Department of Chemistry

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Browsing Department of Chemistry by Subject "03 Chemical Sciences"

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    Conformational Analysis of Fluoro-, Chloro-, and Proteo-Alkene Gly-Pro and Pro-Pro Isosteres to Mimic Collagen
    Arcoria, Paul J.; Ware, Rachel I.; Makwana, Sunny V.; Troya, Diego; Etzkorn, Felicia A. (American Chemical Society, 2021-12-30)
    Collagen is the most abundant human protein, with the canonical sequence (Gly-Pro-Hyp)n in its triple helix region. Cis-trans isomerization of the Xaa-Pro amide has made two of these amide bonds the target of alkene replacement: the Gly-Pro and the Pro-Hyp positions. The conformations of Gly-Pro and Pro-Pro (as a Pro-Hyp model) fluoro-, chloro-, and proteo-alkene mimic models were investigated computationally to determine whether these alkenes can stabilize the polyproline type II (PPII) conformation of collagen. Second-order Møller-Plesset (MP2) calculations with various basis sets were used to perform the conformational analyses and locate stationary points. The calculation results predict that fluoro- and chloro-alkene mimics of Gly-Pro and Pro-Pro can participate in n→π* donation to stabilize PPII conformations, yet they are poor n→π* acceptors, shifting the global minima away from PPII conformations. For the proteo-alkene mimics, the lack of significant n→π* interactions and unstable PPII-like geometries explains their known destabilization of the triple helix in collagen-like peptides.
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    Design Strategies for Enhanced Conductivity in Metal-Organic Frameworks
    Johnson, Eric M.; Ilic, Stefan; Morris, Amanda J. (American Chemical Society, 2021-03-24)
    Metal-organic frameworks (MOFs) are a class of materials which exhibit permanent porosity, high surface area, and crystallinity. As a highly tunable middle ground between heterogeneous and homogeneous species, MOFs have the potential to suit a wide variety of applications, many of which require conductive materials. The continued development of conductive MOFs has provided an ever-growing library of materials with both intrinsic and guest-promoted conductivity, and factors which limit or enhance conductivity in MOFs have become more apparent. In this Outlook, the factors which are believed to influence the future of MOF conductivity most heavily are highlighted along with proposed methods of further developing these fields. Fundamental studies derived from these methods may provide pathways to raise conductivity across a wide range of MOF structures.
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    Emission Spectroscopy as a Probe into Photoinduced Intramolecular Electron Transfer in Polyazine Bridged Ru(II),Rh(III) Supramolecular Complexes
    White, Travis A.; Arachchige, Shamindri M.; Sedai, Baburam; Brewer, Karen J. (MDPI, 2010-08-01)
    Steady-state and time-resolved emission spectroscopy are valuable tools to probe photochemical processes of metal-ligand, coordination complexes. Ru(II) polyazine light absorbers are efficient light harvesters absorbing in the UV and visible with emissive MLCT excited states known to undergo excited state energy and electron transfer. Changes in emission intensity, energy or band-shape, as well as excited state lifetime, provide insight into excited state dynamics. Photophysical processes such as intramolecular electron transfer between electron donor and electron acceptor sub-units may be investigated using these methods. This review investigates the use of steady-state and timeresolved emission spectroscopy to measure excited state intramolecular electron transfer in polyazine bridged Ru(II),Rh(III) supramolecular complexes. Intramolecular electron transfer in these systems provides for conversion of the emissive MLCT (metal-to-ligand charge transfer) excited state to a non-emissive, but potentially photoreactive, MMCT (metal-to-metal charge transfer) excited state. The details of the photophysics of Ru(II),Rh(III) and Ru(II),Rh(III),Ru(II) systems as probed by steady-state and timeresolved emission spectroscopy will be highlighted. © 2010 by the authors. 3 3 3