4"-Hydroxyl group, chemical modification

Physically or chemically modifying the surface of PET fiber is another route to diversified products. Hydrophilicity, moisture absorption, moisture transport, soil release, color depth, tactile aesthetics, and comfort all can be affected by surface modification. Examples iaclude coatiag the surface with multiple hydroxyl groups (40), creatiag surface pores and cavities by adding a gas or gas-forming additive to the polymer melt (41), roughening the surface... 

Semisynthetic Derivatives. No significant improvements in activity have resulted from modifications of the 3-, 9-, 2and/01 4"-hydioxyl groups (314). 3 -0-Acyl derivatives have not been found via fermentation, but chemical acylation of the 3 -hydroxyl group yields products having good antibiotic activity and better pharmacokinetics than the patent macroHdes. Two such compounds have been developed (315,316) ... 

Hydroformylation of nitrile rubber is another chemical modification that can incorporate a reactive aldehyde group into the diene part and further open up new synthetic routes to the formation of novel nitrile elastomers with a saturated backbone containing carboxyl or hydroxyl functionalities. 

The objective of this work is to determine the surface concentration of the hydroxyl groups of cellulose and PVA films utilizing their chemical modification. We chose these polymers mainly because the hydroxyl group is their sole functional group. Recently we have reported that a cellulose film is more excellent in wettability towards water than PVA, though cellulose is insoluble in water, in contrast to PVA(4). Since only the chemical composition of the surface must be responsible for water... 

Surface Modification of Cellulose and PVA Films. Cellulose, as well as PVA,is known to be a typical non-ionic, hydrophilic polymer possessing hydroxyl groups. As this group has a high reactivity,chemical modification of these polymers is relatively easy and, in fact, has been the subject of extensive research. However, so far as we know, no work has been reported concerned with reactions occurring only at the surface of films or fibers from these polymers. 

Most of the chemical modification methods investigated to date have involved the chemical reaction of a reagent with the cell wall polymer hydroxyl groups. This can result in the formation of a single chemical bond with one OH group (Figure 2. Id), or cross-linking between two... 

A very large number of reagents have been studied for their potential for the chemical modification of wood. In almost all cases, these involve reaction with the cell wall polymeric hydroxyl groups. In the main, reactions described in this chapter are unlikely to be suitable for scale-up to industrial processes. In many cases, the cost of reagent and/or difficulties in handling large quantities of potentially toxic reagent remain considerable barriers to exploitation. 

Chemical modification of cyclodextrins is achieved through reactions of their hydroxyl groups. Of the 21 hydroxyls ofP-CD, the seven primary ones (C-6) can easily be reacted. In addition, the C-2 secondary hydroxyl groups are also fairly reactive while the ones at C-3 resist modification (e.g. by methylation). Several CD derivatives are available commercially in large quantities including -among others- randomly methylated P-cylodextrin and hydroxypropyl-P-cylodextrin [2]. Chemical modifications substantially alter the solubility of cyclodextrins in water. For example, the solubility of P-CD... 

Chemical modification takes place and carboxyl, hydroxyl and carbonyl groups are produced on the fiber surface. 

In general, the silanization of hydroxyl-terminated substrates such as silica or glass is an effective method which is used quite often for chemical modification of the substrate surface for immobilization of biomolecules. The main focus for silanization procedures is once again the examination of the self-organizing silane-monolayers. The properties of the monolayer depend on the chemical structure of the silanization reagent, the density of silanol-groups which are available on the surface and the physical surface structure on a nano-scale level. 

It is generally accepted that the only important polar adsoiption sites on the silica surface are the silanol functions, i.e., hydroxyl groups, that are attached to silicon atoms (2). They can interact with the sample molecules by hydrogen bonding and various physical observations ctAi be used to prove this statement. Complete dehydration of silica by beating, i.e., removal of all surface hydroxyl groups, yields a hydrophobia silica which no longer shows adsorption for unsaturated and polar molecules and is no more wetted by water (15). Chemical modification of the surface hydroxyls such as used in the preparation of chemically bonded phases also eliminates the selective adsorption properties of the silica. ... 

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