Designing Multifunctional Expanded Pyridiniums: Properties of Branched and Fused Head-to-Tail Bipyridiniums

Author:

Fortage Jérôme1,Peltier Cyril1,Nastasi Francesco1,Puntoriero Fausto1,Tuyèras Fabien1,Griveau Sophie1,Bedioui Fethi1,Adamo Carlo1,Ciofini Ilaria1,Campagna Sebastiano1,Lainé Philippe P.1

Affiliation:

1. Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques (CNRS UMR-8601), Université Paris Descartes, 45 rue des Saints Pères, F-75270 Paris Cedex 06, France, Institut Parisien de Chimie Moléculaire (CNRS UMR-7201), Equipe Chimie Supramoléculaire, Case 42, Université Pierre et Marie Curie, 4 Place Jussieu, 75252 Paris Cedex 05, France, LECIME, Laboratoire d′Électrochimie, Chimie des Interfaces et Modélisation pour l′Énergie (CNRS UMR-7575), École Nationale Supérieure de Chimie de Paris...

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Reference141 articles.

1. Quaternary Salts of Pyridines and Related Compounds

2. When performing a bibliometric analysis through the ISI Web of Knowledge, a striking point is the close correlation observed in the evolution over the years of the number of publications (and related citations) dealing with the following topics: “viologen” or “bipyridinium” and “ruthenium bipyridine”. Two remarkable inflection points are found around 1980 and 1990. They are ascribable to the launching of two related topics: “water splitting” and “artificial photosynthesis”, on the one hand, and “molecular devices” including “molecular machines”, on the other; see also ref3.

3. From the photochemistry of coordination compounds to light-powered nanoscale devices and machines

4. For selected references dealing with pyridinium-based solvatochromic dyes, see:

5. Solvatochromic Dyes as Solvent Polarity Indicators

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