2020
DOI: 10.1016/j.apsusc.2020.145916
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2D mesoporous atomic monolayers of phenyleneethynylene oligomers on pyrolytic graphite surfaces analyzed by scanning tunneling microscopy

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Cited by 2 publications
(2 citation statements)
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“…We 11 and others 12 also previously reported that the supramolecular organization of phenyleneethynylenes depends strongly on the number of repetitive units and the termini or side chains. In particular, we demonstrated the effect of benzyl or carboxylic acid terminal groups in trimers and pentamers with a dodecanoxy lateral chain in the central phenyl group.…”
Section: Introductionmentioning
confidence: 64%
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“…We 11 and others 12 also previously reported that the supramolecular organization of phenyleneethynylenes depends strongly on the number of repetitive units and the termini or side chains. In particular, we demonstrated the effect of benzyl or carboxylic acid terminal groups in trimers and pentamers with a dodecanoxy lateral chain in the central phenyl group.…”
Section: Introductionmentioning
confidence: 64%
“…However, at least two supramolecular interactions could be considered (vide infra), as shown in Figure d. In this respect, we and others recently published that (benzyl) benzoate and carboxylic acid-terminated phenyleneethynylene macromolecules bearing dodecanoxy (or hexyloxy) side chains form stable 2D films on HOPG. , We found that for the (benzyl) benzoate-terminated oligomers, a staggered arrangement of molecules occurs endorsed by the π–π interaction between the benzyls. In contrast, for the carboxylic acid-terminated oligomers, a linear-type arrangement is promoted by the hydrogen bond created between the carboxylic acid groups.…”
Section: Resultsmentioning
confidence: 98%