Synthesis and Characterization of Poly(N-Arylenebenzimidazole Ketone)

2012 ◽  
Vol 204-208 ◽  
pp. 4211-4214 ◽  
Author(s):  
Ye Wei Xu ◽  
Jie Tang ◽  
Guan Jun Chang ◽  
Fang Hua Zhu ◽  
Lin Zhang
Keyword(s):  
Weight Loss ◽  
Chemical Structure ◽  
Synthesis And Characterization ◽  
The Novel ◽  
Displacement Reaction ◽  
Good Solubility ◽  
Nucleophilic Displacement ◽  
Ft Ir ◽  
Good Agreement

Using 1,4-bis(2-benzimidazolyl) benzene (BBIB) and 4,4'-difluorobenzophenone as the monomers, poly(N-arylenebenzimidazole ketone) (PNABIK) has been prepared via the aromatic nucleophilic displacement reaction. The chemical structure of PNABIK was confirmed by FT-IR, elemental analysis and 1H NMR. The results show a good agreement with the proposed structures. The polymer was obtained in quantitative yields with Mn value 12500 and Mw value 28600, respectively. DSC and TGA measurements show that the glass transition temperature (Tg) is 202 °C and 5% weight loss temperature is 550°C in nitrogen and 571 °C in air, respectively. In addition, the novel polymer exhibit good solubility.

Synthesis and Characterization of Poly(N-arylenebenzimidazole sulfone)

2012 ◽  
Vol 174-177 ◽  
pp. 473-477
Author(s):  
Ye Wei Xu ◽  
Jie Tang ◽  
Guan Jun Chang ◽  
Fang Hua Zhu ◽  
Lin Zhang
Keyword(s):  
Nmr Spectroscopy ◽  
Chemical Structure ◽  
Polyphosphoric Acid ◽  
High Resolution Mass Spectrometry ◽  
Gel Permeation Chromatography ◽  
The Novel ◽  
Good Solubility ◽  
Nucleophilic Displacement ◽  
Ft Ir

Poly(N-arylenebenzimidazole sulfone), PNABIS, has been prepared via the aromatic nucleophilic displacement reaction of 1,4-bis(2-benzimidazolyl) benzene (BBIB) with bis(4-fluorophenyl) sulfone. BBIB was synthesized by the reaction of terephthalaldehydic acid with 1,2-phenylenediamine in polyphosphoric acid. The chemical structure of BBIB was confirmed by FT-IR, high resolution mass spectrometry (HRMS) and NMR spectroscopy. The characterization of the polymer was performed with FT-IR, NMR spectroscopy, gel permeation chromatography (GPC), thermogravimetric analysis (TGA) and solubility tests. The polymer was obtained in quantitative yield with Mn value 11000 and Mw value 25300, respectively. TGA measurements show that 5% weight loss temperature is 532 °C in nitrogen and 331 °C in air, respectively. In addition, the novel polymer exhibits good solubility, which can be dissolved in common organic solvent at room temperature.

Synthesis and Characterization of Novel Degradable Responsive Polyurethane Microsphere

2013 ◽  
Vol 750-752 ◽  
pp. 1271-1275 ◽  
Author(s):  
Lian Hai Shan ◽  
Yuan Yuan Cui ◽  
Shuai Huang ◽  
Zhi Bin Zhang
Keyword(s):  
Drug Delivery ◽  
Molecular Weight ◽  
Chemical Structure ◽  
Solvent Polarity ◽  
Toluene Diisocyanate ◽  
Synthesis And Characterization ◽  
The Novel ◽  
Swelling Ratio ◽  
Swelling Properties

The present study describes degradable polyurethane (PU) microspheres fabricated using toluene diisocyanate, polycaprolactone, polyethylene glycol, 2, 2-hydroxymethyl-2-propionic acid and triethylamine for drug delivery. The novel microspheres were synthesized using self-emulsion and condensed phase separation method. Fourier-Transform Infrared Spectrum analysis (FTIR) was performed revealing the chemical structure of polyurethane microspheres with special chains changing. Swelling properties influenced by solvent polarity, PEG content, PEG molecular weight, were evaluated, suggesting that the swelling ratio (SR) of PU microspheres increased with the increase in solvent polarity, PEG content and PEG molecular weight respectively.

