4.4 Article Proceedings Paper

Adsorption-induced conformational changes of porphyrin derivatives and formation of twin superstructures on a copper surface

Journal

THIN SOLID FILMS
Volume 464, Issue -, Pages 393-397

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.tsf.2004.06.084

Keywords

chirality; isomer; porphyrin; STM; adsorption

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The adsorbed structures and assembly behavior of porphyrin derivatives on Cu substrates were studied using low-temperature scanning tunneling microscopy (STM). The STM images showed that a porphyrin molecule with four tert-butyl-phenyl groups (H-2-TBPP) forms twin domains of a square superstructure. The deformation of H-2-TBPP required to explain the STM images forms a pair of corresponding chiral conformations. The conformation determines which of the twin domains is formed. In contrast, porphyrin molecules with two tert-butylphenyl and two vinyl-phenyl groups (H-2-TBPVPP) showed no form of ordered assembly due to the strong interaction between the vinyl phenyl and substrate. STM observation showed that cis- and trans-H-2-TBPVPP undergo different conformational changes, leading to mirror and two-fold symmetry, respectively. (C) 2004 Elsevier B.V. All rights reserved.

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