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Literature DB >> 16086351

Energetics and mechanism of a room-temperature catalytic process for ammonia synthesis (Schrock cycle): comparison with biological nitrogen fixation.

Felix Studt¹, Felix Tuczek.

Abstract

Entities: Chemical

Mesh：

Substances：

Year: 2005 PMID： 16086351 DOI： 10.1002/anie.200501485

Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN： 1433-7851 Impact factor: 15.336

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13 in total

1. Identification of altered metabolic pathways of γ-irradiated rice mutant via network-based transcriptome analysis.

Authors: Sun-Goo Hwang; Dong Sub Kim; Jung Eun Hwang; Hyeon Mi Park; Cheol Seong Jang
Journal: Genetica Date: 2015-09-11 Impact factor: 1.082

Review 2. Catalytic N₂-to-NH₃ (or -N₂H₄) Conversion by Well-Defined Molecular Coordination Complexes.

Authors: Matthew J Chalkley; Marcus W Drover; Jonas C Peters
Journal: Chem Rev Date: 2020-04-30 Impact factor: 60.622

3. Experimental and theoretical EPR study of Jahn-Teller-active [HIPTN(3)N]MoL complexes (L = N(2), CO, NH(3)).

Authors: Rebecca L McNaughton; Michael Roemelt; Jia Min Chin; Richard R Schrock; Frank Neese; Brian M Hoffman
Journal: J Am Chem Soc Date: 2010-06-30 Impact factor: 15.419

Review 4. Insight into the Iron-Molybdenum Cofactor of Nitrogenase from Synthetic Iron Complexes with Sulfur, Carbon, and Hydride Ligands.

Authors: Ilija Čorić; Patrick L Holland
Journal: J Am Chem Soc Date: 2016-06-03 Impact factor: 15.419

Energetics and mechanism of a room-temperature catalytic process for ammonia synthesis (Schrock cycle): comparison with biological nitrogen fixation.

1. Identification of altered metabolic pathways of γ-irradiated rice mutant via network-based transcriptome analysis.

Review 2. Catalytic N₂-to-NH₃ (or -N₂H₄) Conversion by Well-Defined Molecular Coordination Complexes.

3. Experimental and theoretical EPR study of Jahn-Teller-active [HIPTN(3)N]MoL complexes (L = N(2), CO, NH(3)).

Review 4. Insight into the Iron-Molybdenum Cofactor of Nitrogenase from Synthetic Iron Complexes with Sulfur, Carbon, and Hydride Ligands.

5. Catalytic reduction of dinitrogen to ammonia at a single molybdenum center.

6. Synthesis of diamidopyrrolyl molybdenum complexes relevant to reduction of dinitrogen to ammonia.

7. EPR/ENDOR and Theoretical Study of the Jahn-Teller-Active [HIPTN₃N]Mo^VL Complexes (L = N^-, NH).

Review 8. The discovery of Mo(III) in FeMoco: reuniting enzyme and model chemistry.

9. Catalytic N₂-to-NH₃ Conversion by Fe at Lower Driving Force: A Proposed Role for Metallocene-Mediated PCET.

Review 10. Theoretical studies of homogeneous catalysts mimicking nitrogenase.

Energetics and mechanism of a room-temperature catalytic process for ammonia synthesis (Schrock cycle): comparison with biological nitrogen fixation.

1. Identification of altered metabolic pathways of γ-irradiated rice mutant via network-based transcriptome analysis.

Review 2. Catalytic N2-to-NH3 (or -N2H4) Conversion by Well-Defined Molecular Coordination Complexes.

3. Experimental and theoretical EPR study of Jahn-Teller-active [HIPTN(3)N]MoL complexes (L = N(2), CO, NH(3)).

Review 4. Insight into the Iron-Molybdenum Cofactor of Nitrogenase from Synthetic Iron Complexes with Sulfur, Carbon, and Hydride Ligands.

5. Catalytic reduction of dinitrogen to ammonia at a single molybdenum center.

6. Synthesis of diamidopyrrolyl molybdenum complexes relevant to reduction of dinitrogen to ammonia.

7. EPR/ENDOR and Theoretical Study of the Jahn-Teller-Active [HIPTN3N]MoVL Complexes (L = N-, NH).

Review 8. The discovery of Mo(III) in FeMoco: reuniting enzyme and model chemistry.

9. Catalytic N2-to-NH3 Conversion by Fe at Lower Driving Force: A Proposed Role for Metallocene-Mediated PCET.

Review 10. Theoretical studies of homogeneous catalysts mimicking nitrogenase.

Review 2. Catalytic N₂-to-NH₃ (or -N₂H₄) Conversion by Well-Defined Molecular Coordination Complexes.

7. EPR/ENDOR and Theoretical Study of the Jahn-Teller-Active [HIPTN₃N]Mo^VL Complexes (L = N^-, NH).

9. Catalytic N₂-to-NH₃ Conversion by Fe at Lower Driving Force: A Proposed Role for Metallocene-Mediated PCET.