Heat Resistant Poly(amide-imide)s Derived from N,N′-(4,4′-Pyromellitoyl)-bis-L-phenyl Acetic Acid and Aromatic Diamines: Synthesis and Properties

2013 ◽  
Vol 32 (1) ◽  
pp. 51-57
Author(s):  
Khalil Faghihi ◽  
Mohsen Hajibeygi

AbstractSix new heat resistant and optically active poly(amide-imide)s 5a–f were prepared by the direct polycondensation reaction of N,N′-(4,4′-pyromellitoyl)-bis-L-phenyl acetic acid 3 with various different diamines 4a–f in a medium consisting of triphenyl phosphite, N-methyl-2-pyrrolidone, pyridine and calcium chloride. These polymers were obtained in high yields and had inherent viscosities between 0.35–0.50 dL/g. The resulting polymers were characterized by viscosity measurements, thermal gravimetric analysis (TGA and DTG), differential scanning calorimeter (DSC), solubility test, specific rotation, FT-IR and 1H NMR spectroscopy. N,N′-(4,4′-pyromellitoyl)-bis-L-phenyl acetic acid 3 was prepared by an one-stop reaction of pyromellitic anhydride 1 with L-phenyl acetic acid 3 in acetic acid solution in quantitative yield.

e-Polymers ◽  
2009 ◽  
Vol 9 (1) ◽  
Author(s):  
Khalil Faghihi ◽  
Meisam Shabanian ◽  
Mohsen Hajibeygi

AbstractNew optically active aromatic poly(amide-imide)s (PAIs) were prepared from newly synthesized N,N΄-(bicyclo[2,2,2]oct-7-ene-2,3,5,6-tetracrboxylic)-bis-Lvaline diacid (4) via polycondensation with various aromatic diamines. The diacid (4) was synthesized by the condensation reaction of bicyclo[2,2,2]oct-7-ene- 2,3,5,6-tetracarboxylic dianhydride (1) with L-valine (2) in acetic acid. All polymers were obtained in quantitative (high) yields with inherent viscosities of 0.24-0.36 dL/g. All of these polymers were highly organosoluble in solvents like N-methyl-2- pyrrolidone (NMP), dimethylformamide (DMF), N,N'-dimethylacetamide (DMAc) and dimethylsulfoxide (DMSO) at room temperature and were fully characterized by means of NMR spectroscopy, FTIR spectroscopy, elemental analyses, inherent viscosity, solubility test, specific rotation and thermal properties of the poly(amideimide) s were investigated using TGA/DTG.


1965 ◽  
Vol 43 (5) ◽  
pp. 1306-1317 ◽  
Author(s):  
Allan S. Hay ◽  
Harry S. Blanchard

Cobalt acetate bromide in acetic acid solution is an extraordinarily active catalyst for the autoxidation of hydrocarbons. Carboxylic acids and ketones are readily prepared in high yields at moderate temperatures and at atmospheric pressure. In addition, benzylic and allylic groups can be converted to esters of the corresponding alcohols, and the oxidation of tetralin can be controlled to give either α-tetralone or 1,2-dihydronaphthalene as the major product. A mechanism for these reactions is postulated.


2007 ◽  
Vol 85 (12) ◽  
pp. 1070-1074 ◽  
Author(s):  
Kirill A Kolmakov

Two reaction pathways in acetic acid solution containing cyanuric chloride, aniline, and some hydrogen chloride acceptors (triethylamine, sodium acetate, pyridine) were studied. Both aryl amination and acylation can be performed with high yields under proper reaction conditions. Contrary to the only known literature report on the reactions between carbonic acids and cyanuric chloride in the presence of a hydrogen chloride acceptor (triethylamine), it was established that acid chlorides are not formed. A scheme involving the replacement of chlorine atoms by acetate ion in the initial stage was proposed for the acylation of aniline promoted by cyanuric chloride.Key words: acetic acid, acylation, aniline, cyanuric chloride, aryl amination.


