Phosphate Substituted Phosphazenes as Dispersants in Colloidal Ceramic Processing

1991 ◽  
Vol 249 ◽  
Author(s):  
Sarah D. Burton ◽  
William D. Samuels ◽  
Gregory J. Exarhos
Keyword(s):  
Raman Spectroscopy ◽  
31P Nmr ◽  
Synthesis And Characterization ◽  
Ceramic Processing ◽  
Reaction Conditions ◽  
Solution State

ABSTRACTA new phosphate substituted phosphazene trimer [N3P3Cl5(OP(O)Ph2)] has been synthesized and characterized by 31p NMR and Raman spectroscopy. The course of each solution-state substitution was followed with 31P NMR, and this technique was used to determine the best reaction conditions for the experiment. Information such as phosphorus to phosphorus connectivity and purity were analyzed. This paper will discuss the synthesis and characterization of phosphazene moieties which are substituted by phosphorus(V) centered substituents.

Synthesis and Characterization of Substituted μ-oxo-bis[tetra-phenylporphyrinatoiron] Compounds

2015 ◽  
Vol 748 ◽  
pp. 183-186
Author(s):  
Zhi Cheng Sun ◽  
Shu Ying Chen ◽  
Zhi Peng Guo ◽  
Mei Juan Cao ◽  
Lu Hai Li
Keyword(s):  
Infrared Spectra ◽  
Elemental Analysis ◽  
Aromatic Aldehydes ◽  
Synthesis And Characterization ◽  
Visible Spectroscopy ◽  
Reaction Conditions ◽  
One Pot ◽  
Optimum Reaction ◽  
Novel Method

A novel one-pot method for the synthesis of substituted μ-oxo-bis [tetraphenyl porphyrinatoiron] compounds ([TRPPFe]2O) from pyrrole and aromatic aldehydes was proposed and investigated in this paper. Four kinds of [TRPPFe]2O were designed and synthesized by one-pot reaction and characterized by elemental analysis, infrared spectra and ultraviolet-visible spectroscopy. Moreover, the [TRPPFe]2O yields of 18.7~22.4% could be obtained with this novel method under the optimum reaction conditions.

Synthesis and Characterization of Polysulfonyldiphenylene Phenylphosphonate with High Melting Range

2011 ◽  
Vol 396-398 ◽  
pp. 2342-2345
Author(s):  
Zhong Wei Wang ◽  
Hao Dong Duan ◽  
Qing Yu
Keyword(s):  
Thermal Stability ◽  
Reaction Time ◽  
Thermogravimetric Analysis ◽  
Synthesis And Characterization ◽  
Target Product ◽  
High Melting ◽  
Melting Range ◽  
Reaction Conditions ◽  
Good Thermal Stability

Polysulfonyldiphenylene phenylphosphonate (PSPPP) with high melting range of 197 to 205 °C was synthesized via molten polycondensation method. The effect of material ratio, reaction temperature and reaction time of the method was studied, and the preferred reaction conditions were obtained. The target product was characterized by FTIR and thermogravimetric analysis (TGA) was carried out to confirm the thermal stability. The PSPPP synthesized in this paper showed fairly good thermal stability.

scholarly journals Synthesis and Characterization of Mercury(II) Complexes Containing 2,9-Dimethyl-1,10-phenanthroline by Sonochemical Method

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
M. Ranjbar ◽  
E. Malakooti ◽  
S. Sheshmani
Keyword(s):  
Thermal Analysis ◽  
Stainless Steel ◽  
Synthesis And Characterization ◽  
Particle Sizes ◽  
Sonochemical Method ◽  
Reaction Conditions ◽  
Mercury Acetate ◽  
Crystalline Complexes Of ◽  
Chemical Formulas

Synthesis and characterization of microstructured crystalline complexes of [HgI2(C14H12N2)] and [HgBr2(C14H12N2)] were carried out from the reaction between 2,9-dimethyl-1,10-phenanthroline, mercury acetate, KI, and KBr, respectively, in methanol by sonochemical method. The reaction conditions were optimized under ultrasonic irradiations and without it. Characterization of the complexes was performed by elemental analysis, XRD, SEM, FTIR, and thermal analysis (TG/DTA). The results showed that sonochemical method caused significant reduction of the reaction time. Then the products were put under supercritical condition in a Teflon-lined, stainless-steel Parr bomb container and heated at 150°C for 48 h. The results showed that the chemical formulas of the complexes were not changed; however, the particle sizes were reduced and porosity increased.

