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Results: 1-8 |
Results: 8
Reversible switching of the first hyperpolarisability of an NLO-active donor-acceptor molecule based on redox interconversion of the octamethylferrocene donor unit
Authors: Malaun, M Reeves, ZR Paul, RL Jeffery, JC McCleverty, JA Ward, MD Asselberghs, I Clays, K Persoons, AE
Citation: M. Malaun et al., Reversible switching of the first hyperpolarisability of an NLO-active donor-acceptor molecule based on redox interconversion of the octamethylferrocene donor unit, CHEM COMMUN, (01), 2001, pp. 49-50
Polynuclear osmium-dioxolene complexes: comparison of electrochemical and spectroelectrochemical properties with those of their ruthenium analogues
Authors: Barthram, AM Reeves, ZR Jeffery, JC Ward, MD
Citation: Am. Barthram et al., Polynuclear osmium-dioxolene complexes: comparison of electrochemical and spectroelectrochemical properties with those of their ruthenium analogues, J CHEM S DA, (18), 2000, pp. 3162-3169
Effects of metal co-ordination geometry on self-assembly: a dinuclear double helicate complex and a tetranuclear cage complex of a new bis-bidentate bridging ligand
Authors: Paul, RL Couchman, SM Jeffery, JC McCleverty, JA Reeves, ZR Ward, MD
Citation: Rl. Paul et al., Effects of metal co-ordination geometry on self-assembly: a dinuclear double helicate complex and a tetranuclear cage complex of a new bis-bidentate bridging ligand, J CHEM S DA, (6), 2000, pp. 845-851
Spectroelectrochemical studies and molecular orbital calculations on mononuclear complexes [Mo(Tp(Me,Me))(NO)Cl(py)] (where py is a substituted pyridine derivative): electrochromism in the near-infrared region of the electronic spectrum
Authors: Kowallick, R Jones, AN Reeves, ZR Jeffery, JC McCleverty, JA Ward, MD
Citation: R. Kowallick et al., Spectroelectrochemical studies and molecular orbital calculations on mononuclear complexes [Mo(Tp(Me,Me))(NO)Cl(py)] (where py is a substituted pyridine derivative): electrochromism in the near-infrared region of the electronic spectrum, NEW J CHEM, 23(9), 1999, pp. 915-921
Copper(II) complexes of new potentially hexadentate N3S3- or N-6-donor podand ligands based on the tris(pyrazolyl)borate or tris(pyrazolyl)methane core
Authors: Humphrey, ER Mann, KLV Reeves, ZR Behrendt, A Jeffery, JC Maher, JP McCleverty, JA Ward, MD
Citation: Er. Humphrey et al., Copper(II) complexes of new potentially hexadentate N3S3- or N-6-donor podand ligands based on the tris(pyrazolyl)borate or tris(pyrazolyl)methane core, NEW J CHEM, 23(4), 1999, pp. 417-423
Lanthanide complexes of a new sterically hindered potentially hexadentate podand ligand based on a tris(pyrazolyl)borate core; crystal structures, solution structures and luminescence properties
Authors: Reeves, ZR Mann, KLV Jeffery, JC McCleverty, JA Ward, MD Barigelletti, F Armaroli, N
Citation: Zr. Reeves et al., Lanthanide complexes of a new sterically hindered potentially hexadentate podand ligand based on a tris(pyrazolyl)borate core; crystal structures, solution structures and luminescence properties, J CHEM S DA, (3), 1999, pp. 349-355
Structural, electrochemical and UV/VIS/NIR spectroelectrochemical properties of diastereomerically pure dinuclear ruthenium complexes based on the bridging ligand phenanthroline-5,6-diimine, and a mononuclear by-product witha peripheral isoimidazole group
Authors: Fletcher, NC Robinson, TC Behrendt, A Jeffery, JC Reeves, ZR Ward, MD
Citation: Nc. Fletcher et al., Structural, electrochemical and UV/VIS/NIR spectroelectrochemical properties of diastereomerically pure dinuclear ruthenium complexes based on the bridging ligand phenanthroline-5,6-diimine, and a mononuclear by-product witha peripheral isoimidazole group, J CHEM S DA, (17), 1999, pp. 2999-3006
Effects of metal co-ordination geometry on self-assembly: a monomeric complex with trigonal prismatic metal co-ordination vs. tetrameric complexes with octahedral metal co-ordination
Authors: Paul, RL Amoroso, AJ Jones, PL Couchman, SM Reeves, ZR Rees, LH Jeffery, JC McCleverty, JA Ward, MD
Citation: Rl. Paul et al., Effects of metal co-ordination geometry on self-assembly: a monomeric complex with trigonal prismatic metal co-ordination vs. tetrameric complexes with octahedral metal co-ordination, J CHEM S DA, (10), 1999, pp. 1563-1568
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