Polymer difunctional

Aromatic radical anions, such as lithium naphthalene or sodium naphthalene, are efficient difunctional initiators (eqs. 6,7) (3,20,64). However, the necessity of using polar solvents for their formation and use limits their utility for diene polymerization, since the unique abiUty of lithium to provide high 1,4-polydiene microstmcture is lost in polar media (1,33,34,57,63,64). Consequentiy, a significant research challenge has been to discover a hydrocarbon-soluble dilithium initiator which would initiate the polymerization of styrene and diene monomers to form monomodal a, CO-dianionic polymers at rates which are faster or comparable to the rates of polymerization, ie, to form narrow molecular weight distribution polymers (61,65,66). 

Eig. 1. Schematic bioactive polyphosphazenes. (a) General stmcture, where X = hydrophilic /hydrophobic group that hydrolyzes with concurrent polymer breakdown, Y = difunctional group for attaching bioactive agent to polymer, and T = bioactive agent, (b) Actual example where X = —OC H, Y = and... 

After polymeri2ation is carried out by blending mono- and difunctional chlorosilanes ia excess water, the siloxanes are separated from the water and neutraH2ed. Ratio of the mono-chain stopper to di-chain extender controls the length of the polymer. Once an equiHbrium mixture of chain lengths is catalyticaHy formed, volatile light ends are removed and the desired product results. 

In this example, X is difunctional and the product is linear. If the fiinctionahty of X is higher, the product is branched, ie, it is a star polymer. 

Gel-permeation chromatography studies of epoxy resins prepared by the taffy process shown n values = 0, 1, 2, 3, etc, whereas only even-numbered repeat units are observed for resins prepared by the advancement process. This is a consequence of adding a difunctional phenol to a diglycidyl ether derivative of a difunctional phenol in the polymer-forming step. 

Acid chlorides are useful reagents, but when the pyrazole is N- unsubstituted a dimerization occurs and the diketopiperazine (254) is isolated (Section 4.04.2.3.3(x)). However, (254) reacts with many compounds as an acid chloride would, for example with amines to yield amides (67HC(22)l). The difunctional pyrazole derivative (441) affords polymers by reaction with diphenols (69RRC763). Cyanopyrazoles can be hydrolyzed to the corresponding carboxylic acids (68CB829). 

The elastomers consist of very high moleculcU weight (-0.5 X 10 ) linecu gums cross-linked after fabrication. In order to achieve such polymers it is necessary that very pure difunctional monomers be employed since the presence of monofunctional material will limit the molecular weight while trifunctional material will lead to cross-linking. Where dimethylsilicone rubbers are being prepared, the cyclic tetramer, octamethylcyclotetrasiloxane, which may be obtained free from mono- and trifunctional impurities, is often used. This tetramer occurs to the extent of about 25% during the hydrolysis of dichlorosilanes into polymers. 

The earliest SIS block copolymers used in PSAs were nominally 15 wt% styrene, with an overall molecular weight on the order of 200,000 Da. The preparation by living anionic polymerization starts with the formation of polystyryl lithium, followed by isoprene addition to form the diblock anion, which is then coupled with a difunctional agent, such as 1,2-dibromoethane to form the triblock (Fig. 5a, path i). Some diblock material is inherently present in the final polymer due to inefficient coupling. The diblock is compatible with the triblock and acts... 

Literature articles, which report the formation and evaluation of difunctional cyanoacrylate monomers, have been published. The preparation of the difunctional monomers required an alternative synthetic method than the standard Knoevenagel reaction for the monofunctional monomers, because the crosslinked polymer thermally decomposes before it can revert back to the free monomer. The earliest report for the preparation of a difunctional cyanoacrylate monomer involved a reverse Diels-Alder reaction of a dicyanoacrylate precursor [16,17]. Later reports described a transesterification with a dicyanoacrylic acid [18] or their formation from the oxidation of a diphenylselenide precursor, seen in Eq. 3 for the dicyanoacrylate ester of butanediol, 7 [6]. 

Solvent swelling experiments, with CH2CI2 and ECA polymer crosslinked with 7, demonstrate that the addition of a difunctional cyanoacrylate monomer does improve solvent resistance [6], shown in Fig. 1. 

