RESUMO
A pentacyclic quadruply fused polymer topology has been constructed for the first time through alkyne-azide addition (click) and olefin metathesis (clip) reactions in conjunction with an electrostatic self-assembly and covalent fixation (ESA-CF) process. Thus, a spiro-type, tandem tetracyclic poly(tetrahydrofuran), poly(THF), precursor having two allyloxy groups at the opposite positions of the four ring units was prepared by the click-linking of one unit of an eight-shaped precursor having alkyne groups at the opposite positions with two units of a single-cyclic counterpart having an azide and an alkene group at the opposite positions. Both are obtainable through ESA-CF. The subsequent metathesis clip-folding of the tetracyclic precursor could afford a pentacyclic quadruply fused polymer product, of "shippo" form, in 19% yield.
Assuntos
Alcenos/química , Furanos/química , Polímeros/química , Alcenos/síntese química , Alcinos/síntese química , Alcinos/química , Azidas/síntese química , Azidas/química , Química Click , Ciclização , Furanos/síntese química , Polímeros/síntese químicaRESUMO
Unprecedented tetracyclic polymer topologies with spiro- and a bridged-type quatrefoil forms are effectively constructed through an alkyne-azide, click-linking reaction by employing a kyklo-telechelic poly(tetrahydrofuran), poly(THF), precursor having an azide group, obtained through an electrostatic self-assembly and covalent fixation (ESA-CF) process, and complementary tetrafunctional alkyne reagents of either a pentaerythritol derivative or a four-armed star telechelic polymer precursor.
Assuntos
Química Click , Polímeros/química , Alcinos/química , Azidas/química , Catálise , Reação de Cicloadição , Polímeros/síntese química , Compostos de Espiro/química , Eletricidade EstáticaRESUMO
We report a new methodology for studying diffusion of individual polymer chains in a melt state, with special emphasis on the effect of chain topology. A perylene diimide fluorophore was incorporated into the linear and cyclic poly(THF)s, and real-time diffusion behavior of individual chains in a melt of linear poly(THF) was measured by means of a single-molecule fluorescence imaging technique. The combination of mean squared displacement (MSD) and cumulative distribution function (CDF) analysis demonstrated the broad distribution of diffusion coefficient of both the linear and cyclic polymer chains in the melt state. This indicates the presence of spatiotemporal heterogeneity of the polymer diffusion which occurs at much larger time and length scales than those expected from the current polymer physics theory. We further demonstrated that the cyclic chains showed marginally slower diffusion in comparison with the linear counterparts, to suggest the effective suppression of the translocation through the threading-entanglement with the linear matrix chains. This coincides with the higher activation energy for the diffusion of the cyclic chains than of the linear chains. These results suggest that the single-molecule imaging technique provides a powerful tool to analyze complicated polymer dynamics and contributes to the molecular level understanding of the chain interaction.
Assuntos
Transição de Fase , Polímeros/química , Difusão , Movimento (Física) , Propriedades de SuperfícieRESUMO
A regioselective nucleophilic esterification upon six-membered, thus considered unstrained, azacyclohexane quaternary salts has been disclosed by DFT calculations using a model compound and subsequent experimental studies of nucleophilic substitution on N-phenyl-3,3-dimethylpiperidinium salt groups at the polymer chain ends by carboxylate anions. An exclusive ring-emitting esterification was proposed theoretically and confirmed experimentally to produce a simple ester group, in contrast to less robust amino-ester linkages through an alternative ring-opening process with strained five-membered ammonium salts. This reaction was subsequently applied to a prototypical process of an electrostatic self-assembly and covalent fixation (ESA-CF) technique to produce a ring polymer having simple ester linking units.
