Solvent- and Substrate-Induced Chiroptical Inversion in Amphiphilic,Biocompatible Glycoconjugate Supramolecules: Shape-Persistent Gelation,Self-Healing,and Antibacterial Activity

We have shown solvent- and substrate-dependent chiral inversion of a few glycoconjugate supramolecules. (Z)-F-Gluco, in which d -glucosamine has been attached chemically to Cbz-protected l -phenylalanine at the C terminus, forms a self-healing hydrogel through intertwining of the nanofibers wherein the gelators undergo lamellar packing in the β-sheet secondary structures with a single chiral handedness. Dihybrid (Z)-F-gluco nanocomposite gel was prepared by in-situ formation of silver nanoparticles AgNPs in the gel; this enhances the mechanical properties of the composite gel through physical crosslinking without altering the packing pattern. In contrast, (Z)-L-gluco bearing an l -leucine moiety does not form a hydrogel but an organogel. Interestingly, the chiral handedness of the aggregates of (Z)-L-gluco can be reversed by choosing suitable solvents. In addition to self-healing behavior, (Z)-L-gluco gel revealed shape persistency. Further, (Z)-F-gluco hydrogel is benign, nontoxic, non-immunogenic, and non-allergenic in animal cells. AgNP-loaded (Z)-F-gluco hydrogel showed antibacterial activity against both Gram-positive and Gram-negative bacteria.     

Synthesis and Characterization of New Phosphorus Containing Sulfonated Polytriazoles for Proton Exchange Membrane Application

Sulfonated polytriazoles have drawn a great attention as high performance polymers and their good film forming ability. In the present study, a phosphorus containing new diazide monomer namely, bis-[4-(4′-aminophenoxy)phenyl]phenylphosphine was synthesized and accordingly, a series of phosphorus containing sulfonated polytriazoles (PTPBSH-XX) was synthesized by reacting equimolar amount of this diazide monomer (PAZ) in combination with another sulfonated diazide monomer (DSAZ) and a terminal bis-alkyne (BPALK) by the Cu (I) catalyzed azide–alkyne click polymerization. The polymers were characterized by nuclear magnetic resonance (¹H, ¹³C, ³¹P NMR) and Fourier transform infrared spectroscopic techniques. The sulfonic acid content of the copolymers also determined from the different integral values obtained from the ¹H NMR signals. The small-angle X-ray scattering results unfolded the well-separated dispersion of the hydrophilic and hydrophobic domains of the polymers. As a whole, the copolymer membranes displayed sufficient thermal, mechanical, and oxidative stabilities high with high proton conductivity and low water uptake that are essential for proton exchange membrane applications. The copolymers exhibited oxidative stability in the range of 15–24 h and had proton conductivity values were found as high as 38–110 mS cm⁻¹ at 80 °C in completely hydrated condition. Among the all copolytriazoles, PTPBSH-90 (BPALK:DSAZ:PAZ = 100:90:10) having IEC_W = 2.44 mequiv g⁻¹, showed proton conductivity as high as 119 mS cm⁻¹ at 90 °C with an activation energy of 10.40 kJ mol⁻¹ for the proton conduction. © 2020 Wiley Periodicals, Inc. J. Polym. Sci. 2020 , 58, 263–279     

Boron-Containing Lipids and Liposomes: New Conjugates of Cholesterol with Polyhedral Boron Hydrides

A series of boron-containing lipids were prepared by reactions of cyclic oxonium derivatives of polyhedron boranes and metallacarboranes (closo-dodecaborate anion, cobalt and iron bis(dicarbollides)) with amine and carboxylic acids which are derived from cholesterol. Stable liposomal formulations, on the basis of synthesized boron-containing lipids, hydrogenated soybean l -α-phosphatidylcholine and (HSPC) 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[methoxy(polyethylene glycol)-2000] (DSPE-PEG) as excipients, were prepared and then characterized by dynamic light scattering (DLS) that revealed the formation of particles to be smaller than 200 nm in diameter. The resulting liposomal formulations showed moderate to excellent loading and entrapment efficiency, thus justifying the design of the compounds to fit in the lipid bilayer and ensuring ease of in vivo use for future application. The liposomal formulations based on cobalt and iron bis(dicarbollide)-based lipids were found to be nontoxic against both human breast normal epithelial cells MCF-10A and human breast cancer cells MCF-7.     

From CO2 activation to catalytic reduction: a metal-free approach

Over exploitation of natural resources and human activities are relentlessly fueling the emission of CO₂ in the atmosphere. Accordingly, continuous efforts are required to find solutions to address the issue of excessive CO₂ emission and its potential effects on climate change. It is imperative that the world looks towards a portfolio of carbon mitigation solutions, rather than a single strategy. In this regard, the use of CO₂ as a C1 source is an attractive strategy as CO₂ has the potential to be a great asset for the industrial sector and consumers across the globe. In particular, the reduction of CO₂ offers an alternative to fossil fuels for various organic industrial feedstocks and fuels. Consequently, efficient and scalable approaches for the reduction of CO₂ to products such as methane and methanol can generate value from its emissions. Accordingly, in recent years, metal-free catalysis has emerged as a sustainable approach because of the mild reaction conditions by which CO₂ can be reduced to various value-added products. The metal-free catalytic reduction of CO₂ offers the development of chemical processes with low cost, earth-abundant, non-toxic reagents, and low carbon-footprint. Thus, this perspective aims to present the developments in both the reduction and reductive functionalization chemistry of CO₂ during the last decade using various metal-free catalysts.

