Low molecular weight crosslinker

The use of phenolic polymers in photocrosslinkable systems usually involves multicomponent systems which incorporate polyfunctional low molecular weight crosslinkers. For example, Feely et al. [9] have used hydroxymethyl melamine in combination with a photoactive diazonaphthoquinone which produces an indene carboxylic acid upon irradiation to crosslink a novolac resin. Similarly, Iwayanagi et al. [10] have used photoactive bisazides in combination with poly(p-hydroxy-sty-rene) to afford a negative-tone resist material which does not swell upon development in aqueous base. 

Using a low molecular weight crosslinking agent such as DETA, a ma-... 

As an alternative, side-chain functionalized polymer chains can associate by (c) low molecular weight crosslinkers or (d) mutual heterocomplementary polymer-polymer binding... 

Disclosing the binding motif of multiblock RAFT polymers on AuNPs from citrate reduction raises the questimi of whether the polymer binding can vary for different types of AuNPs. It is known that AuNPs from the two-phase Brust-Schiffrin synthesis can assemble into spherical particle networks when treated with low molecular weight crosslinking agent [106, 107]. When tetraocty-lammonium bromide-capped AuNPs from this two-phase method are functionalized in toluene dispersion with multiblock RAFT polymers of styrene, the formation of spherical AuNP assemblies can be observed by TEM (Fig. 9) [108]. It can be concluded from these TEM images that the particle density inside... 

Film stability is a primary concern for applications. LB films of photopoly-merizable polymeric amphiphiles can be made to crosslink under UV radiation to greatly enhance their thermal stability while retaining the ordered layered structure [178]. Low-molecular-weight perfluoropolyethers are important industrial lubricants for computer disk heads. These small polymers attached to a polar head form continuous films of uniform thickness on LB deposi-... 

Furfural reacts with ketones to form strong, crosslinked resins of technical interest in the former Soviet Union the U.S. Air Force has also shown some interest (42,43). The so-called furfurylidene acetone monomer, a mixture of 2-furfurylidene methyl ketone [623-15-4] (1 )> bis-(2-furfurylidene) ketone [886-77-1] (14), mesityl oxide, and other oligomers, is obtained by condensation of furfural and acetone under basic conditions (44,45). Treatment of the "monomer" with an acidic catalyst leads initially to polymer of low molecular weight and ultimately to cross-linked, black, insoluble, heat-resistant resin (46). 

Positive-Tone Photoresists based on Dissolution Inhibition by Diazonaphthoquinones. The intrinsic limitations of bis-azide—cycHzed mbber resist systems led the semiconductor industry to shift to a class of imaging materials based on diazonaphthoquinone (DNQ) photosensitizers. Both the chemistry and the imaging mechanism of these resists (Fig. 10) differ in fundamental ways from those described thus far (23). The DNQ acts as a dissolution inhibitor for the matrix resin, a low molecular weight condensation product of formaldehyde and cresol isomers known as novolac (24). The phenoHc stmcture renders the novolac polymer weakly acidic, and readily soluble in aqueous alkaline solutions. In admixture with an appropriate DNQ the polymer s dissolution rate is sharply decreased. Photolysis causes the DNQ to undergo a multistep reaction sequence, ultimately forming a base-soluble carboxyHc acid which does not inhibit film dissolution. Immersion of a pattemwise-exposed film of the resist in an aqueous solution of hydroxide ion leads to rapid dissolution of the exposed areas and only very slow dissolution of unexposed regions. In contrast with crosslinking resists, the film solubiHty is controUed by chemical and polarity differences rather than molecular size. 

The presence of these low molecular weight tackifiers and plasticizers may also have other negative effects on the PSA performance. For example, the reduced entanglement of the polymer typically reduces the cohesive strength of the PSA, although crosslinking may be used to compensate for this loss in property. Plasticizers and tackifiers may also be susceptible to migration and/or oxidation, both... 

Through the addition of a low-molecular weight component that may promote copolymer formation and crosslinking or co-crosslinking reactions. 

For example, the molecular weight of unsaturated polyesters is controlled to less than 5000 g/mol. The low molecular weight of the unsaturated polyester allows solvation in vinyl monomers such as styrene to produce a low-viscosity resin. Unsaturated polyesters are made with monomers containing carbon-carbon double bonds able to undergo free-radical crosslinking reactions with styrene and other vinyl monomers. Crosslinking the resin by free-radical polymerization produces the mechanical properties needed in various applications. 

Finkelmann et al. 256 274,2781 have also investigated the synthesis and the characteristics of siloxane based, crosslinked, liquid crystalline polymers. This new type of materials displays both liquid crystallinity and rubber elasticity. The synthesis of these networks is achieved by the hydrosilation of dimethylsiloxane-(hydrogen, methyl)siloxane copolymers and vinyl terminated mesogenic molecules in the presence of low molecular weight a,co-vinyl terminated dimethylsiloxane crosslinking agents156 ... 

Various zirconium compounds are used as delayed crosslinkers, (see Table 17-12). The initially formed complexes with low-molecular-weight compounds are exchanged with intermolecular polysaccharide complexes, which cause delayed crosslinking. 

Figure 17-16. Delayed crosslinking by exchange of hydroxyl groups (idealized). If two low-molecular-weight hydroxyl compounds are exchanged with high-moiecuiar-weight compounds, the hydroxyl units belonging to different molecules, then a crosslink is formed.

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