MECHANISM of REACTION of METALLOPORPHYRINS, FERROCENES and METAL CYANIDES
Main researcher
: AŠPERGER, SMILJKO (994) Assistants
CETINA-ČIŽMEK, BISERKA (121030)
Type of research: basic Duration from: 01/01/91. to 12/31/95. Papers on project (total): 27
Papers on project quoted in Current Contents: 3
Institution name: Hrvatska akademija znanosti i umjetnosti, Zagreb (101) Department/Institute: Research Center Address: Ante Kovačića 5 City: 10000 - Zagreb, Croatia
Communication
Fax: 385 (0)1-44-93-78
Phone: 385 (0)1-44-90-93
Summary: Study of mechanism of reactions of metallo-porphyrins,
especially of cobalt(III)(protoporphyrin IX dimethyl ester)(L1)(L2) with
amine entering ligands of various basicity and pi-bonding ebility with
special emphasis on the nature of the transition states. Also the kinetic
and mechanism of solvolyses of ferrocenylmethyl esters has been studied by
secondary alfa-deuterium kinetic isotope effects. The possibility of
contribution of tunneling to large alfa-D isotope effects has been
investigated.
Research goals: The aim was to determine the nature of the
transition states in the reactions of the metalloporphyrins with piridine
and imidazole and their derivatives, because the metal-imidazolenitrogen
is of great biological interest (hemoglobin, mioglobin,cytochromes,
cobalamins). Also, the study of secondary alfa-D kinetic isotope effect in
solvolyses of ferrocenyl-methyl esters was planned, as well as the study
of tunneling contribution to the large alfa-D isotope effects.
COOPERATION - INSTITUTIONS
Name of institution
: Farmaceutsko-biokemijski fakultet,
Sveučilište u Zagrebu Type of institution: University/Faculty Type of cooperation: Joint publishing of scientific papers City: 10000 - Zagreb, Croatia
Name of institution
: Department of Chemistry, University of
Rochester, Rochester, N.Y. Type of institution: University/Faculty Type of cooperation: Occasional exchange of information City: Rochester, SAD Other information about the project.