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Multi-ring aromatic compounds

The following chemical stractures characterize some plasticizers obtained from mnlti-ring aromatic compounds  [Pg.58]

R3 = C3 to C 2 alkyls R, Ri, Rz- R3 = C4 to C2Z alkyls alkyl substituted anthracene tetraester of benzophenone-tetracarboxylic acid [Pg.58]

Alkyl substituted anthracene has found application in plasticization of poly(N-vinyl carba-zole) residing in photoconductive layer of imaging member. [Pg.58]

The tetraester of benzophenone-tetracarboxylic acid has found application as nonmigrating plasticizer of polyvii rlchloride.  [Pg.58]

A process for making naphthalene hydrodimer mixtures from tetralin or alkyltetralin is available. The resultant mixture was found to be a good PVC plasticizer which may replace part of There is a good compatibility between the plasticizer of an [Pg.58]


Allelopathic compounds consist of a wide variety of chemical types which arise through either the acetate or the shikimic acid pathway (5 ). These compounds range from very simple gases and aliphatic compounds to complex multi-ringed aromatic compounds. Oniy a few examples are mentioned below. [Pg.15]

Attempts to test the extension of the Selectivity Treatment to other multi-ring aromatic hydrocarbons are frustrated by the paucity of data. The information for naphthalene, the only compound for which data for... [Pg.113]

Attention in fundamental and applied research on shape-selective catalysis has been largely focused on open-chain and monocyclic compounds. However, we have observed the rapid developments in polymer materials containing multi-ring aromatic units and the need to develop the monomers and other specialty chemicals from polyaromatic hydrocarbons that are rich in coal-derived liquids [Song and Schobert, 1993, 1996]. Scheme 1 shows the structures of some advanced polymer materials containing aromatic ring in the main-chain. [Pg.164]

Using lor detection and identificatic n of multi-ring aromatic hydrocarbons and highly nitrated compounds S6. -rav struct urc of X7 Chiral nitrammcs 355 Chlorine oxides 457. 458 (II 477) Commercial (Mining) explosives 515-557 tin 395-526)... [Pg.679]

The molar volumes are in some cases at the stated temperature and in other cases at the normal boiling point. Certain calculated molecular volumes are also used thus the reader is cautioned to ensure that when using a molar volume in any correlation, it is correctly selected. In the case of polynuclear aromatic hydrocarbons, the Le Bas molar volume is regarded as suspect because of the compact nature of the multi-ring compounds. It should thus be regarded as merely an indication of relative volume, not an absolute volume. [Pg.29]

Chiraldex G -DA Aromatic amines containing 2 or more rings, large eyelie diols. Some heterocyclics, multi-ring compounds and those with bulky substituents. [Pg.445]

Hydroxylation of Aromatics The aromatic compounds photoadsorbed on the catalyst surface undergo two competing reaction pathways (a) hydroxylation of the aromatic ring or (b) multi-step oxidation reactions to complete mineralization. In the first case, the OH radical attack follows the selectivity rules known for homogeneous electrophilic aromatic substitution when the oxidized compound contains an electron donor group. Hence the only ortho- and para-isomers are obtained. In the presence of an... [Pg.1443]


See other pages where Multi-ring aromatic compounds is mentioned: [Pg.326]    [Pg.595]    [Pg.58]    [Pg.326]    [Pg.595]    [Pg.58]    [Pg.135]    [Pg.258]    [Pg.47]    [Pg.243]    [Pg.169]    [Pg.5018]    [Pg.55]    [Pg.678]    [Pg.417]    [Pg.1097]    [Pg.55]    [Pg.560]    [Pg.20]    [Pg.119]    [Pg.480]    [Pg.204]    [Pg.162]    [Pg.81]    [Pg.588]    [Pg.2]    [Pg.162]    [Pg.253]    [Pg.42]    [Pg.181]    [Pg.73]    [Pg.348]    [Pg.34]    [Pg.708]    [Pg.106]    [Pg.638]    [Pg.69]    [Pg.135]    [Pg.124]    [Pg.18]    [Pg.328]    [Pg.53]    [Pg.59]    [Pg.94]    [Pg.584]   
See also in sourсe #XX -- [ Pg.58 ]




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