Polyacetylene: Myth and Reality

聚乙炔 激发态 化学物理 单重态 材料科学 直接的 凝聚态物理 分子物理学 化学 物理 聚合物 量子力学 复合材料
作者
Bruce S. Hudson
出处
期刊:Materials [MDPI AG]
卷期号:11 (2): 242-242 被引量:31
标识
DOI:10.3390/ma11020242
摘要

Polyacetylene, the simplest and oldest of potentially conducting polymers, has never been made in a form that permits rigorous determination of its structure. Trans polyacetylene in its fully extended form will have a potential energy surface with two equivalent minima. It has been assumed that this results in bond length alternation. It is, rather, very likely that the zero-point energy is above the Peierls barrier. The experimental studies that purport to show bond alternation are reviewed and shown to be compromised by serious experimental inconsistencies or by the presence, for which there is considerable evidence, of finite chain polyenes. In this view, addition of dopants results in conductivity by facilitation of charge transport between finite polyenes. The double minimum potential that necessarily occurs for polyacetylene, if viewed as the result of elongation of finite chains, originates from admixture of the 1¹Ag ground electronic state with the 2¹Ag excited electronic singlet state. This excitation is diradical (two electron) in character. The polyacetylene limit is an equal admixture of these two ¹Ag states making theory intractable for long chains. A method is outlined for preparation of high molecular weight polyacetylene with fully extended chains that are prevented from reacting with neighboring chains.
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