Physical Sciences and Mathematics Commons^™

Hall And Wolynes Reply [Reply To Comment On ‘‘Microscopic Theory Of Network Glasses’’], Randall W. Hall, Peter G. Wolynes

Randall W. Hall

Targeting The Transcriptional Machinery With Unique Artificial Transcriptional Activators, Brian Brennan, Zhiqian Wu, Garrette Belanger, Jenifer Lum, Aaron Minter, Steven Rowe, Annette Plachetka, Chinmay Majmudar, Anna Mapp

Brian B. Brennan

The link between a growing number of human diseases and misregulation of gene expression has spurred intense interest in artificial transcriptional activators that could be used to restore controlled expression of affected genes. To expand the repertoire of activation domains available for the construction of artificial transcriptional regulators, a selection strategy was used to identify two unique activation domain motifs. These activation domains bear little sequence homology to endogenous counterparts and bind to unique sites within the transcriptional machinery. A comparison with two well-characterized activation domains, VP2 and P201, demonstrated for the first time that functional potency is not solely …

Reductivedesorption Of 11-Mercaptoundecanoic Acid Monolayers Modified By Covalent Attachment Of 1,3- And 1,4-Phenylenediamine, Mark Anderson, Richard Baltzersen

Mark R. Anderson

1,3- and 1,4-phenylenediamine were covalently attached to a self-assembled monolayer of 11-mercaptoundecanoic acid by formation of an amide bond. Bonding of the phenylenediamine isomers was confirmed by the presence of infrared features attributable to ring vibrational modes, the amide I vibration, and the amide II vibration in the reflection–absorption infrared spectrum of the modified interface. Reductivedesorption peak potentials were shifted by 120 mV for the monolayer modified by 1,4-phenylenediamine and by 90 mV for the monolayer modified by 1,3-phenylenediamine relative to the desorption potential of the unmodified 11-mercaptoundecanoic acid monolayer. These potential shifts represent 23 and 17 kJ/mol stabilization of …

A Solvent-Free Claisen Condensation Reaction For The Organic Laboratory, John Esteb, Matthew Stockton

John Esteb

An experiment involving the Claisen condensation reaction for a first-year organic chemistry laboratory is presented. Claisen condensations are routinely covered in organic textbooks but owing to the long reaction times required to reach equilibrium in solution they are seldom explored in the undergraduate teaching laboratory. In this experiment, potassium tert-butoxide and ethyl phenylacetate are heated to 100 °C for 30 minutes under solvent-free conditions to produce 2,4-diphenyl acetoacetate in 80% yield. The solvent-free nature of this procedure greatly reduces the quantity of waste generated by students relative to typical carbonyl condensation experiments.

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A Solvent-Free Oxidation Of Alcohols In An Organic Laboratory, John Esteb, Michael Schelle, Anne Wilson

John Esteb

An oxidation experiment for a first-year organic chemistry class is presented. This oxidation utilizes a solid mixture of CuSO4•5H2O and KMnO4 prepared by mortar and pestle. The oxidations take place under solvent-free conditions and near quantitative yields are obtained for the reactions. Thin-layer chromatography is used to monitor the progress of the reaction. This experiment provides for the simple oxidation of a secondary alcohol to a ketone using a relatively nontoxic oxidizing agent under solvent-free conditions.

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