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Synthesis, structures and photophysical properties of Cu(I) phosphine complexes with various diimine ligands
- Source :
- Polyhedron. 127:203-211
- Publication Year :
- 2017
- Publisher :
- Elsevier BV, 2017.
-
Abstract
- A series of triphenylphosphine Cu(I) complexes with various diimine ligands, [Cu(N–N)(PPh3)2](ClO4) [N–N = dmp (2); Ph2Phen (3); Ph2dmp (4); dpq (5); dppz (6); phenCN (7); phenOH (8)] are synthesized by the ligand substitution reactions of [Cu(MeCN)4](ClO4) with 2 mole equiv. of PPh3 ligand and 1.2 mole equiv. of diimine ligand. {Cu(dpq)[P(XPh)3]2}(ClO4) [X = Me (5a); OMe (5b); Cl (5c)] and {Cu(phenOH)[P(XPh)3]2}(ClO4) [X = Me (8a); OMe (8b)] are also obtained by using various substituted phosphine ligands. These mixed-ligand complexes have been characterized using 1H and 31P NMR spectroscopy, IR spectroscopy, mass spectrometry and elemental analysis. Three of these complexes have been structurally characterized by X-ray crystallography. The photophysical and electrochemical properties of these complexes have been studied. These complexes exhibit MLCT phosphorescence with emission energy, lifetimes and quantum yields showing strong dependence on the nature of diimine and phosphine ligands. In particular, both the electronic and steric effects of the substituting groups in phosphine ligands are also found to affect the emission properties of the complexes. Our study provides structural-properties information for the future design of luminescent Cu(I) complexes.
- Subjects :
- Substitution reaction
Steric effects
010405 organic chemistry
Ligand
Infrared spectroscopy
010402 general chemistry
Photochemistry
01 natural sciences
0104 chemical sciences
Inorganic Chemistry
Crystallography
chemistry.chemical_compound
chemistry
Materials Chemistry
Electronic effect
Physical and Theoretical Chemistry
Triphenylphosphine
Phosphine
Diimine
Subjects
Details
- ISSN :
- 02775387
- Volume :
- 127
- Database :
- OpenAIRE
- Journal :
- Polyhedron
- Accession number :
- edsair.doi...........076446f8c10d0c6bdf119fdb8b7716bf
- Full Text :
- https://doi.org/10.1016/j.poly.2017.01.046