Synthesis and optimization of chitosan-incorporated semisynthetic polymer/α-FeO nanoparticle hybrid polymer to explore optimal efficacy of fluorescence resonance energy transfer/charge transfer for Co(II) and Ni(II) sensing.

Initially, four synthetic fluorescent polymers (SFPs) are synthesized from α-methacrylic acid and methanolacrylamide monomers carrying -C(=O)OH and -C(=O)NH subfluorophores, respectively. Among SFPs, ∼1:1 incorporation of subfluorophores in the optimum SFP3 is explored by spectroscopic analyses. Subsequently, chitosan is incorporated in SFP3 to produce five semi-synthetic fluorescent polymers (SSFPs).

Nontraditional Redox Active Aliphatic Luminescent Polymer for Ratiometric pH Sensing and Sensing-Removal-Reduction of Cu(II): Strategic Optimization of Composition.

Here, redox active aliphatic luminescent polymers (ALPs) are synthesized via polymerization of N,N-dimethyl-2-propenamide (DMPA) and 2-methyl-2-propenoic acid (MPA). The structures and properties of the optimum ALP3, ALP3-aggregate and Cu(I)-ALP3, ratiometric pH sensing, redox activity, aggregation enhanced emission (AEE), Stokes shift, and oxygen-donor selective coordination-reduction of Cu(II) to Cu(I) are explored via spectroscopic, microscopic, density functional theory-reduced density gradient (DFT-RDG), fluorescence quenching, adsorption isotherm-thermodynamics, and electrochemical methods. The intense blue and green fluorescence of ALP3 emerges at pH = 7.

Fluorescent Terpolymers Using Two Non-Emissive Monomers for Cr(III) Sensors, Removal, and Bio-Imaging.

The nonconventional purely aliphatic intrinsically fluorescent multifunctional terpolymers, such as 2-acrylamido-2-methylpropane sulfonic acid--2-(3-acrylamidopropylamido)-2-methylpropane sulfonic acid--acrylamide (AMPS--APMPS--AM, ), acrylic acid--3-acrylamidopropanoic acid--acrylamide (AA--APA--AM, ), and methacrylic acid--3-acrylamido-2-methyl propanoic acid--acrylamide (MAA--AMPA--AM, ), were synthesized via N- functionalized multi-C-C/N-C coupled in situ attachments of fluorophore monomers, that is, APMPS, APA, and AMPA, in solution polymerization of two non-fluorescent monomers. These terpolymers were suitable for selective Cr(III) sensors, high-performance exclusions of Cr(III), and fluorescence imaging of human osteosarcoma cancer cells. The structures of , , and , in situ attachments of fluorescent amino acid monomers, locations of fluorophores, aggregation-induced enhanced emissions, and the superadsorption mechanism were understood via microstructural analyses.

Nonconjugated Biocompatible Macromolecular Luminogens for Sensing and Removals of Fe(III) and Cu(II): DFT Studies on Selective Coordination(s) and On-Off Sensing.

This work reports the design and synthesis of two nonaromatic biocompatible macromolecular luminogens, i.e., 2-(dimethylamino)ethyl methacrylate-co-2-(dimethylamino)ethyl 3-(N-(methylol)acrylamido)-2-methylpropanoate-co-N-(methylol)acrylamide/DMAEMA-co-DMAENMAMP-co-NMA (P1) and methacrylic acid-co-3-(N-(methylol)acrylamido)-2-methylpropanoic acid-co-N-(methylol)acrylamide/MEA-co-NMAMPA-co-NMA (P2), prepared through in situ anchored acrylamido-ester/DMAENMAMP and acrylamido-acid/NMAMPA third comonomers, respectively, in a facile polymerization of two non-luminous monomers in water medium to circumvent the drawbacks related to aggregation-caused quenching of aromatic luminogens.

Synthesis of Biocompatible Aliphatic Terpolymers via In Situ Fluorescent Monomers for Three-in-One Applications: Polymerization of Hydrophobic Monomers in Water.

