scholarly journals Synthesis and Characterization of Graphene Oxide Derivatives via Functionalization Reaction with Hexamethylene Diisocyanate

Proceedings ◽  
2018 ◽  
Vol 3 (1) ◽  
pp. 8 ◽  
Author(s):  
José A. Luceño-Sánchez ◽  
Georgiana Maties ◽  
Camino Gonzalez-Arellano ◽  
Ana M. Díez-Pascual
Keyword(s):  
Graphene Oxide ◽  
High Performance ◽  
Organic Molecules ◽  
Hexamethylene Diisocyanate ◽  
Reaction Conditions ◽  
Ft Ir ◽  
Oxygen Groups ◽  
Functionalization Reaction ◽  
Ft Ir Spectroscopy

Graphene oxide (GO), the oxidized form of graphene, shows unique properties, such as strong mechanical strength, high thermal conductivity, amphiphilicity, and surface functionalization capability that make it very attractive in various fields, ranging from medicine to optoelectronic devices and solar cells. However, its insolubility in non-polar and polar aprotic solvents hinders some applications. To solve this issue, novel functionalization strategies are pursued. In this regard, the current study deals with the preparation and characterization of hexamethylene diisocyanate (HDI)-functionalized GO. Different reaction conditions were tested to optimize the functionalization degree (FD), and detailed characterization was conducted via Fourier-transformed infrared (FT-IR) spectroscopy to confirm the success of the functionalization reaction. The HDI-GO could further react with other organic molecules or polymers via the remaining oxygen groups, which makes them ideal candidates as nanofillers for high-performance GO-based polymer nanocomposites.

scholarly journals Synthesis and Characterization of Graphene Oxide Derivatives via Functionalization Reaction with Hexamethylene Diisocyanate

Nanomaterials ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 870 ◽  
Author(s):  
Jose Luceño-Sánchez ◽  
Georgiana Maties ◽  
Camino Gonzalez-Arellano ◽  
Ana Diez-Pascual
Keyword(s):  
Graphene Oxide ◽  
High Performance ◽  
Hexamethylene Diisocyanate ◽  
Covalent Attachment ◽  
Aprotic Solvents ◽  
Transmission Electron ◽  
Device Applications ◽  
Oxygen Groups ◽  
Functionalization Reaction

Graphene oxide (GO), the oxidized form of graphene, shows unique properties including high mechanical strength, optical transparency, amphiphilicity and surface functionalization capability that make it attractive in fields ranging from medicine to optoelectronic devices and solar cells. However, its insolubility in non-polar and polar aprotic solvents hinders some applications. To solve this issue, novel functionalization strategies are pursued. In this regard, this study deals with the preparation and characterization of hexamethylene diisocyanate (HDI)-functionalized GO. Different reaction conditions were tested to optimize the functionalization degree (FD), and detailed characterizations were conducted via elemental analysis, Fourier-transformed infrared (FT-IR) and Raman spectroscopies to confirm the success of the functionalization reaction. The morphology of HDI-GO was investigated by transmission electron microscopy (TEM), which revealed an increase in the flake thickness with increasing FD. The HDI-GO showed a more hydrophobic nature than pristine GO and could be suspended in polar aprotic solvents such as N,N-dimethylformamide (DMF), N-methylpyrrolidone (NMP) and dimethyl sulfoxide (DMSO) as well as in low polar/non-polar solvents like tetrahydrofuran (THF), chloroform and toluene; further, the dispersibility improved upon increasing FD. Thermogravimetric analysis (TGA) confirmed that the covalent attachment of HDI greatly improves the thermal stability of GO, ascribed to the crosslinking between adjacent sheets, which is interesting for long-term electronics and electrothermal device applications. The HDI-GO samples can further react with organic molecules or polymers via the remaining oxygen groups, hence are ideal candidates as nanofillers for high-performance GO-based polymer nanocomposites.

scholarly journals Synthesis, Structures, Electrochemistry, and Catalytic Activity towards Cyclohexanol Oxidation of Mono-, Di-, and Polynuclear Iron(III) Complexes with 3-Amino-2-Pyrazinecarboxylate

