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Francis Hereward Burstall

Bio: Francis Hereward Burstall is an academic researcher. The author has contributed to research in topics: Selenium & Ruthenium. The author has an hindex of 11, co-authored 22 publications receiving 626 citations.


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Journal ArticleDOI
TL;DR: The ferroin group has been known to react as bidentate ligands with certain metal ions such as ferrous, cuprous, and cobaltous, to give colored complex species.
Abstract: -N=C&N-, have been known to react as bidentate ligands with certain metal ions such as ferrous, cuprous, and cobaltous, to give colored complex species (1-6). This effect was first noticed with the ferrous ion ( I ) , and since this complex of a given compound is generally of a more intense color than are those with other ions (7), the atomic configuration in question was given the trivial name of the ferroin group. During the last century, hundreds of compounds containing the ferroin group have been synthesized (7), the majority of which demonstrate the ability to form complexes with the ferrous ion. Most of these complexes are only weakly colored, are unstable under normal physical conditions, or are formed over a very narrow pH range. A few of these compounds, however, form stable, intensely colored species with the ferrous ion and are, therefore, suitable for the quantitative determination of iron (8). Examples of compounds which have found acceptance for such use are 1,lOphenanthroline (9), 4,7-diphenyl-l,lO-phenanthroline (IO), 2,2‘-bipyridine (I]), 2,6-bis(2-pyridyl)-pyridine (11). 2,4,6tris(2-pyridyl)-1,3,5-triazine (12), and phenyl 2-pyridyl ketoxime (13, 14). Many of these reagents are the product of difficult and tedious organic syntheses and, hence, are high in cost (14). Although for even the most expensive of these reagents, the cost of a single manual analysis is fairly low, when one considers automated continuous instrumental analysis, a lowcost yet highly sensitive reagent would be desirable, since the cost of maintaining such an analytical instrument with I

4,332 citations

Book ChapterDOI
TL;DR: In this article, a review is concerned with the neglected class of inorganic compounds, which contain ions of the same element in two different formal states of oxidation, and a number of references cite that many individual examples of this class have been studied, yet they have very rarely been treated as a class, and there has never before, to our knowledge, been a systematic attempt to classify their properties in terms of their electronic and molecular structures.
Abstract: Publisher Summary This review is concerned with the neglected class of inorganic compounds, which contain ions of the same element in two different formal states of oxidation. Although the number of references cited in our review show that many individual examples of this class have been studied, yet they have very rarely been treated as a class, and there has never before, to our knowledge, been a systematic attempt to classify their properties in terms of their electronic and molecular structures. In the past, systems containing an element in two different states of oxidation have gone by various names, the terms “mixed valence,” nonintegral valence,” “mixed oxidation,” “oscillating valency,” and “controlled valency” being used interchangeably. Actually, none of these is completely accurate or all-embracing, but in our hope to avoid the introduction of yet another definition, we have somewhat arbitrarily adopted the phrase “mixed valence” for the description of these systems. The concept of resonance among various valence bond structures is one of the cornerstones of modern organic chemistry.

2,208 citations

Journal ArticleDOI
TL;DR: Proton-coupled electron transfer is an important mechanism for charge transfer in a wide variety of systems including biology- and materials-oriented venues and several are reviewed.
Abstract: ▪ Abstract Proton-coupled electron transfer (PCET) is an important mechanism for charge transfer in a wide variety of systems including biology- and materials-oriented venues. We review several are...

2,182 citations

Journal ArticleDOI
TL;DR: Transition metal photocatalysis represents a promising strategy towards the development of practical, scalable industrial processes with great environmental benefits.
Abstract: Light can be considered an ideal reagent for environmentally friendly, 'green' chemical synthesis; unlike many conventional reagents, light is non-toxic, generates no waste, and can be obtained from renewable sources. Nevertheless, the need for high-energy ultraviolet radiation in most organic photochemical processes has limited both the practicality and environmental benefits of photochemical synthesis on industrially relevant scales. This perspective describes recent approaches to the use of metal polypyridyl photocatalysts in synthetic organic transformations. Given the remarkable photophysical properties of these complexes, these new transformations, which use Ru(bpy)(3)(2+) and related photocatalysts, can be conducted using almost any source of visible light, including both store-bought fluorescent light bulbs and ambient sunlight. Transition metal photocatalysis thus represents a promising strategy towards the development of practical, scalable industrial processes with great environmental benefits.

2,036 citations