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Iridium Cyclooctene Complex That Forms a Hyperpolarization Transfer Catalyst before Converting to a Binuclear C-H Bond Activation Product Responsible for Hydrogen Isotope Exchange.Achieving High Levels of NMR-Hyperpolarization in Aqueous Media With Minimal Catalyst Contamination Using SABRE.A Ruthenium(II)-Copper(II) Dyad for the Photocatalytic Oxygenation of Organic Substrates Mediated by Dioxygen Activation.Extending the Scope of 19F Hyperpolarization through Signal Amplification by Reversible Exchange in MRI and NMR Spectroscopy.Achieving Biocompatible SABRE: An in vitro Cytotoxicity Study.Using parahydrogen to hyperpolarize amines, amides, carboxylic acids, alcohols, phosphates, and carbonates.Synthesis of planar chiral iridacycles by cationic metal π-coordination: facial selectivity, and conformational and stereochemical consequences.Direct and indirect hyperpolarisation of amines using parahydrogen.Quantification of hyperpolarisation efficiency in SABRE and SABRE-Relay enhanced NMR spectroscopyFine-tuning the efficiency of para-hydrogen-induced hyperpolarization by rational N-heterocyclic carbene designIridium α -Carboxyimine Complexes Hyperpolarized with para -Hydrogen Exist in Nuclear Singlet States before Conversion into Iridium CarbonatesFrontispiece: Achieving High Levels of NMR-Hyperpolarization in Aqueous Media With Minimal Catalyst Contamination Using SABRECatalyst-Substrate Effects on Biocompatible SABRE HyperpolarizationCharge-induced facial-selectivity in the formation of new cationic planar chiral iridacycles derived from anilineThe inhibition of iridium-promoted water oxidation catalysis (WOC) by cucurbit[n]urilsRoom temperature tandem hydroamination and hydrosilation/protodesilation catalysis by a tricarbonylchromium-bound iridacycleRapid 13C NMR hyperpolarization delivered from para-hydrogen enables the low concentration detection and quantification of sugarsRelayed hyperpolarization from para-hydrogen improves the NMR detectability of alcoholsHyperpolarising Pyruvate through Signal Amplification by Reversible Exchange (SABRE)
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Q40083383-0ECA1032-C559-46A7-B9CE-40EA65F8B9F6Q41602230-E16B1775-05A0-41C2-9AEE-652115EC85EDQ46723634-704C8058-D3A7-47F3-BBA2-1CCD5DB6D1C3Q47741815-1FA83348-D258-407E-B40E-178F4528F930Q47786721-9C1D6A2D-ECAB-46E5-BD0E-1B7CCF90B702Q48257022-2FAD3EC0-E4A1-4F7D-B68C-E36EB073E124Q53898877-AB2F5364-D8A6-4CB3-B815-ED9864CCA878Q55399876-C5B900A9-7CAF-4E23-B603-885E8B5C2E46Q57285942-3E6F0294-DCA1-461C-B705-4549148CFF92Q57471953-04161E3E-EA32-4AFC-9964-D7929BB8FBBEQ58067928-CA981128-3911-405B-B257-ECE1E7C097FDQ58067997-BB29AEEB-4E72-4089-9578-28A075345E1DQ60206188-61C7075B-9C83-4427-A1CB-D21BE4898626Q83404639-14B5C57D-C701-4C91-B9C0-2390DE9CEB4DQ84890824-01E17023-210F-4D97-A7BA-942A762E3A7DQ84977427-B34484E8-DB4A-4E9A-B50F-3B53AC11E329Q89940992-0631E62B-5889-4C18-9455-B53E4875F44FQ90535107-548C5652-337D-4F07-8D46-62397BB350BCQ92211156-E047FC19-1E1B-4124-86C0-3F95655317D6
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description
researcher
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wetenschapper
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հետազոտող
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name
Wissam Iali
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Wissam Iali
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Wissam Iali
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Wissam Iali
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Wissam Iali
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type
label
Wissam Iali
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Wissam Iali
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Wissam Iali
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Wissam Iali
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Wissam Iali
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Wissam Iali
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Wissam Iali
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Wissam Iali
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Wissam Iali
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Wissam Iali
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P1053
V-2698-2017
P106
P31
P3829
P496
0000-0002-9428-2023