Assuntos
Compostos Aza/química , Cicloexanos/química , Ésteres/síntese química , Polímeros/síntese química , Teoria Quântica , Ésteres/química , Estrutura Molecular , Polímeros/química , Sais/química , Eletricidade Estática , EstereoisomerismoRESUMO
A tandem alkyne-azide addition, i.e., click, and an olefin metathesis condensation, i.e., clip, reactions in conjunction with an electrostatic self-assembly and covalent fixation (ESA-CF) process, have been demonstrated as effective means to produce constructions of programmed folding of polymers having doubly fused tricyclic and triply fused tetracyclic topologies. Thus, a series of cyclic poly(tetrahydrofuran), poly(THF), precursors having an allyloxy group and an alkyne group (Ia), an allyloxy group and an azide group (Ib), and two alkyne groups (Ic) at the opposite positions was prepared by means of the ESA-CF method. The subsequent click reactions of Ia with a linear telechelic poly(THF) precursor having azide end groups (Id) and of Ib with Ic afforded a bridged dicyclic polymer (IIa) and a tandem spiro tricyclic precursor (IIb), respectively, both having two allyloxy groups at the opposite positions of the ring units. Finally, the intramolecular metathesis condensation reaction of IIa and of IIb in the presence of a Grubbs catalyst was performed to construct effectively a doubly fused tricyclic and a triply fused tetracyclic polymer topologies (III and IV), respectively.
Assuntos
Alcinos/química , Azidas/química , Polímeros/química , Alcenos/química , Ciclização , Espectroscopia de Ressonância Magnética , Conformação Molecular , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz , Eletricidade EstáticaRESUMO
A theoretical background is provided for the methods of the analysis and topological separation of complex macrocyclic polymers by means of size exclusion chromatography (SEC), liquid adsorption chromatography, and liquid chromatography at the critical condition. We focus on a particular problem of the separation of theta-shaped polymers from its three-armed star analogues. Based on the theory, we simulate chromatograms for model mixtures of polydisperse theta- and star-polymers and analyze conditions for good separation of these polymers by topology. A theory is compared with the behavior of star- and theta-shaped poly(THF)s in size exclusion and interactive chromatography, and a good qualitative agreement between theory and experiment is observed. In particular, it is shown that in both SEC and interactive chromatography theta-polymers elute after the corresponding stars of the same molar mass. According to theory and experiment, chromatography under the critical and near-critical interaction conditions is especially promising for the separation of polydisperse macrocyclic polymers from their linear or branched analogues.
Assuntos
Butileno Glicóis/análise , Butileno Glicóis/química , Cromatografia Líquida/métodos , Polímeros/análise , Polímeros/química , Cromatografia em GelRESUMO
We demonstrate a method for the synthesis of cyclic polymers and a protocol for characterizing their diffusive motion in a melt state at the single molecule level. An electrostatic self-assembly and covalent fixation (ESA-CF) process is used for the synthesis of the cyclic poly(tetrahydrofuran) (poly(THF)). The diffusive motion of individual cyclic polymer chains in a melt state is visualized using single molecule fluorescence imaging by incorporating a fluorophore unit in the cyclic chains. The diffusive motion of the chains is quantitatively characterized by means of a combination of mean-squared displacement (MSD) analysis and a cumulative distribution function (CDF) analysis. The cyclic polymer exhibits multiple-mode diffusion which is distinct from its linear counterpart. The results demonstrate that the diffusional heterogeneity of polymers that is often hidden behind ensemble averaging can be revealed by the efficient synthesis of the cyclic polymers using the ESA-CF process and the quantitative analysis of the diffusive motion at the single molecule level using the MSD and CDF analyses.
Assuntos
Polímeros , Difusão , Congelamento , Movimento (Física) , Eletricidade Estática , TemperaturaRESUMO
A collection of recent developments in topological polymer chemistry is presented. First, topological isomerism occurring on randomly coiled, flexible polymer molecules having cyclic and linear structures is discussed. Second, an electrostatic self-assembly and covalent fixation strategy has been developed for the synthesis of polymeric topological isomers. These isomers have double cyclic, manacle-, and theta-shaped constructions, and are prepared by using either linear or star telechelic polymer precursors having moderately strained cyclic ammonium salt groups, which carry multifunctional carboxylate counteranions. A technique of reversed-phase chromatography (RPC) is demonstrated as an effective means to separate polymers with different topologies, especially polymeric topological isomers. A further extension of topological polymer chemistry has been observed by dynamic selection from electrostatic polymer self-assembly to enable the effective formation of tadpole-shaped, cyclic-linear hybrid topologies.