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Journal articles on the topic 'Ground state redox potential'

Author: Grafiati

Published: 10 March 2023

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1

Mohammadpourasl, Sanaz, Fabrizia Fabrizi de Biani, Carmen Coppola та ін. "Ground-State Redox Potentials Calculations of D-π-A and D-A-π-A Organic Dyes for DSSC and Visible-Light-Driven Hydrogen Production". Energies 13, № 8 (2020): 2032. http://dx.doi.org/10.3390/en13082032.

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The prediction of ground-state redox potentials by quantum chemical methods has a prominent role in the rational design of novel organic photosensitizers both for dye-sensitized solar cells (DSSCs) and photocatalytic systems for the production of H2. Indeed, the ground-state redox potential of the photosensitizers is one of the key parameters to identify the most promising candidates for such applications. Here, the ground-state redox potentials of 16 organic donor-π-acceptor D-π-A and donor-acceptor-π-acceptor D-A-π-A dyes having a medium to large size of the conjugated scaffold are evaluated

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2

Kim, Dooyoung, and Thomas S. Teets. "Strategies for accessing photosensitizers with extreme redox potentials." Chemical Physics Reviews 3, no. 2 (2022): 021302. http://dx.doi.org/10.1063/5.0084554.

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Photoredox catalysis has been prominent in many applications, including solar fuels, organic synthesis, and polymer chemistry. Photocatalytic activity directly depends on the photophysical and electrochemical properties of photocatalysts in both the ground state and excited state. Controlling those properties, therefore, is imperative to achieve the desired photocatalytic activity. Redox potential is one important factor that impacts both the thermodynamic and kinetic aspects of key elementary steps in photoredox catalysis. In many challenging reactions in organic synthesis, high redox potenti

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3

Vlcek, A. A., Elaine S. Dodsworth, William J. Pietro, and A. B. P. Lever. "Excited State Redox Potentials of Ruthenium Diimine Complexes; Correlations with Ground State Redox Potentials and Ligand Parameters." Inorganic Chemistry 34, no. 7 (1995): 1906–13. http://dx.doi.org/10.1021/ic00111a043.

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4

Bednářová, Eva, Logan R. Beck, Tomislav Rovis, et al. "Tuning the Electrochemical and Photophysical Properties of Osmium-Based Photoredox Catalysts." Synlett 33, no. 03 (2022): 247–58. http://dx.doi.org/10.1055/s-0041-1737792.

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AbstractThe use of low-energy deep-red (DR) and near-infrared (NIR) light to excite chromophores enables catalysis to ensue across barriers such as materials and tissues. Herein, we report the detailed photophysical characterization of a library of OsII polypyridyl photosensitizers that absorb low-energy light. By tuning ligand scaffold and electron density, we access a range of synthetically useful excited state energies and redox potentials.1 Introduction1.1 Scope1.2 Measuring Ground-State Redox Potentials1.3 Measuring Photophysical Properties1.4 Synthesis of Osmium Complexes2 Properties of

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Medina, Edinson, and Balazs Pinter. "A DFT Study on the Redox Active Behavior of Carbene and Pyridine Ligands in the Oxidative and Reductive Quenching Cycles of Ruthenium Photoredox Catalysts." Catalysts 10, no. 1 (2020): 80. http://dx.doi.org/10.3390/catal10010080.

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In this study, a detailed look at the electronic structure changes induced by photon absorption and of the succeeding redox events of the oxidative and reductive quenching cycles of ruthenium–carbene and ruthenium–pyridine photoredox catalysts is provided through an arsenal of density functional theory-based techniques including electron density difference Δρ(r) maps, spin-density distributions, and the non-covalent interaction analysis. We introduced an efficient computational protocol to obtain accurate equilibrium structures and ground-state reduction potentials for these types of complexes

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Hammond, Timothy G., Patricia L. Allen, and Holly H. Birdsall. "Validation of Assays for Reactive Oxygen Species and Glutathione in Saccharomyces cerevisiae during Microgravity Simulation." Gravitational and Space Research 3, no. 2 (2015): 42–53. http://dx.doi.org/10.2478/gsr-2015-0010.

