TY - JOUR
T1 - Synthesis and study of the fluxional behavior of octahedral manganese(I) complexes with a monodentate 1,8-naphthyridine ligand. X-ray crystal structure of fac-[Mn(η1-1,8-naph)(η2-phen)(CO)3]ClO4·½CH2Cl2 (naph = 1,8-naphthyridine, phen = o-phenanthroline)
AU - Bermejo, María José
AU - Ruiz, José Ignacio
AU - Vinaixa Serra, J.
AU - Solans, Xavier
PY - 1988/11/1
Y1 - 1988/11/1
N2 - The addition of 1,8-naphthyridine (naph) to a solution of [Mn(OClO3)(chel)(CO)3] (chel = o-phenanthroline (phen), 2,2′-bipyridyl (bpy)) affords the octahedral complexes [Mn(η-naph)(η-chel)(CO)3]ClO4. The crystal structure of [Mn(η1-naph)(η2-phen)-(CO)3]ClO4·½CH2Cl2 (monoclinic, space group P21/a, a = 19.019 (4) Å, b = 16.120 (3) Å, c = 8.368 (2) Å, β = 90.68 (2)°, Z = 4) shows that in the complex ion the manganese atom displays a slightly distorted octahedral coordination, being linked to three carbonyl ligands in a fac position, to two nitrogen atoms of a bidentate o-phenanthroline ligand (η-phen), and to another nitrogen atom of a monodentate 1,8-naphthyridine ligand (η-naph). A detailed variable-temperature lH NMR study shows that this structure persists in solution at low temperature for both complexes. At higher temperature these complexes are fluxional species in which there is a rapid exchange of the site of manganese coordination between the two nitrogen atoms of the monodentate 1,8-naphthyridine. For this process an approximate activation energy of 63 kJ/mol has been obtained for both complexes. The mechanism for the 1,3-shift is, apparently, intramolecular and is such that the manganese-naphthyridine interaction is probably never lost during the process.
AB - The addition of 1,8-naphthyridine (naph) to a solution of [Mn(OClO3)(chel)(CO)3] (chel = o-phenanthroline (phen), 2,2′-bipyridyl (bpy)) affords the octahedral complexes [Mn(η-naph)(η-chel)(CO)3]ClO4. The crystal structure of [Mn(η1-naph)(η2-phen)-(CO)3]ClO4·½CH2Cl2 (monoclinic, space group P21/a, a = 19.019 (4) Å, b = 16.120 (3) Å, c = 8.368 (2) Å, β = 90.68 (2)°, Z = 4) shows that in the complex ion the manganese atom displays a slightly distorted octahedral coordination, being linked to three carbonyl ligands in a fac position, to two nitrogen atoms of a bidentate o-phenanthroline ligand (η-phen), and to another nitrogen atom of a monodentate 1,8-naphthyridine ligand (η-naph). A detailed variable-temperature lH NMR study shows that this structure persists in solution at low temperature for both complexes. At higher temperature these complexes are fluxional species in which there is a rapid exchange of the site of manganese coordination between the two nitrogen atoms of the monodentate 1,8-naphthyridine. For this process an approximate activation energy of 63 kJ/mol has been obtained for both complexes. The mechanism for the 1,3-shift is, apparently, intramolecular and is such that the manganese-naphthyridine interaction is probably never lost during the process.
UR - http://www.scopus.com/inward/record.url?scp=0000203340&partnerID=8YFLogxK
U2 - 10.1021/ic00297a012
DO - 10.1021/ic00297a012
M3 - Article
AN - SCOPUS:0000203340
SN - 0020-1669
VL - 27
SP - 4385
EP - 4389
JO - Inorganic Chemistry
JF - Inorganic Chemistry
IS - 24
ER -