International audienceIn this paper, we investigate the self-organization of NTCDI molecules on Au(111) surface by combining Density Functional Theory (DFT) and experiments based on scanning tunneling microscopy (STM) and infrared spectroscopy measurements. The competition between the cohesive and adsorption energy on the flat surface is discussed. It was shown that the network is mainly stabilized by cohesive interactions explaining the mobility of the network over the surface. The comparison between experimental and infrared spectra enables confirmation of the effect and importance of the H-bonds in the network stability. STM images at different voltages and in ambient conditions were interpreted by projected density of states calculations and compared with experiment. The theoretically proposed network geometry was characterized at the molecular level reproducing the experimental STM image
The synthesis of five light absorbing triazolobithiophenic thiols, which were utilized for producing self-assembled monolayers (SAMs) on gold surfaces, is presented. The monolayer formation was monitored by cyclic voltammetry, indicating excellent surface coverage. The new triazolobithiophenic compounds exhibited an absorption maximum around 340 nm, which is close to the emission wavelength of a standard nitrogen laser. Consequently these compounds could be used to aid ionization in laser desorption mass spectrometry (MS).
The current manuscript presents 3-[5'-(methylthio)-2,2'-bithiophen-5-ylthio]propanenitrile (MT3P), as a novel matrix molecule, which facilitates the selective ionization of alkaloids in matrix-assisted laser desorption/ionization mass spectrometry. Exhibiting strong ionizing properties at low levels of laser energy, MT3P was evaluated on 55 compounds belonging to various chemical families. The observed molecular ion yields induced by MT3P were compared with those obtained by commercially available matrices such as 1,8-dihydroxy-9,10-dihydroanthracen-9-one, α-cyano-4-hydroxycinnamic acid, 2,2':5',2"-terthiophene and 2,5-dihydroxybenzoic acid. In conclusion, MT3P displayed excellent ionization properties for 23 out of 25 investigated alkaloids, while showing little to no interaction with compounds from different chemical origin. Further, in comparison to other tested matrices, MT3P generally facilitated better ionization of alkaloids. Eventually, levels of laser energy were adjusted to obtain spectra with significantly reduced matrix noise.
Mainly based on electrochemical investigations, this work provides evidence of discrimination between self‐assembled monolayers (SAMs) prepared from alkanethiols or symmetrical dialkyl disulfides on gold. Gravimetric experiments carried out by quartz crystal microbalance during the elaboration of ferrocene based SAMs (from alkanethiols FcC15SH and dialkyl disulfides FcC15SSC15Fc), showed significant differences between monolayers made from the two precursors. The recorded mass was almost 60 % more important with FcC15SH by comparison with FcC15SSC15Fc. The resulting cyclic voltammograms also highlighted a 60 % difference concerning the surface coverage of ferrocene heads. Moreover, dialkyl disulfide and thiol anchoring groups led to symmetrical and dissymmetrical peaks, respectively, suggesting not insignificant differences concerning interactions between adsorbed species into the two kinds of elaborated monolayers. These observations were confirmed on SAMs obtained from other precursors possessing shorter chain length or another functional moiety.
Within the last 25 years, matrix-assisted laser desorption ionization (MALDI) has become a powerful analytical tool in mass spectrometry (MS). While the method has been successfully applied to characterize large organic molecules such as proteins, sugars and polymers, its utilization for small molecules (≤ 600 Da) is significantly impaired by the coformation of matrix ions. Reducing or eliminating matrix-related signals has been subject of many studies. Some of which propose the enhancement of so-called matrix suppression effects, while others suggest the replacement of matrix molecules by materials such as microporous silicon. Alternatively, the immobilization of matrix molecules by utilizing them as self-assembled monolayers (SAMs) has been discussed. In continuation of this research, the current manuscript focuses on the elucidation of ion formation processes occurring on the surface of light absorbing SAMs. Ion yields obtained by free and immobilized matrix molecules as well as those generated by matrix-free gold film-assisted laser desorption ionization (GF-LDI) were compared. Experiments showed that the formation of strong analyte signals essentially required the presence of free matrix molecules, while the immobilization of the latter severely impaired ionization. The observed effect inversely correlated with the surface coverage of SAMs determined by cyclic voltammetry (CV). Based on these findings, the MS signal generated on light absorbing SAMs could be used supplementary to CV for determining the surface coverage of light absorbing SAMs.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.