scholarly journals Microwave-Promoted Synthesis of Sulfonated Metallophthalocyanines and Aggregation in Different Solvents

2015 ◽  
Vol 2015 ◽  
pp. 1-6
Author(s):  
Zhenhua Cheng ◽  
Na Cui ◽  
Shengjuan Jiang ◽  
Hongxiao Zhang ◽  
Lijun Zhu ◽  
...  

Five metallosulfophthalocyanines (Fe, Ni, Zn, Co, and Cu) compounds were synthesized by microwave irradiation. Compared to the conventional method of synthesis in terms of reaction time and yields, the microwave-promoted synthesis is preferred with high product yield and short reaction time. All synthesized products were characterized with MALDI-TOF mass spectrum, Fourier transform infrared spectroscopy (FT-IR), ultraviolet-visible spectroscopy (UV-Vis), and X-ray diffraction (XRD). Aggregation behavior of the five metallosulfophthalocyanines (MSPc) in different solvents was studied by UV-Vis spectroscopy separately in N,N-dimethyl formamide (DMF) and NaOH aqueous solution (5%wt). A redshift of maximum absorption wavelength and deviations from Lambert-Beer law with increasing the concentration were observed. The dimerization equilibrium constants (K) of the five MSPc were determined, respectively.

2020 ◽  
Vol 1 (4) ◽  
pp. 22-25
Author(s):  
Azwan Morni

This study reports a green method for the synthesis of gold nanoparticles (AuNPs) using the aqueous extract of Salix aegyptiaca extract. The effects of gold salt concentration, extract concentration and extract quantity were investigated on nanoparticles synthesis. Novel methods of ideally synthesizing AuNPs are thus thought that are formed at ambient temperatures, neutral pH, low costs and environmentally friendly fashion. AuNPs were characterized with different techniques such as UV–vis spectroscopy, FT-IR spectroscopy, X-ray diffraction, and TEM. FT-IR spectroscopy revealed that gold nanoparticles were functionalized with biomolecules that have primary carbonyl group, -OH groups and other stabilizing functional groups. TEM experiments showed that these nanoparticles are formed with various shapes and X-ray diffraction pattern showed high purity and face centered cubic structure of AuNPs. For electrochemical properties of AuNPs, a modified glassy carbon electrode using AuNPs (AuNPs/GCE) was investigated. The results show that electronic transmission rate between the modified electrode and [Fe (CN)6]3-/4- increased.


2018 ◽  
Vol 15 (1) ◽  
pp. 73-80 ◽  
Author(s):  
Baghdad Science Journal

Polyaniline membranes of aniline were produced using an electrochemical method in a cell consisting of two poles. The effect of the vaccination was observed on the color of membranes of polyaniline, where analysis as of blue to olive green paints. The sanction of PANI was done by FT-IR and Raman techniques. The crystallinity of the models was studied by X-ray diffraction technique. The different electronic transitions of the PANI were determined by UV-VIS spectroscopy. The electrical conductivity of the manufactured samples was measured by using the four-probe technique at room temperature. Morphological studies have been determined by Atomic force microscopy (AFM). The structural studies have been measured by (SEM).


2015 ◽  
Vol 33 (1) ◽  
pp. 163-168 ◽  
Author(s):  
Nitin R. Dighore ◽  
Priyanka L. Anandgaonker ◽  
Suresh T. Gaikwad ◽  
Anjali S. Rajbhoj

AbstractCrystalline MoO3 nanoparticles were obtained by electrochemical synthesis process using tetrapropylammonium bromide as a stabilizer and structure-directing agent in ACN:THF(4:1) solvent. Formation of MoO3 nanoparticles took place at a constant supply current of 14 mA/cm2. These synthesized MoO3 nanoparticles were characterized by UV-Vis spectroscopy, FT-IR spectroscopy, powder X-ray diffraction (XRD), scanning electron microscopy (SEM). So prepared MoO3 nanoparticles were used as a heterogeneous catalyst for the synthesis of 2,6-bis(benzylidene)cyclohexanone derivatives. This protocol offers several advantages, such as simple work-up procedure, recyclability of the catalyst, excellent product yield in a short reaction time and purification of products with a non-chromatographic method.


