Photoinduced oxidation reactions of the pendent macrocyclic complexes: Al(III) phthalocyanine and Ni(II) annulene mechanistic considerations. (15th October 2016)

• Record Type: Journal Article
• Authors: Ferraudi, Guillermo; Lappin, Alexander G.; Ruiz, Gustavo T.; Matsuhiro, Betty
• Is Part Of: Polyhedron. Volume 117(2016)
• Page Start: 381
• Page End: 387
• Publication Date: 2016-10-15
• Subjects: Pendent Ni(II) annulene complex -- Pendent Al(III) phthalocyanine -- Photoinduced redox processes -- Saccharides oxidation -- Kinetics and mechanism; Chemistry, Inorganic -- Periodicals; Chimie inorganique -- Périodiques; Organometaalverbindingen; Anorganische chemie; 546.05
• DOI: 10.1016/j.poly.2016.06.014
• Languages: English
• ISSNs: 0277-5387

Abstract

Graphical abstract: The photoinduced redox reactions of the Al(III) sulfonated phthalocyanine, HOAl III tspc, and Ni(II) tertramethyldibenzotetraazaannnulene, [Ni II (tmdbTAA)], grafted into polymeric structures were investigated in this work. Poly(ethyleneimino) and poly(isobutyl-alt-maleate) were the respective backbones of poly(HOAl III tspc) and poly([Ni II (tmdbTAA)]). Saccharide and flavonoid glycosides were used as probes of the reactions of radicals generated in the case of poly(HOAl III tspc), or the charge-separated intermediate, CS, in the case of poly([Ni II (tmdbTAA)]). While the phthalocyanine-centered radicals were reduced by saccharide, flavonoid glycosides, dAMP (adenosine-5-monophosphate) and CT-DNA, only saccharide and flavonoid glycosides reduced the CS intermediate. In addition to the failure of the CS intermediate to oxidize CT-DNA and dAMP, the intensity of the upper conversion luminescence ( λ em < 500 nm), is modulated by the concentration of dAMP. The modulation is attributed to the formation of adducts of poly([Ni II (tmdbTAA)]) with dAMP which affect the deactivation of the electronically excited Ni(II) tetraazaannnulene pendants before the formation of the CS intermediate. Specific rate constants of the various processes were determined and their values were rationalized on the basis of the reactants intrinsic structural features. Abstract: The goal of the work was to expand the understanding of the photoinduced redox reactions of the Al(III) sulfonated phthalocyanine, HOAl III tspc, and Ni(II) tertramethyldibenzotetraazaannnulene, [Ni II (tmdbTAA)], as components of polymeric structures in which poly(ethyleneimino) and poly(isobutyl-alt-maleate) are the respective backbones of poly(HOAl III tspc) and poly([Ni II (tmdbTAA)]). Saccharide and flavonoid glycosides form adducts that quench the photo-generated oxidizing radicals in the case of poly(HOAl III tspc) with rate constants ≈ 1 × 10 4 s −1, largely independent of reductant structure. The charge-separated intermediate, CS, in the case of poly([Ni II (tmdbTAA)]) shows greater reactivity with the saccharides and flavonoid glycosides, particularly with the flavonoid glycoside rutin where the rate constant is 2.7 × 10 6 s −1 . While phthalocyanine-centered radicals in poly(HOAl III tspc) were reduced by dAMP (adenosine-5-monophosphate) and CT-DNA, energy transfer with these reagents competed with the formation of the CS intermediate in poly([Ni II (tmdbTAA)]). A study of the intensity of the upper conversion luminescence ( λ em < 500 nm), modulated by the concentration of dAMP suggests that this is attributed to the formation of adducts of poly([Ni II (tmdbTAA)]) with dAMP that affect the deactivation of the electronically excited Ni(II) tetraazaannnulene pendants before the formation of the CS intermediate.