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X-Y Zhu

Publications and source records attributed to X-Y Zhu.

3 recordsLinked to original sources

The surface chelate effect.

The presence of a surface chelate effect is established in the model system of Cu2+ adsorption on a self-assembled monolayer of 16-mercaptohexadecanoic acid (MHA) on Au. The formation constant of Cu2+ with the MHA surface was found to be 119 +/- 3.2 times greater than that of Cu2+ with succinic acid (HOOC-(CH2)2-COOH), and 213 +/- 4.0 times greater than that of Cu2+ with glutaric acid (HOOC-(CH2)3-COOH) in aqueous solutions. Both of these molecules are known to chelate to metal ions forming seven- and eight-membered rings. The greater surface chelate effect is attributed to the presence of the two-dimensional array of ligands on the surface. We believe the surface chelate effect demonstrated here is of general significance to adsorption on molecular surfaces and should depend strongly on chemical functionality and monolayer structure.

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Immobilization of oligonucleotides on poly(ethylene glycol) brush-coated Si surfaces.

High-density poly(ethylene glycol) (PEG) molecules are grafted onto Si surfaces in a brush-like configuration. We demonstrate that this surface is an excellent substrate for oligonucleotide immobilization. p-Maleimidophenyl isocyanate is used as a heterobifunctional cross-linker to tether thiol-modified oligonucleotides to terminal OH groups on the PEG brush. This approach gives excellent immobilization specificity and low background. The immobilized oligonucleotides show high sensitivity for the detection of complementary targets.

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Electron transfer at molecule-metal interfzces: a two-photon photoemission study.

Electron transfer between a molecular resonance and a metal surface is a ubiquitous process in many chemical disciplines, ranging from molecular electronics to surface photochemistry. This problem has been probed recently by two-photon photoemission spectroscopy. The first photon excites an electron from an occupied metal state to an unoccupied molecular resonance. Subsequent evolution of the excited electronic wavefunction is probed in energy, momentum, and time domains by the absorption of a second photon, which ionizes the electron for detection. These experiments reveal the important roles of molecule-metal wavefunction mixing, intermolecular band formation, polarization, and localization in interfacial electron transfer.

Journal Article↗