Toward Ligand-Driven Light-Induced Spin Changing. Influence of the Configuration of 4 Styrylpyridine (stpy) on the Magnetic Properties of FeII(stpy)4(NCS)2 Complexes. Crystal Structures of the Spin-Crossover Species Fe(trans-stpy)4(NCS)2 and of the High-Spin Species Fe(cis-stpy)4(NCS)2

1994 ◽  
Vol 33 (10) ◽  
pp. 2273-2279 ◽  
Author(s):  
Cecile Roux ◽  
Jacqueline Zarembowitch ◽  
Bernard Gallois ◽  
Thierry Granier ◽  
Renee Claude
2006 ◽  
Vol 73 (1) ◽  
Author(s):  
Y. Moritomo ◽  
M. Kamiya ◽  
A. Nakamura ◽  
A. Nakamoto ◽  
N. Kojima

1973 ◽  
Vol 26 (5) ◽  
pp. 951 ◽  
Author(s):  
EJ Halbert ◽  
CM Harris ◽  
E Sinn ◽  
GJ Sutton

Substituents at and adjacent to the nitrogen atoms in 2,2?-bipyridyl and 1,10-phenanthroline are most likely to cause drastic changes in the magnetic properties of complexes with these ligands. Complexes of the N-oxides (2,2?-bipyridine 1,1?-dioxide, and 1,10-phenanthroline 1- oxide) with copper, and of 2-substituted phen (substituent = Cl, CONH2) with iron(II) are investigated, and a new one-step reaction to convert phno into cphn is reported. The copper complex Cu(bpyo)Br2 shows antiferromagnetic interactions, but other complexes Cu(bpyo)X2 (X = Cl, NO3) with this ligand are magnetically normal, as are Cu(phno)Cl2 and Cu(phno)Br2. The complex [Fe(cphn)3] (ClO4)2 lies near the high spin-low spin crossover for iron(II), and its magnetic moment is normal at room temperature but falls with decreasing temperature. The dioxide of phen appears not to be formed by the literature method and no successful synthesis can be reported here.


2001 ◽  
Vol 40 (16) ◽  
pp. 3986-3991 ◽  
Author(s):  
Nicolás Moliner ◽  
Ana B. Gaspar ◽  
M. Carmen Muñoz ◽  
Virginie Niel ◽  
Joan Cano ◽  
...  

Crystals ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 87 ◽  
Author(s):  
Mohd. Muddassir ◽  
You Song

A new four-coordinated high-spin Co(II) complex was synthesized through the reactions of Co(NSC)2 with bathocuproine, by the diffusion method, resulting in an infinite one-dimension chain. Both static and dynamic magnetic properties were measured. The magnetic properties investigation shows that the single CoII ion properties dominate the magnetic behavior in the complex. Despite the presence of a four-coordinated single CoII ion, no SMM properties were exhibited by the complex.


2003 ◽  
Vol 64 (6) ◽  
pp. 1003-1013 ◽  
Author(s):  
O Roubeau ◽  
M deVos ◽  
A.F Stassen ◽  
R Burriel ◽  
J.G Haasnoot ◽  
...  

2022 ◽  
Vol 8 (1) ◽  
pp. 8
Author(s):  
Komala Pandurangan ◽  
Anthony B. Carter ◽  
Paulo N. Martinho ◽  
Brendan Gildea ◽  
Tibebe Lemma ◽  
...  

Structural and magnetic properties of a new spin crossover complex [Mn(4,6-diOMe-sal2323)]+ in lattices with ClO4−, (1), NO3−, (2), BF4−, (3), CF3SO3−, (4), and Cl− (5) counterions are reported. Comparison with the magnetostructural properties of the C6, C12, C18 and C22 alkylated analogues of the ClO4− salt of [Mn(4,6-diOMe-sal2323)]+ demonstrates that alkylation effectively switches off the thermal spin crossover pathway and the amphiphilic complexes are all high spin. The spin crossover quenching in the amphiphiles is further probed by magnetic, structural and Raman spectroscopic studies of the PF6− salts of the C6, C12 and C18 complexes of a related complex [Mn(3-OMe-sal2323)]+ which confirm a preference for the high spin state in all cases. Structural analysis is used to rationalize the choice of the spin quintet form in the seven amphiphilic complexes and to highlight the non-accessibility of the smaller spin triplet form of the ion more generally in dilute environments. We suggest that lattice pressure is a requirement to stabilize the spin triplet form of Mn3+ as the low spin form is not known to exist in solution.


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