Biocompatible, nonconventional, multifunctional, purely aliphatic, light-emitting terpolymers, i.e., acrylonitrile--3-(-isopropylacrylamido)propanenitrile---isopropylacrylamide (AN--NIPAMPN--NIPA, ) and acrylonitrile--3-(-hydroxymethylacrylamido)propanenitrile---hydroxymethylacrylamide (AN--NHMAMPN--NHMA, ), were designed and synthesized via N-H-functionalized C-C + N-C-coupled in situ protrusions/grafting of fluorophore monomers, i.

Fluorescent Guar Gum--Terpolymer via In Situ Acrylamido-Acid Fluorophore-Monomer in Cell Imaging, Pb(II) Sensor, and Security Ink.

The nonconventional purely aliphatic scalable and reusable fluorescent guar gum (GRGM)--acrylic acid--3-(-isopropylacrylamido)propanoic acid (NIPAPA)---isopropylacrylamide (GRGM--, i.e., ), was synthesized via of the optimum amount of GRGM and N- functionalized in situ protrusion of acrylamido-acid fluorophore-monomer, i.

Light-Emitting Multifunctional Maleic Acid--2-(-(hydroxymethyl)acrylamido)succinic Acid---(hydroxymethyl)acrylamide for Fe(III) Sensing, Removal, and Cell Imaging.

The intrinsically fluorescent highly hydrophilic multifunctional aliphatic terpolymer, maleic acid (MA)--2-(-(hydroxymethyl)acrylamido)succinic acid (NHASA)---(hydroxymethyl)acrylamide (NHMA), that is, , was designed and synthesized via C-C/N-C-coupled in situ allocation of a fluorophore monomer, that is, NHASA, composed of amido and carboxylic acid functionalities in the polymerization of two nonemissive MA and NHMA. The scalable and reusable intrinsically fluorescent biocompatible was suitable for sensing and high-performance adsorptive exclusion of Fe(III), along with the imaging of Madin-Darby canine kidney cells. The structure of , in situ fluorophore monomer, aggregation-induced enhanced emission, cell-imaging ability, and superadsorption mechanism were studied via microstructural analyses using H/C NMR, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, atomic absorption spectroscopy, ultraviolet-visible spectroscopy, thermogravimetric analysis, dynamic light scattering, high-resolution transmission electron microscopy, solid-state fluorescence, fluorescence lifetime, and fluorescence imaging, along with measuring kinetics, isotherms, and thermodynamic parameters.

In Situ Attachment of Acrylamido Sulfonic Acid-Based Monomer in Terpolymer Hydrogel Optimized by Response Surface Methodology for Individual and/or Simultaneous Removal(s) of M(III) and Cationic Dyes.

Herein, grafting of starch (STR) and in situ strategic inclusion of 2-(3-(acrylamido)propylamido)-2-methylpropane sulfonic acid (APMPS) via solution polymerization of 2-(acrylamido)-2-methylpropanesulfonic acid (AMPS) and acrylamide (AM) have resulted in the synthesis of smart STR-grafted-AMPS--APMPS--AM (i.e., STR--TerPol) interpenetrating terpolymer (TerPol) network hydrogels.

Tetrapolymer Network Hydrogels via Gum Ghatti-Grafted and N-H/C-H-Activated Allocation of Monomers for Composition-Dependent Superadsorption of Metal Ions.

Herein, gum ghatti (GGTI)--[sodium acrylate (SA)--3-(-(4-(4-methyl pentanoate))acrylamido)propanoate (NMPAP)--4-(acrylamido)-4-methyl pentanoate (AMP)---isopropylacrylamide (NIPA)] (i.e., GGTI--TetraP), a novel interpenetrating tetrapolymer network-based sustainable hydrogel, possessing extraordinary physicochemical properties and excellent recyclability, has been synthesized via grafting of GGTI and in situ strategic protrusion of NMPAP and AMP during the solution polymerization of SA and NIPA, through systematic multistage optimization of ingredients and temperature, for ligand-selective superadsorption of hazardous metal ions (M(II)), such as Sr(II), Hg(II), and Cu(II).

