We present here a study of the magnetic properties of the antiferromagnetic dimer material CuVOF 4 ( H 2 O ) 6 ⋅ H 2 O , in which the dimer unit is composed of two different S = 1 / 2 species, Cu(II) and V(IV). An applied magnetic field of μ 0 H c 1 = 13.1 ( 1 ) T is found to close the singlet-triplet energy gap, the magnitude of which is governed by the antiferromagnetic intradimer J 0 ≈ 21 K, and interdimer J ′ ≈ 1 K, exchange energies, determined from magnetometry and electron-spin resonance measurements. The results of density functional theory (DFT) calculations are consistent with the experimental results. The DFT calculations predict antiferromagnetic coupling along all nearest-neighbo...
We report on a comprehensive characterization of the newly synthesized Cu2+-based molecular magnet [...
Spin-state energetics of exchange-coupled copper complexes pose a persistent challenge for applied q...
Most interpretations of the magnetic coupling J between two unpaired electrons rest upon simple val...
We present here a study of the magnetic properties of the antiferromagnetic dimer material CuVOF 4(H...
We present here a study of the magnetic properties of the antiferromagnetic dimer material CuVOF4(H2...
We present here a study of the magnetic properties of the antiferromagnetic dimer material CuVOF4(H2...
Cu(pyz)(NO3)2 is a quasi-one-dimensional molecular antiferromagnet that exhibits three-dimensional l...
We investigate the structural and magnetic properties of two molecule-based magnets synthesized from...
We report on a comprehensive characterization of the newly synthesized Cu2+-based molecular magnet ...
The quasi-one-dimensional molecule-based Heisenberg antiferromagnet Cu(NO3)2(pyz)3 has an intrachain...
This work describes a homometallic spin-urn:x-wiley:09476539:media:chem202200855:chem202200855-math-...
We investigate the structural and magnetic properties of two molecule-based magnets synthesized from...
The 3d-4f exchange interaction plays an important role in many lanthanide based molecular magnetic m...
The accurate electron density distribution and magnetic properties of two metal-organic polymeric ma...
We report on the magnetic properties of HoCo dimers as a model system for the smallest intermetallic...
We report on a comprehensive characterization of the newly synthesized Cu2+-based molecular magnet [...
Spin-state energetics of exchange-coupled copper complexes pose a persistent challenge for applied q...
Most interpretations of the magnetic coupling J between two unpaired electrons rest upon simple val...
We present here a study of the magnetic properties of the antiferromagnetic dimer material CuVOF 4(H...
We present here a study of the magnetic properties of the antiferromagnetic dimer material CuVOF4(H2...
We present here a study of the magnetic properties of the antiferromagnetic dimer material CuVOF4(H2...
Cu(pyz)(NO3)2 is a quasi-one-dimensional molecular antiferromagnet that exhibits three-dimensional l...
We investigate the structural and magnetic properties of two molecule-based magnets synthesized from...
We report on a comprehensive characterization of the newly synthesized Cu2+-based molecular magnet ...
The quasi-one-dimensional molecule-based Heisenberg antiferromagnet Cu(NO3)2(pyz)3 has an intrachain...
This work describes a homometallic spin-urn:x-wiley:09476539:media:chem202200855:chem202200855-math-...
We investigate the structural and magnetic properties of two molecule-based magnets synthesized from...
The 3d-4f exchange interaction plays an important role in many lanthanide based molecular magnetic m...
The accurate electron density distribution and magnetic properties of two metal-organic polymeric ma...
We report on the magnetic properties of HoCo dimers as a model system for the smallest intermetallic...
We report on a comprehensive characterization of the newly synthesized Cu2+-based molecular magnet [...
Spin-state energetics of exchange-coupled copper complexes pose a persistent challenge for applied q...
Most interpretations of the magnetic coupling J between two unpaired electrons rest upon simple val...