Open Access. Powered by Scholars. Published by Universities.®
Articles 1 - 3 of 3
Full-Text Articles in Life Sciences
Special Issue: Intramolecular Hydrogen Bonding 2017, Steve Scheiner
Special Issue: Intramolecular Hydrogen Bonding 2017, Steve Scheiner
Chemistry and Biochemistry Faculty Publications
Even after more than a century of study [1–6], scrutiny, and detailed examination, the H-bond continues [7–12] to evoke a level of fascination that surpasses many other phenomena. Perhaps it is the ability of the simple H atom, with but a single electron, to act as a glue that maintains contact between much more complicated species. Or it might be its geometry, which prefers to hold the bridging proton on a direct line between the two heavy atoms. Not to be ignored are the spectral features of the H-bond: the large red shift of the stretching frequency of the covalent …
A Bipyridine-Ligated Zinc(Ii) Complex With Bridging Flavonolate Ligation: Synthesis, Characterization, And Visible-Light-Induced Co Release Reactivity, Shayne Sorenson, Marina Popova, Atta M. Arif, Lisa M. Berreau
A Bipyridine-Ligated Zinc(Ii) Complex With Bridging Flavonolate Ligation: Synthesis, Characterization, And Visible-Light-Induced Co Release Reactivity, Shayne Sorenson, Marina Popova, Atta M. Arif, Lisa M. Berreau
Chemistry and Biochemistry Faculty Publications
Metal-flavonolate compounds are of significant current interest as synthetic models for quercetinase enzymes and as bioactive compounds of importance to human health. Zinc-3-hydroxyflavonolate compounds, including those of quercetin, kampferol, and morin, generally exhibit bidentate coordination to a single ZnII center. The bipyridine-ligated zinc-flavonolate compound reported herein, namely bis(μ-4-oxo-2-phenyl-4H-chromen-3-olato)-κ3O3:O3,O4;κ3O3,O4:O3-bis[(2,2′-bipyridine-κ2N,N′)zinc(II)] bis(perchlorate), {[Zn2(C15H9O3)2(C10H8N2)2](ClO4)2}n, (1), provides an unusual example of bridging 3-hydroxyflavonolate ligation in a dinuclear metal complex. The symmetry-related ZnII centers of (1) exhibit a distorted octahedral geometry, with weak coordination of a perchlorate anion trans to the bridging deprotonated O atom of the flavonolate ligand. Variable-concentration conductivity measurements provide evidence that, when …
Unraveling The Interactions Of The Physiological Reductant Flavodoxin With The Different Conformations Of The Fe Protein In The Nitrogenase Cycle, Natasha Pence, Monika Tokmina-Lukaszewska, Zhi-Yong Yang, Rhesa N. Ledbetter, Lance C. Seefeldt, Brian Bothner, John W. Peters
Unraveling The Interactions Of The Physiological Reductant Flavodoxin With The Different Conformations Of The Fe Protein In The Nitrogenase Cycle, Natasha Pence, Monika Tokmina-Lukaszewska, Zhi-Yong Yang, Rhesa N. Ledbetter, Lance C. Seefeldt, Brian Bothner, John W. Peters
Chemistry and Biochemistry Faculty Publications
Nitrogenase reduces dinitrogen (N2) to ammonia in biological nitrogen fixation. The nitrogenase Fe protein cycle involves a transient association between the reduced, MgATP-bound Fe protein and the MoFe protein and includes electron transfer, ATP hydrolysis, release of Pi, and dissociation of the oxidized, MgADP-bound Fe protein from the MoFe protein. The cycle is completed by reduction of oxidized Fe protein and nucleotide exchange. Recently, a kinetic study of the nitrogenase Fe protein cycle involving the physiological reductant flavodoxin reported a major revision of the rate-limiting step from MoFe protein and Fe protein dissociation to release of Pi. Because the Fe …