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ABSTRACT The effects of spaceflight on yeast have high concordance with agents that induce a very low intracellular redox state and induce a massive efflux of glutathione. These results raise important issues. Can the reduced redox state during spaceflight be reproduced and modulated in ground-based simulations? Will this allow definition of unique drug pathways as a low redox potential state mirrors the electrophilic properties of mitochondria where many drugs are metabolized? Unfortunately, assays for redox status and its major cellular determinant—glutathione—are diverse and often cell-type

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7

Bourotte, Christine, Reginaldo Bertolo, Marta Almodovar, and Ricardo Hirata. "Natural occurrence of hexavalent chromium in a sedimentary aquifer in Urânia, State of São Paulo, Brazil." Anais da Academia Brasileira de Ciências 81, no. 2 (2009): 227–42. http://dx.doi.org/10.1590/s0001-37652009000200009.

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Anomalous concentrations of hexavalent chromium have been detected in ground-water of the Adamantina Aquifer inat least 54 municipalities located in the northwestern region of the State of São Paulo, southeast Brazil, occasionallyexceeding the permitted limit for human consumption (0.05 mg.L-1). An investigation was conducted in the municipality of Urânia, where the highest concentrations of chromium were detected regionally. It was defined that the originof this contamination is natural, since high concentrations of chromium were detected in aquifer sandstones (averageof 221 ppm) and also in

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Creutz, Carol, and Mei H. Chou. "Solvent Dependence of the Reduction Potential of Ground- and Excited-State Redox Couples: trans- Dioxo(1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane)osmium(VI/V)." Inorganic Chemistry 33, no. 14 (1994): 3199–200. http://dx.doi.org/10.1021/ic00092a033.

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Bumpus, Peter B., and Sarah E. Kruse. "Self-potential monitoring for hydrologic investigations in urban covered-karst terrain." GEOPHYSICS 79, no. 6 (2014): B231—B242. http://dx.doi.org/10.1190/geo2013-0354.1.

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In the covered karst of west-central Florida, USA, sinkholes (sandy collapse conduits) provide locally concentrated recharge to underlying aquifers. For water management, it would be beneficial to understand the rates at which collapse conduits recharge an underlying aquifer. Self-potential (SP) monitoring has promise as a noninvasive, relatively low-cost method for assessing temporal variability in flow. Previous studies suggested that negative SP anomalies over collapse conduits correspond to downward-flowing groundwater; however, before SP surveys can be reliable indicators of conduit flow,

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10

Yang, Jing, John H. Enemark, and Martin L. Kirk. "Metal–Dithiolene Bonding Contributions to Pyranopterin Molybdenum Enzyme Reactivity." Inorganics 8, no. 3 (2020): 19. http://dx.doi.org/10.3390/inorganics8030019.

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Here we highlight past work on metal–dithiolene interactions and how the unique electronic structure of the metal–dithiolene unit contributes to both the oxidative and reductive half reactions in pyranopterin molybdenum and tungsten enzymes. The metallodithiolene electronic structures detailed here were interrogated using multiple ground and excited state spectroscopic probes on the enzymes and their small molecule analogs. The spectroscopic results have been interpreted in the context of bonding and spectroscopic calculations, and the pseudo-Jahn–Teller effect. The dithiolene is a unique liga

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Karipidis, Paraskevas, Athanassios C. Tsipis, and Constantinos A. Tsipis. "Density Functional Study of the Electronic Structure and Related Properties of Pt(NO)/Pt(NO2) Redox Couples." Collection of Czechoslovak Chemical Communications 68, no. 3 (2003): 423–46. http://dx.doi.org/10.1135/cccc20030423.

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Density functional calculations at the B3LYP level of theory, using the SDD basis set, provide satisfactory description of geometric, energetic, electronic and spectroscopic properties of the Pt(NO)/Pt(NO2) redox couple. The neutral Pt(NO) species adopts a bent 2A' ground state, while the cationic [Pt(NO)]+ species adopts a linear 1Σ+ ground state. The B3LYP/SDD- predicted Pt-N bond lengths are 2.016 and 1.777 Å for Pt(NO) (2A') and [Pt(NO)]+ (1Σ+), respectively, while the ∠Pt-N-O bent angle for [Pt(NO)] (2A') is 119.6°. On the other hand, the anionic [Pt(NO)]- species adopts the bent 1A' grou

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YANG, SUNG IK, JYOTI SETH, JON-PAUL STRACHAN, et al. "Ground and Excited State Electronic Properties of Halogenated Tetraarylporphyrins: Tuning the Building Blocks for Porphyrin-based Photonic Devices." Journal of Porphyrins and Phthalocyanines 03, no. 02 (1999): 117–47. http://dx.doi.org/10.1002/(sici)1099-1409(199902)3:2<117::aid-jpp110>3.0.co;2-x.

