Formation of self-assembled monolayer of curcuminoid molecules on gold surfaces
Creators
- 1. Departamento de Física, Facultad de Ciencias Físicas y Matemáticas, Universidad de Chile, Av. Blanco Encalada 2008, Santiago (Chile)
- 2. Departamento de Ciencia de los Materiales, Facultad de Ciencias Físicas y Matemáticas, Universidad de Chile, Beaucheff 851, Santiago (Chile)
- 3. CSIC-ICMAB (Institut de Ciència dels Materials de Barcelona), Campus de la Universitat Autònoma de Barcelona, 08193 Bellaterra (Spain)
- 4. ICREA (Institució Catalana de Recerca i Estudis Avançats), Passeig Lluís Companys, 23, 08018, Barcelona (Spain)
Description
Highlights: • Thiophene curcuminoid molecules deposited on a gold surface by immersion. • Molecular dynamic studies of the molecular arrangement approaching the surface. • XPS and STM studies showing different arrangement of the molecules on the surface. • Molecular Interaction with surface depends on the sulfur position in thiophene rings. • Temporal evolution of the molecular arrangement on the surface. - Abstract: We investigated the formation of self-assembled monolayers of two thiophene curcuminoid molecules, 2-thphCCM (1) and 3-thphCCM (2), on polycrystalline gold substrates prepared by immersion of the surfaces in a solution of the molecules during 24 h. The functionalized surfaces were studied by scanning tunneling microscopy (STM) and X-ray photoelectron spectroscopy (XPS). Despite the fact that both molecules have the same composition and almost the same structure, these molecules exhibit different behavior on the gold surface, which can be explained by the different positions of the sulfur atoms in the terminal aromatic rings. In the case of molecule 1, the complete formation of a SAM can be observed after 24 h of immersion. In the case of molecule 2, the transition from flat-lying to upright configuration on the surface is still in process after 24 h of immersion. This is attributed to the fact that molecule 2 have the sulfur atoms more exposed than molecule 1.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.apsusc.2016.09.077Additional details
Identifiers
- DOI
- 10.1016/j.apsusc.2016.09.077;
- PII
- S0169-4332(16)31946-8;
Publishing Information
- Journal Title
- Applied Surface Science
- Journal Volume
- 392
- Journal Page Range
- p. 834-840
- ISSN
- 0169-4332
- CODEN
- ASUSEE
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48077676
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Descriptors DEI
- CONFIGURATION; CURCUMIN; GOLD; INTERACTIONS; MOLECULAR DYNAMICS METHOD; MOLECULES; POLYCRYSTALS; POLYCYCLIC SULFUR HETEROCYCLES; SCANNING TUNNELING MICROSCOPY; SUBSTRATES; SULFUR; SURFACES; THIOPHENE; TUNNEL EFFECT; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- AROMATICS; CALCULATION METHODS; CRYSTALS; DYES; ELECTRON SPECTROSCOPY; ELEMENTS; ETHERS; HETEROCYCLIC COMPOUNDS; HYDROCARBONS; HYDROXY COMPOUNDS; KETONES; METALS; MICROSCOPY; NONMETALS; ORGANIC COMPOUNDS; ORGANIC OXYGEN COMPOUNDS; ORGANIC SULFUR COMPOUNDS; PHENOLS; PHOTOELECTRON SPECTROSCOPY; POLYPHENOLS; SPECTROSCOPY; TRANSITION ELEMENTS
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.