z-logo
Premium
Studies on thermal stabilities of coordination compounds by gas chromatography: XVIII. Activation and hydrogenation of coordinated CN −
Author(s) -
Niu JunNing,
Xin XinQuan,
Dai AnBang,
Tai A. P.
Publication year - 1986
Publication title -
acta chimica sinica english edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 0256-7660
DOI - 10.1002/cjoc.19860040408
Subject(s) - chemistry , bimetal , thermal decomposition , metal , inorganic chemistry , ligand (biochemistry) , crystal structure , reaction mechanism , ion , coordination complex , hydrogen , crystallography , catalysis , organic chemistry , biochemistry , receptor
Various metal (Cr, Mn, Fe, Co, Ni, Cu, Zn, Ag, Sn, La) ferrocyanides and ferricyanides may be considered as a multibond activation model of bimetal coordination, since CN − acts as a typical ambident ligand bonded at the two ends with two metal ions. In accordance with hydrogenation reactions of CN − taking place during thermal decomposition in hydrogen, the activation effect of bimetal coordination and the mechanism of hydrogenation reaction of CN − are discussed from the viewpoint of the crystal structure and the electron structure of the complexes. The activation degree of CN − bonded with various metal ions has been investigated. It was found that the temperature at which the triple bond of CN − breaks with top speed to evolve NH 3 correlates closely with the standard electrode potential, and d electron configuration of the metal ions.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom