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Complexation Equilibria: The Chelate Effect01:19

Complexation Equilibria: The Chelate Effect

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In complexation reactions, metal atoms or cations interact with ligands to form donor-acceptor adducts called metal complexes. Ligands that bind through one donor site are monodentate, ligands with two donor sites are bidentate, and those with more than two donor sites are polydentate ligands. For example, ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms, forming a five-membered ring. EDTA is a polydentate ligand that binds through four oxygen and two nitrogen...
1.5K
Complexation Equilibria: Factors Influencing Stability of Complexes01:09

Complexation Equilibria: Factors Influencing Stability of Complexes

965
In complexation reactions, metal cations are the electron pair acceptors, and the ligands are the electron pair donors. The stability of the metal complexes depends primarily on the complexing ability of the central metal ion and the nature of the ligands. Generally, the complexing ability of the metal ion depends on the size and charge of the ion. As the metal ion size increases, the stability of the metal complexes decreases, provided that the valency of the metal ion and the ligands remain...
965
Metal-Ligand Bonds02:51

Metal-Ligand Bonds

25.6K
The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
25.6K
EDTA: Chemistry and Properties01:22

EDTA: Chemistry and Properties

3.9K
Polydentate ligands are most widely used in complexometric titrations because they form more stable complexes with the metal ions than mono- or bidentate ligands due to the chelate effect. Examples of polydentate ligands are ethylenediaminetetraacetic acid (EDTA), crown ethers, and cryptands. The most important feature of optimal polydentate ligands is the ability to form 1:1 complexes in a single-step process. Amino carboxylic acid derivatives are frequently used as complexing agents. EDTA is...
3.9K
Valence Bond Theory02:42

Valence Bond Theory

11.7K
Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
11.7K
Complexometric Titration: Ligands00:43

Complexometric Titration: Ligands

2.6K
Different monodentate and polydentate ligands are used as complexing agents in complexometric titration reactions. The formation of complexes by mono- and bidentate ligands involves two or more intermediate steps, limiting their use as complexing agents. In comparison, polydentate ligands can form complexes with metal ions in a single-step process, facilitating sharper end points. This means polydentate ligands, such as amino carboxylic acid derivatives, are most commonly employed in...
2.6K

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Related Experiment Video

Updated: Mar 28, 2026

Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
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Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates

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Functionalised Clathrochelate Complexes--New Building Blocks for Supramolecular Structures.

Matthew D Wise, Kay Severin

    Chimia
    |December 16, 2015
    PubMed
    Summary
    This summary is machine-generated.

    Iron(II) clathrochelate complexes with pyridyl groups serve as versatile building blocks for self-assembling supramolecular structures. These metalloligands enable the creation of molecular squares, 3D polymers, and cage compounds capable of encapsulating anions.

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    Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
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    Area of Science:

    • Coordination Chemistry
    • Supramolecular Chemistry
    • Materials Science

    Background:

    • Tris(dioxime) iron(II) clathrochelate complexes offer tunable properties for constructing advanced materials.
    • Coordination-driven self-assembly is a powerful strategy for designing complex molecular architectures.
    • Pyridyl functionalization provides specific binding sites for metal-mediated assembly.

    Purpose of the Study:

    • To synthesize and characterize pyridyl-functionalized iron(II) clathrochelate metalloligands.
    • To demonstrate the utility of these clathrochelates as building blocks for supramolecular structures.
    • To explore the structure-directing capabilities of clathrochelates in forming discrete and extended frameworks.

    Main Methods:

    • Synthesis of tris(dioxime) iron(II) clathrochelate complexes with 3- and 4-pyridyl groups.
    • Preparation of clathrochelate-based 4,4'-bipyridyl metalloligands of varying lengths (1.5-5.4 nm).
    • Coordination-driven self-assembly to form molecular squares, 3D coordination polymers, and octahedral cage compounds.

    Main Results:

    • Successfully synthesized pyridyl-functionalized iron(II) clathrochelates and derived metalloligands.
    • Demonstrated the formation of a discrete molecular square and a 3D coordination polymer using these building blocks.
    • Synthesized octahedral cage compounds capable of encapsulating the tetraphenylborate (BPh4-) anion in aqueous media.

    Conclusions:

    • Pyridyl-functionalized iron(II) clathrochelates are effective and versatile building blocks for coordination-driven self-assembly.
    • These clathrochelates enable the construction of diverse supramolecular architectures, including cages with encapsulation capabilities.
    • The clathrochelate motif provides significant structural control in the self-assembly process.