| 1. |
- Gao, Y. L., et al.
(författare)
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Crystal structure and electrochemical behavior of copper complex with 6-hydroxymethyl-substituted tris(2-pyridylmethyl) amine, CuCl(C19H20N4O) ClO4
- 2004
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Ingår i: Chinese journal of structural chemistry. - 0254-5861. ; 23:11, s. 1262-1265
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Tidskriftsartikel (refereegranskat)abstract
- A Cu(II) complex [CuCl(C19H20N40)]ClO4 1 containing hydroxymethyl substituted TPA (TPA = tris(2-pyridylmethyl)amine) was prepared. It crystallizes in monoclinic, space group P2(1)/c with a = 11.7628(2), b = 13.0083(3), c = 15.11280(10) Angstrom, beta = 108.724(2)degrees, V = 2190.09(7) Angstrom(3), M-r = 518.83, Z = 4, T = 293 (2) K, D-c = 1.574 g/cm(3), mu = 1.280 mm(-1), F(000) = 1060 and S = 1.085. The final R = 0.0543 and wR = 0.1433 for 2693 observed reflections with I >2sigma(I). The penta-coordinated copper (H) complex. assumes an approximate square pyramidal geometry. Cyclic voltammetry measurement of the complex showed a quasi-reversible Cu-II/Cu-I redox couple with E-1/2 -0.467 v and DeltaE = 68 mv.
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| 2. |
- Shi, F., et al.
(författare)
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Synthesis and spectral properties of a new ruthenium(II) tris-bipyridine with four ester groups and substituted phenol
- 2004
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Ingår i: Huaxue xuebao. - 0567-7351. ; 62:7, s. 713-719
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Tidskriftsartikel (refereegranskat)abstract
- A new ruthenium(II) complex (1) with four ester groups have been designed and synthesized, in which a phenol substituted by {[(2-hydroxy-3-(morpholin-4-ylmethyl)-5-tent-butylbenzyl) (pyridyl-2-methyl) amino]methyl} groups was covalently linked to ruthenium (II) tris-bipyridine. The structure of complex 1 was characterized by electrospray ionization mass spectrometer (ESI-MS) and 1D-NMR, 2D-NMR (gCOSY, HSQC and HMBC) spectra. The electrochemical and spectral properties were also studied. Introduction of the four carboxyl acid groups and the donor ligand tuned the spectra and the redox properties of compound 1. The MLCT transition was turned from 451 to 474 nm and the complex had long lifetime of the (MLCT)-M-3 state emission. Moreover, the oxidation potential of Ru3+/Ru2 + of compound 1 was similar to 360 mV higher than that of [Ru(bpy)(3)](2+) which would enhance the driving-force of electron transfer. These results showed that the compound 1 had proper redox potentials and was suitable for being used as photosensitizer of solar cell.
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| 3. |
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| 4. |
- Sun, S. G., et al.
(författare)
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Electrospray ionization mass spectrometry of rhenium(I) bipyridyl complexes
- 2003
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Ingår i: Youji huaxue. - 0253-2786. ; 23:10, s. 1135-1138
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Tidskriftsartikel (refereegranskat)abstract
- The electrospray ionization mass spectrometry (ESI-MS) of a series of rhenium(I) bipyridyl complexes [(4,4'-(COOEt)(2)-bPY)Re(CO)(3)RPF6], where bpy is 2,2'-bipyridine and R is pyridine, 4-methylpyridine, 4-hydroxypyridine, 4-aminopyridine or 10-(4-picolyl)phenothiazine (py-PTZ) was studied. The dissociation of the ligands (R) forms the fragment of [(4, 4'-( COOEt)(2)-bpy) Re (CO)3](+) at different voltages of in-source collision induced dissociation (CID). The dissociation tendency is in an order: pyridine > 4-methylpyridine > 4-hydroxypyridine > 4-aminopyridine > py-PTZ. It might be used to deduce the stability of these complexes when they are used as photosensitizers in solar cells.
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| 5. |
- Sun, S. G., et al.
(författare)
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Studies on a series of rhenium(I) bipyridyl photosensitive dyes
- 2004
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Ingår i: Youji huaxue. - 0253-2786. ; 24:8, s. 953-956
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Tidskriftsartikel (refereegranskat)abstract
- A series of rhemium(I) 2,2'-bipyridyl complexes [fac-(4,4'-di-COOEt-bpy)Re(CO)(3)(Xpy)PF6] (bpy = 2, 2'-bipyridine; py = pyridine; X = 3-methyl, 3-hydroxy, 3-amino, H) were synthesized. Their electrochemical properties, ground state electronic spectra and emission spectra were studied in acetonitrile. As the X group became more electron donating from H to 3-methyl, 3-hydroxy or 3-amino, the Re(II/I) oxidation potentials declined, the MLCT absorption maximum of the complex was changed little, the emission maximum blue-shifted, and the emission intensity and the fluorescence lifetime were decreased.
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| 6. |
- Sun, S. G., et al.
