Amine Position Research Articles

A comprehensive synthetic library of poly-N-acetyl glucosamines enabled vaccine against lethal challenges of Staphylococcus aureus

Poly-β-(1–6)-N-acetylglucosamine (PNAG) is an important vaccine target, expressed on many pathogens. A critical hurdle in developing PNAG based vaccine is that the impacts of the number and the position of free amine vs N-acetylation on its antigenicity are not well understood. In this work, a divergent strategy is developed to synthesize a comprehensive library of 32 PNAG pentasaccharides. This library enables the identification of PNAG sequences with specific patterns of free amines as epitopes for vaccines against Staphylococcus aureus (S. aureus), an important human pathogen. Active vaccination with the conjugate of discovered PNAG epitope with mutant bacteriophage Qβ as a vaccine carrier as well as passive vaccination with diluted rabbit antisera provides mice with near complete protection against infections by S. aureus including methicillin-resistant S. aureus (MRSA). Thus, the comprehensive PNAG pentasaccharide library is an exciting tool to empower the design of next generation vaccines.

Microwave assisted self-repairable vitrimeric coating for anti-corrosive applications

Vitrimeric coatings are revolutionary and most widely emerging materials for metal corrosion inhibition. As harsh environmental conditions damages polymer-derived protective films and results into micro cracks and corroded metal surfaces. In this work, an active microwave responsive vitrimeric epoxy coating embedded with weathering resistant properties is introduced along with systematic comparative study for the effect of ortho and para position of amine in hardening agent. The developed microwave radiation responsive coating system felicitates self-healing due to disulfide exchange mechanism and corrosion inhibition properties in marine environments. Compared to conventional coatings, prepared graphene oxide (GO) incorporated vitrimeric network showed more promising protection against corrosion in offshore applications with 95.4 % protection efficiency and hydrophobicity with 96-degree contact angle. This study covers the self-healing properties, thermal mechanical study, hydrophobicity measurement, and thorough corrosion examination of synthesized material coated on 304 grade SS substrate. The coating reports excellent self-healing efficiency, reliable mechanical strength (storage modulus-129GPa and loss modulus-83GPa), fast stress relaxation and low activation energy (63KJ/mol) for dynamic disulfide exchange reaction, furthermore low corrosion rate of 1.20 × 10−3mm/y was observed for the coating. Thus, demonstrates its importance for self-healable anti-corrosive application for the marine environment.

Copper catalyzed Shono-type oxidation of proline residues in peptide.

Since the initial report in 1975, the Shono oxidation has become a powerful tool to functionalize the α position of amines, including proline derivatives, by electrochemical oxidation. However, the application of electrochemical Shono oxidations is restricted to the preparation of simple building blocks and homogeneous Shono-type oxidation of proline derivatives remains challenging. The late-stage functionalization at proline residues embedded within peptides is highly important as substitutions about the proline ring are known to affect biological and pharmacological activities. Here, we show that homogenous copper-catalyzed oxidation conditions complement the Shono oxidation and this general protocol can be applied to a series of formal C-C coupling reactions with a variety of nucleophiles using a one-pot procedure. This protocol shows good tolerance toward 19 proteinogenic amino acids and was used to functionalize several representative bioactive peptides, including captopril, enalapril, Smac, and endomorphin-2. Last, peptide cyclization can also be achieved by using an appropriately positioned side-chain hydroxyl moiety.

Ab Initio Calculations of Chitosan Effects on the Electronic Properties of Unpassivated Triangular ZnO Nanowires Oriented along [0001] Directions.

In recent years, both chitosan and ZnO nanostructures have been identified as potential antibacterial substances; however, the potential applications of chitosan adsorbed on ZnO nanowires have not been explored and could offer exciting new perspectives for both materials, for example, in biocompatible electronic circuits. In this work, we investigate the effect of chitosan on the electronic properties of triangular ZnO nanowires (ZnO NWs) from a theoretical perspective. All calculations were performed using density functional theory within the generalized gradient approximation. We considered six different positions of the chitosan molecule (CS) on the nanowire surface. We varied the amine position of CS, viewing it parallel, perpendicular, and at a 45° angle with respect to the NW axis. Our results show that all configurations are chemically stable; moreover, the interaction of the NW surface with the OH radical of CS creates flat states within the band gap energy of the ZnO NWs that might resemble p-doping. In addition, these states induce changes in the band gap energy of the ZnO NWs. All NWs show high chemical stability regardless of the CS position; hence, the adsorption results of all NW assemblies appear to be chemically favorable.

