TIGER

Journal Articles: 11 results
Synthesis of Albendazole Metabolite: Characterization and HPLC Determination  Graciela Mahler, Danilo Davyt, Sandra Gordon, Marcelo Incerti, Ivana Núñez, Horacio Pezaroglo, Laura Scarone, Gloria Serra, Mauricio Silvera, and Eduardo Manta
In this laboratory activity, students are introduced to the synthesis of an albendazole metabolite obtained by a sulfide oxidation reaction. Albendazole as well as its metabolite, albendazole sulfoxide, are used as anthelmintic drugs. The oxidation reagent is H2O2 in acetic acid. The reaction is environmental friendly, fast, and proceeds with high yield. The crude reaction is analyzed by HPLC chromatography to determine purity. The simplicity of the experiment allows students to study chiral concepts, physicochemical and spectroscopic properties of the compounds, and HPLC determinations.
Mahler, Graciela; Davyt, Danilo; Gordon, Sandra; Incerti, Marcelo; Núñez, Ivana; Pezaroglo, Horacio; Scarone, Laura; Serra, Gloria; Silvera, Mauricio; Manta, Eduardo. J. Chem. Educ. 2008, 85, 1652.
Chirality / Optical Activity |
Drugs / Pharmaceuticals |
HPLC |
Medicinal Chemistry |
Organosulfur Compounds |
Oxidation / Reduction |
Synthesis
From the Research Bench to the Teaching Laboratory: Gold Nanoparticle Layering  Maria Oliver-Hoyo and Ralph W. Gerber
The procedures presented here involve the synthesis of gold colloidal suspensions, attachment of a functional group to glass with subsequent creation of self-assembled monolayers through deposition of gold nanoparticles, and measurements of wavelengths, absorbance, and conductivity.
Oliver-Hoyo, Maria; Gerber, Ralph W. J. Chem. Educ. 2007, 84, 1174.
Nanotechnology |
Surface Science |
Synthesis |
UV-Vis Spectroscopy
The Discovery and Development of Cisplatin  Rebecca A. Alderden, Matthew D. Hall, and Trevor W. Hambley
Cisplatin is currently one of the most widely used anticancer drugs in the world. The unlikely events surrounding the discovery of its anticancer activity, subsequent introduction into the clinic, and the continuing research into platinum compounds is the subject of this review.
Alderden, Rebecca A.; Hall, Matthew D.; Hambley, Trevor W. J. Chem. Educ. 2006, 83, 728.
Bioinorganic Chemistry |
Coordination Compounds |
Drugs / Pharmaceuticals |
Medicinal Chemistry |
Metallic Bonding |
Oxidation State |
Synthesis
Volatile Organic Sulfur Compounds of Environmental Interest: Dimethyl Sulfide and Methanethiol. An Introductory Overview  Thomas G. Chasteen and Ronald Bentley
Volatile organic sulfur compounds and their degradation products play important environmental roles in global warming, acid precipitation, and cloud formation. Two important members of this group, dimethyl sulfide, DMS, and methanethiol, MT, are formed by living organisms as well as by abiotic processes. The chemical reactions responsible for the biosynthesis of DMS and MT are emphasized here, as well as means for their degradation. Since sulfur compounds are often ignored in normal course work, this article provides a basic foundation for an understanding of these interesting and environmentally significant compounds.
Chasteen, Thomas G.; Bentley, Ronald. J. Chem. Educ. 2004, 81, 1524.
Atmospheric Chemistry |
Bioorganic Chemistry |
Gases |
Oxidation / Reduction
Functional Group Wordsearch  Terry L. Helser
This puzzle contains 24 names and terms from organic chemistry in a 12 ? 12 letter matrix. A descriptive narrative with underlined spaces to be filled gives clues to the terms students need to find.
Helser, Terry L. J. Chem. Educ. 2004, 81, 517.
Nomenclature / Units / Symbols |
Enrichment / Review Materials
Learning the Functional Groups: Keys to Success  Shannon Byrd and David P. Hildreth
Classification activity and scheme for learning functional groups.
Byrd, Shannon; Hildreth, David P. J. Chem. Educ. 2001, 78, 1355.
Nomenclature / Units / Symbols
Kinetics of Papain: An Introductory Biochemistry Laboratory Experiment  Kathleen Cornely, Eric Crespo, Michael Earley, Rachel Kloter, Aime Levesque, and Mary Pickering
In this experiment, we investigate the kinetics of the thiol protease papain. A specific substrate, Na-benzoyl-arginine-p-nitroanilide (BAPNA), is used, which takes advantage of the fact that papain interacts with a phenylalanine residue two amino acids away from the peptide bond cleaved. Upon hydrolysis by papain, a bright yellow product is released, p-nitroaniline. This allows the reaction to be monitored spectrophotometrically by measuring the rate of formation of the p-nitroaniline product as a function of the increase in absorbance of the solution at the lmax of p-nitroaniline (400 nm) over time at various substrate concentrations. These data are used to plot a Lineweaver-Burk plot from which the vmax and KM are obtained.
Cornely, Kathleen; Crespo, Eric; Earley, Michael; Kloter, Rachel; Levesque, Aime; Pickering, Mary. J. Chem. Educ. 1999, 76, 644.
Enzymes |
Kinetics |
UV-Vis Spectroscopy
Kinetics of the reaction of p-nitrobenzyl chloride with cyanide ion: An undergraduate organic chemistry experiment  Hurst, Michael O.; Hill, John W.
The title reaction is used to develop an undergraduate organic kinetics experiment in which the student determines the order and rate constant of the reaction, as well as the effect of solvent upon the rate of the reaction.
Hurst, Michael O.; Hill, John W. J. Chem. Educ. 1993, 70, 429.
Reactions |
Rate Law |
Kinetics |
Aromatic Compounds |
Alcohols |
Solutions / Solvents |
Organosulfur Compounds
Basic organic nomenclature  Breneman, G. L.
A series of three computer programs have been developed in the Basic Language to give students practice in naming branched alkanes, compounds with various functional groups, and benzene derivatives.
Breneman, G. L. J. Chem. Educ. 1978, 55, 224.
Nomenclature / Units / Symbols
Synthesis of a photochromic benzothiazolinic spiropyran  Guglielmetti, R.; Meyer, R.; Dupuy, C.
The purpose of this type of experiment is to elucidate structure of the different compounds gradually prepared starting from reaction mechanisms and chiefly from spectroscopic data given perviously to students.
Guglielmetti, R.; Meyer, R.; Dupuy, C. J. Chem. Educ. 1973, 50, 413.
Photochemistry |
Synthesis |
Mechanisms of Reactions |
Molecular Properties / Structure
Polymer synthesis in the undergraduate organic laboratory  Sorenson, Wayne R.
Presents a series of experiments on polymer synthesis for the undergraduate organic laboratory.
Sorenson, Wayne R. J. Chem. Educ. 1965, 42, 8.
Synthesis |
Polymerization |
Reactions |
Mechanisms of Reactions