Polymers ◽  
2019 ◽  
Vol 11 (9) ◽  
pp. 1498 ◽  
Author(s):  
Abdul Hafeez ◽  
Zareen Akhter ◽  
John F. Gallagher ◽  
Nawazish Ali Khan ◽  
Asghari Gul ◽  
...  

Bis-aldehyde monomers 4-(4′-formyl-phenoxy)benzaldehyde (3a), 3-methoxy-4-(4′-formyl-phenoxy)benzaldehyde (3b), and 3-ethoxy-4-(4′-formyl-phenoxy)benzaldehyde (3c) were synthesized by etherification of 4-fluorobenzaldehyde (1) with 4-hydroxybenzaldehyde (2a), 3-methoxy-4-hydroxybenzaldehyde (2b), and 3-ethoxy-4-hydroxybenzaldehyde (2c), respectively. Each monomer was polymerized with p-phenylenediamine and 4,4′-diaminodiphenyl ether to yield six poly(azomethine)s. Single crystal X-ray diffraction structures of 3b and 3c were determined. The structural characterization of the monomers and poly(azomethine)s was performed by FT-IR and NMR spectroscopic techniques and elemental analysis. Physicochemical properties of polymers were investigated by powder X-ray diffraction, thermogravimetric analysis (TGA), viscometry, UV–vis, spectroscopy and photoluminescence. These polymers were subjected to electrical conductivity measurements by the four-probe method, and their conductivities were found to be in the range 4.0 × 10−5 to 6.4 × 10−5 Scm−1, which was significantly higher than the values reported so far.


2019 ◽  
Vol 37 (3) ◽  
pp. 304-309
Author(s):  
Azeezaa Varsha Mohammed ◽  
Suresh Sagadevan

AbstractL-cysteine hydrogen fluoride (LCHF) single crystals were grown from aqueous solution. Single crystal X-ray diffraction, FT-IR, UV-Vis-NIR, and TG-DTA were used to test the grown crystals. The specimen dielectric and mechanical behaviors were also studied. Powder X-ray diffraction of the grown crystal was recorded and indexed. The optical properties of the LCHF crystal were determined using UV-Vis spectroscopy. It was found that the optical band gap of LCHF was 4.8 eV. The crystal functional groups were identified using FT-IR. Second harmonic generation (SHG) efficiency of the LCHF was three times higher than that of KDP. The dielectric constant, dielectric loss and AC conductivity were measured at different frequencies and temperatures.


2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
G. Sathiyadevi ◽  
B. Loganathan ◽  
B. Karthikeyan

The solvent-mediated eco-friendly monodispersed Ag/Pd bimetallic nanocomposites (BNCs) having thick core and thin shell have been prepared through novel green chemical solvent reduction method. Reducing solvent, dimethyl formamide (DMF) is employed for the controlled green synthesis. Characterization of the synthesized Ag/Pd BNCs has been done by x-ray diffraction (XRD) studies, high-resolution scanning electron microscopy (HR-SEM), energy-dispersive X-ray analysis (EDX), and high-resolution transmission electron microscopy (HR-TEM) with selected area electron diffraction (SAED) pattern. The nature of the interaction of L-cysteine with Ag/Pd BNCs has been studied by using surface plasmon spectroscopy, Fourier transform-infrared spectroscopy (FT-IR), cyclic voltammetry (CV), and theoretical methods.


