个人简介

Education BSc, Pacific Lutheran University, 1986 PhD, University of California at Berkeley, 1991 Professional Experience Associate Professor, University of Missouri-Columbia, 2000-present Research Investigator, Missouri University Research Reactor, 1996- Assistant Professor, University of Missouri-Columbia, 1995-2000 Postdoctoral Fellow, Pennsylvania State University, 1993-1995 Postdoctoral Fellow, University of Texas at Austin, 1992-1993 Honors and Awards 2000 Alpha Phi Sorority Professor of the Year 1999 Provost's Outstanding Junior Faculty Teaching Award. 1998 National Science Foundation Career Award 1991 Lawrence Berkeley Laboratory Technology Transfer Award 1989 Raychem Corporation Graduate Student Fellowship

研究领域

Inorganic, Solid-State, Materials, Supramolecular

The thread running through all of my research projects is the combination of molecular species with extended solids to create new, fundamentally interesting, and technologically useful materials. Historically, high temperature ceramic processing methods have been employed in the synthesis of solid-state materials. Under such extreme conditions it is often difficult (or impossible) to isolate anything but the thermodynamically favored product. By using "pre-formed" molecular species in concert with lower reaction temperatures, more rationally designed materials can be prepared, often with desired physical properties. Geomimetic Coordination Polymers: figure 1 Rational design of extended solids often cannot be realized under traditional, "heat-and-beat" solid-solid reaction conditions. By connecting soluble, transition-metal building blocks with ligands having specific geometry, we are preparing extended solid-state metal-organic framework structures that are topologically similar to silicate minerals such as quartz and/or zeolites. Our strategy is akin to "tinker toy" chemistry on a molecular level. Chemists have developed a very accurate understanding of the molecular structure, just as one can see how many sticks are attached to one wooden tinker-toy spool and in which directions they point, and synthetic chemists are wonderfully adept and clever at making incredibly complex molecules. But given ten billion spools and sticks (or molecules), predicting the spatial arrangement is not trivial, and preliminary results suggest that non-covalent interactions (hydrogen bonding, anion-framework interactions p-p stacking) can often be responsible for determining the final structure, and hence their physical properites. In addition, we are targeting the construction of scaffold-like materials that will contain cavities capable of absorbing specific guest molecules or ions (like a molecular sponge) that may find important uses in environmental remediation or remote chemical sensing, as the tunnel structure shown in Figure 1. Here Cu(I) cations (red) are linked into a three-dimensional acentric array via coordination to four bridging pyrimidine ligands. In another project we are investigating the behavior of small, magnetic oxide particles. The magnetic properties of such materials are very different than their bulk counterparts, and the differences influence greatly the performance of magneto-optical recording devices. Specifically, we seek to control the size distribution and orientation of the particles by synthesizing them within inorganic matrices. Two-dimensional layered hosts might be expected to produce pancake-like particles, whose spacing can be controlled by controlling the reaction conditions. In addition, we hope to prepare ultra-small magnetic oxide particles within the cages of zeolites similar to the semiconductor clusters of Ozin and co-workers. Instead of electronic coupling between cages, we hope to induce magnetic coupling, and with it, create new types of magnetic three dimensional "supralattices" (see figure). The neutron diffraction capabilities at the Missouri University Research Reactor (MURR) will be invaluable in the determination of the structure and magnetic ordering in these systems.

近期论文

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Chad Inman, Jacqueline M. Knaust, and Steven W. Keller, "A Polyoxometallate-Templated Cu(I) Coordination Polymer: Synthesis and Crystal Structure of Cu3(4,4'-bipyridine)]PW12O40", Chemical Communications, 2002, 156. Jacqueline M. Knaust, Susan Lopez and Steven W. Keller* (invited), "Dimensional Control over bis-1,2-(4-pyridyl)ethylene Cu(I) Coordination Networks", Inorganica Chimica Acta, 2001, 324, 81. S. Lopez and S. W. Keller Subtle Changes, Profound Effects: Synthesis and Crystal Structures of Helical Copper(I):4,7-Phenanthroline Coordination Polymers Cryst. Eng. 1999, 2, 101-114. S. W. Keller, S. Lopez A Two-Dimensional Coordination Polymer Containing Pentagonal Cavities J. Am. Chem. Soc. 1999, 126, 6303-6304. S. Lopez and S. W. Keller Novel One-Dimensional Coordination Polymers Based on Cu(I) and 4,7-Phenanthroline: Structural Dependence on Solvent and Counteranion Inorg. Chem. 1999, 38, 1883. S. Lopez, I. Muravyov, S. R. Pulley and S. W. Keller The (-)-Sparteine Copper(II) Chloride Isomer Acta. Cryst. 1998, C54, 355. S. Lopez and S. W. Keller, Synthesis and Crystal Structure of [Cu4(3-aminopyridine)8(?3-OH)4]4BF4.2MeCN: a Novel Copper(II) Cubane Supramol. Chem. 1998, 9, 239-244. S. W. Keller, An Acentric, Three-Dimensional Coordination Polymer: [Cu(pyrimidine)2]BF4 Angew. Chem. Int Ed. Eng. 1997, 36, 247.