2016 ◽  
Vol 10 (2) ◽  
pp. 135-139 ◽  
Author(s):  
Valentina Chernova ◽  
◽  
Angela Shurshina ◽  
Elena Kulish ◽  
Gennady Zaikov ◽  
...  

Some ways of estimating the values of the intrinsic viscosity of chitosan were analyzed. It was shown that the method of Irzhak and Baranov for estimating the current value of the intrinsic viscosity allows to adequately estimates the conformational state of the macromolecular coil and its degree of swelling.


2019 ◽  
Author(s):  
Jingjing Yan ◽  
Rick Homan ◽  
Corrianna Boucher ◽  
Prem N. Basa ◽  
Katherine Fossum ◽  
...  

Recently, we demonstrated that triphenylacetic acid could be used to seal dye molecules within MOF-5, but guest release required digestion of the framework by treatment with acid. We prepared the sterically bulky photocapping group [bis-(3-nitro-benzyl)-amino]-(3-nitro-phenyl)-acetic acid (PC1) can prevent Crystal violet dye diffusion from inside MOF-5 until removed by photolysis.


2019 ◽  
Author(s):  
Jingjing Yan ◽  
Rick Homan ◽  
Corrianna Boucher ◽  
Prem N. Basa ◽  
Katherine Fossum ◽  
...  

Recently, we demonstrated that triphenylacetic acid could be used to seal dye molecules within MOF-5, but guest release required digestion of the framework by treatment with acid. We prepared the sterically bulky photocapping group [bis-(3-nitro-benzyl)-amino]-(3-nitro-phenyl)-acetic acid (PC1) can prevent Crystal violet dye diffusion from inside MOF-5 until removed by photolysis.


2018 ◽  
Vol 69 (2) ◽  
pp. 297-299
Author(s):  
Adriana Nita ◽  
Delia Mirela Tit ◽  
Lucian Copolovici ◽  
Carmen Elena Melinte (Frunzulica) ◽  
Dana Maria Copolovici ◽  
...  

The aim of this study was to develop and validate a rapid, accurate, and exact method for the quantitative determination of famotidine in pharmaceutical products. The HPLC analyses were performed by using a mobile phase containing methanol:1% acetic acid solution=30:7 (v/v), at a flow rate of 0.4 mL/min.The total time of the method was 10 min, and the retention time of famotidine was 4.16 min. The detection was evaluated at l=267 nm. The method has been validated by using different validation parameters. The linear response of the detector for famotidine peak area was observed at concentrations ranging from 0.1 to 0.0001 mg mL-1 , resulting in a correlation coefficient of 0.99998. The values of the detection limit and of the quantification limit are 0.00048 mg mL-1 and 0.00148 mg mL-1, respectively. The method proposed allowed accurate (with a relative error of less than 2%) and precise (RSD values less than 2.0%) determination of famotidine content in pharmaceutical products and can be used for its rapid quantitative analysis.


BMC Chemistry ◽  
2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Arefeh Dehghani Tafti ◽  
Bi Bi Fatemeh Mirjalili ◽  
Abdolhamid Bamoniri ◽  
Naeimeh Salehi

AbstractNano-eggshell/Ti(IV) as a novel naturally based catalyst was prepared, characterized and applied for the synthesis of dihydropyrano[2,3-c]pyrazole derivatives. The characterization of nano-eggshell/Ti(IV) was performed using Fourier Transform Infrared spectroscopy, X-ray Diffraction, Field Emission Scanning Electron Microscopy, Energy-Dispersive X-ray Spectroscopy, and Thermo Gravimetric Analysis. Dihydropyrano[2,3-c]pyrazoles were synthesized in the presence of nano-eggshell/Ti(IV) via a four component reaction of aldehydes, ethyl acetoacetate, malononitrile and hydrazine hydrate at room temperature under solvent free conditions. The principal affairs of this procedure are mild condition, short reaction times, easy work-up, high yields, reusability of the catalyst and the absence of toxic organic solvents.


Sign in / Sign up

Export Citation Format

Share Document