Double-Diamond Inclusion Compounds of 2,6-Dimethylydeneadamantane-1,3,5,7-tetracarboxylic Acid

1991 ◽  
Vol 74 (4) ◽  
pp. 825-877 ◽  
Author(s):  
Otto Ermer ◽  
Lorenz Lindenberg
Keyword(s):  
Inclusion Compounds ◽  
Tetracarboxylic Acid ◽  
Diamond Inclusion ◽  
Double Diamond

Synthesis and characterization of some polyimide-epoxy composites

e-Polymers ◽  
2011 ◽  
Vol 11 (1) ◽  
Author(s):  
Toheed Akhter ◽  
Humaira Masood Siddiqi ◽  
Zareen Akhter ◽  
M. Saeed Butt
Keyword(s):  
Thermal Behavior ◽  
Epoxy Resins ◽  
Analytical Techniques ◽  
Char Yield ◽  
Epoxy Composites ◽  
Hydroxyl Group ◽  
Synthesis And Characterization ◽  
Tetracarboxylic Acid ◽  
Epoxy Amine

AbstractComposites from some novel polyimide and commercial epoxy were prepared aiming to improve the thermal behavior of epoxy resins. Two diamines namely 4-4'-diamino-4''-hydroxytriphenyl methane (DHTM) and 4-4'- diaminotriphenyl methane (DTM) were synthesized by reacting aniline and aldehydes according to a reported method. The synthesized diamines were blended with commercially available epoxy 1, 4-butanedioldiglycidylether (BDDE) to synthesize model epoxy amine networks which were compared with polyimideepoxy composites. The polyimides were synthesized by reaction of these diamines with aromatic anhydride namely 3,3',4,4'-benzophenone tetracarboxylic acid dianhydride (BTDA). These synthesized polyimides were dispersed in epoxy diamine networks to prepare composites. All the monomers and composites were characterized by making use of various analytical techniques including FTIR, NMR, TGA, DSC and XRD. Presence of hydroxyl group in the diamine helped in better dispersion of polyimide leading to high Tg and high char yield at 600 °C.

Perylene and perinone pigments

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Robert Christie ◽  
Adrian Abel
Keyword(s):  
High Performance ◽  
Heat Stability ◽  
High Heat ◽  
Structural Features ◽  
Fastness Properties ◽  
Tetracarboxylic Acid ◽  
Organic Pigments ◽  
Orange Color ◽  
Cis Isomer ◽  
Chemical Class

Abstract Perylenes and perinones are separate groups of pigments categorized within the carbonyl chemical class. The two pigment groups show similarities, for example, in their chemical structural features and, to an extent, in their technical and application properties as high-performance organic pigments. Perylenes constitute a series of firmly established high-performance pigments, offering red and violet colors, and also extending to black. Synthetically, they are derived from perylene-1,4,5,8-tetracarboxylic acid. The perylenes tend to be quite expensive pigments, but their high levels of fastness properties mean that they are suitable for highly demanding applications. In particular, they offer very high heat stability. Two perinone pigments are used commercially. In their synthesis from naphthalene-1,4,5,8-tetracarboxylic acid, they are formed as mixtures of the two isomers, which can be separated. The trans isomer, CI Pigment Orange 43, is a highly important commercial pigment, especially for plastics, while the cis isomer, CI Pigment Red 194, is bordeaux in color and is of much lesser importance. The perinone, CI Pigment Orange 43, provides a brilliant orange color and has very good fastness properties. Its commercial manufacture involves a challenging multistage procedure and consequently it is one of the most expensive organic pigments on the market.

scholarly journals 1-D calcium, 2-D zinc and 3-D manganese coordination polymers derived from pyrazine-2,3,5,6-tetracarboxylic acid

2017 ◽  
Vol 467 ◽  
pp. 163-168 ◽  
Author(s):  
Saki T. Golafale ◽  
Conrad W. Ingram ◽  
Alvin A. Holder ◽  
Wei-Ya Chen ◽  
Z. John Zhang
Keyword(s):  
Coordination Polymers ◽  
Tetracarboxylic Acid
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