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2000

Organic Chemistry

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Articles 1 - 21 of 21

Full-Text Articles in Chemistry

Fourier Transform Raman Spectroscopy For Process Control In The Petroleum Industry, Kent Lawson Wise Oct 2000

Fourier Transform Raman Spectroscopy For Process Control In The Petroleum Industry, Kent Lawson Wise

Chemistry & Biochemistry Theses & Dissertations

As early as 1950, Raman spectroscopy was proposed as a method to determine aromatics and olefins in hydrocarbon mixtures. Until recently, extensive use of Raman spectroscopy in the characterization of hydrocarbons has not been practical due to several limitations. One early limitation to Raman analysis was the absence of a high intensity and stable excitation source. This problem has been overcome with the advent of lasers. Another limitation was the presence of fluorescence in hydrocarbon fuels when excited by visible lasers. However, the development of Fourier-transform Raman spectrometers now allows Raman spectra to be collected using near-IR lasers (e.g …


Risk Assessments For Chemical Stockpile Incinerators: Is The Supporting Guidance Adequate, Lawrence V. Tannenbaum Sep 2000

Risk Assessments For Chemical Stockpile Incinerators: Is The Supporting Guidance Adequate, Lawrence V. Tannenbaum

RISK: Health, Safety & Environment (1990-2002)

The author identifies potential deficiencies in guidance used in the United States for risk assessments of chemical weapons incinerators.


Fertilisers For Wine Grapes : An Information Package To Promote Efficient Fertiliser Practices, B. H. Goldspink, Neil Lantzke, Bob Paulin, Diana Louise Fisher, Colin Gordon, N. Cross, J M. Campbell-Clause Apr 2000

Fertilisers For Wine Grapes : An Information Package To Promote Efficient Fertiliser Practices, B. H. Goldspink, Neil Lantzke, Bob Paulin, Diana Louise Fisher, Colin Gordon, N. Cross, J M. Campbell-Clause

Bulletins 4000 -

No abstract provided.


The Vaporization Enthalpies Of Some Crown And Polyethers By Correlation Gas Chromatography, Gary Nichols, Jennifer Orf, Sarah M. Reiter, James Chickos, George W. Gokel Feb 2000

The Vaporization Enthalpies Of Some Crown And Polyethers By Correlation Gas Chromatography, Gary Nichols, Jennifer Orf, Sarah M. Reiter, James Chickos, George W. Gokel

James Chickos

No abstract provided.


9-Phenyl-3,4,4a,9a-Tetrahydrotriptycene And 9-Phenyl-1,2,3,4,4a,9a-Hexahydrotriptycene, John Masnovi, Shaoming Duan, Ronald J. Baker Jan 2000

9-Phenyl-3,4,4a,9a-Tetrahydrotriptycene And 9-Phenyl-1,2,3,4,4a,9a-Hexahydrotriptycene, John Masnovi, Shaoming Duan, Ronald J. Baker

Chemistry Faculty Publications

The structure of 9-phenyl-3,4,4a,9a-tetrahydrotriptycene, C26H22, (I), exhibits regiochemistry consistent with a stepwise mechanism for its formation from photocycloaddition of 1,3- cyclohexadiene and 9-phenylanthracene. Bond distances involving the bridgehead C atoms are similar in (I) and the hydrogenated derivative, 9-phenyl-1,2,3,4,4a,9a-hexahydrotriptycene, C26H24, (II), with bonds to the quaternary-C atoms exhibiting significant elongation [1.581 (2) A Ê in (I) and 1.585 (2) A Ê in (II)]. The molecular geometry precludes significant overlap between the phenyl groups and the interannular bonds in both compounds, indicating that the origin of the bond lengthening is steric in nature.


Isolation Of Curcumin From Tumeric, Ram Mohan, Andrew Anderson, Matthew Mitchell Jan 2000

Isolation Of Curcumin From Tumeric, Ram Mohan, Andrew Anderson, Matthew Mitchell

Scholarship

No abstract provided.


