Home

királyi család talaj Közelítés nhc nickel ii reduction to nikkel 0 Harcos Nehézsé tegye túllépés

Electrocatalytic reduction of CO2 with CCC-NHC pincer nickel complexes -  Chemical Communications (RSC Publishing)
Electrocatalytic reduction of CO2 with CCC-NHC pincer nickel complexes - Chemical Communications (RSC Publishing)

Electrocatalytic CO 2 reduction with nickel complexes supported by tunable  bipyridyl-N-heterocyclic carbene donors: understanding redox-active macrocy  ... - Chemical Communications (RSC Publishing) DOI:10.1039/C8CC00266E
Electrocatalytic CO 2 reduction with nickel complexes supported by tunable bipyridyl-N-heterocyclic carbene donors: understanding redox-active macrocy ... - Chemical Communications (RSC Publishing) DOI:10.1039/C8CC00266E

Methyl (Alkyl)-Coenzyme M Reductases: Nickel F-430-Containing Enzymes  Involved in Anaerobic Methane Formation and in Anaerobic Oxidation of  Methane or of Short Chain Alkanes | Biochemistry
Methyl (Alkyl)-Coenzyme M Reductases: Nickel F-430-Containing Enzymes Involved in Anaerobic Methane Formation and in Anaerobic Oxidation of Methane or of Short Chain Alkanes | Biochemistry

Nickel-catalyzed reductive coupling of homoenolates and their higher  homologues with unactivated alkyl bromides | Nature Communications
Nickel-catalyzed reductive coupling of homoenolates and their higher homologues with unactivated alkyl bromides | Nature Communications

Coligand role in the NHC nickel catalyzed C–F bond activation:  investigations on the insertion of bis(NHC) nickel into the C–F bond of  hexafluorobenze ... - Chemical Science (RSC Publishing)  DOI:10.1039/D0SC04237D
Coligand role in the NHC nickel catalyzed C–F bond activation: investigations on the insertion of bis(NHC) nickel into the C–F bond of hexafluorobenze ... - Chemical Science (RSC Publishing) DOI:10.1039/D0SC04237D

An Unsaturated Nickel(0) NHC Catalyst: Facile Preparation and Structure of  Ni(0)(NHC)2, Featuring a Reduction Process from Ni(II)(NHC)(acac)2 |  Organometallics
An Unsaturated Nickel(0) NHC Catalyst: Facile Preparation and Structure of Ni(0)(NHC)2, Featuring a Reduction Process from Ni(II)(NHC)(acac)2 | Organometallics

Well-defined nickel(II) tetrazole-saccharinate complex as homogeneous  catalyst on the reduction of aldehydes: scope and reaction mechanism
Well-defined nickel(II) tetrazole-saccharinate complex as homogeneous catalyst on the reduction of aldehydes: scope and reaction mechanism

Synthesis and structural characterization of nickel(II) complexes of  20-membered macrocyclic rings bearing chelating bis(N-heterocyclic carbene)  ligands - ScienceDirect
Synthesis and structural characterization of nickel(II) complexes of 20-membered macrocyclic rings bearing chelating bis(N-heterocyclic carbene) ligands - ScienceDirect

Redox‐Neutral Nickel(II) Catalysis: Hydroarylation of Unactivated Alkenes  with Arylboronic Acids - Wang - 2020 - Angewandte Chemie - Wiley Online  Library
Redox‐Neutral Nickel(II) Catalysis: Hydroarylation of Unactivated Alkenes with Arylboronic Acids - Wang - 2020 - Angewandte Chemie - Wiley Online Library

Nickel(II) NHC-complexes with tridentate, dianionic ligands - ScienceDirect
Nickel(II) NHC-complexes with tridentate, dianionic ligands - ScienceDirect

Nickel N-heterocyclic carbene complexes in homogeneous catalysis
Nickel N-heterocyclic carbene complexes in homogeneous catalysis

The Synthesis and Catalytic Activity of New Mixed NHC-Phosphite Nickel(0)  Complexes | Organometallics
The Synthesis and Catalytic Activity of New Mixed NHC-Phosphite Nickel(0) Complexes | Organometallics

Redox‐Neutral Nickel(II) Catalysis: Hydroarylation of Unactivated Alkenes  with Arylboronic Acids - Wang - 2020 - Angewandte Chemie - Wiley Online  Library
Redox‐Neutral Nickel(II) Catalysis: Hydroarylation of Unactivated Alkenes with Arylboronic Acids - Wang - 2020 - Angewandte Chemie - Wiley Online Library

Redox‐Neutral Nickel(II) Catalysis: Hydroarylation of Unactivated Alkenes  with Arylboronic Acids - Wang - 2020 - Angewandte Chemie - Wiley Online  Library
Redox‐Neutral Nickel(II) Catalysis: Hydroarylation of Unactivated Alkenes with Arylboronic Acids - Wang - 2020 - Angewandte Chemie - Wiley Online Library

