Substituted phenanthrolines and their metal chelates

1973 ◽  
Vol 26 (5) ◽  
pp. 951 ◽  
Author(s):  
EJ Halbert ◽  
CM Harris ◽  
E Sinn ◽  
GJ Sutton
Keyword(s):  
Magnetic Properties ◽  
High Spin ◽  
Copper Complex ◽  
Magnetic Moment ◽  
Room Temperature ◽  
Spin Crossover ◽  
Metal Chelates ◽  
One Step

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.

The Flexibility of Long Chain Substituents Influences Spin-Crossover in Isomorphous Lipid Bilayer Crystals

2021 ◽  
Author(s):  
Iurii Galadzhun ◽  
Rafal Kulmaczewski ◽  
Namrah Shahid ◽  
Oscar Cespedes ◽  
Mark J Howard ◽  
...  
Keyword(s):  
Lipid Bilayer ◽  
High Spin ◽  
Room Temperature ◽  
Spin Crossover ◽  
Pyridine Derivatives ◽  
Long Chain

[Fe(bpp)2][BF4]2 (bpp = 2,6-di{pyrazol-1-yl}pyridine) derivatives bearing a bent geometry of hexadec-1-ynyl or hexadecyl substituents pyrazole are isomorphous, and high-spin at room temperature. However, only the latter compound undergoes an abrupt,...

scholarly journals Co-Substitution Effect in Room-Temperature Ferromagnetic Oxide Sr3.1Y0.9Co4O10.5

Materials ◽  
2020 ◽  
Vol 13 (10) ◽  
pp. 2301
Author(s):  
Akihiro Tsuruta ◽  
Shuji Kawasaki ◽  
Masashi Mikami ◽  
Yoshiaki Kinemuchi ◽  
Yoshitake Masuda ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Saturation Magnetization ◽  
High Spin ◽  
Spin State ◽  
Room Temperature ◽  
High Spin State ◽  
Substitution Effect ◽  
Co Substitution ◽  
Intermediate Spin ◽  
Intermediate Spin State

We investigated the Co substitution effect for the magnetic properties in room-temperature ferromagnetic oxide Sr3.1Y0.9Co4O10.5. The substituted element (Al and Ga) and low-spin state Co3+, which was changed from a high-spin or intermediate-spin state by Al or Ga substitution, reduced the Curie temperature to even 1.5 times lower than the temperature estimated from a simple dilution effect. Al3+ preferentially substituted for intermediate-spin-state Co3+ in the ferrimagnetic CoO6 layer and deteriorated the saturation magnetization of Sr3.1Y0.9Co4O10.5. By contrast, Ga3+ substituted for high-spin-state Co3+ in the CoO6 layer and/or the antiferromagnetic CoO4.25 layer and enhanced the saturation magnetization per Co ion. These results indicate that the magnetic properties of Sr3.1Y0.9Co4O10.5 can be controlled by selectively substituting for Co3+ with different spin states.

Spin Crossover Meets Diarylethenes: Efficient Photoswitching of Magnetic Properties in Solution at Room Temperature

2013 ◽  
Vol 52 (19) ◽  
pp. 11585-11592 ◽  
Author(s):  
Magdalena Milek ◽  
Frank W. Heinemann ◽  
Marat M. Khusniyarov
Keyword(s):  
Magnetic Properties ◽  
Room Temperature ◽  
Spin Crossover

Strain effects on spin magnetic moment of cubic bixbyite In2O3:C

2015 ◽  
Vol 29 (19) ◽  
pp. 1550099 ◽  
Author(s):  
Hai-Bin Wang ◽  
Zhong-Xiang Xie ◽  
Xia Yu ◽  
Yong Zhang ◽  
Dan Wang
Keyword(s):  
Magnetic Properties ◽  
High Spin ◽  
Magnetic Moment ◽  
First Principles ◽  
Spin Moment ◽  
First Principles Calculations ◽  
Sharp Transition ◽  
Spin Magnetic Moment ◽  
Spin Devices ◽  
Design Pressure

First-principles calculations are performed to study the effect of isotropic stress on the electronic and magnetic properties of cubic bixbyite Indium oxide [Formula: see text] doped with substitution C impurities. In comparison with undoped [Formula: see text] materials, the defects can induce a spin moment with 2 [Formula: see text]B when two C atoms substitutes for two O atoms in the system. In addition, the spin moment remains the same under the condition of strain less than 2%. When the strain is more than 2%, there is a sharp transition to a high-spin magnetic moment with 4 [Formula: see text]B and it stays in this position with the increase of strain. This high magnetoelastic effect could be utilized to design pressure-tunable spin devices based on C-doped [Formula: see text].

