sameAs
Better than platinum? Fuel cells energized by enzymes.Understanding the factors affecting the activation of alkane by Cp'Rh(CO)2 (Cp' = Cp or Cp*).Self-assembly of dinitrosyl iron units into imidazolate-edge-bridged molecular squares: characterization including Mössbauer spectroscopy.Computational studies of [NiFe] and [FeFe] hydrogenases.Unexpected Importance of Aromatic-Aliphatic and Aliphatic Side Chain-Backbone Interactions in the Stability of Amyloids.Redox active iron nitrosyl units in proton reduction electrocatalysis.Refining the active site structure of iron-iron hydrogenase using computational infrared spectroscopy.Mechanism of electrocatalytic hydrogen production by a di-iron model of iron-iron hydrogenase: a density functional theory study of proton dissociation constants and electrode reduction potentials.Analysis of a pentacoordinate iron dicarbonyl as synthetic analogue of the Hmd or mono-iron hydrogenase active site.Kinetic C-H oxidative addition vs thermodynamic C-X oxidative addition of chlorobenzene by a neutral Rh(I) system. A density functional theory study.Monoiron hydrogenase catalysis: hydrogen activation with the formation of a dihydrogen, Fe-H(delta-)...H(delta+)-O, bond and methenyl-H4MPT+ triggered hydride transfer.Stacking interactions of Ni(acac) chelates with benzene: calculated interaction energies.The theoretical transition state structure of a model complex bears a striking resemblance to the active site structure of DMSO reductase.Modeling the active sites in metalloenzymes 5. The heterolytic bond cleavage of H(2) in the [NiFe] hydrogenase of desulfovibrio gigas by a nucleophilic addition mechanism.Series of mixed valent Fe(II)Fe(I) complexes that model the Hox state of [FeFe]hydrogenase: redox properties, density-functional theory investigation, and reactivities with extrinsic CO.How electron flow controls the thermochemistry of the addition of olefins to nickel dithiolenes: predictions by density functional theory.Experimental and computational evidence for a boron-assisted, sigma-bond metathesis pathway for alkane borylation.Investigating the electronic structure of the Atox1 copper(I) transfer mechanism with density functional theory.Carbon monoxide induced reductive elimination of disulfide in an N-heterocyclic carbene (NHC)/thiolate dinitrosyl iron complex (DNIC).A reexamination of the propensities of amino acids towards a particular secondary structure: classification of amino acids based on their chemical structure.Density functional calculations on the conversion of azide and carbon monoxide to isocyanate and dinitrogen by a nickel to sulfur rebound mechanism.Nickel-manganese sulfido carbonyl cluster complexes. synthesis, structure, and properties of the unusual paramagnetic complexes Cp2Ni2Mn(CO)3(mu 3-E)2, E = S, Se.Bimetallic cluster complexes: the synthesis, structures, and bonding of ruthenium carbonyl cluster complexes containing palladium and platinum with the bulky tri-tert-butyl-phosphine ligand.Dinuclear ruthenium and iron complexes containing palladium and platinum with tri-tert-butylphosphine ligands: synthesis, structures, and bonding.Apparent anti-Woodward-Hoffmann addition to a nickel bis(dithiolene) complex: the reaction mechanism involves reduced, dimetallic intermediates.Reaction of the 1,8-bis(diphenylmethylium)naphthalenediyl dication with fluoride: formation of a cation containing a C-F-->C bridge.Reaction products of W(CO)(6) with formamidines; electronic structure of a W(2)(mu-CO)(2) core with unsymmetric bridging carbonyls.Superloading of tin ligands into rhodium and iridium carbonyl cluster complexes.Electronic effects steer the mechanism of asymmetric hydrogenations of unfunctionalized aryl-substituted alkenes.Rhodium boryl complexes in the catalytic, terminal functionalization of alkanes.Ambidentate thiocyanate and cyanate ligands in dinitrosyl iron complexes.Mechanism of the formation of carboxylate from alcohols and water catalyzed by a bipyridine-based ruthenium complex: a computational study.Carbon-hydrogen vs. carbon-halogen oxidative addition of chlorobenzene by a neutral iridium complex explored by DFT.Measuring the internal energies of species emitted from hypervelocity nanoprojectile impacts on surfaces using recalibrated benzylpyridinium probe ions.Thermally Stable Homogeneous Catalysts for Alkane Dehydrogenation S.O. thanks the German Academic Exchange Service (DAAD) for financing a research stay with W.C.K. in the USA. This work was supported by the National Science Foundation (CHE 9800184 tThe osmium-silicon triple bond: synthesis, characterization, and reactivity of an osmium silylyne complex.Density functional theory study of the reaction mechanism for competitive carbon-hydrogen and carbon-halogen bond activations catalyzed by transition metal complexes.Transformations and reactions of Re2(CO)8(mu-SbPh2)(mu-H) induced by the addition of a platinum(tri-t-butylphosphine) group.Biomimetics of [NiFe]-Hydrogenase: Nickel- or Iron-Centered Proton Reduction Catalysis?Understanding Pd-Pd bond length variation in (PNP)Pd-Pd(PNP) dimers.
