Phosphorus(V)corrole- Porphyrin Based Hetero Trimers: Synthesis, Spectroscopy and Photochemistry (original) (raw)

New aspects of porphyrins and related compounds: self-assembled structures in two-dimensional molecular arrays

Journal of Porphyrins and Phthalocyanines, 2009

We have synthesized a series of tetrakis(arylvinylene)phthalocyanines from the corresponding phthalonitriles. According to 1 H and 19 F NMR data, the cis-or trans-conformations of the starting materials retain du ring condensation, thus phthalocyanines formed are in all-cis or all-trans form. The cis-trans photoisomerization occurs easily for phthalonitriles, while phthalocyanines retain their conformations under UV beam.

Chlorophyll-porphyrin heterodimers with orthogonal. pi. systems: Solvent polarity dependent photophysics

Journal of The American Chemical Society, 1990

The synthesis and properties of a series of fixed-distance chlorophyll-porphyrin molecules are described. These molecules consist of a methyl pyrochlorophyllide a moiety which is directly bonded at its 2-position to the 5-position of a 2,8,12,18-tetraethyl-3,7,13,17-tetramethyl-15-(p-tolyl)porphyrin. Steric hindrance between adjacent substituents rigidly positions the Ï systems of both macrocycles perpendicular to one another. The macrocycles were selectively metalated with zinc to

Click made porphyrin–corrole dyad: a system for photo-induced charge separation

Dalton Trans., 2015

The preparation of the first porphyrin-corrole dyad through click chemistry is described. The absorption, the emission and the electrochemical properties were investigated and suggested an efficient excited state interaction between the porphyrin and the corrole unit. Theoretical calculations were performed and proved that the dyad can potentially act as a molecular system for solar energy conversion schemes.

Synthesis, Electrochemical, and Photophysical Study of Covalently Linked Porphyrin Dimers with Two Different Macrocycles

Inorganic Chemistry, 1998

Synthesis of a new symmetrical 1,4,8,11,15,18,22,25-octahexyloxy-2,3,9,10,16,17,23,24-octa-(3,5-dichlorophenyl)phthalocyaninato zinc(II), ZnPc, has been described and characterized by 1 H NMR, 13 C NMR, MS, UVeVis, and IR spectrometry. The newly prepared ZnPc is soluble in organic solvents and is not aggregated in solution. The photophysical properties were studied by steady-state absorption and emission, cyclic voltammetry, and nanosecond transient absorption techniques. The prepared ZnPc absorbs and emits at longer wavelengths compared to that of reported phthalocyanine derivatives. The electron-donating properties of the ZnPc have been examined by mixing it with the electron-accepting dicyanoperylene-3,4,9,10-bis(dicarboximide), PDICN 2 . The recorded nanosecond transient spectra in the visible/near-IR region showed clearly the electron-transfer from the triplet-excited state of the ZnPc to PDICN 2 with a rate of 3.40 Â 10 8 M À1 s À1 . Light absorption in a wide section of the solar spectrum, favorable redox properties, and the electron-transfer properties suggest usefulness of the ZnPc in lightenergy harvesting and developing optoelectronic devices.