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Journal ArticleDOI

Dielectric properties of single crystals of the substituted diacetylene pTS: effect of the solid-state polymerization and phase transitions

TLDR
In this paper, the authors measured the dielectric permittivities of p TS diacetylene in the directions parallel and perpendicular to the direction of polymer chain growth and identified the transition as an antiferroelectric one, the sublattice polarization being most probably the order parameter.
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This article is published in Chemical Physics.The article was published on 1986-05-15. It has received 26 citations till now. The article focuses on the topics: Dielectric & Polymerization.

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Citations
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Journal ArticleDOI

Reinvestigation of generation and transport of charge carriers in crystalline polydiacetylenes (PDAs)

TL;DR: In this paper, the authors re-examined data on stationary and pulsed photoconduction in PDA-TS and re-enforce the occurrence of geminate pair recombination, yet show that the conventional onedimensional version of Onsager's theory is inappropriate because it ignores ballistic electron-hole pair separation and geminate 1D-recombination of a pair of Coulombically unbound charges on the same chain.
Journal ArticleDOI

Anisotropy of the charge-carrier mobility in polydiacetylene crystals

TL;DR: In this paper, the anisotropic mobility of excess charge carriers in pure and mixed polydiacetylene derivatives was determined by time-resolved measurement of the microwave conductivity.
Book ChapterDOI

Chapter 4 – Polydiacetylenes

TL;DR: In this article, the authors discuss polydiacetylenes (PDAs), which constitute a class of conjugated polymers that continue to attract a significant amount of scientific attention.
Journal ArticleDOI

Dynamic Stark effect as a probe of the evolution of geminate electron-hole pairs in a conjugated polymer

TL;DR: In this paper, a transient Stark shift of the absorption band was observed and related to kinetics of generated excitons and electron-hole pairs, which provided unique information on the charge redistribution in excited states.
References
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Journal ArticleDOI

Optical Nonlinearities in One-Dimensional-Conjugated Polymer Crystals.

TL;DR: The one-dimensional electronic delocalization that results from the solid-state polymerization of diacetylenes produces a dramatic enhancement of the optical nonlinearities of these compounds as discussed by the authors.
Journal ArticleDOI

Topochemical reactions of monomers with conjugated triple-bonds. IV. Polymerization of bis-(p-toluene sulfonate) of 2.4-hexadiin-1.6-diol†‡

TL;DR: In this article, the formation of nuclei must be an important feature of the reaction mechanism of 2.4-hexadiin-1.6-diol-bis-p-toluene sulfonate.
Journal ArticleDOI

Solid state polymerization of bis-(p-toluene sulphonate) of 2,4-hexadiyne-1,6-diol: Part 1 X-ray diffraction and spectroscopic observations

TL;DR: In this article, the thermal polymerization of bis-(p-toluene sulphonate) of 2,4-hexadiyne-1,6-diol has been studied by optical and Raman spectroscopy and X-ray diffraction.
Journal ArticleDOI

Solid‐state polymerization of a diacetylene crystal: Thermal, ultraviolet, and γ‐ray polymerization of 2,4‐hexadiyne‐1,6‐diol bis‐(p‐toluene sulfonate)

TL;DR: In this paper, the authors used the triplet excited state of the diacetylene monomer as the chain initiation species to obtain the activation energy of 2,4hexadiyne-1,6-diol bis-(p-toluene sulfonate) (PTS).
Journal ArticleDOI

Investigation of the topochemical solid‐state polymerization of a diacetylene by X‐ray methods and brillouin‐spectroscopy

TL;DR: In this paper, the crystal structure of a polymerizable diacetylene monomer has been solved and the coordinates of all atoms prior and after the reaction have been determined, and the length of the growing polymer chains and their distribution in the monomer matrix can be determined by the evaluation of the Brillouin spectra in terms of a model which considers the polymerizing crystal as a composite material of high modulus rod-like macromolecules dispersed in the low-modulus matrix of the residual monomer.
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