Layer-by-layer assembly of nanofilms from colloidally stable amine-functionalized silica nanoparticles

The assembly of uniform thin films with functional silica nanoparticles (FSNPs) by the layer-by-layer (LbL) technique has been studied to provide rough, robust, and functional surfaces. Initially, monodisperse silica nanoparticles (SNPs) have been synthesized by the reverse microemulsion method. Then SNPs have been functionalized using amino silane coupling agents with various chain lengths and amine positions such as (3-aminopropyl)trimethoxy silane (APS), N-[3-(trimethoxysilyl)propyl]-N,N,N-trimethylammonium chloride (NPC), N -(6-aminohexyl)aminopropyltrimethoxy silane (AHAPS), and 3-aminopropyl(dimethyl)ethoxy silane (APDMES). The amine-functionalized silica nanoparticles have been characterized using zeta potential, Fourier Transform-Infrared Spectroscopy (FT-IR), and 1 H Nuclear Magnetic Resonance (NMR) spectroscopy to prove the existence of amine groups on the silica surface. Scanning electron microscopy (SEM) images have revealed that the LbL assembled thin film coatings of FSNPs are uniform and monodisperse. The thickness measurements of the coatings have been conducted by spectroscopic ellipsometry. Water contact angle measurements were performed to analyze the alteration of surface features with functional groups. The roughness, topography, and elastic modulus of the assembled thin-film coatings were probed by atomic force microscopy (AFM). The dispersion of AHAPS-FSNPs has indicated superior colloidal stability than other FSNPs because of their secondary amines creating steric hindrance. Moreover, AHAPS-FSNPs film exhibited the lowest coating thickness and the highest elastic modulus comparing with the other FSNPS because of their crosslinking and hydrogen-bonding ability. Briefly, in this work, LbL assembly of the amine FSNPs was established by an extensive investigation to form rough and functional surfaces for many demanding applications.

π-Dimers of core-unsubstituted perylene diimide radical anion: Synthesis, dissociation and high current-responsive to alkyl primary amine vapor

π-dimer dissociation Purely organic radical ions dimerize in solution at low temperature, to form the isolated dimers with long multi-center bonds, which shows the metastability in solution. The metastability of radical π-dimers in solution limits the research on its properties and application. The isolated π-dimers of two types of core-unsubstituted perylene diimide radical anion in solution at room temperature were first found in here. The diamagnetic π-dimers with hydroxyl at amine position can be dissociated into its radical anions in solution when adding alkyl primary amines. Moreover, the thin film device of the π-dimer2 showed current-responsive of 11,800 times within volatile alkyl primary amines at voltage of 1 V, and the limit of detection was 209 ppb.

Synthesis and Cu(I)/Mo(VI) Reactivity of a Bifunctional Heterodinucleating Ligand on a Xanthene Platform.

In an effort to probe the feasibility of a model of Mo-Cu CODH (CODH = carbon monoxide dehydrogenase) lacking a bridging sulfido group, the new heterodinucleating ligand LH2 was designed and its Cu(I)/Mo(VI) reactivity was investigated. LH2 ((E)-3-(((5-(bis(pyridin-2-ylmethyl)amino)-2,7-di-tert-butyl-9,9-dimethyl-9H-xanthen-4-yl)imino)methyl)benzene-1,2-diol) features two different chelating positions bridged by a xanthene linker: bis(pyridyl)amine for Cu(I) and catecholate for Mo(VI). LH2 was synthesized via the initial protection of one of the amine positions, followed by two consecutive alkylations of the second position, deprotection, and condensation to attach the catechol functionality. LH2 was found to exhibit dynamic cooperativity between two reactive sites mediated by H-bonding of the catechol protons. In the free ligand, catechol protons exhibit H-bonding with imine (intramolecular) and with pyridine (intermolecular in the solid state). The reaction of LH2 with [Cu(NCMe)4]+ led to the tetradentate coordination of Cu(I) via all nitrogen donors of the ligand, including the imine. Cu(I) complexes were characterized by multinuclear NMR spectroscopy, high-resolution mass spectrometry (HRMS), X-ray crystallography, and DFT calculations. Cu(I) coordination to the imine disrupted H-bonding and caused rotation away from the catechol arm. The reaction of the Cu(I) complex [Cu(LH2)]+ with a variety of monodentate ligands X (PPh3, Cl-, SCN-, CN-) released the metal from coordination to the imine, thereby restoring imine H-bonding with the catechol proton. The second catechol proton engages in H-bonding with Cu-X (X = Cl, CN, SCN), which can be intermolecular (XRD) or intramolecular (DFT). The reaction of LH2 with molybdate [MoO4]2- led to incorporation of [MoVIO3] at the catecholate position, producing [MoO3(L)]2-. Similarly, the reaction of [Cu(LH2)]+ with [MoO4]2- formed the heterodinuclear complex [CuMoO3(L)]-. Both complexes were characterized by multinuclear NMR, UV-vis, and HRMS. HRMS in both cases confirmed the constitution of the complexes, containing molecular ions with the expected isotopic distribution.