The Discovery-Oriented Approach To Organic Chemistry. 3. Boron-Trifluoride Catalyzed Rearrangement Of Cis- And Trans-Stilbene Oxides. An Exercise In 1H Nmr Spectroscopy For Sophomore Organic Laboratories, Ram Mohan, Erik Sgariglia, Regina Schopp, Kostas Gavardinas Jan 2000

The Discovery-Oriented Approach To Organic Chemistry. 3. Boron-Trifluoride Catalyzed Rearrangement Of Cis- And Trans-Stilbene Oxides. An Exercise In 1H Nmr Spectroscopy For Sophomore Organic Laboratories, Ram Mohan, Erik Sgariglia, Regina Schopp, Kostas Gavardinas

Scholarship

Epoxides, or oxiranes, are among the most versatile intermediates in organic synthesis. Yet very few examples of laboratory experiments involving reactions of epoxides are to be found in lab texts. We have developed a discovery-oriented laboratory experiment that involves the rearrangement of both cis- and trans-stilbene oxides with boron trifluoride etherate. The identity of the product can be easily determined by 1H NMR spectroscopy and, in case of the trans isomer, by preparation of the semicarbazone derivative as well. In spite of the simplicity of the experiment, the element of discovery ensures that student interest and enthusiasm are retained.


Hammett Correlations Of The Amide Proton Chemical Shift In A Series Of 1-Tosyl-3-(4-Substituted Phenyl)Ureas, Frank L. Setliff, Melody K. Harrison Jan 2000

Hammett Correlations Of The Amide Proton Chemical Shift In A Series Of 1-Tosyl-3-(4-Substituted Phenyl)Ureas, Frank L. Setliff, Melody K. Harrison

Journal of the Arkansas Academy of Science

No abstract provided.


Double Cysteine Mutations In Staphylococcal Nuclease: The Effect Of Artificially Introduced Disulfide Bonds On Protein Structure And Stability, Anna Terry Jan 2000

Double Cysteine Mutations In Staphylococcal Nuclease: The Effect Of Artificially Introduced Disulfide Bonds On Protein Structure And Stability, Anna Terry

Inquiry: The University of Arkansas Undergraduate Research Journal

Since a protein's function depends on its structure, basic research in protein structure facilitates the solution of many practical problems, such as the synthesis of more effective medicines. With this larger goal in sight, the purpose of this research project is to understand better the chemical principles that underlie protein structure and stability. Disulfide bonds are a potentially stabilizing feature of many proteins. They may form between cysteine residues in close proximity to one another if the orientation is favorable. Often found in proteins produced by organisms that grow at high temperatures, disulfide bonds may anchor side chains together, making …


Bismuth(Iii) Oxide Perchlorate Promoted Rearrangement Of Epoxides To Aldehydes And Ketones, Ram Mohan, Andrew Anderson, Jesse Blazek, Parie Garg, Brian Payne Jan 2000

Bismuth(Iii) Oxide Perchlorate Promoted Rearrangement Of Epoxides To Aldehydes And Ketones, Ram Mohan, Andrew Anderson, Jesse Blazek, Parie Garg, Brian Payne

Scholarship

Aryl-substituted epoxides and aliphatic epoxides with a tertiary epoxide carbon undergo smooth rearrangement in the presence of 10–50 mol% bismuth(III) oxide perchlorate, BiOClO4•xH2O, to give carbonyl compounds. The rearrangement is regioselective with aryl substituted epoxides and a single carbonyl compound arising from cleavage of benzylic C―O bond is formed. BiOClO4•xH2O is relatively non-toxic, insensitive to air and inexpensive, making this catalyst an attractive alternative to more corrosive and toxic Lewis acids such as BF3•Et2O or InCl3 currently used to effect epoxide rearrangements.


Preparation Of An Electrophilic 3-Methylindole Derivative: Difficulties In Forming A Stable, Suitable Material For The Preparation Of Tryptophan, Jason Boggs, Mariah Mcmasters, Robert W. Curley Jr., Michael J. Panigot Jan 2000

Preparation Of An Electrophilic 3-Methylindole Derivative: Difficulties In Forming A Stable, Suitable Material For The Preparation Of Tryptophan, Jason Boggs, Mariah Mcmasters, Robert W. Curley Jr., Michael J. Panigot

Journal of the Arkansas Academy of Science

In an attempt to prepare stereoselectively beta-deuterated tryptophan, N-protected indole-3-methanol compounds were prepared with model studies being done on undeuterated material. Conversion of these compounds to electrophilic species proved exceptionally difficult and resulted in very low yields or recovered starting material only. A summary of the current results utilizing N-tosyl indole-3-methanol will be presented as well as efforts using N-Boc indole-3-methanol.


