TY - JOUR
T1 - Synthesis of a macrocyclic metal complex incorporating peripheral hydroxyethyl tails
T2 - The X-ray structure of [Mn(L1)Cl][BF4]·4H2O
AU - Ansell, Christopher W.G.
AU - Lewis, Jack
AU - Raithby, Paul R.
AU - O'Donoghue, Timothy D.
PY - 1983
Y1 - 1983
N2 - Reaction of 2,9-dichloro-1,10-phenanthroline with 2-hydroxyethylhydrazine leads to the isolation of 2,9-di(N-2′-hydroxyethylhydrazino)-1,10-phenanthroline in moderate yield. This species undergoes a template condensation reaction with 2,6-diacetylpyridine in the presence of MnCl2·4H2O to give the title complex of the macrocyclic ligand L1. The X-ray structure of the complex shows the six-co-ordinate nature of the metal ion which is bound by five N-donors of the macrocycle and is displaced 0.51 Å towards the axial chlorine ligand. The hydroxyethyl tails extend up on the same side of the ligand as the axial chlorine. The complex crystallises in orthorhombic space group Pnma with a = 13.225(4), b = 25.011(4), and c = 17.343(4) Å. The structure was refined to R = 0.103 for 1 323 reflections.
AB - Reaction of 2,9-dichloro-1,10-phenanthroline with 2-hydroxyethylhydrazine leads to the isolation of 2,9-di(N-2′-hydroxyethylhydrazino)-1,10-phenanthroline in moderate yield. This species undergoes a template condensation reaction with 2,6-diacetylpyridine in the presence of MnCl2·4H2O to give the title complex of the macrocyclic ligand L1. The X-ray structure of the complex shows the six-co-ordinate nature of the metal ion which is bound by five N-donors of the macrocycle and is displaced 0.51 Å towards the axial chlorine ligand. The hydroxyethyl tails extend up on the same side of the ligand as the axial chlorine. The complex crystallises in orthorhombic space group Pnma with a = 13.225(4), b = 25.011(4), and c = 17.343(4) Å. The structure was refined to R = 0.103 for 1 323 reflections.
UR - http://www.scopus.com/inward/record.url?scp=37049104156&partnerID=8YFLogxK
U2 - 10.1039/DT9830000177
DO - 10.1039/DT9830000177
M3 - Article
AN - SCOPUS:37049104156
SN - 1472-7773
SP - 177
EP - 179
JO - Journal of the Chemical Society, Dalton Transactions
JF - Journal of the Chemical Society, Dalton Transactions
IS - 1
ER -