Synthesis of new fused heterocyclic aromatic hydrocarbons via C–S and C–C bond formation by C–H bond activation in the presence of new Pd( ii ) Schiff's base complexes
The Schiff's base aza-macrocyclic Pd(DPTTP)Cl 2 and Pd(TPTTP)Cl 2 complexes are efficient photocatalysts for the activation of the C–H bond and the formation of both intramolecular C–C bond and C–S bonds to obtain the fused heterocyclic system. Both ligands and Pd( ii ) complexes are well chara...
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Veröffentlicht in: | RSC advances 2016-01, Vol.6 (91), p.88321-88331 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The Schiff's base aza-macrocyclic Pd(DPTTP)Cl
2
and Pd(TPTTP)Cl
2
complexes are efficient photocatalysts for the activation of the C–H bond and the formation of both intramolecular C–C bond and C–S bonds to obtain the fused heterocyclic system. Both ligands and Pd(
ii
) complexes are well characterized by experimental and theoretical techniques such as microanalyses, mass, surface area, SEM, TGA, XPS, IR, UV-visible,
1
H-NMR, DFT and TDDFT methods. C–H bond activation was confirmed by sequential reactions and the data were supported by a one-pot synthesis product. Optimization of the intensity of visible light of the photocatalytic reactions. Finally, the sp
2
-H bond activation
via
the formation of the C–S and intramolecular C–C bonds in the presence of both the complexes were performed under visible light irradiation to obtain the new fused system, pyrido[3′,2′:6,7][1,4]thiazepino[2,3-
h
][1,6]naphthyridine. It is also shown that the performance of the Pd(TPTTP)Cl
2
is better than that of Pd(DPTT)Cl
2
due to its high surface area and low bandgap energy. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/C6RA15609F |