about
A Combined Experimental/Computational Study of the Mechanism of a Palladium-Catalyzed Bora-Negishi Reaction.Expanded ring diaminocarbene palladium complexes: synthesis, structure, and Suzuki-Miyaura cross-coupling of heteroaryl chlorides in water.Enabling and Probing Oxidative Addition and Reductive Elimination at a Group 14 Metal Center: Cleavage and Functionalization of E-H Bonds by a Bis(boryl)stannylene.Highly Electron-Rich β-Diketiminato Systems: Synthesis and Coordination Chemistry of Amino-Functionalized "N-nacnac" Ligands.A Systematic Study of Structure and E-H Bond Activation Chemistry by Sterically Encumbered Germylene Complexes.Reactivity of a frustrated lewis pair and small-molecule activation by an isolable Arduengo carbene-B{3,5-(CF3)2C6H3}3 complex.Facile reversibility by design: tuning small molecule capture and activation by single component frustrated Lewis pairs.A β-Diketiminate-Stabilized Sila-Acyl Chloride: Systematic Access to Base-Stabilized Silicon Analogues of Classical Carbonyl CompoundsIridium(I) Complexes with Anionic N-Heterocyclic Carbene Ligands as Catalysts for the Hydrogenation of Alkenes in Nonpolar MediaDual reactivity of N-heterocyclic carbenes towards copper(II) saltsCatalytic B-N Dehydrogenation Using Frustrated Lewis Pairs: Evidence for a Chain-Growth Coupling MechanismExperimental and quantum chemical studies of anionic analogues of N-heterocyclic carbenesOn the Viability of Catalytic Turnover via Al-O/B-H Metathesis: The Reactivity of β-Diketiminate Aluminium Hydrides towards CO2 and BoranesBorylated N-Heterocyclic Carbenes: Rearrangement and Chemical TrappingSynthesis of highly-specific stable nanocrystalline goethite-like hydrous ferric oxide nanoparticles for biomedical applications by simple precipitation methodSynthetic, structural and reaction chemistry of N-heterocyclic germylene and stannylene compounds featuring N-boryl substituentsReversible borohydride formation from aluminium hydrides and {H(9-BBN)}2: structural, thermodynamic and reactivity studiesHematite Nanoparticles from Unexpected Reaction of Ferrihydrite with Concentrated Acids for Biomedical Applications
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Q38658819-6BA8A13C-C6DA-43E2-8BEB-8556E6727E0BQ46046443-0CEB8594-533E-4D7C-9B1A-AABF5BF12C3CQ46579227-644790E7-5F52-4EED-B4CD-BE3AF3836778Q48168762-0559206F-E220-4403-A157-856FA9AC91ACQ50788422-230E9318-6638-4D0E-9DCD-77683823C675Q53134329-F32BD481-2B75-447F-A002-DB4B43539038Q53196802-CEE5ACED-7C09-4067-89CA-F01887156FE4Q57461223-B9758016-1EE5-47B9-A2DC-44781B669C6BQ62111899-72C86B84-AD52-46C0-911F-740722EF6A42Q83424986-FED8B37D-502B-448B-827B-0B95518A2195Q87376413-BA55FCFB-2462-4140-928A-0545CC29B7DAQ88754229-5B38CDC1-BA05-48F1-A06A-276B61753343Q89544110-3F4489B1-9B54-4DBC-9200-010E39DD9AD5Q90406771-414506E7-C974-4414-899D-A3027F94A0CDQ91237994-40ECF62F-396C-4D83-9D1D-7D1242E43892Q91985993-191B3625-AA7C-43FF-829B-285A5BA1998FQ92217989-B26D6D9F-3A62-41D2-9E55-825AF9F8C707Q93263926-21EC41F8-1F9A-4D2D-B60F-5421CDF3C762
P50
description
investigador
@es
researcher
@en
name
Eugene L Kolychev
@en
type
label
Eugene L Kolychev
@en
prefLabel
Eugene L Kolychev
@en
P31
P496
0000-0002-8420-5067