An Unsaturated Nickel(0) NHC Catalyst: Facile Preparation and Structure of  Ni(0)(NHC)2, Featuring a Reduction Process from Ni(II)(NHC)(acac)2 |  Organometallics
An Unsaturated Nickel(0) NHC Catalyst: Facile Preparation and Structure of Ni(0)(NHC)2, Featuring a Reduction Process from Ni(II)(NHC)(acac)2 | Organometallics

A surprising mechanism lacking the Ni(0) state during the Ni(II)-catalyzed  P–C cross-coupling reaction performed in the absence of a reducing agent –  An experimental and a theoretical study
A surprising mechanism lacking the Ni(0) state during the Ni(II)-catalyzed P–C cross-coupling reaction performed in the absence of a reducing agent – An experimental and a theoretical study

Recent developments in nickel-catalyzed intermolecular  dicarbofunctionalization of alkenes - Chemical Science (RSC Publishing)  DOI:10.1039/C9SC06006E
Recent developments in nickel-catalyzed intermolecular dicarbofunctionalization of alkenes - Chemical Science (RSC Publishing) DOI:10.1039/C9SC06006E

Catalysts | Free Full-Text | Effect of the Gallium and Vanadium on the  Dibenzothiophene Hydrodesulfurization and Naphthalene Hydrogenation  Activities Using Sulfided NiMo-V2O5/Al2O3-Ga2O3
Catalysts | Free Full-Text | Effect of the Gallium and Vanadium on the Dibenzothiophene Hydrodesulfurization and Naphthalene Hydrogenation Activities Using Sulfided NiMo-V2O5/Al2O3-Ga2O3

Recent developments in nickel-catalyzed intermolecular  dicarbofunctionalization of alkenes - Chemical Science (RSC Publishing)  DOI:10.1039/C9SC06006E
Recent developments in nickel-catalyzed intermolecular dicarbofunctionalization of alkenes - Chemical Science (RSC Publishing) DOI:10.1039/C9SC06006E

An Unsaturated Nickel(0) NHC Catalyst: Facile Preparation and Structure of  Ni(0)(NHC)2, Featuring a Reduction Process from Ni(II)(NHC)(acac)2 |  Organometallics
An Unsaturated Nickel(0) NHC Catalyst: Facile Preparation and Structure of Ni(0)(NHC)2, Featuring a Reduction Process from Ni(II)(NHC)(acac)2 | Organometallics

Mechanisms of Nickel-Catalyzed Coupling Reactions and Applications in  Alkene Functionalization | Accounts of Chemical Research
Mechanisms of Nickel-Catalyzed Coupling Reactions and Applications in Alkene Functionalization | Accounts of Chemical Research

Redox‐Neutral Nickel(II) Catalysis: Hydroarylation of Unactivated Alkenes  with Arylboronic Acids - Wang - 2020 - Angewandte Chemie - Wiley Online  Library
Redox‐Neutral Nickel(II) Catalysis: Hydroarylation of Unactivated Alkenes with Arylboronic Acids - Wang - 2020 - Angewandte Chemie - Wiley Online Library

Phosphine-functionalized NHC Ni(ii) and Ni(0) complexes: synthesis,  characterization and catalytic properties - Dalton Transactions (RSC  Publishing)
Phosphine-functionalized NHC Ni(ii) and Ni(0) complexes: synthesis, characterization and catalytic properties - Dalton Transactions (RSC Publishing)

Mechanism of nickel-catalyzed direct carbonyl-Heck coupling reaction: the  crucial role of second-sphere interactions - Dalton Transactions (RSC  Publishing)
Mechanism of nickel-catalyzed direct carbonyl-Heck coupling reaction: the crucial role of second-sphere interactions - Dalton Transactions (RSC Publishing)

An Unsaturated Nickel(0) NHC Catalyst: Facile Preparation and Structure of  Ni(0)(NHC)2, Featuring a Reduction Process from Ni(II)(NHC)(acac)2 |  Organometallics
An Unsaturated Nickel(0) NHC Catalyst: Facile Preparation and Structure of Ni(0)(NHC)2, Featuring a Reduction Process from Ni(II)(NHC)(acac)2 | Organometallics

An Unsaturated Nickel(0) NHC Catalyst: Facile Preparation and Structure of  Ni(0)(NHC)2, Featuring a Reduction Process from Ni(II)(NHC)(acac)2 |  Organometallics
An Unsaturated Nickel(0) NHC Catalyst: Facile Preparation and Structure of Ni(0)(NHC)2, Featuring a Reduction Process from Ni(II)(NHC)(acac)2 | Organometallics