Poly spacers

Properties have been determined for a series of block copolymers based on poly[3,3-bis(ethoxymethyl)oxetane] and poly [3,3-bis(methoxymethyl)oxetane]- (9-tetrahydrofuran. The block copolymers had properties suggestive of a thermoplastic elastomer (308). POX was a good main chain for a weU-developed smectic Hquid crystalline state when cyano- or fluorine-substituted biphenyls were used as mesogenic groups attached through a four-methylene spacer (309,310). Other side-chain Hquid crystalline polyoxetanes were observed with a spacer-separated azo moiety (311) and with laterally attached mesogenic groups (312). 

The effect of lateral methyl groups in the spacer on the phase behavior has been studied in several polybibenzoates [18,19] derived from poly(tetramethy]ene p,p bibenzoate), P4MB. The branched polymers display transition temperatures significantly lower than P4MB. Moreover, the substituents have a clear effect on the kind of mesophase formed. Thus, P4MB displays a smectic A mesophase, while the lateral methyl groups... 

The phase behavior of several polybibenzoates with oxyalkylene spacers has been reported [11,14,15,20-27]. These spacers include the dimer of trimethylene glycol and different ethylene oxide oligomers. The most noticeable characteristic of these polybibenzoates with ether groups in the spacer is the considerable decrease of the rate of the mesophase-crystal transformation. Thus, Fig. 8 shows the DSC curves corresponding to a sample of poly[oxybis(trimethylene)p,p -bibenzoate], PDTMB, with a structure similar to that of P7MB but with the... 

The presence of three oxyethylene units in the spacer of PTEB slows down the crystallization from the meso-phase, which is a very rapid process in the analogous polybibenzoate with an all-methylene spacer, P8MB [13]. Other effects of the presence of ether groups in the spacer are the change from a monotropic behavior in P8MB to an enantiotropic one in PTEB, as well as the reduction in the glass transition temperature. This rather interesting behavior led us to perform a detailed study of the dynamic mechanical properties of copolymers of these two poly bibenzoates [41]. 

Polyacetylene is considered to be the prototypical low band-gap polymer, but its potential uses in device applications have been hampered by its sensitivity to both oxygen and moisture in its pristine and doped states. Poly(thienylene vinylene) 2 has been extensively studied because it shares many of the useful attributes of polyacetylene but shows considerably improved environmental stability. The low band gap of PTV and its derivatives lends itself to potential applications in both its pristine and highly conductive doped state. Furthermore, the vinylene spacers between thiophene units allow substitution on the thiophene ring without disrupting the conjugation along the polymer backbone. 

Hydrosilation reactions have been one of the earlier techniques utilized in the preparation of siloxane containing block copolymers 22,23). A major application of this method has been in the synthesis of polysiloxane-poly(alkylene oxide) block copolymers 23), which find extensive applications as emulsifiers and stabilizers, especially in the urethane foam formulations 23-43). These types of reactions are conducted between silane (Si H) terminated siloxane oligomers and olefinically terminated poly-(alkylene oxide) oligomers. Consequently the resulting system contains (Si—C) linkages between different segments. Earlier developments in the field have been reviewed 22, 23,43> Recently hydrosilation reactions have been used effectively by Ringsdorf 255) and Finkelmann 256) for the synthesis of various novel thermoplastic liquid crystalline copolymers where siloxanes have been utilized as flexible spacers. Introduction of flexible siloxanes also improved the processibility of these materials. 

Poly(epichlorohydrin) (PECH) and poly(2,6 - dimethyl-1,4-phenylene oxide) (PPO) containing pendant mesogenic units separated form the main chain through spacers of zero to ten methylene units were synthesized and characterized in order to test the "spacer concept." Both polymers were modified by phase transfer catalyzed esterifications of the chloromethyl groups (PECH) or the bromobenzyl groups (brominated PPO) with potassium co -(4-oxybiphenyl) alkanoates and potassium u-(4-methoxy-4-oxybiphenyl)-alk.an oates. While PPO required ten methylene units as a spacer and 4,4 -methoxybiphenyl as mesogen to present thermotropic liquid crystalline mesomorphism,... 