Amino acids change solute affinity for lipid bilayers

Time-resolved fluorescence and differential scanning calorimetry (DSC) were used to examine how two amino acids, L-phenylalanine (L-PA) and N-acetyl-DL-tryptophan (NAT), affect the temperature-dependent membrane affinity of two structurally similar coumarin solutes for 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) vesicles. The 7-aminocoumarin solutes, coumarin 151 (C151) and coumarin 152 (C152), differ in their substitution at amine position—C151 is a primary amine, and C152 is a tertiary amine—and both solutes show different tendencies to associate with lipid bilayers consistent with differences in their respective log-P-values. Adding L-PA to the DPPC vesicle solution did not change C151’s propensity to remain freely solvated in aqueous solution, but C152 showed a greater tendency to partition into the hydrophobic bilayer interior at temperatures below DPPC’s gel-liquid crystalline transition temperature (Tgel-lc). This finding is consistent with L-PA’s ability to enhance membrane permeability by disrupting chain-chain interactions. Adding NAT to DPPC-vesicle-containing solutions changed C151 and C152 affinity for the DPPC membranes in unexpected ways. DSC data show that NAT interacts strongly with the lipid bilayer, lowering Tgel-lc by up to 2°C at concentrations of 10 mM. These effects disappear when either C151 or C152 is added to solution at concentrations below 10 μM, and Tgel-lc returns to a value consistent with unperturbed DPPC bilayers. Together with DSC results, fluorescence data imply that NAT promotes coumarin adsorption to the vesicle bilayer surface. NAT’s effects diminish above Tgel-lc and imply that unlike L-PA, NAT does not penetrate into the bilayer but instead remains adsorbed to the bilayer’s exterior. Taken in their entirety, these discoveries suggest that amino acids—and by inference, polypeptides and proteins—change solute affinity for lipid bilayers with specific effects that depend on individualized amino-acid-lipid-bilayer interactions.

Ligand-Enabled δ-C(sp3 )-H Borylation of Aliphatic Amines.

Directed C-H functionalization has been realized as a complimentary technique to achieve borylation at a distal position of aliphatic amines. Here, we demonstrated the oxidative borylation at the distal δ-position of aliphatic amines using various borylating agents, a palladium catalyst, and a rightly tuned ligand in the presence of a cheap oxidant. Moreover, an organopalladium δ-C(sp3 )-H-activated intermediate has been isolated and crystallographically characterized to get mechanistic insight.

Ligand‐Enabled δ‐C(sp3)−H Borylation of Aliphatic Amines

AbstractDirected C−H functionalization has been realized as a complimentary technique to achieve borylation at a distal position of aliphatic amines. Here, we demonstrated the oxidative borylation at the distal δ‐position of aliphatic amines using various borylating agents, a palladium catalyst, and a rightly tuned ligand in the presence of a cheap oxidant. Moreover, an organopalladium δ‐C(sp3)‐H‐activated intermediate has been isolated and crystallographically characterized to get mechanistic insight.

