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Spectral Рeculiarities of NH-Tautomerism in Isocycle-Containing Porphyrins and their Covalently Linked DimersIt has been found experimentally that a whole class of isocycle-containing porphyrins, including

Formation and optical properties of self-organized pentameric porphyrin arrays(II)l,4-bis[5-(10,15,20-tri-p-hexylphenylporphyrinyl)]-benzene ((ZnHTPP)₂) are bound via one molecule of a

Complexation and interchromophoric interactions in self-organized porphyrin and chlorin triads studied in methylcyclohexane at room temperature. The ability of the dimers bridged by a -CH2-CH2- spacer

Energy transfer in ethane-bisporphyrins studied by fluorescence line narrowing and spectral hole burning burning, has been compared with the calculated value and a conclusion of nonconsistency with the Forster

NH-Tautomerism and Visible Absorption Spectra of Porphyrins with Nonsymmetrical substitution.O) electronic transition intensities in NH tautomers as a consequence of the inversion of LUMO coefficients c₁

Spectroscopy of interchromophoric interactions in self-organized porphyrin and chlorin complexes between macrocycles (-CH₂-CH₂- or phenyl ring) have been studied in methylcyclohexane solutions in a

Molecular analysis of gibberellin receptor gene GID1 in Dasypyrum villosum and development of DNA marker for its identification on the long arm of the first V chromosome. A phenotypic assessment of common wheat lines carrying substituted

Fluorescence line narrowing study of cyclopentaneporphyrin chemical dimers at 4.2 KOEP-cycle) and acceptor (A, ZnOEP-cycle=CH2) subunits in Zn-cyclodimers manifests itself in the strong fluorescence

Poster: Intensive learning technologies as a trend in education digitalizationPoster: Intensive learning technologies as a trend in education digitalization

Maks Aizikovich Akivis

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