![Polymers | Free Full-Text | [Rh(L-alaninate)(1,5-Cyclooctadiene)] Catalyzed Helix-Sense-Selective Polymerizations of Achiral Phenylacetylenes | HTML](https://www.mdpi.com/polymers/polymers-10-01223/article_deploy/html/images/polymers-10-01223-g001.png "Polymers | Free Full-Text | [Rh(L-alaninate)(1,5-Cyclooctadiene)] Catalyzed Helix-Sense-Selective Polymerizations of Achiral Phenylacetylenes | HTML")
Polymers | Free Full-Text | [Rh(L-alaninate)(1,5-Cyclooctadiene)] Catalyzed Helix-Sense-Selective Polymerizations of Achiral Phenylacetylenes | HTML
Ir-Catalyzed Asymmetric Allylic Dearomatization Reactions---State Key Laboratory of Organometallic Chemistry 345 Lingling Lu, Shanghai
Iridium | Syntheticnature
![Ir(COD)Cl]2 as a Catalyst Precursor for the Intramolecular Hydroamination of Unactivated Alkenes with Primary Amines and Secondary Alkyl- or Arylamines: A Combined Catalytic, Mechanistic, and Computational Investigation | Journal of the American](https://pubs.acs.org/cms/10.1021/ja908316n/asset/images/medium/ja-2009-08316n_0012.gif "Ir(COD)Cl]2 as a Catalyst Precursor for the Intramolecular Hydroamination of Unactivated Alkenes with Primary Amines and Secondary Alkyl- or Arylamines: A Combined Catalytic, Mechanistic, and Computational Investigation | Journal of the American")
Ir(COD)Cl]2 as a Catalyst Precursor for the Intramolecular Hydroamination of Unactivated Alkenes with Primary Amines and Secondary Alkyl- or Arylamines: A Combined Catalytic, Mechanistic, and Computational Investigation | Journal of the American
![Allylic amination catalyzed by [Ir(COD)Cl] 2 and L1 | Download Table](https://www.researchgate.net/profile/Alan-Goldman/publication/251330064/figure/tbl13/AS:668932327342083@1536497303136/Allylic-amination-catalyzed-by-IrCODCl-2-and-L1.png "Allylic amination catalyzed by [Ir(COD)Cl] 2 and L1 | Download Table")
Allylic amination catalyzed by [Ir(COD)Cl] 2 and L1 | Download Table
![Catalysts | Free Full-Text | Strong Solvent Effects on Catalytic Transfer Hydrogenation of Ketones with [Ir(cod)(NHC)(PR3)] Catalysts in 2-Propanol-Water Mixtures | HTML](https://www.mdpi.com/catalysts/catalysts-10-00017/article_deploy/html/images/catalysts-10-00017-g001.png "Catalysts | Free Full-Text | Strong Solvent Effects on Catalytic Transfer Hydrogenation of Ketones with [Ir(cod)(NHC)(PR3)] Catalysts in 2-Propanol-Water Mixtures | HTML")
Catalysts | Free Full-Text | Strong Solvent Effects on Catalytic Transfer Hydrogenation of Ketones with [Ir(cod)(NHC)(PR3)] Catalysts in 2-Propanol-Water Mixtures | HTML
Scheme 3 | Luminescent Iridium Complexes Used in Light-Emitting Electrochemical Cells (LEECs) | SpringerLink
![Reactivity of Phosphane–Imidazolium Salts Towards [Ir(COD)Cl]2: Preparation of New Hydridoiridium(III) Complexes Bearing Abnormal Carbenes - Wolf - 2008 - European Journal of Inorganic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/7d35c1e7-977c-43c1-bcee-fbe7d329cb1a/mfig000.jpg "Reactivity of Phosphane–Imidazolium Salts Towards [Ir(COD)Cl]2: Preparation of New Hydridoiridium(III) Complexes Bearing Abnormal Carbenes - Wolf - 2008 - European Journal of Inorganic Chemistry - Wiley Online Library")
Reactivity of Phosphane–Imidazolium Salts Towards [Ir(COD)Cl]2: Preparation of New Hydridoiridium(III) Complexes Bearing Abnormal Carbenes - Wolf - 2008 - European Journal of Inorganic Chemistry - Wiley Online Library
Cyclooctadiene iridium chloride dimer - Wikipedia
Cyclooctadiene iridium methoxide dimer - Wikipedia
![Ir(COD)Cl]2 as a Catalyst Precursor for the Intramolecular Hydroamination of Unactivated Alkenes with Primary Amines and Secondary Alkyl- or Arylamines: A Combined Catalytic, Mechanistic, and Computational Investigation | Journal of the American](https://pubs.acs.org/cms/10.1021/ja908316n/asset/images/medium/ja-2009-08316n_0017.gif "Ir(COD)Cl]2 as a Catalyst Precursor for the Intramolecular Hydroamination of Unactivated Alkenes with Primary Amines and Secondary Alkyl- or Arylamines: A Combined Catalytic, Mechanistic, and Computational Investigation | Journal of the American")
Ir(COD)Cl]2 as a Catalyst Precursor for the Intramolecular Hydroamination of Unactivated Alkenes with Primary Amines and Secondary Alkyl- or Arylamines: A Combined Catalytic, Mechanistic, and Computational Investigation | Journal of the American
