GET THE APP

Ru-Polypyridyl Complexes: Promising Candidates for Electrochemical Co2 Reduction
..

Journal of Material Sciences & Engineering

ISSN: 2169-0022

Open Access

Editorial Note - (2021) Volume 10, Issue 10

Ru-Polypyridyl Complexes: Promising Candidates for Electrochemical Co2 Reduction

Debashis Ghosh*
*Correspondence: Debashis Ghosh, Department of Electrical Engineering, St. Joseph’s College, India, Email:
Department of Electrical Engineering, St. Joseph’s College, India

Received: 07-Oct-2021 Published: 28-Oct-2021

Introduction

Reduction of Co2 to produce CO, HCOOH, alcohols etc. have been pursued to alleviate the global crisis caused by depletion of fossil fuels and the rising atmospheric concentration of Co2. The design and synthesis of new and simpler catalysts having a capability for selective Co2 reduction photochemically and/or electro-chemically to produce either CO or HCOOH has received increased attention from the global research community. Among various metal complexes as active electrocatalysts, Ru-polypyridyl complexes have received much attention, due to their efficiency and stability. Moreover, Ru-polypyridyl complexes have significantly lower overpotentials associated with Co2 reduction compared to those of other active metal complexes. In spite of these major advancement, only a very few reports are available to for showing dependency of Co2 reduction selectivity on the structure of ligand In a Rupolypyridyl complex. Methodology & Theoretical Orientation: New RuIINAD (NAD = nicotinamide adenine dinucleotide) polypyridyl complexes were developed and explored their electrocatalytic activity for selective Co2 reduction to HCOOH in MeCN/H2O mixed solvents. Further, by tuning the ligand structure another new type of Ru-polypyridyl complex has been developed and explored its electrocatalytic activity for selective Co2 reduction to CO in MeCN/H2O. Findings: Different new Ru-polypyridyl complexes have been developed which were able to reduce Co2 to either HCOOH or CO depending on the ligand structure. Conclusion & Significance: By simple tuning in the ligand structure of new Ru-polypyridyl complexes selectivity for Co2 reduction has successfully been altered to either HCOOH or CO. Keywords Ru-polypyridyl, Co2 reduction, Catalysts. Polypyridine complexes are coordination complexes containing polypyridine ligands, such as 2,2'-bipyridine, 1,10-phenanthroline, or 2,2';6'2"-terpyridine. Polypyridines are multidentate ligands that confer characteristic properties to the metal complexes that they form. Some complexes strongly absorb light via a process called metal-to-ligand charge transfer (MLCT).[1] The properties of these complexes can be tuned by changes in substituents. For example, electron donation, electron withdrawal, and Ï?-conjugating groups, to the polypyridine moiety. The MLCT absorption band can be shifted, the emission wavelength can be changed, and the emission lifetime can be extended.[2] Tris(bipyridine)ruthenium(II) is the preeminent example of a polypyridine complex. A well-known example of a polypyridine complex is the tris(bipyridine) derivative of ruthenium(II), [Ru[(bpy)3]2+. This complex exhibits intense luminescence at room temperature in aqueous solution. Another example is a platinum-bipyridine-dithiolate complex, Pt(bpy)(bdt), in which bdt denotes a 1,2-benzenedithiolate anion. This complex also exhibits photoluminescence at room temperature, and its wavelength and lifetime can be tuned by substitution of either bipyridine or dithiolate moieties. Structural control is easier than for ruthenium complexes due to the square planar structure of the platinum complex. Ruthenium(II) polypyridine complexes are one of the most extensively studied and developed systems in the family of luminescent transitionmetal complexes. Notably, there has been a large amount of interest in the biological applications of these luminescent ruthenium(II) complexes because of their rich photophysical and photochemical properties. In this Viewpoint, we explore past and recent works on the possible biological and cellular applications of these promising complexes, with a focus on their use as bioimaging reagents, biomolecular probes, and phototherapeutic agents. Ruthenium(II) polypyridine complexes are one of the most extensively studied and developed systems because of their interesting photophysical and photochemical properties. In this Viewpoint, we explore past and recent works on the spectroscopic, photophysical, and photochemical characteristics of these complexes and their possible biological and cellular applications with a focus on their use as bioimaging reagents, biomolecular probes, and phototherapeutic agents.

Keywords

Ru-polypyridyl, Co2 reduction, Catalysts.

XXXXXX

Figure 1. Co2 reduction using catalyst with structural modification at a) 2,2’-bipyridyl ligand; b) 2,2';6'2"-terpyridine ligand

Polypyridine complexes are coordination complexes containing polypyridine ligands, such as 2,2'-bipyridine, 1,10-phenanthroline, or 2,2';6'2"-terpyridine.

Polypyridines are multidentate ligands that confer characteristic properties to the metal complexes that they form. Some complexes strongly absorb light via a process called metal-to-ligand charge transfer (MLCT).[1] The properties of these complexes can be tuned by changes in substituents. For example, electron donation, electron withdrawal, and π-conjugating groups, to the polypyridine moiety. The MLCT absorption band can be shifted, the emission wavelength can be changed, and the emission lifetime can be extended.[2]

Equation

Tris(bipyridine)ruthenium(II) is the preeminent example of a polypyridine complex.

A well-known example of a polypyridine complex is the tris(bipyridine) derivative of ruthenium(II), [Ru[(bpy)3]2+. This complex exhibits intense luminescence at room temperature in aqueous solution. Another example is a platinum-bipyridine-dithiolate complex, Pt(bpy)(bdt), in which bdt denotes a 1,2-benzenedithiolate anion. This complex also exhibits photoluminescence at room temperature, and its wavelength and lifetime can be tuned by substitution of either bipyridine or dithiolate moieties. Structural control is easier than for ruthenium complexes due to the square planar structure of the platinum complex.

Ruthenium(II) polypyridine complexes are one of the most extensively studied and developed systems in the family of luminescent transitionmetal complexes. Notably, there has been a large amount of interest in the biological applications of these luminescent ruthenium(II) complexes because of their rich photophysical and photochemical properties. In this Viewpoint, we explore past and recent works on the possible biological and cellular applications of these promising complexes, with a focus on their use as bioimaging reagents, biomolecular probes, and phototherapeutic agents. Ruthenium(II) polypyridine complexes are one of the most extensively studied and developed systems because of their interesting photophysical and photochemical properties. In this Viewpoint, we explore past and recent works on the spectroscopic, photophysical, and photochemical characteristics of these complexes and their possible biological and cellular applications with a focus on their use as bioimaging reagents, biomolecular probes, and phototherapeutic agents.

Google Scholar citation report
Citations: 3677

Journal of Material Sciences & Engineering received 3677 citations as per Google Scholar report

Journal of Material Sciences & Engineering peer review process verified at publons

Indexed In

 
arrow_upward arrow_upward