Novel Synthetic Cathinone Eutylone and its Structural Isomers Interact with Monoamine Transporters and Induce Locomotor Stimulation in Mice

Synthetic cathinones are a class of new psychoactive substances that produce psychostimulant effects and pose public health risks. Currently, derivatives of the synthetic cathinone, methylone, are being confiscated worldwide. Eutylone is a popular emerging methylone analog with ethyl substitutions at the a-carbon and amine positions. Little information is presently available about the pharmacological effects of eutylone. Therefore, based on its structure we hypothesized that the compound interacts with monoamine transporters in the brain and produces locomotor stimulation akin to other cathinone psychostimulants. To test this hypothesis, we compared the effects of eutylone and its structural isomers, pentylone and dibutylone, using in vitro transporter assays in rat brain synaptosomes and in vivo locomotor activity assessments in mice. All drugs displayed dose-dependent inhibition of [3H]neurotransmitter uptake at dopamine transporters (DAT) and norepinephrine transporters (NET), with 10-fold more potent effects at DAT (IC50 = ~120 nM). Contrary to dibutylone, which displayed no effects at serotonin transporters (SERT), eutylone and pentylone inhibited uptake at SERT (0.69 & 1.24 μM respectively) and displayed weak partial releasing actions at SERT (both ~50% of maximal response). All drugs stimulated dose-dependent locomotion in mice, with eutylone displaying the most potent and efficacious effects (ED50 = 2.1 mg/kg, s.c.). Rank order of ED50 potency values for locomotor stimulation was eutylone ≥ pentylone > cocaine > dibutylone. Our results demonstrate that eutylone is a potent monoamine transporter inhibitor that displays preference for DAT and induces locomotor stimulation. Eutylone displayed pharmacological effects very similar to those produced by pentylone, which suggests that eutylone will exhibit similar abuse liability and pose risks for psychostimulant side-effects in human users.

Eutylone and Its Structural Isomers Interact with Monoamine Transporters and Induce Locomotor Stimulation

Synthetic cathinones are a class of new psychoactive substances that induce psychostimulant effects and pose risk for hospitalizations, overdose, and death. At the present time, derivatives of the synthetic cathinone, methylone, are being confiscated in nonmedical (i.e., recreational) drug markets worldwide. In particular, eutylone is a newly emerging methylone analog that possesses ethyl groups at the α-carbon and amine positions. Little information is available about the pharmacological effects of eutylone, but based on its structure, we surmised that the compound interacts with monoamine transporters in the brain. To test this hypothesis, we compared the effects of eutylone and its structural isomers, dibutylone and pentylone, using in vitro transporter assays in rat brain synaptosomes and in vivo locomotor activity assessments in mice. All drugs displayed dose-related inhibition of [3H]neurotransmitter uptake at dopamine transporters (DAT) and norepinephrine transporters (NET), but effects at DAT were 10-fold more potent (IC50 = 120 nM). Eutylone and pentylone inhibited uptake at serotonin transporters (SERT), while dibutylone did not. Additionally, eutylone and pentylone displayed weak partial releasing actions at SERT which achieved 50% of maximal response. All drugs stimulated dose-related locomotion in mice, and eutylone was most potent and efficacious in this regard (ED50 = 2 mg/kg, sc). Our results demonstrate that eutylone is a hybrid transporter compound with uptake inhibition properties at DAT and NET but substrate activity at SERT. The effects of eutylone are similar to those produced by pentylone, which suggests that eutylone will exhibit abuse liability and pose risks for psychostimulant side-effects in human users.

Nano cobalt-copper ferrite catalyzed regioselective α-C(sp3)–H cyanation of amines: Secondary, tertiary, and drug molecules

Oxidative cyanation of sp3C–H bonds at the α position of amines was achieved using CoCuFe2O4 as a catalyst and NaCN as an inexpensive cyanide source at room temperature.CoCuFe2O4 was found to be an active catalyst for Csp [3]-Csp coupling, efficiently delivering valuable α-aminonitriles from tertiary/secondary amines in good yields. The corresponding products were obtained with high selectivity toward α position. In addition, functional group tolerance offered the opportunity for application in late-stage functionalization of biologically active molecules. This transformation proceeds convenient on a gram-scale, and the catalyst can be reused for several runs with consistent catalytic activity.

Azido-Desferrioxamine Siderophores as Functional Click-Chemistry Probes Generated in Culture upon Adding a Diazo-Transfer Reagent.

