Anion Sensing in Aqueous Media by Photo-active Transition-Metal Bipyridyl Rotaxanes

2012 ◽  
Vol 18 (36) ◽  
pp. 11277-11283 ◽  
Author(s):  
Laura M. Hancock ◽  
Enrico Marchi ◽  
Paola Ceroni ◽  
Paul D. Beer
Keyword(s):  
Transition Metal ◽  
Aqueous Media ◽  
Anion Sensing ◽  
Active Transition

Transition-Metal-Free Synthetic Strategies for the Cross-Coupling Reactions in Water: A Green Approach

2020 ◽  
Vol 07 ◽  
Author(s):  
Tanmay Chatterjee ◽  
Nilanjana Mukherjee
Keyword(s):  
Transition Metal ◽  
Organic Solvents ◽  
Aqueous Media ◽  
Cross Coupling ◽  
Transition Metal Catalysts ◽  
Synthetic Methods ◽  
Coupling Reactions ◽  
Organic Transformations ◽  
Green Approach ◽  
Dehydrogenative Coupling

Abstract: A natural driving force is always working behind the synthetic organic chemists towards the development of ‘green’ synthetic methodologies for the synthesis of useful classes of organic molecules having potential applications. The majority of the essential classes of organic transformations, including C-C and C-X (X = heteroatom) bond-forming crosscoupling reactions, cross dehydrogenative-coupling (CDC) mostly rely on the requirement of transition-metal catalysts and hazardous organic solvents. Hence, the scope in developing green synthetic strategies by avoiding the use of transitionmetal catalysts and hazardous organic solvents for those important and useful classes of organic transformations is very high. Hence, several attempts are made so far. Water being the most abundant, cheap, and green solvent in the world; numerous synthetic methods have been developed in an aqueous medium. In this review, the development of transitionmetal- free green synthetic strategies for various important classes of organic transformations such as C-C and C-X bondforming cross-coupling, cross dehydrogenative-coupling, and oxidative-coupling in an aqueous media is discussed.

Development of silica-supported frustrated Lewis pairs: highly active transition metal-free catalysts for the Z-selective reduction of alkynes

2016 ◽  
Vol 6 (3) ◽  
pp. 882-889 ◽  
Author(s):  
Kai C. Szeto ◽  
Wissam Sahyoun ◽  
Nicolas Merle ◽  
Jessica Llop Castelbou ◽  
Nicolas Popoff ◽  
...  
Keyword(s):  
Transition Metal ◽  
Lewis Acid ◽  
Selective Reduction ◽  
Frustrated Lewis Pairs ◽  
Acid Base ◽  
Metal Free ◽  
Highly Active ◽  
Active Transition ◽  
Lewis Pairs

Supported Lewis acid/base systems based have been prepared and characterized.

scholarly journals Interactions of atrazine with transition metal ions in aqueous media: experimental and computational approach

3 Biotech ◽  
2015 ◽  
Vol 5 (5) ◽  
pp. 791-798 ◽  
Author(s):  
Vijay Kumar ◽  
Virender Kumar ◽  
Niraj Upadhyay ◽  
Sitansh Sharma
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Aqueous Media ◽  
Transition Metal Ions ◽  
Computational Approach

scholarly journals Density-Based Descriptors of Redox Reactions Involving Transition Metal Compounds as a Reality-Anchored Framework: A Perspective

Molecules ◽  
2021 ◽  
Vol 26 (18) ◽  
pp. 5541
Author(s):  
Daniel Koch ◽  
Mohamed Chaker ◽  
Manabu Ihara ◽  
Sergei Manzhos
Keyword(s):  
Transition Metal ◽  
Metal Ion ◽  
Redox Reactions ◽  
Rational Design ◽  
Chemical Properties ◽  
Transition Metal Ions ◽  
Blind Spot ◽  
Transition Metal Compounds ◽  
Metal Compounds ◽  
Active Transition

Description of redox reactions is critically important for understanding and rational design of materials for electrochemical technologies, including metal-ion batteries, catalytic surfaces, or redox-flow cells. Most of these technologies utilize redox-active transition metal compounds due to their rich chemistry and their beneficial physical and chemical properties for these types of applications. A century since its introduction, the concept of formal oxidation states (FOS) is still widely used for rationalization of the mechanisms of redox reactions, but there exists a well-documented discrepancy between FOS and the electron density-derived charge states of transition metal ions in their bulk and molecular compounds. We summarize our findings and those of others which suggest that density-driven descriptors are, in certain cases, better suited to characterize the mechanism of redox reactions, especially when anion redox is involved, which is the blind spot of the FOS ansatz.

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