Synthesis and structure of palladium(II) complexes supported by bis-NHC pincer ligands for the electrochemical activation of CO2-Reference-Cited by-同舟云学术

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Synthesis and structure of palladium(II) complexes supported by bis-NHC pincer ligands for the electrochemical activation of CO2

Published:2017-10 Issue: Volume:135 Page:134-143
ISSN:0277-5387
Container-title:Polyhedron
language:en
Short-container-title:Polyhedron

Author:

Andrade Gabriel A.,DiMeglio John L.,Guardino Eric T.,Yap Glenn P.A.,Rosenthal Joel

Funder

NSF

National Science Foundation

University of Delaware Research Foundation

NIGMS

NIH

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Physical and Theoretical Chemistry

Reference44 articles.

1. A Pd complex of a tridentate pincer CNC bis-carbene ligand as a robust homogenous Heck catalyst

2. Palladium Complexes with Tridentate Pincer Bis-Carbene Ligands as Efficient Catalysts for C−C Coupling

3. Catalysis by Palladium Pincer Complexes

4. The Privileged Pincer-Metal Platform: Coordination Chemistry & Applications;Farrell,2016

5. Development of Transition Metal Phosphine Complexes as Electrocatalysts for CO2and CO Reduction

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1. Molecular catalysts for CO2 Electroreduction: Progress and prospects with pincer type complexes;Coordination Chemistry Reviews;2023-10

2. Cationic ruthenium(II)-CNC pincer complexes as phosphine-free catalysts for nitrile hydration to amides in aqueous medium;Molecular Catalysis;2023-10

3. Role of ancillary ligands in selectivity towards acceptorless dehydrogenation versus dehydrogenative coupling of alcohols and amines catalyzed by cationic ruthenium(ii)–CNC pincer complexes;Dalton Transactions;2023

4. Pincer‐Type Mesoionic Carbene Nickel(II) Complexes: Synthesis, Properties, Reactions, and Catalytic Application to the Suzuki–Miyaura Coupling Reaction of Aryl Bromides;European Journal of Inorganic Chemistry;2022-02-18

5. Heterobimetallic Pd/Mn and Pd/Co complexes as efficient and stereoselective catalysts for sequential Cu-free Sonogashira coupling–alkyne semi-hydrogenation reactions;Dalton Transactions;2022

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