This work aimed to undertake the in situ conversion of the terminal amine groups of bacterial desferrioxamine (DFO) siderophores, including desferrioxamine B (DFOB), to azide groups to enable downstream click chemistry. Initial studies trialed a precursor-directed biosynthesis (PDB) approach. Supplementing Streptomyces pilosus culture with blunt-end azido/amine non-native substrates designed to replace 1,5-diaminopentane as the native diamine substrate in the terminal amine position of DFOB did not produce azido-DFOB. Addition of the diazo-transfer reagent imidazole-1-sulfonyl azide hydrogen sulfate to spent S. pilosus medium that had been cultured in the presence of 1,4-diaminobutane, as a viable native substrate to expand the suite of native DFO-type siderophores, successfully generated the cognate suite of azido-DFO analogues. CuI -mediated or strain-promoted CuI -free click chemistry reactions between this minimally processed mixture and the appropriate alkyne-bearing biotin reagents produced the cognate suite of 1,4-disubstituted triazole-linked DFO-biotin compounds as potential molecular probes, detected as FeIII -loaded species. The amine-to-azide transformation of amine-bearing natural products in complex mixtures by the direct addition of a diazo-transfer reagent to deliver functional click chemistry reagents adds to the toolbox for chemical proteomics, chemical biology, and drug discovery.

Metal Ion (NiII vs CoII)-Mediated Unusual Amine-Imine Interconversion in Conjugated Amine-ene-imine Ligand: Synthesis, Structure, and Characterization.

Two configurationally isomeric ligands, namely, 2-((E)-benzylideneamino)-3-((pyridin-2-ylmethyl)amino)maleonitrile (HL1) and 2-(benzylamino)-3-((E)-(pyridin-2-ylmethylene)amino)maleonitrile (HL2), were synthesized and fully characterized, which are malenonitrile-tethered, N atom donors tridentate ligands. Structurally, they differ in the interchangeable position of amine and imine group only. Under the same reaction condition, Ni(II) invoked the transformation of (L1)- to (L2)- via simultaneous oxidation of amine to imine and the reduction of imine to amine. Two sequential 1,5-proton transfer pathways were anticipated for this type of unusual amine-imine oxidation/reduction process under acidic medium. In contrast, Co(II) was silent to such amine-imine interconversion reactions under both HL1 and HL2 ligand environment. The variation in electronic requirement might differentiate between both ligands such that HL2 influenced the arial oxidation of Co(II) to Co(III) but HL1 could not. The redox chemistry of Co(II)/Co(III) complexes with either HL1 or HL2 was explained using cyclic voltammetry and UV-vis spectroscopy.

The Effect of Methyl and Chloro Substituent Compounds in Amida Derivatives Synthesis from p-Metoxicynamic Acid with Microwaves Irradiation

Background: The difference in the nature of these aromatic amine substituents, i.e. methyl and chloro will affect the N atom of aniline as a nucleophile to attack the carbonyl C atom in the p -methoxcycinnamoyl chloride in the synthesis two amides derivate of p -methoxycinnamic acid, namely N -( p -methylphenyl)- p -methoxycinnamide and N- ( p -chlorophenyl)- p -methoxycinnamide. Aim: to obtain the N -( p -methylphenyl)- p -methoxycinnamide and the N- ( p -chlorophenyl)- p -metoxicinamide compound from p -methoxycinamic acid using the microwave irradiation method as source of energy. Beside that, it also to determine the effect of the presence of methyl and chloro substituents in para position of aromatic amines in the yields of reactions. Method: The reactions were carried out by microwave irradiation at three powers, i.e 120 watts, 200 watts, 280 watts. After separation and purification steps, the products were identified by spectrometric methods. Result: At power of 200 watts for reaction time of 7.5 minutes, the yield of N -( p -methylphenyl)- p -methoxycinamide is larger than N -( p -chlorophenyl)- p -methoxycinnamamide. The percentage of the product synthesis of N -( p -methylphenyl)- p -methoxycinamide was 51.84% and the percentage of N -( p -chlorophenyl)- p -methoxycinnamamide was to 47.20%. Conclusion: The effect of substituent methyl is increase the percentage yield of N -( p -methylphenyl)- p -methoxycinamide compound than that substituent chloro of N -( p -chlorophenyl)- p -methoxycinamide compound under the same reaction conditions. Based on the identification of the structure of the synthesized compound using a UV spectrophotometer, infrared spectrophotomers and 1 H-NMR spectrometer it can be concluded that the synthesized compounds are N -( p -methylphenyl)- p -methoxycinnamide and N - ( p -chlorophenyl)- p -methoxycinnamide.