Synthesis and Characterization of Temperature-Sensitive TSPU/PNIPAAm Semi-IPN Polymer

2011 ◽  
Vol 399-401 ◽  
pp. 359-362 ◽  
Author(s):  
Yi Chun Wang ◽  
Zheng Wei Dai ◽  
Yuan Xue
Keyword(s):  
Chemical Structure ◽  
In Situ Polymerization ◽  
Phenyl Isocyanate ◽  
Chain Extender ◽  
Synthesis And Characterization ◽  
Temperature Sensitive ◽  
Sensitive Material ◽  
Ft Ir

Thermo-sensitive polyurethane (TSPU) was synthesized from poly(ε-caprolactone) and 4,4’-methylenebis (phenyl isocyanate) by a two-step process with 1,4-butanediol as the chain extender. Following that, a novel temperature-sensitive material was created by the strategy of IPN from TSPU and PNIPAAm in the method of in situ polymerization. The chemical structure and thermo properties of the semi-IPN were characterized with FT-IR and DSC. The results prove that intensive inter-molecular interactions exist between TSPU and PNIPAAm chains, which have significant influence on the phase transition behaviors of the material. According to these results, the transition temperature of the semi-IPN can be adjusted in the range of 30~40 °C by controlling the composition of TSPU and the semi-IPNs.

Synthesis and characterization of novel tetrakis (3-hydroxypropylmercapto)-substituted phthalocyanines

2013 ◽  
Vol 17 (06n07) ◽  
pp. 573-586 ◽  
Author(s):  
Çiğdem Yağcı ◽  
Ahmet Bilgin
Keyword(s):  
Differential Scanning Calorimetry ◽  
Thermal Properties ◽  
Synthesis And Characterization ◽  
The Novel ◽  
Scanning Calorimetry ◽  
Metal Free ◽  
Visible Spectra ◽  
Ft Ir ◽  
Aromatic Nitro

A phthalonitrile precursor 4-(3-hydroxypropylmercapto)phthalonitrile (3) was synthesized via a base-catalyzed nucleophilic aromatic nitro displacement of 4-nitrophthalonitrile with the 3-mercapto-1-propanol. A novel tetrasubstituted metal-free phthalocyanine (4) ( M = 2 H ) and its metal complexes (5–8) ( M = Zn , Ni , Cu and Co ) bearing 3-hydroxypropylmercapto moieties were prepared by the cyclotetramerization reaction of (3) with the appropriate materials. The visible spectra of the zinc(II) phthalocyanine (5) was recorded with different concentrations and different ions as Ag +, Hg 2+ and Pb 2+ in DMF and also with different solvents as dimethylformamide and pyridine. Fluorescence spectrum of the compound (5) was also studied. Temperature and frequency dependence of AC conductivity for (4–8) was investigated in air and under vacuum and were found to be ~10-8–10-5 S.m-1. Thermal properties of the phthalocyanines were examined by differential scanning calorimetry. All the novel compounds have been characterized by elemental analysis, UV-vis, FT-IR, NMR and MS spectral data and DSC techniques.

SYNTHESIS AND CHARACTERIZATION OF A RODLIKE LIQUID CRYSTALLINE POLYURETHANE OLIGOMER

2010 ◽  
Vol 03 (03) ◽  
pp. 169-172
Author(s):  
CHUN WEI ◽  
QIU-SHAN GAO ◽  
YONG-YANG GONG ◽  
XUE-MEI XIONG ◽  
XIN SHEN
Keyword(s):  
Weight Loss ◽  
Liquid Crystalline ◽  
Room Temperature ◽  
Decomposition Temperature ◽  
Synthesis And Characterization ◽  
Smectic A ◽  
Smectic A Phase ◽  
Ft Ir ◽  
Dimethylformamide Solution

A novel rodlike liquid crystalline polyurethane (LCPU) oligomer was synthesized by polyaddition of hexane-1,6-diylbis(4-hydroxybenzoate) with toluene 2,4-diissocyanate in N, N′-dimethylformamide solution. The properties of the LCPU oligomer were investigated by FT-IR, DSC, TGA, POM, WAXD and SEM. The LCPU oligomer was a yellow powder at room temperature, which maintained a stable rodlike microstructure below its melting point, and had high crystallinity. The LCPU oligomer exhibited thermotropic liquid crystalline properties between 166–183°C, and the smectic-A phase with focal conic fan textures at the liquid crystal state was observed by POM. The decomposition temperature of the LCPU oligomer at 5% weight loss was 282°C.

