Benzylic amide [2] catenane (CAT1) deposited from a methanol solution onto highly oriented pyrolitic graphite (HOPG) has been investigated by ambient scanning tunneling microscopy (STM). Submolecular features are resolved which suggest that the adsorption of CAT1 is driven by the electrostatic attraction of carbonyl groups and HOPG. Our evidence shows that CAT1 is mobile at RT on HOPG surface. A statistical analysis of the observed features reveals a bimodal distribution of the lateral size which correlates with the expected diameter of a single macrocycle and the catenane respectively.

STM investigation of flexible supramolecules: benzylic amide [2] catenanes

Biscarini F;Zamboni R
1999

Abstract

Benzylic amide [2] catenane (CAT1) deposited from a methanol solution onto highly oriented pyrolitic graphite (HOPG) has been investigated by ambient scanning tunneling microscopy (STM). Submolecular features are resolved which suggest that the adsorption of CAT1 is driven by the electrostatic attraction of carbonyl groups and HOPG. Our evidence shows that CAT1 is mobile at RT on HOPG surface. A statistical analysis of the observed features reveals a bimodal distribution of the lateral size which correlates with the expected diameter of a single macrocycle and the catenane respectively.
1999
Istituto per lo Studio dei Materiali Nanostrutturati - ISMN
Inglese
102
1-3
1466
1467
2
http://www.sciencedirect.com/science/article/pii/S0379677998005396
Sì, ma tipo non specificato
Adsorption; Amines; Methanol; Molecular structure; Molecules; Scanning tunneling microscopy; Solutions; Statistical methods; Surfaces
Synthetic Metals Volume 102, Issue 1-3, June 1999, Pages 1466-1467 Proceedings of the 1998 International Conference on Science and Technology of Synthetic Metals (ICSM-98); Montpellier; ; 12 July 1998 through 18 July 1998; Code 55266
2
info:eu-repo/semantics/article
262
Biscarini, F.; Gebauer, W.; Di Domenico, D.; Zamboni, R.
01 Contributo su Rivista::01.01 Articolo in rivista
none
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/310005
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