2020 ◽  
Vol 10 (8) ◽  
pp. 2692
Author(s):  
Anirban Karmakar ◽  
Luísa M.D.R.S. Martins ◽  
Yuliya Yahorava ◽  
M. Fátima C. Guedes da Silva ◽  
Armando J. L. Pombeiro
Keyword(s):  
Coordination Polymer ◽  
Heterogeneous Catalysts ◽  
Saturated Calomel Electrode ◽  
Two Dimensional ◽  
Reaction Conditions ◽  
Ability To Act ◽  
Tert Butyl Hydroperoxide ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

The synthesis and characterization of a set of iron(III) complexes, viz. the mononuclear [Fe(L)3] (1) and [NHEt3][Fe(L)2(Cl)2] (2), the dinuclear methoxido-bridged [Fe(L)2(μ-OMe)]2.DMF.1.5MeOH (3), and the heteronuclear Fe(III)/Na(I) two-dimensional coordination polymer [Fe(N3)(μ-L)2(μ-O)1/2(Na)(μ-H2O)1/2]n (4), are reported. Reactions of 3-amino-2-pyrazinecarboxylic acid (HL) with iron(III) chloride under different reaction conditions were studied, and the obtained compounds were characterized by elemental analysis, Fourier Transform Infrared (FT-IR) spectroscopy, and X-ray single-crystal diffraction. Compound 1 is a neutral mononuclear complex, whereas 2 is mono-anionic with its charge being neutralized by triethylammonium cation. Compounds 3 and 4 display a di-methoxido-bridged dinuclear complex and a two-dimensional heterometallic Fe(III)/Na(I) polynuclear coordination polymer, respectively. Compounds 3 and 4 are the first examples of methoxido- and oxido-bridged iron(III) complexes, respectively, with 3-amino-2-pyrazinecarboxylate ligands. The electrochemical study of these compounds reveals a facile single-electron reversible Fe(III)-to-Fe(II) reduction at a positive potential of 0.08V vs. saturated calomel electrode (SCE), which is in line with their ability to act as efficient oxidants and heterogeneous catalysts for the solvent-free microwave-assisted peroxidative oxidation (with tert-butyl hydroperoxide) of cyclohexanol to cyclohexanone (almost quantitative yields after 1 h). Moreover, the catalysts are easily recovered and reused for five consecutive cycles, maintaining a high activity and selectivity.

Synthesis and Characterization of Structure of Fe3O4@Graphene Oxide Nanocomposites

2016 ◽  
Vol 25 (6) ◽  
pp. 096369351602500 ◽  
Author(s):  
Ruimin Fu ◽  
Mingfu Zhu
Keyword(s):  
Graphene Oxide ◽  
Drug Carrier ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Ft Ir ◽  
Co Precipitation ◽  
Ft Ir Spectroscopy

Nowadays, the hummers method for preparation of graphene oxide (GO) was improved. The grapheme oxide @ Fe3O4 magnetic nanocomposites were synthesized by co-precipitation method. After analysing the morphology and structure of obtained nanocomposites by X-ray diffraction (XRD), transmission electron microscope (TEM) and Fourier transform infrared (FT-IR) spectroscopy, the result was shown as follows. The particle size of Fe3O4 in nanocomposites is 30 nm. Many functional groups are found in grapheme oxide, and such groups could be used to bind with the drug. In the test for magnetic properties, the nanocomposites gathered rapidly in the vicinity of the permanent magnet. The nanocomposites, with high superparamagnetism, can be used in the following applications: drug targeting transports, drug carrier, and diagnosis assistant system.

Synthesis and Characterization of Triethanolamine Borate

2013 ◽  
Vol 709 ◽  
pp. 28-31
Author(s):  
Cheng Xue Wang ◽  
Tian Tian Liang ◽  
Chun Qiao Wei
Keyword(s):  
Mass Spectrometry ◽  
Differential Scanning Calorimetry ◽  
Synthesis And Characterization ◽  
Spectroscopy Analysis ◽  
Scanning Calorimetry ◽  
Reaction Conditions ◽  
Different Types ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

Starting with boric acid and triethanolamine , the effect of the different types of the water-carrying agent on the yield was invested, and influences of dosage of water-carrying agent ,the mole ratio of reactants, reaction time on yield were discussed, the optimized reaction conditions were confirmed. The structure of the product was described by Fourier transform-infrared (FT-IR) spectroscopy, NMR Spectroscopy analysis, mass spectrometry (MS) and thermodynamic properties was analyzed by differential scanning calorimetry (DSC) and thermogravimetry (TG).