P50
Q34144832-C9EDEE93-5AE0-4E51-9AD0-957D92CBA217Q34377181-DB15CE02-28FC-4877-8874-94DADB86E2FAQ35621553-00ADF22F-10C8-457A-BF72-9E00E0DE8FEDQ36967143-8894BE50-7ACF-45E7-B5AF-3CDECE814462Q38705428-36F00E50-A1FD-4CEF-A918-7F61ECD1CA0AQ39200623-F00BD64C-748E-4FD6-8543-2F8A7F0634D5Q40118845-284F939E-D518-48A8-837B-B63E35515F11Q43134247-DD06A7DE-FD21-4414-8116-22FF1897548AQ43179017-6CC1EA76-D945-4474-9A54-F5C86D6B9317Q43268667-F8ED6B85-1027-428A-A12E-5E1099FBC321Q43282555-EC9A47A4-936A-4BC0-9E88-37A8FC7B2B2BQ43568516-CDCFEA5D-F091-4098-A981-525F8388E3ACQ43638094-B9ABA085-E84A-4455-8CA0-E926120BB3D6Q43795503-7D09BF03-E368-444C-933B-62E0B0E8F30FQ43845154-19525E81-7324-440B-BC51-A80B24517B2DQ44173219-8157D810-AE07-4AB5-9C38-E554517C422AQ44284577-EE34D17A-162C-401F-A694-A6BD2B687174Q44386096-7DEF438D-B402-46E1-B82A-2CF3CE4FE0D0Q44423245-0A1CA99C-901C-4616-81A5-F4DEA43F597DQ44529130-F4B48A00-0096-492F-871E-A57356ED0FF0Q44822879-C3EBF759-CC5C-4C76-82FE-57C874ACA745Q44837874-4A195D4C-B0E1-48D1-A543-8321E5E359CAQ44852440-E4FDFB2E-D9A3-4D8B-A3AE-0C57FDA63EC8Q44944140-BC4BC7E7-CEA1-4715-9FB3-6CEEA88180D1Q44956345-6C2B8E44-BADF-40A8-BB32-00C1471B8F75Q44957515-111674A6-FB49-4D50-8538-5986880DDD29Q45120507-4E7BEA22-92DA-4127-BC1C-25648D991DA5Q45156633-29060445-7DFE-453E-822A-8BAF6EB2815EQ45196733-1BBFEA5E-D1D6-4365-BBFF-EBC9B83F4E49Q45277972-19464E55-2E9F-493C-83DE-4416E69C0E17Q45729445-5D896FCB-6269-4B68-B7B9-3342EB59DE4DQ45829257-A797ACE1-8AE1-4698-88CA-42EFBF38CE15Q45923559-65864161-5776-4E15-8482-3FD0D2D48042Q45940139-D6BF5CCE-4D5A-4D1C-91C9-68BF51AC1529Q46050158-F7870C03-DDA2-4FF0-85F5-461C2148A8CCQ46110834-6C8C4E74-D085-4326-8AEA-03A21C9F0B8BQ46149902-8EDABA40-D5C2-4D50-9CEB-D72A1D4AFAFCQ46204004-B422566D-9F73-43E7-A658-3880CD161F62Q46261779-E8893FE3-3C54-48FE-ADF3-6BE6B21D0A4BQ46653653-38625F64-AFC1-428C-9B61-2F7D5F07B56C
P50
description
Ameerika Ühendriikide keemik
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American chemist
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Amerikaans scheikundige
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Usana kemiisto
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amerikansk kemiker
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amerikansk kemist
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amerikansk kjemikar
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amerikansk kjemiker
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chimist american
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chimiste américain
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Michael B. Hall
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Michael B. Hall
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Michael B. Hall
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Michael B. Hall
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Michael B. Hall
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Michael B. Hall
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Michael B. Hall
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Michael B. Hall
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Michael B. Hall
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Michael B. Hall
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label
Michael B. Hall
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Michael B. Hall
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Michael B. Hall
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Michael B. Hall
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Michael B. Hall
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Michael B. Hall
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Michael B. Hall
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Michael B. Hall
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Michael B. Hall
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Michael B. Hall
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prefLabel
Michael B. Hall
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Michael B. Hall
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Michael B. Hall
@da
Michael B. Hall
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Michael B. Hall
@en
Michael B. Hall
@es
Michael B. Hall
@fr
Michael B. Hall
@it
Michael B. Hall
@nb
Michael B. Hall
@nl
P1053
B-9118-2013
P106
P1153
35479131200
P21
P2381
P31
P3829
P496
0000-0003-3263-3219