Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Valence Bond Theory02:42

Valence Bond Theory

8.8K
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...
8.8K
Colors and Magnetism03:02

Colors and Magnetism

12.0K
Color in Coordination Complexes
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
12.0K
Atomic Nuclei: Nuclear Spin State Overview01:03

Atomic Nuclei: Nuclear Spin State Overview

1.8K
NMR-active nuclei have energy levels called 'spin states' that are associated with the orientations of their nuclear magnetic moments. In the absence of a magnetic field, the nuclear magnetic moments are randomly oriented, and the spin states are degenerate. When an external magnetic field is applied, the spin states have only 2 + 1 orientations available to them. A proton with = ½ has two available orientations. Similarly, for a quadrupolar nucleus with a nuclear spin value of one, the...
1.8K
Spin–Spin Coupling: Two-Bond Coupling (Geminal Coupling)01:20

Spin–Spin Coupling: Two-Bond Coupling (Geminal Coupling)

1.5K
Two NMR-active nuclei bonded to a central atom can be involved in geminal or two-bond coupling. Geminal coupling is commonly seen between diastereotopic protons in chiral molecules and unsymmetrical alkenes, among others.
The central atom need not be NMR-active because its electrons are affected by the electron polarization of the spin-active atoms. However, spin information is transmitted less effectively than in one-bond coupling, and 2J values are usually weaker than 1J values. The energy of...
1.5K
Spin–Spin Coupling Constant: Overview01:08

Spin–Spin Coupling Constant: Overview

1.2K
In bromoethane, the three methyl protons are coupled to the two methylene protons that are three bonds away. In accordance with the n+1 rule, the signal from the methyl protons is split into three peaks with 1:2:1 relative intensities. The methylene protons appear as a quartet, with the relative intensities of 1:3:3:1.
Qualitatively, any spin plus-half nucleus polarizes the spins of its electrons to the minus-half state. Consequently, the paired electron in the hydrogen–carbon bond must...
1.2K
Spin–Spin Coupling: One-Bond Coupling01:17

Spin–Spin Coupling: One-Bond Coupling

1.2K
Coupling interactions are strongest between NMR-active nuclei bonded to each other, where spin information can be transmitted directly through the pair of bonding electrons. While nuclei polarize their electrons to the opposite spins, the bonding electron pair has opposite spins. Configurations with antiparallel nuclear spins are expected to be lower in energy. When coupling makes antiparallel states more favorable, J is considered to have a positive value. The one-bond coupling constant, 1J,...
1.2K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Metal-Dependent Formation of Heteropoly Blue Anions in Keggin Polyoxometalate Catalysts for Enhanced H<sub>2</sub> Evolution with Iron(II)- and Cobalt(II)-Containing Counterions.

Inorganic chemistry·2026
Same author

Tunable magnons in a dual-gated 2D antiferromagnet.

Nature communications·2026
Same author

Quantum Materials from an Inorganic Chemistry Perspective.

Inorganic chemistry·2026
Same author

Cobalt polyoxometalate-LDH hybrids: pH-switchable molecular catalysts to confined cobalt oxide oxygen evolution layers.

Chemical communications (Cambridge, England)·2026
Same author

One-Dimensional Materials Supported in Two-Dimensional Van der Waals Metal-Organic Frameworks with Optical Anisotropy Switching via Twist-Engineering.

Advanced materials (Deerfield Beach, Fla.)·2026
Same author

Gapless Superconductivity From Extremely Dilute Magnetic Disorder in 2H-NbSe<sub>2-x</sub>S<sub>x</sub>.

Advanced materials (Deerfield Beach, Fla.)·2026

Related Experiment Video

Updated: Apr 21, 2026

Optimizing Magnetic Force Microscopy Resolution and Sensitivity to Visualize Nanoscale Magnetic Domains
07:42

Optimizing Magnetic Force Microscopy Resolution and Sensitivity to Visualize Nanoscale Magnetic Domains

Published on: July 20, 2022

2.5K

One-dimensional and two-dimensional anilate-based magnets with inserted spin-crossover complexes.

Alexandre Abhervé1, Miguel Clemente-León, Eugenio Coronado

  • 1Instituto de Ciencia Molecular (ICMol), Universidad de Valencia , Catedrático José Beltrán 2, 46980 Paterna, Spain.

Inorganic Chemistry
|October 29, 2014
PubMed
Summary

New bimetallic compounds with spin-crossover iron complexes exhibit ferrimagnetic ordering. Some iron ions show high-spin or low-spin states, while others undergo gradual spin crossover with magnetic ordering.

More Related Videos

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
06:53

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks

Published on: June 9, 2023

2.5K
Chemical Vapor Deposition of an Organic Magnet, Vanadium Tetracyanoethylene
08:25

Chemical Vapor Deposition of an Organic Magnet, Vanadium Tetracyanoethylene

Published on: July 3, 2015

11.3K

Related Experiment Videos

Last Updated: Apr 21, 2026

Optimizing Magnetic Force Microscopy Resolution and Sensitivity to Visualize Nanoscale Magnetic Domains
07:42

Optimizing Magnetic Force Microscopy Resolution and Sensitivity to Visualize Nanoscale Magnetic Domains

Published on: July 20, 2022

2.5K
Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
06:53

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks

Published on: June 9, 2023

2.5K
Chemical Vapor Deposition of an Organic Magnet, Vanadium Tetracyanoethylene
08:25

Chemical Vapor Deposition of an Organic Magnet, Vanadium Tetracyanoethylene

Published on: July 3, 2015

11.3K

Area of Science:

  • Inorganic Chemistry
  • Materials Science
  • Magnetochemistry

Background:

  • Anilate-based compounds offer versatile platforms for constructing complex magnetic materials.
  • Incorporating spin-crossover (SCO) complexes into inorganic frameworks allows for the design of stimuli-responsive magnetic materials.

Purpose of the Study:

  • To synthesize and characterize a series of bimetallic anilate-based compounds featuring inserted spin-crossover cationic iron complexes.
  • To investigate the structural and magnetic properties of these novel materials, focusing on their magnetic ordering and spin-state transitions.

Main Methods:

  • Single-crystal X-ray diffraction for structural determination.
  • SQUID magnetometry for magnetic property measurements.
  • Variable-temperature magnetic susceptibility studies to probe spin crossover phenomena.

Main Results:

  • Compounds 1-4, featuring two-dimensional anionic networks with inserted Fe(III) SCO complexes, exhibit long-range ferrimagnetic ordering around 10 K.
  • The inserted Fe(III) ions in 1-4 remain predominantly in either high-spin or low-spin states.
  • Compound 5, containing [Mn(II)Cl2Cr(III)(Cl2An)3](3-) chains and Fe(II) SCO complexes, shows a gradual spin crossover in half of the Fe(II) cations from 280 to 90 K, alongside magnetic ordering below 2.5 K.

Conclusions:

  • The study successfully demonstrates the integration of spin-crossover iron complexes within bimetallic anilate frameworks.
  • The synthesized compounds exhibit diverse magnetic behaviors, including ferrimagnetism and temperature-dependent spin crossover, highlighting their potential for advanced magnetic applications.