Steric Trapping of the High Spin State in FeIII Quinolylsalicylaldimine Complexes

2014 ◽  
Vol 67 (11) ◽  
pp. 1574 ◽  
Author(s):  
Darunee Sertphon ◽  
David J. Harding ◽  
Phimphaka Harding ◽  
Keith S. Murray ◽  
Boujemaa Moubaraki ◽  
...  
Keyword(s):  
Schiff Base ◽  
Electronic Properties ◽  
High Spin ◽  
Spin State ◽  
Schiff Base Ligand ◽  
Room Temperature ◽  
Spin Crossover ◽  
High Spin State ◽  
Electrochemical Studies ◽  
Magnetic Studies

A new sterically bulky Schiff base ligand, N-(8-quinolyl)-5-tert-butylsalicylaldimine (Hqsal-5-tBu) has been prepared and a series of FeIII complexes, [Fe(qsal-5-tBu)2]Y (Y = Cl 1, ClO4 2, NO3 3, BF4 4) utilising this ligand are reported and fully characterised. UV-vis spectroscopic and electrochemical studies indicate that 1–4 are high spin (HS) in solution at room temperature and further suggest that the tBu group only slightly alters the electronic properties of 1–4 compared with related [Fe(qsal-5-X)2]+ systems. The structures of [Fe(qsal-5-tBu)2]Cl·4MeOH·H2O 1, [Fe(qsal-5-tBu)2]ClO4·MeOH 2, and [Fe(qsal-5-tBu)2]NO3 3 determined at 100 K reveal HS FeIII centres in all cases. Four-fold parallel aryl embraces and π–π interactions serve to link the cations forming 2D sheets mirroring the motifs found in other [Fe(qsal-5-X)2]+ complexes. Despite this the tBu group causes strong distortions at the Fe centre which as magnetic studies reveal prevent spin crossover trapping 1–4 in the HS state.

Light- and Thermal-Induced Spin Crossover in {Fe(abpt)2[N(CN)2]2}. Synthesis, Structure, Magnetic Properties, and High-Spin ↔ Low-Spin Relaxation Studies

2001 ◽  
Vol 40 (16) ◽  
pp. 3986-3991 ◽  
Author(s):  
Nicolás Moliner ◽  
Ana B. Gaspar ◽  
M. Carmen Muñoz ◽  
Virginie Niel ◽  
Joan Cano ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
High Spin ◽  
Spin Relaxation ◽  
Spin Crossover ◽  
Relaxation Studies

scholarly journals First Cobalt(II) Spin Crossover Compound with N4S2-Donorset

Molecules ◽  
2020 ◽  
Vol 25 (4) ◽  
pp. 855 ◽  
Author(s):  
Fabian Fürmeyer ◽  
Danny Münzberg ◽  
Luca M. Carrella ◽  
Eva Rentschler
Keyword(s):  
Magnetic Moment ◽  
Metal Ion ◽  
Room Temperature ◽  
Spin Crossover ◽  
Synthesis And Characterization ◽  
Metal Centers ◽  
Mononuclear Complexes

Herein we report the synthesis and characterization of a novel bis-tridentate 1,3,4-thiadiazole ligand (L = 2,5-bis[(2-pyridylmethyl)thio]methyl-1,3,4-thiadiazole). Two new mononuclear complexes of the type [MII(L)2](ClO4)2 (with M = FeII (C1) and CoII (C2)) have been synthesized, containing the new ligand (L). In both complexes the metal centers are coordinated by an N4S2-donorset and each of the two ligands is donating to the metal ion with just one of the tridentate pockets. The iron(II) complex (C1) is in the low spin [LS] state below room temperature and shows an increase in the magnetic moment only above 300 K. In contrast, the cobalt(II) complex (C2) shows a gradual spin crossover (SCO) with T1/2 = 175 K. To our knowledge, this is the first cobalt(II) SCO complex with an N4S2-coordination.

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