Physical Sciences and Mathematics Commons^™

Physical Adsorption Of Linear Hydrocarbon Quadrupoles On Graphite And Mgo (100): Effects Of The Compatibility Of Surface And Molecular Symmetries, Andrew J. Pedersen

Doctoral Dissertations

The process of physical adsorption finds a practical role in wide-ranging fields from catalysis, to lubrication, and even optoelectronics. Furthermore, it provides a mechanism to probe the fundamental understanding of intermolecular forces and how symmetries can play a role in the behavior of a system. Linear quadrupoles preferentially adopt square-T configurations when confined in two dimensions. This would lead the system to adopt a four-fold symmetry in the molecular lattice.

Two archetypal surfaces often studied in physisorption research are MgO (100), which has a four-fold symmetry of alternating charges, and the basal plane of graphite, which has a six-fold symmetry …

Mechanism Study On The Electrocatalytic Oxidation Of Acetylene To Oxalic Acid, Xiu-Li Song, Rui-Long Jia, Wen-Yan Dong, Zhen-Hai Liang

Journal of Electrochemistry

A new method of electrocatalytic synthesis oxalic acid from acetylene was explored and the synthesized oxalic acid was characterized by Ultraviolet-visible spectrophotometry (Uv-vis) and Infrared spectroscopy (IR). First-principles calculations were carried out to examine the adsorption of acetylene over the Pt(111) surface. The electrocatalytic oxidation behavior of acetylene has been investigated on a Pt electrode by cyclic voltammetry (CV) and steady-state polarization in Na₂SO₄ solution. The formation mechanism of oxalic acid in the Na₂SO₄ solution was proposed and the transfer coefficients of the reaction were calculated. The results show that acetylene molecule tends to …

Analysis Of The Electron Withdrawing Capability Of Acetylene Groups For Promoting Nucleophilic Aromatic Substitution, Eric D. Braunstein

Honors Theses

It is well known that electron withdrawing groups, such as nitro or carbonyl groups, activate benzene rings for nucleophilic aromatic substitution. However, little research has been done to investigate the electron withdrawing capability of acetylene groups for substitution of aromatic halides. Experimental and computational investigations on the reactivity of halogenated phenylacetylenes with oxygen and other nucleophiles will be described.

Fragmentation Processes Following Core Excitation In Acetylene And Ethylene By Partial Ion Yield Spectroscopy, Maria Novella Piancastelli, Wayne C. Stolte, Gunnar Ohrwall, S-W Yu, D. Bull, K. Lantz, Alfred S. Schlachter, Dennis W. Lindle

Chemistry and Biochemistry Faculty Research

Partial ion yield spectroscopy provides a very detailed picture of fragmentation processes following core excitation in isolated molecules. We exploit this potential in the analysis of decay processes following C1s→π and C1s→Rydberg excitations in ethylene and acetylene. We show that the relative intensity of spectral features related to the excitation to empty molecular orbitals or to Rydberg states is a function of the time variation of the fragmentation process. Namely, we see an intensity increase in the Rydberg states compared to the molecular orbitals as the fragmentation process becomes more extensive, a result attributable to the diffuse nature of the …