Later, Kricheldorf and coworkers [93,94] extensively demonstrated the use of 0-silylated bifunctional monomers, such as diphenols, for synthesis of a wide variety of polycondensation polymers. The silylated oxygen of difunctional phenols may be condensed with activated... 

Step-growth polymers, such as polyamides and polyesters, are prepared by reactions between difunctional molecules. Polyamides (nylons) are formed by reaction between a diacid and a diamine polyesters are formed from a diacid and a diol. 

Chains with uttdesired functionality from termination by combination or disproportionation cannot be totally avoided. Tn attempts to prepare a monofunctional polymer, any termination by combination will give rise to a difunctional impurity. Similarly, when a difunctional polymer is required, termination by disproportionation will yield a monofunctional impurity. The amount of termination by radical-radical reactions can be minimized by using the lowest practical rate of initiation (and of polymerization). Computer modeling has been used as a means of predicting the sources of chain ends during polymerization and examining their dependence on reaction conditions (Section 7.5.612 0 J The main limitations on accuracy are the precision of rate constants which characterize the polymerization. 

The process may be used to form linear polymers. Nuyken and Volkel224 225 described a method for tclcchclic production, based on the radical initiated reaction of difunctional transfer agents with dienes (e.g. divinyl benzene (13), dimethacrylate esters). However, currently the most common use of thiol-ene... 

The preparation of ABA triblock polymers requires use of a telechelie bisthiol prepared by termination of anionic polymerization initiated by a difunctional initiator. The relative yields of homopolymer, di- and triblock obtained in these experiments depend critically on conversion.273... 

Another class of hydrocarbon binders used in propints are the carboxy-terminated polybutadiene polymers which are cross-linked with either tris[l-(2-methyl)aziridinyl] phosphine oxide (MAPO) or combinations with phenyl bis [l -(2-methyl)aziridinyl] phosphine oxide (Phenyl MAPO). Phenyl MAPO is a difunctional counterpart of MAPO which makes possible chain extension of polymers with two carboxylic acid groups. A typical propint formulation with ballistic properties is in Table 11 (Ref 83) Another class of composites includes those using hydroxy-terminated polybutadienes cross-linked with toluene diisocyanate as binders. The following simplified equations illustrate typical reactions involved in binder formation... 

A difunctional monomer commonly employed to cross-link ion-exchange polymers. 

The molecular weight of a polymer will be reduced if either die extent of conversion or the average functionality is decreased. At 95% conversion of difunctional monomers, for example, Xn is only 20.25 The molecular weight is also related to a stoichiometric imbalance, r, which is normally defined to be less than 1.0 ... 

The number-average molecular weight of a polymer may be controlled by offsetting the stoichiometry of two dissimilar mutually reactive difunctional monomers. The polymer will have the same endgroup functionality as that of the monomer used in excess. For a generic polymer made from a difunctional monomer AA with A functional groups and an excess of difunctional monomer BB widt B functional groups, r is defined as... 

Polystyrene-polytetrahydrofuran block copolymers121122 are an interesting case of coupling between functional polymers The mutual deactivation of living anionic polystyrene and living cationic polyoxolane occurs quantitatively to yield polystyrene-polyoxolane block copolymers. Since either of the initial polymer species can be mono- or difunctional, diblock, triblock or multiblock copolymers can be obtained. 

Condensation polymers are often formed from two distinct monomers, each of which is difunctional. The monomers have the forms AMA and BNB where A and B are functional groups that react to couple the M and N units and form a condensation by-product, AB. M and N are the mer units that form the polymer chain. The first step in the polymerization forms dimer ... 

The most common form of step growth polymerization is condensation polymerization. Condensation polymers are generally formed from simple reactions involving two different monomers. The monomers are difunctional, having a chemically reactive group on each end of their molecules. Examples of condensation polymerization are the formation of nylon 66, a polyamide, and of poly(ethylene terephthalate), a polyester. Because condensation poly-... 

Most aromatic difunctional reagents react with N3P3Cl6 to afford spirocyclic products (20,176,180,181,189,190). With catechol, the trispiro product is observed (190). This product was shown to function as a host in the formation of several inclusion adducts, including polymers (191). Ring degradation of the cyclophosphazene ring occurs in the reaction with o-amino phenol as well as in the reaction with catechol in the presence of a triethylamine (192). 

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