Complexes of a Noncyclic Carbazole-based N5-donor Schiff base: Structures, Redox, EPR and Poor Activity as Hydrogen Evolution Electrocatalysts-Reference-Cited by-同舟云学术

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Complexes of a Noncyclic Carbazole-based N5-donor Schiff base: Structures, Redox, EPR and Poor Activity as Hydrogen Evolution Electrocatalysts

Published:2024-09-03 Issue: Volume: Page:
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Akogun Folaranmi S.¹^ORCID,Judd Martyna²,Mort Alexandra G. C.²,Malthus Stuart J.¹^ORCID,Robb Matthew G.¹^ORCID,Cox Nicholas²^ORCID,Brooker Sally¹^ORCID

Affiliation:

1. Department of Chemistry and MacDiarmid Institute for Advanced Materials and Nanotechnology, University of Otago, PO Box 56, Dunedin 9054, New Zealand

2. Research School of Chemistry, The Australian National University, Canberra, ACT 0200, Australia

Funder

National Computational Infrastructure

MacDiarmid Institute for Advanced Materials and Nanotechnology

University of Otago

He Honoka Hauwai / German-New Zealand Green Hydrogen Centre

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.inorgchem.4c02657

Reference79 articles.

1. Perspective on carbazole-based organic compounds as emitters and hosts in TADF applications

2. Bromomethylthioindole Inspired Carbazole Hybrids as Promising Class of Anti-MRSA Agents

3. First row transition metal complexes of di-o-substituted-diarylamine-based ligands (including carbazoles, acridines and dibenzoazepines)

4. LNL-Carbazole Pincer Ligand: More than the Sum of Its Parts

5. 3d Metal Complexes in T-shaped Geometry as a Gateway to Metalloradical Reactivity

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