Effect of positional isomerism on the spectroelectrochemical response of 3,6-bis(2-pyridyl)-diketopyrrolopyrrolate bridged bis(carbonylhydridoruthenium) compounds-Reference-Cited by-同舟云学术

Effect of positional isomerism on the spectroelectrochemical response of 3,6-bis(2-pyridyl)-diketopyrrolopyrrolate bridged bis(carbonylhydridoruthenium) compounds

Published:2018 Issue:39 Volume:47 Page:14078-14084
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Hazari Arijit Singha¹²³⁴,Ghosh Prabir¹²³⁴,Beyer Katharina⁵⁶⁷⁸,Schwederski Brigitte⁵⁶⁷⁸,Kaim Wolfgang⁵⁶⁷⁸^ORCID,Lahiri Goutam Kumar¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. Indian Institute of Technology Bombay

3. Mumbai 400076

4. India

5. Institut für Anorganische Chemie

6. Universität Stuttgart

7. D-70550 Stuttgart

8. Germany

Abstract

Small but notable differences accompany the ligand-based oxidation of green and blue isomers1and2.

Funder

Science and Engineering Research Board

University Grants Commission

Council of Scientific and Industrial Research

Baden-Württemberg Stiftung

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/DT/C8DT02806K

Reference29 articles.

1. Diketopyrrolopyrrole: brilliant red pigment dye-based fluorescent probes and their applications

2. Isomeric Diruthenium Complexes Bridged by Deprotonated Indigo in cis and trans Configuration

3. A structurally characterised redox pair involving an indigo radical: indigo based redox activity in complexes with one or two [Ru(bpy)2] fragments

4. 1,5-Diamido-9,10-anthraquinone, a Centrosymmetric Redox-Active Bridge with Two Coupled β-Ketiminato Chelate Functions: Symmetric and Asymmetric Diruthenium Complexes

5. Evidence for Bidirectional Noninnocent Behavior of a Formazanate Ligand in Ruthenium Complexes

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