Reaction Of Alpine-Borane With Aldehydes: Reactivity Rate Assessment By Observation Of The Disappearance Of The Carbonyl N - Pi* Peak By Uv-Visible Spectroscopy, Layla Bland, Michael J. Panigot Jan 2000

Reaction Of Alpine-Borane With Aldehydes: Reactivity Rate Assessment By Observation Of The Disappearance Of The Carbonyl N - Pi* Peak By Uv-Visible Spectroscopy, Layla Bland, Michael J. Panigot

Journal of the Arkansas Academy of Science

Due to an unexpectedly difficult reduction of indole-3-carbaldehyde and of isobutyraldehyde using the chiral reducing agent Alpine-Borane, the reactivity of several aliphatic, aromatic, and unsaturated aldehydes was investigated. This was done in order to determine whether there was a relationship between aldehyde structure and reduction rate. It was found that aliphatic aldehydes and aromatic aldehydes with no strongly electron-donating groups on the arene ring reduced faster than unsaturated aldehydes.


Hammett Correlations Of The Sulfonamide Proton Chemical Shift In A Series Of N-(Substituted Aryl)-P-Toluenesulfonamides, Frank L. Setliff, Tyson K. Spradlin Jan 2000

Hammett Correlations Of The Sulfonamide Proton Chemical Shift In A Series Of N-(Substituted Aryl)-P-Toluenesulfonamides, Frank L. Setliff, Tyson K. Spradlin

Journal of the Arkansas Academy of Science

No abstract provided.


On The Vertical And Adiabatic Excitation Energies Of The 21a(G), State Of Trans-1,3-Butadiene, Jason Lappe '00, Robert J. Cave Jan 2000

On The Vertical And Adiabatic Excitation Energies Of The 21a(G), State Of Trans-1,3-Butadiene, Jason Lappe '00, Robert J. Cave

All HMC Faculty Publications and Research

The excitation energy to the 21Ag state of trans-1,3-butadiene is examined using a variety of ab initio electronic structure techniques. While analogous states have been shown to be the lowest singlet excited states for all longer polyenes, for butadiene the position of the 21Ag state relative to the HOMO → LUMO excitation (11Bu) has been difficult to establish theoretically. We employ a variety of methods (CASSCF, CASPT2, MRSDCI, QDVPT) to examine both the vertical and adiabatic excitation energies for this state. At the ground-state geometry, the vertical excitation energies …


Studies Of Tryptophans In Membrane- Spanning "Walp" Peptides By Deuterium Nmr Spectroscopy, Nichole Reed Jan 2000

Studies Of Tryptophans In Membrane- Spanning "Walp" Peptides By Deuterium Nmr Spectroscopy, Nichole Reed

Inquiry: The University of Arkansas Undergraduate Research Journal

WALP pep tides of sequence acetyl-Gly-Trp-Trp-(Leu-Ala)-Trp-Trp-Ala-ethanolamine insert into lipid bilayers as membrane-spanning a-helices and modulate the lipid phase behavior as functions of n and the lipid acyl chain length. A key feature of the WALP peptides is the positioning of tryptophan (Trp) indole rings at the membrane/water interface. For the examples WALP19 with n = 6.5 and WALP23 with n = 8.5, we have labeled individual indoles with deuterium and incorporated the labeled peptides in oriented, hydrated bilayers of Dimyristoyl-phosphatidylcholine (DMPC). Deuterium NMR spectra from these samples show sharp resonances when the membrane normal is aligned either parallel (Beta = …


The Attempted Synthesis Of A Phenolphthalein-Capped Beta-Cyclodextrin, Susan Elizabeth Miller Jan 2000

The Attempted Synthesis Of A Phenolphthalein-Capped Beta-Cyclodextrin, Susan Elizabeth Miller

Dissertations, Theses, and Masters Projects

No abstract provided.


