2004
DOI: 10.1016/j.tetlet.2004.02.019
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Synthesis of a multitopic pyrene–thiophene–anthracene-2,2′:6′,2″-terpyridine array

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Cited by 14 publications
(9 citation statements)
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“…This, together with the less positive potentials for the oxidation of the polyaromatic alkynes (+ 1.0 to + 1.2 V) [46] relative to that of 1,3,5-(HCCC 6 H 4 CC) 3 C 6 H 3 (approximately + 1.35 V), suggested that the first oxidation waves of complexes 9-14 are probably derived from the ligand-centered oxidation of the polyaromatic alkynyl ligands. The large shift in the potential for the first oxidation of 14 (+ 0.86 V) relative to that of the branched chloroplatinum(ii) complex 1 (+ 1.27 V) is indicative of an oxidation that is predominantly ligand-centered in character.…”
Section: Resultsmentioning
confidence: 99%
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“…This, together with the less positive potentials for the oxidation of the polyaromatic alkynes (+ 1.0 to + 1.2 V) [46] relative to that of 1,3,5-(HCCC 6 H 4 CC) 3 C 6 H 3 (approximately + 1.35 V), suggested that the first oxidation waves of complexes 9-14 are probably derived from the ligand-centered oxidation of the polyaromatic alkynyl ligands. The large shift in the potential for the first oxidation of 14 (+ 0.86 V) relative to that of the branched chloroplatinum(ii) complex 1 (+ 1.27 V) is indicative of an oxidation that is predominantly ligand-centered in character.…”
Section: Resultsmentioning
confidence: 99%
“…The large shift in the potential for the first oxidation of 14 (+0.86 V) relative to that of the branched chloroplatinum( II ) complex 1 (+1.27 V) is indicative of an oxidation that is predominantly ligand‐centered in character. This, together with the less positive potentials for the oxidation of the polyaromatic alkynes (+1.0 to +1.2 V)46 relative to that of 1,3,5‐(HCCC 6 H 4 CC) 3 C 6 H 3 (approximately +1.35 V), suggested that the first oxidation waves of complexes 9 – 14 are probably derived from the ligand‐centered oxidation of the polyaromatic alkynyl ligands. However, an involvement of some metal‐centered character could not be completely ruled out.…”
Section: Resultsmentioning
confidence: 99%
“…The particular redox and photophysical properties of the metal ions complexes of terpyridine [20][21][22] make them attractive in photochemistry for the design of luminescent devices or as light sensitizers [23]; terpyridine and its derivative can form polymetallic complex species used in electrochemical sensors. In the fields of medicinal chemistry and biochemistry [24][25][26][27][28], functionalized terpyridines are applied to the colorimetric determination of metal ions [29], and to DNA binding agents in cancer diagnos and anti-tumor therapy [30,31]. The affinity of gadolinium(III) for terpyridine is strong [32,33].…”
Section: Introductionmentioning
confidence: 99%
“…The coordination chemistry of multidentate ␣-terpyridine-based ligands (tpy) is interesting because of their application in emitters for electroluminescence devices and in molecular probes for biochemical research [1][2][3][4][5][6]. Along with the structural features, these ligands and their complexes have interesting electrochemical, catalytic and optical properties [7][8][9].…”
Section: Introductionmentioning
confidence: 99%