Radical Recombination

Radical recombination is a chemical reaction in which two species containing unpaired electrons join to form a new, more stable molecule, often terminating a radical chain reaction. The process occurs when radicals encounter one another through molecular diffusion and collide with suitable orientation and energy, allowing their unpaired electrons to pair and create a covalent bond. In chemistry, recombination helps explain reaction kinetics, product distributions, and the lifetimes of reactive intermediates. It is important in combustion, atmospheric chemistry, radiation chemistry, and polymerization, where the balance between radical generation and recombination influences reaction rates, material properties, and environmental transformations.

Radical Recombination - Related Videos

Research

JoVE Journal - Chemistry
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Free Radicals in Chemical Biology: from Chemical Behavior to Biomarker Development

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Cited by 9 •

2013

Radical-based biomimetic chemistry has been applied to building-up libraries necessary for biomarker development.

Education

JoVE Science Education - Chemistry

Photochemical Initiation Of Radical Polymerization Reactions

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2023

Source: David C. Powers, Tamara M. Powers, Texas A&M In this video, we will carry out the photochemically initiated polymerization of styrene to generate polystyrene, which is an important commodity plastic. We will learn the fundamentals of photochemistry and use simple photochemistry to initiate radical polymerization reactions. Specifically, in this module we will examine the photochemistry of benzoyl peroxide and its role as a photo-initiator of styrene polymerization reactions. In the...

Recombineering Homologous Recombination Constructs in Drosophila

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Cited by 9 •

2013

Homologous recombination techniques greatly advance Drosophila genetics by enabling the creation of molecularly precise mutations. The recent adoption of recombineering allows one to manipulate large pieces of DNA and transform them into Drosophila6. The methods presented here combine these techniques to rapidly generate large homologous recombination vectors.

Radical Reactivity: Electrophilic Radicals

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2023

Radicals adjacent to electron‐withdrawing groups are called electrophilic radicals. These radicals readily react with nucleophilic alkenes. For example, the malonate radical, in which the radical center is flanked by two electron‐withdrawing groups, reacts readily with butyl vinyl ether, which consists of an electron‐donating oxygen substituent. The reaction between electrophilic malonate radical and nucleophilic vinyl ether is favored because the radical has a low‐energy SOMO, which interacts...

Radical Reactivity: Nucleophilic Radicals

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2023

Radicals adjacent to electron-donating groups are called nucleophilic radicals. These radicals readily react with electrophilic alkenes. The SOMO–LUMO interactions are the driving force for the reaction, where the high-energy SOMO of the electron-rich, nucleophilic radicals interacts with the low-energy LUMO of the electron-deficient, electrophilic alkenes. Such SOMO–LUMO interactions are the basis of reactive radical traps, affecting the selectivity in radical reactions. For instance, consider...

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