Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Ester and Amide Polymers

Ch1orocarhony1trime11itic acid 1,2-anhydride [1204-28-0] (9), is used in the preparation of esters and amide—imide polymers. TriaHyl trimellitate [2694-54-4] (10) is used as a cross-linking or co-curing agent for ethylene-derived mbbers and plastics. [Pg.498]

Another important type of condensation polymer are the linear polyesters, such as poly (ethylene terephthalate) (PET) and poly (butylene terephthalate) (PBT). Copolymers of polyesters and PA have been studied in detail, and it has been shown that random copolyesteramides have a low structural order and a low melting temperature. This is even the case for structurally similar systems such as when the group between the ester unit is the same as that between the amide unit, as in caprolactam-caprolactone copolymers (Fig. 3.10).22 Esters and amide units have different cell structures and the structures are not therefore isomorphous. If block copolymers are formed of ester and amide segments, then two melting temperatures are present. [Pg.146]

The Heck reaction on polymer-bound iodoarenes is assisted by the addition of a catalytic amount of tetra-n-butylammonium bromide and has been employed in the synthesis of 4-carboxycinnamic esters and amides [33], and 4-aminosulphonyl-cinnamic esters [34], It has also been reported that the presence of an equimolar equivalent of benzyltriethylammonium chloride aids the Pd(II)-mediated reaction of A -acyl-2-iodoanilines with vinylidene carbonate, which leads to A -acyl-2-hydroxy-indolines providing a convenient route to the indoles (80-90%) [35], The catalysed reaction of 2-hydroxy- and 2-tosylaminoiodobenzene with 1,2-dienes produces 1,2-dihydrobenzofurans and 1,2-dihydroindoles, respectively [36]. [Pg.293]

Figure 5.7, (a) Widely used biological probes of the TICT type. 4, s4 s7> (b) TICT compounds with dual fluorescence and interesting properties amenable to tailor-making of fluorescence probes. Functionalization and inclusion in larger molecular assemblies is easily possible, e.g., at the positions indicated by R. This holds especially for esters and amides which have been used as probes in large polymers 97-1011 or in TICT-labeled cyclodextrins.(l49)... [Pg.119]

The search for RNAs with new catalytic functions has been aided by the development of a method that rapidly searches pools of random polymers of RNA and extracts those with particular activities SELEX is nothing less than accelerated evolution in a test tube (Box 26-3). It has been used to generate RNA molecules that bind to amino acids, organic dyes, nucleotides, cyano-cobalamin, and other molecules. Researchers have isolated ribozymes that catalyze ester and amide bond formation, Sn2 reactions, metallation of (addition of metal ions to) porphyrins, and carbon-carbon bond formation. The evolution of enzymatic cofactors with nucleotide handles that facilitate their binding to ribozymes might have further expanded the repertoire of chemical processes available to primitive metabolic systems. [Pg.1028]

The second method is the most widely used to prepare optically active vinyl polymers (poly-a-olefins, poly-vinyl-ethers, polyacrylic esters and amides etc.. ... [Pg.395]

FIGURE 20. Main and side chain LC polymers with ester and amide attachment groups... [Pg.443]

The hydrolysis of esters and amides easily proceeds with the help of mineral adds. Polymer acids are expected to be effident catal3rsts because of the high local density of protons around the pol3mier chain. [Pg.165]

The characterization of polymer chemical composition is important in numerous practical applications. The polymer identification can be done using various techniques. One of them is the chemical method, which involves reagents that are able to react with the polymer. Oxidation, for example using periodic acid or lead tetraacetate, can be applied to polymers containing 1,2 diol groups, ozonolysis can be applied to polymers containing double bonds, hydrolysis can be applied to esters and amides [4]. [Pg.26]


See other pages where Ester and Amide Polymers is mentioned: [Pg.87]    [Pg.89]    [Pg.91]    [Pg.93]    [Pg.95]    [Pg.97]    [Pg.99]    [Pg.101]    [Pg.103]    [Pg.105]    [Pg.109]    [Pg.111]    [Pg.113]    [Pg.115]    [Pg.117]    [Pg.119]    [Pg.121]    [Pg.123]    [Pg.125]    [Pg.127]    [Pg.129]    [Pg.131]    [Pg.133]    [Pg.135]    [Pg.87]    [Pg.89]    [Pg.91]    [Pg.93]    [Pg.95]    [Pg.97]    [Pg.99]    [Pg.101]    [Pg.103]    [Pg.105]    [Pg.109]    [Pg.111]    [Pg.113]    [Pg.115]    [Pg.117]    [Pg.119]    [Pg.121]    [Pg.123]    [Pg.125]    [Pg.127]    [Pg.129]    [Pg.131]    [Pg.133]    [Pg.135]    [Pg.192]    [Pg.492]    [Pg.734]    [Pg.74]    [Pg.250]    [Pg.1]    [Pg.130]    [Pg.75]    [Pg.445]    [Pg.14]    [Pg.93]    [Pg.178]    [Pg.629]    [Pg.5]    [Pg.734]    [Pg.36]   


SEARCH



Amidation, esters

Amides and esters

Amides polymers

Esters amides

Polymer esters

© 2024 chempedia.info