Crosslinking side chain

Liaw [4] synthesized norbornene monomers containing crosslinkable side chains (VII), which underwent a ROMP reaction with a ruthenium-based... 

In the latter two phases backbones have the spindle-like conformation, i.e., the prolate shape with (R%) > R p), the characteristic of main chain liquid crystalline polymers. Important means of investigating the conformations of side chain liquid crystalline polymers include small angle neutron scattering from deuterium-labeled chains (Kirst Ohm, 1985), or small angle X-ray scattering on side chain liquid crystalline polymers in a small molecular mass liquid crystal solvent (Mattossi et al., 1986), deuterium nuclear resonance (Boeffel et al., 1986), the stress- or electro-optical measurements on crosslinked side chain liquid crystalline polymers (Mitchell et al., 1992), etc. Actually, the nematic (or smectic modifications) phases of the side chain liquid crystalline polymers have been substantially observed by experiments. 

Sanchez-Ferrer A, Fischl T, Stubenrauch M, Wurmus H, Hoffmann M, Finkelmann H (2009) Photo-crosslinked side-chain liquid-crystalline elastomers for microsystems. Macromol ChemPhys 210(20) 1671-1677. doi 10.1002/macp.200900308... 

Results similar to the ones described above are also obtained for the V3-crosslinked side-chain LCEs, i.e. LCEs with different crosslinker geometry and functionality. The measurements of these LCEs showed that the critical point is shifted to essentially lower crosslinking densities in the case of flexible trifunctional crosslinkers, as significantly smaller latent-heat values have been observed already at lower V3 densities [4] (See Eig. 21). 

Fluorosilicones consist of PDMS backbones with some degree of fluoro-aliphatic side chains. The fluorinated group can be trifluoropropyl, nonafluorohexylmethyl, or fluorinated ether side group [78,28,79]. These polymers differ not only in substituent group, but also in the amount of fluoro-substitution relative to PDMS, the overall molecular weight and crosslink density, and the amount of branching. In most commercially available cases, these polymers are addition cure systems and the reactions are those discussed previously for silicone networks. 

From the data of DTA and TGA analyses illustrated in Fig. 4, its evident that the visible exo-peaks in the range of 140-150°C appear in DTA curves (Fig. 4a), which can be taken as evidence of a crosslinking reaction of acylated macromolecules at the expense of side chain... 

The structural versatility of pseudopoly (amino acids) can be increased further by considering dipeptides as monomeric starting materials as well. In this case polymerizations can be designed that involve one of the amino acid side chains and the C terminus, one of the amino acid side chains and the N terminus, or both of the amino acid side chains as reactive groups. The use of dipeptides as monomers in the manner described above results in the formation of copolymers in which amide bonds and nonamide linkages strictly alternate (Fig. 3). It is noteworthy that these polymers have both an amino function and a carboxylic acid function as pendant chains. This feature should facilitate the attachment of drug molecules or crosslinkers,... 

The inhibition of C a2+-ATPase at the active site by ATP-Im or ADP-Im with the participation of Ca2+ is illustrated by the following model. In the reaction of ATP-imidazolide with the carboxylate of Asp 351, a mixed anhydride is formed with the aspartate residue, followed by presumably nucleophilic attack of a lysine side chain, thereby displacing the nucleotide and leading to an intramolecular crosslink.[1]... 

A host of scientists in universities and industrial laboratories are finding that by adding side chains to the crosslinked chains or otherwise altering their structure they can control when and how the materials respond. It is therefore to be expected that they will design new smart gels and ideas for gel-using systems in the future. 

The initial drying of currently applied alkyd paints is accomplished by evaporation of solvent (physical drying). Subsequently, the eventual curing of the alkyd paint is completed by the formation of a polymer network, which is mainly formed by chemical crosslinks (oxidative drying) but in some cases also physical interactions between the fatty acid side chains occur, such as crystallization or proton-bridge formation [129]. Efficient network formation is crucial in the formation of dry films with good mechanical properties. Due to the presence of unsaturated units in the investigated LOFA- and TOFA-PHA bin-... 

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