Perylene diimide derivative regulate the antimony sulfide morphology and electrochemical sensing for hydrazine

Sb2S3/perylene diimide derivatives composite micro-spheres composed of slight dendrites were synthesized by solvothermal reaction. Perylene diimide derivative with two carboxyl groups at amine position as morphology-controlling reagent is the key factor for determining the microscopic morphology of Sb2S3 in this system. Time-dependent experiments have been conducted to track the formation of Sb2S3 micro-spheres. Moreover, the composite material showed an excellent sensitivity of 29.8 μA mM−1 cm2 with a low detection limit of 50 pM, it also showed better stability and selectivity in hydrazine detection. This approach not only regulate the morphology and composition of Sb2S3 submicron materials effectively, but also provide new ideas for the manufacture of metal sulfide- perylenediimide amino acid derivative materials, which will be suitable for sensing, catalysis, and photovoltaic applications.

Functionalizing Cellulose Nanocrystals with Click Modifiable Carbohydrate-Binding Modules.

Functionalized cellulose nanocrystals (CNC) have unique properties that make them attractive in various applications such as drug delivery, hydrogels, and emulsions. However, the predominant chemical methods currently used to functionalize cellulose nanocrystals have a large environmental footprint. Although greener methods are desirable, the relatively inert nature of cellulose crystals presents a major challenge to their potential modification in aqueous media. In the work reported here, carbohydrate binding modules (CBMs) were used to introduce new functionality to cellulose surfaces. CBM2a, which has a strong affinity for crystalline cellulose, was functionalized with an alkyne at the terminal amine position. The alkyne group, which was introduced onto the cellulose surface with CBM2a, underwent a Click reaction with polyethylene glycol (PEG) to modify CNC surfaces. This provided a strong, non-covalent modification of cellulose surfaces that was carried out in a one-pot reaction in aqueous media. The CBM-PEG modification of cellulose surfaces increased CNC redispersion after drying and improved suspension stability based on steric interactions. It was apparent that hybrid polysaccharide-protein, self-assembled nanoparticles could be effectively produced, with potential for nanomedicine, immunoassay, and drug delivery applications.

Multivalent Sialosides: A Tool to Explore the Role of Sialic Acids in Biological Processes.

Sialic acids (Sias) are fascinating nine‐carbon monosaccharides that are primarily found on the terminus of the oligosaccharide chains of glycoproteins and glycolipids on cell surfaces. These Sias undergo a variety of structural modifications at their hydroxy and amine positions, thereby resulting in structural diversity and, hence, coordinating a variety of biological processes. However, deciphering the structural functions of such interactions is highly challenging, because the monovalent binding of Sias is extremely weak. Over the last decade, several multivalent Sia ligands have been synthesized to modulate their binding affinity with proteins/lectins. In this Minireview, we highlight recent developments in the synthesis of multivalent Sia probes and their potential applications. We will discuss four key multivalent families, that is, polymers, dendrimers, liposomes, and nanoparticles, and will emphasize the major parameters that are essential for the specific interactions of these molecules with proteins in biological systems.

Plasticized and plasticizer free lithium acetate doped polyvinyl alcohol–chitosan blend solid polymer electrolytes: Comparative studies

In this work, two systems (plasticized and plasticizer free) of polyvinyl alcohol (PVA)–chitosan blend based solid polymer electrolytes containing lithium acetate (LiOAc) are successfully prepared through solution casting method. In Fourier transform infrared (FTIR) spectroscopy studies, the changes in peak position of amine and hydroxyl band signify the saltpolymer and plasticizer-salt-polymer interactions. The room temperature conductivity of each electrolyte is investigated by impedance analysis in the frequency range of 50 Hz – 1 MHz. Upon addition of 30 wt.% LiOAc, a conductivity of (6.46 ± 1.80) × 10−5 S cm−1 is achieved. The conductivity increases to (1.15 ± 0.19) × 10−3 S cm−1 with the addition 70 wt.% ethylene carbonate (EC). The temperature dependence of conductivity is found to follow Vogel-Tammann-Fulcher (VTF) rule. From the VTF plot, the glass transition temperature (Tg) was analyzed and the highest conducting electrolyte is found to possess the lowest Tg value.