2007
DOI: 10.1134/s1070363207110175
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Synthesis and properties of lanthanide complexes with tetrapyrazinoporphyrazine and its substituted derivatives

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Cited by 9 publications
(6 citation statements)
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“…The Al III complex [TPyz1PzAl (OH)] was prepared [122] with 80% yield by template cyclotetramerization of the dinitrile Pyz1 with AlCl 3 in 1,2-dichlorobenzene in the presence of ammonium molybdate. The lanthanide complexes [TPyz1PzLn (acac)] with Ln = Er III , Tm III , Yb III , Lu III [78] and [TPyz1PzLu(Cl)] [188] were also obtained in similar yields (60-75%) in the complexation reaction between [TPyz1PzH 2 ] and the corresponding lanthanide acetylacetonate or chloride. The sandwich complex [(TPyz1Pz) 2 Lu] has been prepared from the dinitrile precursor by the "isoindoline" method [188].…”
Section: Page 9 Of 66mentioning
confidence: 76%
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“…The Al III complex [TPyz1PzAl (OH)] was prepared [122] with 80% yield by template cyclotetramerization of the dinitrile Pyz1 with AlCl 3 in 1,2-dichlorobenzene in the presence of ammonium molybdate. The lanthanide complexes [TPyz1PzLn (acac)] with Ln = Er III , Tm III , Yb III , Lu III [78] and [TPyz1PzLu(Cl)] [188] were also obtained in similar yields (60-75%) in the complexation reaction between [TPyz1PzH 2 ] and the corresponding lanthanide acetylacetonate or chloride. The sandwich complex [(TPyz1Pz) 2 Lu] has been prepared from the dinitrile precursor by the "isoindoline" method [188].…”
Section: Page 9 Of 66mentioning
confidence: 76%
“…The Zn II complexes of symmetrical 3-pyridyl substituted TPyzPz [121] and non-symmetrical TPyzPzs with four 2-thienyl rings [121], also in combination with 3-pyridyl radicals [121] and maleimide moieties [180], were also later reported by this group [118]. Complexes of octa(2-pyridyl)substituted TPyzPzs with Er III and Yb III were briefly reported by Russian authors [78]. Further, the metal free TPyzPzs bearing 2-thienyl or oligo-2,5-thienyl (bis-and tris-) moieties and the corresponding Zn II and Cu II complexes were also announced as perspective organic conducting materials [203] but no characterization details were reported.…”
Section: Hetaryl Substituted Tpyzpzsmentioning
confidence: 92%
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“…Now various methods for preparing substituted tetrapyrazinoporphyrazines with different donor substituents were developed. [22][23][24][25][26][27] Electron-withdrawing substituents such as cyano-, sulfophenyl-, 2-pyridyl and 2-(N-methyl)-pyridiniumyl are used to increase the acceptor ability of tetrapyrazinoporphyrazines. [21,[28][29][30][31] Molecular structure of pyridine substituted tetrapyrazinoporphyrazine is determined by single-crystal X-ray analysis for cobalt(II) tetrakis[5,6-di(2-pyridyl)-2,3-pyrazino}porphyrazine, Co II TPyzPAPy 8 .…”
Section: Introductionmentioning
confidence: 99%