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The rational design of molecular photonic devices relies on the ability to select components with predictable electronic structure, excited state lifetimes and redox chemistry. Electronic communication in multiporphyrin arrays depends critically on the relative energies and electron density distributions of the frontier molecular orbitals, especially the energetically close highest occupied molecular orbitals (a2u and a1u). To explore how these ground and excited state properties can be modulated, we have synthesized and characterized 40 free base ( Fb ), magnesium and zinc tetraarylporphyrins

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Njogu, Rachael, Peter Fodran, Yuxi Tian, et al. "Electronically Divergent Triscyclometalated Iridium(III) 2-(1-naphthyl)pyridine Complexes and Their Application in Three-Component Methoxytrifluoromethylation of Styrene." Synlett 30, no. 07 (2019): 792–98. http://dx.doi.org/10.1055/s-0037-1611716.

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A systematic study of the photophysical and electrochemical properties of triscyclometalated homoleptic iridium(III) complexes based on 2-(1-naphthyl)pyridine (npy) ligands is presented. A systematic investigation of ligand substitution patterns showed an influence on the lifetime of the excited state, with slight changes in the absorption and emission spectral features. Specifically, the emission lifetime of a complex of an npy ligand substituted with a strongly electron-withdrawing trifluoromethyl group was longer than that of the corresponding complex with the electronically nonperturbed li

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Grover, Nitika, Pinki Rathi, and Muniappan Sankar. "Spectral investigations of meso-tetraalkylporphyrin-fullerene host–guest complexes." Journal of Porphyrins and Phthalocyanines 19, no. 09 (2015): 997–1006. http://dx.doi.org/10.1142/s1088424615500716.

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Meso-tetraalkylporphyrins and their Zn(II) complexes were synthesized and characterized by various spectroscopic techniques. Single crystal X-ray structure of meso-tetrapropylporphyrin (3) revealed the orientation of alkyl chains and planar conformation of porphyrin macrocycle. Spectroscopic, photophysical and electrochemical redox properties of self-assembled donor–acceptor dyads formed by meso-tetraalkylporphyrins and fullerene C 60 were investigated. These studies revealed 1:1 supramolecular dyad formation between the electron donor porphyrins and the electron acceptor, fullerene entities.

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Jaszczyński, Jacek. "The relationship between dissolved organic carbon and hydro-climatic factors in peat-muck soil." Journal of Water and Land Development 24, no. 1 (2015): 27–33. http://dx.doi.org/10.1515/jwld-2015-0004.

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Abstract The object of this study was the concentration of dissolved organic carbon (DOC) in soil solution related to groundwater table, soil temperature, moisture, redox potential and intensive storm rain and their changes during ten years (2001–2010). The studies were localized in drained and agriculturally used Kuwasy Mire situated in the middle basin of the Biebrza River, north-eastern Poland. The study site was situated on a low peat soil managed as intensively used grassland. The soil was recognized as peat-muck in the second stage of the mucking process. DOC concentration was determined

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16

Re, Viviana, Myat Mon Thin, Chiara Tringali, Mya Mya, Enrico Destefanis, and Elisa Sacchi. "Laying the Groundwork for Raising Awareness on Water Related Issues with a Socio-Hydrogeological Approach: The Inle Lake Case Study (Southern Shan State, Myanmar)." Water 13, no. 17 (2021): 2434. http://dx.doi.org/10.3390/w13172434.

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Translating scientific findings into concrete action for (ground)water protection should be fundamental component of any hydrogeological and hydrogeochemical assessment, thus ensuring that scientific outcomes have a positive impact in the real world. To this purpose, understanding the water-related issues and the perceived criticalities by the water users is an asset, especially for earth scientists who are often the first contact with local communities during in situ measurements. By presenting the results of a socio-hydrogeological assessment in the Inle Lake area, this paper aims at demonst

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17

Milanesio, M. Elisa, Miguel Gervaldo, Luis A. Otero, Leonides Sereno, Juana J. Silber, and Edgardo N. Durantini. "Synthesis of a diporphyrin dyad bearing electron-donor and electron-withdrawing substituents with potential use in the spectral sensitization of semiconductor solar cells." Journal of Porphyrins and Phthalocyanines 07, no. 01 (2003): 42–51. http://dx.doi.org/10.1142/s1088424603000070.