Preparation and Characterization of PA6-PEG/Li High Performance Static Dissipation Composites

2017 ◽  
Vol 70 (6) ◽  
pp. 669
Author(s):  
Chongling Yang ◽  
Shouzai Tan ◽  
Gengen Chen ◽  
Litao Guan
Keyword(s):  
High Performance ◽  
Condensation Reaction ◽  
Polyamide 6 ◽  
Decomposition Temperature ◽  
Reaction Conditions ◽  
Comprehensive Properties ◽  
Ft Ir ◽  
Optimal Reaction ◽  
Resistivity Testing

A copolymer of PA6 (polyamide 6) and PEG (polyethylene glycol) was synthesized by a condensation reaction. The optimal reaction conditions were determined as the following: a reaction temperature of 255°C, –0.04 MPa vacuum, and a condensation time of 40 min. A series of novel PA6-PEG/Li composites were developed by melt blending the PA6-PEG copolymer (10 wt-% PEG) with three different kinds of colourless lithium salts (LiCl, C18H35LiO2, LiAc). FT-IR, NMR, thermogravimetric (TGA), electronic universal testing, and resistivity analyses were employed to investigate the comprehensive properties of the copolymers and composites. The results of FT-IR and 1H NMR analyses revealed that the PEG was copolymerized with PA6 successfully. TGA results indicated that the decomposition temperature of the PA6-PEG copolymer was above 350°C. Resistivity testing revealed that the surface resistivity (Rs) of the copolymer decreased from 1 × 1014 to 5.67 × 109 Ω square–1 with an increase of the content of PEG. The PA6-PEG/LiCl composite showed an excellent static dissipation performance of 2.71 × 108 Ω square–1.

scholarly journals Phenotypic Characterization of Shewanella oneidensis MR-1 under Aerobic and Anaerobic Growth Conditions by Using Fourier Transform Infrared Spectroscopy and High-Performance Liquid Chromatography Analyses

2010 ◽  
Vol 76 (18) ◽  
pp. 6266-6276 ◽  
Author(s):  
Hui Wang ◽  
Katherine Hollywood ◽  
Roger M. Jarvis ◽  
Jonathan R. Lloyd ◽  
Royston Goodacre
Keyword(s):  
Ir Spectroscopy ◽  
High Performance ◽  
Shewanella Oneidensis ◽  
Anaerobic Respiration ◽  
Electron Acceptors ◽  
Redox Mediators ◽  
Ft Ir ◽  
Aerobic And Anaerobic ◽  
Ft Ir Spectroscopy

ABSTRACT Shewanella oneidensis is able to conserve energy for growth by reducing a wide variety of terminal electron acceptors during anaerobic respiration, including several environmentally hazardous pollutants. This bacterium employs various electron transfer mechanisms for anaerobic respiration, including cell-bound reductases and secreted redox mediators. The aim of this study was to develop rapid tools for profiling the key metabolic changes associated with these different growth regimes and physiological responses. Initial experiments focused on comparing cells grown under aerobic and anaerobic conditions. Fourier transform infrared (FT-IR) spectroscopy with cluster analysis showed that there were significant changes in the metabolic fingerprints of the cells grown under these two culture conditions. FT-IR spectroscopy clearly differentiated cells of S. oneidensis MR-1 cultured at various growth points and cells grown using different electron acceptors, resulting in different phenotypic trajectories in the cluster analysis. This growth-related trajectory analysis is applied successfully for the first time, here with FT-IR spectroscopy, to investigate the phenotypic changes in contrasting S. oneidensis cells. High-performance liquid chromatography (HPLC) was also used to quantify the concentrations of flavin compounds, which have been identified recently as extracellular redox mediators released by a range of Shewanella species. The partial least-squares regression (PLSR) multivariate statistical technique was combined with FT-IR spectroscopy to predict the concentrations of the flavins secreted by cells of S. oneidensis MR-1, suggesting that this combination could be used as a rapid alternative to conventional chromatographic methods for analysis of flavins in cell cultures. Furthermore, coupling of the FT-IR spectroscopy and HPLC techniques appears to offer a potentially useful tool for rapid characterization of the Shewanella cell metabolome in various process environments.

