Signaling Recognition Events with Fluorescent Sensors and Switches.

In this review, we highlight the use of organic photoredox catalysts in a myriad of synthetic transformations with a range of applications. This overview is arranged by catalyst class where the photophysics and electrochemical characteristics of each is discussed to underscore the differences and advantages to each type of single electron redox agent. We highlight both net reductive and oxidative as well as redox neutral transformations that can be accomplished using purely organic photoredox-active catalysts. An overview of the basic photophysics and electron transfer theory is presented in order to provide a comprehensive guide for employing this class of catalysts in photoredox manifolds.

Organic Photoredox Catalysis

Graphitic carbon nitride, g-C3N4, can be made by polymerization of cyanamide, dicyandiamide or melamine. Depending on reaction conditions, different materials with different degrees of condensation, properties and reactivities are obtained. The firstly formed polymeric C3N4 structure, melon, with pendant amino groups, is a highly ordered polymer. Further reaction leads to more condensed and less defective C3N4 species, based on tri-s-triazine (C6N7) units as elementary building blocks. High resolution transmission electron microscopy proves the extended two-dimensional character of the condensation motif. Due to the polymerization-type synthesis from a liquid precursor, a variety of material nanostructures such as nanoparticles or mesoporous powders can be accessed. Those nanostructures also allow fine tuning of properties, the ability for intercalation, as well as the possibility to give surface-rich materials for heterogeneous reactions. Due to the special semiconductor properties of carbon nitrides, they show unexpected catalytic activity for a variety of reactions, such as for the activation of benzene, trimerization reactions, and also the activation of carbon dioxide. Model calculations are presented to explain this unusual case of heterogeneous, metal-free catalysis. Carbon nitride can also act as a heterogeneous reactant, and a new family of metal nitride nanostructures can be accessed from the corresponding oxides.

/pdf/graphitic-carbon-nitride-materials-variation-of-structure-2o5pjcr9g6.pdf

Graphitic carbon nitride materials: variation of structure and morphology and their use as metal-free catalysts

The interaction between an electronically excited photocatalyst and an organic molecule can result in the genertion of a diverse array of reactive intermediates that can be manipulated in a variety of ways to result in synthetically useful bond constructions. This Review summarizes dual-catalyst strategies that have been applied to synthetic photochemistry. Mechanistically distinct modes of photocatalysis are discussed, including photoinduced electron transfer, hydrogen atom transfer, and energy transfer. We focus upon the cooperative interactions of photocatalysts with redox mediators, Lewis and Bronsted acids, organocatalysts, enzymes, and transition metal complexes.

http://pubs.acs.org/doi/pdf/10.1021/acs.chemrev.6b00018

Dual Catalysis Strategies in Photochemical Synthesis

4.2. Solid-Supported Electrolytes 2280 4.3. Solid-Supported Mediators 2282 4.4. Supported Substrate-Product Capture 2283 4.5. A Unique Electrolyte/Solvent System 2285 5. Reaction Conditions 2285 5.1. Supercritical Fluids 2285 5.1.1. Electrochemical Properties of scCO2 2285 5.1.2. Electroreductive Carboxylation in scCO2 2286 5.1.3. Electrochemical Polymerization in scCO2 2286 5.2. The Cation-Pool Method 2286 5.2.1. Generation of N-Acyliminium Ion Pools 2286 5.2.2. Generation of Alkoxycarbenium Ion Pools 2287 5.2.3. Generation of Diarylcarbenium Ion Pools 2288 5.2.4. Generation of Other Cation Pools 2289 6. Electrochemical Devices 2289 6.1. Electrode Materials 2289 6.2. Ultrasound and Centrifugal Fields 2290 6.3. Electrochemical Microflow Systems 2290 7. Combinatorial Electrochemical Synthesis 2292 7.1. Parallel Electrolysis Using a Macrosystem 2292 7.2. Parallel Electrolysis Using a Microsystem 2293 7.3. Serial Electrolysis Using a Microsystem 2294 8. Conclusions 2294 9. Acknowledgments 2294 10. References 2294

Modern Strategies in Electroorganic Synthesis

Photo-oxygenation of 1,2-diarylcyclopropanes via electron transfer

A novel photosubstitution of dicyanobenzenes by allylic and benzylic silanes

La reaction tolere la presence de divers groupes fonctionnels et peut etre appliquee a des composes avec des fonctions carbonylees et lactones

Regioselective double vicinal carbon-carbon bond forming reactions of electron-deficient alkenes by use of allylic stannanes and organoiodo compounds

The photochemical reactions of 9,10-dicyanoanthracene (DCA)-1,2-diarylcyclopropane (CP) systems have been investigated In degassed acetonitrile solution, (4π+2σ) photocycloaddition between DCA and CP occurred to give cis- and trans-2,4-diaryl-1,5-dicyano-6,7:8,9-dibenzobicyclo[322]nona-6,8-dienes in a 3:1 ratio in good chemical yields although the quantum yields were not high (Φ=0002-004) Thisphotocycloaddition did not occur in benzene

Photochemistry of 9,10-dicyanoanthracene-1,2-diarylcyclopropane systems. Photocycloaddition and photoisomerization

Alkenylidenecyclopropanes have been prepared in a stereospecific manner by the reaction of 1,1-disubstituted 2,2-dibromocyclopropanes with sodium hydroxide under phase-transfer conditions in the presence of alkenes.

General and convenient route to alkenylidenecyclopropanes: generation of alkenylidenecarbenes from 1,1-dibromocyclopropanes under phase-transfer conditions

Yoshio Otsuji

Papers

Photo-oxygenation of 1,2-diarylcyclopropanes via electron transfer

A novel photosubstitution of dicyanobenzenes by allylic and benzylic silanes

Regioselective double vicinal carbon-carbon bond forming reactions of electron-deficient alkenes by use of allylic stannanes and organoiodo compounds

Photochemistry of 9,10-dicyanoanthracene-1,2-diarylcyclopropane systems. Photocycloaddition and photoisomerization

General and convenient route to alkenylidenecyclopropanes: generation of alkenylidenecarbenes from 1,1-dibromocyclopropanes under phase-transfer conditions