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A new dyad 9( ZnP - P ) has been synthesized linking 5,15-bis(4-carboxyphenyl)-10,20-bis(4-nitrophenyl) porphyrin 4( P ) and Zn(II) 5-(4-aminophenyl)-10,15,20-tris(4-methoxylphenyl) porphyrin 8 (ZnP) by an amide bond. The structural moieties of dyad 9( ZnP-P ) present both different singlet state energy and redox properties. Dyad 9 was designed to improve the intramolecular electron transfer capacity. The ZnP moiety bears electron-donating methoxy groups and a zinc ion, while the other porphyrin structure, P , is substituted by electron-withdrawing nitro groups. On the other hand, structure P

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18

Farah, Salim F., Robert A. McClelland, Michael R. Peterson, and Imre G. Csizmadia. "Molecular structure and relative proton and electron affinities of isomeric nitroimidazoles." Canadian Journal of Chemistry 67, no. 10 (1989): 1666–71. http://dx.doi.org/10.1139/v89-255.

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The isomeric 2-nitro, 4-nitro, and 5-nitroimidazoles have been studied in their planar ground state, C—NO2 rotational transition state, 3-H protonated conjugate acid and radical anion forms, with abinitio computations at the split-valence 3-21G basis set level. The stabilities of the parent compounds follow the order 5-NO2 ~ 4-NO2 > 2-NO2. In solution 4-nitro is more stable than 5-nitro; the calculations suggest that this is a solvation effect, since the 4-nitro isomer has a considerably higher dipole moment. Barriers for nitro group rotation range from 10 to 16 kcal/mol. However, the relat

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Oprea, Corneliu I., Petre Panait, Zahraa M. Essam, Reda M. Abd El-Aal, and Mihai A. Gîrțu. "Photoexcitation Processes in Oligomethine Cyanine Dyes for Dye-Sensitized Solar Cells—Synthesis and Computational Study." Nanomaterials 10, no. 4 (2020): 662. http://dx.doi.org/10.3390/nano10040662.

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We report density functional theory (DFT) calculations of three newly synthesized oligomethine cyanine-based dyes as potential TiO2-sensitizers in dye-sensitized solar cells. The three dyes have π-symmetry and the same acceptor side, terminating in the carboxylic anchor, but they differ through the π-bridge and the donor groups. We perform DFT and time-dependent DFT studies and present the electronic structure and optical properties of the dyes alone as well as adsorbed to the TiO2 nanocluster, to provide some predictions on the photovoltaic performance of the system. We analyze theoretically

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Yamada, Atsuo. "(Battery Division Research Award) Structure-Property Relationships: A Journey From LFP to Lithium Metal." ECS Meeting Abstracts MA2022-02, no. 3 (2022): 209. http://dx.doi.org/10.1149/ma2022-023209mtgabs.

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Conceptual importance of “Matastable Phase Diagram” and “Liquid Madelung Potential” will be demonstrated by picking up some of my mechanism-solving works on LFP and lithium metal. In Li x FePO4, the ground state phase separation and metastable solid solution are energetically competitive, and the solid solution phase is induced in a non-equilibrium electrochemical reaction, playing critical role for fast kinetics. However, there had been no discussion or experimental report of the crystal structure, optical and transport properties of the metastable solid solution phase due to the extreme tech

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21

Sakai, Hayato, Mohammad Gulam Rabbani, and Taku Hasobe. "Porphyrin hexamer with a triphenylene core unit: Spectroscopy, electrochemistry and controllable supramolecular formation." Journal of Porphyrins and Phthalocyanines 15, no. 07n08 (2011): 639–51. http://dx.doi.org/10.1142/s1088424611003574.

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A series of free-base and zinc porphyrin hexamers, where six porphyrin units are linked to a triphenylene core through amide or ester linkage, was designed and synthesized in an effort to study their spectroscopic and electrochemical properties, and aggregate formation. The distances between triphenylene core and porphyrin moieties are tuned by changing the lengths of spacer alkyl chains. The absorption spectral studies indicates that the porphyrin units in a hexamer behave like monomeric porphyrins, while a strong fluorescence quenching of triphenylene core was observed suggesting the deactiv

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22

Islam, Ashraful, Surya Prakash Singh та Liyuan Han. "Synthesis and Application of New Ruthenium Complexes Containingβ-Diketonato Ligands as Sensitizers for Nanocrystalline TiO2Solar Cells". International Journal of Photoenergy 2011 (2011): 1–8. http://dx.doi.org/10.1155/2011/204639.

