Synthesis, Structural Characterization, Magnetic Behavior, and Single Crystal EPR Spectra of Three New One-Dimensional Manganese Azido Systems with FM, Alternating FM-AF, and AF Coupling

1999 ◽  
Vol 38 (25) ◽  
pp. 5716-5723 ◽  
Author(s):  
Morsy A. M. Abu-Youssef ◽  
Albert Escuer ◽  
Dante Gatteschi ◽  
Mohamed A. S. Goher ◽  
Franz A. Mautner ◽  
...  
2004 ◽  
Vol 54 (S4) ◽  
pp. 327-330
Author(s):  
J. Prokleška ◽  
J. Vejpravová ◽  
V. Sechovský ◽  
Y. Isikawa

2016 ◽  
Vol 118 ◽  
pp. 404-409 ◽  
Author(s):  
Dmitrijs Stepanovs ◽  
Zenta Tetere ◽  
Irisa Rāviņa ◽  
Viktors Kumpiņš ◽  
Daina Zicāne ◽  
...  

2015 ◽  
Vol 70 (12) ◽  
pp. 851-856 ◽  
Author(s):  
Chun-Hua Dai ◽  
Fu-Lin Mao

AbstractThe tridentate N-donor ligand 2,6-di(2-oxazolyl)pyridine (L) reacts with AgClO4 and AgPF6 to yield two new complexes, {[Ag5(L)5](ClO4)5}n (1) and {[Ag5(L)5](PF6)5}n (2), which have been characterized by single-crystal and powder X-ray diffractions, IR spectroscopy, and elemental and thermogravimetric analyses. Complexes 1 and 2 are isotypic, displaying helical chain structures. The fluorescence properties of 1 and 2 were investigated.


2012 ◽  
Vol 16 (01) ◽  
pp. 154-162 ◽  
Author(s):  
Edwin W.Y. Wong ◽  
Daniel B. Leznoff

The reduction of magnesium phthalocyanine (MgPc) with 2.2 equivalents of potassium graphite in 1,2-dimethoxyethane (DME) gives [K2(DME)4]PcMg(OH)(1) in 67% yield. Compound 1 was structurally characterized using single crystal X-ray crystallography and was found to be a monomeric, heterometallic complex consisting of a μ3-OH ligand that bridges a [MgIIPc3-]- anion to two potassium cations solvated by four DME molecules. An absorption spectrum of 1 confirms the Pc ligand is singly reduced and has a 3–charge. The solid-state structure of 1 does not indicate breaking of the aromaticity of the Pc ligand. Compound 1 is only the second Pc3- complex and the first reduced MgPc to be isolated and structurally characterized.


Author(s):  
Ahmet Karadag ◽  
Hümeyra Pasaoglu ◽  
Gökhan Kastas ◽  
Orhan Büyükgüngör

AbstractThe cyano-bridged heteronuclear coordination polymer of zinc(II)/nickel(II) has been prepared by N-(2-hydroxyethyl)-ethylendiamine (hydet-en), alternatively named 2-(2-aminoethylamino)-ethanol and characterised by IR and thermal analysis. In the bimetallic complex, the decomposition of hydet-en ligands is seen to be endothermic whereas that of the cyano ligands is found to be exothermic. The crystal structure of the complex has been determined by single-crystal X-ray diffraction. The crystal structure of the zinc(II)-nickel(II) complex consists of a one-dimensional polymeric chain –Zn(hydet-en)


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