Structures, Properties, and Performances-Relationships of Polymeric Membranes for Pervaporative Desalination.

For the fulfilment of increasing global demand and associated challenges related to the supply of clean-and-safe water, PV has been considered as one of the most attractive and promising areas in desalinating salty-water of varied salinities. In pervaporative desalination, the sustainability, endurance, and structural features of membrane, along with operating parameters, play the dominant roles and impart paramount impact in governing the overall PV efficiency. Indeed, polymeric- and organic-membranes suffer from several drawbacks, including inferior structural stability and durability, whereas the fabrication of purely inorganic membranes is complicated and costly.

Carbohydrate and collagen-based doubly-grafted interpenetrating terpolymer hydrogel via N-H activated in situ allocation of monomer for superadsorption of Pb(II), Hg(II), dyes, vitamin-C, and p-nitrophenol.

Herein, guar gum (GG)-g-(acrylic acid (AA)-co-3-acrylamido propanoic acid (AMPA)-co-acrylamide (AM))-g-cow buffing dust (CBD)/(GGTPCBD), a smart carbohydrate and protein-based doubly-grafted interpenetrating terpolymer hydrogel showing excellent physicochemical properties and recyclability was synthesized by in situ strategic allocation of AMPA during solution polymerization of AA and AM through systematic optimization of the amounts of components and reaction temperature for superadsorption of Hg(II), Pb(II), methyl violet (MV), methylene blue (MB), p-nitrophenol (PNP), and vitamin-C (vit.C). The in situ strategic protrusion of AMPA, grafting of both GG and CBD into AA-co-AMPA-co-AM, and ligand-selective superadsorption was inferred by advanced microstructural analyses of unadsorbed- and/or adsorbed-GGTPCBD using FTIR, H/C NMR, O1s-/N1s-/C1s-/Pb4f-/Hg4f-XPS, UV-vis, TGA, DSC, XRD, DLS, SEM, EDX, % gel content, % -COOH, and pH.

In Situ Allocation of a Monomer in Pectin--Terpolymer Hydrogels and Effect of Comonomer Compositions on Superadsorption of Metal Ions/Dyes.

Pectin--(sodium acrylate--3-(-isopropylacrylamido) sodium propanoate---isopropylacrylamide) interpenetrating polymer networks (PANIPNs) were synthesized through systematic multistage optimization of equilibrium swelling ratio by response surface methodology for individual and/or synergistic removal(s) of cationic safranine (SF), anionic methyl orange, and M(II/III), such as Hg(II), Cd(II), and Cr(III). The relative effects of copolymer compositions on ligand-selective adsorption, strong/weak H-bonds, thermal stabilities, crystallinity, surface properties, swelling abilities, cross-link densities, network parameters, hydrophilic-hydrophobic characteristics, and adsorption capacities (ACs) were measured through extensive microstructural analyses of adsorbed and/or unadsorbed PANIPN41 and PANIPN21 bearing sodium acrylate and -isopropylacrylamide (SA/NIPAm) in 4:1 and 2:1 ratios, respectively, using Fourier transform infrared, H and C NMR, X-ray photoelectron spectroscopy, thermogravimetric analysis, differential scanning calorimetry, X-ray diffraction, scanning electron microscopy, and energy dispersive X-ray spectroscopy, along with measuring lower critical solution temperature, % gel content (% GC), % -COOH, and pH. Extensive UV-vis measurements were carried out at varying copolymer compositions, initial pH (pH), and dyes, interpreted considering monomer-dimer and azonium-ammonium equilibrium of dye, dye-dye complexation, ligand-selective PANIPNs-dye adduct formation, π-π stacking interactions, and orientation effect of dyes.