In order to determine the necessity and/or the length of the spacer that is required to achieve liquid crystalline behavior from flexible vs. rigid polymers, we have introduced mesogenic units to the backbones of a rigid [poly(2,6-dimethyl-l,4-phenylene oxide) (PPO)] and a flexible [poly(epichlorohydrin) (PECH)] polymer through spacers of from 0 to 10 methylene groups via polymer analogous reactions. 

One of the most successful conjugate polymer systems was developed by Duncan and Kopecek (25). The polymer carrier used in their system is poly [N(2-hydroxypropyl) methacrylamide] a biocompatible polymer that was originally developed as a plasma extender. They have evaluated a number of polymer conjugated drugs for cancer chemotherapy with interesting results. The attachment of the drug is through a peptidyl spacer pendent to the polymer backbone. These peptides links are stable in aqueous media but are readily hydrolyzed intracellularly... 

A number of bis(tacn) ligands, composed of pairs of covalently linked tacn macrocycles, can form similar structures, provided the linker group between the sandwiching macrocycles is sufficiently flexible (e.g., (556)).1411-1413 In particular, several Ni11 complexes of poly(tacn) derivatives with a central benzene have been studied, where the Ni is sandwiched between pairs of tacn macrocycles when these are attached to the ortho positions of the aromatic spacer group (e.g., (557)).1412,1413... 

Before treatment with alcohol, the ionic conductivity of lithium borate polymers was 6.23 X 10-5 to 2.07 X 10-7 Scm-1 at 50°C. The maximum ionic conductivity was observed for the polymer with a PE040o spacer unit. After the polymer reaction with alcohols, glass-transition temperatures of these polymers were found to be -52 to 39°C, which was higher than that of poly(lithium mesitylhydroborate) ( 69°C). 

To increase efficiency and ease of product separation from reaction mixtures, we also prepared styryl-substituted TADDOL-dendrimers that can act as crosslinkers in styrene suspension polymerizations, and thus lead to beads with intimately incorporated TADDOL sites [106,107]. Due to the presence of the con-formationally flexible dendritic spacers between the chiral ligand and the poly-... 

The synthesis and structure of a dendrimer can be illustrated by the well-known poly (amidoamine) type (called PAMAM), which describes the monomers making up the complete polymer. The synthesis starts from a core diamine (or ammonia) molecule. The diamine can be of various lengths and spacer arm properties and even contain cleavable components. Typically, the core... 

Miller and co-workers have recently prepared nanometer-scaled molecular dumbbells based on poly(benzyl ether) dendrons (G1-G4) and oligoimide spacers [64], Their synthetic approach involved the coupling of amine-terminated oligoimides to dendrons with a carboxylic acid focal point. The resulting hybrid materials were found to be quite soluble thus allowing their analysis by cyclic voltammetry in DMF. Consistent with Roncali s observation, the kinetics of reduction of the oligoimide core was not found to be limited by the presence of the dendritic wedges. 

Similar results have been presented by Miller and co-workers, who capped the ends of oligo(dihexylfluorene)s and poly(dihexylfluorene)s with Frechet-type dendrons (Figure 7.17C) [73], Annealing experiments coupled with emission studies revealed that G-3 and G-4 dendrons were effective at preventing excimer formation, even when the poly(fluorene) spacer was 50-80 repeat units long. 

The desired long spacer necessary to allow multiple branch construction, was obtained with commercial tetra(ethylene glycol) which was readily modified into aminoacetal 21 in five steps (Scheme 8). Using 21 as an amine source, poly(amidoamine) (PAMAM) dendrons were prepared according to published protocol using reiterative cycles of methyl acrylate and ethylenediamine reactions. The terminal amines of each generation (G = 1, G = 2 and G = 3, 22a-c) were obtained quantitatively from each of the half generation methyl ester precursors. 

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