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Nonplanar porphyrins: synthesis, properties, and unique functionalities
Porphyrins are variously substituted tetrapyrrolic macrocycles, with wide-ranging biological
and chemical applications derived from metal chelation in the core and the 18π aromatic …
and chemical applications derived from metal chelation in the core and the 18π aromatic …
Porphyrins as molecular electronic components of functional devices
The proposal that molecules can perform electronic functions in devices such as diodes,
rectifiers, wires and capacitors, or serve as functional materials for electronic or magnetic …
rectifiers, wires and capacitors, or serve as functional materials for electronic or magnetic …
Self-organized porphyrinic materials
“Anything that exists must be possible.” is often referred to as KE Boulding's First Law. 1 For
example, nanoscale photonic devices exist that harvest light and convert it to …
example, nanoscale photonic devices exist that harvest light and convert it to …
Conformational control of cofactors in nature–the influence of protein-induced macrocycle distortion on the biological function of tetrapyrroles
Tetrapyrrole-containing proteins are one of the most fundamental classes of enzymes in
nature and it remains an open question to give a chemical rationale for the multitude of …
nature and it remains an open question to give a chemical rationale for the multitude of …
Modulating the chemical reactivity of gold complexes in living systems: from concept to biomedical applications
Conspectus Over the past few decades, research on the chemistry of gold has progressed
rapidly, encompassing topics like catalysis, supramolecular chemistry, molecular …
rapidly, encompassing topics like catalysis, supramolecular chemistry, molecular …
Exercises in molecular gymnastics—bending, stretching and twisting porphyrins
MO Senge - Chemical Communications, 2006 - pubs.rsc.org
The functional versatility of tetrapyrroles as natural cofactors is related to their
conformational flexibility where manipulation of the macrocycle conformation allows a fine …
conformational flexibility where manipulation of the macrocycle conformation allows a fine …
Naphthyl-Fused π-Elongated Porphyrins for Dye-Sensitized TiO2 Cells
S Hayashi, M Tanaka, H Hayashi, S Eu… - The Journal of …, 2008 - ACS Publications
Novel unsymmetrically π-elongated porphyrins, in which the naphthyl moiety is fused to the
porphyrin core at the naphthyl bridge with a carboxyl group (fused-Zn-1) or at the opposite …
porphyrin core at the naphthyl bridge with a carboxyl group (fused-Zn-1) or at the opposite …
Ultrafast excited state relaxation of a metalloporphyrin revealed by femtosecond X-ray absorption spectroscopy
Photoexcited Nickel (II) tetramesitylporphyrin (NiTMP), like many open-shell
metalloporphyrins, relaxes rapidly through multiple electronic states following an initial …
metalloporphyrins, relaxes rapidly through multiple electronic states following an initial …
meso-Tetra(pentafluorophenyl)porphyrin as an Efficient Platform for Combinatorial Synthesis and the Selection of New Photodynamic Therapeutics using a Cancer …
D Samaroo, M Vinodu, X Chen… - Journal of combinatorial …, 2007 - ACS Publications
The four para fluoro groups on 5, 10, 15, 20-tetrakis-(2, 3, 4, 5, 6-pentafluorophenyl)-
porphyrin (TPPF20) are known to react with a variety of nucleophiles, but the reaction …
porphyrin (TPPF20) are known to react with a variety of nucleophiles, but the reaction …
Structures and photoinduced electron transfer of protonated complexes of porphyrins and metallophthalocyanines
S Fukuzumi, T Honda, T Kojima - Coordination Chemistry Reviews, 2012 - Elsevier
Porphyrins and phthalocyanines are planar two-dimensional π-compounds, which are
normally difficult to protonate because of the low basicity. When many bulky substituents are …
normally difficult to protonate because of the low basicity. When many bulky substituents are …