2010 ◽  
Vol 658 ◽  
pp. 109-112 ◽  
Author(s):  
Hyun Soo Lee ◽  
Byung Ha Lee

The aim of the present investigations was to synthesize pigments based on Ni-doped forsterite (Mg2SiO4) for high temperature underglaze colors by ceramic route. In forsterite Mg2+ can be replaced by Fe2+, Ni2+, Co2+ ion since their ionic radious are close or coincide. NiO doped forsterite green pigments pigments were prepared by ceramic method from mixture of MgO and SiO2 and H3BO3 as mineralizer and the colour properties of the pigments was also investigated. In this experiment, very brilliant and fluorescent light green color hue of pigment was obtained at 1300°C for 3 hours. According to various firing condition, crystalline structure of pigments were chracterised by X-ray diffraction and FT-IR, Raman spectroscopy. And their color characterization were analized by UV-Vis spectroscopy on the ground of CIE L*a*b* measurement.


2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Murugan Saranya ◽  
Chella Santhosh ◽  
Rajendran Ramachandran ◽  
Andrews Nirmala Grace

CuS nanostructures have been successfully synthesized by hydrothermal route using copper nitrate and sodium thiosulphate as copper and sulfur precursors. Investigations were done to probe the effect of cationic surfactant, namely, Cetyltrimethylammonium bromide (CTAB) on the morphology of the products. A further study has been done to know the effect of reaction time on the morphology of CuS nanostructures. The FE-SEM results showed that the CuS products synthesized in CTAB were hexagonal plates and the samples prepared without CTAB were nanoplate like morphology of sizes about 40–80 nm. Presence of nanoplate-like structure of size about 40–80 nm was observed for the sample without CTAB. The synthesized CuS nanostructures were characterized by X-ray diffraction (XRD), FE-SEM, DRS-UV-Vis spectroscopy, and FT-IR spectroscopy. A possible growth mechanism has been elucidated for the growth of CuS nanostructures.


2014 ◽  
Vol 926-930 ◽  
pp. 270-273
Author(s):  
Zhen Hua Cheng ◽  
Na Cui ◽  
Hong Xiao Zhang ◽  
Li Jun Zhu ◽  
Dao Hong Xia

Zinc phthalocyanine was prepared with improved method with high yields and characterized by XRD and FT-IR analysis. The SEM analysis was also conducted to demonstrate the apparent morphology of the synthesized compound. Dimerization of the zinc phthalocyanine was measured by UV-Vis spectroscopy in N, N-dimethyl formamide (DMF). The red–shift of maximum absorption wavelength and deviation from Lambert-Beer law was observed with increasing the concentration.


2021 ◽  
Author(s):  
Faiza Lughmani ◽  
Farzana Nazir ◽  
Shahid Ali Khan ◽  
Mudassir Iqbal

Abstract In this study, microcrystalline cellulose (MCC) was modified to oxidized cellulose (OC), 6-deoxycellulose hydrazide and 6-deoxycellulose(N,N-diethyl)amine (MCC-Hyd and MCC-DEM) derivatives and employed as supporting material for the synthesis of copper nanoparticles (NPs). Copper ions from aqueous solution were adsorbed and then reduced to zero valent copper (ZVC) NPs using sodium borohydride on films of prepared derivatives. The characterization of prepared derivatives and Cu NPs embedded films was performed using Fourier Transform Infrared Spectroscopy (FT-IR), Elemental analysis, X-ray diffraction (XRD), Scanning Electron Microscopy (SEM) and Nuclear Magnetic Resonance (NMR) spectroscopy. Ultraviolet/Visible (UV-VIS) spectroscopy was performed for the degradation studies of 4-nitrophenol (4-NP) and various azo dyes viz. Congo Red (CR), Methylene Blue (MB), and Methyl orange (MO). Results revealed that all the films showed degradation only in the presence of ZVC NPs. Oxidized cellulose, MCC-Hyd and MCC-DEM showed excellent degradation efficiencies (> 85%) in all the cases. Our findings revealed that MCC derivatives could be efficient and renewable candidates for removal of water pollutants in future.


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