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Related Concept Videos

Phosphoinositides and PIPs01:42

Phosphoinositides and PIPs

Phosphoinositides are a group of phospholipids containing a glycerol backbone with two fatty acid chains and a phosphate attached to a myoinositol sugar ring. The inositol head group extends into the cytoplasm, where it is modified by adding phosphate groups to form phosphatidylinositol phosphates or PIPs.
Different phosphoinositides are synthesized and recruited on the cytosolic face of the plasma membrane. The localization of specific phosphoinositides concentrated in separate membrane...
Phosphorylation01:02

Phosphorylation

The addition or removal of phosphate groups from proteins is the most common chemical modification that regulates cellular processes. These modifications can affect the structure, activity, stability, and localization of proteins within cells as well as their interactions with other proteins.
During phosphorylation, protein kinases transfer the terminal phosphate group of ATP to specific amino acid side chains of substrate proteins. Serine, threonine, and tyrosine are the most commonly...
Phosphorylation01:02

Phosphorylation

The addition or removal of phosphate groups from proteins is the most common chemical modification that regulates cellular processes. These modifications can affect the structure, activity, stability, and localization of proteins within cells as well as their interactions with other proteins.
During phosphorylation, protein kinases transfer the terminal phosphate group of ATP to specific amino acid side chains of substrate proteins. Serine, threonine, and tyrosine are the most commonly...

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A High Resolution Method to Monitor Phosphorylation-dependent Activation of IRF3
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A High Resolution Method to Monitor Phosphorylation-dependent Activation of IRF3

Published on: January 24, 2016

Ferrocenyl-phospho-nic acid.

Bao-Zhang Yang, Chao Xu, Tai-Ke Duan

    Acta Crystallographica. Section E, Structure Reports Online
    |November 18, 2011
    PubMed
    Summary
    This summary is machine-generated.

    This study details a novel ferrocene derivative with a phosphate group linked by a P-C bond. Six molecules self-assemble via hydrogen bonds into a distorted octahedral cage, showcasing unique crystal packing in organometallic compounds.

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    Area of Science:

    • Organometallic Chemistry
    • Crystal Engineering
    • Supramolecular Chemistry

    Background:

    • Ferrocene derivatives are versatile building blocks in coordination chemistry and materials science.
    • Understanding intermolecular interactions is crucial for designing crystalline architectures.
    • Phosphorus-containing ferrocenes offer unique electronic and structural properties.

    Purpose of the Study:

    • To synthesize and characterize a novel ferrocenyl-phospho-nic acid compound.
    • To investigate the crystal structure and intermolecular interactions of the title compound.
    • To explore the self-assembly behavior of ferrocene derivatives in the solid state.

    Main Methods:

    • Single-crystal X-ray diffraction analysis to determine molecular and crystal structure.
    • Spectroscopic methods for compound characterization (e.g., NMR, IR).
    • Analysis of hydrogen bonding networks and cage formation.

    Main Results:

    • The compound [Fe(C(5)H(5))(C(5)H(6)O(3)P)] features a direct P-C bond (1.749(3) Å) between the phosphate and ferrocene units.
    • Six molecules form a highly distorted octahedral cage through 12 strong intermolecular O-H⋯O hydrogen bonds.
    • The determined cage volume is approximately 270 ų.

    Conclusions:

    • The study reveals a novel organometallic compound with a unique P-C linkage to ferrocene.
    • Intermolecular hydrogen bonding drives the self-assembly into a discrete, albeit distorted, cage structure.
    • This work contributes to the understanding of crystal engineering principles in ferrocene-based systems.