvent molecules on lithium, sodium and potassium metal anodes. We find that two dominant products form during the early SEI formation of cyclical carbonates on alkali metal anodes, carbon monoxide and alkali‐carbonate. The carbonate‐producing reaction is thermodynamically favorable for all tested metals, however, Na and K exhibit a much stronger selectivity than Li towards carbonate formation. Furthermore, we propose a previously unknown reaction mechanism for the CO polymerization on metallic lithium.

Chloroform (CF) is a widely used chemical reagent and disinfectant and a probable human carcinogen. The extensive literature on halocarbon reduction with zerovalent iron (ZVI) shows that transformation of CF is slow, even with nano, bimetallic, sulfidated, and other modified forms of ZVI. In this study, an alternative method of ZVI modification─involving simultaneous sulfidation and nitridation through mechanochemical ball milling─was developed and shown to give improved degradation of CF (i.e., higher degradation rate and inhibited H2 evolution reaction). The composite material (denoted as S-N(C)-ZVI) gave synergistic effects of nitridation and sulfidation on CF degradation. A complete chemical reaction network (CRN) analysis of CF degradation suggests that O-nucleophile-mediated transformation pathways may be the main route for the formation of the terminal nonchlorinated products (formate, CO, and glycolic polymers) that have been used to explain the undetected products needed for mass balance. Material characterizations of the ZVI recovered after batch experiments showed that sulfidation and nitridation promoted the formation of Fe3O4 on the S-N(C)-ZVI particles, and the effect of aging on CF degradation rates was minor for S-N(C)-ZVI. The synergistic benefits of sulfidation and nitridation on CF degradation were also observed in experiments performed with groundwater.

Alzheimer's disease (AD) is a major neurodegenerative disorder primarily characterized by the β-amyloid (Aβ42) misfolding and aggregation-associated multifaceted amyloid toxicity encompassing oxidative stress, neuronal death, and severe cognitive impairment. Modulation of Aβ42 aggregation via various structurally anisotropic macromolecular systems is considered effective in protecting neuronal cells. In this regard, we have developed a cyclic dipeptide (CDP)-based copolymer (CP) and explored its material and biomedical properties. Owing to the structural versatility, CDP-CP forms solvent-dependent anisotropic architectures ranging from dense fibers and mesosheets to vesicles, which are shown to interact with dyes and nanoparticles and mimic synthetic protocells, providing a conceptually new approach to achieve advanced functional materials with the hierarchical organization. CP upon interaction with gold nanoparticles (GNP) and polyoxometalate (POM) generated faceted architectures (CP-GNP) and the nanocomposite (CP-POM), respectively. CP-GNP and CP-POM have shown remarkable ability to inhibit Aβ42 aggregation, dissolve the preformed aggregates, and scavenge reactive oxygen species (ROS) to ameliorate multifaceted amyloid toxicity. In cellulo studies show that CP-GNP and CP-POM protect neuronal cells from Aβ42-induced toxicity and reduce lipopolysaccharide (LPS)-activated neuroinflammation at sub-micromolar concentration. To our knowledge, this is the first report on the hierarchical organization of CDP-CP into 1D-to-2D architectures and their organic-inorganic hybrid nanocomposites to combat the multifaceted amyloid toxicity.

Structurally stable and surface-textured polylactic acid/copolymer/poly (ε-caprolactone) blend-based electrospun constructs with tunable hydroxyapatite responsiveness

Anode Catalytic Dependency Behavior on Ionomer Content in Direct CO Polymer Electrolyte Membrane Fuel Cell

Polymerization of CO₄ groups in carbonates

To formulate, design, and chemically characterize a novel denture base resin (DBR) copolymer containing triazine-based antimicrobial comonomer and also to evaluate the double bond conversion (DC) in the copolymer with various concentrations of the comonomer by fourier transform infrared (FTIR) spectroscopy. The study groups comprise a control group G0 in which the specimens (n = 10) were polymerized without the triazine comonomer and trial groups G10 and G20 where the polymerized specimens (n = 10 each) contained 10 and 20% triazine comonomer, respectively. FTIR was employed to ascertain and evaluate copolymerization (CP) and DC. The obtained DC values were subjected to statistical analysis. A new denture base copolymer containing antimicrobial triazine comonomer was formed with ascertained copolymerization and higher DC than the control group. Twenty percent triazine comonomer in the copolymer exhibited the maximum DC. Incorporation of the antimicrobial comonomer copolymerized with DBR to form a novel denture base copolymer exhibiting high DC. The novel denture base copolymer may prevent the microbial adhesion on the denture surface thereby preventing denture-induced stomatitis in the edentulous patients. Nonetheless, this novel copolymer may enhance the other necessary properties of the DBR and would ameliorate the living quality of the senile geriatric population with good in vivo serviceability.

