We demonstrate that the functionalization of carbon nanotubes dramatically alters their sorption characteristics. The effect of covalent functionalization of multiwalled carbon nanotubes (MWNTs) on the gas phase adsorption and desorption of polar and nonpolar organics is presented. Carboxylation and nitration led to the generation of polar functional groups on the nanotube surface. The derivati...

A theoretical study of the peri interactions, both intramolecular hydrogen (HB) and chalcogen bonds (YB), in 1-hydroxy-8YH-naphthalene, 1,4-dihydroxy-5,8-di-YH-naphthalene, and 1,5-dihydroxy-4,8-di-YH-naphthalene, with Y = O, S, and Se was carried out. The systems with a OH:Y hydrogen bond are the most stable ones followed by those with a chalcogen O:Y interaction, those with a YH:O hydrogen bo...

We have used temperature-dependent single molecule force spectroscopy to stretch covalently anchored carboxymethylated amylose (CMA) polymers attached to an amino-functionalized AFM cantilever. Using an Arrhenius kinetics model based on a Morse potential as a one-dimensional representation of covalent bonds, we have extracted kinetic and structural parameters of the bond rupture process. With 3...

Mass spectrometry is a valuable tool for the analysis and identification of chemical compounds, particularly proteins and peptides. Lichenysins G, the major cyclic lipopeptide of lichenysin, and the non-covalent complex of lichenysins G and 4-ethylguaiacol were investigated with negative ion ESI tandem mass spectrometry. The different fragmentation mechanisms for these compounds were investigat...

We have performed an experimental structure determination of the ordered p(sqrt[3] x sqrt[3])R30 degrees structures of chlorine and iodine on Au{111} using low-energy electron diffraction (LEED). Despite great similarities in the structure of the underlying substrate, which shows only minor deviations from the bulk positions in both cases, chlorine and iodine are found to adsorb in different ad...

In dynamic covalent chemistry, reactions follow a thermodynamically controlled pathway through equilibria. Reversible covalent-bond formation and breaking in process enables the interconversion of products formed under kinetic control to more stable isomers. Notably, enantioselective catalysis transformations has not been reported applied complex molecule synthesis. We describe discovery metal-...

A precursor film has been fabricated from TGA (thiolglycolic acid)-stabilized CdTe nanoparticles and NDR (nitro-containing diazoresin) using electrostatic interactions and the standard layer-by-layer assembly method; covalent bonds are formed under ultraviolet irradiation. XPS provided evidence for the presence of CdTe nanoparticles within the polymer ultrathin films. UV-visible spectroscopy an...

The role of organometallic intermediates during on-surface polymerization via Ullmann coupling was studied on Ag(111). The polymerization progress was monitored by X-ray photoelectron spectroscopy (XPS). Scanning Tunneling Microscopy (STM) was used to characterize organometallic and covalent networks and to identify the temperature regimes for organometallic and covalent bond formation.