Some Studies in Inorganic Complexes. XII. Manganese(II) and Iron(II) with 2-Aminomethylpyridine (2-Picolylamine)

1961 ◽  
Vol 14 (4) ◽  
pp. 550 ◽  
Author(s):  
GJ Sutton

Almost colourless complexes of the type [MnpicCl2], [Mnpic2X2], [Mnpic3]I2 and [Mnpic3][ClO4]2, as well as the brown complexes [Fepic3]Br2 and [Fepic3]I2 have been prepared and studied ; pic being the chelating ligand 2-picolylamine (2-aminomethyl-pyridine) and X the halogen. Conductance and absorption spectroscopy in the near-ultraviolet region measurements, using nitromethane as solvent, indicate that all complexes investigated have a 6-coordinate structure, excepting the chloride [MnpicCl2], the structure of which is uncertain. The latter substance could be tetrahedral or octahedral by polymerization. This substance as well as the bischelate complexes behave as non-electrolytes in nitromethane, although they are ionized to bi-univalent electrolytes in methanol. The complexes containing three molecules of ligand to metal atom are bi-univalent electrolytes in both solvents. Measurements of magnetic susceptibility show that both the iron and manganese complexes have spin-free metal atoms.

1963 ◽  
Vol 16 (3) ◽  
pp. 371 ◽  
Author(s):  
GJ Sutton

The following complexes of the chelating ligands 2-methyl-6-aminomethylpyridine (6-methyl-2-picolylamine or mepic) and 2-thioamidopyridine (thiopic) have been prepared and studied: [Cu mepic2X]X, where X = Cl, Br, I, NO3, ClO4, [Cu mepic2C2O4], [Ni mepic3][ClO4]2, [M(II) thiopic3][ClO4]2, [M(III) thiopic3][ClO4]3, (M(II) = Co, Ni; M(III) = CO, Fe), and [Co thiopic3]Cl2. Conductance measurements in ethanol, nitromethane, and nitrobenzene indicate that the [Cu mepic2X]X complexes are 5-covalent whilst the other complexes studied are 6-covalent. All the complexes are "spin free" excepting those of Co(III). Absorption spectra of the copper complexes in the near ultraviolet region were also made.


1960 ◽  
Vol 13 (1) ◽  
pp. 74 ◽  
Author(s):  
GJ Sutton

Complexes of the type Nipic2X2, Nipic3X2.nH2O, and Nipic3(ClO4)2.H2O have been prepared and studied, where X is Cl, Br, or I and pic is the chelating ligand 2-picolylamine. Conductance measurements in nitrobenzene, nitromethane, methanol, and water show that the blue compounds Nipic2X2, whilst being hexacovalent complexes in the solid state, are progressively ionized in the respective solvents as halogen is replaced by solvent molecules. Conductance measurements also verified a hexacovalent structure for the Ni pic32+ ion complex whose salts are bi-univalent electrolytes. Magnetic measurements show that a11 the complexes are paramagnetic with a mean moment of 3.0 B.M. Their absorption spectra in the near ultraviolet region are characteristic of that of the ligand. A study in the visible spectrum was also made.


Author(s):  
Linyong Xu ◽  
Wuxi Tao ◽  
Heng Liu ◽  
Junhua Ning ◽  
Meihua Huang ◽  
...  

A large-bandgap donor BTBR-2F based on noncovalent conformational lock has been designed and synthesized to achieve more complementary absorption with the PM6: Y6 blend in the near-ultraviolet region. The ternary...


1974 ◽  
Vol 3 (5) ◽  
pp. 419-422 ◽  
Author(s):  
Ken-ichi Hara ◽  
Motomichi Inoue ◽  
Tatsuo Horiba ◽  
Masaji Kubo

2007 ◽  
Vol 201 (15) ◽  
pp. 6655-6659 ◽  
Author(s):  
Keiji Nakamura ◽  
Akira Wakayama ◽  
Ken Yukimura

2006 ◽  
Vol 84 (2) ◽  
pp. 105-110 ◽  
Author(s):  
Javier A Cabeza ◽  
Ignacio del Río ◽  
Pablo García-Álvarez ◽  
Daniel Miguel

The hexanuclear ruthenium cluster [Ru6(µ3-H)2(µ-H)2(µ4-κ2-ampy)2(CO)14] (1) and the octanuclear one [Ru8(µ-H)(µ4-κ2-ampy)3(µ3-κ2-Hampy)(µ-CO)2(CO)15] (2) have been prepared by treating [Ru6(µ3-H)2(µ5-κ2-ampy)(µ-CO)2(CO)14] with 2-amino-6-methylpyridine (H2ampy) in decane at reflux temperature. Their metal atoms are supported by ligands that derive from the activation of one (complex 2) or both N—H bonds (complexes 1 and 2) of the H2ampy amino fragment. Both contain at least one ampy ligand featuring an unprecedented coordination type: the imido N atom caps a triangle of metal atoms while the pyridine nitrogen is attached to an additional metal atom. One of the ampy ligands of cluster 2 also displays another unprecedented coordination type: it caps a distorted square of metal atoms through the imido N atom while the pyridine nitrogen is attached to one of the atoms included in that square.Key words: ruthenium, cluster compounds, amido ligands, imido ligands.


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