This review article documents the key developments in the metal-free catalytic reduction of CO₂ into various energy intensive chemicals and fuels, and reductive functionalization of CO₂ for the formation of new C–N bonds.     

Semi-wet growth and characterization of multi-functional nano-engineered mixed metal oxides for industrial application

This review paper covers the low temperature wet growth of nano-engineered particles of ZnO-based mixed metal oxides, their growth mechanism, and characterization using X-ray diffraction, SEM, TEM and IR, UV–visible, and XPS spectral techniques. Main focus of this article is centered on low temperature semi-wet methods of synthesis that are suitable for large scale production of zinc oxide-based systems mixed with iron oxide, copper oxide, nickel oxide and cobalt oxide. These mixed metal oxides have broad industrial applications as catalyst, semiconductors, adsorbents, superconductors, electro-ceramics, and antifungal agents in addition to extensive applications in medicines. This paper discusses the low-cost and environment friendly synthesis of these mixed metal oxides, measurement of properties and applicability of these materials systems.     

A numerical simulation of mixed convective and arbitrarily oblique radiative stagnation point slip flow of a CNT-water MHD nanofluid

Journal of Thermal Analysis and Calorimetry - Numerical simulation of a non-linear mathematical model governing an arbitrarily oblique slip flow of a nanofluid, with suspended carbon nanotubes in...     

Similarity of L-fuzzy Relations Based on L-topologies Induced by L-fuzzy Rough Approximation Operators

This paper proposes similarity of L-fuzzy relations based on L-topologies induced by L-fuzzy rough approximation operators. First, the notion L-fuzzy rough set is generalized and the relationship between generalized L-fuzzy rough sets and L-topologies on an arbitrary universe is investigated. It shows that Alexandrov L-topologies can be induced by L-fuzzy relations without any preconditions. Second, the concept of similarity of L-fuzzy relations is introduced and variations of an L-fuzzy relation are investigated. Third, algebraic structures on similarity of L-fuzzy relations are obtained. Finally, we prove that the subset of the transitive L-fuzzy relations similar to a fixed L-fuzzy relation is a complete distributive lattice.     

Electrocatalytic Reduction of Nitrogen to Ammonia Using Tiara-like Phenylethanethiolated Nickel Cluster

The fixing of N₂ to NH₃ is challenging due to the inertness of the N≡N bond. Commercially, ammonia production depends on the energy-consuming Haber-Bosch (H−B) process, which emits CO₂ while using fossil fuels as the sources of hydrogen and energy. An alternative method for NH₃ production is the electrochemical nitrogen reduction reaction (NRR) process as it is powered by renewable energy sources. Here, we report a tiara-like nickel-thiolate cluster, [Ni₆(PET)₁₂] (where, PET=2-phenylethanethiol)] as an efficient electro-catalyst for the electrochemical NRR at ambient conditions. Ammonia (NH₃: 16.2±0.8 μg h⁻¹ cm⁻²) was the only nitrogenous product over the potential of −2.3 V vs. F_c⁺/F_c with a Faradaic efficiency of 25%±1.7. Based on theoretical calculations, NRR by [Ni₆(PET)₁₂] proceeds through both the distal and alternating pathways with an onset potential of −1.84 V vs. RHE (i.e., −2.46 V vs. F_c⁺/F_c) which corroborates with the experimental findings.     

Zwitterionic structures of selenocysteine-containing dipeptides and their interactions with Cu(II) ions

The molecular structures of a series of selenocysteine-containing dipeptides in their zwitterionic forms were studied using the B3LYP/6-311++G(d,p) level in the aqueous phase. The B3LYP and BH and HLYP functionals in combination with 6-311++G(d,p) and LANL2DZ basis sets were used to investigate the effects of metal coordination on the structural and molecular properties of the dipeptides by complexing them with bivalent copper ions. The results from this DFT study provide valuable insights into the interaction enthalpies (metal ion-binding affinities) and free energies, the influence of the C-terminal moiety on the backbone structural features, the existence of various types of intramolecular H-bond interactions, harmonic vibrational frequencies, along with various other electronic properties pertaining to the zwitterions of the dipeptide molecules as well as their metallic complexes. Metal coordination via the carboxylate groups tends to enhance the planarity of the amide planes. The participations of the N- and C-terminal side-chain moieties in metal-binding markedly enhance the thermodynamic stability of the metalated dipeptides. The theoretical λ_maxvalues, calculated using the TD/DFT level for all the systems, well represent the occurrence of d-d transitions in the Cu-dipeptide complexes.