Tetracyano complexes of molybdenum(IV)

1968 ◽  
Vol 7 (10) ◽  
pp. 2086-2091 ◽  
Author(s):  
J. Van de Poel ◽  
H. M. Neumann
Keyword(s):  
Tetracyano Complexes

Comparative Bonding and Photophysical Properties of 2,2'-Bipyridine and 2,2'-Bipyrazine in Tetracyano Complexes Containing Ruthenium and Osmium

1995 ◽  
Vol 34 (7) ◽  
pp. 1830-1835 ◽  
Author(s):  
Monica E. Garcia Posse ◽  
Nestor E. Katz ◽  
Luis M. Baraldo ◽  
Diego D. Polonuer ◽  
Claudio G. Colombano ◽  
...  
Keyword(s):  
Photophysical Properties ◽  
Tetracyano Complexes

Preparation and some properties of tetracyano complexes M(en)M′(CN)4 (M=Cd(II), Mn(II);M′=Ni(II), Cd(II))

1994 ◽  
Vol 41 (1) ◽  
pp. 91-98 ◽  
Author(s):  
J. Cernák ◽  
J. Skorsepa ◽  
J. Chomic ◽  
I. Potocnák ◽  
J. Hoppan
Keyword(s):  
Tetracyano Complexes

Inclusion Compounds of Tetracyano Complexes and Their Electrical Properties

1994 ◽  
Vol 59 (11) ◽  
pp. 2436-2446 ◽  
Author(s):  
Mária Reháková ◽  
Anna Sopková ◽  
Vladimír Šály
Keyword(s):  
Electrical Conductivity ◽  
Chemical Composition ◽  
Electrical Properties ◽  
General Formula ◽  
Inclusion Compounds ◽  
High Frequency ◽  
Iodide Ions ◽  
Structure And Morphology ◽  
Composition Structure ◽  
Tetracyano Complexes

The presence of iodine and iodide ions in tetracyanonickelates inclusion compounds with the general formula Ni(B)mNi(CN)4 . n H2O (B = NH3 or ethylenediamine) changes the properties of these compounds. High frequency conductance measurements in the range of 10 - 105 Hz show that the products with ethylenediamine ligands have a higher electrical conductivity than those with NH3 ligands. The differences in the electrical properties between the compounds studied are mainly caused by chemical composition, structure and morphology.

Tetracyano complexes incorporated in natural zeolitic materials

1992 ◽  
Vol 13 (3) ◽  
pp. 233-243 ◽  
Author(s):  
A. Sopková ◽  
P. Mondík ◽  
M. Šingliar
Keyword(s):  
Zeolitic Materials ◽  
Tetracyano Complexes

Clathrates of tetracyanonickelates containing 1,4-dioxane

1987 ◽  
Vol 52 (12) ◽  
pp. 2890-2899 ◽  
Author(s):  
Mária Reháková ◽  
Anna Sopková
Keyword(s):  
Guest Molecule ◽  
Solid Product ◽  
Gc Analysis ◽  
Preparation Conditions ◽  
Direct Addition ◽  
Similar Product ◽  
Host Structure ◽  
Tetracyano Complexes

It was found after study of modifications of tetracyano complexes with 1,4-dioxane that a similar product is formed also by direct addition of 1,4-dioxane to a solution of [Ni(NH3)m][Ni(CN)4] or to solid NiNi(CN)4.nH2O; and 1,4-dioxane is initially bonded as a guest molecule and then as a ligand. The amount of guest component or ligand in the compounds Ni(NH3)m(C4H8O2)aNi(CN)4.(y-a)C4H8O2.nH2O and Ni(C4H8O2)aNi(CN)4.(n-a)C4H8O2 depends on the preparation conditions and on the conditions of storage of the solid product after isolation. The results of TA, IR, and GC analysis confirmed the presence of 1,4-dioxane bonded as a guest component and also 1,4-dioxane entering the host structure as a ligand.

Transition metal tetracyano complexes, their thermal and sorption properties

1986 ◽  
Vol 51 (3) ◽  
pp. 526-538 ◽  
Author(s):  
Anna Sopková ◽  
Michal Šingliar
Keyword(s):  
Organic Compound ◽  
Transition Metal ◽  
Guest Molecule ◽  
Sorption Properties ◽  
Organic Substances ◽  
Hydrated Form ◽  
Complex Lattice ◽  
Lattice Space ◽  
Tetracyano Complexes

The possibility of resorption of a guest molecule (G) or its substitution by other compounds is not known for M(NH3)2N(CN)4.2G (G = C6H6) or M(en)mM'(CN)4.nG clathrates, or even for the parent M(NH3)mM'(CN)4.nH2O, MM'(CN4).nH2O tetracyano complexes. These, however, are capable of sorption, and their lattice space can be reversibly or irreversibly filled with a suitable organic compound if the clathrates or tetracyano complexes in the hydrated form are allowed to be in contact with organic substances whose size and polarity fit the tetracyano complex lattice. The space within the lattice, however, develops as early as their formation from solution or suspension in the presence of the compound G (presence of water is actually sufficient).

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