Probing hydrogen bonding to bound dioxygen in synthetic models for heme proteins: The importance of precise geometry

Chemistry - A European Journal

Volumn 15, Issue 1, 2009, Pages 125-135

  Dube, Henry ^a   Kasumaj, Besnik ^a   Calle, Carlos ^a   Felber, Beatrice ^a   Saito, Makoto ^a   Jeschke, Gunnar ^a   Diederich, François ^a  

^a ETH ZURICH   (Switzerland)

Author keywords

ENDOR spectroscopy; Heme proteins; Hydrogen bonds; Molecular recognition; Porphyrinoids

Indexed keywords

BINDING SITES; CHEMICAL COMPOUNDS; COBALT; COBALT COMPOUNDS; COMPLEXATION; COMPUTATIONAL GEOMETRY; ELECTRON SPIN RESONANCE SPECTROSCOPY; HEMOGLOBIN; HYDROGEN; MOLECULAR BIOLOGY; MOLECULAR RECOGNITION; NONMETALS; PARAMAGNETIC RESONANCE; PORPHYRINS; PROTEINS; TRANSITION METALS;

DIOXYGEN; DIOXYGEN BINDING; ELECTRON PARAMAGNETIC RESONANCE (EPR) SPECTROSCOPY; ENDOR SPECTROSCOPY; HEME PROTEINS; HYDROGEN BONDINGS; MODEL COMPLEXES; MODEL COMPOUNDS; PORPHYRINOIDS; SYNTHETIC MODELS;

HYDROGEN BONDS;

COBALT; HEMOPROTEIN; OXYGEN;

ARTICLE; BINDING SITE; CHEMICAL MODEL; CHEMISTRY; CONFORMATION; HYDROGEN BOND; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SYNTHESIS;

BINDING SITES; COBALT; HEMEPROTEINS; HYDROGEN BONDING; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, CHEMICAL; MOLECULAR CONFORMATION; OXYGEN;

EID: 58449119126     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200802077     Document Type: Article

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