1997
DOI: 10.1107/s0108270196012358
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(Benzoylacetonato-O,O')(2,2'-bipyridine-N,N')(nitrato-O)copper(II)

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Cited by 9 publications
(9 citation statements)
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“…3 and 4 respectively with selected bond dimensions given in Tables 2 and 3 [21] and 2,2 0 -bipyridine complexes of Cu(II) [22,23]. Similarly in 2, the Ni-N(amine) distance in the square The phenyl rings of the ligands are close to the plane of the complexes.…”
Section: Crystal Structuresmentioning
confidence: 99%
“…3 and 4 respectively with selected bond dimensions given in Tables 2 and 3 [21] and 2,2 0 -bipyridine complexes of Cu(II) [22,23]. Similarly in 2, the Ni-N(amine) distance in the square The phenyl rings of the ligands are close to the plane of the complexes.…”
Section: Crystal Structuresmentioning
confidence: 99%
“…Figure 9 presents the optical images of Ppy, P(py‐ co‐ EDOT) and PEDOT films deposited potentiostatically at 1.05, 1.3, and 1.3 V. The Ppy film shows yellow–green color at −0.8 V and blue–violet at 0.8 V [Figure 8(a)] 37. The color of doped and dedoped PEDOT film are light blue (1.0 V) and dark blue (−0.8 V), respectively [Figure 8(c)] 13. It is interesting that the electrochromic phenomena of P(py‐ co‐ EDOT) film is quite different from those of two individual homopolymers, At an applied potential of −0.6 V, the film shows a amaranth color and passes to brown at −0.3 V. With the increase of potential, P(py‐ co‐ EDOT) film turns into dark gray (0.4 V) and light blue at 0.8 V [Figure 8(b)].…”
Section: Resultsmentioning
confidence: 99%
“…Spectroelectrochemistry is a powerful way to investigate the optical properties of a electrochromic conducting polymer under potential change, which also provides information on the electronic structure of the conducting polymer 13, 27. The P(py‐ co‐ EDOT) film is swept between −0.6 and 0.8 V, Figure 9 depicts the Vis‐NIR absorbance spectra.…”
Section: Resultsmentioning
confidence: 99%
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“…Bond angles around the Mn(II) atom greatly deviate from expected values so the coordination geometry may be better described as a distorted pyramid rather than a distorted octahedron. (7) 1.0114 (8) Keto-Enol tautomerism of 1,3-diketones such as bzac has been extensively studied [14]. Neutron diffraction and accurate low temperature X-ray diffraction reveals that within the conjugated enol ring of bzac the C-C bond furthest from the phenyl ring is slightly longer than the C-C bond nearest the phenyl ring [15,16].…”
Section: Crystal Structurementioning
confidence: 99%