Synthesis and Characterization of the Water-Soluble Oleoyl Acetyl Chitosan

2011 ◽  
Vol 284-286 ◽  
pp. 1782-1785
Author(s):  
Wei Chang Ke ◽  
Yi Kun Chen ◽  
Guo Xi Xiong ◽  
Xiang Hong Peng ◽  
Chao Zhu ◽  
...  
Keyword(s):  
Oleic Acid ◽  
Acetic Anhydride ◽  
Chemical Structure ◽  
Water Soluble ◽  
Synthesis And Characterization ◽  
Nmr Spectrum ◽  
Ft Ir ◽  
Oleoyl Chloride ◽  
C Nmr

Oleoyl chloride was synthesized by oleic acid and thionyl dichloride (SOCl2), and then reacted with chitosan in dichloromethane to obtain the oleoyl chitosan. Novel water-soluble oleoyl acetyl chitosan (OACh) was synthesized using oleoyl chloride reacted with acetic anhydride in pyridine. The chemical structure of the OACh was characterized by FT-IR, 1H and 13C NMR. There existed the peaks at 1743.9 cm-1 (C=O) and 1658.1 cm-1(C=C) in FT-IR spectrum, and the peaks at 170.8, 171.6 and 172.5 ppm which were assigned to the C=O of the oleoyl and acetyl groups in 13C NMR spectrum. The results indicated that OACh had oleoyl as hydrophobic moieties and acetyl as hydrophilic moieties.

scholarly journals Fabrication and Characterization of Functional pH-Responsive Poly (S-Co-DEAMVA)-g-Tryptophan

2021 ◽  
pp. 9-19
Author(s):  
Momen S. A. Abdelaty
Keyword(s):  
1H Nmr ◽  
Chemical Structure ◽  
Aldehyde Group ◽  
Biological Molecules ◽  
Ph Responsive ◽  
Investigation Methods ◽  
Vis Spectroscopy ◽  
Ft Ir ◽  
Good Agreement

Vanillin was used to synthesize cationic monomers from the amine group with a tertiary amine. It has both an amine and an aldehyde group. For that, it helps graft to form Schiff base with amino acid-like tryptophan. It is abbreviated by {2-[(diethylamino) methyl]-4-formyl-6-methoxyphenyl acrylate} DEAMVA and evaluated by, e.g., 1H NMR, 13C NMR, and FT IR results were compared with the chemical structure elevated good agreement. 10 and 25 mol % of vanillin monomer was copolymerized with (S). The copolymers of poly (S-co-DEAMVA) were investigated by 1H NMR, FTIR, GPC, and DSC. The grafting with tryptophan has also been modified and exposed to the same investigation methods; further, UV/Vis spectroscopy has designated the pH responsiveness. The study aims to improve the general characterization of polystyrene and produce functional pH-responsive polymer for graft biological molecules in the future.

scholarly journals SYNTHESIS AND CHARACTERIZATION OF BOC-PROTECTED THIO-1,3,4-OXADIAZOL-2-YL DERIVATIVES

2021 ◽  
pp. 5-10
Author(s):  
S. SYED SHAFI ◽  
R. RAJESH ◽  
S. SENTHILKUMAR
Keyword(s):  
Photoluminescence Spectrum ◽  
Chemical Structure ◽  
Phenylacetic Acid ◽  
Industrial Applications ◽  
Powder Xrd ◽  
Synthesis And Characterization ◽  
The Novel ◽  
Structural And Optical Properties ◽  
Good Thermal Stability

