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Eastern Illinois University

Masters Theses

2000

Articles 1 - 5 of 5

Full-Text Articles in Chemistry

A Time Resolved Laser Spectroscopy Study Of Resonance Energy Transfer Between Tb(Iii) And An Organic Dye: 6-Hydroxy-5-[(2-Methoxy-5-Methyl-4-Sulfophenyl)Azo]-2-Naphthalenesulfonic Acid Disodium Salt, Ronald Wesley Tennis Jan 2000

A Time Resolved Laser Spectroscopy Study Of Resonance Energy Transfer Between Tb(Iii) And An Organic Dye: 6-Hydroxy-5-[(2-Methoxy-5-Methyl-4-Sulfophenyl)Azo]-2-Naphthalenesulfonic Acid Disodium Salt, Ronald Wesley Tennis

Masters Theses

Intermolecular energy transfer is a process of crucial importance to photochemistry and photophysics. Complexed lanthanide ions are well suited as energy transfer donors because they display dependable absorption and luminescence qualities with narrow rare-earthion emission in addition to relatively long excited-state lifetimes.

This project used a pulsed nitrogen laser and high speed digital techniques to study energy transfer dynamics between excited state Tb(acac)3 and an ionic organic dye called Red 40. Luminescence decay profiles of excited terbium atoms in the presence of the quencher were measured in both high and low viscosity solvents. The effects of solvent viscosity and …


Degradation Of Trazine Compounds Via Metallic Iron Under Acidic Conditions, Tracy Dombek Jan 2000

Degradation Of Trazine Compounds Via Metallic Iron Under Acidic Conditions, Tracy Dombek

Masters Theses

The degradation of dissolved dimethoxyatrazine (2-chloro-4,6-dimethoxy-1,3,5-triazine), terbutylazine (2-chloro-4-ethylamino-6-terbutylamino-1,3 ,5-triazine) and deisopropylatrazine (2-amino-4-chloro-6-ethylamino-1,3,5-triazine) via metallic iron was studied as a function of solution pH. Generally, degradation was more rapid the lower the solution pH and higher the compound pKa. For dimethoxyatrazine kSA (kSA= k' (min-1)* V (L) / M (g) I SA(m2/g)) was found to be 1.33 (± 0.07) E-4 min-1 m-2 L at pH 2, 6.1 (± 0.6) E-5 min-1 m-2 L at pH 3 and 4.4 (± 0.6) E-5 min-1 m-2 L at pH 4. For …


Equilibrium And Kinetic Studies Of Isomerization Of (Co)5w[Η1-Pph2ch2p(P-Tol)2] And (Co)5w[Η1-P(P-Tol)2ch2pph2], Deliang Chen Jan 2000

Equilibrium And Kinetic Studies Of Isomerization Of (Co)5w[Η1-Pph2ch2p(P-Tol)2] And (Co)5w[Η1-P(P-Tol)2ch2pph2], Deliang Chen

Masters Theses

Unsymmetrical diphosphine tungsten complexes, (CO)5W[η1-PPh2CH2P(p-tol)2] and (CO)5W[η1-P(p-tol)2CH2PPh2], were prepared from (CO)5W(NH2Ph) and Ph2PCH2P(p-tol)2. Two approaches were successfully used to synthesize Ph2PCH2P(p-tol)2. The first utilized PPh2CH2Cl, prepared from PPh2H, CH2Cl2, and KOH under phase transfer conditions, from which Ph2PCH2P(p-tol)2 was …


Investigations Into The Synthesis And Transformations Of An Epoxy Β-Lactone, John Farrell Jan 2000

Investigations Into The Synthesis And Transformations Of An Epoxy Β-Lactone, John Farrell

Masters Theses

In connection with the continuing interests in the stereoselective rearrangements of β-lactones, an investigation of the synthesis and transformations of the epoxy β-lactone 4-(1,2-epoxypentyl)-3-trimethylsilyloxetan-2-one was undertaken. Two synthetic strategies to the desired epoxy β-lactone were studied. The first route was a two-step reaction sequence involving the aldol reaction of trimethylsilylacetic acid with (2R,3S)-epoxyhexanal, followed by lactonization of the resulting β-hydroxy acid with benzenesulfonyl chloride. Complications in preparing the requisite β-hydroxy acids under typical aldol reaction conditions rendered this route unworkable. The complexity and intractability of the aldol reaction mixtures was attributed to the multiple possibilities of …


Validation Of The Thermochemical Cycle Used In Computing Absolute Gas Phase Acidities And A Molecular-Orbital Study Of Protonated Ammonia-Water Cluster Ions, Jeremiah Aeschleman Jan 2000

Validation Of The Thermochemical Cycle Used In Computing Absolute Gas Phase Acidities And A Molecular-Orbital Study Of Protonated Ammonia-Water Cluster Ions, Jeremiah Aeschleman

Masters Theses

This work is comprised of two separate computational projects, an evaluation of the validity of an assumption made when computing absolute gas phase acidities with a thermochemical cycle and a molecular-orbital study of protonated ammonia-water clusters ions.

Relative gas phase acidities are measured experimentally and then adjusted using Hess' law to align them with an absolute scale. In the Hess' law calculation it is assumed that the electron affinity of A• and the ionization energy of H• are independent of temperature. To test this assumption, absolute enthalpies were computed for the anion (A-) and the radical (A•) at …