A versatile catalyst system for enantioselective synthesis of 2-substituted 1,4-benzodioxanes - Chemical Science (RSC Publishing) DOI:10.1039/C8SC05612A
File:Ir2Cl2 cod 2improved.svg - Wikimedia Commons
![Ir(COD)Cl]2 as a Catalyst Precursor for the Intramolecular Hydroamination of Unactivated Alkenes with Primary Amines and Secondary Alkyl- or Arylamines: A Combined Catalytic, Mechanistic, and Computational Investigation | Journal of the American](https://pubs.acs.org/cms/10.1021/ja908316n/asset/images/medium/ja-2009-08316n_0016.gif "Ir(COD)Cl]2 as a Catalyst Precursor for the Intramolecular Hydroamination of Unactivated Alkenes with Primary Amines and Secondary Alkyl- or Arylamines: A Combined Catalytic, Mechanistic, and Computational Investigation | Journal of the American")
Ir(COD)Cl]2 as a Catalyst Precursor for the Intramolecular Hydroamination of Unactivated Alkenes with Primary Amines and Secondary Alkyl- or Arylamines: A Combined Catalytic, Mechanistic, and Computational Investigation | Journal of the American
Figure 1 from In-Depth Study on Chloride Abstractions from (NHC)Ir(COD)Cl Complexes | Semantic Scholar
![Figure 7 from [Ir(COD)Cl]2 as a catalyst precursor for the intramolecular hydroamination of unactivated alkenes with primary amines and secondary alkyl- or arylamines: a combined catalytic, mechanistic, and computational investigation. | Semantic](https://d3i71xaburhd42.cloudfront.net/46356b19fdd1eaa8c5903ce3fbfdabb4098eb769/9-Figure7-1.png "Figure 7 from [Ir(COD)Cl]2 as a catalyst precursor for the intramolecular hydroamination of unactivated alkenes with primary amines and secondary alkyl- or arylamines: a combined catalytic, mechanistic, and computational investigation. | Semantic")
Figure 7 from [Ir(COD)Cl]2 as a catalyst precursor for the intramolecular hydroamination of unactivated alkenes with primary amines and secondary alkyl- or arylamines: a combined catalytic, mechanistic, and computational investigation. | Semantic
![IBIOX6]-IR-(COD)-CL - SpectraBase](https://spectrabase.com/api/compound/ANSKGzPdbWI.png?h=300&w=416 "IBIOX6]-IR-(COD)-CL - SpectraBase")
IBIOX6]-IR-(COD)-CL - SpectraBase
Cyclooctadiene iridium chloride dimer - Wikipedia
![IBIOXME4]-IR-(COD)-CL - SpectraBase](https://spectrabase.com/api/compound/JGXVXMNCehi.png?ph=true&h=300&w=416 "IBIOXME4]-IR-(COD)-CL - SpectraBase")
IBIOXME4]-IR-(COD)-CL - SpectraBase
![Scheme 7 Allylic etherification catalyzed by [Ir(COD)Cl] 2 and a... | Download Scientific Diagram](https://www.researchgate.net/profile/Alan-Goldman/publication/251330064/figure/fig10/AS:668932323164176@1536497302616/Scheme-7-Allylic-etherification-catalyzed-by-IrCODCl-2-and-a-phosphorodiamidite-ligand.png "Scheme 7 Allylic etherification catalyzed by [Ir(COD)Cl] 2 and a... | Download Scientific Diagram")
Scheme 7 Allylic etherification catalyzed by [Ir(COD)Cl] 2 and a... | Download Scientific Diagram
Recent advances and applications of iridium-catalysed asymmetric allylic substitution - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C2OB07086C
Ir(cod)Cl]2 | C16H24Cl2Ir2 | ChemSpider
![The cyclooctadiene ligand in [IrCl(COD)]2 is hydrogenated under transfer hydrogenation conditions: A study in the presence of PPh3 and a strong base in isopropanol - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X16304478-sc1.jpg "The cyclooctadiene ligand in [IrCl(COD)]2 is hydrogenated under transfer hydrogenation conditions: A study in the presence of PPh3 and a strong base in isopropanol - ScienceDirect")
The cyclooctadiene ligand in [IrCl(COD)]2 is hydrogenated under transfer hydrogenation conditions: A study in the presence of PPh3 and a strong base in isopropanol - ScienceDirect
![Figure 6 from [Ir(COD)Cl]2 as a catalyst precursor for the intramolecular hydroamination of unactivated alkenes with primary amines and secondary alkyl- or arylamines: a combined catalytic, mechanistic, and computational investigation. | Semantic](https://d3i71xaburhd42.cloudfront.net/46356b19fdd1eaa8c5903ce3fbfdabb4098eb769/8-Figure6-1.png "Figure 6 from [Ir(COD)Cl]2 as a catalyst precursor for the intramolecular hydroamination of unactivated alkenes with primary amines and secondary alkyl- or arylamines: a combined catalytic, mechanistic, and computational investigation. | Semantic")