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Five heteroleptic ruthenium complexes having differentβ-diketonato ligands, [Ru(tctpy)(dppd)(NCS)] (1), [Ru(tctpy)(pd)(NCS)] (2), [Ru(tctpy)(tdd)(NCS)] (3), [Ru(tctpy)(mepd)(NCS)] (4), and [Ru(tctpy)(tmhd)(NCS)] (5), where tctpy = 4,4′,4′′-tricarboxy-2,2′:6′,2′′-terpyridine, pd = pentane-2,4-dione, mepd = 3-methylpentane-2,4-dione, tmhd = 2,2,6,6-tetramethylheptane-3,5-dione, tdd = tridecane-6,8-dione, and dppd = 1,3-diphenylpropane-1,3-dione, were synthesized and characterized. These heteroleptic complexes exhibit a broad metal-to-ligand charge transfer absorption band over the whole visible

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23

Cantu, Robert, Habtom B. Gobeze, and Francis D’Souza. "Synthesis and photochemical studies of a tris(4-iodophenoxy) subphthalocyaninato boron(III)-fulleropyrrolidine dyad." Journal of Porphyrins and Phthalocyanines 20, no. 08n11 (2016): 987–96. http://dx.doi.org/10.1142/s1088424615500947.

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A subphthalocyanine-fullerene dyad, 1 was newly synthesized through axial functionalization via central boron of subphthalocyanine with [Formula: see text]-hydroxybenzaldehyde, and subsequent dipolar cycloaddition reaction of fullerene. The subphthalocyanine entity was peripherally functionalized with moderately electron rich 4-iodophenoxy substituents to probe their effect on photoinduced processes within the SubPc-C[Formula: see text] dyad. Optical absorbance studies revealed presence of both entities of the dyad while steady-state fluorescence studies revealed quenching of subphthalocyanine

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Rooks, Christine, James Kar-Hei Fang, Pål Tore Mørkved, et al. "Deep-sea sponge grounds as nutrient sinks: denitrification is common in boreo-Arctic sponges." Biogeosciences 17, no. 5 (2020): 1231–45. http://dx.doi.org/10.5194/bg-17-1231-2020.

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Abstract. Sponges are commonly known as general nutrient providers for the marine ecosystem, recycling organic matter into various forms of bioavailable nutrients such as ammonium and nitrate. In this study we challenge this view. We show that nutrient removal through microbial denitrification is a common feature in six cold-water sponge species from boreal and Arctic sponge grounds. Denitrification rates were quantified by incubating sponge tissue sections with 15NO3--amended oxygen-saturated seawater, mimicking conditions in pumping sponges, and de-oxygenated seawater, mimicking non-pumping

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Melnychuk, S. S., and G. G. Trokhymenko. "Peculiarities of migration and accumulation of heavy metals in the system «ground-plant» by the example of the National natural park «Beloberezhye Svyatoslava»." Ecology and Noospherology 28, no. 3-4 (2017): 45–54. http://dx.doi.org/10.15421/031715.

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Heavy metals like ekopolyudanty have a high capacity for bioaccumulation, toxicity and significant mobility in the environment. Since the bulk of the land is plants, it is important to identify the processes of migration and accumulation of heavy metals in them. But keep in mind that the level of heavy metal accumulation in plants of different taxonomic groups are not the same. Cumulative capacity of plants depends on many factors: the type of soil, humidity, altitude, meteorological characteristics of the region and landscape, and more. It should be noted that the migration of heavy metals fr

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Zagal, Jose H., Federico Tasca, and Ingrid Ponce. "(Keynote) Interpretation of Oxygen Reduction Activity Volcano Correlations for MN4 Molecular Catalysts Compared to Those for Metallic Electrodes." ECS Meeting Abstracts MA2022-01, no. 49 (2022): 2057. http://dx.doi.org/10.1149/ma2022-01492057mtgabs.