Abstract The four‐electron oxidation of water (2H2O→O2+4H++4e−) is critical for artificial photosynthesis. In nature, this reaction is efficiently catalyzed by photosystem II via cooperative catalytic centers and charge transporters. However, the integration of water oxidation catalysts and charge transporters in artificial systems remains challenging. In this report, a function‐integrated water oxidation catalyst produced by the electrochemical polymerization of a cobalt phthalocyanine complex bearing carbazole moieties is described. The monomer complex, Co(czPc) (H2czPc=tetrakis(9H‐carbazole‐9‐ethoxy)phthalocyanine), was synthesized and characterized by elemental analysis, matrix‐assisted laser desorption/ionization mass spectrometry, and Fourier transform infrared and ultraviolet‐visible spectroscopy measurements. The electrochemical polymerization of Co(czPc) was confirmed using cyclic voltammetry measurements and yielded poly‐Co(czPc) on the surface of a glassy carbon electrode. Poly‐Co(czPc) showed excellent charge‐transport ability and superior electrocatalytic water oxidation performance to that of the corresponding nonpolymeric system.

Ga and Ti co-doped In2O3 films for flexible amorphous transparent conducting oxides

A novel family of inorganic-organic-hybrid SeFe3(CO)9-dipyridyl two- and one-dimensional Cu polymers was synthesized via the three-component liquid-assisted grinding (LAG) of [Cu(MeCN)4]+, inorganic cluster [SeFe3(CO)9]2- (1), and rigid conjugated dipyridyls 4,4'-dipyridyl (dpy) and 1,2-bis(4-pyridyl)ethylene (bpee) or flexible conjugation-interrupted dipyridyls 1,2-bis(4-pyridyl)ethane (bpea) and 1,3-bis(4-pyridyl)propane (bpp). They included a cluster-linked 2D polymer, [(μ4-Se)Fe3(CO)9Cu2(MeCN)(dpy)1.5]n (1-dpy-2D), a cluster-pendant 1D chain, [(μ3-Se)Fe3(CO)9Cu2(dpy)3]n (1-dpy-1D), cluster-blocked 1D polymers, [(μ3-Se)Fe3(CO)9Cu2(L)]n (1-L-1D, L = bpee, bpea), and a cluster-linked 2D polymer, [(μ4-Se)Fe3(CO)9Cu2(bpp)2]n (1-bpp-2D). The reversible dimensionality transformations of these three types of polymers accompanied by the change in coordination modes of 1 were achieved by the LAG addition of 1/[Cu(MeCN)4]+ or dipyridyl ligands. These polymers were found to possess tunable low-energy gaps (1.49-1.72 eV) that increased in the order regarding their structural features: cluster-linked 1-dpy-2D and 1-bpp-2D, cluster-blocked 1-bpea-1D and 1-bpee-1D, and cluster-pendant 1-dpy-1D and [(μ3-Se)Fe3(CO)9Cu2(L)2.5]n (L = bpee, 1-bpee-2D; bpea, 1-bpea-2D), indicative of the importance of the participation of cluster 1. The measured electrical conductivities of 1-bpp-2D, 1-bpea-1D, and 1-dpy-1D were 3.13 × 10-7, 2.92 × 10-7, and 2.30 × 10-7 S·cm-1, respectively, which were parallel for the trend in their energy gaps, revealing semiconducting behaviors, supported by XPS, XANES, and DFT calculations. The surprising semiconductivity of the conjugation-interrupted bpp-linked 1-bpp-2D was mainly ascribed to electron transport via C-H···O(carbonyl) hydrogen bonds and aromatic C-H···π contacts within its closely packed 2D layers. Water-/light-stable polymers 1-bpp-2D, 1-bpea-2D, and 1-dpy-1D were also demonstrated to exhibit excellent pseudo-first-order photodegradation toward nitroaromatics and organic dyes, where cluster-linked polymer 1-bpp-2D performed the best, as predicted by its structural features and narrow energy gap.