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We have recently developed new classes of compounds based on 2-pyrazolylaniline (pzAn) derivatives that can act as fluorescent sensors for a variety of Lewis acids. Some advantages that these new compounds enjoy over their competition are simple, high yield (nearly quantitative) syntheses, the ability to tune the wavelength of fluorescence by very simple modifications of the ligand backbone, and a selective fluorescence response depending on the nature of the Lewis acid. The fluorescence tunability is exemplified by the picture on the right, which shows a series of diphenylboron complexes of different pzAn derivatives irradiated with 354 nm UV light. The ultimate goals of this research project include using these derivatives as sensitizers for enhancing lanthanide-based emissions, using these fluorescent dyes as biological markers for studies in drug metabolism studies, and incorporating these fluorophores onto semiconductor surfaces to serve as light harvesting antenna in solar cell applications.

Designing components for future use in molecular electronics is another area of interest to our research group. Towards this end, we are investigating the preparation, electrochemistry, and self-assembly capabilities of metal chain compounds, pi-stacked N-heterocycles, and/or combinations thereof as model wire systems. The ultimate goal of this research is to firmly establish the geometric limits and possible metal/heterocycle substitution patterns necessary for efficient intramolecular charge propagation. A primary challenge in this research is to expand the currently known ligand systems that can be used to form metal chain compounds, where neighboring metals are disposed within van der Waals contact. Specifically, it would be desirable to examine discrete systems with increasing number of interacting electroactive centers in order to establish possible trends in the electrochemical or even spectroscopic data. On paper, this would seem to be a simple order to fulfill, however, when dealing with multinucleating ligands one always has to be concerned about the possibility for supramolecular isomerism. This is exemplified in the simplest case scenario in the silver coordination chemistry of some of our dipyrazolyl-based systems in Figure 1. Our group actively investigates the factors that will lead to the preferential formation of supramolecular isomers in these and more complex derivatives. We also examine the differences in the electrochemical and spectroscopic behaviors of each type of supramolecular isomer to gain knowledge in to how to design better systems. Another set of potential wires we look at are based on Jekyll-and-Hyde scorpionates exemplified by the alkali metal salt shown in Figure 2. With these electroactive dipolar ligands, charge can propagate via the pi system of the ligands. We construct one-dimensional chains based on Pearson鈥檚 Hard soft acid-base theory and examine their electrochemical and spectroscopic properties, to evaluate their potential in future wire systems.

Transition metal complexes with d4-d7 electron configurations have the capability of exhibiting two spin states (high spin or low spin) depending on the strength of the ligand field. Strong field ligands tend to favor electron pairing, giving low spin complexes while weak field ligands give rise to high spin complexes with the maximum number of unpaired electrons. Spin crossover (SCO) compounds are special cases where the transition metal complexes have ligands or ligand combinations of intermediate field strength. In such cases, the high or low spin states are in equilibrium and it is possible to access either the high or low spin state depending on external perturbations such as light, heat, or pressure. The change in spin state is accompanied by changes in magnetic moment, color and molecular geometry. The picture to the right shows an example of the thermochromic behavior of an iron(II) SCO compound on warming from 90K to 273K (left to right); it is easy to see why researchers have been fascinated by this sort of compound since their discovery in the 1960鈥檚. The reversible change in magnetic moment and color upon heating, on application of pressure, or upon laser stimulation, holds promise for the use of such materials in different sensing applications. In order to realize such applications several issues need to be addressed, which are the focal points of our and of other鈥檚 research interest around the world. First, can we learn to control the spin crossover behavior (temperature/pressure range) for custom designing future thermochromic or pressure-sensing materials? Secondly, how can we make these SCO materials robust enough for practical sensing applications? Often, but not always, the SCO compounds are susceptible to crystal fracture (via desolvation or stress) which can subsequently change the SCO properties of the material. An example of such a decomposition is shown on the right for a different iron(II) SCO compound going through one heating and cooling cycle; we can show that the magnetic properties of the virgin material are different than the aged sample in many cases- this is clearly not very desirable for incorporation into a reliable device. One example of a strategy we have used is to make robust and potentially useful SCO materials is to incorporate them into polymer matrices, as in Figure 3.

Figure 3