𝔖 Bobbio Scriptorium
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Molecular electronic properties of fused rigid porphyrin-oligomer molecular wires

✍ Scribed by J.R. Reimers; T.X. Lü; M.J. Crossley; N.S. Hush


Book ID
103036264
Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
512 KB
Volume
256
Category
Article
ISSN
0009-2614

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✦ Synopsis


Porphyrin-derived materials may be linked together by fusion to rigid coplanar aromatic bridges such as substituted anthracenes to form linear or branched oligomers. Here, we consider linear oligomers of free-base porphyrin and meso-tetra-aryl derivatives, such as the tetramer. Previously, a number of semi-empirical quantum-chemical methods have been used to determine the geometries and electronic structures of the ground and excited electronic states. Here, the inter-ring coupling responsible for electron or hole conduction is discussed as a function of oligomer size and the predicted molecular-wire characteristics outlined. Comparisons with properties of other linear molecular wires are summarized, and possibilities of introducing switching capacity are indicated. It should be noted that the edge-to-edge length of the tetramer is ca. 56 ]k, sufficient for trans-membrane spanning, while the length of the octamer, ca. 110 A, is sufficient for nano-electrode spanning.


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Molecular orbital (MO) calculations of more than 60 porphyrinic π conjugated structures have been performed within the framework of the Pariser–Parr–Pople approximation. The results of a series of compounds are introduced and summarized in order to show how they vary depending on the systematic chan