scholarly journals SYNTHESIS OF GRAFT COPOLYMER FROM ETHYL METHACRYLATE ONTO DELIGNIFIED GREWIA OPTIVA FIBER

2021 ◽  
pp. 350-365
Author(s):  
Vivek Nandani ◽  
Kinnari Trived
Keyword(s):  
Ascorbic Acid ◽  
Graft Copolymer ◽  
Gravimetric Analysis ◽  
Electron Microscopic ◽  
Reaction Conditions ◽  
Ethyl Methacrylate ◽  
Grewia Optiva ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

Ethyl methacrylate was grafted onto delignified Grewia optiva fiber using ascorbic acid/H2O2 as redox initiators in an aqueous medium. The reaction variables including concentration of ascorbic acid, H2O2, monomer and amount of backbone as well as time and temperature have been varied for establishing grafting. The influence of these reaction conditions on the grafting yield has been discussed. The overall activation energy of grafting has been calculated. The FT-IR spectroscopy, Thermal Gravimetric Analysis (TGA) and Scanning Electron Microscopic (SEM) techniques have been used for the characterization of graft copolymer.

scholarly journals Synthesis and characterization of four N-acylhydrazones as potential O,N,O donors for Cu2+: An experimental and theoretical study

2021 ◽  
Vol 26 (2) ◽  
Author(s):  
Dorian Polo-Cerón ◽  
María Mercedes Hincapié-Otero ◽  
Andrey Joaqui-Joaqui
Keyword(s):  
Organic Molecules ◽  
2D Nmr ◽  
Spectroscopic Techniques ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir ◽  
Multistep Procedure ◽  
Good Agreement ◽  
Ft Ir Spectroscopy

N-acylhydrazones 2-(4-chlorophenyl)-N0 -(2-hydroxybenzylidene)acetohydrazide, N0 -(2-hydroxybenzylidene)-2-(4-methoxyphenyl)acetohydrazide, 2-(4-chlorophenyl)-N0 -(2,4-dihydroxybenzylidene)-acetohydrazide, and N0 -(2,4-dihydroxybenzylidene)-2-(4-methoxyphenyl)acetohydrazide were successfully synthesized by a multistep procedure. The obtained organic molecules were characterized by spectroscopic techniques (FT-IR, 1D and 2D NMR, UV-Vis) and mass spectrometry. The structure of 2-(4-chlorophenyl)-N0 -(2-hydroxybenzylidene)acetohydrazide was also confirmed by X-ray diffraction. Ab initio computational simulations of the ligand spectra were in good agreement with experimental data and validated the hypothesis about the existence of a conformational mixture of each ligand in solution. Finally, the complexation potential of the synthesized ligands to Cu2+ was assessed by continuous variation experiments and FT-IR spectroscopy.

scholarly journals Synthesis and Structural Characterization of (E)-4-[(2-Hydroxy-3-methoxybenzylidene)amino]butanoic Acid and Its Novel Cu(II) Complex

Molbank ◽  
10.3390/m1179 ◽  
2021 ◽  
Vol 2021 (1) ◽  
pp. M1179
Author(s):  
Eleftherios Halevas ◽  
Antonios Hatzidimitriou ◽  
Barbara Mavroidi ◽  
Marina Sagnou ◽  
Maria Pelecanou ◽  
...  
Keyword(s):  
Schiff Base ◽  
Gamma Aminobutyric Acid ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
Polymeric Compound ◽  
Bridging Ligands ◽  
1H And 13C Nmr ◽  
One Dimensional ◽  
Ft Ir

A novel Cu(II) complex based on the Schiff base obtained by the condensation of ortho-vanillin with gamma-aminobutyric acid was synthesized. The compounds are physico-chemically characterized by elemental analysis, HR-ESI-MS, FT-IR, and UV-Vis. The complex and the Schiff base ligand are further structurally identified by single crystal X-ray diffraction and 1H and 13C-NMR, respectively. The results suggest that the Schiff base are synthesized in excellent yield under mild reaction conditions in the presence of glacial acetic acid and the crystal structure of its Cu(II) complex reflects an one-dimensional polymeric compound. The molecular structure of the complex consists of a Cu(II) ion bound to two singly deprotonated Schiff base bridging ligands that form a CuN2O4 chelation environment, and a coordination sphere with a disordered octahedral geometry.

Sign in / Sign up

Export Citation Format

Share Document