(författare)
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Synthesis of a series of rhenium(I) bipyridyl complexes as photosensitive dyes
- 2004
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Ingår i: Gaodeng xuéxiào huàxué xuébào. - 0251-0790. ; 25:5, s. 820-822
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Tidskriftsartikel (refereegranskat)abstract
- In order to study the effects of the substituted groups on the properties of the complexes, a series of rhenium ( I ) 2, 2'-bipyridyl complexes [fac- (4, 4'-di-COOEt-bpy) Re (CO)(3) (X-pyridine) PF6], where bpy is 2,2'-bipyridine and X is 4-methyl, 3-hydroxy, 4-hydroxy, 4-amino, or H, were synthesized with a yield more than 90%, and characterized by H-1 NMR, C-13 NMR, 2D-NMR (H-1-H-1 COSY, HMBC, HSQC), ESI-MS and HRMS. The delta(H) values on the X-pyridine ring were shifted to up-field in H-1 NMR and the MLCT absorbance maxima were red-shifted as the X groups became more electron-donating from H to 4-methyl, 4-hydroxy or 4-amino. The ESI-MS and FIRMS showed the mono-charged peaks and their isotopic peaks of the complexes. The absorption maximum of id(X=4-amino) is 20 nm longer than that of 1e(X=H). It might be used to broaden the absorption range of solar cells.
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| 7. |
- Sun, S. G., et al.
(författare)
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Synthesis of rhenium(I) bipyridyl and ruthenium(II) tris-bipyridyl photosensitive dyes used for solar cells
- 2004
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Ingår i: Gaodeng xuéxiào huàxué xuébào. - 0251-0790. ; 25:1, s. 67-70
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Tidskriftsartikel (refereegranskat)abstract
- There has been a growing effort to convert solar energy into electricity in recent years. In order to get a stable solar cell system and acquire a high incident photon-to-current conversion efficiency(IPCE), two novel rhenium(I) bipyridyl and ruthenium(II) tris-bipyridyl photosensitive dyes were synthesized, the ethoxycarbonyl group in the dyes could be employed for covalently linking to the surface of the nanostructured TiO2. Their structures, photophysical and electrochemical properties were studied. The UV-Vis absorption maxima were 382 and 476 nm; emission maxima were 622 and 672 nm, respectively. The Re(I/II) oxidation potential is significantly positive than that of Ru(II/III) which provides a larger driving force for electron transfer. The results show that they both have proper redox potentials, enough stability and are suitable for being used as photosensitizers of solar cells.
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| 8. |
- Sun, S. G., et al.
(författare)
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Synthesis of two novel rhenium(I) bipyridyl photosensitive dyes
- 2004
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Ingår i: Chinese Chemical Letters. - 1001-8417 .- 1878-5964. ; 15:8, s. 965-968
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Tidskriftsartikel (refereegranskat)abstract
- Two novel rhenium(I) 2, 2'-bipyridyl complexes, [(4,4'-di-COOEt-bipy) Re(CO)3 (NCCH3)PF6] and [(4,4'-di-COOEt-bipy) Re (CO)(3) (NCS)], a model complex [(4,4'-di-COOEt-bipy) Re (CO)(3) (pyridine)PF6], were synthesized. Their ground state electronic spectra and emission spectra were measured in acetonitrile. The MLCT absorption maximum of the complex exhibited a considerable red shift as the ligand changed from pyridine to CNCH3, or SCN.
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| 9. |
- Wang, M., et al.
(författare)
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Preparation, characterization and catalytic oxidation properties of tris 2-(2-pyridyl)benzimidazole iron(II) complexes
- 2004
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Ingår i: Applied organometallic chemistry. - : Wiley. - 0268-2605 .- 1099-0739. ; 18:6, s. 277-281
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Tidskriftsartikel (refereegranskat)abstract
- Complexes [Fe(Hpbi)(3)](ClO4)(2) (1) and [Fe(Hpbi)(3)](SbF6)(2) (2) (Hpbi = 2-(2-pyridyl)benzimidazole) were prepared by a modified method and characterized by IR, H-1 and C-13 NMR, mass spectrometry, electron paramagnetic resonance spectra and elemental analysis. The catalytic activities of 1 and 2 were evaluated for the oxidation of cyclohexene, cyclohexane, ethylbenzene and adamantane with tert-butylhydroperoxide or H2O2 as oxidant, and the results were compared with the properties of their analogue [Fe(bpy)(3)](SbF6)(2) (3). Complexes 1 and 2 both afforded the ketonization product for the oxidation of ethylbenzene and the hydroxylation product for adamantane.
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| 10. |
- Zhang, R., et al.
(författare)
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Electrospray ionization mass spectrometry studies of rhenium(I) bipyridyl complexes
- 2004
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Ingår i: European journal of mass spectrometry. - : SAGE Publications. - 1469-0667 .- 1751-6838. ; 10:5, s. 599-603
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Tidskriftsartikel (refereegranskat)abstract
- Electrospray ionization mass spectrometry has been employed to study the formation of fragment ions from a series of rhenium(I) bipyridyl complexes [(4,4'-di-(COOEt)(2)-bpy) Re(CO)(3)XPyPF6], where bpy is 2,2'-bipyridine, Py is pyridine and X is H, 4-methyl, 3-methyl, 4-hydroxyl, 3-hydroxyl, 4-amino, or 3-amino of the pyridine ligand. The effects of substituents (X) on the stability of the complexes has been investigated with the increase of fragmentor voltages. For different X substitutents, the stability of the complexes increases as X becomes more electron-donating from H to CH3, OH and NH2. For the same substitutent, the p-substituted pyridines have a stronger stabilizing effect than the corresponding m-substituted ones. Ligand exchange reaction was found in acetonitrile, where the pyridine ligand has been replaced by the solvent, indicated by the formation of [M - PF6 - XPy + MeCN](+) in the fragmentation.
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