Syntheses, crystal structures and properties of copper(II) complexes of 1,3-bis[(4-methyl-5-imidazol-1-yl)ethylideneamino]propan-2-ol and 1,3-bis[(4-methyl-5-imidazol-1-yl)ethylideneamino] propane

Citation
Ls. Long et al., Syntheses, crystal structures and properties of copper(II) complexes of 1,3-bis[(4-methyl-5-imidazol-1-yl)ethylideneamino]propan-2-ol and 1,3-bis[(4-methyl-5-imidazol-1-yl)ethylideneamino] propane, TRANSIT MET, 24(4), 1999, pp. 440-444
Citations number
18
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
TRANSITION METAL CHEMISTRY
ISSN journal
03404285 → ACNP
Volume
24
Issue
4
Year of publication
1999
Pages
440 - 444
Database
ISI
SICI code
0340-4285(199908)24:4<440:SCSAPO>2.0.ZU;2-5
Abstract
The syntheses of two polydentate ligands comprising imidazole donors, 1,3-b is[(4-methyl-5-imidazol-1-yl) ethylideneamino]propan-2-ol (BIPO), 1,3-bis[( 4-methyl-5-imidazol-1-yl)ethylideneamino]propane (BIP), and their copper(II ) complexes [Cu(BIPO)(ClO4)(H2O)] (NO3) . H2O (1) and [Cu(BIP)(ClO4)](ClO4) . 2H(2)O (2) are reported. Single-crystal structural analyses show that (1 ) adopts an elongated octahedral geometry with the axial positions occupied by a perchlorate oxygen atom and an aqua ligand, while (2) adopts a distor ted square-pyramidal geometry with the axial positions occupied by a perchl orate oxygen atom. Electronic spectra in aqueous solution indicate that bot h (1) and (2) adopt square-pyramidal geometry. Cyclic voltammetry in aqueou s solution gives reduction waves at -0.07 and -0.08 V versus s.c.e. for (1) and (2), respectively. The low reduction potential and general reversibili ty of the redox reaction of (1) and (2) indicate that BIPO and BIP are flex ible enough to stabilize both Cu-II and Cu-I forms of the complexes.