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Bonding in Metals02:32

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Metallic bonds are formed between two metal atoms. A simplified model to describe metallic bonding has been developed by Paul Drüde called the “Electron Sea Model”. 
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Metallic solids such as crystals of copper, aluminum, and iron are formed by metal atoms. The structure of metallic crystals is often described as a uniform distribution of atomic nuclei within a “sea” of delocalized electrons. The atoms within such a metallic solid are held together by a unique force known as metallic bonding that gives rise to many useful and varied bulk properties.
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Group 1 elements are soft and shiny metallic solids. They are malleable, ductile, and good conductors of heat and electricity. The melting points of the alkali metals are unusually low for metals and decrease going down the group, while the density increases going down the group with the exception of potassium (Table 1).
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Transition metals are defined as those elements that have partially filled d orbitals. As shown in Figure 1, the d-block elements in groups 3–12 are transition elements. The f-block elements, also called inner transition metals (the lanthanides and actinides), also meet this criterion because the d orbital is partially occupied before the f orbitals.
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Walking Metals for Remote Functionalization.

Heiko Sommer1, Francisco Juliá-Hernández2, Ruben Martin2,3

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Remote functionalization enables selective C-H and C-C bond activation using a "metal-walk" mechanism. This innovative approach transforms simple molecules into complex structures, addressing key challenges in organic synthesis.

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Area of Science:

  • Organic Chemistry
  • Catalysis
  • Synthetic Methodology

Background:

  • Selective activation of unreactive C-H and C-C bonds is a major challenge.
  • Remote functionalization offers a strategy to activate bonds distant from an initiation site.

Purpose of the Study:

  • To explore the concept and development of remote functionalization via "metal-walk" or "chain-walk" mechanisms.
  • To highlight the potential of this approach for synthesizing complex molecular scaffolds.

Main Methods:

  • Utilizing iterative hydride shifts (1,2- or 1,3-) of metal complexes along hydrocarbon chains.
  • Developing and refining various catalytic systems, including late-transition metals and sustainable iron/cobalt-based systems.

Main Results:

  • Demonstrated the transformation of simple building blocks into complex scaffolds through a convergent strategy.
  • Showcased the versatility of "metal-walk" for remote bond activation.

Conclusions:

  • Remote functionalization via "metal-walk" is a powerful tool for addressing synthetic challenges.
  • This research area holds significant promise for future advancements in organic synthesis and catalysis.