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A classical well-known reactivity index in electrocatalysis is the binding energy of key intermediates to the active sites. For example, this is well documented for the catalytic activity of metal electrodes for the oxygen reduction reaction (ORR)[1], alloys and metal oxides and less studied for molecular catalysts [2]. The activity at constant potential (log(i)E) plotted versus the M-O2 binding energy has the shape of a volcano. This is well documented in several papers, especially by the group of Norksov for metallic electrodes [1] and can be applied to many electrochemical reactions. This h

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Bitto, Herbert, Dean R. Guyer, William F. Polik, and C. Bradley Moore. "Dissociation on ground-state potential-energy surfaces." Faraday Discussions of the Chemical Society 82 (1986): 149. http://dx.doi.org/10.1039/dc9868200149.

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Jensen, Hans Joergen A., Poul Joergensen, and Trygve Helgaker. "Ground-state potential energy surface of diazene." Journal of the American Chemical Society 109, no. 10 (1987): 2895–901. http://dx.doi.org/10.1021/ja00244a007.

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Šurkus, A. "Ground-state potential energy function of SiCl+." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 60, no. 8-9 (2004): 2185–87. http://dx.doi.org/10.1016/j.saa.2003.09.016.

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Bunker, P. R., Ota Bludsky, Per Jensen, et al. "The H2O++ Ground State Potential Energy Surface." Journal of Molecular Spectroscopy 198, no. 2 (1999): 371–75. http://dx.doi.org/10.1006/jmsp.1999.7970.

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Poznanski, Jaroslaw, Pawel Szczesny, Bartosz Pawlinski, et al. "Arteriovenous oscillations of the redox potential: Is the redox state influencing blood flow?" Redox Report 22, no. 5 (2016): 210–17. http://dx.doi.org/10.1080/13510002.2016.1177933.

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Maiya, Bhaskar G., Anthony Harriman, Jonathan L. Sessler, Gregory Hemmi, Toshiaki Murai, and Thomas E. Mallouk. "Ground- and excited-state spectral and redox properties of cadmium(II) texaphyrin." Journal of Physical Chemistry 93, no. 24 (1989): 8111–15. http://dx.doi.org/10.1021/j100361a027.

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Fahrenbach, Albert C., Carson J. Bruns, Dennis Cao, and J. Fraser Stoddart. "Ground-State Thermodynamics of Bistable Redox-Active Donor–Acceptor Mechanically Interlocked Molecules." Accounts of Chemical Research 45, no. 9 (2012): 1581–92. http://dx.doi.org/10.1021/ar3000629.

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Fahrenbach, Albert C., Carson J. Bruns, Hao Li, Ali Trabolsi, Ali Coskun, and J. Fraser Stoddart. "Ground-State Kinetics of Bistable Redox-Active Donor–Acceptor Mechanically Interlocked Molecules." Accounts of Chemical Research 47, no. 2 (2013): 482–93. http://dx.doi.org/10.1021/ar400161z.

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Yaribeygi, Habib, Stephen L. Atkin, and Amirhossein Sahebkar. "Potential roles of microRNAs in redox state: An update." Journal of Cellular Biochemistry 120, no. 2 (2018): 1679–84. http://dx.doi.org/10.1002/jcb.27475.

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Fajı́n, José Luis Cagide, Javier López Cacheiro, Berta Fernández, and Jan Makarewicz. "Fluorobenzene–argon ground-state intermolecular potential energy surface." Journal of Chemical Physics 120, no. 18 (2004): 8582–86. http://dx.doi.org/10.1063/1.1695553.

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Claudio, Gil C., and Eric R. Bittner. "Ground-state potential energy curves of phenylenevinylene oligomers." Chemical Physics 276, no. 2 (2002): 81–91. http://dx.doi.org/10.1016/s0301-0104(01)00553-5.

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Boatz, Jerry A., Michael W. Schmidt, and Mark S. Gordon. "Ground-state potential energy surface of phosphine oxide." Journal of Physical Chemistry 91, no. 7 (1987): 1743–49. http://dx.doi.org/10.1021/j100291a014.

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Stärck, J., and W. Meyer. "The ground state potential of the beryllium dimer." Chemical Physics Letters 258, no. 3-4 (1996): 421–26. http://dx.doi.org/10.1016/0009-2614(96)00657-4.

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Ramiro Diaz, B., P. Wahnon, and V. Sidis. "A calculated (KrO2)+ ground-state potential energy surface." Chemical Physics Letters 212, no. 3-4 (1993): 218–22. http://dx.doi.org/10.1016/0009-2614(93)89317-b.