The Attempted Synthesis Of 4,4'-Bis(Dimethylamino)Azobenzene-3,3'-Disulfonylchloride As A Cap For Beta-Cyclodextrin, Katherine M. Ross Jan 2000

The Attempted Synthesis Of 4,4'-Bis(Dimethylamino)Azobenzene-3,3'-Disulfonylchloride As A Cap For Beta-Cyclodextrin, Katherine M. Ross

Dissertations, Theses, and Masters Projects

No abstract provided.


Photodecomposition Of Crystal Violet Dye In Water Solution And Suspensions Of Metal Oxides, Tatiana Yurievna Zakharian Jan 2000

Photodecomposition Of Crystal Violet Dye In Water Solution And Suspensions Of Metal Oxides, Tatiana Yurievna Zakharian

Dissertations and Theses @ UNI

Photodecomposition and photodecolorization of crystal violet dye were studied in water solution, hydrogen peroxide solution and suspensions of metal oxides. Spectroscopic evidence for the formation of methylated pararosanilines and demethylated derivatives of Michler's ketone as the reaction intermediates was obtained for the photodecomposition of crystal violet in water solution. The mechanism of formation of the intermediates was discussed in terms of charges of individual atoms calculated using Spartan software.

Photooxidation of crystal violet was shown to occur faster in hydrogen peroxide solution due to the higher oxidation potential of hydrogen peroxide and hydroxyl radicals. A mechanism similar to photooxidation in …


The Discovery-Oriented Approach To Organic Chemistry. 3. Boron-Trifluoride Catalyzed Rearrangement Of Cis- And Trans-Stilbene Oxides. An Exercise In 1H Nmr Spectroscopy For Sophomore Organic Laboratories, Ram S. Mohan, Erik A. Sgariglia, Regina Schopp, Kostas Gavardinas Dec 1999

The Discovery-Oriented Approach To Organic Chemistry. 3. Boron-Trifluoride Catalyzed Rearrangement Of Cis- And Trans-Stilbene Oxides. An Exercise In 1H Nmr Spectroscopy For Sophomore Organic Laboratories, Ram S. Mohan, Erik A. Sgariglia, Regina Schopp, Kostas Gavardinas

Ram S. Mohan

Epoxides, or oxiranes, are among the most versatile intermediates in organic synthesis. Yet very few examples of laboratory experiments involving reactions of epoxides are to be found in lab texts. We have developed a discovery-oriented laboratory experiment that involves the rearrangement of both cis- and trans-stilbene oxides with boron trifluoride etherate. The identity of the product can be easily determined by 1H NMR spectroscopy and, in case of the trans isomer, by preparation of the semicarbazone derivative as well. In spite of the simplicity of the experiment, the element of discovery ensures that student interest and enthusiasm are retained.


Isolation Of Curcumin From Tumeric, Ram S. Mohan, Andrew M. Anderson, Matthew S. Mitchell Dec 1999

Isolation Of Curcumin From Tumeric, Ram S. Mohan, Andrew M. Anderson, Matthew S. Mitchell

Ram S. Mohan

No abstract provided.


Bismuth(Iii) Oxide Perchlorate Promoted Rearrangement Of Epoxides To Aldehydes And Ketones, Ram S. Mohan, Andrew M. Anderson, Jesse M. Blazek, Parie Garg, Brian J. Payne Dec 1999

Bismuth(Iii) Oxide Perchlorate Promoted Rearrangement Of Epoxides To Aldehydes And Ketones, Ram S. Mohan, Andrew M. Anderson, Jesse M. Blazek, Parie Garg, Brian J. Payne

Ram S. Mohan

Aryl-substituted epoxides and aliphatic epoxides with a tertiary epoxide carbon undergo smooth rearrangement in the presence of 10–50 mol% bismuth(III) oxide perchlorate, BiOClO4•xH2O, to give carbonyl compounds. The rearrangement is regioselective with aryl substituted epoxides and a single carbonyl compound arising from cleavage of benzylic C―O bond is formed. BiOClO4•xH2O is relatively non-toxic, insensitive to air and inexpensive, making this catalyst an attractive alternative to more corrosive and toxic Lewis acids such as BF3•Et2O or InCl3 currently used to effect epoxide rearrangements.