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Articles 1 - 7 of 7
Full-Text Articles in Physical Sciences and Mathematics
Odd-Even Effects In Charge Transport Across N-Alkanethiolate-Based Sams, Mostafa Baghbanzadeh, Felice C. Simeone, Carleen M. Bowers, Kung Ching Liao, Martin Thuo, Mahdi Baghbanzadeh, Michael S. Miller, Tricia Breen Carmichael, George M. Whitesides
Odd-Even Effects In Charge Transport Across N-Alkanethiolate-Based Sams, Mostafa Baghbanzadeh, Felice C. Simeone, Carleen M. Bowers, Kung Ching Liao, Martin Thuo, Mahdi Baghbanzadeh, Michael S. Miller, Tricia Breen Carmichael, George M. Whitesides
Chemistry and Biochemistry Publications
This paper compares rates of charge transport across self-assembled monolayers (SAMs) of n-alkanethiolates having odd and even numbers of carbon atoms (nodd and neven) using junctions with the structure MTS/SAM//Ga2O3/EGaIn (M = Au or Ag). Measurements of current density, J(V), across SAMs of n-alkanethiolates on AuTS and AgTS demonstrated a statistically significant odd-even effect on AuTS, but not on AgTS, that could be detected using this technique. Statistical analysis showed the values of tunneling current density across SAMs of n-alkanethiolates on AuTS with nodd and neven belonging to two separate sets, and while there is a significant difference between the …
Ultrasmooth Gold Surfaces Prepared By Chemical Mechanical Polishing For Applications In Nanoscience, Michael S. Miller, Michael Anthony Ferrato, Adrian Niec, Mark C. Biesinger, Tricia Breen Carmichael
Ultrasmooth Gold Surfaces Prepared By Chemical Mechanical Polishing For Applications In Nanoscience, Michael S. Miller, Michael Anthony Ferrato, Adrian Niec, Mark C. Biesinger, Tricia Breen Carmichael
Chemistry and Biochemistry Publications
For over 20 years, template stripping has been the best method for preparing ultrasmooth metal surfaces for studies of nanostructures. However, the organic adhesives used in the template stripping method are incompatible with many solvents, limiting the conditions that may subsequently be used to prepare samples; in addition, the film areas that can be reliably prepared are typically limited to ∼1 cm2. In this article, we present chemical-mechanical polishing (CMP) as an adhesive-free, scalable method of preparing ultrasmooth gold surfaces. In this process, a gold film is first deposited by e-beam evaporation onto a 76-mm-diameter silicon wafer. The CMP process …
Activated Cyclopropanes: A Remarkable Breadth Of Recent Chemistry, James R. Green, Victor Snieckus
Activated Cyclopropanes: A Remarkable Breadth Of Recent Chemistry, James R. Green, Victor Snieckus
Chemistry and Biochemistry Publications
The reactions of cyclopropanes activated by electron-withdrawing groups and electron-donating groups – donor–acceptor (DA) cyclopropanes – and with alkenyl or alkylidene substituents has been an area of recent intense research activity. This Cluster contains contributions from many of the leading research groups in this area, and provides a concise introduction to the rich ring-opening, ring-expansion, dimerization, and cycloaddition chemistry of these compounds.
Synthesis Of Tenuifolin Via Intramolecular Nicholas Reaction, Sinisa Djurdjevic, James R. Green
Synthesis Of Tenuifolin Via Intramolecular Nicholas Reaction, Sinisa Djurdjevic, James R. Green
Chemistry and Biochemistry Publications
The synthesis of the Cinnamomum homosesquiterpenoid tenuifolin has been accomplished by way of an intramolecular Nicholas reaction of the [Co2(CO)6] complex of an alkyne-substituted biaryl for construction of the seven-membered ring. The cyclization features the reaction of a nonactivated arene ring with the propargyldicobalt cation to give the dibenzocycloheptyne-Co2(CO)6.
The Potential Of Quinoline Derivatives For The Treatment Of Toxoplasma Gondii Infection., Sirinart Ananvoranich
The Potential Of Quinoline Derivatives For The Treatment Of Toxoplasma Gondii Infection., Sirinart Ananvoranich
Chemistry and Biochemistry Publications
Here we reported our investigation, as part of our drug repositioning effort, on anti-Toxoplasma properties of newly synthesized quinoline compounds. A collection of 4-aminoquinoline and 4-piperazinylquinoline analogs have recently been synthesized for use in cancer chemotherapy. Some analogs were able to outperform chloroquine, a quinoline derivative drug which is commonly used in the treatment of malaria and other parasitic infections. Herein 58 compounds containing one or two quinoline rings were examined for their effectiveness as potential anti-Toxoplasma compounds. Of these 58 compounds, 32 were efficient at inhibiting Toxoplasma growth (IC50μM). Five compounds with single and simple quinoline rings exhibited similar …
A Multi-Scale Computational Study On The Mechanism Of Streptococcus Pneumoniae Nicotinamidase (Spnic), Bogdan F. Ion, Erum Kazim, James Gauld
A Multi-Scale Computational Study On The Mechanism Of Streptococcus Pneumoniae Nicotinamidase (Spnic), Bogdan F. Ion, Erum Kazim, James Gauld
Chemistry and Biochemistry Publications
Nicotinamidase (Nic) is a key zinc-dependent enzyme in NAD metabolism that catalyzes the hydrolysis of nicotinamide to give nicotinic acid. A multi-scale computational approach has been used to investigate the catalytic mechanism, substrate binding and roles of active site residues of Nic from Streptococcus pneumoniae (SpNic). In particular, density functional theory (DFT), molecular dynamics (MD) and ONIOM quantum mechanics/molecular mechanics (QM/MM) methods have been employed. The overall mechanism occurs in two stages: (i) formation of a thioester enzyme-intermediate (IC2) and (ii) hydrolysis of the thioester bond to give the products. The polar protein environment has a significant effect in stabilizing …
Novel Analogue Of Colchicine Induces Selective Pro-Death Autophagy And Necrosis In Human Cancer Cells, Kristen Elizabeth Larocque, Pamela Ovadje, Sinisa Djurdjevic, Mariam Mehdi, James R. Green, Siyaram Pandey
Novel Analogue Of Colchicine Induces Selective Pro-Death Autophagy And Necrosis In Human Cancer Cells, Kristen Elizabeth Larocque, Pamela Ovadje, Sinisa Djurdjevic, Mariam Mehdi, James R. Green, Siyaram Pandey
Chemistry and Biochemistry Publications
Colchicine, a natural product of Colchicum autumnae currently used for gout treatment, is a tubulin targeting compound which inhibits microtubule formation by targeting fast dividing cells. This tubulin-targeting property has lead researchers to investigate the potential of colchicine and analogs as possible cancer therapies. One major study conducted on an analogue of allocolchicine, ZD 6126, was halted in phase 2 clinical trials due to severe cardio-toxicity associated with treatment. This study involves the development and testing of novel allocolchicine analogues that hold non-toxic anti-cancer properties. Currently we have synthesized and evaluated the anti-cancer activities of two analogues; N-acetyl-O-methylcolchinol (NSC 51046 …