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Goodman, Lionel, Ali G. Ozkabak, and Surya N. Thakur. "A benchmark vibrational potential surface: ground-state benzene." Journal of Physical Chemistry 95, no. 23 (1991): 9044–58. http://dx.doi.org/10.1021/j100176a008.

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Koch, Henrik, Berta Fernández, and Jan Makarewicz. "Ground state benzene–argon intermolecular potential energy surface." Journal of Chemical Physics 111, no. 1 (1999): 198–204. http://dx.doi.org/10.1063/1.479266.

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Šurkus, A. A. "The ground-state potential energy function of PO+." Spectrochimica Acta Part A: Molecular Spectroscopy 48, no. 10 (1992): 1501–2. http://dx.doi.org/10.1016/0584-8539(92)80157-r.

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Akrawy, Dashty T. "α-decay half-lives of some nuclei from ground state to ground state using different nuclear potential". EPJ Nuclear Sciences & Technologies 4 (2018): 5. http://dx.doi.org/10.1051/epjn/2018001.

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Theoretical α-decay half-lives of some nuclei from ground state to ground state are calculated using different nuclear potential model including Coulomb proximity potential (CPPM), Royer proximity potential and Broglia and Winther 1991. The calculated values comparing with experimental data, it is observed that the CPPM model is in good agreement with the experimental data.

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Eberhart, Michael S., Brian T. Phelan, Jens Niklas, et al. "Surface immobilized copper(i) diimine photosensitizers as molecular probes for elucidating the effects of confinement at interfaces for solar energy conversion." Chemical Communications 56, no. 81 (2020): 12130–33. http://dx.doi.org/10.1039/d0cc05972b.

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Hui, Alice K., Richard L. Lord, and Kenneth G. Caulton. "In search of redox non-innocence between a tetrazine pincer ligand and monovalent copper." Dalton Trans. 43, no. 21 (2014): 7958–63. http://dx.doi.org/10.1039/c3dt52490f.

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Khan, Firoz Shah Tuglak, Amy L. Waldbusser, Maria C. Carrasco, Hadi Pourhadi, and Shabnam Hematian. "Synthetic, spectroscopic, structural, and electrochemical investigations of ferricenium derivatives with weakly coordinating anions: ion pairing, substituent, and solvent effects." Dalton Transactions 50, no. 21 (2021): 7433–55. http://dx.doi.org/10.1039/d1dt01192h.

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Kaur, Navjeet, Meenu Devi, Yamini Verma, et al. "Photochemical Synthesis of Fused Five-membered O-heterocycles." Current Green Chemistry 6, no. 3 (2019): 155–83. http://dx.doi.org/10.2174/2213346106666190904145200.

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Some transformations are not possible with ground-state reactions even in the presence of a catalyst, hence they are performed under photochemical conditions. Electron transfer occurs even with the photochemical excitement of one molecule where redox reaction is not possible at the ground state. The side products are obtained from ground-state reactions. For C-C bond formation during photochemical reactions, there is no requirement of any chemical activation of the substrates. Therefore, these reactions are presented here for the synthesis of fused five-membered O-heterocycles in the context o

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Chua, B. H., and B. J. Kleinhans. "Effect of redox potential on protein degradation in perfused rat heart." American Journal of Physiology-Endocrinology and Metabolism 248, no. 6 (1985): E726—E731. http://dx.doi.org/10.1152/ajpendo.1985.248.6.e726.

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The effect of redox potential on protein degradation was assessed in rat hearts supplied either glucose or pyruvate, and the correlation between redox state and proteolysis was examined after the addition of insulin and leucine. In hearts supplied glucose as the sole energy source, the inhibition of protein degradation by a range of concentrations of insulin was associated with increased ratios of perfusate lactate to pyruvate and intracellular lactate to pyruvate, malate to pyruvate, and NADH to NAD. However, the extent of inhibition did not correlate with the redox state. The inhibitory effe

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Javadimanesh, E., H. Hassanabadi, A. A. Rajabi, H. Rahimov, and S. Zarrinkamar. "Alpha Decay Half-Lives of Some Nuclei from Ground State to Ground State with Yukawa Proximity Potential." Communications in Theoretical Physics 58, no. 1 (2012): 146–50. http://dx.doi.org/10.1088/0253-6102/58/1/19.

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