- Home
- Publications
- Publication Search
- Publication Details
Title
Synthesis and reactivity of an N-triphos Mo(0) dinitrogen complex
Authors
Keywords
-
Journal
DALTON TRANSACTIONS
Volume 47, Issue 33, Pages 11386-11396
Publisher
Royal Society of Chemistry (RSC)
Online
2018-07-24
DOI
10.1039/c8dt02471e
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Testing the Push–Pull Hypothesis: Lewis Acid Augmented N2 Activation at Iron
- (2017) Jacob B. Geri et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Remarkable catalytic activity of dinitrogen-bridged dimolybdenum complexes bearing NHC-based PCP-pincer ligands toward nitrogen fixation
- (2017) Aya Eizawa et al. Nature Communications
- Insight into the stereoelectronic parameters of N-triphos ligands via coordination to tungsten(0)
- (2016) Andreas Phanopoulos et al. DALTON TRANSACTIONS
- Molybdenum dinitrogen complexes facially coordinated by linear tridentate PEP ligands (E = N or P): impact of the central E donor in trans-position to N2
- (2016) Svea Hinrichsen et al. DALTON TRANSACTIONS
- Unexpected Formation of Early Late Heterobimetallic Complexes from Transition Metal Frustrated Lewis Pairs
- (2016) Andy M. Chapman et al. INORGANIC CHEMISTRY
- Reactivity of Dinitrogen Bound to Mid- and Late-Transition-Metal Centers
- (2015) Nitesh Khoenkhoen et al. EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
- Recent Progress in Transition-Metal-Catalyzed Reduction of Molecular Dinitrogen under Ambient Reaction Conditions
- (2015) Yoshiaki Nishibayashi INORGANIC CHEMISTRY
- Catalytic Transformation of Levulinic Acid to 2-Methyltetrahydrofuran Using Ruthenium–N-Triphos Complexes
- (2015) Andreas Phanopoulos et al. ACS Catalysis
- (Dinitrogen)molybdenum Complexes Supported by Asymmetric Silicon-Centered Tripod Ligands: Steric and Electronic Influences on the Coordination of Mono- and Diphosphine Coligands
- (2014) Henning Broda et al. EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
- Synthesis, Characterization, and Reactivity of Ruthenium Hydride Complexes of N-Centered Triphosphine Ligands
- (2014) Andreas Phanopoulos et al. INORGANIC CHEMISTRY
- Molybdenum(0)-N2Complexes Supported by the Tripod Ligand 1,1,1-Tris(Diphenyl-Phosphinomethyl)Ethane: Steric Influence on the Coordination of Mono- and Diphosphine Coligands
- (2014) Jan Krahmer et al. ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE
- Molybdenum dinitrogen complexes supported by a silicon-centred tripod ligand and dppm or dmpm: tuning the activation of N2
- (2013) Henning Broda et al. DALTON TRANSACTIONS
- Bonding and Activation of N2 in Mo(0) Complexes Supported by Hybrid Tripod Ligands with Mixed Dialkylphosphine/Diarylphosphine Donor Groups: Interplay of Steric and Electronic Factors
- (2013) Ludger Söncksen et al. INORGANIC CHEMISTRY
- Catalytic Reduction of N2 to NH3 by an Fe–N2 Complex Featuring a C-Atom Anchor
- (2013) Sidney E. Creutz et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Catalytic conversion of nitrogen to ammonia by an iron model complex
- (2013) John S. Anderson et al. NATURE
- Octahedral Molybdenum(0) Monodinitrogen Complexes Facially Coordinated by the Tripodal Ligand 1,1,1-Tris(diphenylphosphanylmethyl)ethane - Influence of Diphosphane Coligands on the Activation of N2
- (2011) Jan Krahmer et al. EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
- Ruthenium-catalysed hydrogenation of esters using tripodal phosphine ligands
- (2011) Martin J. Hanton et al. JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
- The preparation of multimetallic complexes using sterically bulky N-centred tripodal dialkyl phosphino ligands
- (2010) Philip W. Miller et al. JOURNAL OF ORGANOMETALLIC CHEMISTRY
- Energetics and Mechanism of Ammonia Synthesis through the Chatt Cycle: Conditions for a Catalytic Mode and Comparison with the Schrock Cycle
- (2007) Gerald C. Stephan et al. CHEMISTRY-A EUROPEAN JOURNAL
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started