Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Conjugated polymers of intrinsic

A key limitation in the applications of CMPs is the insolubility and poor processability. Recently, Cheng et al. synthesised a conjugated polymer of intrinsic microporosity (C-PIMs) that was soluble and processable. While it cannot be classed as a CMP due to its lack of 3-D network structure, it does open the possibility for similar strategies to be adopted for CMP materials. [Pg.175]

Apart from the tunable color emission covering the full visible range, there are several other aspects supporting the interest in PTs for PLEDs. PTs are examples of classical conjugated polymers with intrinsic one-dimensionality of the polymer chain. Alignment can induce anisotropy in macroscopic properties such as electron transport or optical properties. Polarized... [Pg.202]

Another approach to CPL is the synthesis of conjugated polymers with intrinsic chiro-optical properties. A variety of polymers with CPPL have been synthesized so far. Most of them are based upon well-known conjugated polymers such as poly(thiophene)s [4,111], polyphenylene vinylene)s [123], poly(thienylene vinylene)s [124], ladder polymers [125], PPPs [126], polyphenylene ethynylene)s, [127] and poly(fluorenes) [128]. All of them have been modified with chiral side-chains, which induce the chiro-optical properties. [Pg.472]

Conjugated polymer with intrinsic 3.4 Electro-oxidation of alcohols and ... [Pg.471]

Porous organic frameworks (POFs), such as metal-organic frameworks (MOFs), covalent organic frameworks (COFs), conjugated micro-porous polymers (CMPs), ° polymers of intrinsic microporosity (PIMs), crystalline triazine-based organic frameworks (CTFs), hyper-crosslinked... [Pg.221]

The proposed scenario is mainly based on the molecular approach, which considers conjugated polymer films as an ensemble of short (molecular) segments. The main point in the model is that the nature of the electronic state is molecular, i.e. described by localized wavefunctions and discrete energy levels. In spite of the success of this model, in which disorder plays a fundamental role, the description of the basic intrachain properties remains unsatisfactory. The nature of the lowest excited state in m-LPPP is still elusive. Extrinsic dissociation mechanisms (such as charge transfer at accepting impurities) are not clearly distinguished from intrinsic ones, and the question of intrachain versus interchain charge separation is not yet answered. [Pg.456]

In general. Figure 9-2 b to c show strategies to make conjugated polymers more proeessible but it must be noted that the different synthetic approaches do not only result in different degrees of (a) chemical purity but also alter (b) the physical properties due lo intrinsic differences. Compared to a pure conjugated... [Pg.458]

Conjugated polymers are generally poor conductors unless they have been doped (oxidized or reduced) to generate mobile charge carriers. This can be explained by the schematic band diagrams shown in Fig. I.23 Polymerization causes the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) of the monomer to split into n and n bands. In solid-state terminology these are the valence and conduction bands, respectively. In the neutral forms shown in Structures 1-4, the valence band is filled, the conduction band is empty, and the band gap (Eg) is typically 2-3 eV.24 There is therefore little intrinsic conductivity. [Pg.551]

The linear and nonlinear optical properties of one-dimensional conjugated polymers contain a wealth of information closely related to the structure and dynamics of the ir-electron distribution and to their interaction with the lattice distorsions. The existing values of the nonlinear susceptibilities indicate that these materials are strong candidates for nonlinear optical devices in different applications. However their time response may be limited by the diffusion time of intrinsic conjugation defects and the electron-phonon coupling. Since these defects arise from competition of resonant chemical structures the possible remedy is to control this competition without affecting the delocalization. The understanding of the polymerisation process is consequently essential. [Pg.183]


See other pages where Conjugated polymers of intrinsic is mentioned: [Pg.29]    [Pg.97]    [Pg.185]    [Pg.29]    [Pg.97]    [Pg.185]    [Pg.271]    [Pg.451]    [Pg.545]    [Pg.26]    [Pg.516]    [Pg.6]    [Pg.5]    [Pg.116]    [Pg.143]    [Pg.145]    [Pg.741]    [Pg.2]    [Pg.67]    [Pg.105]    [Pg.107]    [Pg.155]    [Pg.186]    [Pg.287]    [Pg.742]    [Pg.854]    [Pg.191]    [Pg.25]    [Pg.154]    [Pg.162]    [Pg.182]    [Pg.189]    [Pg.226]    [Pg.402]    [Pg.470]    [Pg.553]    [Pg.168]    [Pg.171]    [Pg.2]    [Pg.116]    [Pg.375]   


SEARCH



Conjugated polymers of intrinsic microporosity

Intrinsic polymer

Polymers of intrinsic

© 2024 chempedia.info