Synthesis and characterization of metallophosphazene derivatives: solution state and surface reactions

1993 ◽  
Vol 5 (9) ◽  
pp. 1307-1314 ◽  
Author(s):  
Harry R. Allcock ◽  
Eric N. Silverberg ◽  
Constance J. Nelson ◽  
William D. Coggio
Keyword(s):  
Surface Reactions ◽  
Synthesis And Characterization ◽  
Solution State

scholarly journals Synthesis and characterization of novel mono, bis and tris heteroaryl chalcone derivatives of 1,3,5-trimethoxybenzene

2021 ◽  
Vol 14 (1) ◽  
pp. 39-47
Author(s):  
M. Fatih Polat ◽  
Derya Aktaş Anı
Keyword(s):  
Elemental Analysis ◽  
High Purity ◽  
Synthesis And Characterization ◽  
Spectroscopic Techniques ◽  
Reaction Conditions ◽  
Chalcone Derivatives ◽  
Ft Ir ◽  
Derivatives Of

In this study, a new series consisting of 12 heteroaryl chalcone derivatives of 1,3,5-trimethoxybenzene were synthesised. Chalcones were synthesised in high purity and efficiency, via condensation of mono, bis and tris 2,4,6-trimethoxy acetophenones with hetero-2-carbaldehyde derivatives based on Claisen Schdmit condensation. The reactions feature a good scope for the all products, mild reaction conditions and good yields. The synthesized compounds were characterized by using FT-IR, NMR and elemental analysis spectroscopic techniques.

scholarly journals Synthesis and characterization of new biodegradable gels based on 2,2 '-(ethylenedioxy) diethanethiol and pentaerythritol triacrylate

2022 ◽  
Vol 320 (1) ◽  
pp. 25-31
Author(s):  
R.A. Shulen ◽  
◽  
D.S. Kazybayeva ◽  
Keyword(s):  
Raman Spectroscopy ◽  
Ir Spectroscopy ◽  
Sol Gel ◽  
Polymer Network ◽  
Crosslinking Density ◽  
Mechanical Analysis ◽  
Synthesis And Characterization ◽  
Prolonged Release ◽  
Click Polymerization

The work is devoted to the synthesis and characterization of gels based on the monomers pentaerythritol triaacrylate (PETriA) and 2,2 '-(ethylenedioxy)diethanethiol (EDODET) by thiol-ene "click" polymerization. The properties of the obtained gels were investigated by IR, Raman spectroscopy, mechanical analysis. Sol-gel analysis of obtained networks was carried out and the degradability was investigated. The results of IR spectroscopy confirmed the presence of -C = O and -C-O-C- groups in the composition of the obtained gels. The presence of unreacted C = C bonds conjugated with C = O, as well as thiol groups, varies depending on the composition of the initial monomer mixture (IMM). Raman spectroscopy results correlate well with IR data. Raman spectra also show C-S, S-S and SH characteristic bands that are difficult to identify by IR spectroscopy. It was found that the composition of MM affects the physicochemical properties of the synthesized gels. The highest yield of the gel fraction of obtained polymers was found in samples with an equimolar composition of IMM. The analysis of mechanical properties showed that gels with an excess of PETriA exhibit more elastic properties, and an excess of EDODET leads to the formation of networks with a higher crosslinking density. The study of the ability of obtained PETria-EDODET gels to degrade in a 3% solution of hydrogen peroxide showed that the polymer network degrades by 12% within 60 days. This property of the obtained gels can find application in the creation of targeted drug delivery systems with their prolonged release.

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