Search Results - "PRESTON, Z"

Thermodynamic Trends for Reduction of CO by Molecular Complexes by Wiedner, Eric S, Preston, Andrew Z, Helm, Monte L, Appel, Aaron M

“…Selective reduction of CO2 into fuels and chemical feedstocks is highly desirable to reduce our dependence on fossil fuels. Most molecular catalysts afford 2e–…”
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Enhanced Hydrogenation of Carbon Dioxide to Methanol by a Ruthenium Complex with a Charged Outer-Coordination Sphere by Erickson, Jeremy D, Preston, Andrew Z, Linehan, John C, Wiedner, Eric S

“…We report the hydrogenation of CO2 to MeOH by a Ru­(triphos) catalyst containing a cationic tetraalkylammonium moiety in the outer coordination sphere. This…”
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Highly Regioselective α‑Olefin Dimerization Using Zirconium and Hafnium Amine Bis(phenolate) Complexes by Gunasekara, Thilina, Preston, Andrew Z, Zeng, Manhao, Abu-Omar, Mahdi M

“…Five new structural analogues of a previously studied group IV amine bis­(phenolate) catalyst, Zr­(ONNEt2O)­Bn2, have been synthesized and tested for…”
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Steric and Solvation Effects on Polymerization Kinetics, Dormancy, and Tacticity of Zr-Salan Catalysts by Preston, Andrew Z, Kim, Jungsuk, Medvedev, Grigori A, Delgass, W. Nicholas, Caruthers, James M, Abu-Omar, Mahdi M

“…1-Hexene polymerization using four zirconium-based amine bis­(phenolate) catalysts, Zr­[2-R-4-tBu-ONNO]­Bn2 (where R = methyl (1), ethyl (2), isopropyl (3),…”
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Tachykinins increase [ 3H]acetylcholine release in mouse striatum through multiple receptor subtypes by Preston, Z., Lee, K., Widdowson, L., Richardson, P.J., Pinnock, R.D.

“…Tachykinins have been suggested to play a significant role in the mammalian striatum, at least in part by the control of acetylcholine release from cholinergic…”
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Temperature-sensitive suppressor mutations of the Escherichia coli DNA gyrase B protein by BLANCE, STEPHEN J., WILLIAMS, NICOLA L., PRESTON, ZOË A., BISHARA, JOHN, SMYTH, MICHAEL S., MAXWELL, ANTHONY

“…Escherichia coli strain LE316 contains a mutation in gyrB that results in the substitution of Val164 to Gly and confers both chlorobiocin resistance and…”
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Synthesis and structure of some group VII 1,2-diacyl cyclopentadiene complexes and their pyridazine derivatives by Tice, Nathan C., Snyder, Chad A., Preston, Andrew Z., Wieliczko, Marika B., Young, Jason O. E., Hinson, Daniel F.

“…A series of 1,2-diacyl cyclopentadienyl tricarbonyl manganese and rhenium complexes, [M(CO) 3 {η 5 -1,2-C 5 H 3 (CO-(R) 2 }] ( 3a – c and 4a – b ), were…”
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Synthesis, Characterization, and Structure of Some New Substituted 5,6-Fused Ring Pyridazines by Snyder, Chad A., Tice, Nathan C., Sriramula, Phenahas G., Neathery, James L., Mobley, Justin K., Phillips, Chad L., Preston, Andrew Z., Strain, Jacob M., Vanover, Eric S., Starling, Michael P., Sahi, Nilesh V.

“…Pyridazines are an important class of heterocyclic compounds as a result of their materials and commercial applications. The synthesis of 5,6-fused ring…”
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Tachykinins increase [3H]acetylcholine release in mouse striatum through multiple receptor subtypes by PRESTON, Z, LEE, K, WIDDOWSON, L, RICHARDSON, P. J, PINNOCK, R. D

“…Tachykinins have been suggested to play a significant role in the mammalian striatum, at least in part by the control of acetylcholine release from cholinergic…”
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Adenosine receptor expression and function in rat striatal cholinergic interneurons by Preston, Zoe, Lee, Kevin, Widdowson, Leon, Freeman, Tom C, Dixon, Alistair K, Richardson, Peter J

“…Cholinergic neurons were identified in rat striatal slices by their size, membrane properties, sensitivity to the NK1 receptor agonist (Sar9, Met(O2)11)…”
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Structure-activity Relationships in Olefin Polymerization by Group (IV) Catalysts by Preston, Andrew Z

“…The study of olefin polymerization by homogeneous transition metal catalysts continues to be a field of considerable interest. Much of the success of these…”
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NK-3 receptors are expressed on mouse striatal γ-aminobutyric acid-ergic interneurones and evoke [ 3H] γ-aminobutyric acid release by Preston, Zoe, Richardson, Peter J, Pinnock, Robert D, Lee, Kevin

“…In the present study the ability of tachykinin agonists and antagonists to modulate γ-aminobutyric acid (GABA) release has been correlated with tachykinin…”
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