Objective: The objective of this work is to synthesis thio-1,3,4-oxadiazol-2-yl derivatives for industrial applications. Methods: The synthesis was done by the reaction of (S)-2-amino-2-phenylacetic acid with ethanol-derived ethyl (S)-2-amino-2-phenylacetate. The reaction of ethyl (S)-2-amino-2-phenylacetate with Boc anhydride and hydrazine produces ethyl (S)-2-((tert-butoxycarbonyl)amino)-2-phenylacetate. The intermediate 5-alkyl amino-1,3,4-oxadiazole-2-thiols have been isolated as stable compounds. Results: To study the characteristics of these compounds, they are subjected to 1HNMR, 13CNMR, and IR. These studies examine the chemical structure of synthesized compounds. The mass of the novel compounds was established with the help of the LCMS test. The structural and optical properties were examined by the powder XRD and photoluminescence spectrum respectively. Conclusion: The sharp intense peak in the powder XRD indicates the crystal nature of the sample. The values obtained from the LCMS test indicate that the compounds have good thermal stability. The absorption peak at 358 nm in the PL spectrum indicates that the sample can be used in photoelectronic devices.

Synthesis and Characterization of a New Thermosetting Boric Acid Ester

2011 ◽  
Vol 239-242 ◽  
pp. 1907-1910
Author(s):  
Jian Zhang ◽  
Jia Liu
Keyword(s):  
Weight Loss ◽  
Thermal Properties ◽  
Thermogravimetric Analysis ◽  
Boric Acid ◽  
Acid Ester ◽  
Hydrolytic Stability ◽  
Synthesis And Characterization ◽  
Boric Acid Ester ◽  
Ft Ir

A new thermosetting boric acid ester modifier containing unsaturated bonds (abbreviated TBCE) was prepared. Structure, hydrolytic stability, curing properties and and thermal properties of the boric acid ester were studied by FT-IR, DSC and TGA. The result indicated that the obtained boric acid ester was soluble in most common solvents and was easily processed. The thermogravimetric analysis of silicon-containing arylacetylene resin modified by TBSE (abbreviated MSAR) showed that char yield at 800°C was 87% under nitrogen and 49% under air, and Td5(temperature of 5% weight loss) were 570°C and 580°C respectively.

Preparation and Characterization of Soybean Oil-based Flame Retardant Rigid Polyurethane Foams Containing Phosphaphenanthrene Groups

2020 ◽  
Vol 17 (10) ◽  
pp. 760-771
Author(s):  
Qirui Gong ◽  
Niangui Wang ◽  
Kaibo Zhang ◽  
Shizhao Huang ◽  
Yuhan Wang
Keyword(s):  
Soybean Oil ◽  
Flame Retardant ◽  
Chemical Structure ◽  
Cell Structure ◽  
Polyurethane Foams ◽  
Limiting Oxygen Index ◽  
Rigid Polyurethane Foams ◽  
Degradation Activation Energy ◽  
Ft Ir

A phosphaphenanthrene groups containing soybean oil based polyol (DSBP) was synthesized by epoxidized soybean oil (ESO) and 9,10-dihydro-oxa-10-phosphaphenanthrene-10-oxide (DOPO). Soybean oil based polyol (HSBP) was synthesized by ESO and H2O. The chemical structure of DSBP and HSBP were characterized with FT-IR and 1H NMR. The corresponding rigid polyurethane foams (RPUFs) were prepared by mixing DSBP with HSBP. The results revealed apparent density and compression strength of RPUFs decreased with increasing the DSBP content. The cell structure of RPUFs was examined by scanning electron microscope (SEM) which displayed the cells as spherical or polyhedral. The thermal degradation and flame retardancy of RPUFs were investigated by thermogravimetric analysis, limiting oxygen index (LOI), and UL 94 vertical burning test. The degradation activation energy (Ea) of first degradation stage reduced from 80.05 kJ/mol to 37.84 kJ/mol with 80 wt% DSBP. The RUPF with 80 wt% DSBP achieved UL94 V-0 rating and LOI 28.3. The results showed that the flame retardant effect was mainly in both gas phase and condensed phase.

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